Description

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

Synonyms

wu:fb26e12, wu:fb52h08

Location
INSDC coordinates

chromosome:Zv9:CU651617.3:10855604:10934803:1

About this gene

This gene has 4 transcripts (splice variants), 62 orthologues, 3 paralogues and is a member of 1 Ensembl protein family.

NameTranscript IDbpProteinTranslation IDBiotypeUniProtRefSeqFlags
atrx-001ENSDART0000012759466922011aaENSDARP00000105895
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
E7F4M2 F1QQ67 NM_200653
NP_956947
APPRIS PI5APPRIS candidate principal isoform (longest coding sequence)
Glossary entry for APPRIS
APPRIS website
atrx-202ENSDART0000012586548601620aaENSDARP00000109014
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
F1QJ36 -APPRIS ALT2APPRIS candidate principal isoform that appears to be conserved in fewer than three tested non-primate species
Glossary entry for APPRIS
APPRIS website
atrx-201ENSDART000000619323185995aaENSDARP00000061931
 
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