Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
Ontologies
- GO: Molecular function
- GO: Biological process
- 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: adam12 ENSDARG00000079068

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Description

ADAM metallopeptidase domain 12 [Source:ZFIN;Acc:ZDB-GENE-070809-1]

Gene Synonyms

adam12a

Location

Chromosome 17: 32,158,951-32,334,107 forward strand.

GRCz11:CM002901.2

About this gene

This gene has 3 transcripts (splice variants), 197 orthologues and 18 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000165348.2	adam12-203	3205	941aa	ENSDARP00000135966.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A0R4INJ8	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 P5: Where the APPRIS core modules are unable to choose a clear principal variant and none of the candidate variants are annotated by CCDS, APPRIS selects the longest of the candidate isoforms as 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 P5,
ENSDART00000108736.5	adam12-201	4497	924aa	ENSDARP00000099354.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E7FEZ4	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,
ENSDART00000157347.2	adam12-202	894	48aa	ENSDARP00000129618.1	Nonsense mediated decay	X1WHA6	5' truncation in transcript evidence prevents annotation of the start of the CDS.CDS 5' incomplete,

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Summary

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