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Krt88 Gene Detail
Summary
  • Symbol
    Krt88
  • Name
    keratin 88
  • Synonyms
    1700011A15Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:1913572
    NCBI Gene: 66322
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr15:101345625-101351788 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 15, 56.90 cM, cytoband F3
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    25 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1913572
protein coding gene Chr15:101345605-101351806 (+)
129S1/SvImJ MGP_129S1SvImJ_G0022373
protein coding gene Chr15:103515921-103522319 (+)
A/J MGP_AJ_G0022335
protein coding gene Chr15:99416572-99422734 (+)
AKR/J MGP_AKRJ_G0022311
protein coding gene Chr15:102445746-102451906 (+)
BALB/cJ MGP_BALBcJ_G0022339
protein coding gene Chr15:99520698-99526856 (+)
C3H/HeJ MGP_C3HHeJ_G0022108
protein coding gene Chr15:102530510-102536668 (+)
C57BL/6NJ MGP_C57BL6NJ_G0022787
protein coding gene Chr15:107374556-107380716 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0020312
protein coding gene Chr15:95144531-95150732 (+)
CAST/EiJ MGP_CASTEiJ_G0021634
protein coding gene Chr15:103399377-103408647 (+)
CBA/J MGP_CBAJ_G0022078
protein coding gene Chr15:111095771-111102157 (+)
DBA/2J MGP_DBA2J_G0022205
protein coding gene Chr15:98751313-98757469 (+)
FVB/NJ MGP_FVBNJ_G0022184
protein coding gene Chr15:97802625-97808781 (+)
LP/J MGP_LPJ_G0022276
protein coding gene Chr15:103656769-103662915 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0022205
protein coding gene Chr15:114769040-114775196 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0022801
protein coding gene Chr15:102484549-102490861 (+)
PWK/PhJ MGP_PWKPhJ_G0021373
protein coding gene Chr15:98909890-98916457 (+)
SPRET/EiJ MGP_SPRETEiJ_G0021205
protein coding gene Chr15:102374402-102380458 (+)
WSB/EiJ MGP_WSBEiJ_G0021683
protein coding gene Chr15:103114255-103120633 (+)



Homology
more
  • Human Ortholog
    KRT88P, keratin 88, pseudogene
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    KRT88P, keratin 88, pseudogene
  • Synonyms
    HBC, KRT122P, KRTHBP3
  • Links
    NCBI Gene ID: 85348

  • Chr Location
    12q13.13; chr12:52263781-52268497 (+)  GRCh38

Human Diseases
less
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    30 phenotype references
  • All Mutations and Alleles
    7
  • Chemically induced (other)
    1
  • Endonuclease-mediated
    1
  • Radiation induced
    2
  • Targeted
    3
  • Genomic Mutations
    4 involving Krt88
  • Incidental Mutations
    APF
  • Find Mice (IMSR)
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
  • cDNA Data
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000063971 Ensembl Gene Model | MGI Sequence Detail 6164 C57BL/6J ±  kb
transcript ENSMUST00000023781 Ensembl | MGI Sequence Detail 902 Not Applicable  
polypeptide ENSMUSP00000023781 Ensembl | MGI Sequence Detail 171 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR018039 Intermediate filament protein, conserved site
    IPR039008 Intermediate filament, rod domain
Molecular
Reagents
less
  • All nucleic 11
    cDNA 11

    Microarray probesets 2
References
more
  • Summaries
    All 46
    Diseases 1
    Phenotypes 30
  • Earliest
    J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
  • Latest
    J:274872 Ingham NJ, et al., Mouse screen reveals multiple new genes underlying mouse and human hearing loss. PLoS Biol. 2019 Apr;17(4):e3000194

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory