Submit Data |  Help |  Video Tutorials |  News |  Publications |  FTP Download |  REST API |  Citing RGD |  Contact   
Gene: SPANXN2 (SPANX family member N2) Homo sapiens
Analyze
Symbol: SPANXN2
Name: SPANX family member N2
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: cancer/testis antigen family 11, member 7; CT11.7; nuclear-associated protein SPAN-Xn2; SPANX family, member N2; SPANX-N2; sperm protein associated with the nucleus on the X chromosome N2
Orthologs:
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX143,711,955 - 143,721,423 (-)EnsemblGRCh38hg38GRCh38
GRCh38X143,712,035 - 143,720,668 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X142,795,055 - 142,804,516 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X142,622,721 - 142,632,182 (-)NCBINCBI36hg18NCBI36
CeleraX143,082,347 - 143,091,809 (-)NCBI
Cytogenetic MapXq27.3NCBI
HuRefX131,909,215 - 131,910,047 (-)NCBIHuRef
CHM1_1X142,707,198 - 142,715,825 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


Disease Annotations
Gene-Chemical Interaction Annotations
References - uncurated

Genomics

Comparative Map Data
miRNA Target Status

Expression

RNA-SEQ Expression

Sequence

Nucleotide Sequences
Protein Sequences
Clinical Variants

Additional Information

External Database Links
Nomenclature History
 
More on SPANXN2
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1606620
Created: 2007-04-29
Species: Homo sapiens
Last Modified: 2020-03-24
Status: ACTIVE



NHLBI Logo

RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.