Jaculus jaculus isolate mJacJac1 chromosome 22, mJacJac1.mat.Y.cur, whole genome shotgun sequence.
Jaculus jaculus (lesser Egyptian jerboa)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Glires; Rodentia; Myomorpha; Dipodoidea; Dipodidae; Dipodinae; Jaculus.
REFSEQ INFORMATION: The reference sequence is identical to\nCM036410.1.\nAssembly name: mJacJac1.mat.Y.cur\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Vertebrate Genomes Project on\n2021/11/04. The original whole-genome shotgun project has the\naccession JAJGSA000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Vertebrate Genomes Project\nAssembly Date :: 2021\nAssembly Method :: Trio HiCanu v. 2.1; purge_dups v. 1.2.3;\n Scaff10x v. 4.2; Bionano Solve v. 3.5.1;\n bwa v. 0.7.17; gcpp v. 1.9.0; Longranger\n Align v. 2.2.2; Freebayes v. 1.3.2; gEVAL\n manual curation v. 2021-05--07\nAssembly Name :: mJacJac1.mat.Y.cur\nDiploid :: Principal Pseudohaplotype\nGenome Representation :: Full\nExpected Final Version :: No\nGenome Coverage :: 61.0x\nSequencing Technology :: PacBio Sequel II CLR 101X; 10X Gemonics\n linked reads 78X; Bionano Genomics DLS\n 182X; Arima Genomics Hi-C v1 60X\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Jaculus jaculus Annotation Release\n 102\nAnnotation Version :: 102\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: 10 Proteins, and 9% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
BICD cargo adaptor 1, transcript variant X3
COORDINATES: polyA evidence [ECO:0006239]
BICD cargo adaptor 1, transcript variant X2
BICD cargo adaptor 1, transcript variant X1
BICD cargo adaptor 1, transcript variant X7
BICD cargo adaptor 1, transcript variant X5
BICD cargo adaptor 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins
BICD cargo adaptor 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
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: 16 Proteins, and 8% coverage of the annotated genomic feature by RNAseq alignments
retroelement silencing factor 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
retroelement silencing factor 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
uncharacterized LOC123456426, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
uncharacterized LOC123456426, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
uncharacterized LOC123456426, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
uncharacterized LOC123456426, transcript variant X4
uncharacterized LOC123456426, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
uncharacterized LOC123456426, transcript variant X7
uncharacterized LOC123456426, transcript variant X5
antagonist of mitotic exit network 1 homolog, transcript variant X2
antagonist of mitotic exit network 1 homolog, transcript variant X3
antagonist of mitotic exit network 1 homolog, transcript variant X1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 50% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: bromodomain-containing protein 4-like
DENN domain containing 5B, transcript variant X1
DENN domain containing 5B, transcript variant X2
DENN domain-containing protein 5B isoform X1
DENN domain-containing protein 5B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 62% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00421
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
LOW QUALITY PROTEIN: SIN3-HDAC complex-associated factor
caprin family member 2, transcript variant X2
caprin family member 2, transcript variant X8
caprin family member 2, transcript variant X7
caprin family member 2, transcript variant X11
caprin family member 2, transcript variant X14
caprin family member 2, transcript variant X6
caprin family member 2, transcript variant X1
caprin family member 2, transcript variant X12
caprin family member 2, transcript variant X13
caprin family member 2, transcript variant X9
caprin family member 2, transcript variant X10
caprin family member 2, transcript variant X4
caprin family member 2, transcript variant X5
caprin family member 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 13% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00156
small nucleolar RNA SNORA16B/SNORA16A family
COORDINATES: nucleotide motif:Rfam:12.0:RF00190
mediator of RNA polymerase II transcription subunit 18
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: mediator of RNA polymerase II transcription subunit 18
transmembrane O-mannosyltransferase targeting cadherins 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 64 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ERGIC and golgi 2, transcript variant X2
ERGIC and golgi 2, transcript variant X3
ERGIC and golgi 2, transcript variant X1
endoplasmic reticulum-Golgi intermediate compartment protein 2
fatty acyl-CoA reductase 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fatty acyl-CoA reductase 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
coiled-coil domain containing 91, transcript variant X2
