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Gene: SPANXN3 (SPANX family member N3) Homo sapiens
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Symbol: SPANXN3
Name: SPANX family member N3
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH calcitriol; paracetamol
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: cancer/testis antigen family 11, member 8; CT11.8; nuclear-associated protein SPAN-Xn3; SPANX family, member N3; SPANX-N3; sperm protein associated with the nucleus on the X chromosome N3
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX143,508,735 - 143,517,475 (-)EnsemblGRCh38hg38GRCh38
GRCh38X143,508,735 - 143,517,475 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X142,596,564 - 142,605,307 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X142,424,230 - 142,432,973 (-)NCBINCBI36hg18NCBI36
CeleraX142,883,872 - 142,892,615 (-)NCBI
Cytogenetic MapXq27.3NCBI
HuRefX131,701,462 - 131,709,906 (-)NCBIHuRef
CHM1_1X142,508,450 - 142,517,189 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Position Markers
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Promoters
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SPANXN3
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1603581
Created: 2007-04-28
Species: Homo sapiens
Last Modified: 2020-03-24
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.