Description

alpha thalassemia/mental retardation syndrome X-linked homolog (human) [Source:ZFIN;Acc:ZDB-GENE-030912-11]

Synonyms

wu:fb26e12, wu:fb52h08, wu:fb72g09

JMS, RAD54, XH2, XNP

Location
INSDC coordinates

chromosome:GRCz10:CM002898.1:10350961:10431884:1

About this gene

This gene has 4 transcripts (splice variants), 68 orthologues, 3 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeUniProtRefSeqFlags
atrx-001ENSDART0000012586584162011aaENSDARP00000109014
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
F1QJ36 -APPRIS P5

PRINCIPAL5 - APPRIS candidate principal isoform (longest coding sequence).

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

atrx-202ENSDART0000012759474832013aaENSDARP00000105895
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
E7F4M2 NM_200653
NP_956947
APPRIS P5

PRINCIPAL5 - APPRIS candidate principal isoform (longest coding sequence).

APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods.

atrx-201ENSDART000000619322795731aaENSDARP00000061931
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
F1QQ67 -
atrx-002ENSDART00000146030581No protein-
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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Gene-based displays