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Samd12 Gene Detail
Summary
  • Symbol
    Samd12
  • Name
    sterile alpha motif domain containing 12
  • Synonyms
    A830094I09Rik
  • Feature Type
    protein coding gene
  • IDs
    MGI:2444518
    NCBI Gene: 320679
Location & Maps
more
  • Sequence Map
    Chr15:53461621-53902537 bp, - strand
  • From VEGA annotation of GRCm38

    Mouse Genome Browser

  • Download
    Sequence
      440917 bp   ±  kb flank

  • Genome Browsers
  • Genetic Map
    Chromosome 15, 21.10 cM
  • Mapping Data
    1 experiment
Homology
more
  • Human Ortholog
    SAMD12, sterile alpha motif domain containing 12
  • Vertebrate Orthologs
    10
  • Human Ortholog
    SAMD12, sterile alpha motif domain containing 12
    Orthology source: HomoloGene, HGNC
  • Links
    NCBI Gene ID: 401474
    neXtProt AC: NX_Q8N8I0
    UniProt: Q8N8I0

  • Chr Location
    8q24.11-q24.12; chr8:118131828-118621995 (-)  GRCh38.p7

  • HomoloGene
    Vertebrate Homology Class 35979
    1 human;1 mouse;1 rat;1 chimpanzee;1 cattle;1 dog;1 chicken;1 zebrafish;1 frog, western clawed;1 macaque, rhesus
  • HCOP
    human homology predictions: SAMD12
  • Gene Tree
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    15 phenotype references
Gene Ontology
(GO)
Classifications
less
Expression
less
  • cDNA Data
Interactions
less
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000019492 VEGA Gene Model | MGI Sequence Detail 440917 C57BL/6J ±  kb
transcript OTTMUST00000046537 VEGA | MGI Sequence Detail 1028 Not Applicable  
polypeptide OTTMUSP00000021015 VEGA | MGI Sequence Detail 161 Not Applicable  
For the selected sequence
Polymorphisms
less
  • SNPs within 2kb
    3788 from dbSNP Build 142
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 6
    cDNA 6

    Microarray probesets 1
References
more
  • Summaries
    All 28
    Phenotypes 15
  • Earliest
    J:109968 Roderick TH, et al., Nineteen paracentric chromosomal inversions in mice. Genetics. 1974 Jan;76(1):109-17
  • Latest
    J:155838 Katayama K, et al., Characterization of the chromosomal inversion associated with the Koa mutation in the mouse revealed the cause of skeletal abnormalities. BMC Genet. 2009;10:60

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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last database update
04/11/2017
MGI 6.08
The Jackson Laboratory