Sceloporus undulatus isolate JIND9_A2432 ecotype Alabama chromosome 10, SceUnd_v1.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Lepidosauria; Squamata; Bifurcata; Unidentata; Episquamata; Toxicofera; Iguania; Phrynosomatidae; Phrynosomatinae; Sceloporus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM032828.1.\nAssembly name: SceUnd_v1.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Auburn University on\n2021/07/08. The original whole-genome shotgun project has the\naccession JAGXEY000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Auburn University\nAssembly Date :: 01-AUG-2017\nAssembly Method :: SuperNova v. 2016; HiRise v. August 2017;\n PBJelly v. September 2017\nAssembly Name :: SceUnd_v1.1\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 4859.0x\nSequencing Technology :: Illumina HiSeq; PacBio\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Sceloporus undulatus Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
the sample came from two individuals: brain sample from one juvenile (IND9) and blood, liver, muscle, tail, brain samples from one adult (Adult2432)
Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: polyA evidence [ECO:0006239]
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
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
inositol polyphosphate-5-phosphatase J, 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
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X1
inositol polyphosphate-5-phosphatase J, transcript variant X3
inositol polyphosphate-5-phosphatase J, transcript variant X2
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X2
phosphatidylinositol 4,5-bisphosphate 5-phosphatase A isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
DNA polymerase epsilon, catalytic subunit, 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
DNA polymerase epsilon, catalytic subunit, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
DNA polymerase epsilon catalytic subunit A isoform X1
DNA polymerase epsilon catalytic subunit A isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
proline dehydrogenase 1, mitochondrial-like, transcript variant X1
proline dehydrogenase 1, mitochondrial-like isoform X1
proline dehydrogenase 1, mitochondrial-like, transcript variant X2
proline dehydrogenase 1, mitochondrial-like isoform X2
scavenger receptor class F member 2, transcript variant X1
scavenger receptor class F member 2 isoform X1
scavenger receptor class F member 2, transcript variant X2
scavenger receptor class F member 2, transcript variant X3
scavenger receptor class F member 2 isoform X2
leucine-rich repeat-containing protein 74B
purinergic receptor P2X 6, 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
purinergic receptor P2X 6, transcript variant X1
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 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
apoptosis inducing factor mitochondria associated 3, transcript variant X3
apoptosis inducing factor mitochondria associated 3, transcript variant X2
apoptosis inducing factor mitochondria associated 3, 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 21 samples with support for all annotated introns
NAD-dependent protein lipoamidase sirtuin-4, mitochondrial
hydroxysteroid 11-beta-dehydrogenase 1-like protein A, transcript variant X1
hydroxysteroid 11-beta-dehydrogenase 1-like protein A isoform X1
hydroxysteroid 11-beta-dehydrogenase 1-like protein A, transcript variant X2
hydroxysteroid 11-beta-dehydrogenase 1-like protein A isoform X2
uncharacterized LOC121916429, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121916429, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
phospholipase A2 group IB, transcript variant X3
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
phospholipase A2 group IB, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
phospholipase A2 group IB, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
musashi RNA binding protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
musashi RNA binding protein 1, 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 14 samples with support for all annotated introns
musashi RNA binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
musashi RNA binding protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
RNA-binding protein Musashi homolog 1 isoform X4
RNA-binding protein Musashi homolog 1 isoform X3
RNA-binding protein Musashi homolog 1 isoform X2
RNA-binding protein Musashi homolog 1 isoform X1
cytochrome c oxidase subunit 6A2, mitochondrial
glutamyl-tRNA amidotransferase subunit C, transcript variant X2
glutamyl-tRNA amidotransferase subunit C, transcript variant X1
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial isoform X1
glutamyl-tRNA(Gln) amidotransferase subunit C, mitochondrial isoform X2
serine and arginine rich splicing factor 9, transcript variant X2
serine and arginine rich splicing factor 9, transcript variant X1
2-methoxy-6-polyprenyl-1,4-benzoquinol methylase, mitochondrial
ring finger protein 10, transcript variant X2
ring finger protein 10, transcript variant X3
ring finger protein 10, transcript variant X1
POP5 homolog, ribonuclease P/MRP subunit
calcium binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium binding protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium binding protein 1, 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 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
short-chain specific acyl-CoA dehydrogenase, mitochondrial
signal peptide peptidase like 3, transcript variant X1
signal peptide peptidase like 3, transcript variant X2
signal peptide peptidase-like 3 isoform X2
signal peptide peptidase-like 3 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
TBC1 domain family member 10A, transcript variant X1
TBC1 domain family member 10A, transcript variant X2
TBC1 domain family member 10A, transcript variant X3
TBC1 domain family member 10A, transcript variant X4
TBC1 domain family member 10A isoform X1
TBC1 domain family member 10A isoform X3
TBC1 domain family member 10A isoform X2
TBC1 domain family member 10A isoform X4
protein kinase AMP-activated non-catalytic subunit beta 1, transcript variant X1
protein kinase AMP-activated non-catalytic subunit beta 1, transcript variant X2
5'-AMP-activated protein kinase subunit beta-1
citron rho-interacting serine/threonine kinase
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 93% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: BICD family-like cargo adapter 1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
ribosomal protein lateral stalk subunit P0
coiled-coil domain containing 60, transcript variant X1
coiled-coil domain containing 60, transcript variant X2
coiled-coil domain-containing protein 60 isoform X1
coiled-coil domain-containing protein 60 isoform X2
heat shock protein family B (small) member 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 4
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
SDS3 homolog, SIN3A corepressor complex component, transcript variant X2
SDS3 homolog, SIN3A corepressor complex component, transcript variant X1
sin3 histone deacetylase corepressor complex component SDS3 isoform X2
sin3 histone deacetylase corepressor complex component SDS3 isoform 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 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 4 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 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 1 sample with support for all annotated introns
serine/threonine-protein kinase TAO3 isoform X1
serine/threonine-protein kinase TAO3 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 6 samples with support for all annotated introns
serine/threonine-protein kinase TAO3 isoform X3
phosphatidylethanolamine-binding protein 1-like
deltex E3 ubiquitin ligase 1, transcript variant X1
E3 ubiquitin-protein ligase DTX1 isoform X1
deltex E3 ubiquitin ligase 1, transcript variant X2
E3 ubiquitin-protein ligase DTX1 isoform X2
RAS protein activator like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
RAS protein activator like 1, transcript variant X2
cilia and flagella associated protein 73, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
cilia and flagella associated protein 73, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
