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Gene: SUPT20HL1 (SUPT20H like 1) Homo sapiens
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Symbol: SUPT20HL1
Name: SUPT20H like 1
Description: ENCODES a protein that exhibits transcription coregulator activity (inferred); ASSOCIATED WITH autistic disorder; Neurodevelopmental Disorders; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH valproic acid
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FAM48B1; family with sequence similarity 48, member B1; hypothetical protein LOC100130302; SPT20 homolog, SAGA complex component like 1; SPT20 homolog, SAGA complex component-like 1; SPT20L; suppressor of Ty 20 homolog (S. cerevisiae)-like 1; suppressor of Ty 20 homolog-like 1; transcription factor SPT20 homolog-like 1
Orthologs:
No known orthologs. homologs ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X24,362,683 - 24,367,842 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X24,380,503 - 24,383,557 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X24,290,331 - 24,336,420 (+)NCBINCBI36hg18NCBI36
CeleraX28,503,761 - 28,506,424 (+)NCBI
Cytogenetic MapXp22.11NCBI
HuRefX22,122,907 - 22,125,573 (+)NCBIHuRef
CHM1_1X24,411,915 - 24,414,575 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
Gene Ontology Annotations
References - curated
References - uncurated

Genomics

Position Markers

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SUPT20HL1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 1344534
Created: 2005-03-08
Species: Homo sapiens
Last Modified: 2019-09-12
Status: ACTIVE



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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.