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Gene: FAM236B (family with sequence similarity 236 member B) Homo sapiens
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Symbol: FAM236B
Name: family with sequence similarity 236 member B
Description: ASSOCIATED WITH autistic disorder
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FAM236A; family with sequence similarity 235 member B; uncharacterized LOC100132304; uncharacterized protein FAM236B
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 EnsemblX72,781,865 - 72,782,660 (-)Ensembl
GRCh38X72,781,865 - 72,782,660 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X72,001,640 - 72,002,743 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X71,918,414 - 71,919,295 (-)NCBINCBI36hg18NCBI36
CeleraX72,345,413 - 72,346,296 (-)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX65,755,995 - 65,757,093 (-)NCBIHuRef
CHM1_1X71,894,108 - 71,894,947 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics


Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM236B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 11577064
Created: 2017-01-10
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.