cilia- and flagella-associated protein 73 isoform X1
cilia- and flagella-associated protein 73 isoform X2
RBPJ interacting and tubulin associated 1, transcript variant X2
RBPJ interacting and tubulin associated 1, transcript variant X1
RBPJ-interacting and tubulin-associated protein 1
IQ motif containing D, transcript variant X3
IQ motif containing D, transcript variant X1
IQ motif containing D, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
two pore segment channel 1, transcript variant X1
two pore segment channel 1, transcript variant X2
two pore calcium channel protein 1 isoform X1
two pore calcium channel protein 1 isoform X2
two pore segment channel 1, transcript variant X3
two pore calcium channel protein 1 isoform X3
solute carrier family 8 member B1, transcript variant X3
solute carrier family 8 member B1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
solute carrier family 8 member B1, transcript variant X1
solute carrier family 8 member B1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
mitochondrial sodium/calcium exchanger protein isoform X2
mitochondrial sodium/calcium exchanger protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
L-serine dehydratase/L-threonine deaminase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
RNA binding motif protein 19, 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 3 samples with support for all annotated introns
RNA binding motif protein 19, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
RNA binding motif protein 19, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: T-box transcription factor TBX5
mediator complex subunit 13L, transcript variant X1
mediator complex subunit 13L, transcript variant X2
mediator of RNA polymerase II transcription subunit 13-like isoform X1
mediator of RNA polymerase II transcription subunit 13-like isoform X2
coiled-coil-helix-coiled-coil-helix domain containing 10
coiled-coil-helix-coiled-coil-helix domain-containing protein 10, mitochondrial
V-set and immunoglobulin domain containing 10
V-set and immunoglobulin domain-containing protein 10
WD repeat and SOCS box-containing protein 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
LOW QUALITY PROTEIN: kinase suppressor of Ras 2
nitric oxide synthase 1, transcript variant X4
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 4 samples with support for all annotated introns
nitric oxide synthase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nitric oxide synthase 1, transcript variant X3
nitric oxide synthase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
purinergic receptor P2X 7, 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 1 sample with support for all annotated introns
purinergic receptor P2X 7, 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 3 samples with support for all annotated introns
intraflagellar transport 81, transcript variant X3
intraflagellar transport 81, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
intraflagellar transport 81, transcript variant X2
intraflagellar transport protein 81 homolog
uncharacterized LOC121916401, transcript variant X2
uncharacterized LOC121916401, transcript variant X1
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2, transcript variant X2
ATPase sarcoplasmic/endoplasmic reticulum Ca2+ transporting 2, transcript variant X1
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X1
sarcoplasmic/endoplasmic reticulum calcium ATPase 2 isoform X2
anaphase promoting complex subunit 7, transcript variant X1
anaphase promoting complex subunit 7, transcript variant X2
anaphase-promoting complex subunit 7 isoform X1
anaphase-promoting complex subunit 7 isoform X2
actin related protein 2/3 complex subunit 3
actin-related protein 2/3 complex subunit 3
density regulated re-initiation and release factor
coiled-coil domain containing 62, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
coiled-coil domain containing 62, transcript variant X2
coiled-coil domain containing 62, transcript variant X5
coiled-coil domain-containing protein 62 isoform X1
coiled-coil domain-containing protein 62 isoform X3
coiled-coil domain containing 62, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
coiled-coil domain containing 62, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain-containing protein 62 isoform X2
huntingtin interacting protein 1 related, transcript variant X1
huntingtin interacting protein 1 related, transcript variant X2
huntingtin-interacting protein 1-related protein isoform X1
huntingtin-interacting protein 1-related protein isoform X2
vacuolar protein sorting-associated protein 37B
ATP binding cassette subfamily B member 9
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 5 samples with support for all annotated introns
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X2
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X2
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X3
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X4
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X3
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X4
2-oxoglutarate and iron dependent oxygenase domain containing 2, transcript variant X1
2-oxoglutarate and iron-dependent oxygenase domain-containing protein 2 isoform X1
ADP ribosylation factor like GTPase 6 interacting protein 4, transcript variant X2
ADP ribosylation factor like GTPase 6 interacting protein 4, transcript variant X1
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X1
ADP ribosylation factor like GTPase 6 interacting protein 4, transcript variant X3
ADP-ribosylation factor-like protein 6-interacting protein 4 isoform X2
phosphatidylinositol transfer protein membrane associated 2, transcript variant X8
phosphatidylinositol transfer protein membrane associated 2, transcript variant X4
phosphatidylinositol transfer protein membrane associated 2, transcript variant X6
phosphatidylinositol transfer protein membrane associated 2, transcript variant X2
phosphatidylinositol transfer protein membrane associated 2, transcript variant X9
phosphatidylinositol transfer protein membrane associated 2, transcript variant X7
phosphatidylinositol transfer protein membrane associated 2, transcript variant X3
phosphatidylinositol transfer protein membrane associated 2, transcript variant X5
phosphatidylinositol transfer protein membrane associated 2, transcript variant X1
phosphatidylinositol transfer protein membrane associated 2, transcript variant X11
membrane-associated phosphatidylinositol transfer protein 2 isoform X8
membrane-associated phosphatidylinositol transfer protein 2 isoform X4
membrane-associated phosphatidylinositol transfer protein 2 isoform X6
membrane-associated phosphatidylinositol transfer protein 2 isoform X2
membrane-associated phosphatidylinositol transfer protein 2 isoform X9
membrane-associated phosphatidylinositol transfer protein 2 isoform X7
membrane-associated phosphatidylinositol transfer protein 2 isoform X3
membrane-associated phosphatidylinositol transfer protein 2 isoform X5
membrane-associated phosphatidylinositol transfer protein 2 isoform X1
membrane-associated phosphatidylinositol transfer protein 2 isoform X11
phosphatidylinositol transfer protein membrane associated 2, transcript variant X10
membrane-associated phosphatidylinositol transfer protein 2 isoform X10
M-phase phosphoprotein 9, transcript variant X4
M-phase phosphoprotein 9, transcript variant X1
M-phase phosphoprotein 9, transcript variant X3
M-phase phosphoprotein 9, transcript variant X5
M-phase phosphoprotein 9, transcript variant X2
M-phase phosphoprotein 9, transcript variant X6
M-phase phosphoprotein 9, transcript variant X7
mitochondrial translation release factor in rescue, transcript variant X3
mitochondrial translation release factor in rescue, transcript variant X1
mitochondrial translation release factor in rescue, transcript variant X2
mitochondrial translation release factor in rescue
cyclin dependent kinase 2 associated protein 1, transcript variant X1
cyclin dependent kinase 2 associated protein 1, transcript variant X2
cyclin-dependent kinase 2-associated protein 1 isoform X1
cyclin-dependent kinase 2-associated protein 1 isoform X2
strawberry notch homolog 1, transcript variant X2
strawberry notch homolog 1, transcript variant X1
lysine methyltransferase 5A, transcript variant X2
