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Human (GRCh37.p13)
Description

Fanconi anemia, complementation group B [Source:HGNC Symbol;Acc:3583]

Gene Synonyms

FA2, FAAP90, FAAP95, FAB, FACB, FLJ34064

Location

Chromosome X: 14,861,529-14,891,191 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 4 transcripts (splice variants) and is associated with 5 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
FANCB-201ENST00000398334.13008859aaENSP00000381378.1
 
Protein coding
CCDS14161C9J5X9 Q8NB91 NM_001018113
NP_001018123
GENCODE basic
FANCB-001ENST00000324138.32894859aaENSP00000326819.3
 
Protein coding
CCDS14161C9J5X9 Q8NB91 NM_152633
NP_689846
GENCODE basic
FANCB-002ENST00000452869.12712818aaENSP00000397849.1
 
Protein coding
-C9J5X9 -CDS 3' incomplete
FANCB-003ENST00000489126.1559No protein-
 
Retained intron
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Gene-based displays