Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
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- Gene gain/loss tree
- Orthologues
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Phenotypes
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ID History
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Gene: WDR44 ENSBTAG00000018697

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Description

WD repeat domain 44 [Source:VGNC Symbol;Acc:VGNC:36900]

Location

Primary_assembly X: 2,534,635-2,628,017 forward strand.

ARS-UCD2.0:CM008197.2

About this gene

This gene has 3 transcripts (splice variants) and 200 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000024883.7	WDR44-201	4124	912aa	ENSBTAP00000024883.6	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q9XSC3	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 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,
ENSBTAT00000108090.2	WDR44-202	3857	823aa	ENSBTAP00000086225.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9SQE1	-
ENSBTAT00000096984.1	WDR44-203	3834	887aa	ENSBTAP00000093102.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0AAA9TAR3	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,

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Summary

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