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Gene: GOLGA6L1 (golgin A6 family like 1) Homo sapiens
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Symbol: GOLGA6L1
Name: golgin A6 family like 1
CRRD ID: 3517752
Description: ASSOCIATED WITH Angelman syndrome; autism spectrum disorder; autistic disorder; INTERACTS WITH aflatoxin B1; cadmium atom; sodium arsenite
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FLJ36131; FLJ40198; golgi autoantigen, golgin subfamily a, 6-like 1; golgi autoantigen, golgin subfamily a-like; golgin A6 family-like 1; Golgin subfamily A member 6-like protein 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
GRCh38.p13 Ensembl1523,127,066 - 23,136,822 (-)EnsemblGRCh38hg38GRCh38
GRCh381523,127,066 - 23,136,822 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh371522,736,246 - 22,746,002 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361520,287,610 - 20,296,164 (+)NCBINCBI36hg18NCBI36
Cytogenetic Map15q11.2NCBI
HuRef151,041,836 - 1,051,581 (+)NCBIHuRef
CHM1_11522,685,541 - 22,695,279 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on GOLGA6L1
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 3517752
Created: 2010-07-04
Species: Homo sapiens
Last Modified: 2020-09-16
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.