Catharus ustulatus isolate bCatUst1 chromosome 21, bCatUst1.pri.v2, whole genome shotgun sequence.
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Archelosauria; Archosauria; Dinosauria; Saurischia; Theropoda; Coelurosauria; Aves; Neognathae; Passeriformes; Turdidae; Catharus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM020356.1.\nAssembly name: bCatUst1.pri.v2\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2020/12/22. The original whole-genome shotgun project has the\naccession WNMQ00000000.2.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 06-AUG-2020\nAssembly Method :: FALCON v. DX 1.9.0; FALCON-Unzip v.\n 6.0.0.47841; purge_dups github v.\n purge_haplotig (bitbucket v1.0.3+\n 1.Nov.2018); Scaff10x v. 2; Bionano Solve\n v. 3.2.1_04122018; Salsa2 HiC v. 2.2;\n Arrow polishing and gap filling v.\n Smrtlink_6.0.0.47841; Longranger Align v.\n 2.2.2; freebayes v. 1.3.1; gEVAL manual\n curation v. 2020-08-06; VGP assembly\n pipeline v. 1.5\nAssembly Name :: bCatUst1.pri.v2\nDiploid :: Principal pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 60.58x\nSequencing Technology :: PacBio Sequel I CLR; Illumina NovaSeq;\n Arima Genomics Hi-C; Bionano Genomics DLS\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Catharus ustulatus Annotation\n Release 101\nAnnotation Version :: 101\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 1 EST, 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase
UDP-N-acetylglucosamine pyrophosphorylase 1 like 1
UDP-N-acetylhexosamine pyrophosphorylase-like protein 1
suppressor APC domain containing 2, transcript variant X1
suppressor APC domain containing 2, transcript variant X2
suppressor APC domain-containing protein 2
transmembrane protein 141, transcript variant X4
ectonucleoside triphosphate diphosphohydrolase 2
transmembrane protein 141, transcript variant X3
transmembrane protein 141, transcript variant X2
transmembrane protein 141, transcript variant X1
transmembrane protein 141, transcript variant X5
PAXX non-homologous end joining factor, transcript variant X2
PAXX non-homologous end joining factor, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon
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: chloride intracellular channel protein 3
ATP binding cassette subfamily A member 2, transcript variant X5
ATP binding cassette subfamily A member 2, transcript variant X4
ATP binding cassette subfamily A member 2, transcript variant X3
ATP binding cassette subfamily A member 2, transcript variant X2
ATP binding cassette subfamily A member 2, transcript variant X1
ATP-binding cassette sub-family A member 2 isoform X5
ATP-binding cassette sub-family A member 2 isoform X4
ATP-binding cassette sub-family A member 2 isoform X3
ATP-binding cassette sub-family A member 2 isoform X2
ATP-binding cassette sub-family A member 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
POU domain, class 5, transcription factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 18 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
neural proliferation, differentiation and control 1
neural proliferation differentiation and control protein 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 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; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: lipocalin-like 1 protein
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; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
complement C8 gamma chain, transcript variant X7
complement C8 gamma chain, transcript variant X5
complement C8 gamma chain, transcript variant X6
complement C8 gamma chain, transcript variant X2
complement C8 gamma chain, transcript variant X3
complement component C8 gamma chain isoform X7
complement component C8 gamma chain isoform X6
complement component C8 gamma chain isoform X3
complement C8 gamma chain, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
complement C8 gamma chain, 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 14 samples with support for all annotated introns
complement C8 gamma chain, 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 6 samples with support for all annotated introns
complement C8 gamma chain, transcript variant X8
complement component C8 gamma chain isoform X5
complement component C8 gamma chain isoform X2
complement component C8 gamma chain isoform X4
complement component C8 gamma chain isoform X1
complement component C8 gamma chain isoform X9
complement component C8 gamma chain isoform X8
F-box and WD repeat domain containing 5, transcript variant X1
F-box/WD repeat-containing protein 5 isoform X1
F-box and WD repeat domain containing 5, transcript variant X2
F-box/WD repeat-containing protein 5 isoform X2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 7 bases in 6 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: deleted 7 bases in 6 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: TNF receptor-associated factor 2
endothelial differentiation related factor 1
endothelial differentiation-related factor 1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
LOW QUALITY PROTEIN: apical junction component 1 homolog
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 7 Proteins, and 89% coverage of the annotated genomic feature by RNAseq alignments
notch-regulated ankyrin repeat-containing protein
exonuclease 3'-5' domain containing 3, transcript variant X2
exonuclease 3'-5' domain containing 3, transcript variant X4
exonuclease 3'-5' domain containing 3, transcript variant X3
exonuclease 3'-5' domain containing 3, transcript variant X1
exonuclease 3'-5' domain containing 3, transcript variant X5
exonuclease 3'-5' domain containing 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
NADPH oxidase activator 1, transcript variant X4
NADPH oxidase activator 1, transcript variant X1
NADPH oxidase activator 1, transcript variant X2
NADPH oxidase activator 1, transcript variant X3
NADPH oxidase activator 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
NADPH oxidase activator 1, transcript variant X6
ectonucleoside triphosphate diphosphohydrolase 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 29 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
ectonucleoside triphosphate diphosphohydrolase 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 58% coverage of the annotated genomic feature by RNAseq alignments
NADPH dependent diflavin oxidoreductase 1, transcript variant X2
NADPH dependent diflavin oxidoreductase 1, transcript variant X3
NADPH dependent diflavin oxidoreductase 1, transcript variant X1
NADPH-dependent diflavin oxidoreductase 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat-containing protein 26
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X18
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X12
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X14
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X13
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X11
