Protopterus annectens isolate FY-2018-M chromosome 16.part0, PAN1.0, whole genome shotgun sequence.
Protopterus annectens (West African lungfish)
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Dipnomorpha; Ceratodontiformes; Lepidosirenoidei; Protopteridae; Protopterus.
African lungfish genome sheds light on the vertebrate water-to-land transition
REFSEQ INFORMATION: The reference sequence is identical to\nCM033098.1.\nAssembly name: PAN1.0\nThe genomic sequence for this RefSeq record is from the\nwhole-genome assembly released by the Northwestern Polytechnical\nUniversity on 2021/07/20. The original whole-genome shotgun project\nhas the accession JAGYFI000000000.1.\n\n##Genome-Assembly-Data-START##\nAssembly Provider :: Northwestern Polytechnical University\nAssembly Method :: wtdbg v. huge\nAssembly Name :: PAN1.0\nGenome Representation :: Full\nExpected Final Version :: Yes\nGenome Coverage :: 50.0x\nSequencing Technology :: Oxford Nanopore\n##Genome-Assembly-Data-END##\n\n##Genome-Annotation-Data-START##\nAnnotation Provider :: NCBI\nAnnotation Status :: Full annotation\nAnnotation Name :: Protopterus annectens Annotation\n Release 100\nAnnotation Version :: 100\nAnnotation Pipeline :: NCBI eukaryotic genome annotation\n pipeline\nAnnotation Software Version :: 9.0\nAnnotation Method :: Best-placed RefSeq; Gnomon\nFeatures Annotated :: Gene; mRNA; CDS; ncRNA\n##Genome-Annotation-Data-END##
Derived by automated computational analysis using gene prediction method: Gnomon.
histo-blood group ABO system transferase-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 260 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
histo-blood group ABO system transferase-like, transcript variant X1
histo-blood group ABO system transferase-like isoform X2
histo-blood group ABO system transferase-like isoform X1
Derived by automated computational analysis using gene prediction method: cmsearch.
COORDINATES: nucleotide motif:Rfam:12.0:RF00002
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 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 13 samples with support for all annotated introns
histo-blood group ABO system transferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 267 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: 258 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 29 samples with support for all annotated introns
COORDINATES: polyA evidence [ECO:0006239]
coiled-coil domain-containing protein 180
Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA leucine (anticodon CAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
ral guanine nucleotide dissociation stimulator, transcript variant X2
ral guanine nucleotide dissociation stimulator isoform X2
ral guanine nucleotide dissociation stimulator, transcript variant X1
ral guanine nucleotide dissociation stimulator isoform X1
ral guanine nucleotide dissociation stimulator, transcript variant X3
ral guanine nucleotide dissociation stimulator isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor IIIC subunit 4
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 32 samples with support for all annotated introns
general transcription factor 3C polypeptide 4
adenylate kinase 8, transcript variant X1
adenylate kinase 8, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins
sperm acrosome associated 9, transcript variant X2
sperm acrosome associated 9, 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 15 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
general transcription factor IIIC subunit 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 13 Proteins, and 87% coverage of the annotated genomic feature by RNAseq alignments
general transcription factor 3C polypeptide 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments
transfer RNA alanine (anticodon UGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
growth factor independent 1B transcriptional repressor
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 5 samples with support for all annotated introns
general transcription factor 3C polypeptide 5-like
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
probable ATP-dependent RNA helicase DDX31
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
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
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 26 samples with support for all annotated introns
cilia and flagella associated protein 77
cilia- and flagella-associated protein 77
transfer RNA leucine (anticodon UAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mediator of RNA polymerase II transcription subunit 27
COORDINATES: nucleotide motif:Rfam:12.0:RF00004
probable ribosome biogenesis protein RLP24
Rap guanine nucleotide exchange factor 1
proline rich transmembrane protein 1B, transcript variant X1
proline rich transmembrane protein 1B, transcript variant X2
proline rich transmembrane protein 1B isoform X2
proline rich transmembrane protein 1B isoform X1
protein O-mannosyltransferase 1, transcript variant X3
protein O-mannosyltransferase 1, transcript variant X1
protein O-mannosyltransferase 1, transcript variant X2
protein O-mannosyl-transferase 1 isoform X2
protein O-mannosyl-transferase 1 isoform X1
mediator of RNA polymerase II transcription subunit 12-like, 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
mediator of RNA polymerase II transcription subunit 12-like, transcript variant X2
mediator of RNA polymerase II transcription subunit 12-like
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
protein mono-ADP-ribosyltransferase PARP14-like
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 3 samples with support for all annotated introns
Fc receptor-like protein 5, transcript variant X3
Fc receptor-like protein 5, transcript variant X2
Fc receptor-like protein 5, transcript variant X1
uncharacterized protein LOC122790854 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 80% coverage of the annotated genomic feature by RNAseq alignments, including 37 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 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: 95% coverage of the annotated genomic feature by RNAseq alignments
adenylate cyclase type 2-like, transcript variant X3
adenylate cyclase type 2-like, transcript variant X1
adenylate cyclase type 2-like, transcript variant X2
adenylate cyclase type 2-like isoform X1
adenylate cyclase type 2-like isoform X2
transfer RNA methionine (anticodon CAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
carcinoembryonic antigen-related cell adhesion molecule 5-like
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 UAC); 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: 16 Proteins, and 91% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins
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 7 samples with support for all annotated introns
uncharacterized LOC122790286, 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 1 sample with support for all annotated introns
uncharacterized LOC122790286, transcript variant X1
endonuclease domain-containing 1 protein-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 23 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
H/ACA ribonucleoprotein complex subunit 3
lysophosphatidylcholine acyltransferase 4
ubiquitin carboxyl-terminal hydrolase CYLD-like
ER membrane protein complex subunit 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
E3 ubiquitin-protein ligase CCNB1IP1-like
E3 ubiquitin-protein ligase CCNB1IP1-like, transcript variant X1
E3 ubiquitin-protein ligase CCNB1IP1-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
uncharacterized transmembrane protein DDB_G0289901-like
ubiquitin-conjugating enzyme E2Q-like protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins
leukotriene B4 receptor 1-like, transcript variant X4
leukotriene B4 receptor 1-like, transcript variant X5
leukotriene B4 receptor 1-like, transcript variant X2
leukotriene B4 receptor 1-like, transcript variant X3
leukotriene B4 receptor 1-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
C-terminal-binding protein 2-like, transcript variant X3
C-terminal-binding protein 2-like, transcript variant X4
C-terminal-binding protein 2-like, transcript variant X1
C-terminal-binding protein 2-like, transcript variant X2
C-terminal-binding protein 2-like, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
C-terminal-binding protein 1-like isoform X1
C-terminal-binding protein 2-like isoform X2
family with sequence similarity 53 member C
transfer RNA isoleucine (anticodon AAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
N-acetyllactosaminide alpha-1,3-galactosyltransferase-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
mediator complex subunit 22, transcript variant X1
mediator of RNA polymerase II transcription subunit 22 isoform X1
mediator complex subunit 22, transcript variant X2
mediator of RNA polymerase II transcription subunit 22 isoform X2
transfer RNA threonine (anticodon AGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
COORDINATES: nucleotide motif:Rfam:12.0:RF00069
COORDINATES: nucleotide motif:Rfam:12.0:RF00049
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
protein mono-ADP-ribosyltransferase PARP14-like, 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
protein mono-ADP-ribosyltransferase PARP14-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
protein mono-ADP-ribosyltransferase PARP14-like isoform X1
protein mono-ADP-ribosyltransferase PARP14-like isoform X2
transfer RNA arginine (anticodon CCG); 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: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
short chain dehydrogenase/reductase family 39U member 1
similar to RNA sequence (same species):INSD:GGXP01065439.1
annotated by transcript or proteomic data
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 44 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 16 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
COORDINATES: nucleotide motif:Rfam:12.0:RF00600
COORDINATES: nucleotide motif:Rfam:12.0:RF00090
COORDINATES: nucleotide motif:Rfam:12.0:RF01168
uncharacterized protein LOC122790808 isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 87 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 45 Proteins, and 15% coverage of the annotated genomic feature by RNAseq alignments
probable WRKY transcription factor protein 1
trichohyalin-like, transcript variant X2
trichohyalin-like, transcript variant X1
transfer RNA proline (anticodon CGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon UGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA aspartic acid (anticodon GUC); 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.
