Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Orthologues
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Ontologies
- GO: Anatomical entity
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Genetic Variation
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Gene: Wdr76 ENSRNOG00000022491

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Description

WD repeat domain 76 [Source:RGD Symbol;Acc:1309616]

Gene Synonyms

LOC311361, RGD1309616

Location

Primary_assembly 3: 128,910,503-128,945,239 forward strand.

GRCr8:CM070393.1

About this gene

This gene has 3 transcripts (splice variants), 200 orthologues and is associated with 3 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000155942.1	Wdr76-203	3437	638aa	ENSRNOP00000102214.1	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,
ENSRNOT00000109502.2	Wdr76-202	3249	542aa	ENSRNOP00000097696.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AUS0 A6HPQ1	APPRIS ALT2: 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 appear to be conserved in fewer than 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 ALT2,
ENSRNOT00000036209.5	Wdr76-201	3193	621aa	ENSRNOP00000034184.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	D3ZJT1	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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Summary

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