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Human (GRCh37.p13)
Description

formin 2 [Source:HGNC Symbol;Acc:14074]

Location

Chromosome 1: 240,177,648-240,638,489 forward strand.

GRCh37:CM000663.1

About this gene

This gene has 7 transcripts (splice variants), 12 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000319653.9FMN2-00164341722aaENSP00000318884.9
 
Protein coding
CCDS31069B4DN09 Q96L17 Q9NZ56
NM_020066.4Ensembl CanonicalGENCODE basic
ENST00000543681.1FMN2-201290242aaENSP00000439136.1
 
Protein coding
Q2M1H5 -GENCODE basic
ENST00000545751.1FMN2-2021632318aaENSP00000437918.1
 
Protein coding
B4DP05 Q96L17 -GENCODE basic
ENST00000447095.1FMN2-003906228aaENSP00000409308.1
 
Protein coding
B0QZA8 -CDS 3' incomplete
ENST00000441342.1FMN2-00560299aaENSP00000388922.1
 
Protein coding
B0QZD5 -CDS 3' incomplete
ENST00000496950.1FMN2-002693No protein-
 
Processed transcript
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ENST00000463398.1FMN2-004571No protein-
 
Processed transcript
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