WTAP WT1 associated protein [Macaca mulatta (Rhesus monkey)] - Gene

Summary

Official Symbol: WTAPprovided by VGNC
Official Full Name: WT1 associated proteinprovided by VGNC
Primary source: VGNC:VGNC:83971
See related: Ensembl:ENSMMUG00000012837
Gene type: protein coding
RefSeq status: PROVISIONAL
Organism: Macaca mulatta
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs: human mouse all
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Genomic context

Location:: chromosome: 4

Exon count:: 9

Annotation release	Status	Assembly	Chr	Location
103	current	Mmul_10 (GCF_003339765.1)	4	NC_041757.1 (10843745..10873679, complement)
102	previous assembly	Mmul_8.0.1 (GCF_000772875.2)	4	NC_027896.1 (160846476..160876763)

Chromosome 4 - NC_041757.1 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

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General gene information

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Markers

MARC_17739-17740:1031760457:1 (e-PCR)
- UniSTS:268391

RH45346 (e-PCR)
- UniSTS:75903

RH45351 (e-PCR)
- UniSTS:79551

RH25332 (e-PCR)
- UniSTS:84682

RH45141 (e-PCR)
- UniSTS:48858

Wtap (e-PCR), detects polymorphism
- UniSTS:498921

D6S1433 (e-PCR)
- UniSTS:66286

RH40826 (e-PCR)
- UniSTS:92153

Gene Ontology Provided by RefSeq

Process	Evidence Code	Pubs
involved_in regulation of alternative mRNA splicing, via spliceosome	IEA Inferred from Electronic Annotation more info	PubMed

Component	Evidence Code	Pubs
located_in nucleus	IEA Inferred from Electronic Annotation more info	PubMed

General protein information

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Preferred Names: pre-mRNA-splicing regulator WTAP

Names: Wilms tumor 1 associated protein

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.