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Gene: CXorf51B (chromosome X open reading frame 51B) Homo sapiens
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Symbol: CXorf51B
Name: chromosome X open reading frame 51B
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: CXorf51A; hypothetical protein LOC100133053; uncharacterized protein LOC100133053
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX146,809,771 - 146,810,411 (+)Ensembl
GRCh38X146,809,771 - 146,810,411 (+)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X145,891,302 - 145,891,929 (+)NCBIGRCh37GRCh37hg19GRCh37
Build 36X145,698,995 - 145,699,621 (+)NCBINCBI36hg18NCBI36
Cytogenetic MapXq27.3NCBI
CHM1_1X145,802,661 - 145,802,896 (+)NCBICHM1_1
CHM1_1X145,806,821 - 145,807,248 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
 
More on CXorf51B
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 5508282
Created: 2011-10-11
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.