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Gene: CXorf49B (chromosome X open reading frame 49B) Homo sapiens
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Symbol: CXorf49B
Name: chromosome X open reading frame 49B
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH valproic acid
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: CXorf49; hypothetical protein LOC100132994; uncharacterized protein CXorf49; uncharacterized protein LOC100132994
Orthologs:
Mus musculus (house mouse) : Gm4779 (predicted gene 4779)  MGI  Alliance
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38X71,763,290 - 71,767,201 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X70,983,140 - 70,987,051 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X70,899,692 - 70,903,645 (+)NCBINCBI36hg18NCBI36
CeleraX71,286,613 - 71,290,524 (-)NCBI
Cytogenetic MapXq13.1NCBI
HuRefX64,736,072 - 64,739,983 (+)NCBIHuRef
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
 
More on CXorf49B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

CRRD Object Information
CRRD ID: 2303482
Created: 2009-02-14
Species: Homo sapiens
Last Modified: 2019-10-16
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.