Mauremys mutica isolate MM-2020 ecotype Southern chromosome 23, ASM2049712v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Testudinata; Testudines; Cryptodira; Durocryptodira; Testudinoidea; Geoemydidae; Geoemydinae; Mauremys.
REFSEQ INFORMATION: The reference sequence is identical to\nCM035655.1.\nAssembly name: ASM2049712v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Institute of Zoology,\nGuangdong Academy of Science on 2021/10/14. The original\nwhole-genome shotgun project has the accession JAHDVG000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Institute of Zoology, Guangdong Academy\n of Science\nAssembly Method :: FALCON v. March-2021\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 99.81x\nSequencing Technology :: PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Mauremys mutica Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon AAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA valine (anticodon UAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon UUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon GCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon UGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamine (anticodon CUG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon AGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
transfer RNA arginine (anticodon CCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glutamic acid (anticodon UUC); 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
maestro heat-like repeat family member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transfer RNA arginine (anticodon CCG); 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: 94% 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 57% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123355213, transcript variant X2
uncharacterized LOC123355213, 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 3 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
leucine zipper protein 1, transcript variant X1
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 6 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X2
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 7 samples with support for all annotated introns
leucine zipper protein 1, transcript variant X3
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
heterogeneous nuclear ribonucleoprotein R, transcript variant X1
heterogeneous nuclear ribonucleoprotein R, transcript variant X2
heterogeneous nuclear ribonucleoprotein R, transcript variant X3
heterogeneous nuclear ribonucleoprotein R isoform X2
heterogeneous nuclear ribonucleoprotein R isoform X1
heterogeneous nuclear ribonucleoprotein R isoform X3
ATP synthase inhibitory factor subunit 1
DnaJ heat shock protein family (Hsp40) member C8, transcript variant X1
dnaJ homolog subfamily C member 8 isoform X1
DnaJ heat shock protein family (Hsp40) member C8, transcript variant X2
dnaJ homolog subfamily C member 8 isoform X2
platelet activating factor receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
platelet activating factor receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
platelet activating factor receptor, transcript variant X4
platelet activating factor receptor, transcript variant X5
platelet activating factor receptor, transcript variant X2
platelet-activating factor receptor isoform X1
platelet-activating factor receptor isoform X2
EYA transcriptional coactivator and phosphatase 3, transcript variant X3
EYA transcriptional coactivator and phosphatase 3, transcript variant X2
EYA transcriptional coactivator and phosphatase 3, transcript variant X1
EYA transcriptional coactivator and phosphatase 3, transcript variant X4
EYA transcriptional coactivator and phosphatase 3, transcript variant X5
sphingomyelin phosphodiesterase acid like 3B, transcript variant X1
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 3 samples with support for all annotated introns
acid sphingomyelinase-like phosphodiesterase 3b isoform X1
sphingomyelin phosphodiesterase acid like 3B, transcript variant X2
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
acid sphingomyelinase-like phosphodiesterase 3b isoform X2
replication protein A2, transcript variant X1
replication protein A2, transcript variant X2
replication protein A 32 kDa subunit isoform X1
replication protein A 32 kDa subunit isoform X2
thymocyte selection associated family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 8
nuclear inhibitor of protein phosphatase 1
COORDINATES: nucleotide motif:Rfam:12.0:RF00553
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Cbp/p300 interacting transactivator with Glu/Asp rich carboxy-terminal domain 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% 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 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123355231, transcript variant X2
uncharacterized LOC123355231, transcript variant X4
uncharacterized LOC123355231, transcript variant X3
uncharacterized LOC123355231, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Scm polycomb group protein homolog 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 41 Proteins, 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: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC123355469, transcript variant X1
uncharacterized LOC123355469, transcript variant X2
zinc finger CCHC-type containing 17, transcript variant X2
zinc finger CCHC-type containing 17, transcript variant X4
zinc finger CCHC-type containing 17, transcript variant X3
zinc finger CCHC-type containing 17, transcript variant X1
zinc finger CCHC-type containing 17, transcript variant X5
small nuclear ribonucleoprotein U5 subunit 40
U5 small nuclear ribonucleoprotein 40 kDa protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% 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 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cyclin-dependent kinase 10-like
sodium/potassium transporting ATPase interacting 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
sodium/potassium-transporting ATPase subunit beta-1-interacting protein 1
pumilio RNA binding family member 1, transcript variant X2
pumilio RNA binding family member 1, transcript variant X10
pumilio RNA binding family member 1, transcript variant X1
pumilio RNA binding family member 1, transcript variant X4
pumilio RNA binding family member 1, transcript variant X5
pumilio RNA binding family member 1, transcript variant X7
pumilio RNA binding family member 1, transcript variant X6
pumilio RNA binding family member 1, transcript variant X8
pumilio RNA binding family member 1, transcript variant X3
pumilio RNA binding family member 1, transcript variant X9
COORDINATES: nucleotide motif:Rfam:12.0:RF00188
lysosomal-associated transmembrane protein 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
protein tyrosine phosphatase receptor type U, transcript variant X1
receptor-type tyrosine-protein phosphatase U isoform X1
protein tyrosine phosphatase receptor type U, transcript variant X2
receptor-type tyrosine-protein phosphatase U isoform X2
uncharacterized LOC123355467, transcript variant X3
uncharacterized LOC123355467, transcript variant X2
uncharacterized LOC123355467, transcript variant X1
mitochondrial trans-2-enoyl-CoA reductase, transcript variant X1
mitochondrial trans-2-enoyl-CoA reductase, transcript variant X2
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 6 samples with support for all annotated introns
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X1
enoyl-[acyl-carrier-protein] reductase, mitochondrial isoform X2
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 4 samples with support for all annotated introns
serine and arginine rich splicing factor 4, transcript variant X1
serine/arginine-rich splicing factor 4 isoform X1
serine and arginine rich splicing factor 4, transcript variant X2
