Zootoca vivipara isolate ELT05324 linkage group LG19, UG_Zviv_1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Lepidosauria; Squamata; Bifurcata; Unidentata; Episquamata; Laterata; Lacertibaenia; Lacertidae; Zootoca.
REFSEQ INFORMATION: The reference sequence is identical to\nCM022357.1.\nAssembly name: UG_Zviv_1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the University of Glasgow on\n2020/04/01. The original whole-genome shotgun project has the\naccession JAATIO000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: University of Glasgow\nAssembly Date :: 2018\nAssembly Method :: Platanus v. 1.2.4; OPERA-LG v. 2.0.6;\n AGOUTI v. 0.3.3\nAssembly Name :: UG_Zviv_1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 70.0x\nSequencing Technology :: Illumina HiSeq; PacBio Sequel\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Zootoca vivipara Annotation Release\n 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 8.4\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
United Kingdom: Isle of Cumbrae, Scotland
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cAMP responsive element binding protein 3
cyclic AMP-responsive element-binding protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, 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: 28 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 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 3 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
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
carbonic anhydrase 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carbonic anhydrase 9, 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 1 sample with support for all annotated introns
carbonic anhydrase 9, 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
Rho guanine nucleotide exchange factor 39, transcript variant X1
Rho guanine nucleotide exchange factor 39, 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
rho guanine nucleotide exchange factor 39 isoform X1
rho guanine nucleotide exchange factor 39 isoform X2
39S ribosomal protein L17, mitochondrial
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, 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: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RGP1 homolog, RAB6A GEF complex partner 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RGP1 homolog, RAB6A GEF complex partner 1, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 89% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: sperm-associated antigen 8
histidine triad nucleotide binding protein 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histidine triad nucleotide binding protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
histidine triad nucleotide binding protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
histidine triad nucleotide-binding protein 2, mitochondrial isoform X1
histidine triad nucleotide-binding protein 2, mitochondrial isoform X2
histidine triad nucleotide-binding protein 2, mitochondrial isoform X3
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X2
TATA-box binding protein associated factor, RNA polymerase I subunit C, transcript variant X3
TATA box-binding protein-associated factor RNA polymerase I subunit C isoform X1
TATA box-binding protein-associated factor RNA polymerase I subunit C isoform X2
TATA box-binding protein-associated factor RNA polymerase I subunit C isoform X3
family with sequence similarity 221 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
LDL receptor related protein associated protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
alpha-2-macroglobulin receptor-associated protein
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
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, including 1 sample with support for all annotated introns
B-cell differentiation antigen CD72-like, transcript variant X2
B-cell differentiation antigen CD72-like, transcript variant X1
B-cell differentiation antigen CD72-like, transcript variant X3
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 1 sample with support for all annotated introns
B-cell differentiation antigen CD72-like isoform X1
B-cell differentiation antigen CD72-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
testis associated actin remodelling kinase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dual specificity testis-specific protein kinase 1
family with sequence similarity 166 member B, transcript variant X2
family with sequence similarity 166 member B, 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
RUN and SH3 domain containing 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RUN and SH3 domain containing 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RUN and SH3 domain containing 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RUN and SH3 domain containing 2, transcript variant X2
RUN and SH3 domain containing 2, transcript variant X3
RUN and SH3 domain containing 2, transcript variant X4
phospholipid-transporting ATPase ID-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipid-transporting ATPase ID-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid-transporting ATPase ID-like, transcript variant X3
phospholipid-transporting ATPase ID-like, transcript variant X6
phospholipid-transporting ATPase ID-like, transcript variant X7
phospholipid-transporting ATPase ID-like, transcript variant X1
phospholipid-transporting ATPase ID-like, transcript variant X4
phospholipid-transporting ATPase ID-like, transcript variant X8
phospholipid-transporting ATPase ID-like isoform X2
probable phospholipid-transporting ATPase IM isoform X6
phospholipid-transporting ATPase ID-like isoform X1
phospholipid-transporting ATPase ID-like isoform X5