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X7
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X6
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X5
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X4
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
glutamate receptor ionotropic, NMDA 1 isoform X16
glutamate receptor ionotropic, NMDA 1 isoform X12
glutamate receptor ionotropic, NMDA 1 isoform X14
glutamate receptor ionotropic, NMDA 1 isoform X13
glutamate receptor ionotropic, NMDA 1 isoform X11
glutamate receptor ionotropic, NMDA 1 isoform X7
glutamate receptor ionotropic, NMDA 1 isoform X6
glutamate receptor ionotropic, NMDA 1 isoform X5
glutamate receptor ionotropic, NMDA 1 isoform X4
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X9
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X1
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X2
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X10
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X8
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X3
glutamate receptor ionotropic, NMDA 1 isoform X9
glutamate receptor ionotropic, NMDA 1 isoform X2
glutamate receptor ionotropic, NMDA 1 isoform X10
glutamate receptor ionotropic, NMDA 1 isoform X8
glutamate receptor ionotropic, NMDA 1 isoform X3
glutamate receptor ionotropic, NMDA 1 isoform X1
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X17
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X16
glutamate receptor ionotropic, NMDA 1 isoform X15
zinc finger protein 618, transcript variant X16
zinc finger protein 618, transcript variant X13
zinc finger protein 618, transcript variant X9
zinc finger protein 618, transcript variant X12
zinc finger protein 618, transcript variant X7
zinc finger protein 618, transcript variant X11
zinc finger protein 618, transcript variant X8
zinc finger protein 618, transcript variant X15
zinc finger protein 618, transcript variant X4
zinc finger protein 618, transcript variant X2
zinc finger protein 618, transcript variant X10
zinc finger protein 618, transcript variant X5
zinc finger protein 618, transcript variant X6
zinc finger protein 618, transcript variant X1
zinc finger protein 618, transcript variant X3
zinc finger protein 618, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
regulator of G protein signaling 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 56 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
regulator of G protein signaling 3, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 2 ESTs, 57 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 55 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 54 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 48 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
regulator of G protein signaling 3, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 50 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
regulator of G-protein signaling 3 isoform X2
regulator of G-protein signaling 3 isoform X1
regulator of G-protein signaling 3 isoform X3
regulator of G-protein signaling 3 isoform X4
regulator of G-protein signaling 3 isoform X6
regulator of G-protein signaling 3 isoform X5
regulator of G-protein signaling 3 isoform X7
regulator of G-protein signaling 3 isoform X8
regulator of G-protein signaling 3 isoform X9
DNA polymerase epsilon 3, accessory subunit
aminolevulinate dehydratase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
aminolevulinate dehydratase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
delta-aminolevulinic acid dehydratase isoform X1
delta-aminolevulinic acid dehydratase isoform X2
haloacid dehalogenase like hydrolase domain containing 3
haloacid dehalogenase-like hydrolase domain-containing protein 3
B box and SPRY domain-containing protein
WD repeat domain 31, transcript variant X1
WD repeat domain 31, transcript variant X2
WD repeat domain 31, transcript variant X3
WD repeat domain 31, transcript variant X4
WD repeat-containing protein 31 isoform X1
WD repeat-containing protein 31 isoform X2
pre-mRNA processing factor 4, transcript variant X1
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X1
pre-mRNA processing factor 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
U4/U6 small nuclear ribonucleoprotein Prp4 isoform X2
anaphase-promoting complex subunit CDC26
solute carrier family 31 member 1, transcript variant X2
solute carrier family 31 member 1, transcript variant X1
high affinity copper uptake protein 1 isoform X1
high affinity copper uptake protein 1 isoform X2
FKBP prolyl isomerase family member 15, transcript variant X1
FKBP prolyl isomerase family member 15, transcript variant X2
FKBP prolyl isomerase family member 15, transcript variant X3
leucine rich repeat and sterile alpha motif containing 1, transcript variant X3
leucine rich repeat and sterile alpha motif containing 1, transcript variant X1
leucine rich repeat and sterile alpha motif containing 1, transcript variant X2
E3 ubiquitin-protein ligase LRSAM1 isoform X3
E3 ubiquitin-protein ligase LRSAM1 isoform X1
E3 ubiquitin-protein ligase LRSAM1 isoform X2
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00302
zinc finger MYND domain-containing protein 19
39S ribosomal protein L41, mitochondrial
patatin like phospholipase domain containing 7, transcript variant X1
patatin like phospholipase domain containing 7, transcript variant X2
patatin-like phospholipase domain-containing protein 7 isoform X1
patatin-like phospholipase domain-containing protein 7 isoform X2
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X1
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X3
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X2
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X4
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X1
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X3
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X2
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X4
discoidin domain-containing receptor 2-like, transcript variant X3
discoidin domain-containing receptor 2-like, transcript variant X1
discoidin domain-containing receptor 2-like, transcript variant X2
discoidin domain-containing receptor 2-like isoform X1
discoidin domain-containing receptor 2-like isoform X2
family with sequence similarity 166 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
ectonucleoside triphosphate diphosphohydrolase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
negative elongation factor complex member B
glutamine synthetase, transcript variant X2
glutamine synthetase, transcript variant X1
euchromatic histone lysine methyltransferase 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1 isoform X4
voltage-dependent N-type calcium channel subunit alpha-1B-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
euchromatic histone lysine methyltransferase 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 30 ESTs, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1 isoform X6
