Human (GRCh37.p13)
Description

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

Gene Synonyms

FLJ44669

Location

Chromosome 19: 38,893,775-38,899,728 forward strand.

GRCh37:CM000681.1

About this gene

This gene has 10 transcripts (splice variants), 176 orthologues and 2 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000252530.5FAM98C-0011271349aaENSP00000252530.4
 
Protein coding
CCDS42562Q17RN3 NM_174905.3Ensembl CanonicalGENCODE Basic
ENST00000343358.7FAM98C-0041006267aaENSP00000340348.6
 
Protein coding
Q17RN3 -GENCODE Basic
ENST00000588262.1FAM98C-002826186aaENSP00000467974.1
 
Protein coding
K7EQT7 -GENCODE Basic
ENST00000589408.1FAM98C-007542181aaENSP00000467878.1
 
Protein coding
--CDS 5' and 3' incomplete
ENST00000589029.1FAM98C-00847856aaENSP00000468553.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000585954.1FAM98C-009330No protein-
 
Processed transcript
---
ENST00000586372.1FAM98C-0054133No protein-
 
Retained intron
---
ENST00000588348.1FAM98C-0032530No protein-
 
Retained intron
---
ENST00000589027.1FAM98C-011670No protein-
 
Retained intron
---
ENST00000592992.1FAM98C-010558No protein-
 
Retained intron
---