phospholipid-transporting ATPase ID-like isoform X4
phospholipid-transporting ATPase ID-like isoform X3
phospholipid-transporting ATPase ID-like isoform X7
phospholipid-transporting ATPase ID-like, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipid-transporting ATPase ID-like isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
family with sequence similarity 214 member B, transcript variant X4
family with sequence similarity 214 member B, transcript variant X1
family with sequence similarity 214 member B, transcript variant X3
family with sequence similarity 214 member B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphatidylinositol glycan anchor biosynthesis class O, transcript variant X2
GPI ethanolamine phosphate transferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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 3 samples with support for all annotated introns
transitional endoplasmic reticulum ATPase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
dnaJ homolog subfamily B member 5 isoform X2
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X6
dnaJ homolog subfamily B member 5 isoform X4
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X1
dnaJ homolog subfamily B member 5 isoform X1
DnaJ heat shock protein family (Hsp40) member B5, transcript variant X3
dnaJ homolog subfamily B member 5 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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: 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: 5 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ciliary neurotrophic factor receptor, 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 3 samples with support for all annotated introns
ciliary neurotrophic factor receptor, 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 1 sample with support for all annotated introns
ciliary neurotrophic factor receptor, 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 2 samples with support for all annotated introns
ciliary neurotrophic factor receptor, transcript variant X4
ciliary neurotrophic factor receptor subunit alpha
galactose-1-phosphate uridylyltransferase, transcript variant X2
galactose-1-phosphate uridylyltransferase, transcript variant X1
galactose-1-phosphate uridylyltransferase isoform X2
galactose-1-phosphate uridylyltransferase isoform X1
sigma non-opioid intracellular receptor 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 52% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 3C
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X2
NACHT, LRR and PYD domains-containing protein 3-like, transcript variant X1
NACHT, LRR and PYD domains-containing protein 3-like
ribonuclease P protein subunit p25-like protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 219 member A, transcript variant X1
family with sequence similarity 219 member A, transcript variant X2
linkage group 19 C9orf24 homolog, transcript variant X1
linkage group 19 C9orf24 homolog, transcript variant X3
spermatid-specific manchette-related protein 1 isoform X1
spermatid-specific manchette-related protein 1 isoform X3
linkage group 19 C9orf24 homolog, transcript variant X2
spermatid-specific manchette-related protein 1 isoform X2
myogenesis regulating glycosidase (putative), transcript variant X1
myogenesis regulating glycosidase (putative), transcript variant X3
myogenesis regulating glycosidase (putative), transcript variant X2
myogenesis regulating glycosidase (putative), transcript variant X4
uncharacterized LOC118077248, 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
uncharacterized LOC118077248, transcript variant X2
uncharacterized protein LOC118077248 isoform X1
uncharacterized protein LOC118077248 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
bis(5'-nucleosyl)-tetraphosphatase [asymmetrical]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ubiquitin associated protein 2, transcript variant X1
ubiquitin associated protein 2, transcript variant X2
ubiquitin-associated protein 2 isoform X1
ubiquitin-associated protein 2 isoform X2
ubiquitin associated protein 2, transcript variant X4
ubiquitin associated protein 2, transcript variant X3
ubiquitin-associated protein 2 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF01191
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 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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: nucleolar protein 6
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 3 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 82% coverage of the annotated genomic feature by RNAseq alignments
tubulin polyglutamylase complex subunit 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 72% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: tubulin polyglutamylase complex subunit 2-like
similar to RNA sequence (same species):INSD:GEHX01188897.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 337 bases not found in genome assembly; 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
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 337 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
KIAA1328 ortholog, transcript variant X1
KIAA1328 ortholog, 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 2 samples with support for all annotated introns
KIAA1328 ortholog, transcript variant X2
KIAA1328 ortholog, transcript variant X4
KIAA1328 ortholog, transcript variant X7
KIAA1328 ortholog, transcript variant X5
KIAA1328 ortholog, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X1
phosphatidylinositol 3-kinase catalytic subunit type 3, transcript variant X2
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X1
