Human (GRCh38.p14)
Description

glucocorticoid induced 1 [Source:HGNC Symbol;Acc:HGNC:18713]

Gene Synonyms

FAM117C, GIG18, TSSN1

Location

Chromosome 7: 7,968,796-8,094,272 forward strand.

GRCh38:CM000669.2

About this gene

This gene has 12 transcripts (splice variants), 269 orthologues, 2 paralogues and is associated with 1 phenotype.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000223145.10GLCCI1-2014741547aaENSP00000223145.5
 
Protein coding
CCDS34601Q86VQ1 NM_138426.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000430798.1GLCCI1-203581193aaENSP00000396171.1
 
Protein coding
H7C0Q2 -TSL:3CDS 5' and 3' incomplete
ENST00000414914.5GLCCI1-202575191aaENSP00000406569.1
 
Protein coding
H7C2L5 -TSL:3CDS 5' and 3' incomplete
ENST00000438949.1GLCCI1-204873191aaENSP00000393942.1
 
Nonsense mediated decay
H7C0B2 -TSL:3CDS 5' incomplete
ENST00000474269.5GLCCI1-207691No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000470583.5GLCCI1-206555No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000496617.2GLCCI1-212538No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000482540.1GLCCI1-2083942No protein-
 
Retained intron
--TSL:2
ENST00000489405.5GLCCI1-2091475No protein-
 
Retained intron
--TSL:5
ENST00000492797.5GLCCI1-211495No protein-
 
Retained intron
--TSL:2
ENST00000491947.1GLCCI1-210427No protein-
 
Retained intron
--TSL:1
ENST00000460897.1GLCCI1-205412No protein-
 
Retained intron
--TSL:2