Human (GRCh37.p13)
Description

family with sequence similarity 86, member C1 [Source:HGNC Symbol;Acc:25561]

Gene Synonyms

FAM86C, FLJ10661, FLJ27199

Location

Chromosome 11: 71,498,556-71,512,282 forward strand.

GRCh37:CM000673.1

About this gene

This gene has 6 transcripts (splice variants).

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000359244.4FAM86C1-0022110165aaENSP00000352182.4
 
Protein coding
CCDS41686D6R9N2 Q9NVL1 NM_018172.2Ensembl CanonicalGENCODE Basic
ENST00000346333.6FAM86C1-0012010131aaENSP00000325662.8
 
Protein coding
CCDS8202D6R9N2 Q9NVL1 NM_152563.2GENCODE Basic
ENST00000426628.2FAM86C1-006952158aaENSP00000391329.2
 
Protein coding
CCDS44664D6R9N2 Q9NVL1 NM_001099653.1GENCODE Basic
ENST00000510443.1FAM86C1-003158053aaENSP00000423511.1
 
Nonsense mediated decay
D6R9N2 --
ENST00000526393.1FAM86C1-004129553aaENSP00000432416.1
 
Nonsense mediated decay
D6R9N2 --
ENST00000528685.1FAM86C1-005990125aaENSP00000436598.1
 
Nonsense mediated decay
B4DDJ9 D6R9N2 --