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Gene: TCP11X2 (t-complex 11 family, X-linked 2) Homo sapiens
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Symbol: TCP11X2
Name: t-complex 11 family, X-linked 2
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH 17beta-estradiol (ortholog); bisphenol A (ortholog)
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: T-complex protein 11 homolog
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX102,456,862 - 102,471,842 (-)Ensembl
GRCh38X102,460,319 - 102,471,812 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X101,715,236 - 101,726,732 (-)NCBIGRCh37GRCh37hg19GRCh37
Cytogenetic MapXq22.1NCBI
HuRefX91,380,541 - 91,392,031 (-)NCBIHuRef
CHM1_1X101,608,135 - 101,616,754 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
 
More on TCP11X2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 7243979
Created: 2013-05-21
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.