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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 16 transcripts (splice variants), 170 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000252530.10FAM98C-2011313349aaENSP00000252530.4
 
Protein coding
CCDS42562Q17RN3-1 NM_174905.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000909362.1FAM98C-2111296344aaENSP00000579421.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000909365.1FAM98C-2141211323aaENSP00000579424.1
 
Protein coding
--GENCODE Basic
ENST00000909366.1FAM98C-2151145310aaENSP00000579425.1
 
Protein coding
--GENCODE Basic
ENST00000909364.1FAM98C-2131122293aaENSP00000579423.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000909363.1FAM98C-2121095284aaENSP00000579422.1
 
Protein coding
--GENCODE Basic
ENST00000909367.1FAM98C-2161076288aaENSP00000579426.1
 
Protein coding
--GENCODE Basic
ENST00000343358.11FAM98C-2021006267aaENSP00000340348.6
 
Protein coding
CCDS86763Q17RN3-2 -GENCODE BasicTSL:1
ENST00000588262.5FAM98C-205826186aaENSP00000467974.1
 
Protein coding
K7EQT7 -GENCODE PrimaryGENCODE 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