Choloepus didactylus isolate mChoDid1 chromosome 22, mChoDid1.pri, whole genome shotgun sequence.
Choloepus didactylus (southern two-toed sloth)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Xenarthra; Pilosa; Folivora; Megalonychidae; Choloepus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM026711.1.\nAssembly name: mChoDid1.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/11/03. The original whole-genome shotgun project has the\naccession JADCNF000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 14-SEP-2020\nAssembly Method :: FALCON v. falcon-2018.31.08-03.06;\n FALCON-Unzip v. 6.0.0.47841; purge_dups\n github v.\n ca23030ccf4254dfd2d3a5ea90d0eed41c24f88b;\n Scaff10x v. 4.1.0; Bionano Solve v.\n 3.2.1_04122018; Salsa2 HiC v. 2.2; Polish\n pbgcpp v. 1.9.0; Longranger Align v.\n 2.2.2; freebayes v. 1.3.1; gEVAL manual\n curation v. 2020-09-14; VGP assembly\n pipeline v. 1.6\nAssembly Name :: mChoDid1.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 56.84x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Choloepus didactylus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.5\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
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: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 23% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 36% 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: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: peroxisomal biogenesis factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
H-2 class I histocompatibility antigen, Q10 alpha chain-like, 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 8 samples with support for all annotated introns
H-2 class I histocompatibility antigen, Q10 alpha chain-like, 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 12 samples with support for all annotated introns
H-2 class I histocompatibility antigen, Q10 alpha chain-like, 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 6 samples with support for all annotated introns
H-2 class I histocompatibility antigen, Q9 alpha chain-like isoform X3
H-2 class I histocompatibility antigen, Q10 alpha chain-like isoform X1
H-2 class I histocompatibility antigen, Q10 alpha chain-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
vacuolar protein sorting-associated protein 35
origin recognition complex subunit 6, 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
origin recognition complex subunit 6, 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, including 8 samples with support for all annotated introns
origin recognition complex subunit 6 isoform X1
origin recognition complex subunit 6 isoform X2
myosin light chain kinase 3, 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 4 samples with support for all annotated introns
myosin light chain kinase 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
chromosome 22 C16orf87 homolog, 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 12 samples with support for all annotated introns
UPF0547 protein C16orf87 homolog isoform X2
chromosome 22 C16orf87 homolog, transcript variant X1
UPF0547 protein C16orf87 homolog isoform X1
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
histone-lysine N-methyltransferase SETMAR-like
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
glutamic--pyruvic transaminase 2, 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 8 samples with support for all annotated introns
glutamic--pyruvic transaminase 2, transcript variant X1
DnaJ heat shock protein family (Hsp40) member A2
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 12 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: 7 Proteins
neuropilin and tolloid like 2, 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 2 samples with support for all annotated introns
neuropilin and tolloid like 2, 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 2 samples with support for all annotated introns
neuropilin and tolloid-like protein 2 isoform X2
neuropilin and tolloid-like protein 2 isoform X1
uncharacterized LOC119518406, transcript variant X2
integrin alpha FG-GAP repeat containing 1
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 12 samples with support for all annotated introns
uncharacterized LOC119518406, transcript variant X1
phosphorylase kinase regulatory subunit beta, transcript variant X5
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 10 samples with support for all annotated introns
phosphorylase kinase regulatory subunit beta, transcript variant X7
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
phosphorylase kinase regulatory subunit beta, transcript variant 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 6 samples with support for all annotated introns
phosphorylase kinase regulatory subunit beta, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
phosphorylase kinase regulatory subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit beta isoform X2
phosphorylase b kinase regulatory subunit beta isoform X1
phosphorylase kinase regulatory subunit beta, transcript variant X6
phosphorylase kinase regulatory subunit beta, transcript variant X3
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 12 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit beta isoform X3
phosphorylase kinase regulatory subunit beta, transcript variant X9
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 8 samples with support for all annotated introns
phosphorylase b kinase regulatory subunit beta isoform X5
phosphorylase kinase regulatory subunit beta, transcript variant X8
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
phosphorylase b kinase regulatory subunit beta isoform X4
phosphorylase kinase regulatory subunit beta, transcript variant X10
phosphorylase b kinase regulatory subunit beta isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily C member 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
multidrug resistance-associated protein 9
ATP binding cassette subfamily C member 11, 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 4 samples with support for all annotated introns
ATP binding cassette subfamily C member 11, 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
ATP binding cassette subfamily C member 11, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ATP-binding cassette sub-family C member 11 isoform X2
ATP-binding cassette sub-family C member 11 isoform X1
ATP-binding cassette sub-family C member 11 isoform 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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
siah E3 ubiquitin protein ligase 1, transcript variant X5
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 6 samples with support for all annotated introns
siah E3 ubiquitin protein ligase 1, 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 4 samples with support for all annotated introns
siah E3 ubiquitin protein ligase 1, transcript variant X4
siah E3 ubiquitin protein ligase 1, transcript variant X2
siah E3 ubiquitin protein ligase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
E3 ubiquitin-protein ligase SIAH1 isoform X1
E3 ubiquitin-protein ligase SIAH1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
NEDD4 binding protein 1, transcript variant X6
NEDD4 binding protein 1, transcript variant X5
NEDD4 binding protein 1, transcript variant X4
NEDD4 binding protein 1, transcript variant X3
NEDD4 binding protein 1, 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, including 10 samples with support for all annotated introns
NEDD4 binding protein 1, transcript variant X2
NEDD4 binding protein 1, transcript variant X7
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 8 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 33% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial mRNA pseudouridine synthase RPUSD3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mitochondrial mRNA pseudouridine synthase RPUSD3-like
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 4 samples 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: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: uncharacterized protein C16orf78 homolog
L-lactate dehydrogenase A chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
L-lactate dehydrogenase A chain-like isoform X2
L-lactate dehydrogenase A chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
L-lactate dehydrogenase A chain-like isoform X1
zinc finger protein 423, transcript variant X2
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 6 samples with support for all annotated introns
zinc finger protein 423, transcript variant X1
zinc finger protein 423, 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
zinc finger protein 423, 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
CTD nuclear envelope phosphatase 1 regulatory subunit 1
nuclear envelope phosphatase-regulatory subunit 1
terminal nucleotidyltransferase 4B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
terminal nucleotidyltransferase 4B, 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 10 samples with support for all annotated introns
terminal nucleotidyltransferase 4B isoform X1
terminal nucleotidyltransferase 4B isoform X2
adenylate cyclase 7, transcript variant X6
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 4 samples with support for all annotated introns
adenylate cyclase 7, transcript variant X4
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 10 samples with support for all annotated introns
adenylate cyclase 7, transcript variant X5
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
adenylate cyclase 7, transcript variant X3
adenylate cyclase 7, transcript variant X2
adenylate cyclase 7, transcript variant X8
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 10 samples with support for all annotated introns
adenylate cyclase 7, transcript variant X1
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 12 samples with support for all annotated introns
adenylate cyclase 7, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
bromodomain containing 7, 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 10 samples with support for all annotated introns
bromodomain containing 7, 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 10 samples with support for all annotated introns
bromodomain-containing protein 7 isoform X2
bromodomain-containing protein 7 isoform X1
NKD inhibitor of WNT signaling pathway 1
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
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 8 samples with support for all annotated introns
nucleotide binding oligomerization domain containing 2
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 8 samples with support for all annotated introns
nucleotide-binding oligomerization domain-containing protein 2
CYLD lysine 63 deubiquitinase, transcript variant X1
CYLD lysine 63 deubiquitinase, transcript variant X5
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 10 samples with support for all annotated introns
CYLD lysine 63 deubiquitinase, transcript variant X6
CYLD lysine 63 deubiquitinase, transcript variant X4
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 12 samples with support for all annotated introns
CYLD lysine 63 deubiquitinase, transcript variant X3
CYLD lysine 63 deubiquitinase, transcript variant X2
ubiquitin carboxyl-terminal hydrolase CYLD isoform X1
ubiquitin carboxyl-terminal hydrolase CYLD isoform X2
uncharacterized LOC119518923, transcript variant X4
uncharacterized LOC119518923, transcript variant X2
uncharacterized LOC119518923, transcript variant X3
uncharacterized LOC119518923, transcript variant X1
