Tachyglossus aculeatus isolate mTacAcu1 chromosome 13, mTacAcu1.pri, whole genome shotgun sequence.
Tachyglossus aculeatus (Australian echidna)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Monotremata; Tachyglossidae; Tachyglossus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM027612.1.\nAssembly name: mTacAcu1.pri\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/12/09. The original whole-genome shotgun project has the\naccession JADRJE000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 26-OCT-2020\nAssembly Method :: FALCON v. falcon-2018.31.08-03.06;\n FALCON-Unzip v. 6.0.0.47841; purge_dups\n v. github\n ca23030ccf4254dfd2d3a5ea90d0eed41c24f88b\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. 2020-09-17; Manual Curation\n v. 2020-10-26; VGP assembly pipeline v.\n 1.6\nAssembly Name :: mTacAcu1.pri\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 58.29x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Bionano Genomics DLS; Phase Genomics\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Tachyglossus aculeatus 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##
Australia: Upper Barnard River, New South Wales
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: 9 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: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
sodium channel protein type 5 subunit alpha-like
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: 84 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium channel protein type 5 subunit alpha-like
sodium voltage-gated channel alpha subunit 10
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: 60 Proteins, and 58% 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sodium channel protein type 10 subunit alpha
sodium voltage-gated channel alpha subunit 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 73 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
sodium channel protein type 11 subunit alpha
WD repeat domain 48, 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 6 samples with support for all annotated introns
WD repeat domain 48, 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 8 samples with support for all annotated introns
WD repeat-containing protein 48 isoform X1
WD repeat-containing protein 48 isoform X2
golgi reassembly stacking protein 1, transcript variant X2
golgi reassembly stacking protein 1, 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 9 samples with support for all annotated introns
Golgi reassembly-stacking protein 1 isoform X2
Golgi reassembly-stacking protein 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
chymotrypsin-like elastase family member 1
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 7 samples with support for all annotated introns
cysteine and serine rich nuclear protein 1
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
xin actin-binding repeat-containing protein 1
solute carrier family 22 member 13-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 22 member 13-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 22 member 13-like, transcript variant X3
solute carrier family 22 member 13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 22 member 13-like isoform X3
uncharacterized protein LOC119936336 isoform X1
uncharacterized protein LOC119936336 isoform X2
oxidative stress responsive kinase 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 9 samples with support for all annotated introns
oxidative stress responsive kinase 1, transcript variant X2
serine/threonine-protein kinase OSR1 isoform X1
serine/threonine-protein kinase OSR1 isoform X2
MYD88 innate immune signal transduction adaptor
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 6 samples with support for all annotated introns
myeloid differentiation primary response protein MyD88
mitogen-activated protein kinase kinase kinase 3-like
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
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 9 samples with support for all annotated introns
DLEC1 cilia and flagella associated 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 1 sample with support for all annotated introns
DLEC1 cilia and flagella associated protein, transcript variant X3
DLEC1 cilia and flagella associated protein, transcript variant X6
DLEC1 cilia and flagella associated protein, transcript variant X2
DLEC1 cilia and flagella associated protein, transcript variant X4
DLEC1 cilia and flagella associated protein, transcript variant X1
DLEC1 cilia and flagella associated protein, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
deleted in lung and esophageal cancer protein 1 isoform X5
deleted in lung and esophageal cancer protein 1 isoform X3
deleted in lung and esophageal cancer protein 1 isoform X6
deleted in lung and esophageal cancer protein 1 isoform X2
deleted in lung and esophageal cancer protein 1 isoform X4
deleted in lung and esophageal cancer protein 1 isoform X1
deleted in lung and esophageal cancer protein 1 isoform X7
phospholipase C delta 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X3
phospholipase C delta 1, 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 7 samples with support for all annotated introns
phospholipase C delta 1, 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 7 samples with support for all annotated introns
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X1
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase delta-1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 1 sample with support for all annotated introns
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
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 9 samples with support for all annotated introns
corticotropin releasing hormone receptor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
corticotropin-releasing factor receptor 2
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
ADCYAP receptor type I, 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 3 samples with support for all annotated introns
ADCYAP receptor type I, transcript variant X3
ADCYAP receptor type I, transcript variant X5
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 3 samples with support for all annotated introns
ADCYAP receptor type I, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADCYAP receptor type I, transcript variant X1
ADCYAP receptor type I, transcript variant X7
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 3 samples with support for all annotated introns
ADCYAP receptor type I, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X5
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X2
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X1
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X6
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X4
pituitary adenylate cyclase-activating polypeptide type I receptor isoform X3
growth hormone releasing hormone receptor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 60% coverage of the annotated genomic feature by RNAseq alignments
growth hormone-releasing hormone receptor
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
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: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 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.
