Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
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Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
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- Structural variants
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Molecular interactions
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ID History
- Gene history

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Gene: Wtap ENSRNOG00000019091

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Description

WT1 associated protein [Source:RGD Symbol;Acc:1563824]

Gene Synonyms

LOC499020, RGD1563824

Location

Primary_assembly 1: 50,070,769-50,096,072 forward strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 214 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000102248.2	Wtap-203	2034	395aa	ENSRNOP00000077397.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5XW36	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical,
ENSRNOT00000079312.3	Wtap-202	1872	151aa	ENSRNOP00000072376.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0G2K2U2	-
ENSRNOT00000025936.9	Wtap-201	1446	170aa	ENSRNOP00000025936.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZPY0	APPRIS P1: Transcript(s) expected to code for the main functional isoform based solely on the core modules in the APPRIS. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P1,

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Summary

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