Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Wdr27 ENSRNOG00000015609

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Description

WD repeat domain 27 [Source:RGD Symbol;Acc:1309633]

Gene Synonyms

LOC102547091, LOC308222, RGD1309633

Location

Primary_assembly 1: 64,504,582-64,623,625 reverse strand.

GRCr8:CM070391.1

About this gene

This gene has 3 transcripts (splice variants), 205 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000121631.1	Wdr27-202	3595	817aa	ENSRNOP00000111064.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000021141.9	Wdr27-201	2478	785aa	ENSRNOP00000021141.8	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1M8Z5	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. 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 P2,
ENSRNOT00000142024.1	Wdr27-203	2408	707aa	ENSRNOP00000108767.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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