Ochotona princeps isolate UAM:Mamm:113957 chromosome 1A, OchPri4.0, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Lagomorpha; Ochotonidae; Ochotona.
REFSEQ INFORMATION: The reference sequence is identical to\nCM025746.1.\nAssembly name: OchPri4.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of British\nColumbia Okanagan on 2020/09/21. The original whole-genome shotgun\nproject has the accession JACJUE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: University of British Columbia\n Okanagan\nAssembly Method :: Dovetail HiRise v. 2017\nAssembly Name :: OchPri4.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nReference-guided Assembly :: GCA_000292845.1\nGenome Coverage :: 23.68x\nSequencing Technology :: Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Ochotona princeps Annotation Release\n 102\nAnnotation Version :: 102\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.5\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
USA: Beaverhead-Deerlodge National Forest, Montana
Derived by automated computational analysis using gene prediction method: Gnomon.
A disintegrin and metalloproteinase with thrombospondin motifs 13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
serine/threonine kinase like domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
serine/threonine kinase-like domain-containing protein STKLD1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
mediator complex subunit 22, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins
mediator complex subunit 22, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins
mediator of RNA polymerase II transcription subunit 22 isoform X1
mediator of RNA polymerase II transcription subunit 22 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1 (FORS blood group)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1
ral guanine nucleotide dissociation stimulator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
general transcription factor IIIC subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
general transcription factor 3C polypeptide 5
growth factor independent 1B transcriptional repressor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein
growth factor independent 1B transcriptional repressor, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 8 Proteins
growth factor independent 1B transcriptional repressor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 Protein
sperm acrosome associated 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sperm acrosome-associated protein 9 isoform X2
sperm acrosome associated 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sperm acrosome associated 9, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sperm acrosome-associated protein 9 isoform X1
general transcription factor IIIC subunit 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins
general transcription factor 3C polypeptide 4
probable ATP-dependent RNA helicase DDX31
BarH like homeobox 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 8 Proteins
BarH like homeobox 1, transcript variant X2
cilia and flagella associated protein 77
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins
cilia- and flagella-associated protein 77
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
small nucleolar RNA SNORA30/SNORA37 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00415
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
mediator of RNA polymerase II transcription subunit 27
Rap guanine nucleotide exchange factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein
uridine-cytidine kinase 1, transcript variant X6
uridine-cytidine kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins
uridine-cytidine kinase 1, transcript variant X4
uridine-cytidine kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins
uridine-cytidine kinase 1, transcript variant X3
uridine-cytidine kinase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
proline rich coiled-coil 2B, transcript variant X3
proline rich coiled-coil 2B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins
proline rich coiled-coil 2B, transcript variant X1
proline rich coiled-coil 2B, transcript variant X6
proline rich coiled-coil 2B, transcript variant X4
proline rich coiled-coil 2B, transcript variant X5
COORDINATES: nucleotide motif:Rfam:12.0:RF00153
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins
family with sequence similarity 78 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 2% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
fibrinogen C domain-containing protein 1
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 17 Proteins
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 18 Proteins
exosome component 2, transcript variant X3
exosome component 2, transcript variant X2
exosome component 2, transcript variant X1
exosome complex component RRP4 isoform X3
exosome complex component RRP4 isoform X2
exosome complex component RRP4 isoform X1
PR domain zinc finger protein 12 isoform X2
PR domain zinc finger protein 12 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
formin binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 8 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
formin binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
formin binding protein 1, transcript variant X3
formin binding protein 1, transcript variant X4
formin binding protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
formin binding protein 1, transcript variant X5
formin binding protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
formin binding protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 17 Proteins
ubiquitin carboxyl-terminal hydrolase 20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 3 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
telomere length and silencing protein 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins
ankyrin repeat and SOCS box containing 6
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 mRNAs, 11 Proteins
N-terminal Xaa-Pro-Lys N-methyltransferase 1 isoform X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 3 Proteins
N-terminal Xaa-Pro-Lys N-methyltransferase 1 isoform X2
immediate early response gene 5-like protein
protein phosphatase 2 phosphatase activator, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 15 Proteins
serine/threonine-protein phosphatase 2A activator isoform X1
protein phosphatase 2 phosphatase activator, transcript variant X2
serine/threonine-protein phosphatase 2A activator isoform X2
carnitine O-acetyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
carnitine O-acetyltransferase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
carnitine O-acetyltransferase, transcript variant X4
carnitine O-acetyltransferase isoform X1
carnitine O-acetyltransferase isoform X3
carnitine O-acetyltransferase isoform X4
carnitine O-acetyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
carnitine O-acetyltransferase isoform X2
dolichyldiphosphatase 1, transcript variant X2
dolichyldiphosphatase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins
SH3 domain containing GRB2 like, endophilin B2, transcript variant X1
SH3 domain containing GRB2 like, endophilin B2, transcript variant X2
SH3 domain containing GRB2 like, endophilin B2, transcript variant X3
SH3 domain containing GRB2 like, endophilin B2, transcript variant X4
SH3 domain containing GRB2 like, endophilin B2, transcript variant X5
SH3 domain containing GRB2 like, endophilin B2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 3% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nucleoporin NUP188 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
phytanoyl-CoA dioxygenase domain containing 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X3
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X2
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X1
leucine rich repeat containing 8 VRAC subunit A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 12 Proteins
leucine rich repeat containing 8 VRAC subunit A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 12 Proteins
volume-regulated anion channel subunit LRRC8A
kynurenine aminotransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
kynurenine--oxoglutarate transaminase 1 isoform X1
