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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
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

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

CRRD Object Information
CRRD ID: 1606617
Created: 2007-04-29
Species: Homo sapiens
Last Modified: 2019-10-08
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.