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: Anatomical entity
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: WDHD1 ENSSSCG00000005052

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Description

WD repeat and HMG-box DNA binding protein 1 [Source:VGNC Symbol;Acc:VGNC:94904]

Location

Primary_assembly 1: 184,300,293-184,378,959 reverse strand.

Sscrofa11.1:CM000812.5

About this gene

This gene has 3 transcripts (splice variants) and 210 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSSSCT00000005569.5	WDHD1-202	4107	1129aa	ENSSSCP00000005431.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D1Z902 F1SSP1	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 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,
ENSSSCT00000089298.1	WDHD1-203	3968	1057aa	ENSSSCP00000064203.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A5G2QHD6 A0A8D1ZAN9	-
ENSSSCT00000027382.2	WDHD1-201	3830	1046aa	ENSSSCP00000020519.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8D2CBS3 I3L908	-

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Breeds

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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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