kynurenine aminotransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
kynurenine--oxoglutarate transaminase 1 isoform X2
SPOUT domain containing methyltransferase 1
putative methyltransferase C9orf114 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TBC1 domain family member 13, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 6 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
TBC1 domain family member 13, transcript variant X2
zyg-11 related cell cycle regulator, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 3 Proteins
zyg-11 related cell cycle regulator, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins
zinc finger DHHC-type palmitoyltransferase 12, transcript variant X3
zinc finger DHHC-type palmitoyltransferase 12, transcript variant X2
probable palmitoyltransferase ZDHHC12 isoform X1
probable palmitoyltransferase ZDHHC12 isoform X2
probable palmitoyltransferase ZDHHC12 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
LOW QUALITY PROTEIN: WD repeat-containing protein 34
spectrin alpha, non-erythrocytic 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 7 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 8 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 7 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha, non-erythrocytic 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
spectrin alpha chain, non-erythrocytic 1 isoform X3
spectrin alpha chain, non-erythrocytic 1 isoform X2
spectrin alpha chain, non-erythrocytic 1 isoform X9
spectrin alpha chain, non-erythrocytic 1 isoform X8
spectrin alpha chain, non-erythrocytic 1 isoform X4
spectrin alpha chain, non-erythrocytic 1 isoform X6
spectrin alpha chain, non-erythrocytic 1 isoform X7
spectrin alpha chain, non-erythrocytic 1 isoform X5
spectrin alpha chain, non-erythrocytic 1 isoform X1
DNA polymerase epsilon 4, accessory subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X3
outer dense fiber of sperm tails 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
outer dense fiber of sperm tails 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
cerebral endothelial cell adhesion molecule
inactive glycosyltransferase 25 family member 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 7 Proteins
long-chain fatty acid transport protein 4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 6 Proteins
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial
TruB pseudouridine synthase family member 2
mitochondrial mRNA pseudouridine synthase TRUB2
SWI5 homologous recombination repair protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 3 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 4 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
CDKN1A interacting zinc finger protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
neutrophil gelatinase-associated lipocalin
solute carrier family 25 member 25, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 16 Proteins
solute carrier family 25 member 25, transcript variant X1
solute carrier family 25 member 25, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 15 Proteins
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X2
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X1
solute carrier family 25 member 25, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 15 Proteins
solute carrier family 25 member 25, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X4
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X3
solute carrier family 25 member 25, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 Proteins
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X6
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X5
solute carrier family 25 member 25, transcript variant X7
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X7
actin-related protein 2/3 complex subunit 1A-like
family with sequence similarity 102 member A
dolichyl-phosphate mannosyltransferase subunit 2, regulatory
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dolichol phosphate-mannose biosynthesis regulatory protein
phosphatidylinositol-4-phosphate 5-kinase like 1
phosphatidylinositol 4-phosphate 5-kinase-like protein 1
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 12 Proteins
alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 10 Proteins
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 6 Proteins
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 isoform X1
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6 isoform X2
adenylate kinase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 9 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
adenylate kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 11 Proteins
folylpolyglutamate synthase, transcript variant X3
folylpolyglutamate synthase, transcript variant X2
folylpolyglutamate synthase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins
folylpolyglutamate synthase, mitochondrial isoform X3
folylpolyglutamate synthase, mitochondrial isoform X2
folylpolyglutamate synthase, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 7 Proteins
SH2 domain containing 3C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 Proteins
SH2 domain-containing protein 3C isoform X1
SH2 domain containing 3C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 7 Proteins
SH2 domain-containing protein 3C isoform X2
SH2 domain containing 3C, transcript variant X3
SH2 domain containing 3C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 4 Proteins
SH2 domain-containing protein 3C isoform X3
SH2 domain-containing protein 3C isoform X4
torsin family 2 member A, transcript variant X1
torsin family 2 member A, transcript variant X2
cilia and flagella associated protein 157
cilia- and flagella-associated protein 157
syntaxin binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 11 Proteins
syntaxin binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 5 Proteins
leucine rich repeat and sterile alpha motif containing 1, transcript variant X1
leucine rich repeat and sterile alpha motif containing 1, transcript variant X5
leucine rich repeat and sterile alpha motif containing 1, transcript variant X2
leucine rich repeat and sterile alpha motif containing 1, transcript variant X3
leucine rich repeat and sterile alpha motif containing 1, transcript variant X4
E3 ubiquitin-protein ligase LRSAM1 isoform X5
E3 ubiquitin-protein ligase LRSAM1 isoform X2
E3 ubiquitin-protein ligase LRSAM1 isoform X3
E3 ubiquitin-protein ligase LRSAM1 isoform X4
E3 ubiquitin-protein ligase LRSAM1 isoform X1
ribosomal protein L12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 mRNAs, 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ribosomal protein L12, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 63% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00302
solute carrier family 2, facilitated glucose transporter member 8
GTPase activating Rap/RanGAP domain like 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 6 Proteins
GTPase-activating Rap/Ran-GAP domain-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 8 Proteins
uncharacterized LOC101530474, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC101530474, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger and BTB domain containing 34
zinc finger and BTB domain-containing protein 34
zinc finger and BTB domain containing 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain-containing protein 43
LIM homeobox transcription factor 1 beta, transcript variant X3
LIM homeobox transcription factor 1 beta, transcript variant X2
LIM homeobox transcription factor 1 beta, transcript variant X1
LIM homeobox transcription factor 1-beta isoform X3
LIM homeobox transcription factor 1-beta isoform X2
LIM homeobox transcription factor 1-beta isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 14 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
pre-B-cell leukemia transcription factor 3
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 11 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
target of rapamycin complex 2 subunit MAPKAP1
GTPase activating protein and VPS9 domains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: GTPase-activating protein and VPS9 domain-containing protein 1