euchromatic histone lysine methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1 isoform X2
euchromatic histone lysine methyltransferase 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1, transcript variant X11
euchromatic histone lysine methyltransferase 1, transcript variant X10
euchromatic histone lysine methyltransferase 1, transcript variant X12
euchromatic histone lysine methyltransferase 1, transcript variant X8
euchromatic histone lysine methyltransferase 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 32 ESTs, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
histone-lysine N-methyltransferase EHMT1 isoform X5
histone-lysine N-methyltransferase EHMT1 isoform X1
histone-lysine N-methyltransferase EHMT1 isoform X7
histone-lysine N-methyltransferase EHMT1 isoform X3
histone-lysine N-methyltransferase EHMT1 isoform X8
calcium voltage-gated channel subunit alpha1 B, transcript variant X2
calcium voltage-gated channel subunit alpha1 B, transcript variant X3
calcium voltage-gated channel subunit alpha1 B, transcript variant X7
calcium voltage-gated channel subunit alpha1 B, transcript variant X11
calcium voltage-gated channel subunit alpha1 B, transcript variant X13
calcium voltage-gated channel subunit alpha1 B, transcript variant X15
calcium voltage-gated channel subunit alpha1 B, transcript variant X16
calcium voltage-gated channel subunit alpha1 B, transcript variant X1
calcium voltage-gated channel subunit alpha1 B, transcript variant X9
calcium voltage-gated channel subunit alpha1 B, transcript variant X4
calcium voltage-gated channel subunit alpha1 B, transcript variant X5
calcium voltage-gated channel subunit alpha1 B, transcript variant X6
calcium voltage-gated channel subunit alpha1 B, transcript variant X10
calcium voltage-gated channel subunit alpha1 B, transcript variant X8
calcium voltage-gated channel subunit alpha1 B, transcript variant X12
calcium voltage-gated channel subunit alpha1 B, transcript variant X19
calcium voltage-gated channel subunit alpha1 B, transcript variant X18
calcium voltage-gated channel subunit alpha1 B, transcript variant X14
calcium voltage-gated channel subunit alpha1 B, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
voltage-dependent N-type calcium channel subunit alpha-1B isoform X2
voltage-dependent N-type calcium channel subunit alpha-1B isoform X1
voltage-dependent N-type calcium channel subunit alpha-1B isoform X3
voltage-dependent N-type calcium channel subunit alpha-1B isoform X9
voltage-dependent N-type calcium channel subunit alpha-1B isoform X4
voltage-dependent N-type calcium channel subunit alpha-1B isoform X5
voltage-dependent N-type calcium channel subunit alpha-1B isoform X7
voltage-dependent N-type calcium channel subunit alpha-1B isoform X6
voltage-dependent N-type calcium channel subunit alpha-1B isoform X10
voltage-dependent N-type calcium channel subunit alpha-1B isoform X11
voltage-dependent N-type calcium channel subunit alpha-1B isoform X8
voltage-dependent N-type calcium channel subunit alpha-1B isoform X13
voltage-dependent N-type calcium channel subunit alpha-1B isoform X12
voltage-dependent N-type calcium channel subunit alpha-1B isoform X19
voltage-dependent N-type calcium channel subunit alpha-1B isoform X15
voltage-dependent N-type calcium channel subunit alpha-1B isoform X18
voltage-dependent N-type calcium channel subunit alpha-1B isoform X14
voltage-dependent N-type calcium channel subunit alpha-1B isoform X16
voltage-dependent N-type calcium channel subunit alpha-1B isoform X17
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 5 bases in 3 codons
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; deleted 5 bases in 3 codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: collagen alpha-1(I) chain-like
probable low affinity copper uptake protein 2
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; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 3 Proteins, and 93% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: protein Niban 2-like
syntaxin binding protein 1, transcript variant X1
syntaxin binding protein 1, transcript variant X2
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: microtubule organization protein AKNA
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 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: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 15
tumor necrosis factor ligand superfamily member 8-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
tripartite motif containing 32, transcript variant X1
tripartite motif containing 32, transcript variant X3
tripartite motif containing 32, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 25 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
BMP/retinoic acid inducible neural specific 1, transcript variant X1
BMP/retinoic acid inducible neural specific 1, transcript variant X2
BMP/retinoic acid-inducible neural-specific protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
CDK5 regulatory subunit associated protein 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
CDK5 regulatory subunit associated protein 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
CDK5 regulatory subunit-associated protein 2 isoform X2
CDK5 regulatory subunit-associated protein 2 isoform X1
multiple epidermal growth factor-like domains protein 9
collagen type XXVII alpha 1 chain, transcript variant X1
collagen type XXVII alpha 1 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
collagen alpha-1(XXVII) chain isoform X1
collagen alpha-1(XXVII) chain isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 67% coverage of the annotated genomic feature by RNAseq alignments
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
solute carrier family 25 member 25, transcript variant X2
solute carrier family 25 member 25, transcript variant X1
solute carrier family 25 member 25, transcript variant X4
solute carrier family 25 member 25, transcript variant X3
solute carrier family 25 member 25, transcript variant X6
solute carrier family 25 member 25, transcript variant X5
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X2
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X1
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X4
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X3
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X6
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X5
nuclear apoptosis inducing factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
nuclear apoptosis inducing factor 1, transcript variant X2
nuclear apoptosis inducing factor 1, transcript variant X3
nuclear apoptosis-inducing factor 1 isoform X2
nuclear apoptosis-inducing factor 1 isoform X3
nuclear apoptosis-inducing factor 1 isoform X1
family with sequence similarity 102 member A
dolichyl-phosphate mannosyltransferase subunit 2, regulatory
dolichol phosphate-mannose biosynthesis regulatory protein
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 4, transcript variant X2
alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase isoform X1
alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetyl-galactosaminide alpha-2,6-sialyltransferase isoform X2
ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
alpha-N-acetylgalactosaminide alpha-2,6-sialyltransferase 6
adenylate kinase 1, transcript variant X2
adenylate kinase 1, transcript variant X1
adenylate kinase 1, transcript variant X3
adenylate kinase 1, transcript variant X4
folylpolyglutamate synthase, mitochondrial
SH2 domain containing 3C, transcript variant X1
SH2 domain-containing protein 3C isoform X1
SH2 domain containing 3C, transcript variant X2
SH2 domain-containing protein 3C isoform X2
SH2 domain containing 3C, transcript variant X3
SH2 domain-containing protein 3C isoform X3
torsin family 2 member A, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
torsin family 2 member A, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
torsin family 2 member A, transcript variant X2
peptidyl-tRNA hydrolase 1 homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
peptidyl-tRNA hydrolase 1 homolog, transcript variant X2
peptidyl-tRNA hydrolase 1 homolog, transcript variant X3
probable peptidyl-tRNA hydrolase isoform X3
probable peptidyl-tRNA hydrolase isoform X1
probable peptidyl-tRNA hydrolase isoform X2
cerebral endothelial cell adhesion molecule, transcript variant X1
cerebral endothelial cell adhesion molecule, transcript variant X7
cerebral endothelial cell adhesion molecule, transcript variant X2
cerebral endothelial cell adhesion molecule, transcript variant X3
cerebral endothelial cell adhesion molecule, transcript variant X6
cerebral endothelial cell adhesion molecule, transcript variant X5
cerebral endothelial cell adhesion molecule, transcript variant X4
inactive glycosyltransferase 25 family member 3 isoform X1
inactive glycosyltransferase 25 family member 3 isoform X6
inactive glycosyltransferase 25 family member 3 isoform X2
inactive glycosyltransferase 25 family member 3 isoform X3
inactive glycosyltransferase 25 family member 3 isoform X5
inactive glycosyltransferase 25 family member 3 isoform X4
solute carrier family 27 member 4, transcript variant X3
solute carrier family 27 member 4, transcript variant X1
solute carrier family 27 member 4, transcript variant X2
long-chain fatty acid transport protein 4
transfer RNA arginine (anticodon UCU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial isoform X1
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial isoform X2
TruB pseudouridine synthase family member 2
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mitochondrial mRNA pseudouridine synthase TRUB2
SWI5 homologous recombination repair protein
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 3 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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
CDKN1A interacting zinc finger protein 1, transcript variant X1
CDKN1A interacting zinc finger protein 1, transcript variant X2
CDKN1A interacting zinc finger protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
cip1-interacting zinc finger protein isoform X1
cip1-interacting zinc finger protein isoform X2
cip1-interacting zinc finger protein isoform X3
outer dense fiber of sperm tails 2, transcript variant X2
outer dense fiber of sperm tails 2, transcript variant X3
outer dense fiber of sperm tails 2, transcript variant X4
outer dense fiber of sperm tails 2, transcript variant X5
outer dense fiber of sperm tails 2, transcript variant X1
outer dense fiber of sperm tails 2, transcript variant X6
spectrin alpha, non-erythrocytic 1, transcript variant X1
spectrin alpha, non-erythrocytic 1, transcript variant X3
spectrin alpha, non-erythrocytic 1, transcript variant X2
spectrin alpha, non-erythrocytic 1, transcript variant X4
spectrin alpha chain, non-erythrocytic 1 isoform X1
spectrin alpha chain, non-erythrocytic 1 isoform X3
spectrin alpha chain, non-erythrocytic 1 isoform X2
spectrin alpha chain, non-erythrocytic 1 isoform X4
cytoplasmic dynein 2 intermediate chain 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 ESTs, 16 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 12
zyg-11 related cell cycle regulator, transcript variant X1
zyg-11 related cell cycle regulator, transcript variant X2
SPOUT domain containing methyltransferase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
SPOUT domain containing methyltransferase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
putative methyltransferase C9orf114 homolog isoform X1
putative methyltransferase C9orf114 homolog isoform X2
kynurenine aminotransferase 1, transcript variant X2
kynurenine aminotransferase 1, transcript variant X1
leucine rich repeat containing 8 VRAC subunit A, transcript variant X3
leucine rich repeat containing 8 VRAC subunit A, transcript variant X2
leucine rich repeat containing 8 VRAC subunit A, transcript variant X1
volume-regulated anion channel subunit LRRC8A
phytanoyl-CoA dioxygenase domain containing 1, 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 11 samples with support for all annotated introns
phytanoyl-CoA dioxygenase domain containing 1, 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 19 samples with support for all annotated introns
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X1
phytanoyl-CoA dioxygenase domain-containing protein 1 isoform X2
SH3 domain containing GRB2 like, endophilin B2, transcript variant X10
SH3 domain containing GRB2 like, endophilin B2, transcript variant X9
SH3 domain containing GRB2 like, endophilin B2, transcript variant X8
SH3 domain containing GRB2 like, endophilin B2, transcript variant X6
SH3 domain containing GRB2 like, endophilin B2, transcript variant X4
SH3 domain containing GRB2 like, endophilin B2, transcript variant X2
SH3 domain containing GRB2 like, endophilin B2, transcript variant X7
SH3 domain containing GRB2 like, endophilin B2, transcript variant X5
SH3 domain containing GRB2 like, endophilin B2, transcript variant X3
SH3 domain containing GRB2 like, endophilin B2, transcript variant X1
dolichyldiphosphatase 1, transcript variant X1
dolichyldiphosphatase 1, transcript variant X2
carnitine O-acetyltransferase, transcript variant X1
carnitine O-acetyltransferase, transcript variant X3
carnitine O-acetyltransferase, transcript variant X2
carnitine O-acetyltransferase isoform X1
carnitine O-acetyltransferase isoform X3
carnitine O-acetyltransferase isoform X2
protein phosphatase 2 phosphatase activator
serine/threonine-protein phosphatase 2A activator
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
immediate early response gene 5-like protein
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X2
N-terminal Xaa-Pro-Lys N-methyltransferase 1
ankyrin repeat and SOCS box containing 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
prostaglandin E synthase, transcript variant X4
prostaglandin E synthase, transcript variant X5
prostaglandin E synthase, transcript variant X8
