Human (GRCh38.p14)
Description

SHQ1, H/ACA ribonucleoprotein assembly factor [Source:HGNC Symbol;Acc:HGNC:25543]

Gene Synonyms

FLJ10539, SHQ1P

Location

Chromosome 3: 72,749,277-72,861,914 reverse strand.

GRCh38:CM000665.2

About this gene

This gene has 8 transcripts (splice variants), 202 orthologues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000325599.13SHQ1-2012846577aaENSP00000315182.8
 
Protein coding
CCDS33788Q6PI26-1 NM_018130.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000463369.5SHQ1-2032065549aaENSP00000417452.1
 
Protein coding
Q6PI26-2 -GENCODE basicTSL:2
ENST00000482785.1SHQ1-208502110aaENSP00000418398.1
 
Protein coding
C9J6N3 -TSL:3CDS 3' incomplete
ENST00000444040.6SHQ1-202284450aaENSP00000402447.2
 
Nonsense mediated decay
F8WDZ9 -TSL:2
ENST00000471526.1SHQ1-20655363aaENSP00000417739.1
 
Nonsense mediated decay
F8WBC6 -TSL:4
ENST00000468371.5SHQ1-2054024No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000475558.5SHQ1-207666No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000468347.1SHQ1-204134No protein-
 
Protein coding CDS not defined
--TSL:5