heat shock protein family A (Hsp70) member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 mRNAs, 28 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Rab9 effector protein with kelch motifs, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 28% coverage of the annotated genomic feature by RNAseq alignments
Rab9 effector protein with kelch motifs, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
rab9 effector protein with kelch motifs isoform X2
rab9 effector protein with kelch motifs isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein phosphatase 6 catalytic subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 4 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 10% coverage of the annotated genomic feature by RNAseq alignments
actin related protein 2/3 complex subunit 5 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 7 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
actin-related protein 2/3 complex subunit 5-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: WD repeat-containing protein 38
nuclear receptor subfamily 6 group A member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 47% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 6 group A member 1, transcript variant X3
nuclear receptor subfamily 6 group A member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 6 group A member 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 6 group A member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 6 group A member 1 isoform X5
nuclear receptor subfamily 6 group A member 1 isoform X1
nuclear receptor subfamily 6 group A member 1 isoform X2
nuclear receptor subfamily 6 group A member 1 isoform X3
nuclear receptor subfamily 6 group A member 1 isoform X4
non-histone chromosomal protein HMG-17-like
nuclear receptor subfamily 5 group A member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 15 Proteins
nuclear receptor subfamily 5 group A member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 mRNAs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 7 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins
crumbs cell polarity complex component 2
spermatid perinuclear RNA binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 mRNAs, 15 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
spermatid perinuclear RNA binding protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 8 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
spermatid perinuclear RNA-binding protein isoform X2
spermatid perinuclear RNA-binding protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 23 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 26
zinc finger and BTB domain-containing protein 26
zinc finger and BTB domain-containing protein 6
ring finger and CCCH-type domains 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
ring finger and CCCH-type domains 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
ring finger and CCCH-type domains 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
ring finger and CCCH-type domains 2, transcript variant X6
ring finger and CCCH-type domains 2, transcript variant X5
ring finger and CCCH-type domains 2, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00579
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 11 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 74 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 68 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 16 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosome recycling factor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
ribosome-recycling factor, mitochondrial isoform X1
mitochondrial ribosome recycling factor, transcript variant X2
ribosome-recycling factor, mitochondrial isoform X2
RNA binding motif protein 18, transcript variant X1
RNA binding motif protein 18, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 8 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit A8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 18 Proteins
glycoprotein alpha-galactosyltransferase 1 (inactive)
inactive N-acetyllactosaminide alpha-1,3-galactosyltransferase
N-acetyllactosaminide alpha-1,3-galactosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
N-acetyllactosaminide alpha-1,3-galactosyltransferase-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
erythrocyte band 7 integral membrane protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 21 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 22 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
RAB14, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 mRNAs, 17 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
RAB14, member RAS oncogene family, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins
PHD finger protein 19, transcript variant X2
PHD finger protein 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 5
putative UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase LOC100288842
F-box and WD repeat domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 2 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
F-box and WD repeat domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 12 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
F-box and WD repeat domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 3 Proteins
F-box/WD repeat-containing protein 2 isoform X1
F-box/WD repeat-containing protein 2 isoform X2
F-box and WD repeat domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 2 Proteins
F-box/WD repeat-containing protein 2 isoform X4
F-box/WD repeat-containing protein 2 isoform X3
multiple epidermal growth factor-like domains protein 9
CDK5 regulatory subunit associated protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
CDK5 regulatory subunit-associated protein 2
COORDINATES: nucleotide motif:Rfam:12.0:RF00007
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
BMP/retinoic acid inducible neural specific 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
BMP/retinoic acid-inducible neural-specific protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 11 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
tumor necrosis factor ligand superfamily member 8
tumor necrosis factor ligand superfamily member 15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein 268, transcript variant X2
transmembrane protein 268, transcript variant X1
ATPase H+ transporting V1 subunit G1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATPase H+ transporting V1 subunit G1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
ATPase H+ transporting V1 subunit G1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
V-type proton ATPase subunit G 1 isoform X1
V-type proton ATPase subunit G 1 isoform X3
V-type proton ATPase subunit G 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger protein 618, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 Proteins
zinc finger protein 618, transcript variant X3
zinc finger protein 618, transcript variant X1
zinc finger protein 618, transcript variant X2
zinc finger protein 618, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein
zinc finger protein 618, transcript variant X6
regulator of G protein signaling 3, transcript variant X1
regulator of G protein signaling 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
regulator of G-protein signaling 3 isoform X1
regulator of G-protein signaling 3 isoform X3
regulator of G protein signaling 3, transcript variant X2
regulator of G-protein signaling 3 isoform X2
regulator of G protein signaling 3, transcript variant X5
regulator of G protein signaling 3, transcript variant X4
regulator of G-protein signaling 3 isoform X5
regulator of G-protein signaling 3 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA polymerase epsilon 3, accessory subunit
aminolevulinate dehydratase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 10 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
aminolevulinate dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 77% coverage of the annotated genomic feature by RNAseq alignments
delta-aminolevulinic acid dehydratase isoform X1
delta-aminolevulinic acid dehydratase isoform X2
haloacid dehalogenase like hydrolase domain containing 3
haloacid dehalogenase-like hydrolase domain-containing protein 3