phosphatidylinositol 3-kinase catalytic subunit type 3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
SET binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
SET binding protein 1, transcript variant X2
SET binding protein 1, transcript variant X4
SET binding protein 1, transcript variant X3
SET binding protein 1, transcript variant X5
SET binding protein 1, transcript variant X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
solute carrier family 14 member 1 (Kidd blood group), transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 14 member 1 (Kidd blood group), transcript variant X2
solute carrier family 14 member 1 (Kidd blood group), transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier family 14 member 1 (Kidd blood group), transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ectopic P-granules autophagy protein 5 homolog
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
proline-serine-threonine phosphatase interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
proline-serine-threonine phosphatase-interacting protein 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ATP synthase subunit alpha, mitochondrial
linkage group 19 C18orf25 homolog, transcript variant X4
linkage group 19 C18orf25 homolog, transcript variant X3
linkage group 19 C18orf25 homolog, transcript variant X1
linkage group 19 C18orf25 homolog, transcript variant X2
uncharacterized protein C18orf25 homolog isoform X1
uncharacterized protein C18orf25 homolog isoform X2
uncharacterized protein C18orf25 homolog isoform X3
ring finger protein 165, transcript variant X4
ring finger protein 165, transcript variant X5
E3 ubiquitin-protein ligase RNF165 isoform X4
E3 ubiquitin-protein ligase RNF165 isoform X5
ring finger protein 165, transcript variant X1
ring finger protein 165, transcript variant X3
ring finger protein 165, transcript variant X2
E3 ubiquitin-protein ligase RNF165 isoform X1
E3 ubiquitin-protein ligase RNF165 isoform X3
E3 ubiquitin-protein ligase RNF165 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
lipoxygenase homology domain-containing protein 1
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
alpha-2,8-sialyltransferase 8E isoform X3
alpha-2,8-sialyltransferase 8E isoform X2
alpha-2,8-sialyltransferase 8E isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
protein inhibitor of activated STAT 2, transcript variant X7
protein inhibitor of activated STAT 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein inhibitor of activated STAT 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein inhibitor of activated STAT 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
protein inhibitor of activated STAT 2, transcript variant X5
protein inhibitor of activated STAT 2, transcript variant X6
protein inhibitor of activated STAT 2, transcript variant X3
katanin catalytic subunit A1 like 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
katanin catalytic subunit A1 like 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
katanin catalytic subunit A1 like 2, transcript variant X3
katanin p60 ATPase-containing subunit A-like 2 isoform X1
katanin p60 ATPase-containing subunit A-like 2 isoform X2
katanin p60 ATPase-containing subunit A-like 2 isoform X3
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X7
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X2
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X6
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X1
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X4
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X3
haloacid dehalogenase like hydrolase domain containing 2, transcript variant X5
haloacid dehalogenase-like hydrolase domain-containing protein 2
immediate early response 3 interacting protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
immediate early response 3-interacting protein 1
SKI family transcriptional corepressor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 4% coverage of the annotated genomic feature by RNAseq alignments
SMAD family member 2, transcript variant X2
SMAD family member 2, transcript variant X3
SMAD family member 2, transcript variant X6
SMAD family member 2, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SMAD family member 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
SMAD family member 2, transcript variant X1
mothers against decapentaplegic homolog 2 isoform X2
mothers against decapentaplegic homolog 2 isoform X3
mothers against decapentaplegic homolog 2 isoform X1
zinc finger and BTB domain containing 7C, transcript variant X1
zinc finger and BTB domain containing 7C, transcript variant X2
zinc finger and BTB domain containing 7C, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 7C
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
cap binding complex dependent translation initiation factor, transcript variant X1
cap binding complex dependent translation initiation factor, transcript variant X2
cap binding complex dependent translation initiation factor, transcript variant X3
cap binding complex dependent translation initiation factor, transcript variant X4
cap binding complex dependent translation initiation factor, transcript variant X5
cap binding complex dependent translation initiation factor, transcript variant X6
CBP80/20-dependent translation initiation factor isoform X1
CBP80/20-dependent translation initiation factor isoform X2
CBP80/20-dependent translation initiation factor isoform X3
CBP80/20-dependent translation initiation factor isoform X4
CBP80/20-dependent translation initiation factor isoform X5
CBP80/20-dependent translation initiation factor isoform X6
