Human (GRCh37.p13)
Description

Fanconi anemia, complementation group L [Source:HGNC Symbol;Acc:20748]

Gene Synonyms

FAAP43, FLJ10335, PHF9, POG, Pog

Location

Chromosome 2: 58,386,378-58,468,507 reverse strand.

GRCh37:CM000664.1

About this gene

This gene has 11 transcripts (splice variants) and is associated with 5 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000402135.3FANCL-0021698380aaENSP00000385021.3
 
Protein coding
CCDS46294Q9NW38 NM_001114636.1GENCODE basic
ENST00000233741.4FANCL-0011683375aaENSP00000233741.4
 
Protein coding
CCDS1860Q9NW38 NM_018062.3GENCODE basic
ENST00000403295.3FANCL-0041576347aaENSP00000386097.3
 
Protein coding
B5MC31 -GENCODE basic
ENST00000449070.1FANCL-003964301aaENSP00000401280.1
 
Protein coding
C9JZA9 -CDS 3' incomplete
ENST00000540646.1FANCL-201906127aaENSP00000441431.1
 
Protein coding
B4DN24 -GENCODE basic
ENST00000427708.2FANCL-009864288aaENSP00000400969.2
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000403676.1FANCL-006849258aaENSP00000384046.1
 
Protein coding
B5MCZ6 -GENCODE basic
ENST00000417361.1FANCL-005545145aaENSP00000389448.1
 
Protein coding
C9JPN7 -CDS 3' incomplete
ENST00000446381.1FANCL-007487158aaENSP00000390991.1
 
Protein coding
C9J512 -CDS 3' incomplete
ENST00000481670.1FANCL-008368No protein-
 
Processed transcript
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ENST00000470506.1FANCL-010733No protein-
 
Retained intron
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