uncharacterized LOC119518924, transcript variant X1
uncharacterized LOC119518924, transcript variant X3
uncharacterized LOC119518924, transcript variant X4
uncharacterized LOC119518924, transcript variant X2
spalt like transcription factor 1, 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 6 samples with support for all annotated introns
spalt like transcription factor 1, 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 6 samples with support for all annotated introns
uncharacterized LOC119518904, transcript variant X2
uncharacterized LOC119518904, transcript variant X1
uncharacterized LOC119518904, transcript variant X3
uncharacterized LOC119518904, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
uncharacterized LOC119518971, transcript variant X2
uncharacterized LOC119518971, transcript variant X1
glycine cleavage system H protein, mitochondrial-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
TOX high mobility group box family member 3, 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 2 samples with support for all annotated introns
TOX high mobility group box family member 3 isoform X3
TOX high mobility group box family member 3, transcript variant X2
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 8 samples with support for all annotated introns
TOX high mobility group box family member 3, transcript variant X1
TOX high mobility group box family member 3, 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 2 samples with support for all annotated introns
TOX high mobility group box family member 3 isoform X2
TOX high mobility group box family member 3 isoform X1
TOX high mobility group box family member 3 isoform X4
chromodomain helicase DNA binding protein 9, transcript variant X3
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
chromodomain helicase DNA binding protein 9, transcript variant X2
chromodomain helicase DNA binding protein 9, 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
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
28S ribosomal protein S33, mitochondrial-like
chromodomain-helicase-DNA-binding protein 9 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins
chromodomain helicase DNA binding protein 9, 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 2 samples with support for all annotated introns
chromodomain-helicase-DNA-binding protein 9 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins
chromodomain helicase DNA binding protein 9, transcript variant X4
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 4 samples with support for all annotated introns
chromodomain helicase DNA binding protein 9, transcript variant X6
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 4 samples with support for all annotated introns
chromodomain-helicase-DNA-binding protein 9 isoform X2
chromodomain-helicase-DNA-binding protein 9 isoform X4
chromodomain helicase DNA binding protein 9, transcript variant X7
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 4 samples with support for all annotated introns
chromodomain-helicase-DNA-binding protein 9 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 159 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
RB transcriptional corepressor like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
RB transcriptional corepressor like 2, transcript variant X3
RB transcriptional corepressor like 2, 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 12 samples with support for all annotated introns
retinoblastoma-like protein 2 isoform X1
retinoblastoma-like protein 2 isoform X2
retinoblastoma-like protein 2 isoform X3
RB transcriptional corepressor like 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
retinoblastoma-like protein 2 isoform X4
AKT interacting protein, transcript variant X4
AKT interacting protein, 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, including 12 samples with support for all annotated introns
AKT interacting protein, transcript variant X3
AKT interacting protein, 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 2 samples with support for all annotated introns
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 6 samples with support for all annotated introns
FTO alpha-ketoglutarate dependent dioxygenase, 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 6 samples with support for all annotated introns
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X3
FTO alpha-ketoglutarate dependent dioxygenase, 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 10 samples with support for all annotated introns
FTO alpha-ketoglutarate dependent dioxygenase, transcript variant X2
alpha-ketoglutarate-dependent dioxygenase FTO isoform X1
alpha-ketoglutarate-dependent dioxygenase FTO isoform X2
alpha-ketoglutarate-dependent dioxygenase FTO isoform X3
alpha-ketoglutarate-dependent dioxygenase FTO isoform X4
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 12 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-3
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 4 samples with support for all annotated introns
iroquois-class homeodomain protein IRX-5
iroquois homeobox 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
iroquois homeobox 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
iroquois-class homeodomain protein IRX-6 isoform X2
iroquois-class homeodomain protein IRX-6 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
lysophosphatidylcholine acyltransferase 2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent noradrenaline transporter
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
carboxylesterase 5A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
carboxylesterase 5A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
G protein subunit alpha o1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
G protein subunit alpha o1, transcript variant X2
G protein subunit alpha o1, transcript variant X1
guanine nucleotide-binding protein G(o) subunit alpha isoform X1
guanine nucleotide-binding protein G(o) subunit alpha isoform X2
G protein subunit alpha o1, transcript variant X4
guanine nucleotide-binding protein G(o) subunit alpha isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
cleavage and polyadenylation specificity factor subunit 5
2-oxoglutarate and iron dependent oxygenase domain containing 1, transcript variant X2
2-oxoglutarate and iron dependent oxygenase domain containing 1, 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 12 samples with support for all annotated introns
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins
metallothionein-2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
metallothionein-2-like, 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 12 samples with support for all annotated introns
nuclear pore complex protein Nup93 isoform X1
nuclear pore complex protein Nup93 isoform X2
proteasome subunit alpha type-1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
proteasome subunit alpha type-1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
proteasome subunit alpha type-1-like isoform X1
proteasome subunit alpha type-1-like isoform X2
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
nuclear pore complex protein Nup93 isoform X3
solute carrier family 12 member 3, transcript variant X5
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 2 samples with support for all annotated introns
solute carrier family 12 member 3, 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 2 samples with support for all annotated introns
solute carrier family 12 member 3, transcript variant X9
solute carrier family 12 member 3, transcript variant X7
solute carrier family 12 member 3, transcript variant X3
solute carrier family 12 member 3, transcript variant X10
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 2 samples with support for all annotated introns
solute carrier family 12 member 3, transcript variant X4
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
solute carrier family 12 member 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 12 member 3, transcript variant X2
solute carrier family 12 member 3, transcript variant X8
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
solute carrier family 12 member 3, transcript variant X11
solute carrier family 12 member 3, transcript variant X12
solute carrier family 12 member 3, transcript variant X15
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
solute carrier family 12 member 3, transcript variant X18
solute carrier family 12 member 3 isoform X1
solute carrier family 12 member 3 isoform X3
solute carrier family 12 member 3 isoform X4
solute carrier family 12 member 3 isoform X2
solute carrier family 12 member 3 isoform X5
solute carrier family 12 member 3 isoform X9
solute carrier family 12 member 3 isoform X7
solute carrier family 12 member 3 isoform X10
solute carrier family 12 member 3 isoform X6
solute carrier family 12 member 3 isoform X8
solute carrier family 12 member 3 isoform X11
solute carrier family 12 member 3 isoform X12
solute carrier family 12 member 3 isoform X17
solute carrier family 12 member 3, transcript variant X14
solute carrier family 12 member 3, transcript variant X13
solute carrier family 12 member 3 isoform X13
solute carrier family 12 member 3 isoform X14
solute carrier family 12 member 3, transcript variant X16
solute carrier family 12 member 3 isoform X15
solute carrier family 12 member 3, transcript variant X17
solute carrier family 12 member 3 isoform X16
homocysteine inducible ER protein with ubiquitin like domain 1, transcript variant X1
homocysteine inducible ER protein with ubiquitin like domain 1, 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 12 samples with support for all annotated introns
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 1 protein isoform X1
homocysteine-responsive endoplasmic reticulum-resident ubiquitin-like domain member 1 protein isoform X2
uncharacterized LOC119518954, transcript variant X2
uncharacterized LOC119518954, transcript variant X1
NLR family CARD domain containing 5, transcript variant X10
NLR family CARD domain containing 5, transcript variant X8
NLR family CARD domain containing 5, transcript variant X5
NLR family CARD domain containing 5, transcript variant X1
NLR family CARD domain containing 5, transcript variant X6
NLR family CARD domain containing 5, transcript variant X4
NLR family CARD domain containing 5, transcript variant X7
NLR family CARD domain containing 5, transcript variant X3
NLR family CARD domain containing 5, 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 4 samples with support for all annotated introns
NLR family CARD domain containing 5, transcript variant X9
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 12 samples with support for all annotated introns
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 8 samples with support for all annotated introns
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 6 samples with support for all annotated introns
proteasome activator subunit 3 interacting protein 1, transcript variant X4
proteasome activator subunit 3 interacting protein 1, transcript variant X3
proteasome activator subunit 3 interacting protein 1, transcript variant X6
proteasome activator subunit 3 interacting protein 1, transcript variant X5
proteasome activator subunit 3 interacting protein 1, transcript variant X1
proteasome activator subunit 3 interacting protein 1, transcript variant X7
proteasome activator subunit 3 interacting protein 1, transcript variant X2
ring finger and SPRY domain containing 1, 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 10 samples with support for all annotated introns
