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 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000267430.5FANCM-00171112048aaENSP00000267430.5
 
Protein coding
CCDS32070Q8IYD8 NM_020937.2GENCODE basic
ENST00000542564.2FANCM-00361672022aaENSP00000442493.2
 
Protein coding
B2RTQ9 -GENCODE basic
ENST00000556250.1FANCM-00455771564aaENSP00000452033.1
 
Protein coding
H0YJS3 -CDS 5' incomplete
ENST00000554809.1FANCM-00531121016aaENSP00000450632.1
 
Protein coding
--CDS 5' incomplete
ENST00000556036.1FANCM-0022354669aaENSP00000450596.1
 
Protein coding
Q8IYD8 -GENCODE basic
ENST00000555484.1FANCM-009448106aaENSP00000450797.1
 
Protein coding
H0YJ45 -CDS 5' incomplete
ENST00000557110.1FANCM-010638135aaENSP00000451846.1
 
Nonsense mediated decay
H0YJN7 -CDS 5' incomplete
ENST00000555013.1FANCM-007573No protein-
 
Processed transcript
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ENST00000554030.1FANCM-006917No protein-
 
Retained intron
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ENST00000553551.1FANCM-008603No protein-
 
Retained intron
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