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Human (GRCh38.p14)
Description

XK related 9 [Source:HGNC Symbol;Acc:HGNC:20937]

Location

Chromosome 8: 70,669,332-70,790,371 forward strand.

GRCh38:CM000670.2

About this gene

This gene has 9 transcripts (splice variants), 197 orthologues and 5 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000408926.8XKR9-2013200373aaENSP00000386141.3
 
Protein coding
CCDS34905Q5GH70 NM_001011720.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000920917.1XKR9-2082167373aaENSP00000590976.1
 
Protein coding
CCDS34905--GENCODE BasicAPPRIS P1
ENST00000920916.1XKR9-2071807373aaENSP00000590975.1
 
Protein coding
CCDS34905--GENCODE BasicAPPRIS P1
ENST00000520030.5XKR9-2031799373aaENSP00000431088.1
 
Protein coding
CCDS34905Q5GH70 -GENCODE BasicAPPRIS P1TSL:1
ENST00000920915.1XKR9-2061692373aaENSP00000590974.1
 
Protein coding
CCDS34905--GENCODE BasicAPPRIS P1
ENST00000970137.1XKR9-2091663373aaENSP00000640196.1
 
Protein coding
CCDS34905--GENCODE BasicAPPRIS P1
ENST00000519350.1XKR9-20271689aaENSP00000428904.1
 
Protein coding
E5RFF6 -TSL:3CDS 3' incomplete
ENST00000520092.5XKR9-2041841125aaENSP00000430781.1
 
Nonsense mediated decay
E5RI45 -TSL:2
ENST00000520273.1XKR9-205766No protein-
 
Protein coding CDS not defined
--TSL:3