N-lysine methyltransferase KMT5A isoform X2
lysine methyltransferase 5A, transcript variant X1
N-lysine methyltransferase KMT5A isoform X1
Rab interacting lysosomal protein like 2
small nuclear ribonucleoprotein U11/U12 subunit 35, 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 20 samples with support for all annotated introns
small nuclear ribonucleoprotein U11/U12 subunit 35, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
U11/U12 small nuclear ribonucleoprotein 35 kDa protein isoform X1
U11/U12 small nuclear ribonucleoprotein 35 kDa protein isoform X2
Rab interacting lysosomal protein like 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Rab interacting lysosomal protein like 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Rab interacting lysosomal protein like 1, transcript variant X5
Rab interacting lysosomal protein like 1, transcript variant X3
Rab interacting lysosomal protein like 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
transmembrane p24 trafficking protein 2, transcript variant X3
transmembrane p24 trafficking protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transmembrane p24 trafficking protein 2, transcript variant X1
transmembrane emp24 domain-containing protein 2 isoform X3
transmembrane emp24 domain-containing protein 2 isoform X1
transmembrane emp24 domain-containing protein 2 isoform X2
eukaryotic translation initiation factor 2B subunit alpha
translation initiation factor eIF-2B subunit alpha
general transcription factor IIH subunit 3, transcript variant X1
general transcription factor IIH subunit 3, transcript variant X3
general transcription factor IIH subunit 3, transcript variant X2
general transcription factor IIH subunit 3 isoform X1
general transcription factor IIH subunit 3 isoform X3
general transcription factor IIH subunit 3 isoform X2
uncharacterized LOC121916494, 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
uncharacterized LOC121916494, transcript variant X1
uncharacterized LOC121916494, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized protein LOC121916494 isoform X3
uncharacterized protein LOC121916494 isoform X1
uncharacterized protein LOC121916494 isoform X2
tectonic family member 2, transcript variant X2
tectonic family member 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 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 99% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain containing 92, transcript variant X7
coiled-coil domain containing 92, transcript variant X8
coiled-coil domain containing 92, transcript variant X3
coiled-coil domain containing 92, transcript variant X5
coiled-coil domain containing 92, transcript variant X6
coiled-coil domain containing 92, transcript variant X4
coiled-coil domain containing 92, transcript variant X2
coiled-coil domain containing 92, transcript variant X1
coiled-coil domain-containing protein 92 isoform X2
coiled-coil domain-containing protein 92 isoform X1
coiled-coil domain-containing protein 92 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
nuclear receptor corepressor 2, transcript variant X4
nuclear receptor corepressor 2, transcript variant X2
nuclear receptor corepressor 2, transcript variant X21
nuclear receptor corepressor 2, transcript variant X9
nuclear receptor corepressor 2, transcript variant X24
nuclear receptor corepressor 2, transcript variant X22
nuclear receptor corepressor 2, transcript variant X6
nuclear receptor corepressor 2, transcript variant X8
nuclear receptor corepressor 2, transcript variant X15
nuclear receptor corepressor 2, transcript variant X10
nuclear receptor corepressor 2, transcript variant X13
nuclear receptor corepressor 2, transcript variant X5
nuclear receptor corepressor 2, transcript variant X7
nuclear receptor corepressor 2, transcript variant X25
nuclear receptor corepressor 2, transcript variant X23
nuclear receptor corepressor 2, transcript variant X11
nuclear receptor corepressor 2, transcript variant X16
nuclear receptor corepressor 2, transcript variant X14
nuclear receptor corepressor 2, transcript variant X12
nuclear receptor corepressor 2, transcript variant X1
nuclear receptor corepressor 2, transcript variant X3
nuclear receptor corepressor 2, transcript variant X19
nuclear receptor corepressor 2, transcript variant X20
nuclear receptor corepressor 2, transcript variant X18
nuclear receptor corepressor 2 isoform X17
nuclear receptor corepressor 2 isoform X6
nuclear receptor corepressor 2 isoform X20
nuclear receptor corepressor 2 isoform X18
nuclear receptor corepressor 2 isoform X3
nuclear receptor corepressor 2 isoform X5
nuclear receptor corepressor 2 isoform X12
nuclear receptor corepressor 2 isoform X7
nuclear receptor corepressor 2 isoform X10
nuclear receptor corepressor 2 isoform X2
nuclear receptor corepressor 2 isoform X4
nuclear receptor corepressor 2 isoform X21
nuclear receptor corepressor 2 isoform X19
nuclear receptor corepressor 2 isoform X8
nuclear receptor corepressor 2 isoform X13
nuclear receptor corepressor 2 isoform X11
nuclear receptor corepressor 2 isoform X9
nuclear receptor corepressor 2 isoform X1
nuclear receptor corepressor 2 isoform X15
nuclear receptor corepressor 2 isoform X16
nuclear receptor corepressor 2, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
nuclear receptor corepressor 2 isoform X14
scavenger receptor class B member 1, transcript variant X2
scavenger receptor class B member 1, transcript variant X3
scavenger receptor class B member 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
scavenger receptor class B member 1 isoform X2
scavenger receptor class B member 1 isoform X3
scavenger receptor class B member 1 isoform X1
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
DEAH-box helicase 37, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
probable ATP-dependent RNA helicase DHX37
DEAH-box helicase 37, transcript variant X2
DEAH-box helicase 37, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
transmembrane protein 132B, transcript variant X1
transmembrane protein 132B, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
uncharacterized LOC121916674, transcript variant X1
uncharacterized LOC121916674, transcript variant X2
glycosyltransferase 1 domain containing 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
glycosyltransferase 1 domain-containing 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
RIMS binding protein 2, transcript variant X13
RIMS binding protein 2, transcript variant X6
RIMS binding protein 2, transcript variant X11
RIMS binding protein 2, transcript variant X4
RIMS binding protein 2, transcript variant X1
RIMS binding protein 2, transcript variant X12
RIMS binding protein 2, transcript variant X10
RIMS binding protein 2, transcript variant X2
RIMS binding protein 2, transcript variant X8
RIMS binding protein 2, transcript variant X9
RIMS binding protein 2, transcript variant X15
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
RIMS binding protein 2, transcript variant X14
RIMS binding protein 2, transcript variant X7
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
RIMS binding protein 2, transcript variant X5
RIMS binding protein 2, transcript variant X3
RIMS binding protein 2, transcript variant X16
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 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; deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 88% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; deleted 2 bases in 2 codons; substituted 3 bases at 3 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: adhesion G-protein coupled receptor D1
splicing factor SWAP, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
splicing factor SWAP, 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 23 samples with support for all annotated introns
splicing factor SWAP, transcript variant X2
splicing factor, suppressor of white-apricot homolog isoform X1
splicing factor, suppressor of white-apricot homolog isoform X2
splicing factor, suppressor of white-apricot homolog isoform X3
splicing factor SWAP, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
splicing factor SWAP, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
splicing factor SWAP, transcript variant X5
splicing factor, suppressor of white-apricot homolog isoform X4
transforming acidic coiled-coil-containing protein 3-like
