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ABCR gene
1p22.1-p21
Pathology:
- defects associated with Stargardt disease type 1
Related
retinal-specific ATP-binding cassette transporter; ATP-binding cassette sub-family A member 4; RIM ABC transporter; RIM protein; RmP; Stargardt disease protein (ABCA4 ABCR)
General
unclassified gene
Properties
TEMPLATE-FOR: messenger RNA
TEMPLATE-FOR: retinal-specific ATP-binding cassette transporter
LOCUS: human chromosome-1 P21-13
MOTIF: transcription factor binding site
transcriptional start site
exon
intron
transcriptional termination site
Database Correlations
OMIM 601691
MORBIDMAP 601691
Entrez Gene 24
References
OMIM :accession 601691