coiled-coil domain containing 91, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein 91 isoform X1
coiled-coil domain-containing protein 91 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 40% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC123456427, transcript variant X2
uncharacterized LOC123456427, transcript variant X1
uncharacterized LOC123456427, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 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 97% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
28S ribosomal protein S35, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 6% coverage of the annotated genomic feature by RNAseq alignments
PPFIA binding protein 1, transcript variant X3
PPFIA binding protein 1, transcript variant X1
PPFIA binding protein 1, transcript variant X7
PPFIA binding protein 1, transcript variant X10
PPFIA binding protein 1, transcript variant X6
PPFIA binding protein 1, transcript variant X8
PPFIA binding protein 1, transcript variant X5
PPFIA binding protein 1, transcript variant X4
PPFIA binding protein 1, transcript variant X9
PPFIA binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized protein C12orf71 homolog
single-pass membrane protein with coiled-coil domains 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 78% coverage of the annotated genomic feature by RNAseq alignments
single-pass membrane and coiled-coil domain-containing protein 2
serine/threonine kinase 38 like, transcript variant X1
serine/threonine kinase 38 like, transcript variant X2
serine/threonine kinase 38 like, transcript variant X3
serine/threonine-protein kinase 38-like isoform X1
serine/threonine-protein kinase 38-like isoform X2
phosphodiesterase 3A, transcript variant X1
cGMP-inhibited 3',5'-cyclic phosphodiesterase A isoform X1
phosphodiesterase 3A, transcript variant X2
cGMP-inhibited 3',5'-cyclic phosphodiesterase A isoform X2
solute carrier organic anion transporter family member 1C1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 1C1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
solute carrier organic anion transporter family member 1C1, transcript variant X3
solute carrier organic anion transporter family member 1C1 isoform X1
solute carrier organic anion transporter family member 1C1 isoform X2
solute carrier organic anion transporter family member 1C1 isoform X3
solute carrier organic anion transporter family member 1C1, transcript variant X4
solute carrier organic anion transporter family member 1C1 isoform X4
solute carrier organic anion transporter family member 1B3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
solute carrier organic anion transporter family member 1B3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
solute carrier organic anion transporter family member 1B3
solute carrier organic anion transporter family member 1A2, transcript variant X3
solute carrier organic anion transporter family member 1A2, transcript variant X1
solute carrier organic anion transporter family member 1A2, transcript variant X2
solute carrier organic anion transporter family member 1A2 isoform X1
solute carrier organic anion transporter family member 1A2 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00096
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X1
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform X1
pyridine nucleotide-disulphide oxidoreductase domain 1, transcript variant X2
pyridine nucleotide-disulfide oxidoreductase domain-containing protein 1 isoform X2
RecQ like helicase, transcript variant X3
RecQ like helicase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
RecQ like helicase, transcript variant X2
golgi transport 1B, transcript variant X1
golgi transport 1B, transcript variant X2
vesicle transport protein GOT1B isoform X1
vesicle transport protein GOT1B isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 43% 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 28% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins
CGG triplet repeat-binding protein 1-like
ST8 alpha-N-acetyl-neuraminide alpha-2,8-sialyltransferase 1
alpha-N-acetylneuraminide alpha-2,8-sialyltransferase
sulfotransferase 1C2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
sulfotransferase 1C2, transcript variant X1
cytidine monophosphate N-acetylneuraminic acid synthetase
ATP binding cassette subfamily C member 9
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
ATP-binding cassette sub-family C member 9
potassium inwardly rectifying channel subfamily J member 8
ATP-sensitive inward rectifier potassium channel 8
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 27% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 71% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
C2 calcium dependent domain containing 5, transcript variant X11
C2 calcium dependent domain containing 5, transcript variant X10
C2 calcium dependent domain containing 5, transcript variant X7
C2 calcium dependent domain containing 5, transcript variant X5