transfer RNA leucine (anticodon AAG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA serine (anticodon AGA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA cysteine (anticodon ACA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA phenylalanine (anticodon GAA); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon ACG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA proline (anticodon AGG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA isoleucine (anticodon UAU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
transfer RNA arginine (anticodon CCU); 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: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: zinc-binding protein A33-like
transfer RNA alanine (anticodon CGC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
Ig kappa chain V-VI region NQ6-8.3.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 91% coverage of the annotated genomic feature by RNAseq alignments
Ig heavy chain Mem5-like, transcript variant X2
Ig heavy chain Mem5-like, transcript variant X1
uncharacterized protein LOC122790357 isoform X1
uncharacterized LOC122790321, 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 19 samples with support for all annotated introns
uncharacterized LOC122790321, transcript variant X1
immunoglobulin lambda-1 light chain-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin lambda-1 light chain-like, transcript variant X4
immunoglobulin lambda-1 light chain-like, transcript variant X3
immunoglobulin lambda-1 light chain-like isoform X4
immunoglobulin lambda-1 light chain-like isoform X3
immunoglobulin lambda-1 light chain-like, transcript variant X1
immunoglobulin lambda-1 light chain-like, transcript variant X2
immunoglobulin lambda-1 light chain-like isoform X1
immunoglobulin lambda-1 light chain-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 82% 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 mRNA, 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: 90% coverage of the annotated genomic feature by RNAseq alignments
immunoglobulin kappa light chain-like, transcript variant X3
immunoglobulin kappa light chain-like isoform 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 18 samples with support for all annotated introns
receptor-interacting serine/threonine-protein kinase 2-like, transcript variant X1
receptor-interacting serine/threonine-protein kinase 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
receptor-interacting serine/threonine-protein kinase 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 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 8 samples with support for all annotated introns
receptor-interacting serine/threonine-protein kinase 2-like isoform X1
receptor-interacting serine/threonine-protein kinase 2-like isoform X2
phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1
type 1 phosphatidylinositol 4,5-bisphosphate 4-phosphatase
apurinic/apyrimidinic endodeoxyribonuclease 1, transcript variant X1
apurinic/apyrimidinic endodeoxyribonuclease 1, transcript variant X2
DNA-(apurinic or apyrimidinic site) endonuclease isoform X1
DNA-(apurinic or apyrimidinic site) endonuclease isoform X2
O-sialoglycoprotein endopeptidase, transcript variant X1
O-sialoglycoprotein endopeptidase, transcript variant X3
O-sialoglycoprotein endopeptidase, transcript variant X2
probable tRNA N6-adenosine threonylcarbamoyltransferase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 48 Proteins, and 51% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 110 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
purine nucleoside phosphorylase, transcript variant X1
purine nucleoside phosphorylase, transcript variant X2
purine nucleoside phosphorylase isoform X1
purine nucleoside phosphorylase isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00424
COORDINATES: nucleotide motif:Rfam:12.0:RF00003
pulmonary surfactant-associated protein D-like
pulmonary surfactant-associated protein A1-like, transcript variant X1
pulmonary surfactant-associated protein A1-like, transcript variant X2
pulmonary surfactant-associated protein A1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 Proteins, and 23% coverage of the annotated genomic feature by RNAseq alignments
mannose-binding protein A-like, 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 4 samples with support for all annotated introns
mannose-binding protein A-like, transcript variant X1
mannose-binding protein A-like isoform X2
extracellular calcium-sensing receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 44% 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 26% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 73% 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 25% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122791000, transcript variant X2
uncharacterized LOC122791000, transcript variant X1
uncharacterized LOC122791000, transcript variant X3
platelet endothelial cell adhesion molecule-like
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: 1 Protein, and 8% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 57% coverage of the annotated genomic feature by RNAseq alignments
apolipoprotein L1-like, transcript variant X1
apolipoprotein L1-like, transcript variant X2
apolipoprotein L1-like, 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 4 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 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: 48 Proteins
uncharacterized protein C14orf93 homolog
zinc fingers and homeoboxes protein 3-like, transcript variant X1
zinc fingers and homeoboxes protein 3-like, transcript variant X2
zinc fingers and homeoboxes protein 3-like
homeobox and leucine zipper encoding, transcript variant X1
homeobox and leucine zipper encoding, transcript variant X2
homeobox and leucine zipper protein Homez
abhydrolase domain containing 4, N-acyl phospholipase B, transcript variant X4
abhydrolase domain containing 4, N-acyl phospholipase B, transcript variant X1
abhydrolase domain containing 4, N-acyl phospholipase B, transcript variant X3
abhydrolase domain containing 4, N-acyl phospholipase B, transcript variant X2
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X1
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X3
(Lyso)-N-acylphosphatidylethanolamine lipase isoform X2
transfer RNA lysine (anticodon CUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
von Willebrand factor A domain-containing protein 5A-like, transcript variant X1
von Willebrand factor A domain-containing protein 5A-like, transcript variant X2
von Willebrand factor A domain-containing protein 5A-like, transcript variant X3
von Willebrand factor A domain-containing protein 5A-like isoform X3
von Willebrand factor A domain-containing protein 5A-like isoform X1
von Willebrand factor A domain-containing protein 5A-like isoform X2
von Willebrand factor A domain-containing protein 5A-like
apoptotic chromatin condensation inducer 1, transcript variant X1
apoptotic chromatin condensation inducer 1, transcript variant X2
apoptotic chromatin condensation inducer 1, transcript variant X4
apoptotic chromatin condensation inducer 1, transcript variant X3
apoptotic chromatin condensation inducer in the nucleus isoform X1
apoptotic chromatin condensation inducer in the nucleus isoform X2
apoptotic chromatin condensation inducer in the nucleus isoform X3
chromosome chr16.part0 C14orf119 homolog, 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 15 samples with support for all annotated introns
chromosome chr16.part0 C14orf119 homolog, 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 16 samples with support for all annotated introns
chromosome chr16.part0 C14orf119 homolog, transcript variant X1
chromosome chr16.part0 C14orf119 homolog, transcript variant X2
uncharacterized protein C14orf119 homolog isoform X1
uncharacterized protein C14orf119 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
transcription factor Maf-like, transcript variant X2
transcription factor Maf-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 18% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 54 Proteins, and 63% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 Proteins, and 17% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 47 Proteins, and 10% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 59 Proteins, and 35% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
tubulin polymerization-promoting protein family member 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 27 samples with support for all annotated introns
rho guanine nucleotide exchange factor 40-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 31 Proteins
transfer RNA threonine (anticodon UGU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
coiled-coil domain-containing protein 102A-like
uncharacterized LOC122790982, transcript variant X1
uncharacterized LOC122790982, transcript variant X2
uncharacterized LOC122790982, transcript variant X3
uncharacterized protein LOC122790982 isoform X3
uncharacterized protein LOC122790982 isoform X1
uncharacterized protein LOC122790982 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 5 samples with support for all annotated introns
phosphoenolpyruvate carboxykinase 2, mitochondrial
phosphoenolpyruvate carboxykinase [GTP], mitochondrial
similar to RNA sequence (same species):INSD:GGXP01058382.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 119 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 119 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
fat storage inducing transmembrane protein 1
fat storage-inducing transmembrane protein 1
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
probable N-acetyltransferase CML5, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
probable N-acetyltransferase CML5 isoform X1
probable N-acetyltransferase CML5, 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 9 samples with support for all annotated introns
probable N-acetyltransferase CML5 isoform X2
FH1/FH2 domain-containing protein 3-like
importin subunit alpha-5-like, transcript variant X2
importin subunit alpha-5-like, transcript variant X1
importin subunit alpha-5-like isoform X1
importin subunit alpha-5-like isoform X2
T-cell receptor alpha chain C region-like
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 9 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 22 samples with support for all annotated introns
T cell receptor alpha variable 2-like, transcript variant X2
