Homo sapiens Gene: NIPSNAP1
Summary
InnateDB Gene IDBG-3663.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NIPSNAP1
Gene Name nipsnap homolog 1 (C. elegans)
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000184117
Encoded Proteins
nipsnap homolog 1 (C. elegans)
nipsnap homolog 1 (C. elegans)
nipsnap homolog 1 (C. elegans)
nipsnap homolog 1 (C. elegans)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a member of the NipSnap family of proteins that may be involved in vesicular transport. A similar protein in mice inhibits the calcium channel TRPV6, and is also localized to the inner mitochondrial membrane where it may play a role in mitochondrial DNA maintenance. A pseudogene of this gene is located on the short arm of chromosome 17. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Feb 2011]
Gene Information
Type Protein coding
Genomic Location Chromosome 22:29554808-29581337
Strand Reverse strand
Band q12.2
Transcripts
ENST00000216121 ENSP00000216121
ENST00000437094 ENSP00000403448
ENST00000415100 ENSP00000407851
ENST00000455496 ENSP00000404227
ENST00000496944
ENST00000494966
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 24 experimentally validated interaction(s) in this database.
Experimentally validated
Total 24 [view]
Protein-Protein 24 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0005515 protein binding
GO:0042165 neurotransmitter binding
Biological Process
GO:0019233 sensory perception of pain
Cellular Component
GO:0005739 mitochondrion
GO:0005743 mitochondrial inner membrane
GO:0016020 membrane
GO:0097060 synaptic membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Method
Confidence
Comments
SSD Ortholog
Ortholog supports species divergence
Not yet available
SSD Ortholog
Ortholog supports species divergence
Cross-References
SwissProt
TrEMBL C9JDV8
UniProt Splice Variant
Entrez Gene 8508
UniGene Hs.173878
RefSeq NM_001202502 NM_003634 XM_005261789
HUGO HGNC:7827
OMIM 603249
CCDS CCDS13860
HPRD 10342
IMGT
EMBL AC005529
GenPept
RNA Seq Atlas 8508