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transforming acidic coiled-coil-containing protein 3-like
E1A binding protein p400, transcript variant X1
E1A binding protein p400, 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 9 samples with support for all annotated introns
E1A binding protein p400, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
E1A binding protein p400, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
E1A binding protein p400, transcript variant X2
E1A binding protein p400, transcript variant X6
E1A binding protein p400, transcript variant X7
E1A binding protein p400, transcript variant X8
E1A binding protein p400, transcript variant X9
E1A binding protein p400, transcript variant X13
E1A binding protein p400, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
E1A binding protein p400, transcript variant X17
E1A binding protein p400, transcript variant X16
E1A binding protein p400, transcript variant X10
E1A binding protein p400, transcript variant X11
E1A binding protein p400, transcript variant X18
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
E1A binding protein p400, transcript variant X15
E1A binding protein p400, transcript variant X12
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
unc-51 like autophagy activating kinase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
unc-51 like autophagy activating kinase 1, transcript variant X1
unc-51 like autophagy activating kinase 1, transcript variant X3
unc-51 like autophagy activating kinase 1, transcript variant X2
serine/threonine-protein kinase ULK1 isoform X1
serine/threonine-protein kinase ULK1 isoform X3
serine/threonine-protein kinase ULK1 isoform X2
serine/threonine-protein kinase ULK1 isoform X4
polypeptide N-acetylgalactosaminyltransferase 9, 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 2 samples with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X3
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X1
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
polypeptide N-acetylgalactosaminyltransferase 9, transcript variant X5
polypeptide N-acetylgalactosaminyltransferase 9 isoform X1
polypeptide N-acetylgalactosaminyltransferase 9 isoform X2
polypeptide N-acetylgalactosaminyltransferase 9 isoform X3
autism susceptibility gene 2 protein-like, transcript variant X1
autism susceptibility gene 2 protein-like, transcript variant X6
autism susceptibility gene 2 protein-like, transcript variant X3
autism susceptibility gene 2 protein-like, transcript variant X8
autism susceptibility gene 2 protein-like, transcript variant X12
autism susceptibility gene 2 protein-like, transcript variant X5
autism susceptibility gene 2 protein-like, transcript variant X7
autism susceptibility gene 2 protein-like, transcript variant X4
autism susceptibility gene 2 protein-like, transcript variant X14
autism susceptibility gene 2 protein-like, transcript variant X9
autism susceptibility gene 2 protein-like, transcript variant X11
autism susceptibility gene 2 protein-like, transcript variant X2
autism susceptibility gene 2 protein-like, transcript variant X10
autism susceptibility gene 2 protein-like, transcript variant X13
autism susceptibility gene 2 protein-like isoform X1
autism susceptibility gene 2 protein-like isoform X6
autism susceptibility gene 2 protein-like isoform X3
autism susceptibility gene 2 protein-like isoform X8
autism susceptibility gene 2 protein-like isoform X12
autism susceptibility gene 2 protein-like isoform X5
autism susceptibility gene 2 protein-like isoform X7
autism susceptibility gene 2 protein-like isoform X4
autism susceptibility gene 2 protein-like isoform X14
autism susceptibility gene 2 protein-like isoform X9
autism susceptibility gene 2 protein-like isoform X11
autism susceptibility gene 2 protein-like isoform X2
autism susceptibility gene 2 protein homolog isoform X10
autism susceptibility gene 2 protein homolog isoform X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 70% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: casein kinase I-like
checkpoint with forkhead and ring finger domains
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: E3 ubiquitin-protein ligase CHFR
uncharacterized LOC121916709, transcript variant X3
uncharacterized LOC121916709, transcript variant X4
uncharacterized LOC121916709, transcript variant X1
uncharacterized LOC121916709, transcript variant X2
uncharacterized protein LOC121916709 isoform X3
uncharacterized protein LOC121916709 isoform X1
uncharacterized protein LOC121916709 isoform X2
uncharacterized protein LOC121916709 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
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
ankyrin repeat and LEM domain containing 2, transcript variant X1
ankyrin repeat and LEM domain-containing protein 2 isoform X1
ankyrin repeat and LEM domain containing 2, transcript variant X2
ankyrin repeat and LEM domain-containing protein 2 isoform X2
PGAM family member 5, mitochondrial serine/threonine protein phosphatase, transcript variant X2
PGAM family member 5, mitochondrial serine/threonine protein phosphatase, transcript variant X1
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X2
serine/threonine-protein phosphatase PGAM5, mitochondrial isoform X1
zinc finger DHHC-type palmitoyltransferase 8, transcript variant X1
zinc finger DHHC-type palmitoyltransferase 8, transcript variant X2
RAN binding protein 1, transcript variant X2
RAN binding protein 1, transcript variant X1
RAN binding protein 1, transcript variant X4
RAN binding protein 1, transcript variant X3
ran-specific GTPase-activating protein isoform X2
ran-specific GTPase-activating protein isoform X1
ran-specific GTPase-activating protein isoform X4
ran-specific GTPase-activating protein isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00599
tRNA methyltransferase 2 homolog A, transcript variant X1
tRNA methyltransferase 2 homolog A, transcript variant X2
tRNA (uracil-5-)-methyltransferase homolog A
DGCR8 microprocessor complex subunit, transcript variant X4
DGCR8 microprocessor complex subunit, transcript variant X2
DGCR8 microprocessor complex subunit, transcript variant X1
DGCR8 microprocessor complex subunit, transcript variant X3
DGCR8 microprocessor complex subunit, transcript variant X5
transport and golgi organization 2 homolog, transcript variant X2
transport and golgi organization 2 homolog, transcript variant X3
transport and golgi organization 2 homolog, transcript variant X1
transport and golgi organization 2 homolog, transcript variant X4
transport and Golgi organization protein 2 homolog
ARVCF delta catenin family member, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ARVCF delta catenin family member, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
ARVCF delta catenin family member, transcript variant X1
ARVCF delta catenin family member, transcript variant X9
ARVCF delta catenin family member, transcript variant X6
ARVCF delta catenin family member, transcript variant X5
ARVCF delta catenin family member, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ARVCF delta catenin family member, transcript variant X3
ARVCF delta catenin family member, transcript variant X7
ARVCF delta catenin family member, transcript variant X11
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
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X8
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X1
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X2
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X5
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X6
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X3
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X4
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X7
ARVCF delta catenin family member, transcript variant X10
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X9
armadillo repeat protein deleted in velo-cardio-facial syndrome isoform X10
catechol-O-methyltransferase, transcript variant X3
catechol-O-methyltransferase, transcript variant X6
catechol-O-methyltransferase, transcript variant X2
catechol-O-methyltransferase, transcript variant X4
catechol-O-methyltransferase, transcript variant X1
catechol-O-methyltransferase, transcript variant X7
catechol-O-methyltransferase, transcript variant X5
