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.

Show/hide columns (1 hidden)
  • Transcript ID
  • Name
  • bp
  • Protein
  • Translation ID
  • Biotype
  • CCDS
  • UniProt Match
  • RefSeq
  • Flags
Transcript IDNamebpProteinBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000267430.5FANCM-00171112048aa
 
Protein coding
CCDS32070Q8IYD8 NM_020937.2Ensembl CanonicalGENCODE Basic
ENST00000542564.2FANCM-00361672022aa
 
Protein coding
B2RTQ9 -GENCODE Basic
ENST00000556250.1FANCM-00455771564aa
 
Protein coding
H0YJS3 -CDS 5' incomplete
ENST00000554809.1FANCM-00531121016aa
 
Protein coding
--CDS 5' incomplete
ENST00000556036.1FANCM-0022354669aa
 
Protein coding
Q8IYD8 -GENCODE Basic
ENST00000555484.1FANCM-009448106aa
 
Protein coding
H0YJ45 -CDS 5' incomplete
ENST00000557110.1FANCM-010638135aa
 
Nonsense mediated decay
H0YJN7 -CDS 5' incomplete
ENST00000555013.1FANCM-007573No protein
 
Processed transcript
---
ENST00000554030.1FANCM-006917No protein
 
Retained intron
---
ENST00000553551.1FANCM-008603No protein
 
Retained intron
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