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Gene: FAM106C (family with sequence similarity 106 member C) Homo sapiens
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Symbol: FAM106C
Name: family with sequence similarity 106 member C
RGD ID: 3302126
Description: ASSOCIATED WITH autistic disorder; INTERACTS WITH 2-hydroxypropanoic acid; cadmium atom; pentanal
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: FAM106C pseudogene; FAM106CP; family with sequence similarity 106 member C, pseudogene; FLJ11800 related; MGC120421; MGC120423; putative protein FAM106C
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38.p13 Ensembl1716,788,879 - 16,790,501 (+)EnsemblGRCh38hg38GRCh38
GRCh381716,788,743 - 16,790,501 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh371716,692,057 - 16,693,815 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 361716,632,940 - 16,634,195 (+)NCBINCBI36hg18NCBI36
Cytogenetic Map17p11.2NCBI
CHM1_11716,701,738 - 16,703,496 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data
Position Markers

Expression


Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on FAM106C
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 3302126
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.