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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
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_1X145,806,821 - 145,807,248 (-)NCBICHM1_1
CHM1_1X145,802,661 - 145,802,896 (+)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations

Genomics

Position Markers
miRNA Target Status

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

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