Plutella xylostella chromosome 7, ilPluXylo3.1, whole genome shotgun sequence.
Eukaryota; Metazoa; Ecdysozoa; Arthropoda; Hexapoda; Insecta; Pterygota; Neoptera; Endopterygota; Lepidoptera; Glossata; Ditrysia; Yponomeutoidea; Plutellidae; Plutella.
REFSEQ INFORMATION: The reference sequence is identical to\nOW026571.1.\nAssembly name: ilPluXylo3.1\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the WELLCOME SANGER INSTITUTE on\n2022/03/10. The original whole-genome shotgun project has the\naccession CAKNZZ000000000.1.\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Plutella xylostella Annotation\n Release 103\nAnnotation Version :: 103\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 Protein
acyl-CoA synthetase short-chain family member 3, mitochondrial
COORDINATES: polyA evidence [ECO:0006239]
uncharacterized PE-PGRS family protein PE_PGRS10, transcript variant X1
uncharacterized PE-PGRS family protein PE_PGRS10, transcript variant X2
uncharacterized PE-PGRS family protein PE_PGRS10, transcript variant X3
eukaryotic translation initiation factor 4B2 isoform X1
uncharacterized PE-PGRS family protein PE_PGRS10 isoform X2
uncharacterized PE-PGRS family protein PE_PGRS10 isoform X3
small glutamine-rich tetratricopeptide repeat-containing protein alpha
EH domain-containing protein 1, transcript variant X1
EH domain-containing protein 1, transcript variant X2
EH domain-containing protein 1 isoform X2
EH domain-containing protein 1 isoform 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 67 samples with support for all annotated introns
prostaglandin E2 receptor EP2 subtype, transcript variant X1
prostaglandin E2 receptor EP2 subtype, transcript variant X2
prostaglandin E2 receptor EP2 subtype, transcript variant X3
prostaglandin E2 receptor EP2 subtype, transcript variant X4
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 52 samples with support for all annotated introns
prostaglandin E2 receptor EP2 subtype isoform X1
prostaglandin E2 receptor EP2 subtype isoform X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1, transcript variant X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1, transcript variant X1
adenosine 3'-phospho 5'-phosphosulfate transporter 1 isoform X2
adenosine 3'-phospho 5'-phosphosulfate transporter 1 isoform X1
adenosine 3'-phospho 5'-phosphosulfate transporter 1, transcript variant X3
adenosine 3'-phospho 5'-phosphosulfate transporter 1 isoform 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
uncharacterized LOC105383994, transcript variant X1
uncharacterized protein LOC105383994 isoform X1
uncharacterized LOC105383994, transcript variant X3
uncharacterized LOC105383994, transcript variant X2
uncharacterized protein LOC105383994 isoform X2
uncharacterized protein LOC105383994 isoform X3
uncharacterized LOC105383994, transcript variant X4
uncharacterized protein LOC105383994 isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
hematopoietically-expressed homeobox protein hhex
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 49 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 24 samples with support for all annotated introns
hematopoietically-expressed homeobox protein HHEX-like
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 85 samples with support for all annotated introns
alpha-soluble NSF attachment protein, transcript variant X1
alpha-soluble NSF attachment protein, transcript variant X3
alpha-soluble NSF attachment protein, transcript variant X2
alpha-soluble NSF attachment protein isoform X1
alpha-soluble NSF attachment protein isoform X3
alpha-soluble NSF attachment protein isoform X2
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X7
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X4
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X5
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X2
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X3
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X1
phosphatidylinositol-binding clathrin assembly protein LAP, transcript variant X6
phosphatidylinositol-binding clathrin assembly protein LAP isoform X5
phosphatidylinositol-binding clathrin assembly protein LAP isoform X2
phosphatidylinositol-binding clathrin assembly protein LAP isoform X3
phosphatidylinositol-binding clathrin assembly protein LAP isoform X6
phosphatidylinositol-binding clathrin assembly protein LAP isoform X4
phosphatidylinositol-binding clathrin assembly protein LAP isoform X1
phosphatidylinositol-binding clathrin assembly protein LAP isoform X7
WAS/WASL-interacting protein family member 3
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 69 samples with support for all annotated introns
uncharacterized LOC119690788, 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 36 samples with support for all annotated introns
uncharacterized LOC119690788, 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 41 samples with support for all annotated introns
uncharacterized protein LOC119690788 isoform X2
uncharacterized protein LOC119690788 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 85 samples with support for all annotated introns
transient receptor potential channel pyrexia
LIM domain only protein 7, transcript variant X1
LIM domain only protein 7, transcript variant X3
LIM domain only protein 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA glycine (anticodon GCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LIM domain only protein 7, transcript variant X2
uncharacterized protein LOC105385707 isoform X1
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
uncharacterized LOC105394621, transcript variant X1
uncharacterized LOC105394621, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 42 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 9 samples with support for all annotated introns
jupiter microtubule associated homolog 1, transcript variant X1
jupiter microtubule associated homolog 1, transcript variant X2
jupiter microtubule associated homolog 1
src substrate cortactin, transcript variant X2
src substrate cortactin, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
