Human (GRCh38.p14)
Description

formin like 1 [Source:HGNC Symbol;Acc:HGNC:1212]

Gene Synonyms

C17ORF1, C17ORF1B, FMNL

Location

Chromosome 17: 45,221,444-45,247,319 forward strand.

GRCh38:CM000679.2

About this gene

This gene has 11 transcripts (splice variants), 285 orthologues and 18 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000331495.8FMNL1-20140031100aaENSP00000329219.2
 
Protein coding
CCDS11497O95466-1 NM_005892.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS ALT2TSL:1
ENST00000587489.6FMNL1-20539791104aaENSP00000465474.2
 
Protein coding
CCDS92339O95466-2 -GENCODE basicAPPRIS P3TSL:1
ENST00000586643.5FMNL1-2041475488aaENSP00000465137.1
 
Protein coding
K7EJE6 -TSL:1CDS 5' incomplete
ENST00000589911.1FMNL1-207769127aaENSP00000466711.1
 
Protein coding
K7EMY8 -TSL:3CDS 5' incomplete
ENST00000586092.1FMNL1-203453151aaENSP00000468301.1
 
Protein coding
K7ERL1 -TSL:2CDS 5' and 3' incomplete
ENST00000592006.5FMNL1-209888No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000592415.1FMNL1-210393No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000587856.1FMNL1-2064919No protein-
 
Retained intron
--TSL:2
ENST00000585852.5FMNL1-202877No protein-
 
Retained intron
--TSL:2
ENST00000592527.1FMNL1-211742No protein-
 
Retained intron
--TSL:1
ENST00000591434.1FMNL1-208580No protein-
 
Retained intron
--TSL:4