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4930451I11Rik Gene Detail
Summary
  • Symbol
    4930451I11Rik
  • Name
    RIKEN cDNA 4930451I11 gene
  • Feature Type
    protein coding gene
  • IDs
    MGI:1925368
    NCBI Gene: 78118
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr7:126429640-126430712 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 7, 69.25 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    89 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1925368
protein coding gene Chr7:126429640-126430811 (-)
129S1/SvImJ MGP_129S1SvImJ_G0033002
protein coding gene Chr7:131132488-131133659 (-)
A/J MGP_AJ_G0032985
protein coding gene Chr7:127656453-127657624 (-)
AKR/J MGP_AKRJ_G0032917
protein coding gene Chr7:130891663-130892834 (-)
BALB/cJ MGP_BALBcJ_G0032990
protein coding gene Chr7:127319318-127320489 (-)
C3H/HeJ MGP_C3HHeJ_G0032700
protein coding gene Chr7:130829308-130830479 (-)
C57BL/6NJ MGP_C57BL6NJ_G0033496
protein coding gene Chr7:136228562-136229733 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0030468
protein coding gene Chr7:128850158-128851324 (-)
CAST/EiJ MGP_CASTEiJ_G0032029
protein coding gene Chr7:122615363-122616530 (-)
CBA/J MGP_CBAJ_G0032673
protein coding gene Chr7:140815051-140816222 (-)
DBA/2J MGP_DBA2J_G0032825
protein coding gene Chr7:125631028-125632199 (-)
FVB/NJ MGP_FVBNJ_G0032778
protein coding gene Chr7:125482211-125483382 (-)
LP/J MGP_LPJ_G0032919
protein coding gene Chr7:132601450-132602621 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0032810
protein coding gene Chr7:141992751-141993922 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0033515
protein coding gene Chr7:129901000-129902171 (-)
PWK/PhJ MGP_PWKPhJ_G0031736
protein coding gene Chr7:118625808-118626979 (-)
SPRET/EiJ MGP_SPRETEiJ_G0031582
protein coding gene Chr7:116746678-116747848 (-)
WSB/EiJ MGP_WSBEiJ_G0032141
protein coding gene Chr7:130880827-130881998 (-)



Homology
more
  • Human Ortholog
    C16orf92, chromosome 16 open reading frame 92
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C16orf92, chromosome 16 open reading frame 92
  • Synonyms
    FIMP
  • Links
    NCBI Gene ID: 146378
    neXtProt AC: NX_Q96LL3
    UniProt: Q96LL3

  • Chr Location
    16p11.2; chr16:30023198-30027736 (+)  GRCh38

Human Diseases
less
  • References
    3 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    6 phenotypes from 4 alleles in 3 genetic backgrounds
    49 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.
Male mice homozygous for a null mutation display severely reduced fertility with impaired fertilization due to impaired fusion on sperm with oocytes.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

No experimental evidence to support Molecular Function annotation, following literature review. See J:73796.
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
less
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
  • cDNA Data
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 78118 NCBI Gene Model | MGI Sequence Detail 1073 C57BL/6J ±  kb
    transcript NM_183131 RefSeq | MGI Sequence Detail 475 C57BL/6  
    polypeptide E9Q9R3 UniProt | EBI | MGI Sequence Detail 111 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    • UniProt
      2 Sequences
    • InterPro Domains
      IPR038813 Fertilization-influencing membrane protein
    Molecular
    Reagents
    less
    • All nucleic 8
      cDNA 8

      Microarray probesets 2
    References
    more
    • Summaries
      All 67
      Diseases 3
      Gene Ontology 3
      Phenotypes 49
    • Earliest
      J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
    • Latest
      J:349484 Henis M, et al., The autism susceptibility kinase, TAOK2, phosphorylates eEF2 and modulates translation. Sci Adv. 2024 Apr 12;10(15):eadf7001

    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
    12/10/2024
    MGI 6.24
    The Jackson Laboratory