LOW QUALITY PROTEIN: thioredoxin reductase 2, mitochondrial
G protein subunit beta 1 like, transcript variant X7
G protein subunit beta 1 like, transcript variant X2
G protein subunit beta 1 like, transcript variant X14
G protein subunit beta 1 like, transcript variant X3
G protein subunit beta 1 like, transcript variant X4
G protein subunit beta 1 like, transcript variant X6
G protein subunit beta 1 like, transcript variant X10
G protein subunit beta 1 like, transcript variant X12
G protein subunit beta 1 like, transcript variant X11
G protein subunit beta 1 like, transcript variant X1
G protein subunit beta 1 like, transcript variant X5
G protein subunit beta 1 like, transcript variant X13
G protein subunit beta 1 like, transcript variant X15
G protein subunit beta 1 like, transcript variant X8
G protein subunit beta 1 like, transcript variant X9
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X1
guanine nucleotide-binding protein subunit beta-like protein 1 isoform X2
T-box transcription factor 1, 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
T-box transcription factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
T-box transcription factor TBX1 isoform X2
T-box transcription factor TBX1 isoform X1
glycoprotein Ib platelet subunit beta, 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 16 samples with support for all annotated introns
glycoprotein Ib platelet subunit beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 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: 30 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: 91 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 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: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
cell division control protein 45 homolog
ubiquitin recognition factor in ER associated degradation 1
ubiquitin recognition factor in ER-associated degradation protein 1
39S ribosomal protein L40, mitochondrial
RING-type E3 ubiquitin-protein ligase PPIL2
mitogen-activated protein kinase 1, transcript variant X4
mitogen-activated protein kinase 1, transcript variant X2
mitogen-activated protein kinase 1, transcript variant X1
mitogen-activated protein kinase 1, transcript variant X3
protein phosphatase, Mg2+/Mn2+ dependent 1F
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
stromal cell-derived factor 2-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 116
YdjC chitooligosaccharide deacetylase homolog, transcript variant X1
YdjC chitooligosaccharide deacetylase homolog, transcript variant X2
ubiquitin conjugating enzyme E2 L3, transcript variant X1
ubiquitin conjugating enzyme E2 L3, transcript variant X2
ubiquitin-conjugating enzyme E2 L3 isoform X1
ubiquitin-conjugating enzyme E2 L3 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
HIC ZBTB transcriptional repressor 2, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
HIC ZBTB transcriptional repressor 2, transcript variant X10
HIC ZBTB transcriptional repressor 2, transcript variant X9
HIC ZBTB transcriptional repressor 2, transcript variant X1
HIC ZBTB transcriptional repressor 2, transcript variant X2
HIC ZBTB transcriptional repressor 2, transcript variant X3
HIC ZBTB transcriptional repressor 2, transcript variant X5
HIC ZBTB transcriptional repressor 2, transcript variant X4
HIC ZBTB transcriptional repressor 2, transcript variant X7
HIC ZBTB transcriptional repressor 2, transcript variant X6
clathrin heavy chain like 1, transcript variant X7
clathrin heavy chain like 1, transcript variant X5
clathrin heavy chain like 1, transcript variant X1
clathrin heavy chain like 1, transcript variant X6
clathrin heavy chain like 1, transcript variant X2
clathrin heavy chain like 1, transcript variant X3
clathrin heavy chain like 1, transcript variant X4
tricarboxylate transport protein, mitochondrial
somatomedin-B and thrombospondin type-1 domain-containing protein-like, transcript variant X1
somatomedin-B and thrombospondin type-1 domain-containing protein-like, transcript variant X2
somatomedin-B and thrombospondin type-1 domain-containing protein-like isoform X1
somatomedin-B and thrombospondin type-1 domain-containing protein-like isoform X2
thyroid adenoma-associated protein homolog, transcript variant X3
thyroid adenoma-associated protein homolog, transcript variant X2
thyroid adenoma-associated protein homolog, transcript variant X4
thyroid adenoma-associated protein homolog, transcript variant X1
thyroid adenoma-associated protein homolog, transcript variant X6
thyroid adenoma-associated protein homolog, transcript variant X5
thyroid adenoma-associated protein homolog isoform X3
thyroid adenoma-associated protein homolog isoform X2
thyroid adenoma-associated protein homolog isoform X1
thyroid adenoma-associated protein homolog isoform X6
thyroid adenoma-associated protein homolog isoform X5
thyroid adenoma-associated protein homolog isoform X4
goosecoid homeobox 2, transcript variant X1
goosecoid homeobox 2, transcript variant X3
goosecoid homeobox 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
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
testis-specific serine/threonine-protein kinase 2
testis-specific serine/threonine-protein kinase 1-like
testis-specific serine/threonine-protein kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 55% coverage of the annotated genomic feature by RNAseq alignments
DiGeorge syndrome critical region gene 2, transcript variant X5
DiGeorge syndrome critical region gene 2, transcript variant X1
DiGeorge syndrome critical region gene 2, transcript variant X2
DiGeorge syndrome critical region gene 2, transcript variant X3
DiGeorge syndrome critical region gene 2, transcript variant X4
integral membrane protein DGCR2/IDD isoform X1
integral membrane protein DGCR2/IDD isoform X2
integral membrane protein DGCR2/IDD isoform X3
integral membrane protein DGCR2/IDD isoform X4
integral membrane protein DGCR2/IDD isoform X5
carbonic anhydrase 15-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
carbonic anhydrase 15-like, transcript variant X2
immunoglobulin lambda-1 light chain-like, transcript variant X11
immunoglobulin lambda-1 light chain-like, transcript variant X15
immunoglobulin lambda-1 light chain-like, transcript variant X16
immunoglobulin lambda-1 light chain-like, transcript variant X17
immunoglobulin lambda-1 light chain-like, transcript variant X1
immunoglobulin lambda-1 light chain-like, transcript variant X3
immunoglobulin lambda-1 light chain-like, transcript variant X6
immunoglobulin lambda-1 light chain-like, transcript variant X10
immunoglobulin lambda-1 light chain-like, transcript variant X7
immunoglobulin lambda-1 light chain-like, transcript variant X14
immunoglobulin lambda-1 light chain-like, transcript variant X5
immunoglobulin lambda-1 light chain-like isoform X11
immunoglobulin lambda-1 light chain-like isoform X15
immunoglobulin lambda-1 light chain-like isoform X16
immunoglobulin lambda-1 light chain-like isoform X17
immunoglobulin lambda-1 light chain-like isoform X1
immunoglobulin lambda-1 light chain-like isoform X3
immunoglobulin lambda-1 light chain-like isoform X6
immunoglobulin lambda-1 light chain-like isoform X10
immunoglobulin lambda-1 light chain-like isoform X7
immunoglobulin lambda-1 light chain-like isoform X14
immunoglobulin lambda-1 light chain-like isoform X5
immunoglobulin lambda-1 light chain-like, transcript variant X2
immunoglobulin lambda-1 light chain-like, transcript variant X12
immunoglobulin lambda-1 light chain-like, transcript variant X8
immunoglobulin lambda-1 light chain-like, transcript variant X9
immunoglobulin lambda-1 light chain-like, transcript variant X13
immunoglobulin lambda-1 light chain-like, transcript variant X4
immunoglobulin lambda-1 light chain-like isoform X2
immunoglobulin lambda-1 light chain-like isoform X12
immunoglobulin lambda-1 light chain-like isoform X8
immunoglobulin lambda-1 light chain-like isoform X9
immunoglobulin lambda-1 light chain-like isoform X13
immunoglobulin lambda-1 light chain-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1056 Proteins, and 81% coverage of the annotated genomic feature by RNAseq alignments
probable non-functional immunoglobulin lambda variable 5-48
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 382 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
