Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
- Paralogues
- Strains
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Molecular function
- GO: Biological process
- GO: Cellular component
Phenotypes
Genetic Variation
- Variant table
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- Structural variants
Gene expression
Pathway
Molecular interactions
External references
Supporting evidence
ID 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) and 210 orthologues.

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, 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,
ENSRNOT00000133811.1	Wdr33-202	4569	1331aa	ENSRNOP00000112834.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
ENSRNOT00000168101.1	Wdr33-204	4460	1277aa	ENSRNOP00000102257.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	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,
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	-

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Summary

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