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
  - Paralogues
Ontologies
- GO: Biological process
- GO: Cellular component
- GO: Molecular function
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID History
- Gene history

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Gene: Wdr47 ENSRNOG00000020330

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Description

WD repeat domain 47 [Source:RGD Symbol;Acc:1309181]

Gene Synonyms

LOC310785, RGD1309181

Location

Primary_assembly 2: 198,914,940-198,975,841 forward strand.

GRCr8:CM070392.1

About this gene

This gene has 2 transcripts (splice variants), 273 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000055862.4	Wdr47-201	4159	928aa	ENSRNOP00000052715.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3V9M3	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,
ENSRNOT00000105849.2	Wdr47-202	4319	921aa	ENSRNOP00000077485.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I5Y1M2 A6HV14	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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