Human (GRCh38.p14)
Description

coiled-coil domain containing 169 [Source:HGNC Symbol;Acc:HGNC:34361]

Gene Synonyms

C13ORF38, LOC728591, RP11-251J8.1

Location

Chromosome 13: 36,222,008-36,297,840 reverse strand.

GRCh38:CM000675.2

About this gene

This gene has 13 transcripts (splice variants) and 67 orthologues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000239859.8CCDC169-2011158214aaENSP00000239859.7
 
Protein coding
CCDS45028A6NNP5-1 NM_001144981.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000379864.6CCDC169-2045944139aaENSP00000369193.2
 
Protein coding
CCDS45027A6NNP5-3 -GENCODE basicTSL:1
ENST00000510088.5CCDC169-2131088112aaENSP00000427495.1
 
Protein coding
CCDS45029A6NNP5-5 -GENCODE basicTSL:1
ENST00000503173.5CCDC169-211837241aaENSP00000426174.1
 
Protein coding
CCDS55897A6NNP5-4 -GENCODE basicTSL:1
ENST00000491049.6CCDC169-210753139aaENSP00000425252.1
 
Protein coding
CCDS45027A6NNP5-3 -GENCODE basicTSL:1
ENST00000239860.10CCDC169-202716141aaENSP00000239860.6
 
Protein coding
CCDS53863A6NNP5-6 -GENCODE basicTSL:1
ENST00000379862.6CCDC169-203624112aaENSP00000369191.2
 
Protein coding
CCDS45029A6NNP5-5 -GENCODE basicTSL:5
ENST00000506800.5CCDC169-21285491aaENSP00000420862.1
 
Nonsense mediated decay
E9PBZ7 -TSL:1
ENST00000477250.1CCDC169-2061632No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000479850.6CCDC169-2071306No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000485600.1CCDC169-208887No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000486683.5CCDC169-209541No protein-
 
Protein coding CDS not defined
--TSL:2
ENST00000471781.5CCDC169-205404No protein-
 
Protein coding CDS not defined
--TSL:5