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Human (GRCh37.p13)
Description

Fanconi anemia, complementation group M [Source:HGNC Symbol;Acc:23168]

Gene Synonyms

FAAP250, KIAA1596

Location

Chromosome 14: 45,605,143-45,670,093 forward strand.

GRCh37:CM000676.1

About this gene

This gene has 10 transcripts (splice variants) and is associated with 4 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
FANCM-001ENST00000267430.571112048aaENSP00000267430.5
 
Protein coding
CCDS32070Q8IYD8 NM_020937
NP_065988
GENCODE basic
FANCM-003ENST00000542564.261672022aaENSP00000442493.2
 
Protein coding
-B2RTQ9 -GENCODE basic
FANCM-004ENST00000556250.155771564aaENSP00000452033.1
 
Protein coding
-H0YJS3 -CDS 5' incomplete
FANCM-005ENST00000554809.131121016aaENSP00000450632.1
 
Protein coding
---CDS 5' incomplete
FANCM-002ENST00000556036.12354669aaENSP00000450596.1
 
Protein coding
-Q8IYD8 -GENCODE basic
FANCM-009ENST00000555484.1448106aaENSP00000450797.1
 
Protein coding
-H0YJ45 -CDS 5' incomplete
FANCM-010ENST00000557110.1638135aaENSP00000451846.1
 
Nonsense mediated decay
-H0YJN7 -CDS 5' incomplete
FANCM-007ENST00000555013.1573No protein-
 
Processed transcript
----
FANCM-006ENST00000554030.1917No protein-
 
Retained intron
----
FANCM-008ENST00000553551.1603No protein-
 
Retained intron
----

Gene-based displays