T cell receptor alpha variable 2-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 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: 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
T cell receptor alpha variable 38-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 78% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
T cell receptor alpha variable 26-2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 100% coverage of the annotated genomic feature by RNAseq alignments, including 18 samples with support for all annotated introns
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
probable non-functional immunoglobulin kappa variable 3-7
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
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 23 samples with support for all annotated introns
COORDINATES: nucleotide motif:Rfam:12.0:RF00619
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
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 27 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, including 6 samples with support for all annotated introns
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 16 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 21 samples with support for all annotated introns
T cell receptor alpha variable 12-1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 79% 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: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
T-cell receptor alpha chain V region RL-5-like
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
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 27 samples with support for all annotated introns
T-cell receptor alpha chain V region CTL-F3-like
proto-oncogene Mas-like, transcript variant X2
proto-oncogene Mas-like, transcript variant X3
proto-oncogene Mas-like, 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 24 samples with support for all annotated introns
T cell receptor alpha variable 14/delta variable 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 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 75% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% 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: 85% 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: 1 Protein, and 79% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 81% 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: 81% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
T cell receptor alpha variable 12-3-like
transfer RNA tyrosine (anticodon GUA); 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: 83% 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: 73% 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: 72% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
T cell receptor alpha variable 36/delta variable 7-like
methyltransferase like 17, transcript variant X2
methyltransferase like 17, transcript variant X1
methyltransferase-like protein 17, mitochondrial isoform X2
methyltransferase-like protein 17, mitochondrial isoform X1
flocculation protein FLO11-like, transcript variant X1
flocculation protein FLO11-like, transcript variant X5
flocculation protein FLO11-like, transcript variant X3
flocculation protein FLO11-like, transcript variant X4
flocculation protein FLO11-like isoform X1
flocculation protein FLO11-like, transcript variant X2
flocculation protein FLO11-like isoform X2
tiggy-winkle hedgehog protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
tiggy-winkle hedgehog protein-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 4 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
myb/SANT-like DNA-binding domain-containing protein 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 99% coverage of the annotated genomic feature by RNAseq alignments, including 25 samples with support for all annotated introns
poly(ADP-ribose) polymerase 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 12 samples with support for all annotated introns
poly(ADP-ribose) polymerase 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 10 samples with support for all annotated introns
poly(ADP-ribose) polymerase 2, transcript variant X3
poly [ADP-ribose] polymerase 2 isoform X1
poly [ADP-ribose] polymerase 2 isoform X2
poly [ADP-ribose] polymerase 2 isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 66 Proteins, and 14% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 62 Proteins, and 5% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 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: 117 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 31, transcript variant X1
ring finger protein 31, transcript variant X2
E3 ubiquitin-protein ligase RNF31 isoform X2
E3 ubiquitin-protein ligase RNF31 isoform X1
ER membrane protein complex subunit 9, transcript variant X3
ER membrane protein complex subunit 9, transcript variant X4
ER membrane protein complex subunit 9, transcript variant X2
ER membrane protein complex subunit 9, transcript variant X1
ER membrane protein complex subunit 9 isoform X1
ER membrane protein complex subunit 9 isoform X2
proteasome activator subunit 1, transcript variant X1
proteasome activator subunit 1, transcript variant X2
proteasome activator complex subunit 1 isoform X1
proteasome activator complex subunit 1 isoform X2
protein-glutamine gamma-glutamyltransferase K-like
cell death inducing DFFA like effector b
NOP9 nucleolar protein, transcript variant X9
NOP9 nucleolar protein, transcript variant X8
NOP9 nucleolar protein, transcript variant X3
NOP9 nucleolar protein, transcript variant X4
NOP9 nucleolar protein, transcript variant X1
NOP9 nucleolar protein, transcript variant X2
NOP9 nucleolar protein, transcript variant X5
NOP9 nucleolar protein, transcript variant X6
NOP9 nucleolar protein, transcript variant X7
similar to RNA sequence (same species):INSD:GGXP01056211.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 80 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 80 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
dehydrogenase/reductase SDR family member 1
Rab geranylgeranyltransferase subunit alpha
geranylgeranyl transferase type-2 subunit alpha
TERF1 interacting nuclear factor 2, transcript variant X3
TERF1 interacting nuclear factor 2, transcript variant X1
TERF1 interacting nuclear factor 2, transcript variant X2
TERF1-interacting nuclear factor 2 isoform X1
TERF1-interacting nuclear factor 2 isoform X2
TERF1-interacting nuclear factor 2 isoform X3
transfer RNA serine (anticodon GCU); 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: 23 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 48% 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 12% 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 47% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: inserted 2 bases in 2 codons; deleted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon.
LOW QUALITY PROTEIN: PHD finger protein 19
prostaglandin E synthase, transcript variant X1
prostaglandin E synthase, transcript variant X3
prostaglandin E synthase, transcript variant X2
regulator of G protein signaling 3, transcript variant X1
regulator of G protein signaling 3, transcript variant X2
regulator of G protein signaling 3, transcript variant X4
regulator of G protein signaling 3, transcript variant X3
regulator of G-protein signaling 3 isoform X1
regulator of G-protein signaling 3 isoform X2
regulator of G-protein signaling 3 isoform X4
regulator of G-protein signaling 3 isoform X3
zinc finger and BTB domain containing 26
zinc finger and BTB domain-containing protein 26
zinc finger and BTB domain-containing protein 6
similar to RNA sequence (same species):INSD:GGXP01001188.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 86 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 81 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
similar to RNA sequence (same species):INSD:GGXP01047216.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 100 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 100 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
solute carrier family 2, facilitated glucose transporter member 8
GTPase activating Rap/RanGAP domain like 3
GTPase-activating Rap/Ran-GAP domain-like protein 3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial ribosomal protein L52, transcript variant X1
39S ribosomal protein L52, mitochondrial isoform X1
mitochondrial ribosomal protein L52, transcript variant X2
39S ribosomal protein L52, mitochondrial isoform X2
Y+L amino acid transporter 2-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Y+L amino acid transporter 2-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 76 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
Y+L amino acid transporter 1-like isoform X2
Y+L amino acid transporter 2-like isoform X1
OXA1L mitochondrial inner membrane protein, transcript variant X2
OXA1L mitochondrial inner membrane protein, transcript variant X1
mitochondrial inner membrane protein OXA1L isoform X2
mitochondrial inner membrane protein OXA1L isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00001
angiogenic factor with G-patch and FHA domains 1, transcript variant X1
angiogenic factor with G-patch and FHA domains 1, transcript variant X2
angiogenic factor with G-patch and FHA domains 1, transcript variant X3
angiogenic factor with G patch and FHA domains 1 isoform X1
angiogenic factor with G patch and FHA domains 1 isoform X2
coiled-coil-helix-coiled-coil-helix domain-containing protein 1-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
solute carrier family 25 member 25, transcript variant X1
solute carrier family 25 member 25, transcript variant X2
solute carrier family 25 member 25, transcript variant X3
solute carrier family 25 member 25, transcript variant X4
solute carrier family 25 member 25, transcript variant X5
solute carrier family 25 member 25, transcript variant X6
solute carrier family 25 member 25, transcript variant X7
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X2
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X1
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X3
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X5
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X4
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X6
calcium-binding mitochondrial carrier protein SCaMC-2 isoform X7
protein phosphatase 2 phosphatase activator
serine/threonine-protein phosphatase 2A activator
immediate early response gene 5-like protein
COORDINATES: nucleotide motif:Rfam:12.0:RF00108
uncharacterized LOC122790386, transcript variant X2
uncharacterized LOC122790386, transcript variant X1
uncharacterized protein LOC122790386 isoform X2
uncharacterized protein LOC122790386 isoform X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X5
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X3
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X6
N-terminal Xaa-Pro-Lys N-methyltransferase 1 isoform X2
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X2
N-terminal Xaa-Pro-Lys N-methyltransferase 1, transcript variant X4
N-terminal Xaa-Pro-Lys N-methyltransferase 1 isoform X1
N-terminal Xaa-Pro-Lys N-methyltransferase 1 isoform X3
ankyrin repeat and SOCS box containing 6, transcript variant X1
ankyrin repeat and SOCS box containing 6, transcript variant X2
paired related homeobox 2, transcript variant X2
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 17 samples with support for all annotated introns
paired related homeobox 2, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 16 samples with support for all annotated introns
paired mesoderm homeobox protein 2 isoform X1
paired mesoderm homeobox protein 2 isoform X2
protein CutA homolog, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
protein CutA homolog, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
proteasome 26S subunit, non-ATPase 5, transcript variant X1
proteasome 26S subunit, non-ATPase 5, transcript variant X2
26S proteasome non-ATPase regulatory subunit 5 isoform X1
26S proteasome non-ATPase regulatory subunit 5 isoform 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
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 90% coverage of the annotated genomic feature by RNAseq alignments
calmodulin regulated spectrin associated protein 1, transcript variant X10
calmodulin regulated spectrin associated protein 1, transcript variant X4
calmodulin regulated spectrin associated protein 1, transcript variant X9
calmodulin regulated spectrin associated protein 1, transcript variant X8
calmodulin regulated spectrin associated protein 1, transcript variant X3
calmodulin regulated spectrin associated protein 1, transcript variant X2
calmodulin regulated spectrin associated protein 1, transcript variant X1
calmodulin regulated spectrin associated protein 1, transcript variant X7
calmodulin regulated spectrin associated protein 1, transcript variant X5
calmodulin regulated spectrin associated protein 1, transcript variant X6
calmodulin-regulated spectrin-associated protein 1 isoform X8
calmodulin-regulated spectrin-associated protein 1 isoform X5
calmodulin-regulated spectrin-associated protein 1 isoform X9
calmodulin-regulated spectrin-associated protein 1 isoform X6
calmodulin-regulated spectrin-associated protein 1 isoform X7
calmodulin-regulated spectrin-associated protein 1 isoform X4
calmodulin-regulated spectrin-associated protein 1 isoform X2
calmodulin-regulated spectrin-associated protein 1 isoform X3
calmodulin-regulated spectrin-associated protein 1 isoform X1
TATA-box binding protein associated factor 10
transcription initiation factor TFIID subunit 10
cyclic nucleotide gated channel subunit alpha 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 36 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
cyclic nucleotide-gated cation channel alpha-4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 69% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin-associated domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
transmembrane protein 250, transcript variant X3
transmembrane protein 250, transcript variant X1
transmembrane protein 250, transcript variant X2
LIM/homeobox protein Lhx3, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
LIM/homeobox protein Lhx3, 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 5 samples with support for all annotated introns
LIM/homeobox protein Lhx3, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 17 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
LIM/homeobox protein Lhx3, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 12 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
dehydrogenase/reductase SDR family member 4-like
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 12 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 92% coverage of the annotated genomic feature by RNAseq alignments
G protein signaling modulator 1, transcript variant X1
G protein signaling modulator 1, transcript variant X2
G-protein-signaling modulator 1 isoform X1
G-protein-signaling modulator 1 isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF01210
caspase recruitment domain family member 9, 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 8 samples with support for all annotated introns
caspase recruitment domain family member 9, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
caspase recruitment domain family member 9, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
caspase recruitment domain-containing protein 9 isoform X1
caspase recruitment domain-containing protein 9 isoform X2
small nuclear RNA activating complex polypeptide 4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
snRNA-activating protein complex subunit 4
carnitine O-acetyltransferase, transcript variant X1
carnitine O-acetyltransferase isoform X1
carnitine O-acetyltransferase, transcript variant X2
carnitine O-acetyltransferase, transcript variant X4
carnitine O-acetyltransferase, transcript variant X5
carnitine O-acetyltransferase, transcript variant X3
carnitine O-acetyltransferase, transcript variant X6
carnitine O-acetyltransferase isoform X2
similar to RNA sequence (same species):INSD:GGXP01019705.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 97 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 97 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
SH3 domain containing GRB2 like, endophilin B2, transcript variant X1
SH3 domain containing GRB2 like, endophilin B2, transcript variant X7
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 13 samples with support for all annotated introns
SH3 domain containing GRB2 like, endophilin B2, transcript variant X6
SH3 domain containing GRB2 like, endophilin B2, transcript variant X8
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 12 samples with support for all annotated introns
SH3 domain containing GRB2 like, endophilin B2, transcript variant X3
SH3 domain containing GRB2 like, endophilin B2, transcript variant X4
SH3 domain containing GRB2 like, endophilin B2, transcript variant X2
SH3 domain containing GRB2 like, endophilin B2, transcript variant X9
SH3 domain containing GRB2 like, endophilin B2, transcript variant X5
SH3 domain containing GRB2 like, endophilin B2, transcript variant X10
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins
phytanoyl-CoA dioxygenase domain containing 1
phytanoyl-CoA dioxygenase domain-containing protein 1
TBCC domain-containing protein 1-like, transcript variant X4
TBCC domain-containing protein 1-like, transcript variant X1
TBCC domain-containing protein 1-like, transcript variant X3
TBCC domain-containing protein 1-like, transcript variant X7
TBCC domain-containing protein 1-like, transcript variant X6
TBCC domain-containing protein 1-like, transcript variant X5
TBCC domain-containing protein 1-like, transcript variant X2
TBCC domain-containing protein 1-like, transcript variant X8
TBCC domain-containing protein 1-like isoform X1
TBCC domain-containing protein 1-like isoform X2
TBCC domain-containing protein 1-like isoform X3
leucine rich repeat containing 8 VRAC subunit A, transcript variant X3
leucine rich repeat containing 8 VRAC subunit A, transcript variant X1
leucine rich repeat containing 8 VRAC subunit A, transcript variant X2
volume-regulated anion channel subunit LRRC8A
kynurenine aminotransferase 1, transcript variant X1
kynurenine aminotransferase 1, transcript variant X2
kynurenine aminotransferase 1, transcript variant X6
kynurenine aminotransferase 1, transcript variant X4
kynurenine aminotransferase 1, transcript variant X3
kynurenine aminotransferase 1, transcript variant X7
kynurenine--oxoglutarate transaminase 1 isoform X1
kynurenine aminotransferase 1, transcript variant X5
kynurenine--oxoglutarate transaminase 1 isoform X2
SPOUT domain containing methyltransferase 1
putative methyltransferase C9orf114 homolog
TBC1 domain family member 13, 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 5 samples with support for all annotated introns
TBC1 domain family member 13, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 15 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
zinc finger DHHC-type palmitoyltransferase 12
vav guanine nucleotide exchange factor 2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 89% coverage of the annotated genomic feature by RNAseq alignments, including 14 samples with support for all annotated introns
neural proliferation, differentiation and control 1, transcript variant X1
neural proliferation, differentiation and control 1, transcript variant X2
neural proliferation differentiation and control protein 1 isoform X1
neural proliferation, differentiation and control 1, transcript variant X3
neural proliferation differentiation and control protein 1 isoform X2
POU domain, class 5, transcription factor 3-like
fucosyltransferase 7, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 12 samples with support for all annotated introns
fucosyltransferase 7, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
fucosyltransferase 7, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
fucosyltransferase 7, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 46 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 samples with support for all annotated introns
ATP binding cassette subfamily A member 2
similar to RNA sequence (same species):INSD:GGXP01037466.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 58 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 58 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
ATP-binding cassette sub-family A member 2
chloride intracellular channel protein 4-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 58 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: 1 Protein, and 64% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: substituted 2 bases at 2 genomic stop codons; Derived by automated computational analysis using gene prediction method: Gnomon.
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 44 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: 14 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
dual specificity testis-specific protein kinase 1-like, transcript variant X4
dual specificity testis-specific protein kinase 1-like, transcript variant X5
dual specificity testis-specific protein kinase 1-like, transcript variant X6
dual specificity testis-specific protein kinase 1-like, transcript variant X3
dual specificity testis-specific protein kinase 1-like, transcript variant X2
dual specificity testis-specific protein kinase 1-like, transcript variant X1
dual specificity testis-specific protein kinase 1-like isoform X1
dual specificity testis-specific protein kinase 1-like, transcript variant X7
dual specificity testis-specific protein kinase 1-like isoform X2
ubiquinone biosynthesis protein COQ4 homolog, mitochondrial
folylpolyglutamate synthase, transcript variant X1
folylpolyglutamate synthase, transcript variant X2
folylpolyglutamate synthase, mitochondrial isoform X1
folylpolyglutamate synthase, mitochondrial isoform X2
folylpolyglutamate synthase, transcript variant X3
folylpolyglutamate synthase, mitochondrial isoform X3
zinc finger BED domain-containing protein 5-like
uncharacterized LOC122790798, transcript variant X3
uncharacterized LOC122790798, transcript variant X1
uncharacterized LOC122790798, transcript variant X2
nuclear receptor subfamily 6 group A member 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
nuclear receptor subfamily 5 group A member 2-like, transcript variant X1
nuclear receptor subfamily 5 group A member 2-like isoform X1
nuclear receptor subfamily 5 group A member 2-like, transcript variant X2
nuclear receptor subfamily 5 group A member 2-like isoform X2
adhesion G protein-coupled receptor D2, transcript variant X3
adhesion G protein-coupled receptor D2, transcript variant X1
adhesion G-protein coupled receptor D2 isoform X3
adhesion G-protein coupled receptor D2 isoform X1
adhesion G protein-coupled receptor D2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 1 sample with support for all annotated introns
adhesion G-protein coupled receptor D2 isoform X2
mitochondrial ribosome recycling factor, transcript variant X2
mitochondrial ribosome recycling factor, transcript variant X1
ribosome-recycling factor, mitochondrial isoform X2
ribosome-recycling factor, mitochondrial isoform X1
COORDINATES: nucleotide motif:Rfam:12.0:RF00026
RNA binding motif protein 18, transcript variant X1
RNA binding motif protein 18, transcript variant X3
RNA binding motif protein 18, transcript variant X2
probable RNA-binding protein 18 isoform X2
probable RNA-binding protein 18 isoform X1
probable RNA-binding protein 18 isoform X3
keratin, type I cytoskeletal 18-like, 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 1 sample with support for all annotated introns
keratin, type I cytoskeletal 18-like, transcript variant X4
keratin, type I cytoskeletal 18-like, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
keratin, type I cytoskeletal 18-like, transcript variant X2
keratin, type I cytoskeletal 18-like isoform X1
keratin, type I cytoskeletal 18-like isoform X4
keratin, type I cytoskeletal 18-like isoform X3
keratin, type I cytoskeletal 18-like isoform X2
ring finger and CCCH-type domains 2, transcript variant X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 96% coverage of the annotated genomic feature by RNAseq alignments
ring finger and CCCH-type domains 2, transcript variant X1
ring finger and CCCH-type domains 2, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
The sequence of the model RefSeq 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: olfactomedin-like protein 2A
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 86% 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 92% coverage of the annotated genomic feature by RNAseq alignments
suppressor of cancer cell invasion, transcript variant X7
suppressor of cancer cell invasion, transcript variant X4
suppressor of cancer cell invasion, transcript variant X2
suppressor of cancer cell invasion, transcript variant X8
suppressor of cancer cell invasion, transcript variant X1
suppressor of cancer cell invasion, transcript variant X3
suppressor of cancer cell invasion, transcript variant X6
suppressor of cancer cell invasion, transcript variant X5
protein phosphatase 6 catalytic subunit, transcript variant X1
protein phosphatase 6 catalytic subunit, transcript variant X2
serine/threonine-protein phosphatase 6 catalytic subunit isoform X1
serine/threonine-protein phosphatase 6 catalytic subunit isoform X2
heat shock protein family A (Hsp70) member 5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
GTPase activating protein and VPS9 domains 1, transcript variant X1
GTPase activating protein and VPS9 domains 1, transcript variant X2
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X1
GTPase-activating protein and VPS9 domain-containing protein 1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 27 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 10 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 95% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 115 Proteins, and 47% coverage of the annotated genomic feature by RNAseq alignments
DENN domain containing 1A, transcript variant X1
DENN domain containing 1A, transcript variant X3
DENN domain containing 1A, transcript variant X2
DENN domain containing 1A, transcript variant X4
DENN domain-containing protein 1A isoform X1
DENN domain-containing protein 1A isoform X3
DENN domain-containing protein 1A isoform X2
DENN domain-containing protein 1A isoform X4
transfer RNA lysine (anticodon UUU); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
RAB GTPase activating protein 1, transcript variant X1
RAB GTPase activating protein 1, transcript variant X2
rab GTPase-activating protein 1 isoform X1
rab GTPase-activating protein 1 isoform X2
similar to RNA sequence (same species):INSD:GGXP01061495.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 54 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 54 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
uncharacterized LOC122790461, transcript variant X1
uncharacterized LOC122790461, transcript variant X2
similar to RNA sequence (same species):INSD:GGXP01054589.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 174 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 174 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
ras/Rap GTPase-activating protein SynGAP-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
disabled homolog 2-interacting protein-like
disabled homolog 2-interacting protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 34 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
disabled homolog 2-interacting protein-like, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
disabled homolog 2-interacting protein-like isoform X1
disabled homolog 2-interacting protein-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
carboxyl-terminal PDZ ligand of neuronal nitric oxide synthase protein-like
similar to RNA sequence (same species):INSD:GGXP01002432.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 166 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 166 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
Ral GEF with PH domain and SH3 binding motif 1
ras-specific guanine nucleotide-releasing factor RalGPS1
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 7 samples with support for all annotated introns
zinc finger and BTB domain containing 43
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 21 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 15 samples with support for all annotated introns
zinc finger and BTB domain-containing protein 43
transfer RNA glutamic acid (anticodon UUC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LIM homeobox transcription factor 1 beta, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 26 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
LIM homeobox transcription factor 1 beta, transcript variant X1
LIM homeobox transcription factor 1-beta isoform X2
LIM homeobox transcription factor 1-beta isoform X1
multivesicular body subunit 12B, transcript variant X2
multivesicular body subunit 12B, transcript variant X1
multivesicular body subunit 12B, transcript variant X3
multivesicular body subunit 12B isoform X1
multivesicular body subunit 12B, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
multivesicular body subunit 12B isoform X2
pre-B-cell leukemia transcription factor 3 isoform X1
pre-B-cell leukemia transcription factor 3 isoform X5
pre-B-cell leukemia transcription factor 3 isoform X6
pre-B-cell leukemia transcription factor 3 isoform X8
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 22 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 16 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 19 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X4
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
pre-B-cell leukemia transcription factor 3 isoform 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 14 samples with support for all annotated introns
pre-B-cell leukemia transcription factor 3 isoform X3
pre-B-cell leukemia transcription factor 3 isoform X7
similar to RNA sequence (same species):INSD:GGXP01057903.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 78 bases not found in genome assembly
target of rapamycin complex 2 subunit MAPKAP1
family with sequence similarity 163 member B, transcript variant X4
family with sequence similarity 163 member B, transcript variant X3
family with sequence similarity 163 member B, transcript variant X1
family with sequence similarity 163 member B, transcript variant X2
family with sequence similarity 163 member B, transcript variant X6
COORDINATES: nucleotide motif:Rfam:12.0:RF00015
family with sequence similarity 163 member B, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 10 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 86% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122790871, transcript variant X1
uncharacterized LOC122790871, transcript variant X2
uncharacterized protein LOC122790871 isoform X1
uncharacterized protein LOC122790871 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 49 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
RHO family interacting cell polarization regulator 1, transcript variant X2
RHO family interacting cell polarization regulator 1, 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 7 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X6
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