mothers against decapentaplegic homolog 7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosomal protein L17, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ribosomal protein L17, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00151
lipase G, endothelial type, transcript variant X1
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 1 sample with support for all annotated introns
lipase G, endothelial type, transcript variant X3
lipase G, endothelial type, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00283
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 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: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cilia and flagella associated protein 53
cilia- and flagella-associated protein 53
spindle and kinetochore associated complex subunit 1, transcript variant X1
spindle and kinetochore-associated protein 1 isoform X1
spindle and kinetochore associated complex subunit 1, transcript variant X2
spindle and kinetochore-associated protein 1 isoform X2
spindle and kinetochore associated complex subunit 1, transcript variant X3
spindle and kinetochore-associated protein 1 isoform X3
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 4 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mitogen-activated protein kinase 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NAD-dependent malic enzyme, mitochondrial
SMAD family member 4, transcript variant X1
SMAD family member 4, transcript variant X3
SMAD family member 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
RNA-binding E3 ubiquitin-protein ligase MEX3C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC118077202, transcript variant X2
uncharacterized LOC118077202, transcript variant X1
StAR related lipid transfer domain containing 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
linkage group 19 C18orf54 homolog, transcript variant X2
linkage group 19 C18orf54 homolog, transcript variant X1
lung adenoma susceptibility protein 2 isoform X2
lung adenoma susceptibility protein 2 isoform 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 2 samples with support for all annotated introns
RAB27B, member RAS oncogene family, 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 1 sample with support for all annotated introns
RAB27B, member RAS oncogene family, transcript variant X1
coiled-coil domain containing 68, transcript variant X2
coiled-coil domain containing 68, transcript variant X1
coiled-coil domain containing 68, transcript variant X3
coiled-coil domain-containing protein 68
transcription factor 4, transcript variant X6
transcription factor 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transcription factor 4, transcript variant X4
transcription factor 4, transcript variant X5
transcription factor 4, transcript variant X8
transcription factor 4, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transcription factor 4, transcript variant X2
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 1 sample with support for all annotated introns
transcription factor 4, transcript variant X10
transcription factor 4, transcript variant X7
transcription factor 4, transcript variant X12
transcription factor 4, transcript variant X11
transfer RNA asparagine (anticodon GUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00548
thioredoxin like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
thioredoxin like 1, transcript variant X3
thioredoxin like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sia-alpha-2,3-Gal-beta-1,4-GlcNAc-R:alpha 2,8-sialyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ferrochelatase, mitochondrial isoform X1
ferrochelatase, mitochondrial isoform X2
ATPase phospholipid transporting 8B1, transcript variant X7
ATPase phospholipid transporting 8B1, transcript variant X4
ATPase phospholipid transporting 8B1, transcript variant X8
ATPase phospholipid transporting 8B1, transcript variant X6
ATPase phospholipid transporting 8B1, transcript variant X2
ATPase phospholipid transporting 8B1, transcript variant X3
ATPase phospholipid transporting 8B1, transcript variant X5
ATPase phospholipid transporting 8B1, transcript variant X1
NEDD4 like E3 ubiquitin protein ligase, transcript variant X7
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 2 samples with support for all annotated introns
NEDD4 like E3 ubiquitin protein ligase, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD4 like E3 ubiquitin protein ligase, transcript variant X9
E3 ubiquitin-protein ligase NEDD4-like isoform X7
E3 ubiquitin-protein ligase NEDD4-like isoform X8
E3 ubiquitin-protein ligase NEDD4-like isoform X9
NEDD4 like E3 ubiquitin protein ligase, transcript variant X11
NEDD4 like E3 ubiquitin protein ligase, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD4 like E3 ubiquitin protein ligase, transcript variant X1
NEDD4 like E3 ubiquitin protein ligase, transcript variant X3
NEDD4 like E3 ubiquitin protein ligase, transcript variant X2
NEDD4 like E3 ubiquitin protein ligase, transcript variant X5
NEDD4 like E3 ubiquitin protein ligase, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NEDD4 like E3 ubiquitin protein ligase, transcript variant X6
E3 ubiquitin-protein ligase NEDD4-like isoform X1
E3 ubiquitin-protein ligase NEDD4-like isoform X3
E3 ubiquitin-protein ligase NEDD4-like isoform X4
E3 ubiquitin-protein ligase NEDD4-like isoform X6
E3 ubiquitin-protein ligase NEDD4-like isoform X2
E3 ubiquitin-protein ligase NEDD4-like isoform X5
E3 ubiquitin-protein ligase NEDD4-like isoform X10
mucosa-associated lymphoid tissue lymphoma translocation protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 25% coverage of the annotated genomic feature by RNAseq alignments
SEC11 homolog C, signal peptidase complex subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
