Homo sapiens Gene: NNAT
Summary
InnateDB Gene IDBG-74328.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NNAT
Gene Name neuronatin
Synonyms Peg5
Species Homo sapiens
Ensembl Gene ENSG00000053438
Encoded Proteins
neuronatin
neuronatin
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary The protein encoded by this gene is a proteolipid that may be involved in the regulation of ion channels during brain development. The encoded protein may also play a role in forming and maintaining the structure of the nervous system. This gene is found within an intron of the BLCAP gene, but on the opposite strand. This gene is imprinted and is expressed only from the paternal allele. Two transcript variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Nov 2009]
Gene Information
Type Protein coding
Genomic Location Chromosome 20:37521215-37523693
Strand Forward strand
Band q11.23
Transcripts
ENST00000062104 ENSP00000062104
ENST00000346199 ENSP00000335497
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 5 experimentally validated interaction(s) in this database.
Experimentally validated
Total 5 [view]
Protein-Protein 4 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
Biological Process
GO:0006810 transport
GO:0007420 brain development
GO:0009249 protein lipoylation
GO:0009749 response to glucose
GO:0030182 neuron differentiation
GO:0032024 positive regulation of insulin secretion
GO:0032880 regulation of protein localization
Cellular Component
GO:0005737 cytoplasm
Orthologs
No orthologs found for this gene
Cross-References
SwissProt
TrEMBL
UniProt Splice Variant
Entrez Gene
UniGene
RefSeq NM_005386 NM_181689
HUGO
OMIM
CCDS CCDS13296 CCDS13297
HPRD 04377
IMGT
EMBL
GenPept
RNA Seq Atlas