RHO family interacting cell polarization regulator 1, 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 8 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 2 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 4 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X11
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 25 samples with support for all annotated introns
RHO family interacting cell polarization regulator 1, transcript variant X7
RHO family interacting cell polarization regulator 1, transcript variant X10
RHO family interacting cell polarization regulator 1, transcript variant X8
RHO family interacting cell polarization regulator 1, transcript variant X9
rho family-interacting cell polarization regulator 1 isoform X4
rho family-interacting cell polarization regulator 1 isoform X2
rho family-interacting cell polarization regulator 1 isoform X1
rho family-interacting cell polarization regulator 1 isoform X3
inactive serine/threonine-protein kinase VRK3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 14 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
nuclear pore complex protein Nup98-Nup96-like
ras-specific guanine nucleotide-releasing factor RalGPS1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 86% coverage of the annotated genomic feature by RNAseq alignments
zinc finger and BTB domain containing 34
zinc finger and BTB domain-containing protein 34
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 9 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
similar to RNA sequence (same species):INSD:GGXP01065357.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 297 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 297 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
spectrin alpha chain, non-erythrocytic 1
cytoplasmic dynein 2 intermediate chain 2
SET nuclear proto-oncogene, transcript variant X1
SET nuclear proto-oncogene, transcript variant X2
laminin subunit gamma 3, transcript variant X2
laminin subunit gamma 3, transcript variant X1
TAR DNA-binding protein 43-like, transcript variant X3
TAR DNA-binding protein 43-like, transcript variant X4
TAR DNA-binding protein 43-like, transcript variant X1
TAR DNA-binding protein 43-like, transcript variant X2
TAR DNA-binding protein 43-like isoform X1
TAR DNA-binding protein 43-like isoform X2
TAR DNA-binding protein 43-like isoform X3
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
fibrinogen C domain-containing protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
ABL proto-oncogene 1, non-receptor tyrosine kinase
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 5 Proteins, and 97% coverage of the annotated genomic feature by RNAseq alignments
ubiquitin specific peptidase 20, transcript variant X4
ubiquitin specific peptidase 20, transcript variant X5
ubiquitin specific peptidase 20, transcript variant X3
ubiquitin specific peptidase 20, transcript variant X2
ubiquitin specific peptidase 20, transcript variant X1
ubiquitin carboxyl-terminal hydrolase 20 isoform X2
ubiquitin carboxyl-terminal hydrolase 20 isoform X1
telomere length and silencing protein 1 homolog
neuronal calcium sensor 1, transcript variant X1
neuronal calcium sensor 1, transcript variant X2
exosome component 2, transcript variant X1
exosome component 2, transcript variant X2
exosome complex component RRP4 isoform X1
exosome complex component RRP4 isoform X2
retinoid X receptor alpha, transcript variant X1
retinoid X receptor alpha, transcript variant X3
retinoid X receptor alpha, transcript variant X2
collagen type V alpha 1 chain, transcript variant X2
collagen type V alpha 1 chain, transcript variant X1
protein phosphatase 1 regulatory subunit 26, transcript variant X2
protein phosphatase 1 regulatory subunit 26, transcript variant X3
protein phosphatase 1 regulatory subunit 26, transcript variant X1
protein phosphatase 1 regulatory subunit 26, transcript variant X4
protein phosphatase 1 regulatory subunit 26
mitochondrial ribosomal protein S2, transcript variant X1
28S ribosomal protein S2, mitochondrial isoform X1
mitochondrial ribosomal protein S2, transcript variant X2
28S ribosomal protein S2, mitochondrial isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00560
1-acyl-sn-glycerol-3-phosphate acyltransferase alpha-like, transcript variant X2
1-acyl-sn-glycerol-3-phosphate acyltransferase alpha-like isoform X2
1-acyl-sn-glycerol-3-phosphate acyltransferase alpha-like, transcript variant X1
1-acyl-sn-glycerol-3-phosphate acyltransferase alpha-like isoform X1
EGF like domain multiple 7, transcript variant X2
EGF like domain multiple 7, transcript variant X7
EGF like domain multiple 7, transcript variant X1
EGF like domain multiple 7, transcript variant X3
EGF like domain multiple 7, transcript variant X4
EGF like domain multiple 7, transcript variant X6
EGF like domain multiple 7, transcript variant X5
epidermal growth factor-like protein 7 isoform X2
epidermal growth factor-like protein 7 isoform X1
dipeptidyl peptidase 7, transcript variant X1
dipeptidyl peptidase 7, transcript variant X2
transfer RNA glycine (anticodon UCC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
mannosidase alpha class 1B member 1, 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 16 samples with support for all annotated introns
mannosidase alpha class 1B member 1, transcript variant X4
mannosidase alpha class 1B member 1, 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 23 samples with support for all annotated introns
mannosidase alpha class 1B member 1, transcript variant 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 6 samples with support for all annotated introns
endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase isoform X2
endoplasmic reticulum mannosyl-oligosaccharide 1,2-alpha-mannosidase isoform X1
UDP-N-acetylglucosamine pyrophosphorylase 1 like 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 83% coverage of the annotated genomic feature by RNAseq alignments
UDP-N-acetylhexosamine pyrophosphorylase-like protein 1
amiloride-sensitive sodium channel subunit gamma-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 65% coverage of the annotated genomic feature by RNAseq alignments
suppressor APC domain-containing protein 2
breast cancer anti-estrogen resistance protein 1-like, transcript variant X3
breast cancer anti-estrogen resistance protein 1-like, transcript variant X1
breast cancer anti-estrogen resistance protein 1-like isoform X1
breast cancer anti-estrogen resistance protein 1-like isoform X3
breast cancer anti-estrogen resistance protein 1-like, transcript variant X2
breast cancer anti-estrogen resistance protein 1-like isoform X2
breast cancer anti-estrogen resistance protein 1-like, transcript variant X4
breast cancer anti-estrogen resistance protein 1-like isoform X4
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 96% coverage of the annotated genomic feature by RNAseq alignments
solute carrier family 22 member 17-like, transcript variant X2
solute carrier family 22 member 17-like, transcript variant X1
solute carrier family 22 member 17-like, transcript variant X3
solute carrier family 22 member 17-like, transcript variant X4
solute carrier family 22 member 17-like, transcript variant X5
solute carrier family 22 member 17-like, transcript variant X6
solute carrier family 22 member 17-like isoform X1
solute carrier family 22 member 17-like isoform X2
similar to RNA sequence (same species):INSD:GGXP01046510.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 68 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 29 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 68 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
protein phosphatase 1 regulatory subunit 3E-like
twisted gastrulation protein homolog 1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 17 samples with support for all annotated introns
charged multivesicular body protein 4b-like
transmembrane 9 superfamily member 1, transcript variant X2
transmembrane 9 superfamily member 1, transcript variant X1
family with sequence similarity 102 member A
adenylate kinase isoenzyme 5-like, transcript variant X1
adenylate kinase isoenzyme 5-like, transcript variant X2
adenylate kinase isoenzyme 5-like isoform X1
adenylate kinase isoenzyme 5-like isoform X2
SEC16 homolog A, endoplasmic reticulum export factor
similar to RNA sequence (same species):INSD:GGXP01025251.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 4 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 4 bases not found in genome assembly; 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: 36 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
neurogenic locus notch homolog protein 1
solute carrier family 2, facilitated glucose transporter member 6-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 19 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 20 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 6 Proteins
CDKN1A interacting zinc finger protein 1, transcript variant X4
CDKN1A interacting zinc finger protein 1, transcript variant X5
CDKN1A interacting zinc finger protein 1, transcript variant X6
CDKN1A interacting zinc finger protein 1, transcript variant X2
CDKN1A interacting zinc finger protein 1, transcript variant X3
CDKN1A interacting zinc finger protein 1, transcript variant X7
CDKN1A interacting zinc finger protein 1, transcript variant X1
cip1-interacting zinc finger protein isoform X4
cip1-interacting zinc finger protein isoform X3
cip1-interacting zinc finger protein isoform X2
cip1-interacting zinc finger protein isoform X5
cip1-interacting zinc finger protein isoform X1
calcium channel flower domain containing 1
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
ADAM metallopeptidase with thrombospondin type 1 motif 13
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 5 samples with support for all annotated introns
A disintegrin and metalloproteinase with thrombospondin motifs 13
transfer RNA arginine (anticodon UCG); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
REX4 homolog, 3'-5' exonuclease, transcript variant X2
REX4 homolog, 3'-5' exonuclease, transcript variant X1
REX4 homolog, 3'-5' exonuclease, transcript variant X3
similar to RNA sequence (same species):INSD:GGXP01047301.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 130 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 130 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
low-density lipoprotein receptor-related protein 10
endosome associated trafficking regulator 1, transcript variant X2
endosome associated trafficking regulator 1, transcript variant X1
endosome-associated-trafficking regulator 1 isoform X2
endosome-associated-trafficking regulator 1 isoform X1
peptidase, mitochondrial processing subunit alpha