C2 calcium dependent domain containing 5, transcript variant X4
C2 calcium dependent domain containing 5, transcript variant X2
C2 calcium dependent domain containing 5, transcript variant X3
C2 calcium dependent domain containing 5, transcript variant X1
C2 calcium dependent domain containing 5, transcript variant X12
C2 calcium dependent domain containing 5, transcript variant X9
C2 calcium dependent domain containing 5, transcript variant X13
C2 calcium dependent domain containing 5, transcript variant X8
C2 calcium dependent domain containing 5, transcript variant X6
C2 calcium dependent domain containing 5, transcript variant X15
C2 calcium dependent domain containing 5, transcript variant X14
C2 domain-containing protein 5 isoform X11
C2 domain-containing protein 5 isoform X10
C2 domain-containing protein 5 isoform X7
C2 domain-containing protein 5 isoform X5
C2 domain-containing protein 5 isoform X4
C2 domain-containing protein 5 isoform X2
C2 domain-containing protein 5 isoform X3
C2 domain-containing protein 5 isoform X1
C2 domain-containing protein 5 isoform X12
C2 domain-containing protein 5 isoform X9
C2 domain-containing protein 5 isoform X13
C2 domain-containing protein 5 isoform X8
C2 domain-containing protein 5 isoform X6
C2 domain-containing protein 5 isoform X15
C2 domain-containing protein 5 isoform X14
SRY-box transcription factor 5, transcript variant X3
SRY-box transcription factor 5, transcript variant X1
SRY-box transcription factor 5, transcript variant X5
SRY-box transcription factor 5, transcript variant X7
SRY-box transcription factor 5, transcript variant X2
SRY-box transcription factor 5, transcript variant X8
SRY-box transcription factor 5, transcript variant X4
SRY-box transcription factor 5, transcript variant X6
branched chain amino acid transaminase 1, transcript variant X1
branched chain amino acid transaminase 1, transcript variant X2
branched chain amino acid transaminase 1, transcript variant X3
branched-chain-amino-acid aminotransferase, cytosolic isoform X1
branched-chain-amino-acid aminotransferase, cytosolic isoform X2
branched-chain-amino-acid aminotransferase, cytosolic isoform X3
small nucleolar RNA SNORA2/SNORA34 family
COORDINATES: nucleotide motif:Rfam:12.0:RF00410
four and a half LIM domains protein 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
inositol 1,4,5-triphosphate receptor associated 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00432
dynein axonemal intermediate chain 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
dynein axonemal intermediate chain 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
dynein axonemal intermediate chain 7 isoform X1
dynein axonemal intermediate chain 7 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 50% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 71% 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
tubulin alpha-3 chain, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 71 Proteins, and 61% coverage of the annotated genomic feature by RNAseq alignments
tubulin alpha-3 chain, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 62% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00614
Ras association domain family member 8, transcript variant X2
Ras association domain family member 8, transcript variant X1
ras association domain-containing protein 8 isoform X2
ras association domain-containing protein 8 isoform X1
basic helix-loop-helix family member e41
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 85% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
class E basic helix-loop-helix protein 41
inositol 1,4,5-trisphosphate receptor type 2, 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
inositol 1,4,5-trisphosphate receptor type 2, 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 4 samples with support for all annotated introns
inositol 1,4,5-trisphosphate receptor type 2 isoform X2
inositol 1,4,5-trisphosphate receptor type 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
WW domain binding protein 11, transcript variant X1
WW domain binding protein 11, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
single-pass membrane protein with coiled-coil domains 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
single-pass membrane and coiled-coil domain-containing protein 3
ADP-ribosyltransferase 4 (inactive) (Dombrock blood group)
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 19% coverage of the annotated genomic feature by RNAseq alignments
endoplasmic reticulum resident protein 27
Rho GDP dissociation inhibitor beta, transcript variant X4
Rho GDP dissociation inhibitor beta, transcript variant X2
Rho GDP dissociation inhibitor beta, transcript variant X1
Rho GDP dissociation inhibitor beta, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
retinal cone rhodopsin-sensitive cGMP 3',5'-cyclic phosphodiesterase subunit gamma
RAS like estrogen regulated growth inhibitor
ras-related and estrogen-regulated growth inhibitor