uncharacterized LOC105398726, transcript variant X1
uncharacterized LOC105398726, transcript variant X2
putative peptidyl-prolyl cis-trans isomerase dodo
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 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 66 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 24 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
MAP7 domain-containing protein 2, transcript variant X3
MAP7 domain-containing protein 2, transcript variant X4
MAP7 domain-containing protein 2, transcript variant X5
MAP7 domain-containing protein 2, transcript variant X2
MAP7 domain-containing protein 2, transcript variant X1
MAP7 domain-containing protein 2, transcript variant X6
MAP7 domain-containing protein 1 isoform X3
MAP7 domain-containing protein 2 isoform X4
MAP7 domain-containing protein 2 isoform X5
MAP7 domain-containing protein 2 isoform X2
MAP7 domain-containing protein 2 isoform X1
MAP7 domain-containing protein 2 isoform X6
uncharacterized LOC125488775, transcript variant X1
uncharacterized LOC125488775, 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 49 samples with support for all annotated introns
uncharacterized LOC105398770, transcript variant X1
uncharacterized LOC105398770, transcript variant X2
uncharacterized protein LOC105398770 isoform X1
uncharacterized protein LOC105398770 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
uncharacterized LOC105398810, transcript variant X1
uncharacterized LOC105398810, transcript variant X2
uncharacterized protein LOC105398810 isoform X2
uncharacterized protein LOC105398810 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC105379976, 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 10 samples with support for all annotated introns
uncharacterized LOC105379976, 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 13 samples with support for all annotated introns
uncharacterized protein LOC105379976 isoform X1
uncharacterized protein LOC105379976 isoform X2
general odorant-binding protein 56d-like; Derived by automated computational analysis using gene prediction method: BestRefSeq.
general odorant-binding protein 56d-like
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305524.1
annotated by transcript or proteomic data
The RefSeq transcript has 15 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
Derived by automated computational analysis using gene prediction method: BestRefSeq.
general odorant-binding protein 56d-like precursor
COORDINATES: ab initio prediction:SignalP:4.0
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 33 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
uncharacterized LOC125488719, transcript variant X2
uncharacterized LOC125488719, transcript variant X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
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 23 samples with support for all annotated introns
MICOS complex subunit Mic10, transcript variant X1
MICOS complex subunit Mic10, transcript variant X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00012
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments
transcription initiation factor TFIID subunit 3, transcript variant X1
transcription initiation factor TFIID subunit 3, transcript variant X2
transcription initiation factor TFIID subunit 3
general transcription factor IIH subunit 1
uncharacterized LOC125488744, transcript variant X1
uncharacterized LOC125488744, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
fibroblast growth factor receptor homolog 1, 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 36 samples with support for all annotated introns
fibroblast growth factor receptor homolog 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 47 samples with support for all annotated introns
fibroblast growth factor receptor homolog 1 isoform X1
fibroblast growth factor receptor homolog 1 isoform X2
putative glutathione-specific gamma-glutamylcyclotransferase 2
rho GTPase-activating protein 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
rho GTPase-activating protein 7, 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 5 samples with support for all annotated introns
rho GTPase-activating protein 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
rho GTPase-activating protein 7, transcript variant X4
rho GTPase-activating protein 7, transcript variant X5
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 14 samples with support for all annotated introns
rho GTPase-activating protein 7 isoform X2
rho GTPase-activating protein 7 isoform X1
rho GTPase-activating protein 7 isoform X3
rho GTPase-activating protein 7 isoform X5
rho GTPase-activating protein 7 isoform X4
rho guanine nucleotide exchange factor 17, transcript variant X3
rho guanine nucleotide exchange factor 17, transcript variant X2
rho guanine nucleotide exchange factor 17, transcript variant X1
rho guanine nucleotide exchange factor 17 isoform X3
rho guanine nucleotide exchange factor 17 isoform X2
rho guanine nucleotide exchange factor 17 isoform 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 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
3-oxoacyl-[acyl-carrier-protein] reductase FabG
tubulin monoglutamylase TTLL4, transcript variant X1
tubulin monoglutamylase TTLL4, transcript variant X3
tubulin monoglutamylase TTLL4, transcript variant X4
tubulin monoglutamylase TTLL4, transcript variant X2
tubulin monoglutamylase TTLL4, transcript variant X5
tubulin monoglutamylase TTLL4 isoform X1
tubulin monoglutamylase TTLL4 isoform X2
tubulin monoglutamylase TTLL4 isoform X3
tubulin monoglutamylase TTLL4 isoform X4
tubulin monoglutamylase TTLL4 isoform X5
tubulin monoglutamylase TTLL4, transcript variant X6
tubulin monoglutamylase TTLL4 isoform X6
tubulin monoglutamylase TTLL4, transcript variant X7
tubulin monoglutamylase TTLL4 isoform X7
zinc finger MYM-type protein 3, transcript variant X1
zinc finger MYM-type protein 3, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
serine-arginine protein 55, transcript variant X4
serine-arginine protein 55, transcript variant X2
serine-arginine protein 55, transcript variant X3
