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Gm9507 Gene Detail
Summary
  • Symbol
    Gm9507
  • Name
    predicted gene 9507
  • Feature Type
    protein coding gene
  • IDs
    MGI:3779917
    NCBI Gene: 670880
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:77646801-77647677 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
    13 from dbSNP Build 142
  • Strain Annotations
    14
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3779917
protein coding gene Chr10:77646581-77647723 (-)
129S1/SvImJ no annotation
A/J MGP_AJ_G0017385
protein coding gene Chr10:75489991-75491803 (-)
AKR/J MGP_AKRJ_G0017348
protein coding gene Chr10:77517156-77519773 (-)
BALB/cJ MGP_BALBcJ_G0017347
protein coding gene Chr10:75676290-75676964 (-)
C3H/HeJ MGP_C3HHeJ_G0017170
protein coding gene Chr10:77588042-77588920 (-)
C57BL/6NJ no annotation
CAROLI/EiJ MGP_CAROLIEiJ_G0015494
protein coding gene Chr10:71858440-71859287 (-)
CAST/EiJ MGP_CASTEiJ_G0016740
protein coding gene Chr10:77921658-77922254 (-)
CBA/J MGP_CBAJ_G0017142
protein coding gene Chr10:84031793-84032554 (-)
DBA/2J MGP_DBA2J_G0017250
protein coding gene Chr10:74738817-74740574 (-)
FVB/NJ MGP_FVBNJ_G0017242
protein coding gene Chr10:73908899-73909842 (-)
LP/J MGP_LPJ_G0017322
protein coding gene Chr10:78638697-78639152 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0017269
protein coding gene Chr10:86059463-86060902 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0017845
protein coding gene Chr10:77557033-77557866 (-)
PWK/PhJ no annotation
SPRET/EiJ MGP_SPRETEiJ_G0016307
protein coding gene Chr10:76761671-76763494 (-)
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.p7

  • 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; chr21:44558023-44558760 (-)  GRCh38.p7

  • 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.p7

Human Diseases
less
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    25 phenotype references
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
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000094913 Ensembl Gene Model | MGI Sequence Detail 877 C57BL/6J ±  kb
transcript ENSMUST00000095491 Ensembl | MGI Sequence Detail 877 Not Applicable  
polypeptide ENSMUSP00000093145 Ensembl | MGI Sequence Detail 223 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    2 Sequences
  • InterPro Domains
    IPR002494 Keratin-associated protein
References
more
  • Summaries
    All 32
    Diseases 2
    Phenotypes 25
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:332837 Jewett CE, et al., Trisomy 21 induces pericentrosomal crowding delaying primary ciliogenesis and mouse cerebellar development. Elife. 2023 Jan 19;12

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
03/21/2023
MGI 6.22
The Jackson Laboratory