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Human (GRCh38.p14)
Description

potassium channel tetramerization domain containing 17 [Source:HGNC Symbol;Acc:HGNC:25705]

Gene Synonyms

FLJ12242

Location

Chromosome 22: 37,051,739-37,063,390 forward strand.

GRCh38:CM000684.2

About this gene

This gene has 11 transcripts (splice variants), 190 orthologues, 3 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000403888.8KCTD17-2021760314aaENSP00000385096.4
 
Protein coding
CCDS74854Q8N5Z5-1 NM_001282684.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000851347.1KCTD17-2101740308aaENSP00000521406.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000402077.8KCTD17-2011691290aaENSP00000384391.4
 
Protein coding
CCDS13940Q8N5Z5-2 -GENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000949216.1KCTD17-2111482223aaENSP00000619275.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000610767.5KCTD17-2091477213aaENSP00000480699.2
 
Protein coding
CCDS74855A0A087WX35 -GENCODE PrimaryGENCODE BasicAPPRIS P2TSL:3
ENST00000456470.1KCTD17-2051438180aaENSP00000409638.1
 
Protein coding
H0Y731 -TSL:3CDS 5' incomplete
ENST00000431531.1KCTD17-20455963aaENSP00000402434.1
 
Protein coding
B0QYB2 -TSL:4CDS 3' incomplete
ENST00000421900.5KCTD17-203451104aaENSP00000409116.1
 
Nonsense mediated decay
H7C323 -TSL:5CDS 5' incomplete
ENST00000462640.1KCTD17-206808No protein-
 
Retained intron
--TSL:5
ENST00000478231.5KCTD17-207584No protein-
 
Retained intron
--TSL:5
ENST00000483389.5KCTD17-208546No protein-
 
Retained intron
--TSL:2