ring finger and SPRY domain containing 1, 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 8 samples with support for all annotated introns
RING finger and SPRY domain-containing protein 1
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X1
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X4
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
ADP-ribosylation factor-like protein 2-binding protein isoform X1
ADP-ribosylation factor-like protein 2-binding protein isoform X4
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X5
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 10 samples with support for all annotated introns
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X2
ADP-ribosylation factor-like protein 2-binding protein isoform X2
ADP-ribosylation factor-like protein 2-binding protein isoform X5
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X6
ADP ribosylation factor like GTPase 2 binding protein, transcript variant X3
ADP-ribosylation factor-like protein 2-binding protein isoform X3
ADP-ribosylation factor-like protein 2-binding protein isoform X6
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
C-C motif chemokine ligand 22, transcript variant X2
C-C motif chemokine ligand 22, transcript variant X1
C-X3-C motif chemokine ligand 1, transcript variant X3
C-X3-C motif chemokine ligand 1, transcript variant X2
C-X3-C motif chemokine ligand 1, transcript variant X1
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 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cytokine induced apoptosis inhibitor 1, transcript variant X4
cytokine induced apoptosis inhibitor 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 12 samples with support for all annotated introns
cytokine induced apoptosis inhibitor 1, transcript variant X2
cytokine induced apoptosis inhibitor 1, transcript variant X3
ubiquinone biosynthesis protein COQ9, mitochondrial isoform X1
ubiquinone biosynthesis protein COQ9, mitochondrial isoform X2
RNA polymerase II subunit C, transcript variant X1
RNA polymerase II subunit C, transcript variant X2
DNA-directed RNA polymerase II subunit RPB3 isoform X1
DNA-directed RNA polymerase II subunit RPB3 isoform X2
RNA polymerase II subunit C, transcript variant X3
DNA-directed RNA polymerase II subunit RPB3 isoform 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 8 samples with support for all annotated introns
coiled-coil domain-containing protein 102A
adhesion G protein-coupled receptor G5, transcript variant X1
adhesion G protein-coupled receptor G5, transcript variant X4
adhesion G protein-coupled receptor G5, transcript variant X6
adhesion G protein-coupled receptor G5, transcript variant X5
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
adhesion G protein-coupled receptor G5, transcript variant X7
adhesion G protein-coupled receptor G5, transcript variant X2
adhesion G protein-coupled receptor G5, transcript variant X3
adhesion G-protein coupled receptor G5 isoform X3
adhesion G-protein coupled receptor G5 isoform X5
adhesion G-protein coupled receptor G5 isoform X1
adhesion G-protein coupled receptor G5 isoform X2
adhesion G-protein coupled receptor G5 isoform X4
adhesion G protein-coupled receptor G1, transcript variant X3
adhesion G protein-coupled receptor G1, transcript variant X1
adhesion G protein-coupled receptor G1, 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 4 samples with support for all annotated introns
adhesion G protein-coupled receptor G1, 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 2 samples with support for all annotated introns
adhesion G protein-coupled receptor G1, 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 6 samples with support for all annotated introns
adhesion G protein-coupled receptor G3, transcript variant X1
adhesion G protein-coupled receptor G3, transcript variant X2
adhesion G protein-coupled receptor G3, transcript variant X3
adhesion G protein-coupled receptor G3 isoform X1
adhesion G protein-coupled receptor G3 isoform X3
adhesion G protein-coupled receptor G3 isoform X2
dynein regulatory complex subunit 7, 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 6 samples with support for all annotated introns
dynein regulatory complex subunit 7, transcript variant X3
dynein regulatory complex subunit 7, transcript variant X1
dynein regulatory complex subunit 7 isoform X1
dynein regulatory complex subunit 7 isoform X2
katanin regulatory subunit B1, 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 12 samples with support for all annotated introns
katanin regulatory subunit B1, transcript variant X3
katanin regulatory subunit B1, transcript variant X2
katanin p80 WD40 repeat-containing subunit B1 isoform X1
katanin p80 WD40 repeat-containing subunit B1 isoform X2
katanin regulatory subunit B1, transcript variant X4
katanin p80 WD40 repeat-containing subunit B1 isoform X3
kinesin family member C3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
kinesin family member C3, 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 8 samples with support for all annotated introns
kinesin family member C3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
kinesin family member C3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
kinesin family member C3, transcript variant X4
uncharacterized LOC119518516, 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 10 samples with support for all annotated introns
uncharacterized LOC119518516, transcript variant X5
uncharacterized LOC119518516, transcript variant X4
uncharacterized LOC119518516, transcript variant X2
uncharacterized LOC119518516, transcript variant X1
uncharacterized LOC119518946, transcript variant X2
cyclic nucleotide gated channel subunit beta 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 44% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated cation channel beta-1
uncharacterized LOC119518946, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
testis, prostate and placenta-expressed protein
U6 snRNA biogenesis phosphodiesterase 1, transcript variant X1
U6 snRNA biogenesis phosphodiesterase 1, transcript variant X2
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 10 samples with support for all annotated introns
matrix metallopeptidase 15, transcript variant X1
matrix metallopeptidase 15, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
cilia and flagella associated protein 20
cilia- and flagella-associated protein 20
52 kDa repressor of the inhibitor of the protein kinase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins
casein kinase 2 alpha 2, 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 10 samples with support for all annotated introns
casein kinase 2 alpha 2, transcript variant X1
coiled-coil domain containing 113, 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 8 samples with support for all annotated introns
coiled-coil domain containing 113, transcript variant X3
coiled-coil domain containing 113, transcript variant X2
coiled-coil domain-containing protein 113 isoform X1
coiled-coil domain-containing protein 113 isoform X2
coiled-coil domain-containing protein 113 isoform X3
DNA replication complex GINS protein PSF3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
NDRG family member 4, transcript variant X3
NDRG family member 4, transcript variant X2
NDRG family member 4, transcript variant X1
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 8 samples with support for all annotated introns
NDRG family member 4, transcript variant X4
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 6 samples with support for all annotated introns
NDRG family member 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
SET domain containing 6, protein lysine methyltransferase, transcript variant X3
SET domain containing 6, protein lysine methyltransferase, transcript variant X1
SET domain containing 6, protein lysine methyltransferase, 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 8 samples with support for all annotated introns
N-lysine methyltransferase SETD6 isoform X1
N-lysine methyltransferase SETD6 isoform X2
N-lysine methyltransferase SETD6 isoform X3
CCR4-NOT transcription complex subunit 1, transcript variant X4
CCR4-NOT transcription complex subunit 1, transcript variant X6
CCR4-NOT transcription complex subunit 1, transcript variant X2
CCR4-NOT transcription complex subunit 1, transcript variant X7
CCR4-NOT transcription complex subunit 1, transcript variant X3
CCR4-NOT transcription complex subunit 1, transcript variant X5
CCR4-NOT transcription complex subunit 1, transcript variant X1
CCR4-NOT transcription complex subunit 1 isoform X4
CCR4-NOT transcription complex subunit 1 isoform X6
CCR4-NOT transcription complex subunit 1 isoform X2
CCR4-NOT transcription complex subunit 1 isoform X7
CCR4-NOT transcription complex subunit 1 isoform X3
CCR4-NOT transcription complex subunit 1 isoform X5
CCR4-NOT transcription complex subunit 1 isoform X1
CCR4-NOT transcription complex subunit 1, transcript variant X8
CCR4-NOT transcription complex subunit 1 isoform X8
CCR4-NOT transcription complex subunit 1, transcript variant X9
CCR4-NOT transcription complex subunit 1 isoform X9
COORDINATES: nucleotide motif:Rfam:12.0:RF00404
COORDINATES: nucleotide motif:Rfam:12.0:RF00407
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
solute carrier family 38 member 7, transcript variant X4
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
solute carrier family 38 member 7, transcript variant X3
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 8 samples with support for all annotated introns
solute carrier family 38 member 7, transcript variant X1
solute carrier family 38 member 7, transcript variant X2
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
putative sodium-coupled neutral amino acid transporter 7 isoform X1
solute carrier family 38 member 7, transcript variant X5
putative sodium-coupled neutral amino acid transporter 7 isoform 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 12 samples with support for all annotated introns
aspartate aminotransferase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
endogenous retrovirus group K member 113 Pro protein-like
serine/arginine-rich splicing factor 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 20% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 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: 32 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 32% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 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: 37 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
spermatogenesis-associated protein 2-like protein
thymidine kinase 2, transcript variant X2
thymidine kinase 2, transcript variant X1
thymidine kinase 2, mitochondrial isoform X2
thymidine kinase 2, mitochondrial isoform X1
chemokine like factor, transcript variant X1
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 4 samples with support for all annotated introns
chemokine like factor, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 1, transcript variant X1
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
CKLF-like MARVEL transmembrane domain-containing protein 1, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 1 isoform X1
CKLF-like MARVEL transmembrane domain-containing protein 2 isoform X2
CKLF like MARVEL transmembrane domain containing 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
CKLF-like MARVEL transmembrane domain-containing protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
CKLF like MARVEL transmembrane domain containing 3
CKLF-like MARVEL transmembrane domain-containing protein 3