immunoglobulin lambda variable 5-37-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 471 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
immunoglobulin lambda variable 3-25-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 257 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
vacuolar protein sorting-associated protein 29-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X1
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X8
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X7
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X5
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X6
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X9
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X10
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X4
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X2
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X3
calcium/calmodulin-dependent protein kinase kinase 2 isoform X7
calcium/calmodulin-dependent protein kinase kinase 2 isoform X6
calcium/calmodulin-dependent protein kinase kinase 2 isoform X2
calcium/calmodulin-dependent protein kinase kinase 2 isoform X5
calcium/calmodulin-dependent protein kinase kinase 2 isoform X4
calcium/calmodulin-dependent protein kinase kinase 2 isoform X3
calcium/calmodulin-dependent protein kinase kinase 2 isoform X1
calcium/calmodulin dependent protein kinase kinase 2, transcript variant X11
anaphase-promoting complex subunit 5-like
anaphase promoting complex subunit 5, 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 14 samples with support for all annotated introns
anaphase promoting complex subunit 5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ring finger protein 34, transcript variant X11
ring finger protein 34, transcript variant X1
ring finger protein 34, transcript variant X4
ring finger protein 34, transcript variant X3
ring finger protein 34, transcript variant X5
ring finger protein 34, transcript variant X7
ring finger protein 34, transcript variant X9
ring finger protein 34, transcript variant X10
E3 ubiquitin-protein ligase RNF34 isoform X2
ring finger protein 34, transcript variant X2
ring finger protein 34, transcript variant X8
ring finger protein 34, transcript variant X6
E3 ubiquitin-protein ligase RNF34 isoform X1
lysine demethylase 2B, transcript variant X12
lysine demethylase 2B, transcript variant X4
lysine demethylase 2B, transcript variant X3
lysine demethylase 2B, transcript variant X5
lysine demethylase 2B, transcript variant X2
lysine demethylase 2B, transcript variant X1
lysine demethylase 2B, transcript variant X9
lysine demethylase 2B, transcript variant X11
lysine demethylase 2B, transcript variant X6
lysine demethylase 2B, transcript variant X8
lysine demethylase 2B, transcript variant X7
lysine demethylase 2B, transcript variant X10
lysine demethylase 2B, transcript variant X13
lysine demethylase 2B, transcript variant X14
lysine demethylase 2B, transcript variant X15
lysine-specific demethylase 2B isoform X7
lysine-specific demethylase 2B isoform X4
lysine-specific demethylase 2B isoform X3
lysine-specific demethylase 2B isoform X5
lysine-specific demethylase 2B isoform X2
lysine-specific demethylase 2B isoform X1
lysine-specific demethylase 2B isoform X6
lysine-specific demethylase 2B isoform X8
lysine-specific demethylase 2B isoform X9
ORAI calcium release-activated calcium modulator 1, transcript variant X1
ORAI calcium release-activated calcium modulator 1, transcript variant X2
calcium release-activated calcium channel protein 1
MORN repeat containing 3, transcript variant X1
MORN repeat containing 3, transcript variant X2
MORN repeat-containing protein 3 isoform X1
MORN repeat-containing protein 3 isoform X2
transmembrane protein 120B, transcript variant X2
transmembrane protein 120B, transcript variant X1
ras homolog family member F, filopodia associated
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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
SET domain containing 1B, histone lysine methyltransferase
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 7 bases in 6 codons; deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 7 bases in 6 codons; deleted 3 bases in 2 codons; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: histone-lysine N-methyltransferase SETD1B
4-hydroxyphenylpyruvate dioxygenase, transcript variant X1
4-hydroxyphenylpyruvate dioxygenase, transcript variant X2
4-hydroxyphenylpyruvate dioxygenase isoform X1
4-hydroxyphenylpyruvate dioxygenase isoform X2
proteasome 26S subunit, non-ATPase 9, transcript variant X2
proteasome 26S subunit, non-ATPase 9, transcript variant X1
26S proteasome non-ATPase regulatory subunit 9 isoform X1
26S proteasome non-ATPase regulatory subunit 9 isoform X2
cilia and flagella associated protein 251, transcript variant X1
cilia and flagella associated protein 251, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
cilia and flagella associated protein 251, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
cilia- and flagella-associated protein 251
BAF chromatin remodeling complex subunit BCL7A, transcript variant X2
BAF chromatin remodeling complex subunit BCL7A, transcript variant X1
B-cell CLL/lymphoma 7 protein family member A
MLX interacting protein, 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 14 samples with support for all annotated introns
MLX interacting protein, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: leucine-rich repeat-containing protein 43
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4, transcript variant X4
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 4, 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 13 samples with support for all annotated introns
N-acetyllactosaminide beta-1,3-N-acetylglucosaminyltransferase 4
diablo IAP-binding mitochondrial protein
uncharacterized LOC121916637, transcript variant X1
uncharacterized LOC121916637, transcript variant X2
VPS33A core subunit of CORVET and HOPS complexes
vacuolar protein sorting-associated protein 33A
CAP-Gly domain containing linker protein 1, transcript variant X6
CAP-Gly domain containing linker protein 1, transcript variant X9
CAP-Gly domain containing linker protein 1, transcript variant X13
CAP-Gly domain containing linker protein 1, transcript variant X12
CAP-Gly domain containing linker protein 1, transcript variant X8
CAP-Gly domain containing linker protein 1, transcript variant X1
CAP-Gly domain containing linker protein 1, transcript variant X10
CAP-Gly domain containing linker protein 1, transcript variant X2
CAP-Gly domain containing linker protein 1, transcript variant X11
CAP-Gly domain containing linker protein 1, transcript variant X15
CAP-Gly domain containing linker protein 1, transcript variant X14
CAP-Gly domain containing linker protein 1, transcript variant X4
CAP-Gly domain containing linker protein 1, transcript variant X16
CAP-Gly domain containing linker protein 1, transcript variant X5
CAP-Gly domain containing linker protein 1, transcript variant X3
CAP-Gly domain containing linker protein 1, transcript variant X7
CAP-Gly domain containing linker protein 1, transcript variant X17
CAP-Gly domain-containing linker protein 1 isoform X3
CAP-Gly domain-containing linker protein 1 isoform X11
CAP-Gly domain-containing linker protein 1 isoform X5
CAP-Gly domain-containing linker protein 1 isoform X7
CAP-Gly domain-containing linker protein 1 isoform X6
CAP-Gly domain-containing linker protein 1 isoform X9
CAP-Gly domain-containing linker protein 1 isoform X8
CAP-Gly domain-containing linker protein 1 isoform X2
CAP-Gly domain-containing linker protein 1 isoform X1
CAP-Gly domain-containing linker protein 1 isoform X4
CAP-Gly domain-containing linker protein 1 isoform X10
zinc finger CCHC-type containing 8, transcript variant X2
zinc finger CCHC-type containing 8, transcript variant X1
zinc finger CCHC-type containing 8, transcript variant X3
zinc finger CCHC-type containing 8, transcript variant X4
zinc finger CCHC domain-containing protein 8 isoform X2
zinc finger CCHC domain-containing protein 8 isoform X3
zinc finger CCHC domain-containing protein 8 isoform X1
zinc finger CCHC domain-containing protein 8 isoform X4
arginine and serine rich coiled-coil 2, transcript variant X1