B box and SPRY domain-containing protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA processing factor 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA processing factor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 6 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
pre-mRNA processing factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X1
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X2
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X3
cell division cycle 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division cycle 26, transcript variant X2
cell division cycle 26, transcript variant X3
anaphase-promoting complex subunit CDC26
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
probable low affinity copper uptake protein 2
coenzyme Q-binding protein COQ10 homolog B, mitochondrial-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coenzyme Q-binding protein COQ10 homolog B, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 16% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
KIAA1958 ortholog, transcript variant X2
KIAA1958 ortholog, transcript variant X1
KIAA1958 ortholog, transcript variant X3
uncharacterized protein KIAA1958 homolog isoform X2
uncharacterized protein KIAA1958 homolog isoform X1
uncharacterized protein KIAA1958 homolog isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
hydroxysteroid dehydrogenase-like protein 2
polypyrimidine tract binding protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
polypyrimidine tract binding protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
polypyrimidine tract binding protein 3, transcript variant X3
polypyrimidine tract binding protein 3, transcript variant X4
polypyrimidine tract binding protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
polypyrimidine tract-binding protein 3 isoform X1
polypyrimidine tract-binding protein 3 isoform X2
polypyrimidine tract-binding protein 3 isoform X3
polypyrimidine tract-binding protein 3 isoform X4
polypyrimidine tract-binding protein 3 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
UDP-glucose ceramide glucosyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ceramide glucosyltransferase
protein shortage in chiasmata 1 ortholog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-10
DnaJ heat shock protein family (Hsp40) member C25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 6 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
proteasome adapter and scaffold protein ECM29
LOW QUALITY PROTEIN: olfactory receptor 2K2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 mRNAs, 11 Proteins
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
muscle associated receptor tyrosine kinase, transcript variant X9
muscle associated receptor tyrosine kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs
muscle associated receptor tyrosine kinase, transcript variant X8
muscle associated receptor tyrosine kinase, transcript variant X6
muscle associated receptor tyrosine kinase, transcript variant X7
muscle associated receptor tyrosine kinase, transcript variant X4
muscle associated receptor tyrosine kinase, transcript variant X3
muscle associated receptor tyrosine kinase, transcript variant X2
muscle associated receptor tyrosine kinase, transcript variant X1
muscle, skeletal receptor tyrosine-protein kinase isoform X9
muscle, skeletal receptor tyrosine-protein kinase isoform X6
muscle, skeletal receptor tyrosine-protein kinase isoform X5
muscle, skeletal receptor tyrosine-protein kinase isoform X7
muscle, skeletal receptor tyrosine-protein kinase isoform X4
muscle, skeletal receptor tyrosine-protein kinase isoform X8
muscle, skeletal receptor tyrosine-protein kinase isoform X3
muscle, skeletal receptor tyrosine-protein kinase isoform X2
muscle, skeletal receptor tyrosine-protein kinase isoform X1
sushi, von Willebrand factor type A, EGF and pentraxin domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1
thioredoxin domain containing 8, transcript variant X1
thioredoxin domain containing 8, transcript variant X4
thioredoxin domain containing 8, transcript variant X3
thioredoxin domain containing 8, transcript variant X7
thioredoxin domain containing 8, transcript variant X6
thioredoxin domain containing 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
thioredoxin domain containing 8, transcript variant X5
thioredoxin domain-containing protein 8 isoform X1
thioredoxin domain-containing protein 8 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C9orf152 homolog
PALM2 and AKAP2 fusion, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
PALM2 and AKAP2 fusion, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein tyrosine phosphatase non-receptor type 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase non-receptor type 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 5 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
tyrosine-protein phosphatase non-receptor type 3 isoform X1
tyrosine-protein phosphatase non-receptor type 3 isoform X2
erythrocyte membrane protein band 4.1 like 4B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 245, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 21% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 245, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
transmembrane protein 245, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 22% coverage of the annotated genomic feature by RNAseq alignments
catenin alpha like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 mRNAs, 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
catenin alpha like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 mRNAs, 4 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
elongator acetyltransferase complex subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 11 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 18 Proteins
RAD23 homolog B, nucleotide excision repair protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
UV excision repair protein RAD23 homolog B
zinc finger protein 462, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 2 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 462, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 1 Protein, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
trimeric intracellular cation channel type B
T-cell acute lymphocytic leukemia protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 31% coverage of the annotated genomic feature by RNAseq alignments
fibronectin type III and SPRY domain containing 1 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 44 member 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
choline transporter-like protein 1 isoform X3
solute carrier family 44 member 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 9 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 44 member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 12 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
choline transporter-like protein 1 isoform X4
choline transporter-like protein 1 isoform X2
solute carrier family 44 member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
choline transporter-like protein 1 isoform X1
ATP binding cassette subfamily A member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 18 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily A member 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
phospholipid-transporting ATPase ABCA1 isoform X2
phospholipid-transporting ATPase ABCA1 isoform X1
protein NipSnap homolog 3A, transcript variant X2
protein NipSnap homolog 3A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
protein NipSnap homolog 3A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 13C8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 5 bases in 3 codons; deleted 3 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 13F1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 mRNAs, 9 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
structural maintenance of chromosomes protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 3A
protein phosphatase 3 regulatory subunit B, beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 20, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 8 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 20, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase BRE1A isoform X1
E3 ubiquitin-protein ligase BRE1A isoform X2