LOW QUALITY PROTEIN: probable ubiquitin carboxyl-terminal hydrolase MINDY-4
vasoactive intestinal peptide receptor 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 3 samples with support for all annotated introns
vasoactive intestinal peptide receptor 1, transcript variant X2
vasoactive intestinal polypeptide receptor 1 isoform X1
vasoactive intestinal polypeptide receptor 1 isoform X2
SEC22 homolog C, vesicle trafficking protein
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
natural killer cell triggering receptor, transcript variant X4
natural killer cell triggering receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
natural killer cell triggering receptor, 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 8 samples with support for all annotated introns
natural killer cell triggering receptor, transcript variant X3
natural killer cell triggering receptor, 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 9 samples with support for all annotated introns
zinc finger and BTB domain containing 47, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 47 isoform X1
zinc finger and BTB domain containing 47, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 47 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
hedgehog acyltransferase like, 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 3 samples with support for all annotated introns
hedgehog acyltransferase 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 2 samples with support for all annotated introns
protein-cysteine N-palmitoyltransferase HHAT-like protein isoform X1
protein-cysteine N-palmitoyltransferase HHAT-like protein isoform X2
coiled-coil domain containing 13, transcript variant X3
coiled-coil domain-containing protein 13 isoform X3
coiled-coil domain containing 13, transcript variant X2
coiled-coil domain containing 13, transcript variant X1
coiled-coil domain-containing protein 13 isoform X2
coiled-coil domain-containing protein 13 isoform X1
coiled-coil domain containing 13, transcript variant X4
coiled-coil domain-containing protein 13 isoform X4
HIG1 hypoxia inducible domain family member 1A
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 11 samples with support for all annotated introns
HIG1 domain family member 1A, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 24% coverage of the annotated genomic feature by RNAseq alignments
5-beta-cholestane-3-alpha,7-alpha-diol 12-alpha-hydroxylase
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
obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
basic salivary proline-rich protein 2-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 1 sample with support for all annotated introns
iron-sulfur cluster assembly factor IBA57
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
putative transferase CAF17, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
guanylate kinase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
guanylate kinase 1, 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 3 samples with support for all annotated introns
mitochondrial ribosomal protein L55, 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 10 samples with support for all annotated introns
mitochondrial ribosomal protein L55, transcript variant X2
chromosome 13 C1orf35 homolog, 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 2 samples with support for all annotated introns
39S ribosomal protein L55, mitochondrial isoform X1
39S ribosomal protein L55, mitochondrial isoform X2
chromosome 13 C1orf35 homolog, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
chromosome 13 C1orf35 homolog, transcript variant X1
multiple myeloma tumor-associated protein 2
ADP ribosylation factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ADP ribosylation factor 1, transcript variant X2
ADP ribosylation factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
jumonji domain containing 4, transcript variant X2
jumonji domain containing 4, transcript variant X4
jumonji domain containing 4, transcript variant X3
jumonji domain containing 4, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
jumonji domain containing 4, 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 4 samples with support for all annotated introns
2-oxoglutarate and iron-dependent oxygenase JMJD4 isoform X1
2-oxoglutarate and iron-dependent oxygenase JMJD4 isoform X2
ALS2 C-terminal like, 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 1 sample with support for all annotated introns
ALS2 C-terminal like, transcript variant X3
ALS2 C-terminal like, transcript variant X1
ALS2 C-terminal like, transcript variant X5
ALS2 C-terminal like, transcript variant X4
ALS2 C-terminal like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments
transmembrane inner ear expressed protein
myosin light chain 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
myosin light chain 3, transcript variant X2
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
parathyroid hormone 1 receptor, transcript variant X1
parathyroid hormone 1 receptor, transcript variant X3
parathyroid hormone 1 receptor, transcript variant X2
parathyroid hormone 1 receptor, 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 2 samples with support for all annotated introns
parathyroid hormone/parathyroid hormone-related peptide receptor isoform X1
parathyroid hormone/parathyroid hormone-related peptide receptor isoform X3
parathyroid hormone/parathyroid hormone-related peptide receptor isoform X2
parathyroid hormone 1 receptor, transcript variant X6
parathyroid hormone 1 receptor, transcript variant X7
parathyroid hormone 1 receptor, transcript variant X8
parathyroid hormone 1 receptor, 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 5 samples with support for all annotated introns
parathyroid hormone/parathyroid hormone-related peptide receptor isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
coiled-coil domain containing 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
coiled-coil domain containing 12, transcript variant X2
coiled-coil domain-containing protein 12 isoform X1
coiled-coil domain-containing protein 12 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: 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: neurobeachin-like protein 2
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
SET domain containing 2, histone lysine methyltransferase
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 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: histone-lysine N-methyltransferase SETD2
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
kelch like family member 18, 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 8 samples with support for all annotated introns