prostaglandin E synthase, transcript variant X3
prostaglandin E synthase, transcript variant X2
prostaglandin E synthase, transcript variant X1
prostaglandin E synthase, transcript variant X6
prostaglandin E synthase, transcript variant X7
torsin family 1 member B, transcript variant X1
torsin family 1 member B, transcript variant X3
torsin family 1 member B, transcript variant X2
telomere length and silencing protein 1 homolog
ubiquitin specific peptidase 20, transcript variant X1
ubiquitin specific peptidase 20, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 20
formin binding protein 1, transcript variant X4
formin binding protein 1, transcript variant X7
formin binding protein 1, transcript variant X3
formin binding protein 1, transcript variant X9
formin binding protein 1, transcript variant X5
formin binding protein 1, transcript variant X6
formin binding protein 1, transcript variant X1
formin binding protein 1, transcript variant X10
formin binding protein 1, transcript variant X14
formin binding protein 1, transcript variant X11
formin binding protein 1, transcript variant X8
formin binding protein 1, transcript variant X2
formin binding protein 1, transcript variant X23
formin binding protein 1, transcript variant X18
formin binding protein 1, transcript variant X16
formin binding protein 1, transcript variant X20
formin binding protein 1, transcript variant X19
formin binding protein 1, transcript variant X17
formin binding protein 1, transcript variant X13
formin binding protein 1, transcript variant X12
formin binding protein 1, transcript variant X22
formin binding protein 1, transcript variant X15
formin binding protein 1, transcript variant X21
G protein-coupled receptor 107, transcript variant X1
G protein-coupled receptor 107, transcript variant X5
G protein-coupled receptor 107, transcript variant X4
G protein-coupled receptor 107, transcript variant X2
G protein-coupled receptor 107, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
argininosuccinate synthase 1, transcript variant X1
argininosuccinate synthase 1, transcript variant X2
far upstream element binding protein 3, transcript variant X1
far upstream element binding protein 3, transcript variant X4
far upstream element binding protein 3, transcript variant X2
far upstream element binding protein 3, transcript variant X3
far upstream element-binding protein 3 isoform X1
far upstream element-binding protein 3 isoform X4
far upstream element-binding protein 3 isoform X2
far upstream element-binding protein 3 isoform X3
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X1
ABL proto-oncogene 1, non-receptor tyrosine kinase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
fibrinogen C domain-containing protein 1
laminin subunit gamma 3, transcript variant X3
laminin subunit gamma 3, transcript variant X2
laminin subunit gamma 3, transcript variant X1
nuclear pore complex protein Nup214 isoform X1
nuclear pore complex protein Nup214 isoform X2
family with sequence similarity 78 member A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
phospholipid phosphatase 7 (inactive), transcript variant X2
phospholipid phosphatase 7 (inactive), transcript variant X1
proline rich coiled-coil 2B, transcript variant X1
proline rich coiled-coil 2B, transcript variant X6
proline rich coiled-coil 2B, transcript variant X5
proline rich coiled-coil 2B, transcript variant X2
proline rich coiled-coil 2B, transcript variant X4
proline rich coiled-coil 2B, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 69% coverage of the annotated genomic feature by RNAseq alignments
Rap guanine nucleotide exchange factor 1, transcript variant X14
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X13
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X15
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X11
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 13 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X10
Rap guanine nucleotide exchange factor 1, transcript variant X12
Rap guanine nucleotide exchange factor 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 12 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 11 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X2
Rap guanine nucleotide exchange factor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 10 ESTs, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
Rap guanine nucleotide exchange factor 1, transcript variant X4
Rap guanine nucleotide exchange factor 1, transcript variant X1
rap guanine nucleotide exchange factor 1 isoform X14
rap guanine nucleotide exchange factor 1 isoform X13
rap guanine nucleotide exchange factor 1 isoform X15
rap guanine nucleotide exchange factor 1 isoform X11
rap guanine nucleotide exchange factor 1 isoform X10
rap guanine nucleotide exchange factor 1 isoform X12
rap guanine nucleotide exchange factor 1 isoform X3
rap guanine nucleotide exchange factor 1 isoform X9
rap guanine nucleotide exchange factor 1 isoform X8
rap guanine nucleotide exchange factor 1 isoform X7
rap guanine nucleotide exchange factor 1 isoform X5
rap guanine nucleotide exchange factor 1 isoform X2
rap guanine nucleotide exchange factor 1 isoform X6
rap guanine nucleotide exchange factor 1 isoform X4
rap guanine nucleotide exchange factor 1 isoform X1
mediator of RNA polymerase II transcription subunit 27
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
cilia and flagella associated protein 77
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
cilia- and flagella-associated protein 77
BarH like homeobox 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
BarH like homeobox 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
BarH like homeobox 1, transcript variant X2
BarH like homeobox 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX31
general transcription factor IIIC subunit 4, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
general transcription factor IIIC subunit 4, transcript variant X1
general transcription factor 3C polypeptide 4
adenylate kinase 8, transcript variant X2
adenylate kinase 8, transcript variant X3
adenylate kinase 8, transcript variant X5
adenylate kinase 8, transcript variant X1
adenylate kinase 8, transcript variant X6
adenylate kinase 8, transcript variant X4
adenylate kinase 8, transcript variant X7
sperm acrosome-associated protein 9-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
sperm acrosome-associated protein 9-like, 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 14 samples with support for all annotated introns
sperm acrosome-associated protein 9-like isoform X1
sperm acrosome-associated protein 9-like isoform X2
sperm acrosome-associated protein 9-like
TSC complex subunit 1, transcript variant X5
TSC complex subunit 1, transcript variant X4
TSC complex subunit 1, transcript variant X3
TSC complex subunit 1, transcript variant X2
TSC complex subunit 1, transcript variant X1
growth factor independent 1B transcriptional repressor
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIIC subunit 5