post-GPI attachment to proteins GalNAc transferase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
post-GPI attachment to proteins factor 4
aldolase, fructose-bisphosphate B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 mRNAs, 21 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
aldolase, fructose-bisphosphate B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 mRNAs, 21 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger protein 189, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 6 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 189, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 189, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 6 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 189, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L50, mitochondrial
bile acid-CoA:amino acid N-acyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 5 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase-related protein type 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transmembrane protein with EGF like and two follistatin like domains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Myb/SANT DNA binding domain containing 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 8 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myb/SANT-like DNA-binding domain-containing protein 3
testis expressed 10, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 6 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
testis expressed 10, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 mRNAs, 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
endoplasmic reticulum resident protein 44
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
nuclear receptor subfamily 4 group A member 3, transcript variant X3
nuclear receptor subfamily 4 group A member 3, transcript variant X2
nuclear receptor subfamily 4 group A member 3, transcript variant X1
nuclear receptor subfamily 4 group A member 3 isoform X3
nuclear receptor subfamily 4 group A member 3 isoform X2
nuclear receptor subfamily 4 group A member 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein transport protein Sec61 subunit beta
transforming growth factor beta receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 25 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
polypeptide N-acetylgalactosaminyltransferase 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 8 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat and sterile alpha motif domain containing 6
ankyrin repeat and SAM domain-containing protein 6
gamma-aminobutyric acid type B receptor subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 7 Proteins, and 22% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
acidic nuclear phosphoprotein 32 family member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
acidic nuclear phosphoprotein 32 family member B, transcript variant X1
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X2
acidic leucine-rich nuclear phosphoprotein 32 family member B isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF01225
XPA, DNA damage recognition and repair factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
DNA repair protein complementing XP-A cells
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
thiosulfate sulfurtransferase like domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
thiosulfate sulfurtransferase/rhodanese-like domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 180
stimulated by retinoic acid gene 6 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
insulin like growth factor binding protein like 1
insulin-like growth factor-binding protein-like 1
aldehyde dehydrogenase 1 family member B1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 9 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 Proteins
FERM and PDZ domain-containing protein 1
translocase of outer mitochondrial membrane 5
mitochondrial import receptor subunit TOM5 homolog
glyceraldehyde-3-phosphate dehydrogenase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 20 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 5 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerase I subunit RPA49
zinc finger and BTB domain-containing protein 5
glyoxylate and hydroxypyruvate reductase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
glyoxylate reductase/hydroxypyruvate reductase
zinc finger CCHC-type containing 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
zinc finger CCHC-type containing 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger CCHC domain-containing protein 7 isoform X2
zinc finger CCHC domain-containing protein 7 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 13 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 17 Proteins
maternal embryonic leucine zipper kinase, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 2 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 2 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 5 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 28% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 27% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 3 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
maternal embryonic leucine zipper kinase isoform X5
maternal embryonic leucine zipper kinase isoform X4
maternal embryonic leucine zipper kinase isoform X3
maternal embryonic leucine zipper kinase isoform X1
maternal embryonic leucine zipper kinase isoform X6
maternal embryonic leucine zipper kinase isoform X7
maternal embryonic leucine zipper kinase isoform X2
maternal embryonic leucine zipper kinase isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 15 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
glucosamine (UDP-N-acetyl)-2-epimerase/N-acetylmannosamine kinase
bifunctional UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase
clathrin light chain A, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 mRNAs, 8 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 6 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 2 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 3 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 2 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 4 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 7 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 3 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 5 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 2 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 2 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
clathrin light chain A, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 2 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Golgi-associated plant pathogenesis-related protein 1
reversion inducing cysteine rich protein with kazal motifs
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 10 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
reversion-inducing cysteine-rich protein with Kazal motifs
COORDINATES: nucleotide motif:Rfam:12.0:RF00421
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 13C7-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: olfactory receptor 13J1
small regulatory polypeptide of amino acid response
histidine-rich carboxyl terminus protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 mRNAs, 11 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins
family with sequence similarity 221 member B
histidine triad nucleotide binding protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 9 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histidine triad nucleotide-binding protein 2, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: sperm-associated antigen 8
natriuretic peptide receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
natriuretic peptide receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 9 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
natriuretic peptide receptor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
atrial natriuretic peptide receptor 2 isoform X3
atrial natriuretic peptide receptor 2 isoform X2
atrial natriuretic peptide receptor 2 isoform X1
RGP1 homolog, RAB6A GEF complex partner 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
cAMP responsive element binding protein 3