kelch like family member 18, 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
protein tyrosine phosphatase non-receptor type 23
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
tyrosine-protein phosphatase non-receptor type 23
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; deleted 2 bases in 2 codons; 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 9 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 2 bases in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sterol regulatory element-binding protein cleavage-activating protein
elongator acetyltransferase complex subunit 6, 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 9 samples with support for all annotated introns
elongator acetyltransferase complex subunit 6, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin subfamily c member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
KAT8 regulatory NSL complex subunit 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA cysteine (anticodon GCA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DExH-box helicase 30, 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 4 samples with support for all annotated introns
ATP-dependent RNA helicase DHX30 isoform X1
DExH-box helicase 30, transcript variant X3
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
ATP-dependent RNA helicase DHX30 isoform X3
DExH-box helicase 30, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP-dependent RNA helicase DHX30 isoform 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
microtubule associated protein 4, 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 6 samples with support for all annotated introns
microtubule associated protein 4, transcript variant X5
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
microtubule associated protein 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
microtubule-associated protein 4 isoform X8
microtubule-associated protein 4 isoform X5
microtubule-associated protein 4 isoform X1
microtubule associated protein 4, transcript variant X9
microtubule associated protein 4, transcript variant X6
microtubule associated protein 4, transcript variant X7
microtubule associated protein 4, transcript variant X3
microtubule associated protein 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
microtubule associated protein 4, transcript variant X2
microtubule-associated protein 4 isoform X9
microtubule-associated protein 4 isoform X6
microtubule-associated protein 4 isoform X7
microtubule-associated protein 4 isoform X3
microtubule-associated protein 4 isoform X4
microtubule-associated protein 4 isoform X2
cell division cycle 25A, 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
cell division cycle 25A, 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 3 samples with support for all annotated introns
M-phase inducer phosphatase 1 isoform X2
M-phase inducer phosphatase 1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: unconventional myosin-Ig
uncharacterized LOC119936175, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC119936175, transcript variant X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00411
CCM2 scaffold protein, transcript variant X2
cerebral cavernous malformations 2 protein isoform X2
CCM2 scaffold protein, transcript variant X1
cerebral cavernous malformations 2 protein isoform X1
CCM2 scaffold protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cerebral cavernous malformations 2 protein isoform X3
NAC-alpha domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 54% coverage of the annotated genomic feature by RNAseq alignments
transforming growth factor beta regulator 4
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 9 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00392
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
myb-related transcription factor, partner of profilin-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 73% 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 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 3 Proteins, and 90% 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: 6 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
LOW QUALITY PROTEIN: zinc finger protein 746
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: 3 Proteins, and 97% 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.
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 67% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA serine (anticodon AGA); 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: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 436-like, transcript variant X2
zinc finger protein 436-like, transcript variant X1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% coverage of the annotated genomic feature by RNAseq alignments
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
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
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 8 samples with support for all annotated introns
leucine-rich repeat-containing protein 61
retinoic acid receptor responder 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
retinoic acid receptor responder 2, transcript variant X3
retinoic acid receptor responder 2, transcript variant X1
retinoic acid receptor responder 2, 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 9 samples with support for all annotated introns
retinoic acid receptor responder protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger protein 775
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00020
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 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: 3 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119936315, 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 5 samples with support for all annotated introns
uncharacterized LOC119936315, transcript variant X2
uncharacterized protein LOC119936315 isoform X1
uncharacterized protein LOC119936315 isoform X2
uncharacterized LOC119936280, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC119936280, transcript variant X4
uncharacterized LOC119936280, transcript variant X3
uncharacterized LOC119936280, transcript variant X2
uncharacterized LOC119936280, transcript variant X1
uncharacterized protein LOC119936280 isoform X5
uncharacterized protein LOC119936280 isoform X4
uncharacterized protein LOC119936280 isoform X3
uncharacterized protein LOC119936280 isoform X2
uncharacterized protein LOC119936280 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00409
stonustoxin subunit alpha-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
