Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: WDR45B ENSBTAG00000003695

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Description

WD repeat domain 45B [Source:VGNC Symbol;Acc:VGNC:36901]

Location

Primary_assembly 19: 49,991,255-50,028,477 forward strand.

ARS-UCD1.3:CM008186.2

About this gene

This gene has 4 transcripts (splice variants), 208 orthologues and 3 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000093790.1	WDR45B-203	2088	415aa	ENSBTAP00000100318.1	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,
ENSBTAT00000132987.1	WDR45B-201	2542	405aa	ENSBTAP00000101378.1	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,
ENSBTAT00000004811.5	WDR45B-202	2143	310aa	ENSBTAP00000004811.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F1MW27	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,
ENSBTAT00000106860.1	WDR45B-204	2037	324aa	ENSBTAP00000094322.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	-	-

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Summary

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