Cyprinus carpio isolate SPL01 chromosome A22, ASM1834038v1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Actinopterygii; Neopterygii; Teleostei; Ostariophysi; Cypriniformes; Cyprinidae; Cyprininae; Cyprinus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM031259.1.\nAssembly name: ASM1834038v1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Chinese Academy of Fishery\nSciences on 2021/05/12. The original whole-genome shotgun project\nhas the accession JAEOAB000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Chinese Academy of Fishery Sciences\nAssembly Method :: wtdbg v. 2; quickmerge v. 1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 184.8x\nSequencing Technology :: PacBio; Oxford Nanopore; Illumina HiSeq\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Cyprinus carpio Annotation Release\n 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments
myosin heavy chain, fast skeletal muscle-like
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 143 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
olfactory receptor class A-like protein 1
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins
transforming protein RhoA-like, transcript variant X3
transforming protein RhoA-like, transcript variant X1
transforming protein RhoA-like, transcript variant X2
uncharacterized protein LOC619199 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase complex assembly factor
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 3
NCK-interacting protein with SH3 domain-like, transcript variant X1
NCK-interacting protein with SH3 domain-like, transcript variant X2
NCK-interacting protein with SH3 domain-like
mitochondrial carnitine/acylcarnitine carrier protein
protein kinase, cAMP-dependent, regulatory, type II, alpha, B, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein kinase, cAMP-dependent, regulatory, type II, alpha, B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
protein kinase, cAMP-dependent, regulatory, type II, alpha, B isoform X1
protein kinase, cAMP-dependent, regulatory, type II, alpha, B isoform X2
msx2-interacting protein, transcript variant X4
msx2-interacting protein, transcript variant X2
msx2-interacting protein, transcript variant X3
msx2-interacting protein, transcript variant X1
msx2-interacting protein, transcript variant X5
filamin binding LIM protein 1, transcript variant X2
filamin binding LIM protein 1, transcript variant X1
filamin binding LIM protein 1, transcript variant X3
filamin-binding LIM protein 1 isoform X2
filamin-binding LIM protein 1 isoform X1
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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 82% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: F-box only protein 42
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
39S ribosomal protein L20, mitochondrial
succinate dehydrogenase complex, subunit B, iron sulfur (Ip)
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: 1 Protein, and 83% 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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: succinate dehydrogenase [ubiquinone] iron-sulfur subunit, mitochondrial
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 124 samples with support for all annotated introns
adaptin ear-binding coat-associated protein 2
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 70 samples with support for all annotated introns
SSU72 homolog, RNA polymerase II CTD phosphatase
RNA polymerase II subunit A C-terminal domain phosphatase SSU72
fibronectin type III domain containing 10
fibronectin type III domain-containing protein 10
olfactory receptor class A-like protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 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: 36 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 47-like, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 47-like isoform X1
ubiquitin carboxyl-terminal hydrolase 47-like isoform X2
WAP four-disulfide core domain 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 32 samples with support for all annotated introns
glycine-rich cell wall structural protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
neuroblastoma suppressor of tumorigenicity 1-like, transcript variant X3
neuroblastoma suppressor of tumorigenicity 1-like, transcript variant X2
neuroblastoma suppressor of tumorigenicity 1-like, transcript variant X1
neuroblastoma suppressor of tumorigenicity 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
cadherin EGF LAG seven-pass G-type receptor 2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cadherin EGF LAG seven-pass G-type receptor 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 51% 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 82% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 106 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc finger protein 865-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 ESTs, 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: GTPase IMAP family member 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 25 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
peroxisome proliferator-activated receptor delta-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 228 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
differentially expressed in FDCP 6 homolog
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 61 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 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: 14 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
mediator complex subunit 20, transcript variant X1
mediator complex subunit 20, transcript variant X2
mediator of RNA polymerase II transcription subunit 20 isoform X1
mediator complex subunit 20, transcript variant X3
mediator of RNA polymerase II transcription subunit 20 isoform 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 89 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 49
transmembrane and coiled-coil domains protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
transmembrane and coiled-coil domains protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 38 samples with support for all annotated introns
transmembrane and coiled-coil domains protein 2-like isoform X2
transmembrane and coiled-coil domains protein 2-like isoform X1
cyclin-dependent kinase inhibitor 1-like, transcript variant X1
cyclin-dependent kinase inhibitor 1-like, transcript variant X2
cyclin-dependent kinase inhibitor 1-like
serine and arginine rich splicing factor 3b
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 25 samples with support for all annotated introns
apolipoprotein B mRNA editing enzyme, catalytic polypeptide-like 2a
E74-like factor 3 (ets domain transcription factor, epithelial-specific), transcript variant X1
E74-like factor 3 (ets domain transcription factor, epithelial-specific), transcript variant X2
ETS-related transcription factor Elf-3 isoform X1
ETS-related transcription factor Elf-3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 141 samples with support for all annotated introns
uncharacterized protein LOC768179 homolog, transcript variant X2
uncharacterized protein LOC768179 homolog, transcript variant X1
choline/ethanolaminephosphotransferase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 11 Proteins, and 77% 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 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
calcium/calmodulin-dependent protein kinase type 1D-like, transcript variant X2
calcium/calmodulin-dependent protein kinase type 1D-like, transcript variant X1
calcium/calmodulin-dependent protein kinase type 1D-like
uncharacterized LOC122134836, 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 17 samples with support for all annotated introns
uncharacterized LOC122134836, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
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 35 samples with support for all annotated introns
guanylyl cyclase-activating protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
GTPase IMAP family member 8-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
GTPase IMAP family member 8-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 ESTs, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
GTPase IMAP family member 8-like isoform X1
GTPase IMAP family member 8-like 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 31 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 1 Protein, and 46% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 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: 1 Protein, 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: tRNAscan-SE.
transfer RNA methionine (anticodon CAU); 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.