serine-arginine protein 55, transcript variant X1
serine-arginine protein 55, transcript variant X5
serine-arginine protein 55, transcript variant X7
serine-arginine protein 55, transcript variant X6
serine-arginine protein 55, transcript variant X8
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 76 samples with support for all annotated introns
uncharacterized LOC105382631, transcript variant X3
uncharacterized LOC105382631, transcript variant X1
uncharacterized LOC105382631, transcript variant X2
uncharacterized LOC105382631, transcript variant X4
uncharacterized protein LOC105382631 isoform X1
uncharacterized protein LOC105382631 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
uncharacterized LOC119690783, 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 8 samples with support for all annotated introns
uncharacterized LOC119690783, 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 6 samples with support for all annotated introns
uncharacterized LOC119690783, transcript variant X1
uncharacterized LOC119690783, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
39S ribosomal protein L19, mitochondrial
katanin p60 ATPase-containing subunit A-like 1
trithorax group protein osa, transcript variant X1
trithorax group protein osa, transcript variant X10
trithorax group protein osa, transcript variant X9
trithorax group protein osa, transcript variant X3
trithorax group protein osa, transcript variant X7
trithorax group protein osa, transcript variant X11
trithorax group protein osa, transcript variant X2
trithorax group protein osa, transcript variant X4
trithorax group protein osa, transcript variant X5
trithorax group protein osa, transcript variant X6
trithorax group protein osa, transcript variant X8
serine/threonine-protein kinase PRP4 homolog, transcript variant X1
serine/threonine-protein kinase PRP4 homolog, transcript variant X2
serine/threonine-protein kinase PRP4 homolog isoform X1
serine/threonine-protein kinase PRP4 homolog isoform X2
uncharacterized LOC119694801, transcript variant X2
uncharacterized protein LOC119694801 isoform X2
uncharacterized LOC119694801, transcript variant X1
uncharacterized protein LOC119694801 isoform 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 81 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X6
tight junction protein ZO-1, transcript variant X7
tight junction protein ZO-1, transcript variant X2
tight junction protein ZO-1, transcript variant X1
tight junction protein ZO-1, transcript variant X3
tight junction protein ZO-1, transcript variant X11
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 29 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X12
tight junction protein ZO-1, transcript variant X13
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 35 samples with support for all annotated introns
tight junction protein ZO-1, transcript variant X4
thioredoxin domain-containing protein 12
tight junction protein ZO-1, transcript variant X8
tight junction protein ZO-1, transcript variant X9
PIN2/TERF1-interacting telomerase inhibitor 1
tight junction protein ZO-1, transcript variant X10
uncharacterized LOC105382663, transcript variant X1
uncharacterized LOC105382663, transcript variant X2
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 11 samples with support for all annotated introns
FHIP family protein GJ17503, transcript variant X2
FHIP family protein GJ17503, 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 12 samples with support for all annotated introns
eukaryotic translation initiation factor 2-alpha kinase
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 1 base at 1 genomic stop codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: eukaryotic translation initiation factor 2-alpha kinase
zinc finger CCHC domain-containing protein 10
mitochondrial import inner membrane translocase subunit Tim16
septin-interacting protein 1, transcript variant X1
septin-interacting protein 1, transcript variant X3
septin-interacting protein 1, transcript variant X2
neuronal PAS domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
vesicle-associated membrane protein 2, transcript variant X2
vesicle-associated membrane protein 2 isoform X2
vesicle-associated membrane protein 2, transcript variant X1
vesicle-associated membrane protein 2, transcript variant X3
vesicle-associated membrane protein 2, transcript variant X4
vesicle-associated membrane protein 2 isoform X1
vesicle-associated membrane protein 2 isoform 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 9 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
mediator of RNA polymerase II transcription subunit 24
tRNA (adenine(58)-N(1))-methyltransferase catalytic subunit TRMT61A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 97% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
CCR4-NOT transcription complex subunit 9
ralA-binding protein 1, transcript variant X1
ralA-binding protein 1, transcript variant X2
golgin subfamily A member 5, transcript variant X2
golgin subfamily A member 5, transcript variant X3
golgin subfamily A member 5, transcript variant X1
serine protease inhibitor 27A, 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 61 samples with support for all annotated introns
serine protease inhibitor 27A isoform X1
serine protease inhibitor 27A, transcript variant X2
serine protease inhibitor 27A isoform X2
D-aminoacyl-tRNA deacylase 1, transcript variant X1
D-aminoacyl-tRNA deacylase 1, 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 72 samples with support for all annotated introns
microtubule-associated protein Jupiter, transcript variant X2
microtubule-associated protein Jupiter, transcript variant X1
microtubule-associated protein Jupiter, transcript variant X4
microtubule-associated protein Jupiter, transcript variant X3
microtubule-associated protein Jupiter, transcript variant X5
microtubule-associated protein Jupiter isoform X4
microtubule-associated protein Jupiter isoform X2
microtubule-associated protein Jupiter isoform X1
microtubule-associated protein Jupiter isoform X5