CKLF like MARVEL transmembrane domain containing 4
CKLF-like MARVEL transmembrane domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 29% coverage of the annotated genomic feature by RNAseq alignments
dynein cytoplasmic 1 light intermediate chain 2, 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 12 samples with support for all annotated introns
dynein cytoplasmic 1 light intermediate chain 2, transcript variant X1
dynein cytoplasmic 1 light intermediate chain 2, transcript variant X3
cytoplasmic dynein 1 light intermediate chain 2 isoform X2
cytoplasmic dynein 1 light intermediate chain 2 isoform X1
cytoplasmic dynein 1 light intermediate chain 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
telomere repeat binding bouquet formation protein 1
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
telomere repeats-binding bouquet formation protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
NEDD8 activating enzyme E1 subunit 1, transcript variant X2
NEDD8 activating enzyme E1 subunit 1, transcript variant X1
NEDD8-activating enzyme E1 regulatory subunit isoform X2
NEDD8-activating enzyme E1 regulatory subunit isoform X1
carbonic anhydrase 7, transcript variant X1
carbonic anhydrase 7, transcript variant X4
carbonic anhydrase 7, transcript variant X3
carbonic anhydrase 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehyrogenase phosphatase catalytic subunit 2, transcript variant X1
pyruvate dehyrogenase phosphatase catalytic subunit 2, transcript variant X2
pyruvate dehydrogenase [acetyl-transferring]-phosphatase 2, mitochondrial
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
RRAD, Ras related glycolysis inhibitor and calcium channel regulator
cytosolic iron-sulfur assembly component 2B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
carboxylesterase 2, transcript variant 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 4 samples with support for all annotated introns
carboxylesterase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
carboxylesterase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
carboxylesterase 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
carboxylesterase 3, transcript variant X1
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
carboxylesterase 3, transcript variant X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; substituted 4 bases at 4 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: carboxylesterase 4A
core-binding factor subunit beta, transcript variant X2
core-binding factor subunit beta, transcript variant X1
core-binding factor subunit beta isoform X1
core-binding factor subunit beta isoform X2
chromosome 22 C16orf70 homolog, transcript variant X1
chromosome 22 C16orf70 homolog, 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 10 samples with support for all annotated introns
UPF0183 protein C16orf70 homolog isoform X1
UPF0183 protein C16orf70 homolog isoform X2
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 9
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
tumor necrosis factor receptor type 1-associated DEATH domain protein
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 7 bases in 5 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples 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: inserted 7 bases in 5 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: F-box/LRR-repeat protein 8
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: heat shock factor protein 4
nucleolar protein 3, transcript variant X2
nucleolar protein 3, transcript variant X5
nucleolar protein 3, transcript variant X3
nucleolar protein 3, transcript variant X4
nucleolar protein 3, 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 2 samples with support for all annotated introns
uncharacterized protein KIAA0895-like homolog isoform X2
uncharacterized protein KIAA0895-like homolog isoform X1
exocyst complex component 3-like protein
E2F transcription factor 4, transcript variant X1
E2F transcription factor 4, 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 8 samples with support for all annotated introns
engulfment and cell motility 3, transcript variant X4
engulfment and cell motility 3, transcript variant X5
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 8 samples with support for all annotated introns
engulfment and cell motility 3, transcript variant X2
engulfment and cell motility 3, transcript variant X1
engulfment and cell motility 3, transcript variant X3
engulfment and cell motility protein 3 isoform X4
engulfment and cell motility protein 3 isoform X5
engulfment and cell motility protein 3 isoform X2
engulfment and cell motility protein 3 isoform X1
engulfment and cell motility protein 3 isoform X3
engulfment and cell motility 3, transcript variant X6
engulfment and cell motility protein 3 isoform X6
leucine-rich repeat-containing protein 29
transmembrane protein 208, transcript variant X1
transmembrane protein 208, 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 12 samples with support for all annotated introns
solute carrier family 9 member A5, transcript variant X1
solute carrier family 9 member A5, transcript variant X2
solute carrier family 9 member A5, transcript variant X6
solute carrier family 9 member A5, transcript variant X7
solute carrier family 9 member A5, transcript variant X8
solute carrier family 9 member A5, transcript variant X5
solute carrier family 9 member A5, transcript variant X9
solute carrier family 9 member A5, transcript variant X10
solute carrier family 9 member A5, transcript variant X4
solute carrier family 9 member A5, transcript variant X3
pleckstrin homology and RhoGEF domain containing G4, transcript variant X1
pleckstrin homology and RhoGEF domain containing G4, transcript variant X4
pleckstrin homology and RhoGEF domain containing G4, transcript variant X2
pleckstrin homology and RhoGEF domain containing G4, transcript variant X3
potassium channel tetramerization domain containing 19
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
BTB/POZ domain-containing protein KCTD19
leucine rich repeat containing 36, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
leucine-rich repeat-containing protein 36 isoform X1
leucine rich repeat containing 36, transcript variant X2
leucine-rich repeat-containing protein 36 isoform X2
tubulin polymerization promoting protein family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
tubulin polymerization promoting protein family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tubulin polymerization promoting protein family member 3, transcript variant X3
tubulin polymerization-promoting protein family member 3
zinc finger DHHC-type containing 1, transcript variant X2
zinc finger DHHC-type containing 1, transcript variant X1
corticosteroid 11-beta-dehydrogenase isozyme 2
agouti related neuropeptide, 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 2 samples with support for all annotated introns
agouti related neuropeptide, transcript variant X1
agouti related neuropeptide, transcript variant X4
agouti related neuropeptide, transcript variant X3
RHO family interacting cell polarization regulator 1, transcript variant X1
RHO family interacting cell polarization regulator 1, transcript variant X2
rho family-interacting cell polarization regulator 1 isoform X1
rho family-interacting cell polarization regulator 1 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcriptional repressor CTCF
capping protein regulator and myosin 1 linker 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
LOW QUALITY PROTEIN: capping protein, Arp2/3 and myosin-I linker protein 2
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X2
ACD shelterin complex subunit and telomerase recruitment factor, transcript variant X1
adrenocortical dysplasia protein homolog isoform X2
adrenocortical dysplasia protein homolog isoform X1
par-6 family cell polarity regulator alpha, transcript variant X2
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
par-6 family cell polarity regulator alpha, transcript variant X1
partitioning defective 6 homolog alpha isoform X1
partitioning defective 6 homolog alpha isoform X2
enkurin domain containing 1, transcript variant X2
enkurin domain containing 1, transcript variant X1
enkurin domain-containing protein 1 isoform X2
enkurin domain-containing protein 1 isoform X1
uncharacterized protein C16orf86 homolog
glucose-fructose oxidoreductase domain containing 2, 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 4 samples with support for all annotated introns
glucose-fructose oxidoreductase domain containing 2, transcript variant X5
glucose-fructose oxidoreductase domain-containing protein 2 isoform X4
glucose-fructose oxidoreductase domain-containing protein 2 isoform X3
glucose-fructose oxidoreductase domain containing 2, transcript variant X3
glucose-fructose oxidoreductase domain containing 2, transcript variant X1
glucose-fructose oxidoreductase domain containing 2, transcript variant X2
glucose-fructose oxidoreductase domain containing 2, transcript variant X4
glucose-fructose oxidoreductase domain-containing protein 2 isoform X1
glucose-fructose oxidoreductase domain-containing protein 2 isoform X2
RAN binding protein 10, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
RAN binding protein 10, transcript variant X1
RAN binding protein 10, transcript variant X2
RAN binding protein 10, transcript variant X4
translin associated factor X interacting protein 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 2 samples with support for all annotated introns
translin-associated factor X-interacting protein 1 isoform 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
translin associated factor X interacting protein 1, transcript variant X2
translin-associated factor X-interacting protein 1 isoform X2
centromere protein T, transcript variant X2
centromere protein T, 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
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
nuclear transport factor 2, transcript variant X1
nuclear transport factor 2, transcript variant X2
enhancer of mRNA decapping 4, transcript variant X2
enhancer of mRNA-decapping protein 4 isoform X2
enhancer of mRNA decapping 4, transcript variant X1
enhancer of mRNA-decapping protein 4 isoform 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
protein serine kinase H1, transcript variant X1
protein serine kinase H1, transcript variant X2
protein serine kinase H1, transcript variant X3
serine/threonine-protein kinase H1 isoform X1
serine/threonine-protein kinase H1 isoform X2
serine/threonine-protein kinase H1 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% 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 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: chymotrypsin-like protease CTRL-1
proteasome 20S subunit beta 10, transcript variant X2
proteasome 20S subunit beta 10, transcript variant X1
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 12 samples with support for all annotated introns
proteasome subunit beta type-10 isoform X2
proteasome subunit beta type-10 isoform X1
lecithin-cholesterol acyltransferase, transcript variant X1
lecithin-cholesterol acyltransferase, transcript variant X2
phosphatidylcholine-sterol acyltransferase isoform X1
phosphatidylcholine-sterol acyltransferase isoform X2
solute carrier family 12 member 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 12 member 4, 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 4 samples with support for all annotated introns
solute carrier family 12 member 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
solute carrier family 12 member 4 isoform X3
