Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
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: Wdr37 ENSRNOG00000016834

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Description

WD repeat domain 37 [Source:RGD Symbol;Acc:1306189]

Gene Synonyms

LOC307075

Location

Primary_assembly 17: 66,547,147-66,613,841 forward strand.

GRCr8:CM070407.1

About this gene

This gene has 6 transcripts (splice variants), 261 orthologues, 1 paralogue and is associated with 9 phenotypes.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000123865.1	Wdr37-204	4429	496aa	ENSRNOP00000101152.1	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, 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,
ENSRNOT00000165066.1	Wdr37-206	4453	464aa	ENSRNOP00000105222.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000022688.7	Wdr37-201	4356	449aa	ENSRNOP00000022688.5	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A6KRN7 D3ZQ02	-
ENSRNOT00000100659.2	Wdr37-202	4341	494aa	ENSRNOP00000091653.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AE33	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,
ENSRNOT00000104845.2	Wdr37-203	4182	451aa	ENSRNOP00000086670.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GF74	-
ENSRNOT00000136396.1	Wdr37-205	1631	459aa	ENSRNOP00000107974.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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