microtubule-associated protein Jupiter isoform 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 21 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 31 samples with support for all annotated introns
UDP-glucosyltransferase 2, transcript variant X3
UDP-glucosyltransferase 2, transcript variant X2
UDP-glucosyltransferase 2, transcript variant X4
UDP-glucosyltransferase 2, transcript variant X1
bromodomain-containing protein DDB_G0270170
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 75 samples with support for all annotated introns
histone-lysine N-methyltransferase trithorax
deoxyuridine 5'-triphosphate nucleotidohydrolase, 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 85 samples with support for all annotated introns
deoxyuridine 5'-triphosphate nucleotidohydrolase, 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 63 samples with support for all annotated introns
deoxyuridine 5'-triphosphate nucleotidohydrolase
coiled-coil domain-containing protein 174, transcript variant X1
coiled-coil domain-containing protein 174, transcript variant X2
coiled-coil domain-containing protein 174
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
sodium- and chloride-dependent neutral and basic amino acid transporter B(0+)
glycoprotein 3-alpha-L-fucosyltransferase A, transcript variant X2
glycoprotein 3-alpha-L-fucosyltransferase A, transcript variant X1
glycoprotein 3-alpha-L-fucosyltransferase A isoform X1
glycoprotein 3-alpha-L-fucosyltransferase A isoform X2
coiled-coil domain-containing protein 115
SAFB-like transcription modulator, transcript variant X1
SAFB-like transcription modulator, transcript variant X2
SAFB-like transcription modulator, transcript variant X3
SAFB-like transcription modulator, transcript variant X5
SAFB-like transcription modulator, transcript variant X4
SAFB-like transcription modulator isoform X1
SAFB-like transcription modulator isoform X2
SAFB-like transcription modulator isoform X3
SAFB-like transcription modulator isoform X5
SAFB-like transcription modulator isoform X4
abasic site processing protein HMCES, 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 10 samples with support for all annotated introns
abasic site processing protein HMCES, transcript variant X1
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 49 samples with support for all annotated introns
abasic site processing protein HMCES isoform X1
abasic site processing protein HMCES isoform X2
uncharacterized LOC105390560, transcript variant X2
uncharacterized LOC105390560, transcript variant X1
uncharacterized protein LOC105390560 isoform X1
uncharacterized protein LOC105390560 isoform X2
S-adenosylmethionine sensor upstream of mTORC1
histone acetyltransferase type B catalytic subunit
transfer RNA threonine (anticodon CGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
larval cuticle protein A3A-like, transcript variant X2
larval cuticle protein A3A-like, transcript variant X3
larval cuticle protein A3A-like, transcript variant X1
larval cuticle protein A3A-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 120 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
outer dynein arm-docking complex subunit 4-like
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
cytochrome c oxidase subunit 5B, mitochondrial
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 47 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 69% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 56 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
cysteine-rich hydrophobic domain-containing protein 2
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 79 samples with support for all annotated introns
SH3 domain-containing protein 19, transcript variant X2
SH3 domain-containing protein 19, transcript variant X1
SH3 domain-containing protein 19 isoform X2
SH3 domain-containing protein 19 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 90% coverage of the annotated genomic feature by RNAseq alignments
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 58 samples with support for all annotated introns
activating signal cointegrator 1 complex subunit 3
peptidyl-prolyl cis-trans isomerase FKBP2
transcription initiation factor TFIID subunit 12
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 7 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 85 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 45 samples with support for all annotated introns
ankyrin repeat domain-containing protein 49
trafficking protein particle complex subunit 10
mothers against decapentaplegic homolog 4, 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 42 samples with support for all annotated introns
mothers against decapentaplegic homolog 4, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 22 samples with support for all annotated introns
mothers against decapentaplegic homolog 4, 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 23 samples with support for all annotated introns
mothers against decapentaplegic homolog 4, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
mothers against decapentaplegic homolog 4 isoform X1
mothers against decapentaplegic homolog 4 isoform X2
mothers against decapentaplegic homolog 4 isoform X3
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 80 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 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
serine-aspartate repeat-containing protein D-like
histone acetyltransferase KAT6A, transcript variant X1
histone acetyltransferase KAT6A, transcript variant X3
histone acetyltransferase KAT6A, transcript variant X2
histone acetyltransferase KAT6A, transcript variant X4
histone acetyltransferase KAT6A isoform X1
histone acetyltransferase KAT6A isoform X2
tyrosine-protein kinase receptor Tie-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 75% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
distal membrane-arm assembly complex protein 2
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, including 41 samples with support for all annotated introns
palmitoyltransferase ZDHHC20-B, transcript variant X2
palmitoyltransferase ZDHHC20-B, transcript variant X1
