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Gene: CXorf51A (chromosome X open reading frame 51A) Homo sapiens
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Symbol: CXorf51A
Name: chromosome X open reading frame 51A
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH antirheumatic drug; butanal; methotrexate
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: CXorf51; CXorf51B; hypothetical protein LOC100129239; Uncharacterized protein CXorf51B; uncharacterized protein LOC100129239
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX146,814,106 - 146,814,726 (-)Ensembl
GRCh38X146,814,104 - 146,814,731 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X145,895,622 - 145,896,249 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X145,703,314 - 145,703,940 (-)NCBINCBI36hg18NCBI36
Cytogenetic MapXq27.3NCBI
HuRefX134,860,067 - 134,860,694 (-)NCBIHuRef
CHM1_1X145,802,661 - 145,802,896 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - curated

Genomics

Comparative Map Data
Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on CXorf51A
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 2293161
Created: 2008-05-16
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.