stonustoxin subunit alpha-like, transcript variant X3
stonustoxin subunit alpha-like, transcript variant X2
stonustoxin subunit alpha-like isoform X1
stonustoxin subunit alpha-like isoform 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 11 samples with support for all annotated introns
amiloride-sensitive amine oxidase [copper-containing]-like
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 7 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: amiloride-sensitive amine oxidase [copper-containing]-like
potassium voltage-gated channel subfamily H member 2, transcript variant X2
potassium voltage-gated channel subfamily H member 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 5 samples with support for all annotated introns
potassium voltage-gated channel subfamily H member 2, transcript variant X3
potassium voltage-gated channel subfamily H member 2 isoform X2
potassium voltage-gated channel subfamily H member 2 isoform X1
potassium voltage-gated channel subfamily H member 2 isoform X3
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 42% coverage of the annotated genomic feature by RNAseq alignments
ATP binding cassette subfamily B member 8, transcript variant X2
ATP binding cassette subfamily B member 8, transcript variant X1
mitochondrial potassium channel ATP-binding subunit isoform X1
mitochondrial potassium channel ATP-binding subunit isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: anion exchange protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
transmembrane and ubiquitin like domain 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 9 samples with support for all annotated introns
transmembrane and ubiquitin-like domain-containing protein 1
ArfGAP with GTPase domain, ankyrin repeat and PH domain 3, transcript variant X1
ArfGAP with GTPase domain, ankyrin repeat and PH domain 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ArfGAP with GTPase domain, ankyrin repeat and PH domain 3, transcript variant X4
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 isoform X1
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 isoform X3
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 isoform X4
ArfGAP with GTPase domain, ankyrin repeat and PH domain 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 66% coverage of the annotated genomic feature by RNAseq alignments
arf-GAP with GTPase, ANK repeat and PH domain-containing protein 3 isoform X2
ankyrin repeat and SOCS box containing 10, transcript variant X4
ankyrin repeat and SOCS box protein 10 isoform X4
ankyrin repeat and SOCS box containing 10, transcript variant X2
ankyrin repeat and SOCS box containing 10, transcript variant X1
ankyrin repeat and SOCS box protein 10 isoform X2
ankyrin repeat and SOCS box protein 10 isoform X1
ankyrin repeat and SOCS box containing 10, transcript variant X3
ankyrin repeat and SOCS box protein 10 isoform X3
IQ motif containing with AAA domain 1 like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
IQ and AAA domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 171 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
ATP-binding cassette sub-family F member 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69% coverage of the annotated genomic feature by RNAseq alignments
chondroitin sulfate glucuronyltransferase
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X2
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X4
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 3 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, transcript variant X3
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 3, 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
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X4
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X5
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X2
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 3 isoform X3
negative regulator of ubiquitin like proteins 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: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
LOW QUALITY PROTEIN: NEDD8 ultimate buster 1
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 5 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; 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
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 11 samples with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X2
protein kinase AMP-activated non-catalytic subunit gamma 2, 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 5 samples with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X5
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
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X4
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 1 sample with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, 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 3 samples with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X7
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
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X14
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X10
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 1 sample with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X13
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 5 samples with support for all annotated introns
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X11
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X12
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X9
protein kinase AMP-activated non-catalytic subunit gamma 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
5'-AMP-activated protein kinase subunit gamma-2 isoform X4
5'-AMP-activated protein kinase subunit gamma-2 isoform X2
5'-AMP-activated protein kinase subunit gamma-2 isoform X1
5'-AMP-activated protein kinase subunit gamma-2 isoform X3
5'-AMP-activated protein kinase subunit gamma-2 isoform X10
5'-AMP-activated protein kinase subunit gamma-2 isoform X5
5'-AMP-activated protein kinase subunit gamma-2 isoform X8
5'-AMP-activated protein kinase subunit gamma-2 isoform X7
5'-AMP-activated protein kinase subunit gamma-2 isoform X6
5'-AMP-activated protein kinase subunit gamma-2 isoform X9
jerky protein homolog-like, transcript variant X5
jerky protein homolog-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
jerky protein homolog-like, transcript variant X4
jerky protein homolog-like, transcript variant X3
jerky protein homolog-like, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 11, 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