palmitoyltransferase ZDHHC20-B, transcript variant X4
palmitoyltransferase ZDHHC20-B, transcript variant X3
palmitoyltransferase ZDHHC20-B isoform X3
probable DNA mismatch repair protein Msh6
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 73 samples with support for all annotated introns
mannose-1-phosphate guanyltransferase beta
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial, transcript variant X2
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X1
succinate--CoA ligase [ADP/GDP-forming] subunit alpha, mitochondrial isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 73 samples with support for all annotated introns
probable ATP-dependent RNA helicase DDX43
uncharacterized LOC105391906, transcript variant X2
uncharacterized LOC105391906, transcript variant X1
uncharacterized LOC105391906, transcript variant X5
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 18 samples with support for all annotated introns
uncharacterized LOC105391906, transcript variant X4
uncharacterized LOC105391906, transcript variant X3
uncharacterized LOC105391906, transcript variant X6
uncharacterized protein LOC105391906 isoform X1
uncharacterized protein LOC105391906 isoform X2
uncharacterized protein LOC105391906 isoform X3
uncharacterized protein LOC105391906 isoform X4
uncharacterized protein LOC105391906 isoform X6
uncharacterized protein LOC105391906 isoform X5
cysteine sulfinic acid decarboxylase, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
cysteine sulfinic acid decarboxylase, transcript variant X2
cysteine sulfinic acid decarboxylase isoform X1
cysteine sulfinic acid decarboxylase isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
uncharacterized LOC105390916, 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 22 samples with support for all annotated introns
uncharacterized LOC105390916, 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 33 samples with support for all annotated introns
uncharacterized protein LOC105390916 isoform X1
uncharacterized protein LOC105390916 isoform X2
uncharacterized LOC105390930, transcript variant X1
uncharacterized LOC105390930, transcript variant X2
PF03932 family protein CutC, transcript variant X2
PF03932 family protein CutC, transcript variant X1
PF03932 family protein CutC, transcript variant X3
mitochondrial import inner membrane translocase subunit Tim8
DNA repair protein RAD51 homolog 3, transcript variant X1
DNA repair protein RAD51 homolog 3, transcript variant X4
DNA repair protein RAD51 homolog 3, transcript variant X5
DNA repair protein RAD51 homolog 3, transcript variant X2
DNA repair protein RAD51 homolog 3, transcript variant X3
DNA repair protein RAD51 homolog 3 isoform X3
DNA repair protein RAD51 homolog 3 isoform X2
DNA repair protein RAD51 homolog 3 isoform X1
mediator of RNA polymerase II transcription subunit 29
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
SWI/SNF complex subunit SMARCC2, transcript variant X3
SWI/SNF complex subunit SMARCC2, transcript variant X2
SWI/SNF complex subunit SMARCC2, transcript variant X1
SWI/SNF complex subunit SMARCC2 isoform X3
SWI/SNF complex subunit SMARCC2 isoform X2
SWI/SNF complex subunit SMARCC2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
CCR4-NOT transcription complex subunit 2, transcript variant X2
CCR4-NOT transcription complex subunit 2, transcript variant X3
CCR4-NOT transcription complex subunit 2, transcript variant X1
CCR4-NOT transcription complex subunit 2 isoform X1
CCR4-NOT transcription complex subunit 2 isoform X2
V-type proton ATPase subunit E; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305532.1
The RefSeq transcript has 17 substitutions, 5 non-frameshifting indels compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
similar to AA sequence (same species):RefSeq:NP_001292461.1
The RefSeq protein has 1 substitution compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
mitochondrial glutamate carrier 1, transcript variant X3
mitochondrial glutamate carrier 1, transcript variant X1
mitochondrial glutamate carrier 1, 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 11 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 35 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 30 samples with support for all annotated introns
dopamine receptor 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dopamine receptor 2, transcript variant X2
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 3 samples with support for all annotated introns
dopamine receptor 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 40 samples with support for all annotated introns
uncharacterized LOC105389015, transcript variant X5
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, including 2 samples with support for all annotated introns
uncharacterized LOC105389015, transcript variant X4
uncharacterized LOC105389015, transcript variant X6
uncharacterized protein LOC105389015 isoform X4
uncharacterized protein LOC105389015 isoform X3
uncharacterized LOC105389015, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 ESTs, 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
uncharacterized LOC105389015, transcript variant X1
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, including 18 samples with support for all annotated introns
uncharacterized LOC105389015, transcript variant X3
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, including 29 samples with support for all annotated introns
uncharacterized protein LOC105389015 isoform X1
uncharacterized protein LOC105389015 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 28 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 37 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 77 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00476
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
putative leucine-rich repeat-containing protein DDB_G0290503
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
COX assembly mitochondrial protein 2 homolog, transcript variant X1
COX assembly mitochondrial protein 2 homolog, 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 85 samples with support for all annotated introns
