Human (GRCh38.p14)
Description

FIGNL1 interacting regulator of recombination and mitosis [Source:HGNC Symbol;Acc:HGNC:25565]

Gene Synonyms

APOLO1, C1ORF112, FLIP, FLJ10706, MEICA1

Location

Chromosome 1: 169,662,007-169,854,080 forward strand.

GRCh38:CM000663.2

About this gene

This gene has 9 transcripts (splice variants) and 203 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000359326.9FIRRM-2024011853aaENSP00000352276.4
 
Protein coding
CCDS1285Q9NSG2-1 NM_001320047.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000286031.10FIRRM-2014355853aaENSP00000286031.6
 
Protein coding
CCDS1285Q9NSG2-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000413811.3FIRRM-2032661530aaENSP00000389257.3
 
Protein coding
CCDS86030Q9NSG2-3 -GENCODE basicTSL:1
ENST00000472795.5FIRRM-206925161aaENSP00000490194.1
 
Protein coding
CCDS81401A0A1B0GUP7 -GENCODE basicTSL:2
ENST00000496973.5FIRRM-208782180aaENSP00000490333.1
 
Protein coding
CCDS81400A0A1B0GV14 -GENCODE basicTSL:1
ENST00000459772.5FIRRM-204372756aaENSP00000490589.1
 
Nonsense mediated decay
A0A1B0GTJ9 -TSL:2
ENST00000466580.6FIRRM-20581556aaENSP00000490772.1
 
Nonsense mediated decay
A0A1B0GTJ9 -TSL:4
ENST00000481744.5FIRRM-20775556aaENSP00000489730.1
 
Nonsense mediated decay
A0A1B0GTJ9 -TSL:3
ENST00000498289.5FIRRM-2093849No protein-
 
Protein coding CDS not defined
--TSL:2