cyclic AMP-responsive element-binding protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 19 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 23 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 11 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 25 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Rho guanine nucleotide exchange factor 39
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: coiled-coil domain-containing protein 107
signaling threshold regulating transmembrane adaptor 1
signaling threshold-regulating transmembrane adapter 1
B-cell differentiation antigen CD72-like
testis associated actin remodelling kinase 1
dual specificity testis-specific protein kinase 1
family with sequence similarity 166 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
RUN and SH3 domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 9 Proteins
RUN and SH3 domain containing 2, transcript variant X2
phospholipid-transporting ATPase FetA-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 21% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 214 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 214 member B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 mRNAs, 7 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
stomatin-like protein 2, mitochondrial isoform X1
stomatin-like protein 2, mitochondrial isoform X2
stomatin-like protein 2, mitochondrial isoform X3
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 2 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 9% coverage of the annotated genomic feature by RNAseq alignments
GPI ethanolamine phosphate transferase 3 isoform X1
GPI ethanolamine phosphate transferase 3 isoform X2
GPI ethanolamine phosphate transferase 3 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 133 mRNAs, 19 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
transitional endoplasmic reticulum ATPase
uncharacterized protein C9orf131 homolog
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 16 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 20 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
dnaJ homolog subfamily B member 5 isoform X1
dnaJ homolog subfamily B member 5 isoform X2
PHD finger protein 24, transcript variant X1
PHD finger protein 24, transcript variant X3
PHD finger protein 24, transcript variant X2
family with sequence similarity 205 member C, transcript variant X2
family with sequence similarity 205 member C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118759906, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC118759906, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
galactose-1-phosphate uridylyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
galactose-1-phosphate uridylyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 8 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
galactose-1-phosphate uridylyltransferase isoform X1
galactose-1-phosphate uridylyltransferase isoform X2
sigma non-opioid intracellular receptor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
sigma non-opioid intracellular receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
sigma non-opioid intracellular receptor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
sigma non-opioid intracellular receptor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
sigma non-opioid intracellular receptor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
sigma non-opioid intracellular receptor 1 isoform X1
sigma non-opioid intracellular receptor 1 isoform X5
sigma non-opioid intracellular receptor 1 isoform X2
sigma non-opioid intracellular receptor 1 isoform X4
sigma non-opioid intracellular receptor 1 isoform X3
AT-rich interactive domain-containing protein 3C
dynactin subunit 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynactin subunit 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynactin subunit 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynactin subunit 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
dynactin subunit 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
ribonuclease P protein subunit p25-like protein
ciliary neurotrophic factor receptor subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 219 member A, transcript variant X3
family with sequence similarity 219 member A, transcript variant X1
family with sequence similarity 219 member A, transcript variant X2
family with sequence similarity 219 member A, transcript variant X4
family with sequence similarity 219 member A, transcript variant X5
chromosome 1A C9orf24 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
chromosome 1A C9orf24 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
spermatid-specific manchette-related protein 1 isoform X2
spermatid-specific manchette-related protein 1 isoform X1
chromosome 1A C9orf24 homolog, transcript variant X3
spermatid-specific manchette-related protein 1 isoform X3
chromosome 1A C9orf24 homolog, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
spermatid-specific manchette-related protein 1 isoform X4
myogenesis regulating glycosidase (putative)
nudix hydrolase 2, transcript variant X1
nudix hydrolase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nudix hydrolase 2, transcript variant X2
bis(5'-nucleosyl)-tetraphosphatase [asymmetrical]
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: ubiquitin-associated protein 1
cytochrome c oxidase subunit 7B, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01191
ubiquitin conjugating enzyme E2 R2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 12 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ubiquitin conjugating enzyme E2 R2, transcript variant X2
ubiquitin-conjugating enzyme E2 R2 isoform X2
ubiquitin-conjugating enzyme E2 R2 isoform X1
nucleolar protein 6, transcript variant X1
nucleolar protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 mRNAs, 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
nuclear transcription factor, X-box binding 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 9 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
charged multivesicular body protein 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 mRNAs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
charged multivesicular body protein 5, transcript variant X2
charged multivesicular body protein 5 isoform X1
charged multivesicular body protein 5 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
BAG family molecular chaperone regulator 1
beta-1,4-galactosyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 15 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-galactosyltransferase 1, transcript variant X2
beta-1,4-galactosyltransferase 1 isoform X1
beta-1,4-galactosyltransferase 1 isoform X2
SMU1 DNA replication regulator and spliceosomal factor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 3 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 13 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X1
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 94% coverage of the annotated genomic feature by RNAseq alignments
NADH:ubiquinone oxidoreductase subunit B6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform X1
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform X2
NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 6 isoform X3
TOP1 binding arginine/serine rich protein, E3 ubiquitin ligase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
DExD/H-box helicase 58, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
DExD/H-box helicase 58, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
DExD/H-box helicase 58, transcript variant X2
antiviral innate immune response receptor RIG-I isoform X1
antiviral innate immune response receptor RIG-I isoform X3
antiviral innate immune response receptor RIG-I isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00561
28S ribosomal protein S14, mitochondrial-like
leucine rich repeat and Ig domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 16 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
leucine rich repeat and Ig domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 16 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
leucine-rich repeat and immunoglobulin-like domain-containing nogo receptor-interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 4 Proteins