signal peptidase complex catalytic subunit SEC11C
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
retina and anterior neural fold homeobox
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 46% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
lectin, mannose binding 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
lectin, mannose binding 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 11% coverage of the annotated genomic feature by RNAseq alignments
collagen and calcium binding EGF domains 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
collagen and calcium binding EGF domains 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
collagen and calcium-binding EGF domain-containing protein 1
phorbol-12-myristate-13-acetate-induced protein 1
PDZ domain containing 2, transcript variant X5
PDZ domain containing 2, transcript variant X2
PDZ domain containing 2, transcript variant X3
PDZ domain containing 2, transcript variant X7
PDZ domain containing 2, transcript variant X9
PDZ domain containing 2, transcript variant X1
PDZ domain containing 2, transcript variant X6
PDZ domain containing 2, transcript variant X4
PDZ domain containing 2, transcript variant X10
PDZ domain containing 2, transcript variant X8
PDZ domain containing 2, transcript variant X11
PDZ domain-containing protein 2 isoform X5
PDZ domain-containing protein 2 isoform X3
PDZ domain-containing protein 2 isoform X2
PDZ domain-containing protein 2 isoform X1
PDZ domain-containing protein 2 isoform X4
PDZ domain-containing protein 2 isoform X6
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 3 samples with support for all annotated introns
myotubularin related protein 12, 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 2 samples with support for all annotated introns
myotubularin related protein 12, transcript variant X2
myotubularin-related protein 12 isoform X1
myotubularin-related protein 12 isoform X2
zinc finger RNA binding protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger RNA-binding protein isoform X1
zinc finger RNA binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
zinc finger RNA binding protein, transcript variant X2
zinc finger RNA-binding protein isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00155
activated RNA polymerase II transcriptional coactivator p15
natriuretic peptide receptor 3, transcript variant X2
natriuretic peptide receptor 3, transcript variant X1
atrial natriuretic peptide receptor 3 isoform X2
atrial natriuretic peptide receptor 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X1
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X2
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X4
ADAM metallopeptidase with thrombospondin type 1 motif 12, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 12 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins
solute carrier family 45 member 2, transcript variant X2
solute carrier family 45 member 2, transcript variant X1
membrane-associated transporter protein isoform X1
membrane-associated transporter protein 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 3 samples with support for all annotated introns
C1q and TNF related 3, transcript variant X2
C1q and TNF related 3, transcript variant X1
complement C1q tumor necrosis factor-related protein 3 isoform X2
complement C1q tumor necrosis factor-related protein 3 isoform X1
retinoic acid induced 14, transcript variant X3
retinoic acid induced 14, transcript variant X1
retinoic acid induced 14, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
tetratricopeptide repeat protein 23-like
RAD1 checkpoint DNA exonuclease, transcript variant X2
RAD1 checkpoint DNA exonuclease, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RAD1 checkpoint DNA exonuclease, transcript variant X4
RAD1 checkpoint DNA exonuclease, transcript variant X1
ribosome biogenesis protein BRX1 homolog
DnaJ heat shock protein family (Hsp40) member C21
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: alanine--glyoxylate aminotransferase 2, mitochondrial
prolactin receptor, 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 1 sample with support for all annotated introns
prolactin receptor, transcript variant X1
prolactin receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
interleukin 7 receptor, transcript variant X2
interleukin 7 receptor, transcript variant X1
interleukin-7 receptor subunit alpha isoform X1
interleukin-7 receptor subunit alpha isoform X2
calcyphosine like, transcript variant X2
calcyphosine like, transcript variant X1
LMBR1 domain containing 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LMBR1 domain containing 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
LMBR1 domain containing 2, transcript variant X1
LMBR1 domain containing 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
G-protein coupled receptor-associated protein LMBRD2 isoform X2
G-protein coupled receptor-associated protein LMBRD2 isoform X1
NAD kinase 2, mitochondrial, transcript variant X1
NAD kinase 2, mitochondrial, transcript variant X2
NAD kinase 2, mitochondrial, transcript variant X4
NAD kinase 2, mitochondrial, transcript variant X3
NAD kinase 2, mitochondrial, transcript variant X5
RAN binding protein 3 like, transcript variant X3
RAN binding protein 3 like, transcript variant X6
RAN binding protein 3 like, transcript variant X5
RAN binding protein 3 like, transcript variant X4
RAN binding protein 3 like, transcript variant X2
RAN binding protein 3 like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NIPBL cohesin loading factor, transcript variant X1
NIPBL cohesin loading factor, transcript variant X3
NIPBL cohesin loading factor, transcript variant X2
