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Krtap10-26 Gene Detail
Summary
  • Symbol
    Krtap10-26
  • Name
    keratin associated protein 10-26
  • Synonyms
    Gm7138
  • Feature Type
    protein coding gene
  • IDs
    MGI:3779678
    NCBI Gene: 102640500
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:77612086-77612778 bp, - strand
    From Ensembl 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
    71 from dbSNP Build 142
  • Strain Annotations
    2
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3779678
protein coding gene Chr10:77612046-77612778 (-)
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 no annotation
LP/J no annotation
NOD/ShiLtJ no annotation
NZO/HlLtJ MGP_NZOHlLtJ_G0017842
protein coding gene Chr10:77480312-77480828 (-)
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    KRTAP10-1, keratin associated protein 10-1
  • Vertebrate Orthologs
    13
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    KRTAP10-1, keratin associated protein 10-1
  • Synonyms
    KAP10.1, KAP18-1, KAP18.1, KRTAP10.1, KRTAP18-1, KRTAP18.1
  • Links
    NCBI Gene ID: 386677
    UniProt: P60331

  • Chr Location
    21q22.3; chr21:44538981-44540195 (-)  GRCh38

  • Human Ortholog
    KRTAP10-10, keratin associated protein 10-10
  • Synonyms
    KAP10.10, KAP18.10, KRTAP18-10, KRTAP18.10
  • Links
    NCBI Gene ID: 353333
    UniProt: P60014

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

  • Human Ortholog
    KRTAP10-11, keratin associated protein 10-11
  • Synonyms
    KAP10.11, KAP18.11, KRTAP18-11, KRTAP18.11
  • Links
    NCBI Gene ID: 386678
    UniProt: P60412

  • Chr Location
    21q22.3; chr21:44646414-44647650 (+)  GRCh38

  • Human Ortholog
    KRTAP10-12, keratin associated protein 10-12
  • Synonyms
    KAP10.12, KRTAP18-12, KRTAP18.12
  • Links
    NCBI Gene ID: 386685
    UniProt: P60413

  • Chr Location
    21q22.3; chr21:44697172-44698044 (+)  GRCh38

  • Human Ortholog
    KRTAP10-2, keratin associated protein 10-2
  • Synonyms
    KAP10.2, KAP18-2, KAP18.2, KRTAP10.2, KRTAP18-2, KRTAP18.2
  • Links
    NCBI Gene ID: 386679
    UniProt: P60368

  • Chr Location
    21q22.3; chr21:44550357-44551505 (-)  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
    UniProt: P60369

  • Chr Location
    21q22.3; chr21:44557790-44558795 (-)  GRCh38

  • Human Ortholog
    KRTAP10-4, keratin associated protein 10-4
  • Synonyms
    KAP10.4, KAP18-4, KRTAP10.4, KRTAP18-4, KRTAP18.4
  • Links
    NCBI Gene ID: 386672
    UniProt: P60372

  • Chr Location
    21q22.3; chr21:44573729-44575371 (+)  GRCh38

  • Human Ortholog
    KRTAP10-5, keratin associated protein 10-5
  • Synonyms
    KAP10.5, KAP18-5, KAP18.5, KRTAP10.5, KRTAP18.1, KRTAP18-5, KRTAP18.5
  • Links
    NCBI Gene ID: 386680
    UniProt: P60370

  • Chr Location
    21q22.3; chr21:44579455-44580604 (-)  GRCh38

  • Human Ortholog
    KRTAP10-6, keratin associated protein 10-6
  • Synonyms
    KAP10.6, KAP18.6, KRTAP18-6, KRTAP18.6
  • Links
    NCBI Gene ID: 386674
    UniProt: P60371

  • Chr Location
    21q22.3; chr21:44591268-44592505 (-)  GRCh38

  • Human Ortholog
    KRTAP10-8, keratin associated protein 10-8
  • Synonyms
    KAP10.8, KRTAP18-8, KRTAP18.8
  • Links
    NCBI Gene ID: 386681
    UniProt: P60410

  • Chr Location
    21q22.3; chr21:44612079-44612954 (+)  GRCh38

  • Human Ortholog
    KRTAP10-9, keratin associated protein 10-9
  • Synonyms
    KAP10.9, KAP18.9, KRTAP18-9
  • Links
    NCBI Gene ID: 386676
    UniProt: P60411

  • Chr Location
    21q22.3; chr21:44627093-44628378 (+)  GRCh38

Human Diseases
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  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    32 phenotype references
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
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

No experimental evidence to support Biological Process annotation, following literature review. See J:73796.
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
Sequences &
Gene Models
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  • All Sequences
  • RefSeq
  • UniProt
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000095593 Ensembl Gene Model | MGI Sequence Detail 693 C57BL/6J ±  kb
transcript ENSMUST00000167669 Ensembl | MGI Sequence Detail 693 Not Applicable  
polypeptide ENSMUSP00000130212 Ensembl | MGI Sequence Detail 230 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR002494 Keratin-associated protein
  • GlyGen
    L7N2C3 1 site
Other
Accession IDs
less
MGI:7580646
References
more
  • Summaries
    All 41
    Diseases 2
    Gene Ontology 3
    Phenotypes 32
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

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
03/24/2026
MGI 6.24
The Jackson Laboratory