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Human (GRCh37.p13)
Description

Fanconi anemia, complementation group G [Source:HGNC Symbol;Acc:3588]

Gene Synonyms

FAG, XRCC9

Location

Chromosome 9: 35,073,832-35,080,013 reverse strand.

GRCh37:CM000671.1

About this gene

This gene has 8 transcripts (splice variants) and is associated with 59 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
FANCG-001ENST00000378643.32631622aaENSP00000367910.3
 
Protein coding
CCDS6574C9JSE3 O15287 Q53XM5
NM_004629
NP_004620
GENCODE basic
FANCG-003ENST00000448890.1868215aaENSP00000409607.1
 
Protein coding
-C9JSE3 -CDS 3' incomplete
FANCG-005ENST00000425676.12108106aaENSP00000412793.1
 
Nonsense mediated decay
-F8WC08 --
FANCG-002ENST00000476212.1484No protein-
 
Processed transcript
----
FANCG-004ENST00000462124.1654No protein-
 
Retained intron
----
FANCG-008ENST00000481254.1592No protein-
 
Retained intron
----
FANCG-006ENST00000474894.1572No protein-
 
Retained intron
----
FANCG-007ENST00000461149.1388No protein-
 
Retained intron
----

Gene-based displays