transfer RNA aspartic acid (anticodon GUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); 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: 3 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
lon protease homolog, mitochondrial-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lon protease homolog, mitochondrial-like
lens fiber membrane intrinsic protein-like, transcript variant X1
lens fiber membrane intrinsic protein-like, transcript variant X2
lens fiber membrane intrinsic protein-like
G-protein coupled receptor 55-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 5 samples with support for all annotated introns
G-protein coupled receptor 55-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 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 44% coverage of the annotated genomic feature by RNAseq alignments
GRAM domain-containing protein 2B-like, transcript variant X2
GRAM domain-containing protein 2B-like, transcript variant X1
GRAM domain-containing protein 2B-like, transcript variant X3
GRAM domain-containing protein 2B-like, transcript variant X5
GRAM domain-containing protein 2B-like, transcript variant X4
GRAM domain-containing protein 2A-like isoform X2
GRAM domain-containing protein 2A-like isoform X1
GRAM domain-containing protein 2B-like isoform X3
GRAM domain-containing protein 2B-like isoform X5
GRAM domain-containing protein 2B-like isoform X4
PDZ domain-containing protein GIPC3-like
thromboxane A2 receptor-like, transcript variant X3
thromboxane A2 receptor-like, transcript variant X1
thromboxane A2 receptor-like, transcript variant X2
thromboxane A2 receptor-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
receptor-type tyrosine-protein phosphatase S-like
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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
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
major histocompatibility complex class I-related gene protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 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: 59 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
class I histocompatibility antigen, F10 alpha chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
E3 ubiquitin-protein ligase UHRF1, 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 51 samples with support for all annotated introns
E3 ubiquitin-protein ligase UHRF1, 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 17 samples with support for all annotated introns
TIR domain-containing adapter molecule 1-like, transcript variant X1
TIR domain-containing adapter molecule 1-like, transcript variant X2
TIR domain-containing adapter molecule 1-like
mitochondrial import inner membrane translocase subunit TIM44-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
UV excision repair protein RAD23 homolog B-like, transcript variant X2
UV excision repair protein RAD23 homolog B-like, transcript variant X1
UV excision repair protein RAD23 homolog B-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 2 samples with support for all annotated introns
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 24 samples with support for all annotated introns
SLAM family member 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 86% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SLAM family member 9-like, transcript variant X2
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 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 78% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109110216, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
uncharacterized LOC109110216, 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 73% coverage of the annotated genomic feature by RNAseq alignments
SLAM family member 5-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 81% coverage of the annotated genomic feature by RNAseq alignments
SLAM family member 5-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
uncharacterized LOC122134848, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized LOC122134848, 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 27 samples with support for all annotated introns
uncharacterized protein LOC122134848 isoform X2
uncharacterized protein LOC122134848 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein LOC109072657 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 14 samples with support for all annotated introns
uncharacterized protein C19orf44 homolog
calcium homeostasis endoplasmic reticulum protein, transcript variant X2
calcium homeostasis endoplasmic reticulum protein, transcript variant X1
calcium homeostasis endoplasmic reticulum protein isoform X2
calcium homeostasis endoplasmic reticulum protein isoform X1
NACHT, LRR and PYD domains-containing protein 12-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
retinal homeobox gene 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
retinal homeobox gene 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ATCAY kinesin light chain interacting caytaxin a
nicotinamide riboside kinase 2-like, transcript variant X1
nicotinamide riboside kinase 2-like isoform X1
nicotinamide riboside kinase 2-like, transcript variant X2
nicotinamide riboside kinase 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
tumor necrosis factor alpha-induced protein 8-like protein 1, transcript variant X2
tumor necrosis factor alpha-induced protein 8-like protein 1, transcript variant X1
tumor necrosis factor alpha-induced protein 8-like protein 1 isoform X1
tumor necrosis factor alpha-induced protein 8-like protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
SLAM family member 5, transcript variant X4
SLAM family member 5, transcript variant X3
SLAM family member 5, transcript variant X2
SLAM family member 5, transcript variant X1
uncharacterized protein LOC109076362 isoform X3
uncharacterized protein LOC109076362 isoform X2
uncharacterized protein LOC109076362 isoform X1
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: 1 EST, 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
LOW QUALITY PROTEIN: podocalyxin-like protein 2
DNA replication licensing factor mcm2-like
mitochondrial potassium channel-like, transcript variant X3
mitochondrial potassium channel-like, transcript variant X2
mitochondrial potassium channel-like, transcript variant X1
translation machinery-associated protein 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 87% coverage of the annotated genomic feature by RNAseq alignments
deoxyribonuclease gamma-like, 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 50 samples with support for all annotated introns
deoxyribonuclease gamma-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 75 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-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 41 samples with support for all annotated introns
piggyBac transposable element-derived protein 4-like, transcript variant X1
piggyBac transposable element-derived protein 4-like, transcript variant X2
piggyBac transposable element-derived protein 4-like isoform X1
piggyBac transposable element-derived protein 4-like isoform X2
cytochrome c oxidase assembly protein COX14 homolog
ceramide synthase 5-like, transcript variant X3
ceramide synthase 5-like, transcript variant X1
ceramide synthase 5-like, 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 21 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 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 12% 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
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 63 samples with support for all annotated introns
uncharacterized LOC109054492, transcript variant X1
uncharacterized LOC109054492, transcript variant X2
uncharacterized protein LOC109054492 isoform X1
uncharacterized protein LOC109054492 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 4 samples with support for all annotated introns
uncharacterized LOC109053833, transcript variant X4
uncharacterized LOC109053833, transcript variant X3
uncharacterized LOC109053833, transcript variant X2
uncharacterized LOC109053833, transcript variant X1
uncharacterized protein LOC109053833 isoform X2
uncharacterized protein LOC109053833 isoform 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 LOC122134993, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC122134993, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109061256, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC109061256, transcript variant X3
uncharacterized LOC109061256, transcript variant X2
uncharacterized LOC109061256, transcript variant X1
uncharacterized protein LOC109061256 isoform X2
uncharacterized protein LOC109061256 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
glycerol-3-phosphate dehydrogenase [NAD(+)], cytoplasmic
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 132 samples with support for all annotated introns
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 1
acid-sensing ion channel 1B, transcript variant X5
acid-sensing ion channel 1B, transcript variant X4
acid-sensing ion channel 1B, transcript variant X6
acid-sensing ion channel 1B, transcript variant X3
acid-sensing ion channel 1B, transcript variant X1
acid-sensing ion channel 1B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
uncharacterized LOC109046421, transcript variant X2
uncharacterized LOC109046421, 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 44 samples with support for all annotated introns
uncharacterized protein LOC109046421 isoform X1
uncharacterized protein LOC109046421 isoform X2
natural killer cell receptor 2B4-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
natural killer cell receptor 2B4-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
natural killer cell receptor 2B4-like, transcript variant X2
uncharacterized protein LOC122134982 isoform X2
uncharacterized LOC109046417, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC109046417, transcript variant X2
gastrula zinc finger protein XlCGF57.1-like, transcript variant X3
gastrula zinc finger protein XlCGF57.1-like, transcript variant X2
gastrula zinc finger protein XlCGF57.1-like, transcript variant X1
gastrula zinc finger protein XlCGF57.1-like, transcript variant X4
gastrula zinc finger protein XlCGF57.1-like
gastrula zinc finger protein XlCGF8.2DB-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 86 samples with support for all annotated introns