solute carrier family 12 member 4 isoform X2
solute carrier family 12 member 4 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
dipeptidase 2-like, transcript variant X4
dipeptidase 2-like, transcript variant X13
dipeptidase 2-like, transcript variant X3
dipeptidase 2-like, transcript variant X10
dipeptidase 2-like, transcript variant X11
dipeptidase 2-like, transcript variant X14
dipeptidase 2-like, transcript variant X9
dipeptidase 2-like, transcript variant X5
dipeptidase 2-like, transcript variant X8
dipeptidase 2-like, transcript variant X6
dipeptidase 2-like, transcript variant X12
dipeptidase 2-like, transcript variant X7
dipeptidase 2-like, transcript variant X2
dipeptidase 2-like, transcript variant X1
LOW QUALITY PROTEIN: DPEP2 neighbor protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
probable ATP-dependent RNA helicase DDX28
dihydrouridine synthase 2, transcript variant X1
dihydrouridine synthase 2, transcript variant X2
probable ribosome biogenesis protein RLP24
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X1
dihydrouridine synthase 2, transcript variant X3
tRNA-dihydrouridine(20) synthase [NAD(P)+]-like isoform X2
nuclear factor of activated T cells 3, 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 12 samples with support for all annotated introns
nuclear factor of activated T cells 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
nuclear factor of activated T cells 3, transcript variant X2
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 12 samples with support for all annotated introns
nuclear factor of activated T-cells, cytoplasmic 3 isoform X2
nuclear factor of activated T-cells, cytoplasmic 3 isoform X3
nuclear factor of activated T-cells, cytoplasmic 3 isoform X1
epithelial splicing regulatory protein 2, 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 2 samples with support for all annotated introns
epithelial splicing regulatory protein 2, transcript variant X4
epithelial splicing regulatory protein 2, transcript variant X6
epithelial splicing regulatory protein 2, transcript variant X5
epithelial splicing regulatory protein 2, transcript variant X3
epithelial splicing regulatory protein 2, transcript variant X8
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 6 samples with support for all annotated introns
epithelial splicing regulatory protein 2, transcript variant X7
epithelial splicing regulatory protein 2, transcript variant X1
epithelial splicing regulatory protein 2, transcript variant X9
epithelial splicing regulatory protein 2 isoform X3
epithelial splicing regulatory protein 2 isoform X2
epithelial splicing regulatory protein 2 isoform X1
epithelial splicing regulatory protein 2 isoform X4
phospholipase A2 group XV, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
phospholipase A2 group XV, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipase A2 group XV, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
phospholipase A2 group XV, transcript variant X3
phospholipase A2 group XV, transcript variant X1
solute carrier family 7 member 6, transcript variant X3
solute carrier family 7 member 6, 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 4 samples with support for all annotated introns
solute carrier family 7 member 6, transcript variant X5
solute carrier family 7 member 6, transcript variant X6
solute carrier family 7 member 6, transcript variant X2
solute carrier family 7 member 6, transcript variant X4
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
solute carrier family 7 member 6 opposite strand, transcript variant X2
solute carrier family 7 member 6 opposite strand, transcript variant X1
probable RNA polymerase II nuclear localization protein SLC7A6OS isoform X2
probable RNA polymerase II nuclear localization protein SLC7A6OS isoform X1
protein arginine methyltransferase 7, transcript variant X2
protein arginine methyltransferase 7, transcript variant X1
protein arginine methyltransferase 7, transcript variant X3
protein arginine N-methyltransferase 7 isoform X1
protein arginine N-methyltransferase 7 isoform X2
protein arginine methyltransferase 7, transcript variant X4
39S ribosomal protein L42, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
ZFP90 zinc finger protein, transcript variant X7
ZFP90 zinc finger protein, transcript variant X6
ZFP90 zinc finger protein, transcript variant X2
ZFP90 zinc finger protein, transcript variant X8
ZFP90 zinc finger protein, transcript variant X5
ZFP90 zinc finger protein, transcript variant X1
ZFP90 zinc finger protein, transcript variant X3
ZFP90 zinc finger protein, transcript variant X4
zinc finger protein 90 homolog isoform X2
zinc finger protein 90 homolog isoform X5
zinc finger protein 90 homolog isoform X1
zinc finger protein 90 homolog isoform X4
zinc finger protein 90 homolog 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 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
transport and golgi organization 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
transport and Golgi organization protein 6 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 213 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
hyaluronan synthase 3, 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
hyaluronan synthase 3, transcript variant X1
DERPC proline and glycine rich nuclear protein
decreased expression in renal and prostate cancer protein
chromosome transmission fidelity factor 8
chromosome transmission fidelity protein 8 homolog
UTP4 small subunit processome component, transcript variant X2
UTP4 small subunit processome component, transcript variant X1
U3 small nucleolar RNA-associated protein 4 homolog
vacuolar protein sorting 4 homolog A, transcript variant X2
vacuolar protein sorting 4 homolog A, 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 12 samples with support for all annotated introns
vacuolar protein sorting 4 homolog A, transcript variant X3
vacuolar protein sorting-associated protein 4A isoform X1
vacuolar protein sorting-associated protein 4A isoform X2
vacuolar protein sorting-associated protein 4A isoform X3
component of oligomeric golgi complex 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
conserved oligomeric Golgi complex subunit 8 isoform X2
component of oligomeric golgi complex 8, transcript variant X1
conserved oligomeric Golgi complex subunit 8 isoform X1
nucleolar pre-rRNA processing protein NIP7
60S ribosome subunit biogenesis protein NIP7 homolog
transmembrane emp24 domain-containing protein 6
telomeric repeat binding factor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
telomeric repeat binding factor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
telomeric repeat-binding factor 2 isoform X2
telomeric repeat-binding factor 2 isoform X1
cytochrome b5 type B, transcript variant X4
cytochrome b5 type B, transcript variant X2
cytochrome b5 type B, transcript variant X5
cytochrome b5 type B, transcript variant X3
cytochrome b5 type B, transcript variant X6
cytochrome b5 type B, transcript variant X1
cyclin-dependent kinases regulatory subunit 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples 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 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: nuclear factor of activated T-cells 5
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
NIN1 (RPN12) binding protein 1 homolog, transcript variant X2
NIN1 (RPN12) binding protein 1 homolog, transcript variant X1
WW domain containing E3 ubiquitin protein ligase 2, transcript variant X2
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 10 samples with support for all annotated introns
WW domain containing E3 ubiquitin protein ligase 2, transcript variant X1
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 2 samples with support for all annotated introns
NEDD4-like E3 ubiquitin-protein ligase WWP2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
26S proteasome non-ATPase regulatory subunit 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RNA-binding protein 27-like
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
uncharacterized LOC119518968, transcript variant X1
uncharacterized LOC119518968, transcript variant X2
zinc finger homeobox 3, transcript variant X1
zinc finger homeobox 3, transcript variant X2
zinc finger homeobox 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119518793, transcript variant X2
uncharacterized LOC119518793, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins
polyamine modulated factor 1 binding protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
polyamine-modulated factor 1-binding protein 1
pre-mRNA-splicing factor ATP-dependent RNA helicase PRP16
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
dihydroorotate dehydrogenase (quinone), mitochondrial
IST1 factor associated with ESCRT-III, transcript variant X2
IST1 factor associated with ESCRT-III, transcript variant X1
IST1 factor associated with ESCRT-III, transcript variant X3
IST1 factor associated with ESCRT-III, transcript variant X4
zinc finger protein 821, transcript variant X6
zinc finger protein 821, transcript variant X8
zinc finger protein 821, transcript variant X7
zinc finger protein 821, transcript variant X5
zinc finger protein 821, transcript variant X3
zinc finger protein 821, transcript variant X4
zinc finger protein 821, transcript variant X2
zinc finger protein 821, transcript variant X9
zinc finger protein 821, transcript variant X10
zinc finger protein 821, transcript variant X11
zinc finger protein 821, transcript variant X1
adaptor related protein complex 1 subunit gamma 1, transcript variant X2
adaptor related protein complex 1 subunit gamma 1, transcript variant X1
adaptor related protein complex 1 subunit gamma 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 112 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00576
PH domain and leucine rich repeat protein phosphatase 2, transcript variant X1
PH domain and leucine rich repeat protein phosphatase 2, transcript variant X2
PH domain leucine-rich repeat-containing protein phosphatase 2 isoform X1
PH domain leucine-rich repeat-containing protein phosphatase 2 isoform X2
MARVEL domain containing 3, transcript variant X1
MARVEL domain-containing protein 3 isoform X1
MARVEL domain containing 3, transcript variant X2
MARVEL domain-containing protein 3 isoform X2
tyrosine aminotransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
tyrosine aminotransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 40% 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: 13 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 8 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples 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 8 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 19
zinc finger protein 23, transcript variant X5
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 12 samples with support for all annotated introns
zinc finger protein 23, transcript variant X7
zinc finger protein 23, transcript variant X9
zinc finger protein 23, transcript variant X8
zinc finger protein 23, transcript variant X3
zinc finger protein 23, transcript variant X4
zinc finger protein 23, transcript variant X6
zinc finger protein 23, 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
zinc finger protein 23, 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 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cap methyltransferase 2, transcript variant X1
cap methyltransferase 2, transcript variant X2
cap-specific mRNA (nucleoside-2'-O-)-methyltransferase 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
HYDIN axonemal central pair apparatus protein, transcript variant X3