polypeptide N-acetylgalactosaminyltransferase 11, 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 1 sample with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 11, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 11 isoform X1
polypeptide N-acetylgalactosaminyltransferase 11 isoform 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
chaperonin containing TCP1 subunit 8 like 2
T-complex protein 1 subunit theta-like 2
X-ray repair cross complementing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
X-ray repair cross complementing 2, transcript variant X2
actin related protein 3B, 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
actin related protein 3B, 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 11 samples with support for all annotated introns
dipeptidyl peptidase like 6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X3
dipeptidyl peptidase like 6, transcript variant X5
dipeptidyl peptidase like 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X4
dipeptidyl peptidase like 6, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X1
dipeptidyl aminopeptidase-like protein 6 isoform X5
dipeptidyl peptidase like 6, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dipeptidyl aminopeptidase-like protein 6 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% 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: 10 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC119936396, transcript variant X2
uncharacterized LOC119936396, transcript variant X1
insulin induced gene 1, transcript variant X1
insulin induced gene 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
sonic hedgehog signaling molecule, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
sonic hedgehog signaling molecule, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ring finger protein 32, 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 1 sample with support for all annotated introns
ring finger protein 32, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 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 96% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
nucleolar MIF4G domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
motor neuron and pancreas homeobox protein 1
DnaJ heat shock protein family (Hsp40) member B6, transcript variant X2
DnaJ heat shock protein family (Hsp40) member B6, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member B6, transcript variant X1
dnaJ homolog subfamily B member 6 isoform X3
dnaJ homolog subfamily B member 6 isoform X1
dnaJ homolog subfamily B member 6 isoform X2
protein tyrosine phosphatase receptor type N2
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
receptor-type tyrosine-protein phosphatase N2
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
dynein 2 intermediate chain 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dynein 2 intermediate chain 1, transcript variant X2
dynein 2 intermediate chain 1, transcript variant X3
dynein 2 intermediate chain 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dynein 2 intermediate chain 1, transcript variant X5
dynein 2 intermediate chain 1, transcript variant X6
cytoplasmic dynein 2 intermediate chain 1 isoform X1
cytoplasmic dynein 2 intermediate chain 1 isoform X2
cytoplasmic dynein 2 intermediate chain 1 isoform X3
cytoplasmic dynein 2 intermediate chain 1 isoform X4
cytoplasmic dynein 2 intermediate chain 1 isoform X5
cytoplasmic dynein 2 intermediate chain 1 isoform X6
dynein 2 intermediate chain 1, transcript variant X7
cytoplasmic dynein 2 intermediate chain 1 isoform X7
vasoactive intestinal peptide receptor 2, 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 3 samples with support for all annotated introns
vasoactive intestinal peptide receptor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vasoactive intestinal peptide receptor 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
vasoactive intestinal polypeptide receptor 2 isoform X1
vasoactive intestinal polypeptide receptor 2 isoform X2
vasoactive intestinal polypeptide receptor 2 isoform X3
zinc finger MYND-type containing 11, transcript variant X2
zinc finger MYND-type containing 11, transcript variant X4
zinc finger MYND-type containing 11, transcript variant X13
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
zinc finger MYND-type containing 11, transcript variant X1
zinc finger MYND-type containing 11, transcript variant X14
zinc finger MYND-type containing 11, transcript variant X11
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
zinc finger MYND-type containing 11, transcript variant X6
zinc finger MYND-type containing 11, transcript variant X15
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
zinc finger MYND-type containing 11, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
zinc finger MYND-type containing 11, transcript variant X5
zinc finger MYND-type containing 11, transcript variant X7
zinc finger MYND-type containing 11, transcript variant X10
zinc finger MYND-type containing 11, transcript variant X9
zinc finger MYND-type containing 11, transcript variant X8
zinc finger MYND domain-containing protein 11 isoform X1
zinc finger MYND domain-containing protein 11 isoform X4
zinc finger MYND domain-containing protein 11 isoform X2
zinc finger MYND domain-containing protein 11 isoform X5
zinc finger MYND-type containing 11, transcript variant X12
zinc finger MYND domain-containing protein 11 isoform X3
zinc finger MYND-type containing 11, transcript variant X16
zinc finger MYND domain-containing protein 11 isoform X6
disco interacting protein 2 homolog C, transcript variant X4
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 5 samples with support for all annotated introns
disco interacting protein 2 homolog C, transcript variant X3
disco interacting protein 2 homolog C, 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 5 samples with support for all annotated introns
disco interacting protein 2 homolog C, transcript variant X1
disco-interacting protein 2 homolog C isoform X4
disco-interacting protein 2 homolog C isoform X3
disco-interacting protein 2 homolog C isoform X2
disco-interacting protein 2 homolog C isoform X1
La ribonucleoprotein 4B, transcript variant X3
La ribonucleoprotein 4B, 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 4 samples with support for all annotated introns
La ribonucleoprotein 4B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 53% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
isopentenyl-diphosphate delta isomerase 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 5 samples with support for all annotated introns
isopentenyl-diphosphate delta isomerase 1, transcript variant X1
isopentenyl-diphosphate Delta-isomerase 1
