Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
- Paralogues
- Breeds
  - Gene tree
  - Orthologues
  - Paralogues
Ontologies
- GO: Biological process
- GO: Molecular function
- GO: Cellular component
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: WFDC2 ENSBTAG00000013928

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Description

WAP four-disulfide core domain 2 [Source:VGNC Symbol;Acc:VGNC:36933]

Location

Primary_assembly 13: 74,360,835-74,367,976 forward strand.

ARS-UCD1.3:CM008180.2

About this gene

This gene has 4 transcripts (splice variants) and 100 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSBTAT00000066322.3	WFDC2-201	532	169aa	ENSBTAP00000054125.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	G3MX65	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,
ENSBTAT00000121635.1	WFDC2-203	545	123aa	ENSBTAP00000075848.1	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,
ENSBTAT00000018498.5	WFDC2-202	517	164aa	ENSBTAP00000018498.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	F6R695	-
ENSBTAT00000077883.2	WFDC2-204	504	116aa	ENSBTAP00000068335.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q3T0Z0	-

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Summary

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