protein tyrosine phosphatase receptor type O, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein tyrosine phosphatase receptor type O, transcript variant X2
receptor-type tyrosine-protein phosphatase O isoform X1
receptor-type tyrosine-protein phosphatase O isoform X2
epidermal growth factor receptor pathway substrate 8, transcript variant X1
epidermal growth factor receptor pathway substrate 8, transcript variant X2
epidermal growth factor receptor kinase substrate 8
serine/threonine kinase receptor associated protein, transcript variant X1
serine/threonine kinase receptor associated protein, transcript variant X2
serine-threonine kinase receptor-associated protein isoform X1
serine-threonine kinase receptor-associated protein isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 33% coverage of the annotated genomic feature by RNAseq alignments
LIM domain only 3, transcript variant X8
LIM domain only 3, transcript variant X3
LIM domain only 3, transcript variant X5
LIM domain only 3, transcript variant X6
LIM domain only 3, transcript variant X4
LIM domain only 3, transcript variant X2
LIM domain only 3, transcript variant X1
LIM domain only 3, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
ras-related and estrogen-regulated growth inhibitor-like protein
phosphatidylinositol-4-phosphate 3-kinase catalytic subunit type 2 gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
phosphatidylinositol 4-phosphate 3-kinase C2 domain-containing subunit gamma
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 7% coverage of the annotated genomic feature by RNAseq alignments
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase zeta-1
capping actin protein of muscle Z-line subunit alpha 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
pleckstrin homology domain containing A5, transcript variant X1
pleckstrin homology domain containing A5, transcript variant X3
pleckstrin homology domain containing A5, transcript variant X6
pleckstrin homology domain containing A5, transcript variant X4
pleckstrin homology domain containing A5, transcript variant X5
pleckstrin homology domain containing A5, transcript variant X10
pleckstrin homology domain containing A5, transcript variant X8
pleckstrin homology domain containing A5, transcript variant X9
pleckstrin homology domain containing A5, transcript variant X14
pleckstrin homology domain containing A5, transcript variant X2
pleckstrin homology domain containing A5, transcript variant X7
pleckstrin homology domain containing A5, transcript variant X23
pleckstrin homology domain containing A5, transcript variant X12
pleckstrin homology domain containing A5, transcript variant X11
pleckstrin homology domain containing A5, transcript variant X15
pleckstrin homology domain containing A5, transcript variant X17
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
pleckstrin homology domain containing A5, transcript variant X16
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
pleckstrin homology domain containing A5, transcript variant X18
pleckstrin homology domain containing A5, transcript variant X19
pleckstrin homology domain containing A5, transcript variant X22
pleckstrin homology domain containing A5, transcript variant X21
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
pleckstrin homology domain containing A5, transcript variant X20
pleckstrin homology domain-containing family A member 5 isoform X3
pleckstrin homology domain-containing family A member 5 isoform X1
pleckstrin homology domain-containing family A member 5 isoform X6
pleckstrin homology domain-containing family A member 5 isoform X4
pleckstrin homology domain-containing family A member 5 isoform X5
pleckstrin homology domain-containing family A member 5 isoform X10
pleckstrin homology domain-containing family A member 5 isoform X8
pleckstrin homology domain-containing family A member 5 isoform X9
pleckstrin homology domain-containing family A member 5 isoform X14
pleckstrin homology domain-containing family A member 5 isoform X2
pleckstrin homology domain-containing family A member 5 isoform X7
pleckstrin homology domain-containing family A member 5 isoform X21
pleckstrin homology domain-containing family A member 5 isoform X12
pleckstrin homology domain-containing family A member 5 isoform X11
pleckstrin homology domain-containing family A member 5 isoform X15
pleckstrin homology domain-containing family A member 5 isoform X17
pleckstrin homology domain-containing family A member 5 isoform X16
pleckstrin homology domain-containing family A member 5 isoform X20
pleckstrin homology domain-containing family A member 5 isoform X19
pleckstrin homology domain-containing family A member 5 isoform X18
pleckstrin homology domain containing A5, transcript variant X13
pleckstrin homology domain-containing family A member 5 isoform X13
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 92% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 73% coverage of the annotated genomic feature by RNAseq alignments