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Gene: GOLGA6L22 (golgin A6 family like 22) Homo sapiens
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Symbol: GOLGA6L22
Name: golgin A6 family like 22
Description: ASSOCIATED WITH autistic disorder
Type: protein-coding
RefSeq Status: INFERRED
Also known as: golgin A6 family-like 22; golgin subfamily A member 6-like protein 22; putative golgin subfamily A member 6-like
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 Ensembl1522,458,903 - 22,469,230 (+)Ensembl
GRCh381522,458,903 - 22,467,626 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371523,569,672 - 23,579,379 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 361521,121,113 - 21,130,820 (-)NCBINCBI36hg18NCBI36
Cytogenetic Map15q11.2NCBI
HuRef151,041,878 - 1,050,379 (+)NCBIHuRef
CHM1_11523,354,982 - 23,363,314 (-)NCBICHM1_1
CHM1_11523,519,227 - 23,528,899 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - curated
References - uncurated

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on GOLGA6L22
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 8551349
Created: 2014-04-09
Species: Homo sapiens
Last Modified: 2019-12-25
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.