About   Help   FAQ
Krt16 Gene Detail
Summary
  • Symbol
    Krt16
  • Name
    keratin 16
  • Synonyms
    K16, Krt1-16
  • Feature Type
    protein coding gene
  • IDs
    MGI:96690
    NCBI Gene: 16666
  • Gene Overview
    MyGene.info: KRT16
  • Alliance
Location & Maps
more
  • Sequence Map
    Chr11:100246091-100248902 bp, - strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      2812 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 11, 63.44 cM
  • Mapping Data
    1 experiment
Homology
more
  • Human Ortholog
    KRT16, keratin 16
  • Vertebrate Orthologs
    7
  • Human Ortholog
    KRT16, keratin 16
    Orthology source: HomoloGene, HGNC
  • Synonyms
    CK16, FNEPPK, K16, K1CP, KRT16A, NEPPK, PC1
  • Links
    NCBI Gene ID: 3868
    neXtProt AC: NX_P08779
    UniProt: P08779

  • Chr Location
    17q21.2; chr17:41609778-41612827 (-)  GRCh38.p7

Human Diseases
more
  • Diseases
    2 with Krt16 mouse models; 2 with human KRT16 associations

Human Disease Mouse Models
      
IDs
View 1 model
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    14 phenotypes from 1 allele in 1 genetic background
    13 phenotypes from multigenic genotypes
    13 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 a knock-out allele exhibit partial neonatal and postnatal lethality, decreased body weight, abnormal tongue epithelium and hyperkertotic calluses in areas of physical pressure.
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

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

nucleic acid-templated transcription
carbohydrate derivative metabolism
cell death
cell differentiation
cell proliferation
cellular component organization
establishment of localization
homeostatic process
immune system process
lipid metabolic process
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
non-membrane-bounded organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Interactions
    less
    Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic OTTMUSG00000002540 VEGA Gene Model | MGI Sequence Detail 2812 C57BL/6J ±  kb
    transcript OTTMUST00000004966 VEGA | MGI Sequence Detail 1565 Not Applicable  
    polypeptide OTTMUSP00000002391 VEGA | MGI Sequence Detail 469 Not Applicable  
    For the selected sequence
    Polymorphisms
    less
    • SNPs within 2kb
      52 from dbSNP Build 142
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 23
      cDNA 21
      Primer pair 2

      Microarray probesets 3
    Other
    Accession IDs
    less
    MGD-MRK-11645, MGI:2144125
    References
    more
    • Summaries
      All 52
      Developmental Gene Expression 10
      Diseases 1
      Gene Ontology 7
      Phenotypes 13
    • Earliest
      J:16017 Steinert PM, et al., Complete amino acid sequence of a mouse epidermal keratin subunit and implications for the structure of intermediate filaments. Nature. 1983 Apr 28;302(5911):794-800
    • Latest
      J:261187 Kerns ML, et al., Sexual Dimorphism in Response to an NRF2 Inducer in a Model for Pachyonychia Congenita. J Invest Dermatol. 2018 May;138(5):1094-1100

    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
    Citing These Resources
    Funding Information
    Warranty Disclaimer & Copyright Notice
    Send questions and comments to User Support.
    last database update
    06/12/2018
    MGI 6.12
    The Jackson Laboratory