gastrula zinc finger protein XlCGF57.1-like isoform X1
gastrula zinc finger protein XlCGF8.2DB-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 57 samples with support for all annotated introns
gastrula zinc finger protein XlCGF8.2DB-like isoform X2
uncharacterized LOC109112660, transcript variant X2
uncharacterized LOC109112660, transcript variant X1
NACHT, LRR and PYD domains-containing protein 3-like
SLAM family member 9-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
gastrula zinc finger protein XlCGF49.1-like, transcript variant X4
gastrula zinc finger protein XlCGF49.1-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 2 samples with support for all annotated introns
gastrula zinc finger protein XlCGF49.1-like, transcript variant X2
gastrula zinc finger protein XlCGF49.1-like isoform X4
gastrula zinc finger protein XlCGF49.1-like, 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 18 samples with support for all annotated introns
uncharacterized LOC122134990, transcript variant X2
uncharacterized LOC122134990, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 88 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 54 samples with support for all annotated introns
striatin-interacting protein 1 homolog, transcript variant X2
striatin-interacting protein 1 homolog, transcript variant X1
striatin-interacting protein 1 homolog isoform X2
striatin-interacting protein 1 homolog isoform X1
voltage-dependent calcium channel subunit alpha-2/delta-2-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: voltage-dependent calcium channel subunit alpha-2/delta-2-like
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 12-like, transcript variant X3
NACHT, LRR and PYD domains-containing protein 12-like isoform X2
NACHT, LRR and PYD domains-containing protein 12-like isoform X1
NACHT, LRR and PYD domains-containing protein 3-like isoform X3
uncharacterized LOC122134985, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
uncharacterized protein LOC122134985 isoform X2
uncharacterized LOC122134985, transcript variant X1
uncharacterized protein LOC122134985 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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 13 samples with support for all annotated introns
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 16 samples with support for all annotated introns
muscle M-line assembly protein unc-89-like
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% 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: 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122134857, transcript variant X2
uncharacterized LOC122134857, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
glutaminase kidney isoform, mitochondrial-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
glutaminase kidney isoform, mitochondrial-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
glutaminase kidney isoform, mitochondrial-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
glutaminase kidney isoform, mitochondrial-like isoform X2
glutaminase kidney isoform, mitochondrial-like isoform X1
glutaminase kidney isoform, mitochondrial-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
biogenesis of lysosome-related organelles complex 1 subunit 1
TBC1 domain family member 20-like, transcript variant X4
TBC1 domain family member 20-like, transcript variant X3
TBC1 domain family member 20-like, transcript variant X1
TBC1 domain family member 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 62 samples with support for all annotated introns
TBC1 domain family member 20-like isoform X1
TBC1 domain family member 20-like isoform X2
TBC1 domain family member 20-like isoform X3
ranBP-type and C3HC4-type zinc finger-containing protein 1-like, transcript variant X2
ranBP-type and C3HC4-type zinc finger-containing protein 1-like, transcript variant X1
ranBP-type and C3HC4-type zinc finger-containing protein 1-like
hydroxyacyl-thioester dehydratase type 2, mitochondrial-like
PX domain containing serine/threonine kinase, transcript variant X4
PX domain containing serine/threonine kinase, transcript variant X3
PX domain containing serine/threonine kinase, transcript variant X2
PX domain containing serine/threonine kinase, transcript variant X10
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 15 samples with support for all annotated introns
PX domain containing serine/threonine kinase, transcript variant X1
PX domain containing serine/threonine kinase, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
PX domain containing serine/threonine kinase, transcript variant X8
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 61 samples with support for all annotated introns
PX domain containing serine/threonine kinase, transcript variant X7
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 15 samples with support for all annotated introns
PX domain containing serine/threonine kinase, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 69 samples with support for all annotated introns
PX domain containing serine/threonine kinase, transcript variant X6
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 61 samples with support for all annotated introns
PX domain-containing protein kinase-like protein isoform X1
PX domain-containing protein kinase-like protein isoform X2
PX domain-containing protein kinase-like protein isoform X3
PX domain-containing protein kinase-like protein isoform X4
PX domain-containing protein kinase-like protein isoform X5
PX domain-containing protein kinase-like protein isoform X6
PX domain containing serine/threonine kinase, transcript variant X11
PX domain-containing protein kinase-like protein isoform X7
pyruvate dehydrogenase E1 subunit beta, transcript variant X1
pyruvate dehydrogenase E1 component subunit beta, mitochondrial isoform X1
pyruvate dehydrogenase E1 subunit beta, transcript variant X2
pyruvate dehydrogenase E1 component subunit beta, mitochondrial isoform X2
potassium channel tetramerization domain containing 6a, 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 42 samples with support for all annotated introns
potassium channel tetramerization domain containing 6a, 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 21 samples with support for all annotated introns
BTB/POZ domain-containing protein KCTD6a
uncharacterized LOC109047374, transcript variant X1
uncharacterized LOC109047374, transcript variant X3
uncharacterized LOC109047374, transcript variant X4
uncharacterized LOC109047374, transcript variant X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing glutamate-rich 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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
extracellular matrix protein 2, female organ and adipocyte specific, transcript variant X1
extracellular matrix protein 2, female organ and adipocyte specific, transcript variant X2
inositol 1,3,4,5,6-pentakisphosphate 2-kinase
ATR interacting protein, transcript variant X2
ATR interacting protein, transcript variant X1
protein shisa-5-like, transcript variant X7
protein shisa-5-like, transcript variant X6
uncharacterized protein LOC109093036 isoform X2
uncharacterized protein LOC109093036 isoform X3
protein shisa-5-like, transcript variant X3
protein shisa-5-like, transcript variant X4
protein shisa-5-like, transcript variant X5
protein shisa-5-like, transcript variant X1
protein shisa-5-like, transcript variant X2
ubiquitin carboxyl-terminal hydrolase BAP1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
hyaluronidase-2-like, transcript variant X2
hyaluronidase-2-like, transcript variant X1
abhydrolase domain containing 14A, transcript variant X2
abhydrolase domain containing 14A, transcript variant X1
major facilitator superfamily domain containing 14A 1
hippocampus abundant transcript 1 protein
spindle assembly abnormal protein 6 homolog, transcript variant X2
spindle assembly abnormal protein 6 homolog, transcript variant X1
spindle assembly abnormal protein 6 homolog isoform X2
spindle assembly abnormal protein 6 homolog isoform X1
U6 snRNA-associated Sm-like protein LSm7
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
mitochondrial import inner membrane translocase subunit Tim13-like
rho guanine nucleotide exchange factor 18-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 64 samples with support for all annotated introns
unconventional SNARE in the ER 1 homolog (S. cerevisiae)
uncharacterized LOC109047222, transcript variant X2
uncharacterized LOC109047222, 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 8 samples with support for all annotated introns
uncharacterized protein LOC109047222 isoform X2
uncharacterized protein LOC109047222 isoform X1
uncharacterized LOC109047222, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
uncharacterized protein LOC109047222 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
BCL-6 corepressor-like, transcript variant X2
BCL-6 corepressor-like, transcript variant X1
BCL-6 corepressor-like, transcript variant X3
uncharacterized LOC122134998, transcript variant X1
uncharacterized LOC122134998, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
uncharacterized LOC122134998, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109070454, transcript variant X1
uncharacterized LOC122134998, transcript variant X3
uncharacterized LOC109070454, transcript variant X2
sodium-independent sulfate anion transporter
guanine nucleotide-binding protein G(o) subunit alpha-like
ethanolamine-phosphate cytidylyltransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 84 samples with support for all annotated introns
ethanolamine-phosphate cytidylyltransferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
ethanolamine-phosphate cytidylyltransferase-like isoform X1
ethanolamine-phosphate cytidylyltransferase-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
gamma-crystallin S-like, transcript variant X2
gamma-crystallin S-like, transcript variant X1
keratin, type I cytoskeletal 19-like, transcript variant X1
keratin, type I cytoskeletal 19-like, transcript variant X3
keratin, type I cytoskeletal 19-like, transcript variant X2
keratin, type I cytoskeletal 19-like, transcript variant X5
keratin, type I cytoskeletal 19-like, transcript variant X4
keratin, type I cytoskeletal 19-like isoform X2
keratin, type I cytoskeletal 19-like isoform X1
protein tyrosine phosphatase non-receptor type 4b, transcript variant X1
protein tyrosine phosphatase non-receptor type 4b, transcript variant X2
tyrosine-protein phosphatase non-receptor type 4b
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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
DNA annealing helicase and endonuclease ZRANB3-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: 13 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
LOW QUALITY PROTEIN: DNA annealing helicase and endonuclease ZRANB3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
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: R3H domain-containing protein 1-like
cobalamin trafficking protein CblD-like, transcript variant X1
cobalamin trafficking protein CblD-like, transcript variant X3
cobalamin trafficking protein CblD-like, transcript variant X2
centrosomal protein of 70 kDa-like, transcript variant X2
centrosomal protein of 70 kDa-like, transcript variant X1
centrosomal protein of 70 kDa-like isoform X2
centrosomal protein of 70 kDa-like isoform X1
double-stranded RNA-specific editase 1-like, transcript variant X2
double-stranded RNA-specific editase 1-like, transcript variant X3
double-stranded RNA-specific editase 1-like, transcript variant X1
double-stranded RNA-specific editase 1-like isoform X1
double-stranded RNA-specific editase 1-like isoform X2
double-stranded RNA-specific editase 1-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
CCR4-NOT transcription complex subunit 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 127 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: growth/differentiation factor 8
signal transducer and activator of transcription 1-alpha/beta-like, transcript variant X1
signal transducer and activator of transcription 1-alpha/beta-like, transcript variant X2
signal transducer and activator of transcription 1-alpha/beta-like isoform X1
signal transducer and activator of transcription 1-alpha/beta-like isoform X2
contactin associated protein family member 5b
protein S100-B-like, transcript variant X1
protein S100-B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: aldehyde oxidase 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
basic leucine zipper and W2 domain-containing protein 1-A
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 44 samples with support for all annotated introns
von Willebrand factor D and EGF domain-containing protein-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: von Willebrand factor D and EGF domain-containing protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 80% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
low density lipoprotein receptor-related protein 1Ba
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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: low-density lipoprotein receptor-related protein 1B
uncharacterized LOC109089665, transcript variant X2
uncharacterized LOC109089665, transcript variant X1
protein phosphatase 1 regulatory subunit 29-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
protein phosphatase 1 regulatory subunit 29-like
beta-1,3-N-acetylglucosaminyltransferase manic fringe
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, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 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: 8 Proteins, and 50% 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 63% 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 92% coverage of the annotated genomic feature by RNAseq alignments, including 66 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 10 bases in 8 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 76% 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 10 bases in 8 codons; substituted 2 bases at 2 genomic stop 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: 99 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 82% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: scaffold attachment factor B2-like
mucosa-associated lymphoid tissue lymphoma translocation protein 1 homolog, transcript variant X2
mucosa-associated lymphoid tissue lymphoma translocation protein 1 homolog, transcript variant X1
mucosa-associated lymphoid tissue lymphoma translocation protein 1 homolog
39S ribosomal protein L54, mitochondrial-like
epidermal growth factor receptor substrate 15-like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments, including 52 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 61% coverage of the annotated genomic feature by RNAseq alignments
dual specificity protein phosphatase CDC14AB-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
dual specificity protein phosphatase CDC14AB-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 3 samples with support for all annotated introns
dual specificity protein phosphatase CDC14AB-like isoform X2
dual specificity protein phosphatase CDC14AB-like isoform X1
dual specificity protein phosphatase CDC14AB-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
leucine-rich repeat-containing protein 39-like
tRNA:m(4)X modification enzyme TRM13 homolog
oxysterol-binding protein-related protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
amine sulfotransferase-like, transcript variant X2
amine sulfotransferase-like, transcript variant X3
amine sulfotransferase-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 49% coverage of the annotated genomic feature by RNAseq alignments
glutamic acid-rich protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamic acid-rich protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 97% 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 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 48 samples with support for all annotated introns
ankyrin repeat and MYND domain containing 1
ankyrin repeat and MYND domain-containing protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tropomyosin alpha-1 chain
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 138 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 29% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 81 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 19% coverage of the annotated genomic feature by RNAseq alignments
epidermal growth factor receptor pathway substrate 15-like 1a
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 50 samples with support for all annotated introns
LOW QUALITY PROTEIN: epidermal growth factor receptor substrate 15-like 1
zinc finger and BTB domain-containing protein 37-like, 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 58 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 37-like, 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 76 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 37-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: vascular cell adhesion protein 1-like
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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: probable G-protein coupled receptor 88
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 131 samples with support for all annotated introns
dual specificity protein phosphatase CDC14AB-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 45% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 23% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 44 samples with support for all annotated introns
procathepsin L-like, transcript variant X1
procathepsin L-like, transcript variant X2
ankyrin repeat domain-containing protein 29, transcript variant X2
ankyrin repeat domain-containing protein 29, transcript variant X4
ankyrin repeat domain-containing protein 29, transcript variant X5
ankyrin repeat domain-containing protein 29, transcript variant X1
ankyrin repeat domain-containing protein 29, transcript variant X3
ankyrin repeat domain-containing protein 29 isoform X1
ankyrin repeat domain-containing protein 29 isoform X3
ankyrin repeat domain-containing protein 29 isoform X2
ankyrin repeat domain-containing protein 29 isoform X4
ankyrin repeat domain-containing protein 29 isoform X5
vacuolar protein sorting-associated protein 4B-like
pleckstrin homology domain-containing family B member 2-like
immediate early response gene 5 protein-like
T-cell acute lymphocytic leukemia protein 1 homolog, transcript variant X1
T-cell acute lymphocytic leukemia protein 1 homolog, transcript variant X2
T-cell acute lymphocytic leukemia protein 1 homolog isoform X1
T-cell acute lymphocytic leukemia protein 1 homolog isoform X2
inaD-like protein, transcript variant X3
inaD-like protein, transcript variant X7
inaD-like protein, transcript variant X6
inaD-like protein, transcript variant X5
inaD-like protein, transcript variant X4
inaD-like protein, transcript variant X8
inaD-like protein, transcript variant X1
inaD-like protein, transcript variant X2
nuclear factor 1 A-type, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
nuclear factor 1 A-type, 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 17 samples with support for all annotated introns
nuclear factor 1 A-type, 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 21 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X10
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 23 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X8
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 22 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X12
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 28 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X9
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 10 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X7
nuclear factor 1 A-type, transcript variant X11
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 18 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X5
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 16 samples with support for all annotated introns
nuclear factor 1 A-type, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X1
ATP synthase mitochondrial F1 complex assembly factor 1, transcript variant X2
ATP synthase mitochondrial F1 complex assembly factor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
protein FAM163A-like, transcript variant X2
protein FAM163A-like, transcript variant X1
rab GTPase-activating protein 1-like, transcript variant X3
rab GTPase-activating protein 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 83 samples with support for all annotated introns
rab GTPase-activating protein 1-like isoform X3
rab GTPase-activating protein 1-like isoform X1
rab GTPase-activating protein 1-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 81 samples with support for all annotated introns
rab GTPase-activating protein 1-like, transcript variant X4
rab GTPase-activating protein 1-like isoform X4
uncharacterized protein LOC109112558 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 16 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 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: 14 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X1
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X2
heterogeneous nuclear ribonucleoprotein M-like isoform X1
heterogeneous nuclear ribonucleoprotein M-like isoform X2
heterogeneous nuclear ribonucleoprotein M-like, transcript variant X3
heterogeneous nuclear ribonucleoprotein M-like isoform X3
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X2
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X1
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X3
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X5
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X4
phosphatidylinositol-4-phosphate 5-kinase, type I, gamma a, transcript variant X6
phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform X4
phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform X3
phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform X2
phosphatidylinositol 4-phosphate 5-kinase type-1 gamma isoform X1
RNA polymerase II, I and III subunit E, b
DNA-directed RNA polymerases I, II, and III subunit RPABC1
LOW QUALITY PROTEIN: rho GTPase-activating protein 45
tight junction protein 3, 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 45 samples with support for all annotated introns
tight junction protein 3, 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 27 samples with support for all annotated introns
tight junction protein 3, transcript variant X3
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 14 samples with support for all annotated introns
tight junction protein 3, transcript variant X4
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 18 samples with support for all annotated introns
hyaluronan and proteoglycan link protein 4-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 2 bases in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: neurocan core protein-like
nuclear receptor 2C2-associated protein, transcript variant X2
nuclear receptor 2C2-associated protein, transcript variant X3
nuclear receptor 2C2-associated protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
nuclear receptor 2C2-associated protein, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
nuclear receptor 2C2-associated protein isoform X3
nuclear receptor 2C2-associated protein isoform X2
nuclear receptor 2C2-associated protein isoform X1
nuclear receptor 2C2-associated protein isoform X4
regulatory factor X-associated ankyrin-containing protein, transcript variant X2
regulatory factor X-associated ankyrin-containing protein, transcript variant X1
BLOC-1 related complex subunit 8, 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 46 samples with support for all annotated introns
BLOC-1 related complex subunit 8, transcript variant X2
BLOC-1-related complex subunit 8 isoform X1
BLOC-1-related complex subunit 8 isoform 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 30 samples with support for all annotated introns
myocyte-specific enhancer factor 2B-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
myocyte-specific enhancer factor 2B-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
myocyte-specific enhancer factor 2B-like isoform X1
myocyte-specific enhancer factor 2B-like isoform 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 82 samples with support for all annotated introns
transcriptional repressor p66-alpha-like, transcript variant X1
transcriptional repressor p66-alpha-like isoform X1
transcriptional repressor p66-alpha-like, transcript variant X3
transcriptional repressor p66-alpha-like, transcript variant X2
transcriptional repressor p66-alpha-like isoform X2
transcriptional repressor p66-alpha-like isoform X3
testis-specific serine/threonine-protein kinase 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
yjeF N-terminal domain-containing 3-like
cartilage intermediate layer protein 1-like
granzyme-like protein 1, transcript variant X2
granzyme-like protein 1, transcript variant X3
granzyme-like protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 67% coverage of the annotated genomic feature by RNAseq alignments
cold-inducible RNA-binding protein B-like, transcript variant X2
cold-inducible RNA-binding protein B-like, transcript variant X6
cold-inducible RNA-binding protein-like isoform X2
cold-inducible RNA-binding protein B-like, transcript variant X3
cold-inducible RNA-binding protein B-like, transcript variant X7
cold-inducible RNA-binding protein B-like, transcript variant X8
cold-inducible RNA-binding protein B-like, transcript variant X1
cold-inducible RNA-binding protein B-like, transcript variant X5
cold-inducible RNA-binding protein B-like, transcript variant X4
cold-inducible RNA-binding protein B-like isoform X3
cold-inducible RNA-binding protein B-like isoform X1
cold-inducible RNA-binding protein-like isoform X5
cold-inducible RNA-binding protein B-like isoform X4
ATP synthase subunit delta, mitochondrial-like
voltage-dependent calcium channel beta subunit-associated regulatory protein-like, transcript variant X3
voltage-dependent calcium channel beta subunit-associated regulatory protein-like, transcript variant X1
voltage-dependent calcium channel beta subunit-associated regulatory protein-like, transcript variant X2
voltage-dependent calcium channel beta subunit-associated regulatory protein-like isoform X1
voltage-dependent calcium channel beta subunit-associated regulatory protein-like isoform X2
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 2-like
DNA-directed RNA polymerase, mitochondrial-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 21 Proteins, and 99% 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: 11 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: 13 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: 1 Protein, and 83% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122134869, transcript variant X1
uncharacterized LOC122134869, transcript variant X3
uncharacterized LOC122134869, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 93% coverage of the annotated genomic feature by RNAseq alignments
mast cell protease 1A-like, transcript variant X1
mast cell protease 1A-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 53% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 158 samples with support for all annotated introns
LOW QUALITY PROTEIN: MICOS complex subunit MIC13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
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 131 samples with support for all annotated introns
CUGBP Elav-like family member 5, transcript variant X1
CUGBP Elav-like family member 5, transcript variant X4
CUGBP Elav-like family member 5, transcript variant X5
CUGBP Elav-like family member 5, transcript variant X2
CUGBP Elav-like family member 5, transcript variant X3
CUGBP Elav-like family member 5 isoform X5
CUGBP Elav-like family member 5 isoform X4
CUGBP Elav-like family member 5 isoform X2
CUGBP Elav-like family member 5 isoform X3
CUGBP Elav-like family member 5 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
uncharacterized LOC109084643, transcript variant X3
uncharacterized LOC109084643, transcript variant X2
uncharacterized LOC109084643, transcript variant X1
uncharacterized protein LOC109084643 isoform X3
uncharacterized protein LOC109084643 isoform X2
uncharacterized protein LOC109084643 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Nek7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LIM/homeobox protein Lhx9, transcript variant X2
LIM/homeobox protein Lhx9, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 91% 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 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DENN domain-containing protein 1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
complement factor H-related protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 92% coverage of the annotated genomic feature by RNAseq alignments
homeobox protein HMX1-like, 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 10 samples with support for all annotated introns
homeobox protein HMX1-like, 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 24 samples with support for all annotated introns
homeobox protein HMX1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 71% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122134877, transcript variant X1
uncharacterized LOC122134877, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 41% coverage of the annotated genomic feature by RNAseq alignments
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 25 samples with support for all annotated introns
chromatin assembly factor 1 subunit A-like
abnormal spindle-like microcephaly-associated protein homolog
sushi, von Willebrand factor type A, EGF and pentraxin domain-containing protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
complement factor H-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
complement factor H-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 22 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; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
LOW QUALITY PROTEIN: complement factor H-like
uncharacterized LOC122134871, transcript variant X2
uncharacterized LOC122134871, transcript variant X3
uncharacterized protein LOC122134871 isoform X2
uncharacterized LOC122134871, transcript variant X1
uncharacterized protein LOC122134871 isoform X1
uncharacterized protein LOC122134871 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase isozyme L5-like
regulator of G-protein signaling 21-like
regulator of G-protein signaling 21-like, transcript variant X2
regulator of G-protein signaling 21-like, transcript variant X1
regulator of G-protein signaling 21-like isoform X2
regulator of G-protein signaling 21-like isoform X1
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
LOW QUALITY PROTEIN: platelet glycoprotein V-like
coiled-coil domain-containing protein 50-like, transcript variant X1
coiled-coil domain-containing protein 50-like, transcript variant X2
coiled-coil domain-containing protein 50-like isoform X1
coiled-coil domain-containing protein 50-like isoform X2