guanine nucleotide exchange C9orf72 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 2 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
intraflagellar transport protein 74 homolog
leucine-rich repeat-containing protein 19
phospholipase A2 activating protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 4 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A2 activating protein, transcript variant X3
phospholipase A2 activating protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
phospholipase A-2-activating protein isoform X1
phospholipase A-2-activating protein isoform X2
caspase activity and apoptosis inhibitor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
tumor suppressor candidate gene 1 protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
IZUMO family member 3, transcript variant X1
IZUMO family member 3, transcript variant X2
izumo sperm-egg fusion protein 3 isoform X1
izumo sperm-egg fusion protein 3 isoform X2
ELAV like RNA binding protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 25 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 9 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 14 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 24 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 13 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 23 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 17 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X5
ELAV like RNA binding protein 2, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins, and 28% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X9
ELAV like RNA binding protein 2, transcript variant X12
ELAV like RNA binding protein 2, transcript variant X19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X23
ELAV like RNA binding protein 2, transcript variant X29
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X22
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X27
ELAV like RNA binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 17 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 25 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X20
ELAV like RNA binding protein 2, transcript variant X24
ELAV like RNA binding protein 2, transcript variant X30
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 10 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X28
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 6 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 17 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 25 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 14 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 10 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X26
ELAV like RNA binding protein 2, transcript variant X32
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
ELAV like RNA binding protein 2, transcript variant X31
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 32 Proteins
cyclin-dependent kinase inhibitor 2A, transcript variant X2
cyclin-dependent kinase inhibitor 2A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 32 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinase inhibitor 2A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 mRNAs, 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 17 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: interferon alpha-6-like
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
MLLT3 super elongation complex subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 9 Proteins, and 56% coverage of the annotated genomic feature by RNAseq alignments
MLLT3 super elongation complex subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
MLLT3 super elongation complex subunit, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
40S ribosomal protein S4, X isoform-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 mRNAs, 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DENN domain containing 4C, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X5
DENN domain containing 4C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 10 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 30% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 4C, transcript variant X2
DENN domain containing 4C, transcript variant X3
DENN domain containing 4C, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
DENN domain-containing protein 4C isoform X9
DENN domain-containing protein 4C isoform X10
DENN domain-containing protein 4C isoform X7
DENN domain-containing protein 4C isoform X8
DENN domain-containing protein 4C isoform X5
DENN domain-containing protein 4C isoform X4
DENN domain-containing protein 4C isoform X2
DENN domain-containing protein 4C isoform X3
DENN domain-containing protein 4C isoform X6
DENN domain-containing protein 4C isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00286
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 17 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
SH3 domain containing GRB2 like 2, endophilin A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 13 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
SH3 domain containing GRB2 like 2, endophilin A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 9 Proteins, and 60% coverage of the annotated genomic feature by RNAseq alignments
SH3 domain containing GRB2 like 2, endophilin A1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 6 Proteins, and 25% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 171
COORDINATES: nucleotide motif:Rfam:12.0:RF00322
PC4 and SFRS1 interacting protein 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 9 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PC4 and SFRS1 interacting protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 12 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PC4 and SFRS1 interacting protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PC4 and SFRS1 interacting protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PC4 and SFRS1 interacting protein 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
PC4 and SFRS1 interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PC4 and SFRS1 interacting protein 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
PC4 and SFRS1-interacting protein isoform X1
PC4 and SFRS1-interacting protein isoform X2
PC4 and SFRS1-interacting protein isoform X3
PC4 and SFRS1-interacting protein isoform X5
PC4 and SFRS1-interacting protein isoform X4
small nuclear RNA activating complex polypeptide 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
small nuclear RNA activating complex polypeptide 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
small nuclear RNA activating complex polypeptide 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
small nuclear RNA activating complex polypeptide 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments
snRNA-activating protein complex subunit 3 isoform X3
snRNA-activating protein complex subunit 3 isoform X4
snRNA-activating protein complex subunit 3 isoform X1
snRNA-activating protein complex subunit 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
FRAS1-related extracellular matrix protein 1
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 21, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor I B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA histidin (anticodon GUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
nuclear factor I B, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 14 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor I B, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 14 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear factor I B, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 18 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor I B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 19 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor I B, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor I B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor I B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear factor I B, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 22 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor I B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
nuclear factor I B, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
