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Naip1 Gene Detail
Summary
  • Symbol
    Naip1
  • Name
    NLR family, apoptosis inhibitory protein 1
  • Synonyms
    Birc1a, D13Lsd1, Naip
  • Feature Type
    protein coding gene
  • IDs
    MGI:1298223
    NCBI Gene: 17940
  • Member of
    Naipc cluster
  • Alliance
    gene page
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr13:100544272-100589372 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 13, 53.18 cM, cytoband D1-D3
  • Mapping Data
    13 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1386 from dbSNP Build 142
  • Strain Annotations
    6
  • PCR
    3
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1298223
 protein coding gene Chr13:100544272-100589377 (-)
129S1/SvImJ no annotation
A/J no annotation
AKR/J MGP_AKRJ_G0020811
 protein coding gene Chr13:101341438-101399702 (-)
BALB/cJ MGP_BALBcJ_G0020835
 protein coding gene Chr13:99070452-99114184 (-)
C3H/HeJ no annotation
C57BL/6NJ MGP_C57BL6NJ_G0021269
 protein coding gene Chr13:105341665-105409597 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0018840
 protein coding gene Chr13:93830533-94221211 (-)
CAST/EiJ no annotation
CBA/J MGP_CBAJ_G0020586
 protein coding gene Chr13:109512347-109562912 (-)
DBA/2J no annotation
FVB/NJ no annotation
LP/J no annotation
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    NAIP, NLR family apoptosis inhibitory protein
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    NAIP, NLR family apoptosis inhibitory protein
  • Synonyms
    BIRC1, NLRB1, psiNAIP
  • Links
    NCBI Gene ID: 4671
    neXtProt AC: NX_Q13075
    UniProt: Q13075

  • Chr Location
    5q13.2; chr5:70968166-71025339 (-)  GRCh38
Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    2 phenotypes from 2 alleles in 2 genetic backgrounds
    22 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for disruptions in this gene display a normal phenotype.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
    25
  • GO References
    7
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
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Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
    889
  • Tissues
    123
  • cDNA Data
    10
  • Literature Summary
    7
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 17940 NCBI Gene Model | MGI Sequence Detail 45101 C57BL/6J ±  kb
transcript NM_008670 RefSeq | MGI Sequence Detail 5361 Not Specified  
polypeptide Q9QWK5 UniProt | EBI | MGI Sequence Detail 1403 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 41
    Genomic 21
    cDNA 10
    Primer pair 8
    Other 2

    Microarray probesets 3
Other
Accession IDs
less
MGD-MRK-38374, MGD-MRK-39477, MGI:109329, MGI:109478, MGI:2145401
References
more
  • Summaries
    All 70
    Developmental Gene Expression 7
    Diseases 1
    Gene Ontology 7
    Phenotypes 22
  • Earliest
    J:37707 Scharf JM, et al., The mouse region syntenic for human spinal muscular atrophy lies within the Lgn1 critical interval and contains multiple copies of Naip exon 5. Genomics. 1996 Dec 15;38(3):405-17
  • Latest
    J:358278 Yang Y, et al., Erythrocytic alpha-Synuclein and the Gut Microbiome: Kindling of the Gut-Brain Axis in Parkinson's Disease. Mov Disord. 2024 Jan;39(1):40-52
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory