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Krtap10-22 Gene Detail
Summary
  • Symbol
    Krtap10-22
  • Name
    keratin associated protein 10-22
  • Synonyms
    Gm3238
  • Feature Type
    protein coding gene
  • IDs
    MGI:3781416
    NCBI Gene: 100041261
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr10:77606467-77607159 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 10, 39.72 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    74 from dbSNP Build 142
  • Strain Annotations
    3
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3781416
protein coding gene Chr10:77606467-77607159 (-)
129S1/SvImJ no annotation
A/J no annotation
AKR/J no annotation
BALB/cJ no annotation
C3H/HeJ no annotation
C57BL/6NJ no annotation
CAROLI/EiJ no annotation
CAST/EiJ no annotation
CBA/J no annotation
DBA/2J no annotation
FVB/NJ MGP_FVBNJ_G0017238
protein coding gene Chr10:73845393-73846301 (-)
LP/J MGP_LPJ_G0017320
protein coding gene Chr10:78585512-78588069 (-)
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    KRTAP10-10, keratin associated protein 10-10
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    KRTAP10-10, keratin associated protein 10-10
  • Synonyms
    KAP10.10, KAP18.10, KRTAP18-10, KRTAP18.10
  • Links
    NCBI Gene ID: 353333
    neXtProt AC: NX_P60014
    UniProt: P60014

  • Chr Location
    21q22.3; chr21:44637356-44638455 (+)  GRCh38

  • Human Ortholog
    KRTAP10-3, keratin associated protein 10-3
  • Synonyms
    KAP10.3, KAP18-3, KAP18.3, KRTAP10.3, KRTAP18-3, KRTAP18.3
  • Links
    NCBI Gene ID: 386682
    neXtProt AC: NX_P60369
    UniProt: P60369

  • Chr Location
    21q22.3

  • Human Ortholog
    KRTAP10-7, keratin associated protein 10-7
  • Synonyms
    KAP10.7, KAP18.7, KRTAP18-7
  • Links
    NCBI Gene ID: 386675
    neXtProt AC: NX_P60409
    UniProt: P60409

  • Chr Location
    21q22.3; chr21:44600597-44602174 (+)  GRCh38

Human Diseases
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  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    29 phenotype references
  • All Mutations and Alleles
    4
  • Chemically induced (other)
    1
  • Targeted
    3
  • Genomic Mutations
    4 involving Krtap10-22
  • Incidental Mutations
    APF
  • Find Mice (IMSR)
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
Cellular Component

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 100041261 NCBI Gene Model | MGI Sequence Detail 693 C57BL/6J ±  kb
transcript NM_001101630 RefSeq | MGI Sequence Detail 693 mixed  
polypeptide NP_001095100 RefSeq | MGI Sequence Detail 230 mixed  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR002494 Keratin-associated protein
Other
Accession IDs
less
MGI:7580617
References
more
  • Summaries
    All 37
    Diseases 2
    Gene Ontology 1
    Phenotypes 29
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:357279 Donovan MG, et al., Multimodal analysis of dysregulated heme metabolism, hypoxic signaling, and stress erythropoiesis in Down syndrome. Cell Rep. 2024 Aug 27;43(8):114599

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