Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
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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: Wdr33 ENSRNOG00000011382

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Description

WD repeat domain 33 [Source:RGD Symbol;Acc:1309230]

Gene Synonyms

LOC307524

Location

Primary_assembly 18: 23,706,602-23,809,708 forward strand.

GRCr8:CM070408.1

About this gene

This gene has 6 transcripts (splice variants), 214 orthologues and is associated with 1 phenotype.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000173447.1	Wdr33-206	4635	1343aa	ENSRNOP00000110865.1	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,
ENSRNOT00000133811.1	Wdr33-202	4569	1331aa	ENSRNOP00000112834.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000168101.1	Wdr33-204	4460	1277aa	ENSRNOP00000102257.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000172505.1	Wdr33-205	1210	312aa	ENSRNOP00000110186.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000141009.1	Wdr33-203	1096	275aa	ENSRNOP00000100588.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-
ENSRNOT00000017075.7	Wdr33-201	1063	263aa	ENSRNOP00000017075.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1LT09	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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Strains

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Genomic alignments

Gene tree

Orthologues

Paralogues (Not available)

Families (Not available)

More views of comparative genomics data, such as multiple alignments and synteny, are available on the Location page for this gene.

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Personal Data