general transcription factor 3C polypeptide 5
ral guanine nucleotide dissociation stimulator, transcript variant X5
ral guanine nucleotide dissociation stimulator, transcript variant X3
ral guanine nucleotide dissociation stimulator, transcript variant X4
ral guanine nucleotide dissociation stimulator, transcript variant X2
ral guanine nucleotide dissociation stimulator, transcript variant X1
ral guanine nucleotide dissociation stimulator isoform X5
ral guanine nucleotide dissociation stimulator isoform X3
ral guanine nucleotide dissociation stimulator isoform X4
ral guanine nucleotide dissociation stimulator isoform X2
ral guanine nucleotide dissociation stimulator isoform X1
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like, transcript variant X4
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
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like, transcript variant X3
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like, 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 9 samples with support for all annotated introns
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like isoform X1
globoside alpha-1,3-N-acetylgalactosaminyltransferase 1-like isoform X2
mediator complex subunit 22, transcript variant X2
mediator complex subunit 22, transcript variant X1
mediator of RNA polymerase II transcription subunit 22 isoform X2
mediator of RNA polymerase II transcription subunit 22 isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00069
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
surfeit locus protein 1, transcript variant X2
surfeit locus protein 1, transcript variant X1
serine/threonine kinase like domain containing 1
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
serine/threonine kinase-like domain-containing protein STKLD1
ADAM metallopeptidase with thrombospondin type 1 motif 13, 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 18 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 13, 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 18 samples with support for all annotated introns
ADAM metallopeptidase with thrombospondin type 1 motif 13, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 13 isoform X1
A disintegrin and metalloproteinase with thrombospondin motifs 13 isoform X2
A disintegrin and metalloproteinase with thrombospondin motifs 13 isoform X3
calcium channel flower domain containing 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
calcium channel flower domain containing 1, transcript variant X1
calcium channel flower domain containing 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 2, facilitated glucose transporter member 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 3 ESTs, 7 Proteins
family with sequence similarity 163 member B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 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: 1 mRNA, 14 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
sarcosine dehydrogenase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sarcosine dehydrogenase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
vav guanine nucleotide exchange factor 2, transcript variant X6
vav guanine nucleotide exchange factor 2, transcript variant X4
vav guanine nucleotide exchange factor 2, transcript variant X3
vav guanine nucleotide exchange factor 2, transcript variant X2
vav guanine nucleotide exchange factor 2, transcript variant X5
vav guanine nucleotide exchange factor 2, transcript variant X1
vav guanine nucleotide exchange factor 2, transcript variant X8
guanine nucleotide exchange factor VAV2 isoform X6
guanine nucleotide exchange factor VAV2 isoform X4
guanine nucleotide exchange factor VAV2 isoform X3
guanine nucleotide exchange factor VAV2 isoform X2
guanine nucleotide exchange factor VAV2 isoform X5
guanine nucleotide exchange factor VAV2 isoform X1
guanine nucleotide exchange factor VAV2 isoform X8
vav guanine nucleotide exchange factor 2, transcript variant X7
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 16 samples with support for all annotated introns
guanine nucleotide exchange factor VAV2 isoform X7
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
collagen type V alpha 1 chain, transcript variant X4
collagen type V alpha 1 chain, transcript variant X1
collagen type V alpha 1 chain, transcript variant X2
collagen type V alpha 1 chain, transcript variant X3
protein phosphatase 1 regulatory subunit 26
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 5 bases in 5 codons; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 3 bases in 3 codons; deleted 5 bases in 5 codons; substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: protein phosphatase 1 regulatory subunit 26
chromosome 21 C9orf116 homolog, transcript variant X2
chromosome 21 C9orf116 homolog, transcript variant X3
chromosome 21 C9orf116 homolog, transcript variant X1
UPF0691 protein C9orf116 homolog isoform X2
UPF0691 protein C9orf116 homolog isoform X1
LOW QUALITY PROTEIN: 28S ribosomal protein S2, mitochondrial
COORDINATES: nucleotide motif:Rfam:12.0:RF00560
1-acylglycerol-3-phosphate O-acyltransferase 2
1-acyl-sn-glycerol-3-phosphate acyltransferase beta
EGF like domain multiple 7, transcript variant X2
EGF like domain multiple 7, transcript variant X1
epidermal growth factor-like protein 7 isoform X2
epidermal growth factor-like protein 7 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 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 ESTs, 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 6 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
neurogenic locus notch homolog protein 1 isoform X1
neurogenic locus notch homolog protein 1 isoform X2
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X1
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X3
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X4
SEC16 homolog A, endoplasmic reticulum export factor, transcript variant X2
protein transport protein Sec16A isoform X1
protein transport protein Sec16A isoform X2
protein transport protein Sec16A isoform X3
phosphatidylinositol polyphosphate 5-phosphatase type IV
peptidase, mitochondrial processing subunit alpha
mitochondrial-processing peptidase subunit alpha
endosome associated trafficking regulator 1
endosome-associated-trafficking regulator 1
small nuclear RNA activating complex polypeptide 4
snRNA-activating protein complex subunit 4
caspase recruitment domain family member 9
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
caspase recruitment domain-containing protein 9
LOW QUALITY PROTEIN: DNL-type zinc finger protein
G protein signaling modulator 1, transcript variant X2
G protein signaling modulator 1, transcript variant X1
G protein signaling modulator 1, transcript variant X3
G protein signaling modulator 1, transcript variant X7
G protein signaling modulator 1, transcript variant X5
G protein signaling modulator 1, transcript variant X6
G protein signaling modulator 1, transcript variant X8