serine/arginine-rich splicing factor 4 isoform X2
serine and arginine rich splicing factor 4, transcript variant X3
serine/arginine-rich splicing factor 4 isoform X3
lethal(3)malignant brain tumor-like protein 4, transcript variant X10
lethal(3)malignant brain tumor-like protein 4, transcript variant X7
lethal(3)malignant brain tumor-like protein 4, transcript variant X2
lethal(3)malignant brain tumor-like protein 4, transcript variant X3
lethal(3)malignant brain tumor-like protein 4 isoform X2
lethal(3)malignant brain tumor-like protein 4, transcript variant X4
lethal(3)malignant brain tumor-like protein 4, transcript variant X6
lethal(3)malignant brain tumor-like protein 4, transcript variant X1
lethal(3)malignant brain tumor-like protein 4, transcript variant X5
lethal(3)malignant brain tumor-like protein 4 isoform X4
lethal(3)malignant brain tumor-like protein 4 isoform X3
lethal(3)malignant brain tumor-like protein 4 isoform X1
lethal(3)malignant brain tumor-like protein 4, transcript variant X8
lethal(3)malignant brain tumor-like protein 4, transcript variant X9
lethal(3)malignant brain tumor-like protein 4 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins
transmembrane protein 200B, transcript variant X3
transmembrane protein 200B, transcript variant X1
transmembrane protein 200B, transcript variant X2
erythrocyte membrane protein band 4.1, transcript variant X7
erythrocyte membrane protein band 4.1, transcript variant X20
erythrocyte membrane protein band 4.1, transcript variant X6
erythrocyte membrane protein band 4.1, transcript variant X8
erythrocyte membrane protein band 4.1, transcript variant X32
erythrocyte membrane protein band 4.1, transcript variant X28
erythrocyte membrane protein band 4.1, transcript variant X24
erythrocyte membrane protein band 4.1, transcript variant X15
erythrocyte membrane protein band 4.1, transcript variant X22
erythrocyte membrane protein band 4.1, transcript variant X31
erythrocyte membrane protein band 4.1, transcript variant X18
erythrocyte membrane protein band 4.1, transcript variant X27
erythrocyte membrane protein band 4.1, transcript variant X29
erythrocyte membrane protein band 4.1, transcript variant X30
erythrocyte membrane protein band 4.1, transcript variant X23
erythrocyte membrane protein band 4.1, transcript variant X26
erythrocyte membrane protein band 4.1, transcript variant X14
erythrocyte membrane protein band 4.1, transcript variant X21
erythrocyte membrane protein band 4.1, transcript variant X11
erythrocyte membrane protein band 4.1, transcript variant X25
erythrocyte membrane protein band 4.1, transcript variant X10
erythrocyte membrane protein band 4.1, transcript variant X5
erythrocyte membrane protein band 4.1, transcript variant X4
erythrocyte membrane protein band 4.1, transcript variant X1
erythrocyte membrane protein band 4.1, transcript variant X9
erythrocyte membrane protein band 4.1, transcript variant X2
erythrocyte membrane protein band 4.1, transcript variant X19
erythrocyte membrane protein band 4.1, transcript variant X3
erythrocyte membrane protein band 4.1, transcript variant X17
erythrocyte membrane protein band 4.1, transcript variant X13
erythrocyte membrane protein band 4.1, transcript variant X16
erythrocyte membrane protein band 4.1, transcript variant X12
erythrocyte membrane protein band 4.1, transcript variant X33
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tRNA selenocysteine 1 associated protein 1, transcript variant X1
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 5 samples with support for all annotated introns
tRNA selenocysteine 1 associated protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
tRNA selenocysteine 1-associated protein 1 isoform X1
tRNA selenocysteine 1-associated protein 1 isoform X2
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
COORDINATES: nucleotide motif:Rfam:12.0:RF00405
COORDINATES: nucleotide motif:Rfam:12.0:RF00608
RAB42, member RAS oncogene family, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RAB42, member RAS oncogene family, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
TATA-box binding protein associated factor 12, transcript variant X2
TATA-box binding protein associated factor 12, transcript variant X3
TATA-box binding protein associated factor 12, transcript variant X1
transcription initiation factor TFIID subunit 12 isoform X1
transcription initiation factor TFIID subunit 12 isoform X3
transcription initiation factor TFIID subunit 12 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
discoidin, CUB and LCCL domain-containing protein 1-like, transcript variant X1
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 5 samples with support for all annotated introns
discoidin, CUB and LCCL domain-containing protein 1-like, transcript variant X2
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
discoidin, CUB and LCCL domain-containing protein 1-like isoform X1
discoidin, CUB and LCCL domain-containing protein 1-like isoform X2
glucocorticoid modulatory element binding protein 1, transcript variant X5
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 3 samples with support for all annotated introns
glucocorticoid modulatory element binding protein 1, transcript variant X2
glucocorticoid modulatory element binding protein 1, transcript variant X7
glucocorticoid modulatory element binding protein 1, transcript variant X1
glucocorticoid modulatory element binding protein 1, transcript variant X3
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
glucocorticoid modulatory element binding protein 1, transcript variant X4
glucocorticoid modulatory element binding protein 1, transcript variant X6
glucocorticoid modulatory element binding protein 1, transcript variant X8
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 8 samples with support for all annotated introns
glucocorticoid modulatory element binding protein 1, transcript variant X9
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 9 samples with support for all annotated introns
glucocorticoid modulatory element-binding protein 1 isoform X1
glucocorticoid modulatory element-binding protein 1 isoform X2
glucocorticoid modulatory element-binding protein 1 isoform X3
glucocorticoid modulatory element-binding protein 1 isoform X4
YTH N6-methyladenosine RNA binding protein 2
peptide methionine sulfoxide reductase MsrA-like, transcript variant X4
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
peptide methionine sulfoxide reductase MsrA-like, transcript variant X3
peptide methionine sulfoxide reductase MsrA-like, transcript variant X2
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 3 samples with support for all annotated introns
peptide methionine sulfoxide reductase MsrA-like, transcript variant X5
peptide methionine sulfoxide reductase MsrA-like, transcript variant X6
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 5 samples with support for all annotated introns
peptide methionine sulfoxide reductase MsrA-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mitochondrial peptide methionine sulfoxide reductase-like isoform X1
peptide methionine sulfoxide reductase MsrA-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peptide methionine sulfoxide reductase MsrA-like isoform X2
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
basic salivary proline-rich protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
cation channel sperm associated 4, 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
cation channel sperm associated 4, transcript variant X3
cation channel sperm-associated protein 4 isoform X1
cation channel sperm-associated protein 4 isoform X3
cation channel sperm associated 4, transcript variant X2
cation channel sperm-associated protein 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ArfGAP with SH3 domain, ankyrin repeat and PH domain 3