HYDIN axonemal central pair apparatus protein, transcript variant X2
HYDIN axonemal central pair apparatus protein, transcript variant X1
HYDIN axonemal central pair apparatus protein, transcript variant X5
HYDIN axonemal central pair apparatus protein, transcript variant X4
HYDIN axonemal central pair apparatus protein, transcript variant X7
HYDIN axonemal central pair apparatus protein, transcript variant X8
HYDIN axonemal central pair apparatus protein, transcript variant X9
HYDIN axonemal central pair apparatus protein, transcript variant X10
HYDIN axonemal central pair apparatus protein, transcript variant X11
hydrocephalus-inducing protein homolog isoform X1
hydrocephalus-inducing protein homolog isoform X3
hydrocephalus-inducing protein homolog isoform X2
hydrocephalus-inducing protein homolog isoform X5
hydrocephalus-inducing protein homolog isoform X6
hydrocephalus-inducing protein homolog isoform X7
hydrocephalus-inducing protein homolog isoform X8
HYDIN axonemal central pair apparatus protein, transcript variant X6
hydrocephalus-inducing protein homolog isoform X4
non-histone chromosomal protein HMG-14-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 32% coverage of the annotated genomic feature by RNAseq alignments
DNA-directed RNA polymerases I, II, and III subunit RPABC4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins
VAC14 component of PIKFYVE complex, transcript variant X2
VAC14 component of PIKFYVE complex, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
MTSS I-BAR domain containing 2, transcript variant X4
MTSS I-BAR domain containing 2, transcript variant X3
MTSS I-BAR domain containing 2, transcript variant X2
MTSS I-BAR domain containing 2, transcript variant X1
splicing factor 3b subunit 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
splicing factor 3b subunit 3, transcript variant X1
splicing factor 3b subunit 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 10 samples with support for all annotated introns
splicing factor 3b subunit 3, transcript variant X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00611
component of oligomeric golgi complex 4, transcript variant X2
component of oligomeric golgi complex 4, transcript variant X1
component of oligomeric golgi complex 4, transcript variant X3
component of oligomeric golgi complex 4, transcript variant X4
conserved oligomeric Golgi complex subunit 4 isoform X1
conserved oligomeric Golgi complex subunit 4 isoform X2
conserved oligomeric Golgi complex subunit 4 isoform X3
conserved oligomeric Golgi complex subunit 4 isoform X4
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X1
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X5
ST3 beta-galactoside alpha-2,3-sialyltransferase 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
CMP-N-acetylneuraminate-beta-galactosamide- alpha-2,3-sialyltransferase 2
ATP-dependent RNA helicase DDX19A, transcript variant X3
ATP-dependent RNA helicase DDX19A, 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 12 samples with support for all annotated introns
ATP-dependent RNA helicase DDX19A, transcript variant X2
ATP-dependent RNA helicase DDX19A, transcript variant X4
ATP-dependent RNA helicase DDX19A isoform X3
ATP-dependent RNA helicase DDX19A isoform X1
ATP-dependent RNA helicase DDX19A isoform X2
ATP-dependent RNA helicase DDX19A isoform 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
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 12 samples with support for all annotated introns
alanyl-tRNA synthetase 1, transcript variant X2
alanyl-tRNA synthetase 1, transcript variant X1
alanine--tRNA ligase, cytoplasmic isoform X1
alanine--tRNA ligase, cytoplasmic isoform X2
heterogeneous nuclear ribonucleoprotein C-like 2
C-type lectin domain family 18 member A-like, transcript variant X2
C-type lectin domain family 18 member A-like, transcript variant X3
C-type lectin domain family 18 member A-like, transcript variant X1
C-type lectin domain family 18 member A-like isoform X2
C-type lectin domain family 18 member A-like isoform X3
C-type lectin domain family 18 member A-like isoform X1
C-type lectin domain family 18 member A-like, transcript variant X4
C-type lectin domain family 18 member B-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 244 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pyruvate dehydrogenase phosphatase regulatory subunit, transcript variant X1
pyruvate dehydrogenase phosphatase regulatory subunit, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
golgi glycoprotein 1, transcript variant X2
golgi glycoprotein 1, transcript variant X1
golgi glycoprotein 1, transcript variant X4
golgi glycoprotein 1, transcript variant X3
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
ring finger and WD repeat domain 3, transcript variant X2
ring finger and WD repeat domain 3, transcript variant X1
E3 ubiquitin-protein ligase RFWD3 isoform X2
E3 ubiquitin-protein ligase RFWD3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 39% coverage of the annotated genomic feature by RNAseq alignments
mixed lineage kinase domain like pseudokinase, transcript variant X6
mixed lineage kinase domain like pseudokinase, transcript variant X4
mixed lineage kinase domain-like protein isoform X2
mixed lineage kinase domain-like protein isoform X4
mixed lineage kinase domain like pseudokinase, transcript variant X3
mixed lineage kinase domain like pseudokinase, transcript variant X1
mixed lineage kinase domain like pseudokinase, transcript variant X2
mixed lineage kinase domain like pseudokinase, transcript variant X5
mixed lineage kinase domain-like protein isoform X3
mixed lineage kinase domain-like protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 31% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 59, transcript variant X2
WD repeat domain 59, transcript variant X3
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 10 samples with support for all annotated introns
WD repeat domain 59, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
WD repeat domain 59, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
zinc and ring finger 1, transcript variant X3
zinc and ring finger 1, transcript variant X2
zinc and ring finger 1, transcript variant X1
lactate dehydrogenase D, transcript variant X4
lactate dehydrogenase D, transcript variant X3
lactate dehydrogenase D, transcript variant X1
probable D-lactate dehydrogenase, mitochondrial isoform X3
probable D-lactate dehydrogenase, mitochondrial isoform X1
probable D-lactate dehydrogenase, mitochondrial isoform X4
lactate dehydrogenase D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
probable D-lactate dehydrogenase, mitochondrial isoform X2
ZFP1 zinc finger protein, transcript variant X3
ZFP1 zinc finger protein, transcript variant X1
zinc finger protein 1 homolog isoform X2
ZFP1 zinc finger protein, transcript variant X2
SH3 domain-binding glutamic acid-rich-like protein
zinc finger protein 1 homolog isoform X1
zinc finger protein 1 homolog, transcript variant X3
zinc finger protein 1 homolog, transcript variant X5
zinc finger protein 1 homolog, transcript variant X2
zinc finger protein 1 homolog, transcript variant X4
zinc finger protein 1 homolog, transcript variant X6
zinc finger protein 1 homolog, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 1 homolog, transcript variant X8
zinc finger protein 1 homolog, transcript variant X7
zinc finger protein 1 homolog, transcript variant X9
zinc finger protein 1 homolog, transcript variant 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 8 samples with support for all annotated introns
zinc finger protein 1 homolog isoform X3
zinc finger protein 1 homolog isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 12% coverage of the annotated genomic feature by RNAseq alignments
BCAR1 scaffold protein, Cas family member, transcript variant X2
BCAR1 scaffold protein, Cas family member, transcript variant X4
BCAR1 scaffold protein, Cas family member, 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 10 samples with support for all annotated introns
BCAR1 scaffold protein, Cas family member, transcript variant X1
BCAR1 scaffold protein, Cas family member, transcript variant X5
BCAR1 scaffold protein, Cas family member, transcript variant X6
breast cancer anti-estrogen resistance protein 1 isoform X2
breast cancer anti-estrogen resistance protein 1 isoform X3
breast cancer anti-estrogen resistance protein 1 isoform X1
breast cancer anti-estrogen resistance protein 1 isoform X4
craniofacial development protein 1, transcript variant X2
craniofacial development protein 1, transcript variant X1
craniofacial development protein 1 isoform X2
craniofacial development protein 1 isoform X1
bifunctional 3'-phosphoadenosine 5'-phosphosulfate synthase 1
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
transmembrane protein 170A, transcript variant X2
transmembrane protein 170A, transcript variant X1
carbohydrate sulfotransferase 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carbohydrate sulfotransferase 6, transcript variant X3
carbohydrate sulfotransferase 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carbohydrate sulfotransferase 6, transcript variant X4
GABA type A receptor associated protein like 2
gamma-aminobutyric acid receptor-associated protein-like 2
adenosine deaminase tRNA specific 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
tRNA-specific adenosine deaminase 1 isoform X1
adenosine deaminase tRNA specific 1, transcript variant X2
tRNA-specific adenosine deaminase 1 isoform X2
lysyl-tRNA synthetase 1, transcript variant X2
lysyl-tRNA synthetase 1, transcript variant X1
telomeric repeat-binding factor 2-interacting protein 1
double homeobox protein B-like, transcript variant X7
double homeobox protein B-like, transcript variant X8
double homeobox protein B-like, transcript variant X6
double homeobox protein B-like, transcript variant X5
double homeobox protein B-like, transcript variant X9
double homeobox protein B-like, transcript variant X3
double homeobox protein B-like, transcript variant X4
double homeobox protein B-like, transcript variant X1
double homeobox protein B-like, transcript variant X2
contactin associated protein family member 4, transcript variant X1
contactin associated protein family member 4, transcript variant X3
contactin associated protein family member 4, transcript variant X2
contactin associated protein family member 4, transcript variant X5
contactin-associated protein-like 4 isoform X1
contactin-associated protein-like 4 isoform X3
contactin-associated protein-like 4 isoform X5
contactin-associated protein-like 4 isoform X2
contactin associated protein family member 4, transcript variant X4
contactin-associated protein-like 4 isoform X4
contactin associated protein family member 4, transcript variant X6
contactin-associated protein-like 4 isoform X6
MON1 homolog B, secretory trafficking associated, transcript variant X5
MON1 homolog B, secretory trafficking associated, transcript variant X3
MON1 homolog B, secretory trafficking associated, transcript variant X2
MON1 homolog B, secretory trafficking associated, transcript variant X1
MON1 homolog B, secretory trafficking associated, transcript variant X4
synaptonemal complex central element protein 1 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
synaptonemal complex central element protein 1-like
ADAM metallopeptidase with thrombospondin type 1 motif 18, transcript variant X2
A disintegrin and metalloproteinase with thrombospondin motifs 18 isoform X2
ADAM metallopeptidase with thrombospondin type 1 motif 18, transcript variant X1