COX assembly mitochondrial protein 2 homolog isoform X2
DNA-directed RNA polymerases I, II, and III subunit RPABC2
E3 ubiquitin-protein ligase arkadia-A, transcript variant X1
E3 ubiquitin-protein ligase arkadia-A, 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 3 samples with support for all annotated introns
E3 ubiquitin-protein ligase arkadia-A isoform X2
E3 ubiquitin-protein ligase arkadia-A isoform X1
mitochondrial pyruvate carrier 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 82 samples with support for all annotated introns
mitochondrial pyruvate carrier 2 isoform X2
mitochondrial pyruvate carrier 2, transcript variant X1
mitochondrial pyruvate carrier 2 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 mRNA, 14 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 57 samples with support for all annotated introns
stress protein DDR48, transcript variant X5
stress protein DDR48, transcript variant X3
stress protein DDR48, transcript variant X2
stress protein DDR48, transcript variant X1
stress protein DDR48, transcript variant X4
uncharacterized protein LOC105393945 isoform X4
uncharacterized protein LOC105393945 isoform X5
uncharacterized protein LOC105393945 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
synaptic vesicle glycoprotein 2B, transcript variant X3
synaptic vesicle glycoprotein 2B, transcript variant X2
synaptic vesicle glycoprotein 2B, transcript variant X1
synaptic vesicle glycoprotein 2B isoform X1
synaptic vesicle glycoprotein 2B isoform X2
keratin, type II cytoskeletal 2 epidermal-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 97% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
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: 100% coverage of the annotated genomic feature by RNAseq alignments, including 63 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
atrial natriuretic peptide receptor 1, transcript variant X4
atrial natriuretic peptide receptor 1, transcript variant X5
atrial natriuretic peptide receptor 1, transcript variant X6
atrial natriuretic peptide receptor 1, transcript variant X3
atrial natriuretic peptide receptor 1, transcript variant X2
atrial natriuretic peptide receptor 1, transcript variant X1
atrial natriuretic peptide receptor 1 isoform X2
atrial natriuretic peptide receptor 1 isoform X4
atrial natriuretic peptide receptor 1 isoform X1
atrial natriuretic peptide receptor 1 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: 3-hydroxyacyl-CoA dehydrogenase type-2
FHF complex subunit HOOK interacting protein 2A, 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 42 samples with support for all annotated introns
FHF complex subunit HOOK interacting protein 2A, transcript variant X2
FHF complex subunit HOOK interacting protein 2A isoform X1
FHF complex subunit HOOK interacting protein 2A isoform X2
phosphatidylinositol 4-kinase type 2-beta, transcript variant X1
phosphatidylinositol 4-kinase type 2-beta, transcript variant X2
phosphatidylinositol 4-kinase type 2-beta isoform X1
phosphatidylinositol 4-kinase type 2-beta isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
protein IWS1 homolog, transcript variant X1
protein IWS1 homolog, transcript variant X2
heavy metal-associated isoprenylated plant protein 34-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
coiled-coil domain-containing protein R3HCC1L, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 ESTs, 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 71 samples with support for all annotated introns
coiled-coil domain-containing protein R3HCC1L, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 68 samples with support for all annotated introns
coiled-coil domain-containing protein R3HCC1L isoform X1
coiled-coil domain-containing protein R3HCC1L isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 78 samples with support for all annotated introns
protein phosphatase methylesterase 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
protein phosphatase methylesterase 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 ESTs, 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 72 samples with support for all annotated introns
protein phosphatase methylesterase 1 isoform X1
protein phosphatase methylesterase 1 isoform X2
calcium uptake protein 3, mitochondrial, transcript variant X2
calcium uptake protein 3, mitochondrial, transcript variant X1
calcium uptake protein 3, mitochondrial, transcript variant X4
calcium uptake protein 3, mitochondrial, transcript variant X3
calcium uptake protein 3, mitochondrial isoform X4
calcium uptake protein 3, mitochondrial isoform X3
calcium uptake protein 3, mitochondrial isoform X2
calcium uptake protein 3, mitochondrial isoform X1
uncharacterized LOC119690823, transcript variant X1
uncharacterized LOC119690823, transcript variant X2
uncharacterized protein LOC119690823 isoform X2
uncharacterized protein LOC119690823 isoform X1
fibroblast growth factor 22, transcript variant X1
fibroblast growth factor 22, transcript variant X2
fibroblast growth factor 22, transcript variant X3
putative nuclease HARBI1, 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 78 samples with support for all annotated introns
putative nuclease HARBI1, 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 55 samples with support for all annotated introns
uncharacterized protein LOC125488783 isoform X2
uncharacterized LOC125488784, transcript variant X1
uncharacterized LOC125488784, transcript variant X2
uncharacterized protein LOC125488784 isoform X1
uncharacterized protein LOC125488784 isoform X2
uncharacterized LOC119693424, transcript variant X3
uncharacterized LOC119693424, transcript variant X4
uncharacterized LOC119693424, transcript variant X2
uncharacterized LOC119693424, transcript variant X5
uncharacterized LOC119693424, transcript variant X1
uncharacterized protein LOC119693424 isoform X4
uncharacterized protein LOC119693424 isoform X2
uncharacterized protein LOC119693424 isoform X3
uncharacterized protein LOC119693424 isoform X1