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 5 samples with support for all annotated introns
arf-GAP with SH3 domain, ANK repeat and PH domain-containing protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
transcription elongation factor A protein 3
regulator of G-protein signaling 19-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of G-protein signaling 19-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of G-protein signaling 19-like, transcript variant X3
regulator of G-protein signaling 19-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulator of G-protein signaling 19-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
regulator of G-protein signaling 19-like isoform X1
regulator of G-protein signaling 20-like isoform X2
regulator of G-protein signaling 19-like isoform X3
regulator of G-protein signaling 19-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of chromosome condensation 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
regulator of chromosome condensation 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulator of chromosome condensation isoform X1
regulator of chromosome condensation isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00045
phosphatase and actin regulator 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
phosphatase and actin regulator 4, transcript variant X1
phosphatase and actin regulator 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphatase and actin regulator 4 isoform X3
phosphatase and actin regulator 4 isoform X2
phosphatase and actin regulator 4 isoform X1
phosphatase and actin regulator 4 isoform X4
uncharacterized LOC123355254, transcript variant X4
uncharacterized LOC123355254, transcript variant X2
uncharacterized LOC123355254, transcript variant X3
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 4 samples with support for all annotated introns
uncharacterized LOC123355254, transcript variant X1
family with sequence similarity 76 member A, transcript variant X1
family with sequence similarity 76 member A, transcript variant X2
interferon alpha inducible protein 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 281 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
interferon alpha inducible protein 6, transcript variant X3
interferon alpha inducible protein 6, transcript variant X1
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 6 samples with support for all annotated introns
digestive cysteine proteinase 1-like, transcript variant X1
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
digestive cysteine proteinase 1-like isoform X1
digestive cysteine proteinase 1-like, transcript variant X2
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
digestive cysteine proteinase 1-like isoform X2
FGR proto-oncogene, Src family tyrosine kinase, transcript variant X1
FGR proto-oncogene, Src family tyrosine kinase, transcript variant X3
FGR proto-oncogene, Src family tyrosine kinase, transcript variant X2
AT-hook DNA binding motif containing 1, transcript variant X2
AT-hook DNA binding motif containing 1, transcript variant X1
AT-hook DNA-binding motif-containing protein 1 isoform X1
AT-hook DNA-binding motif-containing protein 1 isoform X2
AT-hook DNA binding motif containing 1, transcript variant X3
AT-hook DNA binding motif containing 1, transcript variant X4
AT-hook DNA-binding motif-containing protein 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
wiskott-Aldrich syndrome protein family member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CD164 molecule like 2, transcript variant X2
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 13 samples with support for all annotated introns
CD164 molecule like 2, transcript variant X1
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 4 samples with support for all annotated introns
CD164 molecule like 2, transcript variant X3
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 16 samples with support for all annotated introns
CD164 sialomucin-like 2 protein isoform X2
CD164 sialomucin-like 2 protein isoform X1
CD164 sialomucin-like 2 protein isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 6, transcript variant X1
mitogen-activated protein kinase kinase kinase 6
synaptotagmin like 1, transcript variant X2
synaptotagmin like 1, transcript variant X1
transmembrane protein 222, transcript variant X2
transmembrane protein 222, transcript variant X1
transmembrane protein 222, transcript variant X3
WD and tetratricopeptide repeats protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 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 93% coverage of the annotated genomic feature by RNAseq alignments
keratinocyte differentiation factor 1, transcript variant X3
keratinocyte differentiation factor 1, transcript variant X1
keratinocyte differentiation factor 1, transcript variant X4
keratinocyte differentiation factor 1, transcript variant X2
nuclear distribution C, dynein complex regulator
nuclear receptor subfamily 0 group B member 2
GPN-loop GTPase 2, transcript variant X1
GPN-loop GTPase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X6
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X2
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X8
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X9
zinc finger DHHC-type palmitoyltransferase 18, transcript variant X4
phosphatidylinositol glycan anchor biosynthesis class V, transcript variant X1
phosphatidylinositol glycan anchor biosynthesis class V, transcript variant X3
phosphatidylinositol glycan anchor biosynthesis class V, transcript variant X2
AT-rich interaction domain 1A, transcript variant X2
AT-rich interaction domain 1A, transcript variant X5
AT-rich interaction domain 1A, transcript variant X3
AT-rich interaction domain 1A, transcript variant X4
AT-rich interaction domain 1A, transcript variant X1
AT-rich interactive domain-containing protein 1A isoform X2
AT-rich interactive domain-containing protein 1A isoform X3
AT-rich interactive domain-containing protein 1A isoform X1
ribosomal protein S6 kinase A1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ribosomal protein S6 kinase A1, transcript variant X3
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
ribosomal protein S6 kinase A1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ribosomal protein S6 kinase A1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
ribosomal protein S6 kinase alpha-1 isoform X4
ribosomal protein S6 kinase alpha-1 isoform X2
ribosomal protein S6 kinase alpha-1 isoform X3
ribosomal protein S6 kinase alpha-1 isoform X1
high mobility group nucleosomal binding domain 2
dehydrodolichyl diphosphate synthase subunit, transcript variant X1
dehydrodolichyl diphosphate synthase subunit, transcript variant X3
dehydrodolichyl diphosphate synthase subunit, transcript variant X2
dehydrodolichyl diphosphate synthase complex subunit DHDDS isoform X1
dehydrodolichyl diphosphate synthase complex subunit DHDDS isoform X2
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 1 sample with support for all annotated introns
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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 21 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 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
tissue-resident T-cell transcription regulator protein ZNF683
crystallin beta-gamma domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
beta/gamma crystallin domain-containing protein 2
uncharacterized LOC123355533, transcript variant X8
uncharacterized LOC123355533, transcript variant X5
uncharacterized LOC123355533, transcript variant X3
uncharacterized LOC123355533, transcript variant X4
uncharacterized LOC123355533, transcript variant X9
uncharacterized LOC123355533, transcript variant X14
uncharacterized LOC123355533, transcript variant X2
uncharacterized LOC123355533, transcript variant X1
uncharacterized LOC123355533, transcript variant X6
