Human (GRCh37.p13)
Description

Fanconi anemia, complementation group D2 [Source:HGNC Symbol;Acc:3585]

Gene Synonyms

FA-D2, FA4, FACD, FAD, FAD2, FANCD

Location

Chromosome 3: 10,068,098-10,143,614 forward strand.

GRCh37:CM000665.1

About this gene

This gene has 13 transcripts (splice variants) and is associated with 77 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000287647.3FANCD2-00152191471aaENSP00000287647.3
 
Protein coding
CCDS2595Q9BXW9 NM_033084.3GENCODE basic
ENST00000419585.1FANCD2-00251851451aaENSP00000398754.1
 
Protein coding
CCDS33696Q9BXW9 -GENCODE basic
ENST00000383807.1FANCD2-20251021451aaENSP00000373318.1
 
Protein coding
CCDS33696Q9BXW9 NM_001018115.1GENCODE basic
ENST00000383806.1FANCD2-20150081249aaENSP00000373317.1
 
Protein coding
Q9BXW9 -GENCODE basic
ENST00000431693.1FANCD2-0032450241aaENSP00000399354.1
 
Protein coding
Q9BXW9 -GENCODE basic
ENST00000421731.1FANCD2-0043425749aaENSP00000389936.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000435522.1FANCD2-00556738aaENSP00000402166.1
 
Nonsense mediated decay
F8WE37 --
ENST00000438741.1FANCD2-008558No protein-
 
Processed transcript
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ENST00000470757.1FANCD2-011547No protein-
 
Processed transcript
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ENST00000483276.1FANCD2-006505No protein-
 
Processed transcript
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ENST00000470028.1FANCD2-012449No protein-
 
Processed transcript
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ENST00000480909.1FANCD2-010603No protein-
 
Retained intron
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ENST00000464934.1FANCD2-007563No protein-
 
Retained intron
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