arginine and serine rich coiled-coil 2, transcript variant X2
arginine and serine rich coiled-coil 2, transcript variant X3
arginine/serine-rich coiled-coil protein 2 isoform X1
arginine/serine-rich coiled-coil protein 2 isoform X2
arginine/serine-rich coiled-coil protein 2 isoform X3
kinetochore associated 1, transcript variant X1
kinetochore associated 1, transcript variant X4
kinetochore associated 1, transcript variant X5
kinetochore associated 1, transcript variant X3
kinetochore associated 1, transcript variant X2
kinetochore-associated protein 1 isoform X1
kinetochore-associated protein 1 isoform X2
kinetochore-associated protein 1 isoform X3
VPS29 retromer complex component, transcript variant X3
VPS29 retromer complex component, transcript variant X2
VPS29 retromer complex component, transcript variant X1
VPS29 retromer complex component, transcript variant X4
vacuolar protein sorting-associated protein 29 isoform X3
vacuolar protein sorting-associated protein 29 isoform X2
vacuolar protein sorting-associated protein 29 isoform X1
vacuolar protein sorting-associated protein 29 isoform X4
cell cycle checkpoint control protein RAD9B
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 3 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein phosphatase PTC7 homolog
hydrogen voltage gated channel 1, transcript variant X2
hydrogen voltage gated channel 1, transcript variant X1
hydrogen voltage gated channel 1, transcript variant X3
uncharacterized LOC121916400, transcript variant X2
uncharacterized LOC121916400, transcript variant X1
uncharacterized LOC121916400, transcript variant X3
protein phosphatase 1 catalytic subunit gamma, transcript variant X2
serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform X2
protein phosphatase 1 catalytic subunit gamma, transcript variant X3
protein phosphatase 1 catalytic subunit gamma, transcript variant X4
protein phosphatase 1 catalytic subunit gamma, transcript variant X1
serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform X4
serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform X1
serine/threonine-protein phosphatase PP1-gamma catalytic subunit isoform X3
myosin regulatory light chain 2, ventricular/cardiac muscle isoform
cut like homeobox 2, transcript variant X2
cut like homeobox 2, transcript variant X1
cut like homeobox 2, transcript variant X3
PH domain containing endocytic trafficking adaptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
PH domain containing endocytic trafficking adaptor 1, transcript variant X3
PH domain containing endocytic trafficking adaptor 1, 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 9 samples with support for all annotated introns
SH2B adaptor protein 3, transcript variant X4
SH2B adaptor protein 3, transcript variant X6
SH2B adaptor protein 3, transcript variant X1
SH2B adaptor protein 3, transcript variant X3
SH2B adaptor protein 3, transcript variant X5
SH2B adaptor protein 3, transcript variant X2
BRCA1 associated protein, transcript variant X3
BRCA1 associated protein, transcript variant X4
BRCA1 associated protein, transcript variant X5
BRCA1 associated protein, transcript variant X2
BRCA1 associated protein, transcript variant X1
serine/arginine repetitive matrix protein 1-like
acyl-CoA dehydrogenase family member 10, transcript variant X1
acyl-CoA dehydrogenase family member 10 isoform X1
acyl-CoA dehydrogenase family member 10, transcript variant X2
acyl-CoA dehydrogenase family member 10 isoform X2
MAPK activated protein kinase 5, transcript variant X1
MAPK activated protein kinase 5, transcript variant X2
MAP kinase-activated protein kinase 5 isoform X1
MAP kinase-activated protein kinase 5 isoform X2
disintegrin and metalloproteinase domain-containing protein 21-like
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
transmembrane protein 116, transcript variant X1
transmembrane protein 116, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
endoplasmic reticulum resident protein 29
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X3
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X4
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X2
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X3
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X2
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X1
N-alpha-acetyltransferase 25, NatB auxiliary subunit isoform X4
N-alpha-acetyltransferase 25, NatB auxiliary subunit, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
TRAF-type zinc finger domain containing 1, transcript variant X3
TRAF-type zinc finger domain-containing protein 1 isoform X3
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
TRAF-type zinc finger domain containing 1, transcript variant X4
TRAF-type zinc finger domain-containing protein 1 isoform X4
TRAF-type zinc finger domain containing 1, transcript variant X1
TRAF-type zinc finger domain containing 1, transcript variant X2
TRAF-type zinc finger domain-containing protein 1 isoform X1
TRAF-type zinc finger domain-containing protein 1 isoform X2
HECT domain E3 ubiquitin protein ligase 4
probable E3 ubiquitin-protein ligase HECTD4
protein tyrosine phosphatase non-receptor type 11
tyrosine-protein phosphatase non-receptor type 11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 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: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC121916413, transcript variant X2
uncharacterized LOC121916413, transcript variant X3
uncharacterized LOC121916413, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chemerin chemokine-like receptor 1, transcript variant X11
chemerin chemokine-like receptor 1, transcript variant X12
chemerin chemokine-like receptor 1, transcript variant X8
chemerin chemokine-like receptor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
chemerin chemokine-like receptor 1, transcript variant X4
chemerin chemokine-like receptor 1, transcript variant X9
chemerin chemokine-like receptor 1, transcript variant X6
chemerin chemokine-like receptor 1, transcript variant X3
chemerin chemokine-like receptor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
chemerin chemokine-like receptor 1, transcript variant X10
chemerin chemokine-like receptor 1, transcript variant X5
chemerin chemokine-like receptor 1, 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 7 samples with support for all annotated introns
FIC domain protein adenylyltransferase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
FIC domain protein adenylyltransferase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
protein adenylyltransferase FICD isoform X1
protein adenylyltransferase FICD isoform X2
spliceosome associated factor 3, U4/U6 recycling protein
squamous cell carcinoma antigen recognized by T-cells 3
squamous cell carcinoma antigen recognized by T-cells 3-like
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 24 samples with support for all annotated introns
iron-sulfur cluster assembly enzyme ISCU, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
immunoglobulin lambda variable 3-21-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 417 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
selectin P ligand, 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 7 samples with support for all annotated introns
selectin P ligand, transcript variant X2
selectin P ligand, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
P-selectin glycoprotein ligand 1 isoform X1
P-selectin glycoprotein ligand 1 isoform X2
slingshot protein phosphatase 1, transcript variant X1
slingshot protein phosphatase 1, transcript variant X3
slingshot protein phosphatase 1, transcript variant X2
protein phosphatase Slingshot homolog 1 isoform X3
protein phosphatase Slingshot homolog 1 isoform X1
protein phosphatase Slingshot homolog 1 isoform X2
D-amino acid oxidase, transcript variant X1
D-amino acid oxidase, transcript variant X3
D-amino acid oxidase, transcript variant X2
SV2 related protein, transcript variant X4
SV2 related protein, transcript variant X3
SV2 related protein, transcript variant X2
SV2 related protein, transcript variant X1
synaptic vesicle 2-related protein isoform X4
synaptic vesicle 2-related protein isoform X3
synaptic vesicle 2-related protein isoform X2
synaptic vesicle 2-related protein isoform X1
ubiquitin specific peptidase 30, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