uncharacterized LOC123355533, transcript variant X12
uncharacterized LOC123355533, transcript variant X10
uncharacterized LOC123355533, transcript variant X11
uncharacterized LOC123355533, transcript variant X7
uncharacterized LOC123355533, transcript variant X13
UBX domain protein 11, transcript variant X1
UBX domain protein 11, transcript variant X4
UBX domain-containing protein 11 isoform X2
UBX domain protein 11, transcript variant X2
UBX domain protein 11, transcript variant X7
UBX domain-containing protein 11 isoform X5
UBX domain protein 11, transcript variant X6
UBX domain-containing protein 11 isoform X4
UBX domain protein 11, transcript variant X3
UBX domain-containing protein 11 isoform X1
UBX domain protein 11, transcript variant X8
UBX domain protein 11, transcript variant X5
UBX domain-containing protein 11 isoform X3
UBX domain protein 11, transcript variant X10
UBX domain protein 11, transcript variant X9
UBX domain-containing protein 11 isoform X6
SH3 domain binding glutamate rich protein like 3
SH3 domain-binding glutamic acid-rich-like protein 3
centrosomal protein 85, transcript variant X4
centrosomal protein 85, transcript variant X1
centrosomal protein 85, transcript variant X5
centrosomal protein 85, transcript variant X3
centrosomal protein 85, transcript variant X6
centrosomal protein 85, transcript variant X2
centrosomal protein of 85 kDa isoform X2
centrosomal protein of 85 kDa isoform X1
connector enhancer of kinase suppressor of Ras 1
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 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C1orf232 homolog
family with sequence similarity 110 member D, transcript variant X1
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 4 samples with support for all annotated introns
family with sequence similarity 110 member D, transcript variant X2
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 2 samples with support for all annotated introns
PDLIM1 interacting kinase 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
PDLIM1 interacting kinase 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
PDLIM1 interacting kinase 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
serine/threonine-protein kinase PDIK1L isoform X1
serine/threonine-protein kinase PDIK1L isoform X2
tripartite motif containing 63, transcript variant X2
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
E3 ubiquitin-protein ligase TRIM63 isoform X2
tripartite motif containing 63, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E3 ubiquitin-protein ligase TRIM63 isoform X1
solute carrier family 30 member 2, transcript variant X3
solute carrier family 30 member 2, transcript variant X2
solute carrier family 30 member 2, transcript variant X1
exostosin like glycosyltransferase 1, transcript variant X2
exostosin like glycosyltransferase 1, transcript variant X1
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 5 samples with support for all annotated introns
platelet activating factor acetylhydrolase 2, transcript variant X1
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X1
platelet activating factor acetylhydrolase 2, transcript variant X3
platelet activating factor acetylhydrolase 2, transcript variant X2
platelet-activating factor acetylhydrolase 2, cytoplasmic isoform X2
progestin and adipoQ receptor family member 7
aurora kinase A and ninein interacting protein, transcript variant X1
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 7 samples with support for all annotated introns
aurora kinase A and ninein interacting protein, transcript variant X2
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 5 samples with support for all annotated introns
aurora kinase A and ninein interacting protein, transcript variant X3
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 6 samples with support for all annotated introns
aurora kinase A and ninein-interacting protein isoform X1
aurora kinase A and ninein-interacting protein isoform X2
mitochondrial fission regulator 1 like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X6
mitochondrial fission regulator 1 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X7
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 4 samples with support for all annotated introns
mitochondrial fission regulator 1 like, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mannosyl-oligosaccharide 1,2-alpha-mannosidase IC
low density lipoprotein receptor adaptor protein 1, transcript variant X3
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 11 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1, transcript variant X6
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 10 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1, transcript variant X11
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 8 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1 isoform X3
low density lipoprotein receptor adapter protein 1 isoform X6
low density lipoprotein receptor adapter protein 1 isoform X9
low density lipoprotein receptor adaptor protein 1, transcript variant X2
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 7 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1, transcript variant X1
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 9 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1 isoform X2
low density lipoprotein receptor adapter protein 1 isoform X1
low density lipoprotein receptor adaptor protein 1, transcript variant X5
low density lipoprotein receptor adapter protein 1 isoform X5
low density lipoprotein receptor adaptor protein 1, transcript variant X4
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 14 samples with support for all annotated introns
low density lipoprotein receptor adapter protein 1 isoform X4
low density lipoprotein receptor adaptor protein 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
low density lipoprotein receptor adaptor protein 1, transcript variant X10
low density lipoprotein receptor adaptor protein 1, transcript variant X7
low density lipoprotein receptor adapter protein 1 isoform X8
low density lipoprotein receptor adapter protein 1 isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 132 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 134 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane protein 50A, transcript variant X2
transmembrane protein 50A, transcript variant X1
arginine and serine rich protein 1, transcript variant X4
arginine and serine rich protein 1, transcript variant X1
arginine and serine rich protein 1, transcript variant X2
arginine and serine rich protein 1, transcript variant X3
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 11 samples with support for all annotated introns
arginine/serine-rich protein 1 isoform X1
arginine/serine-rich protein 1 isoform X2
RUNX family transcription factor 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX family transcription factor 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUNX family transcription factor 3, transcript variant X4
RUNX family transcription factor 3, transcript variant X2
RUNX family transcription factor 3, transcript variant X5
runt-related transcription factor 3 isoform X2
runt-related transcription factor 3 isoform X1
chloride intracellular channel 4, transcript variant X3
chloride intracellular channel 4, transcript variant X1
chloride intracellular channel 4, transcript variant X2
chloride intracellular channel protein 4 isoform X1
chloride intracellular channel protein 4 isoform X2
chloride intracellular channel protein 4 isoform X3
serine and arginine repetitive matrix 1, transcript variant X2
serine and arginine repetitive matrix 1, transcript variant X7
serine and arginine repetitive matrix 1, transcript variant X3
serine and arginine repetitive matrix 1, transcript variant X1
serine and arginine repetitive matrix 1, transcript variant X4