WD repeat domain 37, transcript variant X1
WD repeat domain 37, 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
WD repeat-containing protein 37 isoform X1
WD repeat-containing protein 37 isoform X2
adenosine deaminase RNA specific B2 (inactive)
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 5 samples with support for all annotated introns
phosphofructokinase, platelet, transcript variant X6
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
phosphofructokinase, platelet, transcript variant X2
phosphofructokinase, platelet, transcript variant X5
phosphofructokinase, platelet, transcript variant X1
phosphofructokinase, platelet, transcript variant X3
phosphofructokinase, platelet, transcript variant X4
ATP-dependent 6-phosphofructokinase, platelet type isoform X6
ATP-dependent 6-phosphofructokinase, platelet type isoform X1
ATP-dependent 6-phosphofructokinase, platelet type isoform X3
ATP-dependent 6-phosphofructokinase, platelet type isoform X4
ATP-dependent 6-phosphofructokinase, platelet type isoform X2
ATP-dependent 6-phosphofructokinase, platelet type isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
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
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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
cAMP responsive element modulator, transcript variant X8
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 1 sample with support for all annotated introns
cAMP responsive element modulator, transcript variant X10
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 1 sample with support for all annotated introns
cAMP responsive element modulator, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cAMP responsive element modulator, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cAMP responsive element modulator, transcript variant X2
cAMP responsive element modulator, transcript variant X3
cAMP responsive element modulator, transcript variant X9
cAMP responsive element modulator, transcript variant X5
cAMP responsive element modulator, transcript variant X12
cAMP responsive element modulator, transcript variant X15
cAMP-responsive element modulator isoform X6
cAMP-responsive element modulator isoform X8
cAMP-responsive element modulator isoform X4
cAMP-responsive element modulator isoform X1
cAMP-responsive element modulator isoform X7
cAMP-responsive element modulator isoform X3
cAMP-responsive element modulator isoform X10
cAMP responsive element modulator, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
cAMP-responsive element modulator isoform X11
cAMP-responsive element modulator isoform X13
cAMP responsive element modulator, transcript variant X11
cAMP responsive element modulator, transcript variant X4
cAMP-responsive element modulator isoform X9
cAMP-responsive element modulator isoform X2
cAMP responsive element modulator, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cAMP-responsive element modulator isoform X12
cAMP responsive element modulator, transcript variant X7
cAMP-responsive element modulator isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X4
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 2 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X1
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 5 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X7
par-3 family cell polarity regulator, transcript variant X3
par-3 family cell polarity regulator, transcript variant X9
par-3 family cell polarity regulator, 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 3 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X6
par-3 family cell polarity regulator, transcript variant X10
par-3 family cell polarity regulator, 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 3 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X8
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 4 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
par-3 family cell polarity regulator, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
partitioning defective 3 homolog isoform X4
partitioning defective 3 homolog isoform X1
partitioning defective 3 homolog isoform X7
partitioning defective 3 homolog isoform X3
partitioning defective 3 homolog isoform X9
partitioning defective 3 homolog isoform X2
partitioning defective 3 homolog isoform X6
partitioning defective 3 homolog isoform X10
partitioning defective 3 homolog isoform X5
partitioning defective 3 homolog isoform X8
partitioning defective 3 homolog isoform X14
partitioning defective 3 homolog isoform X13
par-3 family cell polarity regulator, transcript variant X11
par-3 family cell polarity regulator, transcript variant X12
partitioning defective 3 homolog isoform X11
partitioning defective 3 homolog isoform X12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
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 3 samples with support for all annotated introns
integrin subunit beta 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 1 sample with support for all annotated introns
uncharacterized LOC119936235, transcript variant X2
uncharacterized LOC119936235, transcript variant X1
integrin subunit beta 1, transcript variant X3
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 10 samples with support for all annotated introns
integrin subunit beta 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 4 samples with support for all annotated introns
coiled-coil domain containing 7, transcript variant X3
coiled-coil domain containing 7, transcript variant X5
coiled-coil domain containing 7, transcript variant X7
coiled-coil domain containing 7, transcript variant X8
coiled-coil domain containing 7, transcript variant X1
coiled-coil domain containing 7, transcript variant X6
coiled-coil domain containing 7, transcript variant X10
coiled-coil domain containing 7, transcript variant X4
coiled-coil domain containing 7, transcript variant X2
coiled-coil domain-containing protein 7 isoform X1
coiled-coil domain containing 7, transcript variant X9
coiled-coil domain containing 7, transcript variant X11
coiled-coil domain-containing protein 7 isoform X2
enhancer of polycomb homolog 1, transcript variant X3
enhancer of polycomb homolog 1 isoform X3
enhancer of polycomb homolog 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
enhancer of polycomb homolog 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
enhancer of polycomb homolog 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 9 samples with support for all annotated introns
enhancer of polycomb homolog 1 isoform X1
enhancer of polycomb homolog 1 isoform X2
enhancer of polycomb homolog 1 isoform X4
