Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Anatomical entity
Phenotypes
Genetic Variation
- Variant table
- Variant image
- Structural variants
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: Abhd8 ENSRNOG00000000054

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Description

abhydrolase domain containing 8 [Source:RGD Symbol;Acc:1305693]

Gene Synonyms

LOC306338

Location

Primary_assembly 16: 18,178,441-18,191,638 reverse strand.

GRCr8:CM070406.1

About this gene

This gene has 2 transcripts (splice variants), 281 orthologues and 12 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000096877.2	Abhd8-202	2046	459aa	ENSRNOP00000088470.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AIY3	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,
ENSRNOT00000000060.8	Abhd8-201	1982	441aa	ENSRNOP00000000060.4	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B5DEN3 B5DEQ5	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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Paralogues

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