serine and arginine repetitive matrix 1, transcript variant X6
serine and arginine repetitive matrix 1, transcript variant X8
serine and arginine repetitive matrix 1, transcript variant X5
serine and arginine repetitive matrix 1, transcript variant X9
serine/arginine repetitive matrix protein 1 isoform X8
serine/arginine repetitive matrix protein 1 isoform X4
serine/arginine repetitive matrix protein 1 isoform X6
serine/arginine repetitive matrix protein 1 isoform X2
serine/arginine repetitive matrix protein 1 isoform X7
serine/arginine repetitive matrix protein 1 isoform X5
serine/arginine repetitive matrix protein 1 isoform X3
serine/arginine repetitive matrix protein 1 isoform X1
serine/arginine repetitive matrix protein 1 isoform X9
RCAN family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
RCAN family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
RCAN family member 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RCAN family member 3, transcript variant X3
RCAN family member 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
NIPA like domain containing 3, transcript variant X5
NIPA like domain containing 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NIPA like domain containing 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
NIPA like domain containing 3, transcript variant X3
NIPA like domain containing 3, transcript variant X1
grainyhead like transcription factor 3, transcript variant X5
grainyhead like transcription factor 3, transcript variant X4
grainyhead like transcription factor 3, transcript variant X3
grainyhead like transcription factor 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
grainyhead like transcription factor 3, transcript variant X7
grainyhead like transcription factor 3, transcript variant X6
grainyhead like transcription factor 3, transcript variant X9
grainyhead like transcription factor 3, transcript variant X1
grainyhead like transcription factor 3, transcript variant X8
grainyhead-like protein 3 homolog isoform X5
grainyhead-like protein 3 homolog isoform X2
grainyhead-like protein 3 homolog isoform X1
grainyhead-like protein 3 homolog isoform X3
grainyhead-like protein 3 homolog isoform X4
interferon lambda receptor 1, transcript variant X1
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
interferon lambda receptor 1, transcript variant X2
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 4 samples with support for all annotated introns
interleukin 22 receptor subunit alpha 1, transcript variant X3
interleukin 22 receptor subunit alpha 1, transcript variant X2
interleukin-22 receptor subunit alpha-1 isoform X2
interleukin 22 receptor subunit alpha 1, transcript variant X1
interleukin-22 receptor subunit alpha-1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
serine and arginine rich splicing factor 10, transcript variant X5
serine/arginine-rich splicing factor 10 isoform X5
serine and arginine rich splicing factor 10, transcript variant X6
serine/arginine-rich splicing factor 10 isoform X6
serine and arginine rich splicing factor 10, transcript variant X2
serine and arginine rich splicing factor 10, transcript variant X4
serine and arginine rich splicing factor 10, transcript variant X1
serine and arginine rich splicing factor 10, transcript variant X3
serine/arginine-rich splicing factor 10 isoform X1
serine/arginine-rich splicing factor 10 isoform X2
serine/arginine-rich splicing factor 10 isoform X3
serine/arginine-rich splicing factor 10 isoform X4
proline rich nuclear receptor coactivator 2, transcript variant X2
proline rich nuclear receptor coactivator 2, transcript variant X1
proline-rich nuclear receptor coactivator 2 isoform X1
proline-rich nuclear receptor coactivator 2 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
3-hydroxy-3-methylglutaryl-CoA lyase, transcript variant X1
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform X1
3-hydroxy-3-methylglutaryl-CoA lyase, transcript variant X2
hydroxymethylglutaryl-CoA lyase, mitochondrial isoform X2
UDP-galactose-4-epimerase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
UDP-galactose-4-epimerase, transcript variant X2
lysophospholipase 2, transcript variant X3
lysophospholipase 2, transcript variant X1
lysophospholipase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
cyclic GMP-AMP synthase-like, transcript variant X1
cyclic GMP-AMP synthase-like, transcript variant X2
elongation factor 1-alpha, somatic form-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 534 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
elongation factor 1-alpha-like isoform X1
elongation factor 1-alpha, oocyte form-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 515 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
elongation factor 1-alpha, somatic form-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 535 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
elongation factor 1-alpha, somatic form-like isoform X2
sodium-dependent phosphate transport protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium-dependent phosphate transport protein 3-like
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 17 samples with support for all annotated introns
cyclase associated actin cytoskeleton regulatory protein 1, transcript variant X1
cyclase associated actin cytoskeleton regulatory protein 1, transcript variant X2
major facilitator superfamily domain containing 2A, transcript variant X1
major facilitator superfamily domain containing 2A, transcript variant X3
sodium-dependent lysophosphatidylcholine symporter 1 isoform X1
sodium-dependent lysophosphatidylcholine symporter 1 isoform X3
major facilitator superfamily domain containing 2A, transcript variant X2
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 20 samples with support for all annotated introns
sodium-dependent lysophosphatidylcholine symporter 1 isoform X2
MYCL proto-oncogene, bHLH transcription factor
tRNA isopentenyltransferase 1, transcript variant X2
tRNA isopentenyltransferase 1, transcript variant X1
CYFIP-related Rac1 interactor A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
CYFIP-related Rac1 interactor A-like, transcript variant X4
CYFIP-related Rac1 interactor A-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
CYFIP-related Rac1 interactor A-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
CYFIP-related Rac1 interactor A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
CYFIP-related Rac1 interactor A-like isoform X2
CYFIP-related Rac1 interactor A-like isoform X4
CYFIP-related Rac1 interactor A-like isoform X1
CYFIP-related Rac1 interactor A-like isoform X3
5'-nucleotidase, cytosolic IA, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
5'-nucleotidase, cytosolic IA, transcript variant X2
hes related family bHLH transcription factor with YRPW motif like
hairy/enhancer-of-split related with YRPW motif-like protein
poly(A) binding protein cytoplasmic 4, transcript variant X2
poly(A) binding protein cytoplasmic 4, transcript variant X3
polyadenylate-binding protein 4 isoform X2
poly(A) binding protein cytoplasmic 4, transcript variant X1
polyadenylate-binding protein 4 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00431
peptidylprolyl isomerase E, transcript variant X2
peptidyl-prolyl cis-trans isomerase E isoform X2
peptidylprolyl isomerase E, transcript variant X1
peptidyl-prolyl cis-trans isomerase E isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
microtubule actin crosslinking factor 1, transcript variant X11
microtubule actin crosslinking factor 1, transcript variant X10
microtubule actin crosslinking factor 1, transcript variant X16
microtubule actin crosslinking factor 1, transcript variant X18
microtubule actin crosslinking factor 1, transcript variant X15
microtubule actin crosslinking factor 1, transcript variant X14
microtubule actin crosslinking factor 1, transcript variant X17