mitochondrial-processing peptidase subunit alpha
inositol polyphosphate-5-phosphatase E, transcript variant X2
inositol polyphosphate-5-phosphatase E, transcript variant X1
phosphatidylinositol polyphosphate 5-phosphatase type IV isoform X2
phosphatidylinositol polyphosphate 5-phosphatase type IV isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 11 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: 1 Protein, and 5% coverage of the annotated genomic feature by RNAseq alignments
sodium-dependent phosphate transport protein 2C-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins
bcl-2-related ovarian killer protein homolog A-like, 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 9 samples with support for all annotated introns
bcl-2-related ovarian killer protein homolog A-like, transcript variant X1
bcl-2-related ovarian killer protein homolog A-like isoform X1
bcl-2-related ovarian killer protein homolog A-like isoform X2
probable inactive glycosyltransferase 25 family member 3
ubiquitin related modifier 1, transcript variant X2
ubiquitin related modifier 1, transcript variant X1
long-chain fatty acid transport protein 4
similar to RNA sequence (same species):INSD:GGXP01066975.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 262 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 262 bases not found in genome assembly; 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: 30 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine kinase like domain containing 1, transcript variant X1
serine/threonine kinase-like domain-containing protein STKLD1 isoform X1
serine/threonine kinase like domain containing 1, transcript variant X2
serine/threonine kinase-like domain-containing protein STKLD1 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 41 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 35 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77% coverage of the annotated genomic feature by RNAseq alignments
meiotic recombination protein REC8 homolog
RNA-binding protein 39-like, transcript variant X2
RNA-binding protein 39-like, transcript variant X1
RNA-binding protein 39-like, transcript variant X3
receptor-interacting serine/threonine-protein kinase 3-like, transcript variant X1
receptor-interacting serine/threonine-protein kinase 3-like, transcript variant X2
receptor-interacting serine/threonine-protein kinase 3-like, transcript variant X3
receptor-interacting serine/threonine-protein kinase 3-like isoform X1
receptor-interacting serine/threonine-protein kinase 3-like isoform X3
receptor-interacting serine/threonine-protein kinase 3-like isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 3 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 68% coverage of the annotated genomic feature by RNAseq alignments
mannose-specific lectin-like, transcript variant X2
mannose-specific lectin-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
endonuclease domain-containing 1 protein-like, 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 14 samples with support for all annotated introns
endonuclease domain-containing 1 protein-like, transcript variant X3
endonuclease domain-containing 1 protein-like isoform X3
endonuclease domain-containing 1 protein-like isoform X2
endonuclease domain-containing 1 protein-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
endonuclease domain-containing 1 protein-like isoform X1
thiamine triphosphatase, transcript variant X1
thiamine triphosphatase, transcript variant X3
thiamine triphosphatase, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 95% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
AT-rich interactive domain-containing protein 4B
translocase of outer mitochondrial membrane 20
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 16 Proteins, and 75% coverage of the annotated genomic feature by RNAseq alignments
mitochondrial import receptor subunit TOM20 homolog
syntaxin binding protein 1, transcript variant X1
syntaxin binding protein 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 1 Protein, and 72% coverage of the annotated genomic feature by RNAseq alignments
probable low affinity copper uptake protein 2
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 35 samples with support for all annotated introns
ER degradation-enhancing alpha-mannosidase-like protein 3, transcript variant X1
ER degradation-enhancing alpha-mannosidase-like protein 3, transcript variant X2
ER degradation-enhancing alpha-mannosidase-like protein 3 isoform X1
ER degradation-enhancing alpha-mannosidase-like protein 3 isoform X2
negative elongation factor complex member B
LOW QUALITY PROTEIN: negative elongation factor B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
euchromatic histone lysine methyltransferase 1
histone-lysine N-methyltransferase EHMT1
calcium voltage-gated channel subunit alpha1 B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 8 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
voltage-dependent N-type calcium channel subunit alpha-1B
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 90% 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: 93% coverage of the annotated genomic feature by RNAseq alignments
uncharacterized LOC122790830, transcript variant X2
uncharacterized LOC122790830, transcript variant X1
uncharacterized LOC122790830, transcript variant X3
discoidin domain-containing receptor 2-like, transcript variant X3
discoidin domain-containing receptor 2-like, transcript variant X2
discoidin domain-containing receptor 2-like, transcript variant X1
discoidin domain-containing receptor 2-like, transcript variant X4
discoidin domain-containing receptor 2-like isoform X2
discoidin domain-containing receptor 2-like isoform X3
discoidin domain-containing receptor 2-like isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 43 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 8 samples with support for all annotated introns
ectonucleoside triphosphate diphosphohydrolase 2
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: inserted 1 base in 1 codon; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 18 Proteins, and 53% 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: rho GTPase-activating protein 19-like
capping protein regulator and myosin 1 linker 3
capping protein, Arp2/3 and myosin-I linker protein 3
CKLF like MARVEL transmembrane domain containing 5, transcript variant X1
CKLF-like MARVEL transmembrane domain-containing protein 5 isoform X1
CKLF like MARVEL transmembrane domain containing 5, transcript variant X2
CKLF-like MARVEL transmembrane domain-containing protein 5 isoform X2
zinc finger protein 239-like, transcript variant X6
zinc finger protein 239-like, transcript variant X1
zinc finger protein 239-like, transcript variant X3
zinc finger protein 239-like, transcript variant X2
zinc finger protein 239-like, transcript variant X5
zinc finger protein 239-like, transcript variant X4
eukaryotic translation initiation factor 3 subunit A-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 94% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 33 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments, including 29 samples with support for all annotated introns
similar to RNA sequence (same species):INSD:GGXP01073275.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 1329 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 42 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 39 samples with support for all annotated introns
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 173 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
multiple epidermal growth factor-like domains protein 9
zinc finger protein 618-like, transcript variant X5
zinc finger protein 618-like, transcript variant X1
zinc finger protein 618-like, transcript variant X4
zinc finger protein 618-like, transcript variant X7
zinc finger protein 618-like, transcript variant X3
zinc finger protein 618-like, transcript variant X9
zinc finger protein 618-like, transcript variant X10
zinc finger protein 618-like, transcript variant X6
zinc finger protein 618-like, transcript variant X11
zinc finger protein 618-like, transcript variant X12
zinc finger protein 618-like, transcript variant X8
zinc finger protein 618-like, transcript variant X13
zinc finger protein 618-like, transcript variant X2
zinc finger protein 618-like isoform X10
zinc finger protein 618-like isoform X11
zinc finger protein 618-like isoform X12
zinc finger protein 521-like, transcript variant X2
zinc finger protein 521-like, transcript variant X1
uncharacterized protein LOC122790475 isoform X2
BMP/retinoic acid inducible neural specific 1, transcript variant X4
BMP/retinoic acid inducible neural specific 1, transcript variant X1
BMP/retinoic acid inducible neural specific 1, transcript variant X3
BMP/retinoic acid inducible neural specific 1, transcript variant X2
BMP/retinoic acid-inducible neural-specific protein 1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
macrophage migration inhibitory factor-like
tripartite motif containing 32, transcript variant X1
tripartite motif containing 32, transcript variant X2
E3 ubiquitin-protein ligase TRIM32 isoform X1
E3 ubiquitin-protein ligase TRIM32 isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 79% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 85 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: 1 mRNA, 2 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 5 samples with support for all annotated introns
tumor necrosis factor ligand superfamily member 8
tumor necrosis factor ligand superfamily member 15
cyclin dependent kinase 9, transcript variant X1
cyclin dependent kinase 9, transcript variant X2
cholesterol 7-desaturase nvd-like, transcript variant X2
cholesterol 7-desaturase nvd-like isoform X2
cholesterol 7-desaturase nvd-like, transcript variant X1
uncharacterized protein LOC122790793 isoform X1
glutamate receptor ionotropic, NMDA 1-like
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
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 39 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 11 samples with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X1
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X4
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X5
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 7 samples with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X6
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 28 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 6 samples with support for all annotated introns
glutamate ionotropic receptor NMDA type subunit 1, transcript variant X3
glutamate receptor ionotropic, NMDA 1 isoform X1