non-structural maintenance of chromosomes element 1 homolog
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: non-structural maintenance of chromosomes element 1 homolog
multiple PDZ domain crumbs cell polarity complex component, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 37% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 5 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 36% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X6
multiple PDZ domain crumbs cell polarity complex component, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X11
multiple PDZ domain crumbs cell polarity complex component, transcript variant X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
multiple PDZ domain crumbs cell polarity complex component, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 mRNAs, 7 Proteins
5,6-dihydroxyindole-2-carboxylic acid oxidase
protein tyrosine phosphatase receptor type D, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type D, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 9 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type D, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 9 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase delta isoform X1
receptor-type tyrosine-protein phosphatase delta isoform X3
receptor-type tyrosine-protein phosphatase delta isoform X4
receptor-type tyrosine-protein phosphatase delta isoform X2
protein tyrosine phosphatase receptor type D, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 9 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type D, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
receptor-type tyrosine-protein phosphatase delta isoform X5
receptor-type tyrosine-protein phosphatase delta isoform X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00340
distal membrane arm assembly complex 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 64% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
distal membrane arm assembly complex 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 43% coverage of the annotated genomic feature by RNAseq alignments
distal membrane-arm assembly complex protein 1 isoform X2
distal membrane-arm assembly complex protein 1 isoform X1
lysine demethylase 4C, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
lysine demethylase 4C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 Proteins, and 16% coverage of the annotated genomic feature by RNAseq alignments
lysine-specific demethylase 4C isoform X1
lysine-specific demethylase 4C isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 4 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
iron-sulfur cluster assembly 1 homolog, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 51% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 35, NatC auxiliary subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 35, NatC auxiliary subunit, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 mRNAs, 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 35, NatC auxiliary subunit, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
N-alpha-acetyltransferase 35, NatC auxiliary subunit isoform X2
N-alpha-acetyltransferase 35, NatC auxiliary subunit isoform X1
ATP/GTP binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
ATP/GTP binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
ATP/GTP binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 2 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
ATP/GTP binding protein 1, transcript variant X4
neurotrophic receptor tyrosine kinase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 59% coverage of the annotated genomic feature by RNAseq alignments
neurotrophic receptor tyrosine kinase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
neurotrophic receptor tyrosine kinase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
BDNF/NT-3 growth factors receptor isoform X2
BDNF/NT-3 growth factors receptor isoform X1
BDNF/NT-3 growth factors receptor isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 37% coverage of the annotated genomic feature by RNAseq alignments
recQ-mediated genome instability protein 1
heterogeneous nuclear ribonucleoprotein K, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 mRNAs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 mRNAs, 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 mRNAs, 4 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 3 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K isoform X2
heterogeneous nuclear ribonucleoprotein K isoform X4
heterogeneous nuclear ribonucleoprotein K isoform X1
heterogeneous nuclear ribonucleoprotein K isoform X3
heterogeneous nuclear ribonucleoprotein K, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, and 88% coverage of the annotated genomic feature by RNAseq alignments
heterogeneous nuclear ribonucleoprotein K isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 3 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 7 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
FERM domain containing 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 16 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
FERM domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 9 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
FERM domain-containing protein 3 isoform X2
FERM domain-containing protein 3 isoform X1
FERM domain containing 3, transcript variant X3
FERM domain-containing protein 3 isoform X3
spermatogenesis-associated protein 31E1-like
serine palmitoyltransferase long chain base subunit 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 6 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
receptor tyrosine kinase like orphan receptor 2
tyrosine-protein kinase transmembrane receptor ROR2
nuclear factor interleukin-3-regulated protein
AU RNA binding methylglutaconyl-CoA hydratase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
methylglutaconyl-CoA hydratase, mitochondrial
growth arrest and DNA damage inducible gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 mRNAs, 13 Proteins
growth arrest and DNA damage-inducible protein GADD45 gamma
anaphase-promoting complex subunit 15-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 12% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: selenocysteine insertion sequence-binding protein 2
CDC28 protein kinase regulatory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
cyclin-dependent kinases regulatory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 mRNAs, 11 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 mRNAs, 8 Proteins
COORDINATES: nucleotide motif:Rfam:12.0:RF00412
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 mRNAs, 28 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
cyclin dependent kinase 20, transcript variant X1
cyclin dependent kinase 20, transcript variant X4
cyclin dependent kinase 20, transcript variant X2
cyclin dependent kinase 20, transcript variant X3
F-box/WD repeat-containing protein 12-like
hippocampus abundant transcript-like protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: hippocampus abundant transcript-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 13 Proteins, and 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 5 Proteins, and 34% coverage of the annotated genomic feature by RNAseq alignments
constitutive coactivator of PPAR-gamma-like protein 1
FYVE, RhoGEF and PH domain-containing protein 3
caspase recruitment domain family member 19
caspase recruitment domain-containing protein 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 mRNAs, 16 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments
extracellular matrix protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
extracellular matrix protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
extracellular matrix protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
extracellular matrix protein 2 isoform X2
extracellular matrix protein 2 isoform X1
extracellular matrix protein 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 mRNAs, 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF01229
potassium calcium-activated channel subfamily U member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: potassium channel subfamily U member 1