Human (GRCh38.p14)
Description

family with sequence similarity 98 member C [Source:HGNC Symbol;Acc:HGNC:27119]

Gene Synonyms

FLJ44669

Location

Chromosome 19: 38,403,093-38,409,088 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 10 transcripts (splice variants), 174 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000252530.10FAM98C-2011313349aaENSP00000252530.4
 
Protein coding
CCDS42562Q17RN3-1 NM_174905.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000343358.11FAM98C-2021006267aaENSP00000340348.6
 
Protein coding
CCDS86763Q17RN3-2 -GENCODE basicTSL:1
ENST00000588262.5FAM98C-205826186aaENSP00000467974.1
 
Protein coding
K7EQT7 -GENCODE basicTSL:1
ENST00000589408.1FAM98C-209542181aaENSP00000467878.1
 
Protein coding
K7EQL1 -TSL:2CDS 5' and 3' incomplete
ENST00000589029.1FAM98C-20847856aaENSP00000468553.1
 
Nonsense mediated decay
K7ES49 -TSL:3CDS 5' incomplete
ENST00000585954.1FAM98C-203330No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000586372.5FAM98C-2044133No protein-
 
Retained intron
--TSL:2
ENST00000588348.5FAM98C-2062530No protein-
 
Retained intron
--TSL:2
ENST00000589027.1FAM98C-207670No protein-
 
Retained intron
--TSL:2
ENST00000592992.1FAM98C-210558No protein-
 
Retained intron
--TSL:2