glutamate receptor ionotropic, NMDA 1 isoform X4
glutamate receptor ionotropic, NMDA 1 isoform X3
glutamate receptor ionotropic, NMDA 1 isoform X2
glutamate receptor ionotropic, NMDA 1 isoform X5
glutamate receptor ionotropic, NMDA 1 isoform X6
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: anaphase-promoting complex subunit 2
NADPH dependent diflavin oxidoreductase 1
similar to RNA sequence (same species):INSD:GGXP01062811.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 99 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 99 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
NADPH-dependent diflavin oxidoreductase 1
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase 9-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 53 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
ring finger protein 208, transcript variant X2
ring finger protein 208, transcript variant X1
tripartite motif-containing protein 2-like
uncharacterized LOC122790341, transcript variant X2
uncharacterized LOC122790341, transcript variant X1
endothelial differentiation related factor 1
endothelial differentiation-related factor 1
similar to RNA sequence (same species):INSD:GGXP01030884.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 125 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 125 bases not found in genome assembly; 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: 7 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 23 samples with support for all annotated introns
alpha-1-microglobulin/bikunin precursor, transcript variant X1
alpha-1-microglobulin/bikunin precursor, transcript variant X2
notch-regulated ankyrin repeat-containing protein
similar to RNA sequence (same species):INSD:GGXP01057245.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 65 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 94% coverage of the annotated genomic feature by RNAseq alignments
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 65 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
NADPH oxidase activator 1, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments, including 9 samples with support for all annotated introns
NADPH oxidase activator 1, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 8, transcript variant X2
ectonucleoside triphosphate diphosphohydrolase 8, transcript variant X1
ectonucleoside triphosphate diphosphohydrolase 8, transcript variant X3
ectonucleoside triphosphate diphosphohydrolase 8
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X1
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X3
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X3
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X1
NMDA receptor synaptonuclear signaling and neuronal migration factor, transcript variant X2
NMDA receptor synaptonuclear signaling and neuronal migration factor isoform X2
COORDINATES: nucleotide motif:Rfam:12.0:RF00302
zinc finger MYND domain-containing protein 19, transcript variant X3
zinc finger MYND domain-containing protein 19, transcript variant X1
zinc finger MYND domain-containing protein 19 isoform X1
zinc finger MYND domain-containing protein 19, transcript variant X4
zinc finger MYND domain-containing protein 19, transcript variant X2
zinc finger MYND domain-containing protein 19 isoform X2
zinc finger MYND domain-containing protein 19 isoform X3
zinc finger MYND domain-containing protein 19-like
leucine rich repeat and sterile alpha motif containing 1
similar to RNA sequence (same species):INSD:GGXP01071624.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 123 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 123 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
solute carrier family 31 member 1, transcript variant X3
solute carrier family 31 member 1, transcript variant X1
solute carrier family 31 member 1, transcript variant X2
high affinity copper uptake protein 1 isoform X1
high affinity copper uptake protein 1 isoform X2
anaphase-promoting complex subunit CDC26
pre-mRNA processing factor 4, transcript variant X1
vesicle-associated membrane protein 2-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 50 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments, including 32 samples with support for all annotated introns
pre-mRNA processing factor 4, transcript variant X2
U4/U6 small nuclear ribonucleoprotein Prp4
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 13 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 20 samples with support for all annotated introns
B box and SPRY domain-containing protein
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X5
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X4
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X3
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X2
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X1
haloacid dehalogenase like hydrolase domain containing 3, transcript variant X6
haloacid dehalogenase-like hydrolase domain-containing protein 3
LOW QUALITY PROTEIN: delta-aminolevulinic acid dehydratase
DNA polymerase epsilon 3, accessory subunit
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 26 samples with support for all annotated introns
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 3 Proteins, and 76% coverage of the annotated genomic feature by RNAseq alignments
interleukin enhancer-binding factor 3-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 72% coverage of the annotated genomic feature by RNAseq alignments
eosinophil granule major basic protein 2-like
4-galactosyl-N-acetylglucosaminide 3-alpha-L-fucosyltransferase FUT5-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 61 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
beta-1,4-galactosyltransferase galt-1-like, transcript variant X2
beta-1,4-galactosyltransferase galt-1-like, transcript variant X1
beta-1,4-galactosyltransferase galt-1-like
transfer RNA valine (anticodon CAC); Derived by automated computational analysis using gene prediction method: tRNAscan-SE.
LIM domain transcription factor LMO4-A, transcript variant X2
LIM domain transcription factor LMO4-A isoform X2
LIM domain transcription factor LMO4-A, transcript variant X5
LIM domain transcription factor LMO4-A, transcript variant X4
LIM domain transcription factor LMO4-A isoform X4
LIM domain transcription factor LMO4-A, transcript variant X1
LIM domain transcription factor LMO4-A isoform X1
LIM domain transcription factor LMO4-A, transcript variant X3
LIM domain transcription factor LMO4-A isoform X3
LIM domain transcription factor LMO4-A isoform X5
uncharacterized threonine-rich GPI-anchored glycoprotein PJ4664.02-like
trimeric autotransporter adhesin AtaA-like
repetitive proline-rich cell wall protein 2-like
hyaluronan mediated motility receptor-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 96% coverage of the annotated genomic feature by RNAseq alignments
serine/threonine-protein kinase Sgk1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 4 Proteins, and 38% coverage of the annotated genomic feature by RNAseq alignments
family with sequence similarity 78 member A
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 18 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 83% coverage of the annotated genomic feature by RNAseq alignments
COORDINATES: nucleotide motif:Rfam:12.0:RF00153
TOX high mobility group box family member 4, transcript variant X2
TOX high mobility group box family member 4, transcript variant X1
TOX high mobility group box family member 4, transcript variant X3
TOX high mobility group box family member 4 isoform X1
TOX high mobility group box family member 4 isoform X2
TOX high mobility group box family member 4 isoform X3
chromodomain helicase DNA binding protein 8
similar to RNA sequence (same species):INSD:GGXP01057967.1
The sequence of the model RefSeq transcript was modified relative to this genomic sequence to represent the inferred CDS: added 565 bases not found in genome assembly
The sequence of the model RefSeq protein was modified relative to this genomic sequence to represent the inferred CDS: added 565 bases not found in genome assembly; Derived by automated computational analysis using gene prediction method: Gnomon.
chromodomain-helicase-DNA-binding protein 8
dolichyl-diphosphooligosaccharide--protein glycosyltransferase subunit DAD1
SPT16 homolog, facilitates chromatin remodeling subunit
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 51 Proteins, and 100% coverage of the annotated genomic feature by RNAseq alignments
methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit, transcript variant X2
methyltransferase 3, N6-adenosine-methyltransferase complex catalytic subunit, transcript variant X1
N6-adenosine-methyltransferase catalytic subunit isoform X2
N6-adenosine-methyltransferase catalytic subunit isoform X1
heterogeneous nuclear ribonucleoprotein C, transcript variant X1
heterogeneous nuclear ribonucleoprotein C, transcript variant X2
heterogeneous nuclear ribonucleoproteins C1/C2 isoform X1
heterogeneous nuclear ribonucleoproteins C1/C2 isoform X2
DNA repair protein SWI5 homolog, transcript variant X3
DNA repair protein SWI5 homolog isoform X3
DNA repair protein SWI5 homolog, transcript variant X1
DNA repair protein SWI5 homolog, transcript variant X2
DNA repair protein SWI5 homolog, transcript variant X5
DNA repair protein SWI5 homolog, transcript variant X4
DNA repair protein SWI5 homolog isoform X4
DNA repair protein SWI5 homolog isoform X5
DNA repair protein SWI5 homolog isoform X1
DNA repair protein SWI5 homolog isoform X2
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 22 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
cilia- and flagella-associated protein 157-like
Tu translation elongation factor, mitochondrial, transcript variant X2
Tu translation elongation factor, mitochondrial, transcript variant X1
elongation factor Tu, mitochondrial isoform X2
elongation factor Tu, mitochondrial isoform X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 55 Proteins
zinc finger protein 560-like, transcript variant X2
zinc finger protein 560-like, transcript variant X1
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 7 Proteins, and 98% coverage of the annotated genomic feature by RNAseq alignments
gastrula zinc finger protein XlCGF26.1-like
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 77 Proteins, and 99% coverage of the annotated genomic feature by RNAseq alignments
Derived by automated computational analysis using gene prediction method: Gnomon. Supporting evidence includes similarity to: 70 Proteins, and 66% coverage of the annotated genomic feature by RNAseq alignments
LOW QUALITY PROTEIN: zinc finger protein 3-like