Human (GRCh38.p14)
Description

FA complementation group D2 [Source:HGNC Symbol;Acc:HGNC:3585]

Gene Synonyms

FA-D2, FACD, FAD, FANCD

Location

Chromosome 3: 10,026,370-10,101,932 forward strand.

GRCh38:CM000665.2

About this gene

This gene has 18 transcripts (splice variants), 192 orthologues and is associated with 76 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000675286.1FANCD2-21250961451aaENSP00000502379.1
 
Protein coding
CCDS33696Q9BXW9-2 NM_001018115.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P2
ENST00000287647.7FANCD2-20152191471aaENSP00000287647.3
 
Protein coding
CCDS2595Q9BXW9-1 -GENCODE basicAPPRIS ALT2TSL:1
ENST00000419585.5FANCD2-20251851451aaENSP00000398754.1
 
Protein coding
CCDS33696Q9BXW9-2 -GENCODE basicAPPRIS P2TSL:1
ENST00000676013.1FANCD2-21343341414aaENSP00000501999.1
 
Protein coding
A0A6Q8PFY3 -CDS 3' incomplete
ENST00000431693.1FANCD2-2042450241aaENSP00000399354.1
 
Protein coding
Q9BXW9-4 -GENCODE basicTSL:1
ENST00000625535.1FANCD2-21111738aaENSP00000486945.1
 
Protein coding
F8WE37 -GENCODE basicTSL:5
ENST00000421731.5FANCD2-2033425749aaENSP00000389936.1
 
Nonsense mediated decay
H7BZJ7 -TSL:1CDS 5' incomplete
ENST00000682647.1FANCD2-215214538aaENSP00000506736.1
 
Nonsense mediated decay
F8WE37 --
ENST00000435522.5FANCD2-20556738aaENSP00000402166.1
 
Nonsense mediated decay
F8WE37 -TSL:4
ENST00000681997.1FANCD2-2143559No protein-
 
Protein coding CDS not defined
---
ENST00000683263.1FANCD2-2163474No protein-
 
Protein coding CDS not defined
---
ENST00000438741.1FANCD2-206558No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000470757.5FANCD2-209547No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000470028.1FANCD2-208449No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000683312.1FANCD2-2174010No protein-
 
Retained intron
---
ENST00000683933.1FANCD2-218836No protein-
 
Retained intron
---
ENST00000480909.1FANCD2-210603No protein-
 
Retained intron
--TSL:2
ENST00000464934.1FANCD2-207563No protein-
 
Retained intron
--TSL:4