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Gene: SPANXN5 (SPANX family member N5) Homo sapiens
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Symbol: SPANXN5
Name: SPANX family member N5
Description: ASSOCIATED WITH autistic disorder; syndromic X-linked intellectual disability Lubs type; INTERACTS WITH butanal; copper atom; copper(0)
Type: protein-coding
RefSeq Status: VALIDATED
Also known as: cancer/testis antigen family 11, member 10; CT11.10; nuclear-associated protein SPAN-Xn5; SPANX family, member N5; SPANX-N5; sperm protein associated with the nucleus on the X chromosome N5
Orthologs:
Mus musculus (house mouse) : Gm6760 (predicted gene 6760)  MGI
more info ...
Allele / Splice: See ClinVar data
Latest Assembly: GRCh38 - Human Genome Assembly GRCh38
Position:
Human AssemblyChrPosition (strand)SourceGenome Browsers
JBrowseNCBIUCSCEnsembl
GRCh38 EnsemblX52,796,144 - 52,797,427 (-)Ensembl
GRCh38X52,796,144 - 52,797,427 (-)NCBIGRCh38GRCh38hg38GRCh38
GRCh37X52,825,186 - 52,826,388 (-)NCBIGRCh37GRCh37hg19GRCh37
Build 36X52,841,911 - 52,843,113 (-)NCBINCBI36hg18NCBI36
CeleraX56,647,753 - 56,648,955 (-)NCBI
Cytogenetic MapXp11.22NCBI
HuRefX49,890,331 - 49,891,533 (-)NCBIHuRef
CHM1_1X52,815,307 - 52,816,509 (-)NCBICHM1_1
JBrowse: View Region in Genome Browser (JBrowse)
Model


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

Genomics

Comparative Map Data
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 SPANXN5
Alliance Gene
NCBI Gene
Ensembl Gene
JBrowse: hg19 hg38
HGNC Report
NCBI Genome Data Viewer

RGD Object Information
RGD ID: 1606617
Created: 2007-04-29
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.