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Gene: FAM106B (family with sequence similarity 106 member B) Homo sapiens
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Symbol: FAM106B
Name: family with sequence similarity 106 member B
RGD ID: 1604137
Description: ASSOCIATED WITH autistic disorder
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: uncharacterized protein LOC100996259
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh381720,417,020 - 20,418,518 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371720,320,625 - 20,321,742 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361720,261,203 - 20,263,587 (+)NCBINCBI36hg18NCBI36
Cytogenetic Map17p11.2NCBI
CHM1_11720,329,342 - 20,331,100 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
References - uncurated

Genomics

miRNA Target Status

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM106B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1604137
Created: 2007-04-28
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.