microtubule actin crosslinking factor 1, transcript variant X9
microtubule actin crosslinking factor 1, transcript variant X6
microtubule actin crosslinking factor 1, transcript variant X2
microtubule actin crosslinking factor 1, transcript variant X8
microtubule actin crosslinking factor 1, transcript variant X7
microtubule actin crosslinking factor 1, transcript variant X5
microtubule actin crosslinking factor 1, transcript variant X3
microtubule actin crosslinking factor 1, transcript variant X4
microtubule actin crosslinking factor 1, transcript variant X1
microtubule actin crosslinking factor 1, transcript variant X13
microtubule actin crosslinking factor 1, transcript variant X12
microtubule-actin cross-linking factor 1 isoform X10
microtubule-actin cross-linking factor 1 isoform X16
microtubule-actin cross-linking factor 1 isoform X18
microtubule-actin cross-linking factor 1 isoform X17
microtubule-actin cross-linking factor 1 isoform X15
microtubule-actin cross-linking factor 1 isoform X14
microtubule-actin cross-linking factor 1 isoform X11
microtubule-actin cross-linking factor 1 isoform X13
microtubule-actin cross-linking factor 1 isoform X12
microtubule-actin cross-linking factor 1 isoform X2
microtubule-actin cross-linking factor 1 isoform X8
microtubule-actin cross-linking factor 1 isoform X9
microtubule-actin cross-linking factor 1 isoform X7
microtubule-actin cross-linking factor 1 isoform X5
microtubule-actin cross-linking factor 1 isoform X3
microtubule-actin cross-linking factor 1 isoform X4
microtubule-actin cross-linking factor 1 isoform X6
microtubule-actin cross-linking factor 1 isoform X1
NADH:ubiquinone oxidoreductase subunit S5
NADH dehydrogenase [ubiquinone] iron-sulfur protein 5
antizyme inhibitor 2, transcript variant X4
antizyme inhibitor 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 4 samples with support for all annotated introns
antizyme inhibitor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
antizyme inhibitor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ring finger protein 19B, transcript variant X3
ring finger protein 19B, transcript variant X2
ring finger protein 19B, transcript variant X1
E3 ubiquitin-protein ligase RNF19B isoform X2
E3 ubiquitin-protein ligase RNF19B isoform X1
E3 ubiquitin-protein ligase RNF19B isoform X3
adenylate kinase 2, transcript variant X2
adenylate kinase 2, transcript variant X3
adenylate kinase 2, transcript variant X1
adenylate kinase 2, mitochondrial isoform X2
adenylate kinase 2, mitochondrial isoform X3
adenylate kinase 2, mitochondrial isoform X1
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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
neuron-specific calcium-binding protein hippocalcin
fibronectin type III domain containing 5
fibronectin type III domain-containing protein 5
S100P binding protein, transcript variant X5
S100P binding protein, transcript variant X4
S100P binding protein, transcript variant X2
S100P binding protein, transcript variant X1
S100P binding protein, transcript variant X3
KIAA1522 ortholog, transcript variant X1
KIAA1522 ortholog, transcript variant X2
KIAA1522 ortholog, transcript variant X3
uncharacterized protein KIAA1522 homolog isoform X1
uncharacterized protein KIAA1522 homolog isoform X2
uncharacterized protein KIAA1522 homolog isoform X3
syncoilin, intermediate filament protein, transcript variant X3
syncoilin, intermediate filament protein, transcript variant X2
syncoilin, intermediate filament protein, transcript variant X1
RB binding protein 4, chromatin remodeling factor, transcript variant X1
RB binding protein 4, chromatin remodeling factor, transcript variant X2
histone-binding protein RBBP4 isoform X2
histone-binding protein RBBP4 isoform X1
zinc finger and BTB domain containing 8 opposite strand, transcript variant X1
zinc finger and BTB domain containing 8 opposite strand, transcript variant X2
zinc finger and BTB domain-containing protein 8A-like, transcript variant X6
zinc finger and BTB domain-containing protein 8A-like, transcript variant 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 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like isoform X3
zinc finger and BTB domain-containing protein 8A-like, transcript variant X2
zinc finger and BTB domain-containing protein 8A-like, transcript variant X3
zinc finger and BTB domain-containing protein 8A-like, transcript variant X1
zinc finger and BTB domain-containing protein 8A-like, transcript variant X7
zinc finger and BTB domain-containing protein 8A-like isoform X2
zinc finger and BTB domain-containing protein 8A-like isoform X1
zinc finger and BTB domain-containing protein 8A-like, transcript variant X5
zinc finger and BTB domain-containing protein 8A-like isoform X4
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 14 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 8A-like
zinc finger and BTB domain containing 8B, transcript variant X1
zinc finger and BTB domain containing 8B, transcript variant X3
zinc finger and BTB domain containing 8B, transcript variant X4
zinc finger and BTB domain containing 8B, transcript variant X2
zinc finger and BTB domain-containing protein 8B
oligodendrocyte transcription factor 3-like
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
BSD domain containing 1, transcript variant X4
BSD domain containing 1, transcript variant X2
BSD domain containing 1, transcript variant X1
BSD domain-containing protein 1 isoform X1
BSD domain-containing protein 1 isoform X2
BSD domain containing 1, transcript variant X3
BSD domain-containing protein 1 isoform X3
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
testis-specific serine/threonine-protein kinase 3
family with sequence similarity 229 member A, transcript variant X2
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 4 samples with support for all annotated introns
family with sequence similarity 229 member A, transcript variant X4
family with sequence similarity 229 member A, transcript variant X3
family with sequence similarity 229 member A, transcript variant X1
karyopherin subunit alpha 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
karyopherin subunit alpha 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain containing 28B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
coiled-coil domain containing 28B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
coiled-coil domain-containing protein 28B
IQ motif containing C, transcript variant X2
IQ motif containing C, transcript variant X1
IQ domain-containing protein C isoform X1
IQ domain-containing protein C isoform X2
doublecortin domain containing 2B, transcript variant X2
doublecortin domain containing 2B, transcript variant X1
doublecortin domain containing 2B, transcript variant X3
doublecortin domain-containing protein 2B isoform X1
doublecortin domain-containing protein 2B isoform X2
doublecortin domain-containing protein 2B isoform X3
transmembrane protein 234, transcript variant X3
transmembrane protein 234, transcript variant X4
transmembrane protein 234, transcript variant X1
transmembrane protein 234, transcript variant X2
transmembrane protein 234, transcript variant X5
eukaryotic translation initiation factor 3 subunit I
myotubularin-related protein 9-like, transcript variant X2
myotubularin-related protein 9-like, transcript variant X3
myotubularin-related protein 9-like, transcript variant X1
myotubularin-related protein 9-like, transcript variant X4
myotubularin-related protein 9-like, transcript variant X5
myotubularin-related protein 9-like isoform X2
myotubularin-related protein 9-like isoform X1
myotubularin-related protein 9-like isoform X3
family with sequence similarity 167 member B, transcript variant X2
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 15 samples with support for all annotated introns
family with sequence similarity 167 member B, transcript variant X1