uncharacterized LOC119693424, 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 43 samples with support for all annotated introns
uncharacterized LOC125488789, transcript variant X2
uncharacterized LOC125488789, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 76% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
uncharacterized protein K02A2.6-like, transcript variant X1
uncharacterized protein K02A2.6-like, transcript variant X2
uncharacterized protein K02A2.6-like isoform X1
uncharacterized protein LOC105385604 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 49 samples with support for all annotated introns
uncharacterized LOC105389591, transcript variant X1
uncharacterized LOC105389591, transcript variant X2
uncharacterized LOC105389591, transcript variant X4
uncharacterized LOC105389591, transcript variant X3
uncharacterized protein LOC105389591 isoform X1
uncharacterized protein LOC105389591 isoform X2
uncharacterized protein LOC105389591 isoform X3
uncharacterized protein LOC105389591 isoform 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 68 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments
leucine-rich repeat extensin-like protein 6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 83% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 74% coverage of the annotated genomic feature by RNAseq alignments
pseudouridylate synthase 1 homolog, transcript variant X2
pseudouridylate synthase 1 homolog, transcript variant X1
pseudouridylate synthase 1 homolog, transcript variant X3
pseudouridylate synthase 1 homolog isoform X1
pseudouridylate synthase 1 homolog isoform X2
pseudouridylate synthase 1 homolog isoform 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 14 samples with support for all annotated introns
actin-interacting protein 1, transcript variant X1
actin-interacting protein 1, transcript variant X3
actin-interacting protein 1, transcript variant X2
actin-interacting protein 1, transcript variant X5
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 35 samples with support for all annotated introns
actin-interacting protein 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 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 15 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 24 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 21 samples with support for all annotated introns
ankyrin repeat domain-containing protein 49, transcript variant X3
ankyrin repeat domain-containing protein 49, transcript variant X2
ankyrin repeat domain-containing protein 49, transcript variant X1
ankyrin repeat domain-containing protein 49 isoform X1
ankyrin repeat domain-containing protein 49, transcript variant X4
ankyrin repeat domain-containing protein 49 isoform X2
uncharacterized LOC119690789, transcript variant X5
uncharacterized LOC119690789, transcript variant X4
uncharacterized LOC119690789, transcript variant X1
uncharacterized LOC119690789, transcript variant X2
uncharacterized LOC119690789, transcript variant X3
uncharacterized protein LOC119690789 isoform X1
uncharacterized protein LOC119690789 isoform X3
uncharacterized protein LOC119690789 isoform X2
uncharacterized protein LOC119690789 isoform 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 20 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 95% coverage of the annotated genomic feature by RNAseq alignments, including 34 samples with support for all annotated introns
uncharacterized LOC105398711, 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 54 samples with support for all annotated introns
uncharacterized LOC105398711, 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 22 samples with support for all annotated introns
uncharacterized LOC105398711, 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 50 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 88% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
uncharacterized LOC105380261, transcript variant X1
uncharacterized LOC105380261, transcript variant X3
uncharacterized LOC105380261, transcript variant X5
uncharacterized LOC105380261, transcript variant X4
uncharacterized LOC105380261, transcript variant X2
uncharacterized LOC105380261, transcript variant X6
uncharacterized LOC105380261, transcript variant X8
uncharacterized LOC105380261, transcript variant X7
uncharacterized protein LOC105380261 isoform X1
uncharacterized protein LOC105380261 isoform X3
uncharacterized protein LOC105380261 isoform X5
uncharacterized protein LOC105380261 isoform X4
uncharacterized protein LOC105380261 isoform X6
uncharacterized protein LOC105380261 isoform X2
uncharacterized protein LOC105380261 isoform X8
uncharacterized protein LOC105380261 isoform X7
protein krasavietz, transcript variant X1
protein krasavietz, transcript variant X2
probable 39S ribosomal protein L45, mitochondrial
regulator of G-protein signaling loco, transcript variant X1
regulator of G-protein signaling loco isoform X1
regulator of G-protein signaling loco, transcript variant X2
regulator of G-protein signaling loco isoform X2
uncharacterized LOC105386375, 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 33 samples with support for all annotated introns
uncharacterized LOC105386375, transcript variant X2
uncharacterized protein LOC105386375 isoform X1
uncharacterized protein LOC105386375 isoform X2
trafficking protein particle complex subunit 2
DNA-directed RNA polymerase III subunit RPC4, transcript variant X1
DNA-directed RNA polymerase III subunit RPC4, transcript variant X2
DNA-directed RNA polymerase III subunit RPC4 isoform X1
DNA-directed RNA polymerase III subunit RPC4 isoform X2
probable 28S ribosomal protein S26, mitochondrial
proclotting enzyme, 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 26 samples with support for all annotated introns
proclotting enzyme, transcript variant X2
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 18 samples with support for all annotated introns
uncharacterized protein LOC105386416 isoform X1
glutamate-gated chloride channel; Derived by automated computational analysis using gene prediction method: BestRefSeq,Gnomon.