uncharacterized LOC109093518, transcript variant X2
uncharacterized LOC109093518, transcript variant X1
chloride channel CLIC-like protein 1, transcript variant X2
chloride channel CLIC-like protein 1, transcript variant X3
chloride channel CLIC-like protein 1, 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 24 samples with support for all annotated introns
chloride channel CLIC-like protein 1 isoform X2
chloride channel CLIC-like protein 1 isoform X3
chloride channel CLIC-like protein 1 isoform 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 24 samples with support for all annotated introns
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
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 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
afadin- and alpha-actinin-binding protein-like, transcript variant X1
afadin- and alpha-actinin-binding protein-like, transcript variant X2
afadin- and alpha-actinin-binding protein-like isoform X2
afadin- and alpha-actinin-binding protein-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99 Proteins, and 98% 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: 108 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sialoadhesin-like, transcript variant X1
sialoadhesin-like, transcript variant X2
uncharacterized LOC109047597, transcript variant X2
uncharacterized protein LOC109047597 isoform X2
uncharacterized LOC109047597, transcript variant X3
uncharacterized LOC109047597, transcript variant X1
uncharacterized protein LOC109047597 isoform X3
uncharacterized protein LOC109047597 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
neuronal pentraxin receptor-like, transcript variant X1
neuronal pentraxin receptor-like, transcript variant X2
neuronal pentraxin receptor-like isoform X2
neuronal pentraxin receptor-like isoform X1
polymerase (RNA) III (DNA directed) polypeptide F
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: DNA-directed RNA polymerase III subunit RPC6
double zinc ribbon and ankyrin repeat domains 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: double zinc ribbon and ankyrin repeat-containing protein 1
protein PET117 homolog, mitochondrial-like
alanyl-tRNA synthetase 2, mitochondrial (putative)
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 10 bases in 9 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 10 bases in 9 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: alanine--tRNA ligase, mitochondrial
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
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 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 197 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: 5 Proteins, and 54% 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 48% 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 77% 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
uncharacterized LOC122134890, transcript variant X1
uncharacterized LOC122134890, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 82 samples with support for all annotated introns
uncharacterized LOC122135039, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
uncharacterized LOC122135039, 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 64 samples with support for all annotated introns
uncharacterized LOC122135040, transcript variant X1
uncharacterized LOC122135040, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 40 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 97 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC109088898, transcript variant X2
uncharacterized LOC109088898, transcript variant X1
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: 1 EST, 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: transmembrane protein 186
glycerophosphodiester phosphodiesterase 1
MAPK regulated corepressor interacting protein 2-like
structure-specific endonuclease subunit SLX4-like
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: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
LOW QUALITY PROTEIN: structure-specific endonuclease subunit SLX4-like
CREB binding protein a, transcript variant X1
CREB binding protein a, transcript variant X4
CREB binding protein a, transcript variant X2
CREB binding protein a, transcript variant X3
CREB binding protein a, transcript variant X5
histone lysine acetyltransferase CREBBP isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 70 samples with support for all annotated introns
uncharacterized LOC122134899, transcript variant X1
uncharacterized LOC122134899, transcript variant X2
zinc finger protein GLIS2-like, transcript variant X2
zinc finger protein GLIS2-like, transcript variant X1
zinc finger protein GLIS2-like, transcript variant X3
beta-1,3-galactosyltransferase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
beta-1,3-galactosyltransferase 1-like isoform X1
beta-1,3-galactosyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
beta-1,3-galactosyltransferase 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: calpain 2, (m/II) large subunit, like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 69 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 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: 75 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
28S ribosomal protein S28, mitochondrial-like
SDE2 telomere maintenance homolog (S. pombe)
replication stress response regulator SDE2
LOW QUALITY PROTEIN: WD repeat domain-containing protein 83
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 9 samples with support for all annotated introns
coiled-coil domain-containing protein 130 homolog
platelet-derived growth factor subunit A, transcript variant X2
platelet-derived growth factor subunit A, transcript variant X1
platelet-derived growth factor subunit A isoform X1
platelet-derived growth factor subunit A isoform X2
uncharacterized LOC109107388, transcript variant X20
uncharacterized LOC109107388, transcript variant X16
uncharacterized LOC109107388, transcript variant X11
uncharacterized LOC109107388, transcript variant X12
uncharacterized LOC109107388, transcript variant X8
uncharacterized LOC109107388, transcript variant X2
uncharacterized LOC109107388, transcript variant X14
uncharacterized LOC109107388, transcript variant X3
uncharacterized LOC109107388, transcript variant X18
uncharacterized LOC109107388, transcript variant X10
uncharacterized LOC109107388, transcript variant X19
uncharacterized LOC109107388, transcript variant X13
uncharacterized LOC109107388, transcript variant X6
uncharacterized LOC109107388, transcript variant X4
uncharacterized LOC109107388, transcript variant X15
uncharacterized LOC109107388, transcript variant X5
uncharacterized LOC109107388, transcript variant X1
uncharacterized LOC109107388, transcript variant X9
uncharacterized LOC109107388, transcript variant X7
uncharacterized LOC109107388, transcript variant X17
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 20 samples with support for all annotated introns
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 18 samples with support for all annotated introns
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 53 samples with support for all annotated introns
V-set domain-containing T-cell activation inhibitor 1-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 13 samples with support for all annotated introns
V-set domain-containing T-cell activation inhibitor 1-like isoform X2
V-set domain-containing T-cell activation inhibitor 1-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 27 samples with support for all annotated introns
V-set domain-containing T-cell activation inhibitor 1-like isoform X1
V-set domain-containing T-cell activation inhibitor 1-like
adhesion G-protein coupled receptor G7-like
uncharacterized LOC122134903, transcript variant X1
uncharacterized LOC122134903, 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 1 sample with support for all annotated introns
myelin-oligodendrocyte glycoprotein-like, transcript variant X1
myelin-oligodendrocyte glycoprotein-like, transcript variant X2
myelin-oligodendrocyte glycoprotein-like isoform X1
myelin-oligodendrocyte glycoprotein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
interphotoreceptor matrix proteoglycan 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
interphotoreceptor matrix proteoglycan 2-like, transcript variant X2
interphotoreceptor matrix proteoglycan 2-like isoform X1
interphotoreceptor matrix proteoglycan 2-like isoform X2
LOW QUALITY PROTEIN: target of Nesh-SH3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% 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: 94% 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: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
collagen alpha-1(VIII) chain-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
collagen alpha-1(VIII) chain-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 60 samples with support for all annotated introns
apoptosis-stimulating of p53 protein 2-like, transcript variant X3
apoptosis-stimulating of p53 protein 2-like, transcript variant X2
apoptosis-stimulating of p53 protein 2-like, transcript variant X1
apoptosis-stimulating of p53 protein 2-like isoform X1
apoptosis-stimulating of p53 protein 2-like isoform X2
apoptosis-stimulating of p53 protein 2-like isoform X3
apoptosis-stimulating of p53 protein 2-like, transcript variant X4
apoptosis-stimulating of p53 protein 2-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
chromobox protein homolog 6-like, transcript variant X2
chromobox protein homolog 6-like, transcript variant X3
chromobox protein homolog 6-like isoform X3
chromobox protein homolog 6-like isoform X2
chromobox protein homolog 6-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 90 samples with support for all annotated introns
chromobox protein homolog 6-like isoform X1
85/88 kDa calcium-independent phospholipase A2-like, transcript variant X1
85/88 kDa calcium-independent phospholipase A2-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 61 samples with support for all annotated introns
85/88 kDa calcium-independent phospholipase A2-like isoform X1
85/88 kDa calcium-independent phospholipase A2-like isoform X2
85/88 kDa calcium-independent phospholipase A2-like isoform X3
brain-specific angiogenesis inhibitor 1-associated protein 2-like protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
parvalbumin-7-like, transcript variant X2
parvalbumin-7-like, transcript variant X1