ciliogenesis and planar polarity effector 1, transcript variant X2
ciliogenesis and planar polarity effector 1, transcript variant X5
ciliogenesis and planar polarity effector 1, transcript variant X3
ciliogenesis and planar polarity effector 1, transcript variant X7
ciliogenesis and planar polarity effector 1, transcript variant X4
ciliogenesis and planar polarity effector 1, transcript variant X6
ciliogenesis and planar polarity effector 1, transcript variant X1
ciliogenesis and planar polarity effector 1, transcript variant X9
ciliogenesis and planar polarity effector 1, transcript variant X8
ciliogenesis and planar polarity effector 1 isoform X4
ciliogenesis and planar polarity effector 1 isoform X2
ciliogenesis and planar polarity effector 1 isoform X6
ciliogenesis and planar polarity effector 1 isoform X3
ciliogenesis and planar polarity effector 1 isoform X5
ciliogenesis and planar polarity effector 1 isoform X1
ciliogenesis and planar polarity effector 1 isoform X7
glial cell derived neurotrophic factor, transcript variant X2
glial cell derived neurotrophic factor, transcript variant X3
glial cell derived neurotrophic factor, transcript variant X1
glial cell line-derived neurotrophic factor isoform X1
glial cell line-derived neurotrophic factor isoform X2
EGF like, fibronectin type III and laminin G domains, transcript variant X1
EGF like, fibronectin type III and laminin G domains, transcript variant X2
leukemia inhibitory factor receptor-like, transcript variant X2
leukemia inhibitory factor receptor-like, transcript variant X6
leukemia inhibitory factor receptor-like, transcript variant X1
leukemia inhibitory factor receptor-like, transcript variant X5
leukemia inhibitory factor receptor-like, transcript variant X3
leukemia inhibitory factor receptor-like, transcript variant X4
leukemia inhibitory factor receptor-like isoform X2
leukemia inhibitory factor receptor-like isoform X1
oncostatin-M-specific receptor subunit beta-like, transcript variant X1
oncostatin-M-specific receptor subunit beta-like, transcript variant X3
oncostatin-M-specific receptor subunit beta-like, transcript variant X2
oncostatin-M-specific receptor subunit beta-like, transcript variant X4
oncostatin-M-specific receptor subunit beta-like
RPTOR independent companion of MTOR complex 2, transcript variant X5
RPTOR independent companion of MTOR complex 2, transcript variant X3
RPTOR independent companion of MTOR complex 2, transcript variant X2
RPTOR independent companion of MTOR complex 2, transcript variant X1
RPTOR independent companion of MTOR complex 2, transcript variant X4
RPTOR independent companion of MTOR complex 2, transcript variant X6
rapamycin-insensitive companion of mTOR isoform X3
rapamycin-insensitive companion of mTOR isoform X2
rapamycin-insensitive companion of mTOR isoform X1
rapamycin-insensitive companion of mTOR isoform X4
FYN binding protein 1, transcript variant X3
FYN binding protein 1, transcript variant X4
FYN binding protein 1, transcript variant X1
FYN binding protein 1, transcript variant X2
DAB adaptor protein 2, transcript variant X5
DAB adaptor protein 2, transcript variant X2
DAB adaptor protein 2, transcript variant X3
DAB adaptor protein 2, transcript variant X1
DAB adaptor protein 2, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
DAB adaptor protein 2, transcript variant X4
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X1
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 2 samples with support for all annotated introns
protein kinase AMP-activated catalytic subunit alpha 1, transcript variant X2
5'-AMP-activated protein kinase catalytic subunit alpha-1 isoform X1
5'-AMP-activated protein kinase catalytic subunit alpha-1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00577
complement component C6-like, transcript variant X4
complement component C6-like, transcript variant X5
complement component C6-like, transcript variant X2
complement component C6-like, transcript variant X7
complement component C6-like, transcript variant X6
complement component C6-like, transcript variant X3
complement component C6-like, transcript variant X1
phosphatidylinositol specific phospholipase C X domain containing 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
succinyl-CoA:3-ketoacid coenzyme A transferase 1, mitochondrial
growth hormone receptor, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
growth hormone receptor, transcript variant X2
growth hormone receptor, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 119 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 152
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X2
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X3
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X4
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X1
3-hydroxy-3-methylglutaryl-CoA synthase 1, transcript variant X5
hydroxymethylglutaryl-CoA synthase, cytoplasmic isoform X1
hydroxymethylglutaryl-CoA synthase, cytoplasmic isoform X2
hydroxymethylglutaryl-CoA synthase, cytoplasmic isoform X3
transmembrane protein 267, transcript variant X3
transmembrane protein 267, transcript variant X2
transmembrane protein 267, transcript variant X1
linkage group 19 C5orf34 homolog, transcript variant X1
uncharacterized protein C5orf34 homolog isoform X1
linkage group 19 C5orf34 homolog, transcript variant X2
linkage group 19 C5orf34 homolog, transcript variant X3
uncharacterized protein C5orf34 homolog isoform X2
poly(A) binding protein interacting protein 1
polyadenylate-binding protein-interacting protein 1
nicotinamide nucleotide transhydrogenase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