G protein signaling modulator 1, transcript variant X9
G protein signaling modulator 1, transcript variant X4
G-protein-signaling modulator 1 isoform X2
G-protein-signaling modulator 1 isoform X1
G-protein-signaling modulator 1 isoform X3
G-protein-signaling modulator 1 isoform X4
G-protein-signaling modulator 1 isoform X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 187
centrosome-associated protein 350-like, transcript variant X1
centrosome-associated protein 350-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
centrosome-associated protein 350-like isoform X1
centrosome-associated protein 350-like isoform X2
NACC family member 2, transcript variant X2
NACC family member 2, transcript variant X6
NACC family member 2, transcript variant X3
NACC family member 2, transcript variant X7
NACC family member 2, transcript variant X1
NACC family member 2, transcript variant X4
NACC family member 2, transcript variant X8
NACC family member 2, transcript variant X5
UBA domain containing 1, transcript variant X2
UBA domain containing 1, transcript variant X1
ubiquitin-associated domain-containing protein 1 isoform X1
ubiquitin-associated domain-containing protein 1 isoform X2
calmodulin regulated spectrin associated protein 1, transcript variant X1
calmodulin regulated spectrin associated protein 1, transcript variant X2
calmodulin-regulated spectrin-associated protein 1 isoform X1
calmodulin-regulated spectrin-associated protein 1 isoform X2
calmodulin regulated spectrin associated protein 1, transcript variant X3
calmodulin-regulated spectrin-associated protein 1 isoform X3
potassium sodium-activated channel subfamily T member 1, transcript variant X2
potassium sodium-activated channel subfamily T member 1, transcript variant X4
potassium sodium-activated channel subfamily T member 1, transcript variant X3
potassium sodium-activated channel subfamily T member 1, transcript variant X5
potassium sodium-activated channel subfamily T member 1, transcript variant X1
potassium sodium-activated channel subfamily T member 1, transcript variant X10
potassium sodium-activated channel subfamily T member 1, transcript variant X8
potassium sodium-activated channel subfamily T member 1, transcript variant X9
potassium sodium-activated channel subfamily T member 1, transcript variant X7
potassium sodium-activated channel subfamily T member 1, transcript variant X12
potassium sodium-activated channel subfamily T member 1, transcript variant X11
potassium channel subfamily T member 1 isoform X2
potassium channel subfamily T member 1 isoform X4
potassium channel subfamily T member 1 isoform X3
potassium channel subfamily T member 1 isoform X5
potassium channel subfamily T member 1 isoform X1
potassium channel subfamily T member 1 isoform X11
potassium channel subfamily T member 1 isoform X9
potassium channel subfamily T member 1 isoform X7
potassium channel subfamily T member 1 isoform X8
potassium channel subfamily T member 1 isoform X6
potassium channel subfamily T member 1 isoform X10
potassium sodium-activated channel subfamily T member 1, 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 8 samples with support for all annotated introns
26S proteasome non-ATPase regulatory subunit 5
protein CutA homolog, transcript variant X2
protein CutA homolog, transcript variant X3
protein CutA homolog, 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 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: 12 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
RAB14, member RAS oncogene family, transcript variant X1
RAB14, member RAS oncogene family, transcript variant X2
DAB2 interacting protein, transcript variant X2
disabled homolog 2-interacting protein isoform X2
DAB2 interacting protein, transcript variant X3
disabled homolog 2-interacting protein isoform X3
DAB2 interacting protein, transcript variant X6
DAB2 interacting protein, transcript variant X5
DAB2 interacting protein, transcript variant X4
DAB2 interacting protein, transcript variant X1
DAB2 interacting protein, transcript variant X7
disabled homolog 2-interacting protein isoform X5
disabled homolog 2-interacting protein isoform X1
disabled homolog 2-interacting protein isoform X7
disabled homolog 2-interacting protein isoform X4
disabled homolog 2-interacting protein isoform X6
DAB2 interacting protein, transcript variant X11
DAB2 interacting protein, transcript variant X8
disabled homolog 2-interacting protein isoform X8
DAB2 interacting protein, transcript variant X9
disabled homolog 2-interacting protein isoform X9
DAB2 interacting protein, transcript variant X10
DAB2 interacting protein, transcript variant X12
disabled homolog 2-interacting protein isoform X10
tubulin tyrosine ligase like 11, transcript variant X3
tubulin tyrosine ligase like 11, transcript variant X4
tubulin tyrosine ligase like 11, transcript variant X2
tubulin tyrosine ligase like 11, transcript variant X1
tubulin polyglutamylase TTLL11 isoform X3
tubulin polyglutamylase TTLL11 isoform X2
tubulin polyglutamylase TTLL11 isoform X1
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X1
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like, transcript variant X2
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like isoform X1
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like isoform X2
NADH:ubiquinone oxidoreductase subunit A8
NADH dehydrogenase [ubiquinone] 1 alpha subcomplex subunit 8
mitochondrial ribosome recycling factor, transcript variant X1
ribosome-recycling factor, mitochondrial isoform X1
mitochondrial ribosome recycling factor, transcript variant X2
ribosome-recycling factor, mitochondrial isoform X2
prostaglandin-endoperoxide synthase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
prostaglandin-endoperoxide synthase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ring finger and CCCH-type domains 2, transcript variant X1
ring finger and CCCH-type domains 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 5 ESTs, 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00579
zinc finger and BTB domain-containing protein 6
zinc finger and BTB domain containing 26
zinc finger and BTB domain-containing protein 26
RAB GTPase activating protein 1, transcript variant X1
RAB GTPase activating protein 1, transcript variant X2
rab GTPase-activating protein 1 isoform X1
rab GTPase-activating protein 1 isoform X2
RAB GTPase activating protein 1, transcript variant X3
rab GTPase-activating protein 1 isoform X3
spermatid perinuclear RNA binding protein, transcript variant X9
spermatid perinuclear RNA binding protein, transcript variant X5
spermatid perinuclear RNA binding protein, transcript variant X8
spermatid perinuclear RNA binding protein, transcript variant X4
spermatid perinuclear RNA-binding protein isoform X6
spermatid perinuclear RNA-binding protein isoform X7
spermatid perinuclear RNA-binding protein isoform X3
spermatid perinuclear RNA-binding protein isoform X2
spermatid perinuclear RNA binding protein, transcript variant X7