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
A disintegrin and metalloproteinase with thrombospondin motifs 18 isoform X1
nudix hydrolase 7, transcript variant X1
nudix hydrolase 7, 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 12 samples with support for all annotated introns
peroxisomal coenzyme A diphosphatase NUDT7 isoform X1
peroxisomal coenzyme A diphosphatase NUDT7 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
synaptic vesicle membrane protein VAT-1 homolog-like
C-type lectin domain family 3 member A, transcript variant X1
C-type lectin domain family 3 member A isoform X1
C-type lectin domain family 3 member A, transcript variant X2
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 4 samples with support for all annotated introns
C-type lectin domain family 3 member A isoform X2
WW domain containing oxidoreductase, transcript variant X1
WW domain containing oxidoreductase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
WW domain-containing oxidoreductase isoform X1
WW domain-containing oxidoreductase isoform X2
uncharacterized LOC119518938, transcript variant X2
uncharacterized LOC119518938, transcript variant X1
MAF bZIP transcription factor, transcript variant X8
MAF bZIP transcription factor, transcript variant X9
MAF bZIP transcription factor, transcript variant X10
MAF bZIP transcription factor, transcript variant X7
MAF bZIP transcription factor, transcript variant X5
MAF bZIP transcription factor, transcript variant X2
MAF bZIP transcription factor, transcript variant X4
MAF bZIP transcription factor, transcript variant X6
MAF bZIP transcription factor, transcript variant X3
MAF bZIP transcription factor, transcript variant X1
MAF bZIP transcription factor, transcript variant X11
uncharacterized LOC119518937, transcript variant X1
uncharacterized LOC119518937, transcript variant X2
chromodomain Y like 2, transcript variant X3
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 4 samples with support for all annotated introns
chromodomain Y like 2, transcript variant X2
chromodomain Y like 2, 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 2 samples with support for all annotated introns
chromodomain Y-like protein 2 isoform X3
chromodomain Y-like protein 2 isoform X2
chromodomain Y-like protein 2 isoform X1
C-X9-C motif containing 2, transcript variant X2
C-X9-C motif containing 2, transcript variant X3
C-X9-C motif containing 2, transcript variant X1
COX assembly mitochondrial protein 2 homolog isoform X1
COX assembly mitochondrial protein 2 homolog isoform X2
centromere protein N, transcript variant X1
centromere protein N, transcript variant X2
chromosome 22 C16orf46 homolog, transcript variant X3
uncharacterized protein C16orf46 homolog isoform X3
chromosome 22 C16orf46 homolog, transcript variant X2
uncharacterized protein C16orf46 homolog isoform X2
chromosome 22 C16orf46 homolog, transcript variant X6
chromosome 22 C16orf46 homolog, transcript variant X4
chromosome 22 C16orf46 homolog, transcript variant X1
chromosome 22 C16orf46 homolog, transcript variant X5
uncharacterized protein C16orf46 homolog isoform X1
uncharacterized protein C16orf46 homolog isoform X4
glycine cleavage system H protein, mitochondrial
uncharacterized LOC119518438, transcript variant X3
uncharacterized LOC119518438, transcript variant X2
uncharacterized LOC119518438, transcript variant X1
uncharacterized LOC119518438, transcript variant X7
uncharacterized LOC119518438, transcript variant X8
uncharacterized LOC119518438, transcript variant X4
uncharacterized LOC119518438, transcript variant X6
uncharacterized LOC119518438, transcript variant X5
uncharacterized LOC119518438, transcript variant X9
polycystic kidney disease protein 1-like 2
uncharacterized LOC119519005, transcript variant X2
uncharacterized LOC119519005, transcript variant X4
uncharacterized LOC119519005, transcript variant X1
uncharacterized LOC119519005, transcript variant X3
uncharacterized LOC119519005, transcript variant X5
c-Maf inducing protein, transcript variant X1
c-Maf inducing protein, transcript variant X2
c-Maf inducing protein, transcript variant X3
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase gamma-2
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X10
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X9
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 6 samples with support for all annotated introns
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X6
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X8
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X7
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X5
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X4
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X3
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X2
short chain dehydrogenase/reductase family 42E, member 1, transcript variant X1
short-chain dehydrogenase/reductase family 42E member 1
hydroxysteroid 17-beta dehydrogenase 2, transcript variant X1
hydroxysteroid 17-beta dehydrogenase 2, transcript variant X2
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, including 12 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 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119518500, transcript variant X2
uncharacterized LOC119518500, transcript variant X1
malonyl-CoA decarboxylase, transcript variant X2
malonyl-CoA decarboxylase, transcript variant X1
malonyl-CoA decarboxylase, mitochondrial isoform X1
malonyl-CoA decarboxylase, mitochondrial isoform X2
oxidative stress induced growth inhibitor 1, transcript variant X2
oxidative stress induced growth inhibitor 1, transcript variant X1
oxidative stress-induced growth inhibitor 1 isoform X1
oxidative stress induced growth inhibitor 1, transcript variant X3
oxidative stress induced growth inhibitor 1, transcript variant X4
oxidative stress-induced growth inhibitor 1 isoform X2
oxidative stress-induced growth inhibitor 1 isoform X3
N-terminal EF-hand calcium binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
N-terminal EF-hand calcium-binding protein 2 isoform X1
N-terminal EF-hand calcium binding protein 2, transcript variant X2
N-terminal EF-hand calcium-binding protein 2 isoform X2
N-terminal EF-hand calcium binding protein 2, transcript variant X3
N-terminal EF-hand calcium-binding protein 2 isoform X3
solute carrier family 38 member 8, transcript variant X2
solute carrier family 38 member 8, transcript variant X1
putative sodium-coupled neutral amino acid transporter 8 isoform X1
putative sodium-coupled neutral amino acid transporter 8 isoform X2
membrane bound transcription factor peptidase, site 1
membrane-bound transcription factor site-1 protease
hydroxysteroid dehydrogenase like 1, transcript variant X1
hydroxysteroid dehydrogenase like 1, transcript variant X2
inactive hydroxysteroid dehydrogenase-like protein 1
dynein axonemal assembly factor 1, transcript variant X1
dynein axonemal assembly factor 1, transcript variant X2
dynein axonemal assembly factor 1, transcript variant X3
dynein axonemal assembly factor 1, transcript variant X5
dynein assembly factor 1, axonemal isoform X1
dynein assembly factor 1, axonemal isoform X2
dynein assembly factor 1, axonemal isoform X3
dynein assembly factor 1, axonemal isoform X5
dynein axonemal assembly factor 1, transcript variant X4
dynein axonemal assembly factor 1, transcript variant X6
dynein assembly factor 1, axonemal isoform X6
dynein assembly factor 1, axonemal isoform X4
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X1
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X2
TATA box-binding protein-associated factor RNA polymerase I subunit C isoform X1
TATA box-binding protein-associated factor RNA polymerase I subunit C isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
adenosine deaminase domain-containing protein 2
potassium voltage-gated channel modifier subfamily G member 4
potassium voltage-gated channel subfamily G member 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
WAP four-disulfide core domain protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA/RNA-binding protein KIN17-like
ATPase secretory pathway Ca2+ transporting 2, transcript variant X1
calcium-transporting ATPase type 2C member 2 isoform X1
ATPase secretory pathway Ca2+ transporting 2, transcript variant X2
calcium-transporting ATPase type 2C member 2 isoform X2
MTOR associated protein, eak-7 homolog, transcript variant X4
MTOR associated protein, eak-7 homolog, transcript variant X3
MTOR associated protein, eak-7 homolog, transcript variant X1
MTOR associated protein, eak-7 homolog, transcript variant X2
MTOR-associated protein MEAK7 isoform X2
MTOR-associated protein MEAK7 isoform X1
MTOR-associated protein MEAK7 isoform X3
coactosin like F-actin binding protein 1
kelch like family member 36, transcript variant X1
kelch like family member 36, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 10
cysteine rich secretory protein LCCL domain containing 2
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
cysteine-rich secretory protein LCCL domain-containing 2
zinc finger DHHC-type palmitoyltransferase 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 7, transcript variant X1
KIAA0513 ortholog, transcript variant X2
KIAA0513 ortholog, transcript variant X1
KIAA0513 ortholog, transcript variant X3
KIAA0513 ortholog, transcript variant X4
uncharacterized protein KIAA0513 homolog isoform X1
uncharacterized protein KIAA0513 homolog isoform X2
uncharacterized protein KIAA0513 homolog isoform X3
CBY1 interacting BAR domain containing 2, transcript variant X4
CBY1 interacting BAR domain containing 2, transcript variant X2
CBY1-interacting BAR domain-containing protein 2 isoform X4
CBY1-interacting BAR domain-containing protein 2 isoform X2
CBY1 interacting BAR domain containing 2, transcript variant X3
CBY1 interacting BAR domain containing 2, transcript variant X1
CBY1-interacting BAR domain-containing protein 2 isoform X3
CBY1-interacting BAR domain-containing protein 2 isoform X1
uncharacterized LOC119519012, transcript variant X3
uncharacterized LOC119519012, transcript variant X1
uncharacterized LOC119519012, transcript variant X2
uncharacterized protein LOC119519012 isoform X2
uncharacterized protein LOC119519012 isoform X3
uncharacterized protein LOC119519012 isoform X1
uncharacterized LOC119519012, transcript variant X5
uncharacterized LOC119519012, transcript variant X4
uncharacterized protein LOC119519012 isoform X4
Gse1 coiled-coil protein, transcript variant X9
Gse1 coiled-coil protein, transcript variant X5
Gse1 coiled-coil protein, transcript variant X3
Gse1 coiled-coil protein, transcript variant X7
Gse1 coiled-coil protein, transcript variant X4
Gse1 coiled-coil protein, transcript variant X8
Gse1 coiled-coil protein, transcript variant X6
Gse1 coiled-coil protein, transcript variant X2
Gse1 coiled-coil protein, transcript variant X1
DNA replication complex GINS protein PSF2
chromosome 22 C16orf74 homolog, transcript variant X3
chromosome 22 C16orf74 homolog, transcript variant X2
chromosome 22 C16orf74 homolog, transcript variant X1
uncharacterized protein C16orf74 homolog isoform X1
uncharacterized protein C16orf74 homolog isoform X2
ER membrane protein complex subunit 8, transcript variant X1
ER membrane protein complex subunit 8, transcript variant X2
ER membrane protein complex subunit 8 isoform X1
ER membrane protein complex subunit 8 isoform X2
cytochrome c oxidase subunit 4 isoform 1, mitochondrial
interferon regulatory factor 8, transcript variant X1
interferon regulatory factor 8, transcript variant X4
interferon regulatory factor 8, transcript variant X3