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 13 samples with support for all annotated introns
LCK proto-oncogene, Src family tyrosine kinase, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LCK proto-oncogene, Src family tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 105 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LCK proto-oncogene, Src family tyrosine kinase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 104 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane protein 39B, transcript variant X1
transmembrane protein 39B, transcript variant X3
transmembrane protein 39B, transcript variant X2
uncharacterized LOC123355413, transcript variant X1
uncharacterized LOC123355413, transcript variant X2
KH RNA binding domain containing, signal transduction associated 1, transcript variant X2
KH RNA binding domain containing, signal transduction associated 1, transcript variant X3
KH RNA binding domain containing, signal transduction associated 1, transcript variant X1
KH domain-containing, RNA-binding, signal transduction-associated protein 1 isoform X1
KH domain-containing, RNA-binding, signal transduction-associated protein 1 isoform X2
protein tyrosine phosphatase 4A2, transcript variant X3
protein tyrosine phosphatase 4A2, transcript variant X4
protein tyrosine phosphatase 4A2, transcript variant X2
protein tyrosine phosphatase 4A2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
SPOC domain containing 1, transcript variant X1
SPOC domain containing 1, transcript variant X2
SPOC domain containing 1, transcript variant X3
SPOC domain-containing protein 1 isoform X1
SPOC domain-containing protein 1 isoform X2
SPOC domain-containing protein 1 isoform X3
adhesion G protein-coupled receptor B2, transcript variant X1
adhesion G protein-coupled receptor B2, transcript variant X3
adhesion G protein-coupled receptor B2, transcript variant X2
adhesion G protein-coupled receptor B2 isoform X1
adhesion G protein-coupled receptor B2 isoform X2
adhesion G protein-coupled receptor B2, transcript variant X5
adhesion G protein-coupled receptor B2, transcript variant X6
adhesion G protein-coupled receptor B2, transcript variant X4
adhesion G protein-coupled receptor B2 isoform X3
adhesion G protein-coupled receptor B2, transcript variant X7
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 1 sample with support for all annotated introns
adhesion G protein-coupled receptor B2 isoform X4
collagen type XVI alpha 1 chain, transcript variant X4
collagen type XVI alpha 1 chain, transcript variant X2
collagen type XVI alpha 1 chain, transcript variant X1
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
collagen type XVI alpha 1 chain, transcript variant X3
collagen type XVI alpha 1 chain, transcript variant X5
tubulointerstitial nephritis antigen like 1
tubulointerstitial nephritis antigen-like
potassium voltage-gated channel subfamily Q member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium voltage-gated channel subfamily KQT member 4
nuclear transcription factor Y subunit gamma
regulating synaptic membrane exocytosis 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulating synaptic membrane exocytosis protein 3
collagen type IX alpha 2 chain, transcript variant X3
collagen type IX alpha 2 chain, transcript variant X6
collagen type IX alpha 2 chain, transcript variant X1
collagen type IX alpha 2 chain, transcript variant X2
collagen type IX alpha 2 chain, transcript variant X4
collagen type IX alpha 2 chain, transcript variant X5
uncharacterized LOC123355342, transcript variant X2
uncharacterized LOC123355342, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
CUB and sushi domain-containing protein 2
uncharacterized LOC123355343, transcript variant X1
uncharacterized LOC123355344, transcript variant X1
uncharacterized LOC123355344, transcript variant X2
uncharacterized LOC123355343, transcript variant X2
gap junction beta-5 protein-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction beta-5 protein-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction beta-5 protein-like, transcript variant X2
gap junction beta-5 protein-like, transcript variant X7
gap junction beta-5 protein-like, transcript variant X4
gap junction beta-5 protein-like, transcript variant X6
gap junction beta-5 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
gap junction protein beta 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction protein beta 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
gap junction protein alpha 4, transcript variant X4
gap junction protein alpha 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
gap junction protein alpha 4, transcript variant X2
gap junction protein alpha 4, transcript variant X1
gap junction protein alpha 4, transcript variant X3
small integral membrane protein 12, transcript variant X4
small integral membrane protein 12, transcript variant X1
small integral membrane protein 12, transcript variant X2
small integral membrane protein 12, transcript variant X3
small integral membrane protein 12 isoform X1
small integral membrane protein 12 isoform X2
uncharacterized LOC123355371, transcript variant X2
uncharacterized LOC123355371, transcript variant X3
uncharacterized LOC123355371, transcript variant X4
uncharacterized LOC123355371, transcript variant X5
uncharacterized LOC123355371, transcript variant X6
uncharacterized LOC123355371, transcript variant X1
DLG associated protein 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DLG associated protein 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DLG associated protein 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
DLG associated protein 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DLG associated protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DLG associated protein 3, transcript variant X4
disks large-associated protein 3 isoform X2
disks large-associated protein 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 24% coverage of the annotated genomic feature by RNAseq alignments
splicing factor proline and glutamine rich, transcript variant X9
splicing factor proline and glutamine rich, transcript variant X7
splicing factor proline and glutamine rich, transcript variant X8
splicing factor proline and glutamine rich, transcript variant X6
splicing factor proline and glutamine rich, transcript variant X4
splicing factor proline and glutamine rich, transcript variant X5
splicing factor proline and glutamine rich, transcript variant X2
splicing factor proline and glutamine rich, transcript variant X3
splicing factor proline and glutamine rich, transcript variant X1
splicing factor, proline- and glutamine-rich
uncharacterized LOC123355317, transcript variant X1
uncharacterized LOC123355317, transcript variant X2
zinc finger MYM-type containing 4, transcript variant X2
zinc finger MYM-type protein 4 isoform X2
zinc finger MYM-type containing 4, transcript variant X3
zinc finger MYM-type containing 4, transcript variant X1
zinc finger MYM-type protein 4 isoform X1
zinc finger MYM-type protein 4 isoform X3
interferon alpha-inducible protein 27-like protein 2, transcript variant X4
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 5 samples with support for all annotated introns
interferon alpha-inducible protein 27-like protein 2, transcript variant X1
interferon alpha-inducible protein 27-like protein 2, transcript variant X2
interferon alpha-inducible protein 27-like protein 2, transcript variant X3
interferon alpha-inducible protein 27-like protein 2 isoform X2
interferon alpha-inducible protein 27-like protein 2 isoform X1
interferon alpha-inducible protein 27-like protein 2A
interferon alpha-inducible protein 27-like protein 2B
dyslexia-associated protein KIAA0319-like protein homolog
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 3 samples with support for all annotated introns