spermatid perinuclear RNA binding protein, transcript variant X6
spermatid perinuclear RNA-binding protein isoform X5
spermatid perinuclear RNA-binding protein isoform X4
spermatid perinuclear RNA binding protein, transcript variant X2
spermatid perinuclear RNA binding protein, transcript variant X1
spermatid perinuclear RNA binding protein, transcript variant X3
spermatid perinuclear RNA-binding protein isoform X1
crumbs cell polarity complex component 2, transcript variant X6
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 13 samples with support for all annotated introns
crumbs cell polarity complex component 2, transcript variant X5
crumbs cell polarity complex component 2, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
crumbs cell polarity complex component 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
crumbs cell polarity complex component 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
crumbs cell polarity complex component 2, 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 18 samples with support for all annotated introns
DENN domain containing 1A, transcript variant X1
DENN domain containing 1A, transcript variant X2
DENN domain-containing protein 1A isoform X2
DENN domain-containing protein 1A isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 5 group A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 1 EST, 22 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
nuclear receptor subfamily 6 group A member 1, transcript variant X2
nuclear receptor subfamily 6 group A member 1, transcript variant X1
nuclear receptor subfamily 6 group A member 1, transcript variant X3
nuclear receptor subfamily 6 group A member 1 isoform X2
nuclear receptor subfamily 6 group A member 1 isoform X1
nuclear receptor subfamily 6 group A member 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
actin related protein 2/3 complex subunit 5 like
LOW QUALITY PROTEIN: actin-related protein 2/3 complex subunit 5-like protein
serine/threonine-protein phosphatase 6 catalytic subunit
heat shock protein family A (Hsp70) member 5
GTPase activating protein and VPS9 domains 1, transcript variant X2
GTPase activating protein and VPS9 domains 1, transcript variant X1
GTPase activating protein and VPS9 domains 1, transcript variant X5
GTPase activating protein and VPS9 domains 1, transcript variant X3
GTPase activating protein and VPS9 domains 1, transcript variant X4
GTPase activating protein and VPS9 domains 1, transcript variant X6
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X1
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X4
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X2
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X3
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X5
MAPK associated protein 1, 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 19 samples with support for all annotated introns
MAPK associated protein 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 mRNAs, 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
target of rapamycin complex 2 subunit MAPKAP1 isoform X2
target of rapamycin complex 2 subunit MAPKAP1 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 mRNAs, 9 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X1
pre-B-cell leukemia transcription factor 3 isoform X3
pre-B-cell leukemia transcription factor 3 isoform X2
multivesicular body subunit 12B, transcript variant X7
multivesicular body subunit 12B, transcript variant X8
multivesicular body subunit 12B, transcript variant X5
multivesicular body subunit 12B, transcript variant X4
multivesicular body subunit 12B, transcript variant X6
multivesicular body subunit 12B, 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 3 samples with support for all annotated introns
multivesicular body subunit 12B, transcript variant X1
multivesicular body subunit 12B, transcript variant X9
multivesicular body subunit 12B, transcript variant X10
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 17 samples with support for all annotated introns
multivesicular body subunit 12B isoform X2
multivesicular body subunit 12B isoform X1
multivesicular body subunit 12B isoform X4
multivesicular body subunit 12B isoform X5
multivesicular body subunit 12B, transcript variant X3
multivesicular body subunit 12B isoform X3
LIM homeobox transcription factor 1 beta
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 mRNAs, 3 ESTs, 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
LIM homeobox transcription factor 1-beta
zinc finger and BTB domain containing 43, transcript variant X2
zinc finger and BTB domain containing 43, transcript variant X1
zinc finger and BTB domain containing 43, transcript variant X3
zinc finger and BTB domain-containing protein 43
zinc finger and BTB domain containing 34, transcript variant X1
zinc finger and BTB domain containing 34, transcript variant X3
zinc finger and BTB domain containing 34, transcript variant X2
zinc finger and BTB domain containing 34, transcript variant X4
zinc finger and BTB domain-containing protein 34 isoform X1
zinc finger and BTB domain-containing protein 34 isoform X2
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X1
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X4
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X5
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X3
Ral GEF with PH domain and SH3 binding motif 1, transcript variant X2
Ral GEF with PH domain and SH3 binding motif 1, 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 16 samples with support for all annotated introns
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X1
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X3
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X4
ras-specific guanine nucleotide-releasing factor RalGPS1 isoform X2
angiopoietin like 2, transcript variant X2
angiopoietin like 2, transcript variant X1
angiopoietin like 2, transcript variant X3
uncharacterized LOC117005590, transcript variant X5
uncharacterized LOC117005590, transcript variant X3
uncharacterized LOC117005590, transcript variant X2
uncharacterized LOC117005590, transcript variant X4
uncharacterized LOC117005590, transcript variant X1
F-box and WD repeat domain containing 2, transcript variant X1
F-box and WD repeat domain containing 2, transcript variant X2
F-box/WD repeat-containing protein 2 isoform X1
F-box/WD repeat-containing protein 2 isoform X2
GTPase activating Rap/RanGAP domain like 3
GTPase-activating Rap/Ran-GAP domain-like protein 3
uncharacterized LOC117005818, 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 19 samples with support for all annotated introns
uncharacterized LOC117005818, 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 16 samples with support for all annotated introns
uncharacterized LOC117005819, transcript variant X1
uncharacterized LOC117005819, 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 15 samples with support for all annotated introns