Rho GTPase activating protein 12, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rho GTPase activating protein 12, transcript variant X3
Rho GTPase activating protein 12, transcript variant X2
Rho GTPase activating protein 12, 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 7 samples with support for all annotated introns
Rho GTPase activating protein 12, transcript variant X4
rho GTPase-activating protein 12 isoform X1
rho GTPase-activating protein 12 isoform X3
rho GTPase-activating protein 12 isoform X2
rho GTPase-activating protein 12 isoform X5
rho GTPase-activating protein 12 isoform X4
zinc finger E-box binding homeobox 1, transcript variant X4
zinc finger E-box binding homeobox 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger E-box binding homeobox 1, transcript variant X2
zinc finger E-box binding homeobox 1, transcript variant X1
zinc finger E-box binding homeobox 1, transcript variant X8
zinc finger E-box binding homeobox 1, transcript variant X6
zinc finger E-box binding homeobox 1, transcript variant X10
zinc finger E-box binding homeobox 1, transcript variant X7
zinc finger E-box binding homeobox 1, transcript variant X9
zinc finger E-box binding homeobox 1, transcript variant X5
zinc finger E-box binding homeobox 1, transcript variant X11
zinc finger E-box-binding homeobox 1 isoform X4
zinc finger E-box-binding homeobox 1 isoform X3
zinc finger E-box-binding homeobox 1 isoform X2
zinc finger E-box-binding homeobox 1 isoform X1
zinc finger E-box-binding homeobox 1 isoform X6
zinc finger E-box-binding homeobox 1 isoform X5
zinc finger E-box-binding homeobox 1 isoform X7
zinc finger protein 438, 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 1 sample with support for all annotated introns
zinc finger protein 438, transcript variant X7
zinc finger protein 438, transcript variant X6
zinc finger protein 438, transcript variant X3
zinc finger protein 438, 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 3 samples with support for all annotated introns
zinc finger protein 438, transcript variant X8
zinc finger protein 438, transcript variant X2
zinc finger protein 438, transcript variant X4
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
junctional cadherin 5 associated, transcript variant X1
junctional cadherin 5 associated, transcript variant X2
junctional cadherin 5 associated, transcript variant X4
junctional cadherin 5 associated, transcript variant X3
junctional protein associated with coronary artery disease isoform X1
junctional protein associated with coronary artery disease isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mitogen-activated protein kinase kinase kinase 8
uncharacterized LOC119936404, transcript variant X1
uncharacterized LOC119936404, transcript variant X2
BMP and activin membrane bound inhibitor
BMP and activin membrane-bound inhibitor homolog
WW domain containing adaptor with coiled-coil, transcript variant X6
WW domain containing adaptor with coiled-coil, transcript variant X2
WW domain containing adaptor with coiled-coil, transcript variant X1
WW domain containing adaptor with coiled-coil, transcript variant X3
WW domain containing adaptor with coiled-coil, transcript variant X4
WW domain containing adaptor with coiled-coil, transcript variant X5
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
WW domain-containing adapter protein with coiled-coil isoform X5
WW domain-containing adapter protein with coiled-coil isoform X3
WW domain-containing adapter protein with coiled-coil isoform X2
WW domain-containing adapter protein with coiled-coil isoform X4
WW domain-containing adapter protein with coiled-coil isoform X1
WW domain-containing adapter protein with coiled-coil isoform X6
membrane palmitoylated protein 7, transcript variant X1
membrane palmitoylated protein 7, transcript variant X2
outer dynein arm docking complex subunit 2, transcript variant X3
outer dynein arm docking complex subunit 2, transcript variant X1
outer dynein arm docking complex subunit 2, transcript variant X2
outer dynein arm docking complex subunit 2, transcript variant X4
armadillo repeat-containing protein 4 isoform X1
armadillo repeat-containing protein 4 isoform X3
armadillo repeat-containing protein 4 isoform X2
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
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 11 samples with support for all annotated introns
phenolphthiocerol/phthiocerol polyketide synthase subunit B-like
ATP-dependent zinc metalloprotease YME1L1
microtubule associated serine/threonine kinase like, 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
serine/threonine-protein kinase greatwall isoform X1
microtubule associated serine/threonine kinase like, transcript variant X2
serine/threonine-protein kinase greatwall isoform X2
acyl-CoA binding domain containing 5, 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
acyl-CoA binding domain containing 5, transcript variant X3
acyl-CoA binding domain containing 5, 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 1 sample with support for all annotated introns
acyl-CoA-binding domain-containing protein 5 isoform X2
acyl-CoA-binding domain-containing protein 5 isoform 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 3 samples with support for all annotated introns
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 6 samples with support for all annotated introns
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
decaprenyl diphosphate synthase subunit 1
all trans-polyprenyl-diphosphate synthase PDSS1
protein adenylyltransferase SelO-like, transcript variant X1
protein adenylyltransferase SelO-like isoform X1
protein adenylyltransferase SelO-like, transcript variant X2
protein adenylyltransferase SelO-like isoform X2
amyloid beta precursor protein binding family B member 1 interacting protein
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: 10 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: amyloid beta A4 precursor protein-binding family B member 1-interacting protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
enkurin, TRPC channel interacting protein, transcript variant X2
enkurin, TRPC channel interacting protein, transcript variant X1
Rho GTPase activating protein 21, transcript variant X1
Rho GTPase activating protein 21, transcript variant X2
rho GTPase-activating protein 21 isoform X1
rho GTPase-activating protein 21 isoform X2
KIAA1217 ortholog, transcript variant X8
KIAA1217 ortholog, transcript variant X11
KIAA1217 ortholog, transcript variant X12
KIAA1217 ortholog, transcript variant X7
KIAA1217 ortholog, transcript variant X5
KIAA1217 ortholog, transcript variant X3
