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: Wdr7 ENSRNOG00000018387

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Description

WD repeat domain 7 [Source:RGD Symbol;Acc:619836]

Gene Synonyms

Trag, Wd7

Location

Primary_assembly 18: 59,435,768-59,718,800 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 2 transcripts (splice variants), 214 orthologues and 25 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000025325.5	Wdr7-201	7068	1488aa	ENSRNOP00000025325.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9ERH3-1	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, APPRIS ALT1: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that is conserved in at least three tested species. 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 ALT1,
ENSRNOT00000110066.2	Wdr7-202	7054	1465aa	ENSRNOP00000082010.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9ERH3-2	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,

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Orthologues

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