Homo sapiens Gene: NAIP
Summary
InnateDB Gene IDBG-402309.3
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol NAIP
Gene Name NLR family, apoptosis inhibitory protein
Synonyms BIRC1; NLRB1; psiNAIP
Species Homo sapiens
Ensembl Gene ENSG00000249437
Encoded Proteins
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
NLR family, apoptosis inhibitory protein
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This copy of the gene is full length; additional copies with truncations and internal deletions are also present in this region of chromosome 5q13. It is thought that this gene is a modifier of spinal muscular atrophy caused by mutations in a neighboring gene, SMN1. The protein encoded by this gene contains regions of homology to two baculovirus inhibitor of apoptosis proteins, and it is able to suppress apoptosis induced by various signals. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Gene Information
Type Protein coding
Genomic Location Chromosome 5:70968483-71025114
Strand Reverse strand
Band q13.2
Transcripts
ENST00000315147
ENST00000194097 ENSP00000443944
ENST00000447012 ENSP00000429591
ENST00000517649 ENSP00000428657
ENST00000523981 ENSP00000428363
ENST00000508426 ENSP00000429545
ENST00000514857 ENSP00000428226
ENST00000508794
ENST00000519014 ENSP00000429154
ENST00000503719 ENSP00000424913
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
Experimentally validated
Total 10 [view]
Protein-Protein 10 [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:0005524 ATP binding
GO:0017111 nucleoside-triphosphatase activity
GO:0043027 cysteine-type endopeptidase inhibitor activity involved in apoptotic process
GO:0046872 metal ion binding
Biological Process
GO:0006954 inflammatory response
GO:0007399 nervous system development
GO:0008152 metabolic process
GO:0043066 negative regulation of apoptotic process
GO:0043154 negative regulation of cysteine-type endopeptidase activity involved in apoptotic process
GO:0043524 negative regulation of neuron apoptotic process
GO:0045087 innate immune response
Cellular Component
GO:0005737 cytoplasm
GO:0016323 basolateral plasma membrane
GO:0070062 extracellular vesicular exosome
Orthologs
No orthologs found for this gene
Pathways
NETPATH
REACTOME
KEGG
NOD-like receptor signaling pathway pathway
INOH
PID NCI
Cross-References
SwissProt Q13075
TrEMBL B4DHI2
UniProt Splice Variant
Entrez Gene 4671
UniGene Hs.606815 Hs.652859 Hs.654500 Hs.658700 Hs.667693 Hs.710305 Hs.737896
RefSeq NM_022892 NM_004536 XM_005248523 XM_006714628 XM_006714629 XM_006714630
HUGO HGNC:7634
OMIM 600355
CCDS CCDS43327 CCDS4009
HPRD
IMGT
EMBL AB048534 AB209123 AC005031 AC044797 AH003063 AK295115 BC136273 U19251 U80017
GenPept AAA64504 AAC52045 AAC52047 AAC62261 AAI36274 BAB87181 BAD92360 BAG58144
RNA Seq Atlas 4671