KIAA1217 ortholog, transcript variant X2
KIAA1217 ortholog, transcript variant X1
KIAA1217 ortholog, transcript variant X4
KIAA1217 ortholog, transcript variant X6
KIAA1217 ortholog, transcript variant X10
KIAA1217 ortholog, transcript variant X9
KIAA1217 ortholog, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C10orf67 homolog, mitochondrial
pancreas associated transcription factor 1a
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pancreas transcription factor 1 subunit alpha
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
methionine-R-sulfoxide reductase B2, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
armadillo repeat containing 3, transcript variant X2
armadillo repeat containing 3, transcript variant X1
phosphatidylinositol-5-phosphate 4-kinase type 2 alpha
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
phosphatidylinositol 5-phosphate 4-kinase type-2 alpha
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
polycomb complex protein BMI-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 7 samples with support for all annotated introns
polycomb complex protein BMI-1, transcript variant X2
DnaJ heat shock protein family (Hsp40) member C1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119936370, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized LOC119936370, transcript variant X4
uncharacterized LOC119936370, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC119936370, transcript variant X5
uncharacterized LOC119936370, transcript variant X3
uncharacterized LOC119936370, transcript variant X2
MLLT10 histone lysine methyltransferase DOT1L cofactor, 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
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X3
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MLLT10 histone lysine methyltransferase DOT1L cofactor, 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
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X6
MLLT10 histone lysine methyltransferase DOT1L cofactor, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
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
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
tRNA (cytosine(72)-C(5))-methyltransferase NSUN6
calcium voltage-gated channel auxiliary subunit beta 2, 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
calcium voltage-gated channel auxiliary subunit beta 2, transcript variant X2
calcium voltage-gated channel auxiliary subunit beta 2, transcript variant X4
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
calcium voltage-gated channel auxiliary subunit beta 2, transcript variant X1
voltage-dependent L-type calcium channel subunit beta-2 isoform X3
voltage-dependent L-type calcium channel subunit beta-2 isoform X2
voltage-dependent L-type calcium channel subunit beta-2 isoform X4
voltage-dependent L-type calcium channel subunit beta-2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 74% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA tyrosine (anticodon GUA); 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: 2 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
signal transducing adaptor molecule, transcript variant X3
signal transducing adaptor molecule, 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 5 samples with support for all annotated introns
signal transducing adaptor molecule, transcript variant X2
signal transducing adapter molecule 1 isoform X1
signal transducing adapter molecule 1 isoform X2
signal transducing adapter molecule 1 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 6 samples with support for all annotated introns
very-long-chain (3R)-3-hydroxyacyl-CoA dehydratase 1
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 11 samples with support for all annotated introns
ADAM metallopeptidase domain 22, transcript variant X2
ADAM metallopeptidase domain 22, transcript variant X1
disintegrin and metalloproteinase domain-containing protein 22 isoform X2
disintegrin and metalloproteinase domain-containing protein 22 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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 B member 1, transcript variant X1
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
ATP binding cassette subfamily B member 1, transcript variant X2
ATP-dependent translocase ABCB1 isoform X1
ATP-dependent translocase ABCB1 isoform X2
phosphatidylcholine translocator ABCB4-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 109 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylcholine translocator ABCB4-like isoform X3
phosphatidylcholine translocator ABCB4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatidylcholine translocator ABCB4-like isoform X1
phosphatidylcholine translocator ABCB4-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatidylcholine translocator ABCB4-like isoform X2
carnitine O-octanoyltransferase, transcript variant X3
carnitine O-octanoyltransferase, transcript variant X4
carnitine O-octanoyltransferase, transcript variant X2
carnitine O-octanoyltransferase, transcript variant X1
peroxisomal carnitine O-octanoyltransferase isoform X2
peroxisomal carnitine O-octanoyltransferase isoform X1
peroxisomal carnitine O-octanoyltransferase isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
glycylpeptide N-tetradecanoyltransferase 2
family with sequence similarity 171 member A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase MINDY-3
phosphotriesterase related, transcript variant X3
phosphotriesterase related, 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 3 samples with support for all annotated introns
phosphotriesterase related, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Ras suppressor 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 10 samples with support for all annotated introns
Ras suppressor protein 1, transcript variant X2
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: 8 Proteins, and 97% 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 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
tRNA aspartic acid methyltransferase 1, transcript variant X1
tRNA (cytosine(38)-C(5))-methyltransferase isoform X1
tRNA aspartic acid methyltransferase 1, transcript variant X2
tRNA (cytosine(38)-C(5))-methyltransferase isoform X2
tRNA aspartic acid methyltransferase 1, transcript variant X3
tRNA (cytosine(38)-C(5))-methyltransferase isoform X3
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 11 samples with support for all annotated introns
normal mucosa of esophagus-specific gene 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 48% coverage of the annotated genomic feature by RNAseq alignments