glutamate-gated chloride channel, transcript variant X3
similar to RNA sequence, mRNA (same species):RefSeq:NM_001305518.2
The RefSeq transcript has 8 substitutions, 1 non-frameshifting indel compared to this genomic sequence; Derived by automated computational analysis using gene prediction method: BestRefSeq.
glutamate-gated chloride channel, transcript variant X6
glutamate-gated chloride channel, transcript variant X4
glutamate-gated chloride channel, transcript variant X5
glutamate-gated chloride channel, transcript variant X2
glutamate-gated chloride channel, transcript variant X1
glutamate-gated chloride channel isoform X2
glutamate-gated chloride channel isoform X4
glutamate-gated chloride channel isoform X1
similar to AA sequence (same species):RefSeq:NP_001292447.1
glutamate-gated chloride channel precursor
glutamate-gated chloride channel isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 76 samples with support for all annotated introns
small VCP/p97-interacting protein, transcript variant X2
small VCP/p97-interacting protein isoform X2
small VCP/p97-interacting protein, transcript variant X1
small VCP/p97-interacting protein isoform X1
solute carrier organic anion transporter family member 1C1, transcript variant X2
solute carrier organic anion transporter family member 1C1, transcript variant X1
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, transcript variant X3
solute carrier organic anion transporter family member 1C1 isoform X3
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X3
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X1
UTP--glucose-1-phosphate uridylyltransferase isoform X1
UTP--glucose-1-phosphate uridylyltransferase isoform X3
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X4
UTP--glucose-1-phosphate uridylyltransferase isoform X4
UTP--glucose-1-phosphate uridylyltransferase, transcript variant X2
UTP--glucose-1-phosphate uridylyltransferase isoform X2
solute carrier organic anion transporter family member 2A1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 28 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
chromatin target of PRMT1 protein, 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 13 samples with support for all annotated introns
chromatin target of PRMT1 protein, 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 34 samples with support for all annotated introns
chromatin target of PRMT1 protein isoform X2
chromatin target of PRMT1 protein isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
zinc finger BED domain-containing protein 4-like
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X3
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X4
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X2
ubiquitin carboxyl-terminal hydrolase 8, transcript variant X5
ubiquitin carboxyl-terminal hydrolase 8 isoform X1
ubiquitin carboxyl-terminal hydrolase 8 isoform X3
ubiquitin carboxyl-terminal hydrolase 8 isoform X2
ubiquitin carboxyl-terminal hydrolase 8 isoform X4
ubiquitin carboxyl-terminal hydrolase 8 isoform X5
synapse-associated protein of 47 kDa, transcript variant X6
synapse-associated protein of 47 kDa, transcript variant X5
synapse-associated protein of 47 kDa, transcript variant X7
synapse-associated protein of 47 kDa, transcript variant X1
synapse-associated protein of 47 kDa, transcript variant X3
synapse-associated protein of 47 kDa, transcript variant X2
synapse-associated protein of 47 kDa, transcript variant X4
synapse-associated protein of 47 kDa isoform X1
synapse-associated protein of 47 kDa isoform X6
synapse-associated protein of 47 kDa isoform X3
synapse-associated protein of 47 kDa isoform X2
synapse-associated protein of 47 kDa isoform X4
synapse-associated protein of 47 kDa isoform X5
synapse-associated protein of 47 kDa isoform X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 26 samples with support for all annotated introns
trimethyllysine dioxygenase, mitochondrial
cyclin-dependent kinases regulatory subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 EST, 1 Protein, and 98% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC119690300, transcript variant X1
uncharacterized LOC119690300, transcript variant X2
uncharacterized LOC119690300, transcript variant X3
uncharacterized protein LOC119690300 isoform X2
uncharacterized protein LOC119690300 isoform X1
dystrophin, isoforms A/C/F/G/H-like, transcript variant X5
dystrophin, isoforms A/C/F/G/H-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 20 samples with support for all annotated introns
dystrophin, isoforms A/C/F/G/H-like, transcript variant X1
dystrophin, isoforms A/C/F/G/H-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 41 samples with support for all annotated introns
dystrophin, isoforms A/C/F/G/H-like, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 43 samples with support for all annotated introns
dystrophin, isoforms A/C/F/G/H-like isoform X5
dystrophin, isoforms A/C/F/G/H-like isoform X2
dystrophin, isoforms A/C/F/G/H-like isoform X1
dystrophin, isoforms A/C/F/G/H-like isoform X3
dystrophin, isoforms A/C/F/G/H-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 84% coverage of the annotated genomic feature by RNAseq alignments
serine/arginine repetitive matrix protein 1, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
serine/arginine repetitive matrix protein 1, transcript variant X2
serine/arginine repetitive matrix protein 1, transcript variant X1
splicing factor, arginine/serine-rich 19 isoform X1
splicing factor, arginine/serine-rich 19 isoform X2
serine/arginine repetitive matrix protein 1 isoform X3