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: NAD(P) transhydrogenase, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 2 codons; deleted 4 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 39S ribosomal protein S30, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
hyperpolarization activated cyclic nucleotide gated potassium channel 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: 40S ribosomal protein S15-like
poly(ADP-ribose) polymerase family member 8, transcript variant X1
poly(ADP-ribose) polymerase family member 8, transcript variant X2
poly(ADP-ribose) polymerase family member 8, transcript variant X3
poly(ADP-ribose) polymerase family member 8, transcript variant X4
protein mono-ADP-ribosyltransferase PARP8 isoform X1
protein mono-ADP-ribosyltransferase PARP8 isoform X2
protein mono-ADP-ribosyltransferase PARP8 isoform X3
protein mono-ADP-ribosyltransferase PARP8 isoform X4
poly(ADP-ribose) polymerase family member 8, transcript variant X5
poly(ADP-ribose) polymerase family member 8, transcript variant X6
protein mono-ADP-ribosyltransferase PARP8 isoform X5
protein mono-ADP-ribosyltransferase PARP8 isoform X6
ISL LIM homeobox 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ISL LIM homeobox 1, transcript variant X2
insulin gene enhancer protein ISL-1 isoform X1
insulin gene enhancer protein ISL-1 isoform X2
pelota mRNA surveillance and ribosome rescue factor
molybdopterin synthase catalytic subunit-like
molybdopterin synthase sulfur carrier subunit-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 15% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
NADH:ubiquinone oxidoreductase subunit S4
NADH dehydrogenase [ubiquinone] iron-sulfur protein 4, mitochondrial
ADP ribosylation factor like GTPase 15, transcript variant X2
ADP ribosylation factor like GTPase 15, transcript variant X1
ADP-ribosylation factor-like protein 15 isoform X2
ADP-ribosylation factor-like protein 15 isoform X1
ADP ribosylation factor like GTPase 15, transcript variant X3
ADP-ribosylation factor-like protein 15 isoform X3
ADP ribosylation factor like GTPase 15, transcript variant X4
ADP-ribosylation factor-like protein 15 isoform X4
heat shock protein family B (small) member 3, transcript variant X1
heat shock protein family B (small) member 3, transcript variant X3
heat shock protein family B (small) member 3, transcript variant X4
heat shock protein family B (small) member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chondroitin sulfate proteoglycan 4-like, transcript variant X1
chondroitin sulfate proteoglycan 4-like, transcript variant X2
chondroitin sulfate proteoglycan 4-like, transcript variant X4
chondroitin sulfate proteoglycan 4-like, transcript variant X3
chondroitin sulfate proteoglycan 4-like isoform X1
chondroitin sulfate proteoglycan 4-like isoform X2
chondroitin sulfate proteoglycan 4-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 84% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
cell division cycle protein 20 homolog B
multiciliate differentiation and DNA synthesis associated cell cycle protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 24% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
DExH-box helicase 29, transcript variant X2
DExH-box helicase 29, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ATP-dependent RNA helicase DHX29 isoform X1
ATP-dependent RNA helicase DHX29 isoform X2
phospholipid phosphatase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
phospholipid phosphatase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 52 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier family 38 member 9, transcript variant X1
solute carrier family 38 member 9, transcript variant X2
sodium-coupled neutral amino acid transporter 9 isoform X1
sodium-coupled neutral amino acid transporter 9 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
DEAD-box helicase 4, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DEAD-box helicase 4, transcript variant X4
DEAD-box helicase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
probable ATP-dependent RNA helicase DDX4 isoform X1
DEAD-box helicase 4, transcript variant X2
DEAD-box helicase 4, transcript variant X5
DEAD-box helicase 4, transcript variant X6
DEAD-box helicase 4, transcript variant X3
probable ATP-dependent RNA helicase DDX4 isoform X2
probable ATP-dependent RNA helicase DDX4 isoform X3
interleukin 31 receptor A, transcript variant X3
interleukin 31 receptor A, transcript variant X2
interleukin 31 receptor A, transcript variant X6
interleukin 31 receptor A, transcript variant X5
interleukin 31 receptor A, transcript variant X7
interleukin 31 receptor A, transcript variant X4
interleukin 31 receptor A, transcript variant X1
interleukin-31 receptor subunit alpha isoform X1
interleukin-31 receptor subunit alpha isoform X2
interleukin-31 receptor subunit alpha isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
ankyrin repeat domain-containing protein 55
mitogen-activated protein kinase kinase kinase 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71% coverage of the annotated genomic feature by RNAseq alignments
mitogen-activated protein kinase kinase kinase 1, transcript variant X2
mitogen-activated protein kinase kinase kinase 1, transcript variant X1
mitogen-activated protein kinase kinase kinase 1 isoform X1
mitogen-activated protein kinase kinase kinase 1 isoform X2
SET domain containing 9, transcript variant X2
SET domain containing 9, transcript variant X1
SET domain-containing protein 9 isoform X1
SET domain-containing protein 9 isoform X2
MIER family member 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
MIER family member 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
mesoderm induction early response protein 3 isoform X1
