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: fam219aa ENSDARG00000016396

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Description

family with sequence similarity 219 member Aa [Source:NCBI gene;Acc:445197]

Gene Synonyms

fam219a, zgc:101028

Location

Chromosome 21: 13,093,136-13,123,185 reverse strand.

GRCz11:CM002905.2

About this gene

This gene has 4 transcripts (splice variants), 206 orthologues and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSDART00000024616.9	fam219aa-201	1303	186aa	ENSDARP00000002156.7	Gene/transcipt that contains an open reading frame (ORF).Protein coding	Q6DC60	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,
ENSDART00000144866.3	fam219aa-204	886	185aa	ENSDARP00000123113.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	E9QD86	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,
ENSDART00000135623.2	fam219aa-202	406	64aa	ENSDARP00000115661.1	Nonsense mediated decay	E9QFS7	-
ENSDART00000140281.2	fam219aa-203	678	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron	-	-

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Summary

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