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Insc Gene Detail
Summary
  • Symbol
    Insc
  • Name
    INSC spindle orientation adaptor protein
  • Synonyms
    3830422K02Rik, Inscuteable
  • Feature Type
    protein coding gene
  • IDs
    MGI:1917942
    NCBI Gene: 233752
  • Alliance
  • Transcription Start Sites
    17 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:114342931-114449615 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 7, 60.23 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    3307 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1917942
protein coding gene Chr7:114342929-114449618 (+)
129S1/SvImJ MGP_129S1SvImJ_G0032886
protein coding gene Chr7:118427913-118537857 (+)
A/J MGP_AJ_G0032869
protein coding gene Chr7:115451915-115560215 (+)
AKR/J MGP_AKRJ_G0032801
protein coding gene Chr7:118369166-118479830 (+)
BALB/cJ MGP_BALBcJ_G0032874
protein coding gene Chr7:115157038-115264806 (+)
C3H/HeJ MGP_C3HHeJ_G0032584
protein coding gene Chr7:118334854-118443742 (+)
C57BL/6NJ MGP_C57BL6NJ_G0033380
protein coding gene Chr7:123181931-123292784 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0030352
protein coding gene Chr7:116968683-117079367 (+)
CAST/EiJ MGP_CASTEiJ_G0031912
protein coding gene Chr7:109983586-110108219 (+)
CBA/J MGP_CBAJ_G0032557
protein coding gene Chr7:127298291-127411129 (+)
DBA/2J MGP_DBA2J_G0032709
protein coding gene Chr7:113499174-113605816 (+)
FVB/NJ MGP_FVBNJ_G0032662
protein coding gene Chr7:113365534-113472325 (+)
LP/J MGP_LPJ_G0032803
protein coding gene Chr7:119928841-120036948 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0032694
protein coding gene Chr7:128900929-129012622 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0033400
protein coding gene Chr7:117359509-117466646 (+)
PWK/PhJ MGP_PWKPhJ_G0031620
protein coding gene Chr7:106377268-106521673 (+)
SPRET/EiJ MGP_SPRETEiJ_G0031467
protein coding gene Chr7:104090624-104222207 (+)
WSB/EiJ MGP_WSBEiJ_G0032025
protein coding gene Chr7:118223624-118333633 (+)



Homology
more
  • Human Ortholog
    INSC, INSC spindle orientation adaptor protein
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    INSC, INSC spindle orientation adaptor protein
  • Links
    NCBI Gene ID: 387755
    neXtProt AC: NX_Q1MX18
    UniProt: Q1MX18

  • Chr Location
    11p15.2; chr11:15111416-15269676 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    20 phenotypes from 4 alleles in 2 genetic backgrounds
    16 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.
Homozygous inactivation of this gene leads to abnormal cochlear hair cell morphology.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 233752 NCBI Gene Model | MGI Sequence Detail 106685 C57BL/6J ±  kb
    transcript NR_175961 RefSeq | MGI Sequence Detail 2390 C57BL/6  
    polypeptide Q3HNM7 UniProt | EBI | MGI Sequence Detail 579 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 13
      cDNA 12
      Primer pair 1

      Microarray probesets 2
    References
    more
    • Summaries
      All 50
      Developmental Gene Expression 9
      Gene Ontology 6
      Phenotypes 16
    • Earliest
      J:61682 Hagiwara N, et al., Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4180-5
    • Latest
      J:308321 Lau EO, et al., DIAPH3 deficiency links microtubules to mitotic errors, defective neurogenesis, and brain dysfunction. Elife. 2021 Apr 26;10:e61974

    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)
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    Funding Information
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    last database update
    11/12/2024
    MGI 6.24
    The Jackson Laboratory