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Protein Coding Gene : Wtap WT1 associating protein
Primary Identifier  MGI:1926395 Organism  mouse, laboratory
Chromosome  17 NCBI Gene Number  60532
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 8.0.0)

Predicted to enable identical protein binding activity. Predicted to be involved in mRNA modification; mRNA processing; and regulation of alternative mRNA splicing, via spliceosome. Located in cytoplasm and nucleoplasm. Part of RNA N6-methyladenosine methyltransferase complex. Is expressed in several structures, including early conceptus; embryo mesoderm; hemolymphoid system gland; hindlimb; and jaw epithelium. Orthologous to human WTAP (WT1 associated protein).
PHENOTYPE: Mice homozygous for a mutation display lethality during embryogenesis with abnormalities appearing during gastrulation. [provided by MGI curators]
  • synonyms:
  • WT1 associating protein,
  • MGI:1924525,
  • MGI:1922064,
  • RIKEN cDNA 2810408K05 gene,
  • 2810408K05Rik,
  • RIKEN cDNA 9430038B09 gene,
  • 9430038B09Rik,
  • Wtap
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Features --> Cross References

Genome

Sequence Feature Displayer

JG Browse Displayer

0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

1 Involved In Mutations

Trail: ProteinCodingGene

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

2 Pathways

Trail: ProteinCodingGene

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For





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