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
argonaute RISC component 4, transcript variant X2
argonaute RISC component 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein argonaute-3, transcript variant X1
protein argonaute-3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein argonaute-3, transcript variant X2
protein argonaute-3, transcript variant X5
protein argonaute-3, transcript variant X4
collagen type VIII alpha 2 chain, transcript variant X4
collagen type VIII alpha 2 chain, transcript variant X2
collagen type VIII alpha 2 chain, transcript variant X1
collagen type VIII alpha 2 chain, transcript variant X3
trafficking protein particle complex subunit 3, transcript variant X1
trafficking protein particle complex subunit 3, transcript variant X2
trafficking protein particle complex subunit 3 isoform X1
trafficking protein particle complex subunit 3 isoform X2
angiopoietin-2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
angiopoietin-2-like, transcript variant X1
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 1 sample with support for all annotated introns
probable beta-D-xylosidase 7, transcript variant X2
probable beta-D-xylosidase 7, transcript variant X1
MAP7 domain containing 1, transcript variant X3
MAP7 domain containing 1, transcript variant X1
MAP7 domain containing 1, transcript variant X2
MAP7 domain containing 1, transcript variant X5
MAP7 domain containing 1, transcript variant X6
MAP7 domain containing 1, transcript variant X4
MAP7 domain-containing protein 1 isoform X1
MAP7 domain-containing protein 1 isoform X4
MAP7 domain-containing protein 1 isoform X3
MAP7 domain-containing protein 1 isoform X2
MAP7 domain-containing protein 1 isoform X5
MAP7 domain-containing protein 1 isoform X6
thyroid hormone receptor associated protein 3, transcript variant X1
thyroid hormone receptor associated protein 3, transcript variant X3
thyroid hormone receptor associated protein 3, transcript variant X2
thyroid hormone receptor-associated protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase 40, transcript variant X2
serine/threonine kinase 40, transcript variant X4
serine/threonine kinase 40, transcript variant X6
serine/threonine kinase 40, transcript variant X1
serine/threonine kinase 40, transcript variant X3
serine/threonine kinase 40, transcript variant X5
serine/threonine kinase 40, transcript variant X7
serine/threonine kinase 40, transcript variant X8
serine/threonine-protein kinase 40 isoform X1
serine/threonine-protein kinase 40 isoform X2
LSM10, U7 small nuclear RNA associated, transcript variant X1
LSM10, U7 small nuclear RNA associated, transcript variant X2
U7 snRNA-associated Sm-like protein LSm10
organic solute carrier partner 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
organic solute carrier partner 1, transcript variant X2
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 6 samples with support for all annotated introns
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 20 samples with support for all annotated introns
28S ribosomal protein S15, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
granulocyte colony-stimulating factor receptor
glutamate ionotropic receptor kainate type subunit 3, transcript variant X2
glutamate ionotropic receptor kainate type subunit 3, transcript variant X1
glutamate receptor ionotropic, kainate 3 isoform X2
glutamate receptor ionotropic, kainate 3 isoform X1
glutamate ionotropic receptor kainate type subunit 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MYST/Esa1 associated factor 6, transcript variant X1
MYST/Esa1 associated factor 6, transcript variant X3
chromatin modification-related protein MEAF6 isoform X1
MYST/Esa1 associated factor 6, transcript variant X2
chromatin modification-related protein MEAF6 isoform X2
dynein axonemal light intermediate chain 1, transcript variant X2
axonemal dynein light intermediate polypeptide 1 isoform X2
dynein axonemal light intermediate chain 1, transcript variant X1
axonemal dynein light intermediate polypeptide 1 isoform X1
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
chromosome 23 C1orf109 homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized protein C1orf109 homolog isoform X2
chromosome 23 C1orf109 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
chromosome 23 C1orf109 homolog, transcript variant X1
uncharacterized protein C1orf109 homolog isoform X1
cell division cycle associated 8, transcript variant X1
cell division cycle associated 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 57 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: 62 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: 27 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: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
glycoprotein endo-alpha-1,2-mannosidase-like protein
yrdC N6-threonylcarbamoyltransferase domain containing, transcript variant X2
yrdC N6-threonylcarbamoyltransferase domain containing, transcript variant X1
yrdC domain-containing protein, mitochondrial isoform X2
yrdC domain-containing protein, mitochondrial isoform X1
uncharacterized LOC123355352, transcript variant X2
uncharacterized LOC123355352, transcript variant X3
uncharacterized LOC123355352, transcript variant X1
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 3 samples with support for all annotated introns
inositol polyphosphate-5-phosphatase B, transcript variant X3
inositol polyphosphate-5-phosphatase B, transcript variant X2
inositol polyphosphate-5-phosphatase B, transcript variant X1
inositol polyphosphate-5-phosphatase B, transcript variant X4
inositol polyphosphate-5-phosphatase B, transcript variant X9
inositol polyphosphate-5-phosphatase B, transcript variant X7
inositol polyphosphate-5-phosphatase B, transcript variant X8
inositol polyphosphate-5-phosphatase B, transcript variant X6
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X4
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X2
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X3
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X1
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X5
type II inositol 1,4,5-trisphosphate 5-phosphatase isoform X6
inositol polyphosphate-5-phosphatase B, transcript variant X5
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 21 samples with support for all annotated introns
four and a half LIM domains 3, transcript variant X1
four and a half LIM domains 3, transcript variant X2
four and a half LIM domains protein 3 isoform X1
four and a half LIM domains protein 3 isoform 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 9 samples with support for all annotated introns
UTP11 small subunit processome component
probable U3 small nucleolar RNA-associated protein 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
POU domain, class 3, transcription factor 1
Ras related GTP binding C, transcript variant X1
Ras related GTP binding C, transcript variant X2
ras-related GTP-binding protein C isoform X2
ras-related GTP-binding protein C isoform X1
Ras related GTP binding C, transcript variant X3
ras-related GTP-binding protein C isoform X3
MYC binding protein, transcript variant X1
MYC binding protein, transcript variant X2
rhomboid-related protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
gap junction alpha-9 protein-like isoform X1
rhomboid-related protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
rhomboid-related protein 2-like isoform X2
uncharacterized LOC123355359, transcript variant X1
uncharacterized LOC123355359, transcript variant X2
uncharacterized LOC123355362, transcript variant X2
uncharacterized LOC123355362, transcript variant X1
uncharacterized LOC123355502, transcript variant X3
uncharacterized LOC123355502, transcript variant X4
uncharacterized LOC123355502, transcript variant X2
uncharacterized LOC123355502, transcript variant X1