Homo sapiens Gene: NAIP | |||||||||||||||||||
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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
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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] |
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Gene Information | |||||||||||||||||||
Type | Protein coding | ||||||||||||||||||
Genomic Location | Chromosome 5:70968483-71025114 | ||||||||||||||||||
Strand | Reverse strand | ||||||||||||||||||
Band | q13.2 | ||||||||||||||||||
Transcripts | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 10 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||||
No orthologs found for this gene | |||||||||||||||||||
Pathways | |||||||||||||||||||
NETPATH | |||||||||||||||||||
REACTOME | |||||||||||||||||||
KEGG |
NOD-like receptor signaling pathway pathway
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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 | ||||||||||||||||||