adenylate cyclase, terminal-differentiation specific-like, transcript variant X1
adenylate cyclase, terminal-differentiation specific-like, transcript variant X2
adenylate cyclase, terminal-differentiation specific-like isoform X1
adenylate cyclase, terminal-differentiation specific-like isoform X2
SHOC2 leucine rich repeat scaffold protein, transcript variant X2
SHOC2 leucine rich repeat scaffold protein, transcript variant X1
SHOC2 leucine rich repeat scaffold protein, transcript variant X3
RNA-binding protein 20-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 10 samples with support for all annotated introns
RNA-binding protein 20-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
RNA-binding protein 20-like, 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 16 samples with support for all annotated introns
structural maintenance of chromosomes protein 3
fibroin heavy chain-like, transcript variant X8
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
fibroin heavy chain-like, transcript variant X14
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
fibroin heavy chain-like, transcript variant X9
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
fibroin heavy chain-like, transcript variant X10
fibroin heavy chain-like, transcript variant X6
fibroin heavy chain-like, transcript variant X4
fibroin heavy chain-like, transcript variant X11
fibroin heavy chain-like, transcript variant X17
fibroin heavy chain-like, transcript variant X5
fibroin heavy chain-like, transcript variant X13
fibroin heavy chain-like, transcript variant X22
fibroin heavy chain-like, transcript variant X23
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
fibroin heavy chain-like, transcript variant X16
fibroin heavy chain-like, transcript variant X19
fibroin heavy chain-like, transcript variant X31
fibroin heavy chain-like, 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 3 samples with support for all annotated introns
fibroin heavy chain-like, transcript variant X12
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
fibroin heavy chain-like, transcript variant X2
fibroin heavy chain-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
fibroin heavy chain-like, transcript variant X7
fibroin heavy chain-like, transcript variant X32
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
fibroin heavy chain-like, transcript variant X29
fibroin heavy chain-like, transcript variant X33
fibroin heavy chain-like, transcript variant X38
fibroin heavy chain-like, transcript variant X36
fibroin heavy chain-like, transcript variant X37
fibroin heavy chain-like, transcript variant X26
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
fibroin heavy chain-like, transcript variant X24
fibroin heavy chain-like, transcript variant X18
fibroin heavy chain-like, transcript variant X35
fibroin heavy chain-like, transcript variant X30
fibroin heavy chain-like, transcript variant X15
fibroin heavy chain-like, transcript variant X20
fibroin heavy chain-like, transcript variant X21
fibroin heavy chain-like, transcript variant X28
fibroin heavy chain-like, transcript variant X25
fibroin heavy chain-like, transcript variant X27
fibroin heavy chain-like, transcript variant X46
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
fibroin heavy chain-like, transcript variant X34
fibroin heavy chain-like, transcript variant X43
fibroin heavy chain-like, transcript variant X39
fibroin heavy chain-like, transcript variant X40
fibroin heavy chain-like, transcript variant X41
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
fibroin heavy chain-like, transcript variant X44
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
fibroin heavy chain-like, transcript variant X47
fibroin heavy chain-like, transcript variant X42
fibroin heavy chain-like, transcript variant X45
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized protein LOC109047611 isoform X32
uncharacterized protein LOC109047611 isoform X4
uncharacterized protein LOC109047611 isoform X8
uncharacterized protein LOC109047611 isoform X14
uncharacterized protein LOC109047611 isoform X19
uncharacterized protein LOC109047611 isoform X31
uncharacterized protein LOC109047611 isoform X11
uncharacterized protein LOC109047611 isoform X9
uncharacterized protein LOC109047611 isoform X10
uncharacterized protein LOC109047611 isoform X17
uncharacterized protein LOC109047611 isoform X29
uncharacterized protein LOC109047611 isoform X38
uncharacterized protein LOC109047611 isoform X33
uncharacterized protein LOC109047611 isoform X36
uncharacterized protein LOC109047611 isoform X37
uncharacterized protein LOC109047611 isoform X6
uncharacterized protein LOC109047611 isoform X5
uncharacterized protein LOC109047611 isoform X13
uncharacterized protein LOC109047611 isoform X46
fibroin heavy chain-like, transcript variant X48
fibroin heavy chain-like, transcript variant X49
fibroin heavy chain-like, transcript variant X50
uncharacterized protein LOC109047611 isoform X48
uncharacterized protein LOC109047611 isoform X49
uncharacterized protein LOC109047611 isoform X50
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
gamma-adducin-like, transcript variant X2
gamma-adducin-like, transcript variant X4
gamma-adducin-like, transcript variant X3
gamma-adducin-like, transcript variant X1
gamma-adducin-like, transcript variant X8
gamma-adducin-like, transcript variant X7
gamma-adducin-like, transcript variant X9
gamma-adducin-like, transcript variant X5
gamma-adducin-like, transcript variant X6
max-interacting protein 1, transcript variant X1
max-interacting protein 1, transcript variant X2
max-interacting protein 1, transcript variant X3
max-interacting protein 1, transcript variant X4
interferon-induced very large GTPase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
interferon-induced very large GTPase 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
interferon-induced very large GTPase 1-like
interleukin-8-like, transcript variant X1
interleukin-8-like, transcript variant X2
epidermal differentiation-specific protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 27% 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 75% coverage of the annotated genomic feature by RNAseq alignments
cullin-associated NEDD8-dissociated protein 1-like
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cullin-associated NEDD8-dissociated protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
SEC13 homolog, nuclear pore and COPII coat complex component
glutamate receptor-interacting protein 2-like
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
sodium- and chloride-dependent taurine transporter-like, transcript variant X1
sodium- and chloride-dependent taurine transporter-like, transcript variant X2
sodium- and chloride-dependent taurine transporter-like isoform X1
sodium- and chloride-dependent taurine transporter-like isoform X2
CD276 antigen homolog, transcript variant X3
CD276 antigen homolog, transcript variant X2
CD276 antigen homolog, transcript variant X1
uncharacterized protein LOC109092420 isoform X1
CD276 antigen homolog, transcript variant X4
GPI-anchored hemophore cfmA-like, transcript variant X4
GPI-anchored hemophore cfmA-like, transcript variant X1
GPI-anchored hemophore cfmA-like, transcript variant X3
GPI-anchored hemophore cfmA-like, transcript variant X6
GPI-anchored hemophore cfmA-like, transcript variant X2
GPI-anchored hemophore cfmA-like, transcript variant X5
GPI-anchored hemophore cfmA-like isoform X1
GPI-anchored hemophore cfmA-like isoform X3
GPI-anchored hemophore cfmA-like isoform X6
GPI-anchored hemophore cfmA-like isoform X2
hyphally-regulated protein-like isoform X5
hyphally-regulated protein-like isoform X4
uncharacterized LOC122134455, transcript variant X2
uncharacterized LOC122134455, transcript variant X3
uncharacterized LOC122134455, transcript variant X1
uncharacterized protein LOC122134455 isoform X3
uncharacterized protein LOC122134455 isoform X1
uncharacterized protein LOC122134455 isoform X2
uncharacterized LOC109045643, transcript variant X2
uncharacterized LOC109045643, transcript variant X3
uncharacterized LOC109045643, transcript variant X4
uncharacterized protein LOC109045643 isoform X2
uncharacterized protein LOC109045643 isoform X3
uncharacterized LOC109045643, transcript variant X1
uncharacterized protein LOC109045643 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 4 bases in 2 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: dedicator of cytokinesis protein 3-like
mesencephalic astrocyte-derived neurotrophic factor-like
poly(rC)-binding protein 4-like, transcript variant X3
poly(rC)-binding protein 4-like, transcript variant X2
poly(rC)-binding protein 4-like, transcript variant X1
poly(rC)-binding protein 4-like isoform X2
poly(rC)-binding protein 4-like isoform X1
poly(rC)-binding protein 4-like isoform X3
poly(rC)-binding protein 4-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
poly(rC)-binding protein 2-like isoform X4
dystroglycan-like, transcript variant X2
dystroglycan-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
metabotropic glutamate receptor 7-like, transcript variant X2
metabotropic glutamate receptor 7-like, transcript variant X1
metabotropic glutamate receptor 7-like, transcript variant X4
metabotropic glutamate receptor 7-like isoform X3
metabotropic glutamate receptor 7-like isoform X1
metabotropic glutamate receptor 7-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
metabotropic glutamate receptor 7-like isoform X2
uncharacterized LOC122134920, transcript variant X2
uncharacterized LOC122134920, transcript variant X1
E3 ubiquitin-protein ligase RNF123-like, transcript variant X1
E3 ubiquitin-protein ligase RNF123-like, transcript variant X5
E3 ubiquitin-protein ligase RNF123-like, transcript variant X3
E3 ubiquitin-protein ligase RNF123-like, transcript variant X2
E3 ubiquitin-protein ligase RNF123-like, transcript variant X6
E3 ubiquitin-protein ligase RNF123-like, transcript variant X4
E3 ubiquitin-protein ligase RNF123-like isoform X1
amphoterin-induced protein 3-like, 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 21 samples with support for all annotated introns
amphoterin-induced protein 3-like, transcript variant X1
amphoterin-induced protein 3-like, transcript variant X2
amphoterin-induced protein 3-like isoform X2
amphoterin-induced protein 3-like isoform X1
E3 ubiquitin-protein ligase RNF123-like, 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 6 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF123-like isoform X2