ubiquitin specific peptidase 30, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
ubiquitin specific peptidase 30, transcript variant X7
ubiquitin specific peptidase 30, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 30 isoform X2
ubiquitin specific peptidase 30, transcript variant X6
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 18 samples with support for all annotated introns
ubiquitin specific peptidase 30, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
ubiquitin specific peptidase 30, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
ubiquitin carboxyl-terminal hydrolase 30 isoform X1
ubiquitin carboxyl-terminal hydrolase 30 isoform X3
ubiquitin carboxyl-terminal hydrolase 30 isoform X4
uracil DNA glycosylase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uracil DNA glycosylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
MORC family CW-type zinc finger 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
MORC family CW-type zinc finger 2, transcript variant X4
MORC family CW-type zinc finger 2, transcript variant X1
MORC family CW-type zinc finger 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger protein 34-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
zinc finger protein 34-like, transcript variant X1
zinc finger protein 34-like, transcript variant X3
trichohyalin-like, transcript variant X3
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X1
uncharacterized protein LOC121916384 isoform X1
uncharacterized protein LOC121916384 isoform X2
oxysterol binding protein 2, transcript variant X1
oxysterol binding protein 2, transcript variant X2
oxysterol binding protein 2, transcript variant X5
oxysterol binding protein 2, transcript variant X3
oxysterol binding protein 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 77% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
synergin gamma-like, transcript variant X2
synergin gamma-like, transcript variant X1
uncharacterized protein LOC121916367 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
pescadillo ribosomal biogenesis factor 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
LOW QUALITY PROTEIN: galactosylceramide sulfotransferase
zona pellucida sperm-binding protein 3-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zona pellucida sperm-binding protein 3-like, transcript variant X2
zona pellucida sperm-binding protein 3-like isoform X1
zona pellucida sperm-binding protein 3-like isoform X2
mitochondrial fission process 1, transcript variant X1
mitochondrial fission process 1, transcript variant X2
mitochondrial fission process protein 1 isoform X1
mitochondrial fission process protein 1 isoform X2
SEC14 like lipid binding 2, transcript variant X2
SEC14 like lipid binding 2, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 6 bases in 4 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 57% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 6 bases in 4 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: RING finger protein 215
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 157
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
LOW QUALITY PROTEIN: RNA-binding protein EWS
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
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 23 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 81% coverage of the annotated genomic feature by RNAseq alignments
THO complex subunit 5 homolog isoform X1
THO complex subunit 5 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 60 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 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 23 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 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC121916634, transcript variant X2
uncharacterized LOC121916634, transcript variant X1
uncharacterized protein LOC121916634 isoform X1
uncharacterized protein LOC121916634 isoform X2
tRNA modification GTPase GTPBP3, mitochondrial-like
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
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
coiled-coil domain-containing protein 194
polypyrimidine tract binding protein 1, transcript variant X1
polypyrimidine tract binding protein 1, transcript variant X2
polypyrimidine tract-binding protein 1 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
LOW QUALITY PROTEIN: uncharacterized protein LOC121916679
polypyrimidine tract-binding protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
phospholipid phosphatase-related protein type 3
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 13 samples with support for all annotated introns
mediator of RNA polymerase II transcription subunit 16
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
AT-rich interactive domain-containing protein 3A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
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 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
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 1 base in 1 codon; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: DNA-directed RNA polymerases I, II, and III subunit RPABC1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 2 bases in 2 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: rho GTPase-activating protein 45
regulatory factor X associated ankyrin containing protein, transcript variant X2
regulatory factor X associated ankyrin containing protein, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: transmembrane protein 161A
solute carrier family 25 member 42, transcript variant X1
solute carrier family 25 member 42, 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 13 samples with support for all annotated introns
solute carrier family 25 member 42, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
mitochondrial coenzyme A transporter SLC25A42
LOW QUALITY PROTEIN: armadillo repeat-containing protein 6
SURP and G-patch domain containing 2, transcript variant X3
SURP and G-patch domain containing 2, transcript variant X1
SURP and G-patch domain containing 2, transcript variant X2
SURP and G-patch domain-containing protein 2
probable ATP-dependent RNA helicase DDX49
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: coatomer subunit epsilon
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
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: 85% coverage of the annotated genomic feature by RNAseq alignments
regulator of nonsense transcripts 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 65% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: cartilage oligomeric matrix protein
CREB regulated transcription coactivator 1
CREB-regulated transcription coactivator 1
kelch-like protein 26, transcript variant X2
kelch-like protein 26, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cytokine receptor like factor 1, transcript variant X2
cytokine receptor like factor 1, transcript variant X1
cytokine receptor like factor 1, transcript variant X4
cytokine receptor-like factor 1 isoform X1
cytokine receptor-like factor 1 isoform X2
cytokine receptor-like factor 1 isoform X4
cytokine receptor like factor 1, transcript variant X3
cytokine receptor-like factor 1 isoform X3
required for excision 1-B domain containing
required for excision 1-B domain-containing protein
ubiquitin A-52 residue ribosomal protein fusion product 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
cAMP-specific 3',5'-cyclic phosphodiesterase 4C-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 38 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase 4C-like isoform X1
cAMP-specific 3',5'-cyclic phosphodiesterase 4C-like, 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 11 samples with support for all annotated introns
cAMP-specific 3',5'-cyclic phosphodiesterase 4C-like isoform X2
uncharacterized LOC121916638, transcript variant X3
uncharacterized LOC121916638, transcript variant X4
uncharacterized protein LOC121916638 isoform X2
uncharacterized LOC121916638, transcript variant X2
uncharacterized LOC121916638, transcript variant X1
uncharacterized protein LOC121916638 isoform X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 7 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 8 bases in 7 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: insulin receptor-like