interferon regulatory factor 8, transcript variant X2
interferon regulatory factor 8 isoform X1
interferon regulatory factor 8 isoform X2
interferon regulatory factor 8, transcript variant X5
interferon regulatory factor 8 isoform X3
methenyltetrahydrofolate synthetase domain containing, transcript variant X1
methenyltetrahydrofolate synthetase domain containing, transcript variant X2
methenyltetrahydrofolate synthase domain-containing protein isoform X1
methenyltetrahydrofolate synthase domain-containing protein isoform X2
chromosome 22 C16orf95 homolog, transcript variant X2
chromosome 22 C16orf95 homolog, transcript variant X1
uncharacterized protein C16orf95 homolog isoform X2
uncharacterized protein C16orf95 homolog isoform X1
microtubule associated protein 1 light chain 3 beta
microtubule-associated proteins 1A/1B light chain 3B
zinc finger CCHC-type containing 14, transcript variant X2
zinc finger CCHC-type containing 14, transcript variant X1
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 8 samples with support for all annotated introns
zinc finger CCHC domain-containing protein 14 isoform X1
zinc finger CCHC-type containing 14, transcript variant X3
zinc finger CCHC domain-containing protein 14 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples 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 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
kelch domain containing 4, transcript variant X3
kelch domain containing 4, transcript variant X2
kelch domain containing 4, transcript variant X1
kelch domain containing 4, transcript variant X4
kelch domain-containing protein 4 isoform X2
kelch domain-containing protein 4 isoform X1
kelch domain-containing protein 4 isoform X3
kelch domain-containing protein 4 isoform X4
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 10 samples with support for all annotated introns
large neutral amino acids transporter small subunit 1
carbonic anhydrase 5A, transcript variant X3
carbonic anhydrase 5A, transcript variant X1
carbonic anhydrase 5A, transcript variant X2
carbonic anhydrase 5A, mitochondrial isoform X3
carbonic anhydrase 5A, mitochondrial isoform X1
carbonic anhydrase 5A, mitochondrial isoform X2
BTG3 associated nuclear protein, transcript variant X1
BTG3 associated nuclear protein, transcript variant X2
BTG3 associated nuclear protein, transcript variant X3
uncharacterized LOC119518736, transcript variant X2
uncharacterized protein LOC119518736 isoform X2
uncharacterized LOC119518736, transcript variant X1
uncharacterized LOC119518736, transcript variant X4
uncharacterized LOC119518736, transcript variant X3
uncharacterized LOC119518736, transcript variant X5
uncharacterized protein LOC119518736 isoform X1
zinc finger protein, FOG family member 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; 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, including 10 samples 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: inserted 1 base in 1 codon; deleted 3 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein ZFPM1
protein diaphanous homolog 1-like, transcript variant X1
protein diaphanous homolog 1-like, transcript variant X3
protein diaphanous homolog 1-like, transcript variant X2
protein diaphanous homolog 1-like, transcript variant X5
protein diaphanous homolog 1-like, transcript variant X4
zinc finger CCCH-type containing 18, transcript variant X3
zinc finger CCCH-type containing 18, transcript variant X1
zinc finger CCCH-type containing 18, transcript variant X2
zinc finger CCCH domain-containing protein 18 isoform X1
zinc finger CCCH domain-containing protein 18 isoform X2
zinc finger CCCH domain-containing protein 18 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
mevalonate diphosphate decarboxylase, transcript variant X2
mevalonate diphosphate decarboxylase, transcript variant X1
diphosphomevalonate decarboxylase isoform X2
diphosphomevalonate decarboxylase isoform X1
snail family transcriptional repressor 3, transcript variant X5
snail family transcriptional repressor 3, transcript variant X1
snail family transcriptional repressor 3, transcript variant X3
snail family transcriptional repressor 3, transcript variant X4
snail family transcriptional repressor 3, transcript variant X2
cytosolic thiouridylase subunit 2, transcript variant X1
cytosolic thiouridylase subunit 2, transcript variant X2
cytoplasmic tRNA 2-thiolation protein 2 isoform X1
cytoplasmic tRNA 2-thiolation protein 2 isoform X2
piezo type mechanosensitive ion channel component 1, transcript variant X2
piezo type mechanosensitive ion channel component 1, transcript variant X1
piezo-type mechanosensitive ion channel component 1 isoform X2
piezo-type mechanosensitive ion channel component 1 isoform X1
basic proline-rich protein-like, transcript variant X3
basic proline-rich protein-like, transcript variant X2
basic proline-rich protein-like, transcript variant X1
chromatin licensing and DNA replication factor 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LOW QUALITY PROTEIN: DNA replication factor Cdt1
nascent polypeptide-associated complex subunit alpha, muscle-specific form-like
uncharacterized LOC119518553, transcript variant X2
uncharacterized LOC119518553, transcript variant X1
uncharacterized protein LOC119518553 isoform X1
uncharacterized protein LOC119518553 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 118 Proteins
acyl-CoA synthetase family member 3, transcript variant X2
acyl-CoA synthetase family member 3, transcript variant X3
acyl-CoA synthetase family member 3, transcript variant X8
acyl-CoA synthetase family member 3, transcript variant X10
acyl-CoA synthetase family member 3, transcript variant X9
acyl-CoA synthetase family member 3, transcript variant X7
acyl-CoA synthetase family member 3, transcript variant X6
acyl-CoA synthetase family member 3, transcript variant X5
acyl-CoA synthetase family member 3, transcript variant X4
acyl-CoA synthetase family member 3, transcript variant X1
malonate--CoA ligase ACSF3, mitochondrial isoform X1
malonate--CoA ligase ACSF3, mitochondrial isoform X4
malonate--CoA ligase ACSF3, mitochondrial isoform X3
malonate--CoA ligase ACSF3, mitochondrial isoform X5
malonate--CoA ligase ACSF3, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 28% 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; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: putative solute carrier family 22 member 31
ankyrin repeat domain 11, transcript variant X5
ankyrin repeat domain 11, transcript variant X7
ankyrin repeat domain 11, transcript variant X8
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
ankyrin repeat domain 11, transcript variant X4
ankyrin repeat domain 11, transcript variant X3
ankyrin repeat domain 11, transcript variant X6
ankyrin repeat domain 11, transcript variant X2
ankyrin repeat domain 11, transcript variant X1
ankyrin repeat domain 11, transcript variant X9
ankyrin repeat domain-containing protein 11 isoform X1
ankyrin repeat domain-containing protein 11 isoform X2
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X3
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X1
SPG7 matrix AAA peptidase subunit, paraplegin, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00324
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cyclin dependent kinase 10, transcript variant X2
cyclin dependent kinase 10, transcript variant X1
cyclin dependent kinase 10, transcript variant X3
cyclin dependent kinase 10, transcript variant X8
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 10 samples with support for all annotated introns
cyclin dependent kinase 10, transcript variant X9
cyclin dependent kinase 10, transcript variant X10
cyclin dependent kinase 10, transcript variant X5
cyclin dependent kinase 10, transcript variant X7
cyclin dependent kinase 10, transcript variant X6
cyclin dependent kinase 10, transcript variant X4
spermatogenesis associated 2 like, transcript variant X1
spermatogenesis associated 2 like, transcript variant X2
VPS9 domain containing 1, transcript variant X5
VPS9 domain containing 1, transcript variant X2
VPS9 domain containing 1, transcript variant X4
VPS9 domain containing 1, transcript variant X1
VPS9 domain containing 1, transcript variant X3
VPS9 domain-containing protein 1 isoform X4
VPS9 domain-containing protein 1 isoform X2
VPS9 domain-containing protein 1 isoform X3
VPS9 domain-containing protein 1 isoform X1
VPS9 domain containing 1, transcript variant X6
zinc finger protein 276, transcript variant X1
zinc finger protein 276, transcript variant X2
zinc finger protein 276, transcript variant X3
zinc finger protein 276, transcript variant X5
zinc finger protein 276, transcript variant X4
FA complementation group A, transcript variant X2
FA complementation group A, transcript variant X3
FA complementation group A, transcript variant X4
FA complementation group A, transcript variant X1
FA complementation group A, transcript variant X7
FA complementation group A, transcript variant X6
FA complementation group A, transcript variant X8
FA complementation group A, transcript variant X11
FA complementation group A, transcript variant X9
FA complementation group A, transcript variant X10
Fanconi anemia group A protein isoform X2
Fanconi anemia group A protein isoform X3
Fanconi anemia group A protein isoform X4
Fanconi anemia group A protein isoform X1
Fanconi anemia group A protein isoform X6
Fanconi anemia group A protein isoform X8
Fanconi anemia group A protein isoform X7
FA complementation group A, transcript variant X5
Fanconi anemia group A protein isoform X5
FA complementation group A, transcript variant X12
Fanconi anemia group A protein isoform X9
FA complementation group A, transcript variant X13
FA complementation group A, transcript variant X14
Fanconi anemia group A protein isoform X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
FA complementation group A, transcript variant X15
Fanconi anemia group A protein isoform X11
FA complementation group A, transcript variant X17
FA complementation group A, transcript variant X16
spire type actin nucleation factor 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
spire type actin nucleation factor 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
spire type actin nucleation factor 2, transcript variant X2
spire type actin nucleation factor 2, transcript variant X3
spire type actin nucleation factor 2, transcript variant X1
spire type actin nucleation factor 2, transcript variant X4
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
LOW QUALITY PROTEIN: transcription factor 25
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 158 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
differentially expressed in FDCP 8 homolog, transcript variant X2
differentially expressed in FDCP 8 homolog, transcript variant X1
differentially expressed in FDCP 8 homolog isoform X2
differentially expressed in FDCP 8 homolog isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: CENPB DNA-binding domain-containing protein 1
dysbindin domain containing 1, transcript variant X2
dysbindin domain containing 1, transcript variant X1
dysbindin domain-containing protein 1 isoform X1
dysbindin domain-containing protein 1 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: dynein regulatory complex subunit 4
5-hydroxyisourate hydrolase-like, transcript variant X1
5-hydroxyisourate hydrolase-like, transcript variant X2
5-hydroxyisourate hydrolase-like isoform X2
uncharacterized protein LOC119518677 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 13% coverage of the annotated genomic feature by RNAseq alignments
probable histone-lysine N-methyltransferase PRDM7