mesoderm induction early response protein 3 isoform X2
RAB3C, member RAS oncogene family, transcript variant X2
RAB3C, member RAS oncogene family, transcript variant X1
phosphodiesterase 4D, transcript variant X1
phosphodiesterase 4D, transcript variant X2
phosphodiesterase 4D, transcript variant X4
phosphodiesterase 4D, transcript variant X3
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 1 sample with support for all annotated introns
phosphodiesterase 4D, transcript variant X8
phosphodiesterase 4D, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phosphodiesterase 4D, transcript variant X6
phosphodiesterase 4D, transcript variant X7
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X1
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X3
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X2
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X7
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X4
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X5
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X6
transfer RNA isoleucine (anticodon GAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
phosphodiesterase 4D, transcript variant X11
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X10
phosphodiesterase 4D, transcript variant X10
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X9
phosphodiesterase 4D, transcript variant X9
cAMP-specific 3',5'-cyclic phosphodiesterase 4D isoform X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
elongation of very long chain fatty acids protein 7
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X1
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X3
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X4
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X5
ERCC excision repair 8, CSA ubiquitin ligase complex subunit, transcript variant X2
DNA excision repair protein ERCC-8 isoform X1
DNA excision repair protein ERCC-8 isoform X3
DNA excision repair protein ERCC-8 isoform X2
DNA excision repair protein ERCC-8 isoform X5
DNA excision repair protein ERCC-8 isoform X4
NADH:ubiquinone oxidoreductase complex assembly factor 2
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex assembly factor 2
small integral membrane protein 15, transcript variant X6
small integral membrane protein 15, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
small integral membrane protein 15, transcript variant X1
small integral membrane protein 15, transcript variant X3
small integral membrane protein 15, transcript variant X2
small integral membrane protein 15, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
zinc finger SWIM domain-containing protein 6
kinesin family member 2A, transcript variant X3
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
kinesin family member 2A, transcript variant X1
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 2 samples with support for all annotated introns
kinesin family member 2A, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
DIMT1 rRNA methyltransferase and ribosome maturation factor
leucine rich repeat containing 70, transcript variant X2
leucine rich repeat containing 70, transcript variant X1
leucine-rich repeat-containing protein 70 isoform X1
leucine-rich repeat-containing protein 70 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins
ring finger protein 180, transcript variant X1
ring finger protein 180, transcript variant X3
E3 ubiquitin-protein ligase RNF180 isoform X1
E3 ubiquitin-protein ligase RNF180 isoform X3
ring finger protein 180, transcript variant X2
E3 ubiquitin-protein ligase RNF180 isoform X2
regulator of G protein signaling 7 binding protein, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of G protein signaling 7 binding protein, transcript variant X1
regulator of G-protein signaling 7-binding protein isoform X1
regulator of G-protein signaling 7-binding protein isoform X3
regulator of G protein signaling 7 binding protein, transcript variant X2
regulator of G-protein signaling 7-binding protein isoform X2
CWC27 spliceosome associated cyclophilin
spliceosome-associated protein CWC27 homolog
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X8
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X7
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X6
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X5
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X1
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X2
ADAM metallopeptidase with thrombospondin type 1 motif 6, transcript variant X3
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X5
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X4
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X3
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 6 isoform X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
peptidylprolyl isomerase domain and WD repeat containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peptidylprolyl isomerase domain and WD repeat-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
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
trafficking protein particle complex 13, transcript variant X1
trafficking protein particle complex 13, transcript variant X2
trafficking protein particle complex 13, transcript variant X3
trafficking protein particle complex 13, transcript variant X4
trafficking protein particle complex subunit 13 isoform X1
trafficking protein particle complex subunit 13 isoform X2
trafficking protein particle complex subunit 13 isoform X3
trafficking protein particle complex subunit 13 isoform X4
small glutamine rich tetratricopeptide repeat containing beta
small glutamine-rich tetratricopeptide repeat-containing protein beta