telomeric repeat-binding factor 2-interacting protein 1-like
Fc receptor-like protein 5, transcript variant X3
Fc receptor-like protein 5, transcript variant X1
Fc receptor-like protein 5, transcript variant X4
Fc receptor-like protein 5, transcript variant X2
leukocyte immunoglobulin-like receptor subfamily B member 1 isoform X3
immunoglobulin superfamily member 1-like isoform X1
ligand-dependent corepressor-like, transcript variant X2
ligand-dependent corepressor-like, transcript variant X1
ligand-dependent corepressor-like isoform X1
ligand-dependent corepressor-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
armadillo-like helical domain-containing protein 3
EGF-containing fibulin-like extracellular matrix protein 1, transcript variant X1
EGF-containing fibulin-like extracellular matrix protein 1, transcript variant X2
EGF-containing fibulin-like extracellular matrix protein 1
serum response factor-like, transcript variant X3
serum response factor-like, transcript variant X1
serum response factor-like, transcript variant X2
E3 ubiquitin-protein ligase RNF13-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 59 samples with support for all annotated introns
E3 ubiquitin-protein ligase RNF13-like, transcript variant X1
E3 ubiquitin-protein ligase RNF13-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 30% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 12 bases in 10 codons; deleted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 45% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 12 bases in 10 codons; deleted 4 bases in 3 codons; substituted 2 bases at 2 genomic stop 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, 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
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X3
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like isoform X1
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like isoform X3
run domain Beclin-1-interacting and cysteine-rich domain-containing protein-like isoform X2
5-hydroxytryptamine receptor 3A-like, transcript variant X3
5-hydroxytryptamine receptor 3A-like, transcript variant X2
5-hydroxytryptamine receptor 3A-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
dynein light chain Tctex-type protein 2B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
aminoacylase-1-like, transcript variant X1
aminoacylase-1-like, transcript variant X3
aminoacylase-1-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like isoform X1
aminoacylase-1-like, transcript variant X6
aminoacylase-1-like, transcript variant X5
aminoacylase-1-like, transcript variant X4
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
interferon-induced protein 44-like, transcript variant X4
interferon-induced protein 44-like, transcript variant X1
interferon-induced protein 44-like, transcript variant X2
interferon-induced protein 44-like, transcript variant X3
interferon-induced protein 44-like isoform X2
interferon-induced protein 44-like isoform X1
cocaine- and amphetamine-regulated transcript protein-like
lysosome-associated membrane glycoprotein 3-like
methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial-like
phospholipid-transporting ATPase IF-like, transcript variant X5
phospholipid-transporting ATPase IF-like, transcript variant X8
phospholipid-transporting ATPase IF-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
phospholipid-transporting ATPase IF-like isoform X6
phospholipid-transporting ATPase IF-like isoform X3
phospholipid-transporting ATPase IF-like, transcript variant X3
phospholipid-transporting ATPase IF-like, transcript variant X6
phospholipid-transporting ATPase IF-like, transcript variant X1
phospholipid-transporting ATPase IF-like, transcript variant X9
phospholipid-transporting ATPase IF-like, transcript variant X7
phospholipid-transporting ATPase IF-like, transcript variant X11
phospholipid-transporting ATPase IF-like, transcript variant X4
phospholipid-transporting ATPase IF-like isoform X9
phospholipid-transporting ATPase IF-like isoform X5
phospholipid-transporting ATPase IF-like isoform X2
phospholipid-transporting ATPase IF-like, transcript variant X10
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 17 samples with support for all annotated introns
phospholipid-transporting ATPase IF-like isoform X4
phospholipid-transporting ATPase IF-like isoform X1
phospholipid-transporting ATPase IF-like isoform X7
phospholipid-transporting ATPase IF-like isoform X8
uncharacterized LOC109047878, transcript variant X2
uncharacterized LOC109047878, transcript variant X1
DnaJ (Hsp40) homolog, subfamily C, member 19
mitochondrial import inner membrane translocase subunit TIM14
fragile X mental retardation syndrome-related protein 1-like, transcript variant X1
fragile X mental retardation syndrome-related protein 1-like, transcript variant X2
fragile X mental retardation syndrome-related protein 1-like isoform X2
fragile X mental retardation syndrome-related protein 1-like isoform X1
integumentary mucin C.1-like, transcript variant X2
integumentary mucin C.1-like, transcript variant X1
26S proteasome non-ATPase regulatory subunit 1, transcript variant X1
26S proteasome non-ATPase regulatory subunit 1, transcript variant X2
26S proteasome non-ATPase regulatory subunit 1 isoform X1
26S proteasome non-ATPase regulatory subunit 1 isoform X2
5-hydroxytryptamine (serotonin) receptor 2B, G protein-coupled
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 5 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X3
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X8
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X8
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X3
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X6
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X5
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X4
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X2
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X7
arf-GAP with coiled-coil, ANK repeat and PH domain-containing protein 2-like isoform X1
alkaline phosphatase, intestinal, tandem duplicate 2
intestinal-type alkaline phosphatase-like, transcript variant X2
intestinal-type alkaline phosphatase-like, transcript variant X1
intestinal-type alkaline phosphatase-like isoform X2
intestinal-type alkaline phosphatase-like isoform 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 42 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 7-like
LOW QUALITY PROTEIN: lisH domain-containing protein ARMC9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 6% coverage of the annotated genomic feature by RNAseq alignments
dynein light chain Tctex-type protein 2B
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
lisH domain-containing protein ARMC9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
potassium voltage-gated channel subfamily H member 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC122134932, transcript variant X1
uncharacterized LOC122134932, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
WW domain-containing transcription regulator protein 1-like, transcript variant X2
WW domain-containing transcription regulator protein 1-like, transcript variant X1
WW domain-containing transcription regulator protein 1-like isoform X1
WW domain-containing transcription regulator protein 1-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 43% coverage of the annotated genomic feature by RNAseq alignments
HPS3 biogenesis of lysosomal organelles complex 2 subunit 1, transcript variant X1
HPS3 biogenesis of lysosomal organelles complex 2 subunit 1, transcript variant X2
Hermansky-Pudlak syndrome 3 protein isoform X2
Hermansky-Pudlak syndrome 3 protein isoform X1
REST corepressor 3-like, transcript variant X2
REST corepressor 3-like, 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 38 samples with support for all annotated introns
serine/threonine-protein kinase MARK1-like, transcript variant X1
serine/threonine-protein kinase MARK1-like, transcript variant X2
serine/threonine-protein kinase MARK1-like, transcript variant X3
serine/threonine-protein kinase MARK1-like isoform X3
serine/threonine-protein kinase MARK1-like isoform X2
serine/threonine-protein kinase MARK1-like isoform X1
kinesin light chain 1-like, transcript variant X1
kinesin light chain 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
phosphofurin acidic cluster sorting protein 2-like
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
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, including 9 samples with support for all annotated introns
tripartite motif-containing protein 16-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
sentrin-specific protease 5-like, transcript variant X1
sentrin-specific protease 5-like, transcript variant X3
sentrin-specific protease 5-like, transcript variant X2
sentrin-specific protease 5-like isoform X1
sentrin-specific protease 5-like isoform X2
nuclear cap-binding protein subunit 2, transcript variant X2
nuclear cap-binding protein subunit 2 isoform X2
nuclear cap-binding protein subunit 2, 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 152 samples with support for all annotated introns
nuclear cap-binding protein subunit 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
nuclear cap-binding protein subunit 2 isoform X1
nuclear cap-binding protein subunit 2 isoform X3
NAD-dependent protein deacetylase sirtuin-7-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
rho guanine nucleotide exchange factor 3-like, transcript variant X1
rho guanine nucleotide exchange factor 3-like isoform X1
rho guanine nucleotide exchange factor 3-like, transcript variant X3
rho guanine nucleotide exchange factor 3-like isoform X3
rho guanine nucleotide exchange factor 3-like, transcript variant X2
rho guanine nucleotide exchange factor 3-like isoform X2
coiled-coil domain-containing protein 66-like, transcript variant X1
coiled-coil domain-containing protein 66-like, transcript variant X2
coiled-coil domain-containing protein 66-like, transcript variant X3
coiled-coil domain-containing protein 66-like isoform X2
coiled-coil domain-containing protein 66-like isoform X1
coiled-coil domain-containing protein 66-like isoform X3
inositol hexakisphosphate kinase 1-like, transcript variant X1
inositol hexakisphosphate kinase 1-like, transcript variant X2
mannose-1-phosphate guanyltransferase beta