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Gm7735 Gene Detail
Summary
  • Symbol
    Gm7735
  • Name
    predicted gene 7735
  • Feature Type
    protein coding gene
  • IDs
    MGI:3649168
    NCBI Gene: 102637417
  • Alliance
Location &
Maps
more
  • Sequence Map
    Chr16:89169490-89169648 bp, + strand
  • From NCBI annotation of GRCm38

    View this region in JBrowse

  • Genome Browsers
  • Genetic Map
    Chromosome 16, 51.42 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    25 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3649168
protein coding gene Chr16:89169490-89169648 (+)
129S1/SvImJ MGP_129S1SvImJ_G0023015
protein coding gene Chr16:90013492-90013650 (+)
A/J MGP_AJ_G0022983
protein coding gene Chr16:85842031-85842177 (+)
AKR/J MGP_AKRJ_G0022953
protein coding gene Chr16:88466294-88466452 (+)
BALB/cJ MGP_BALBcJ_G0022985
protein coding gene Chr16:86369570-86369728 (+)
C3H/HeJ MGP_C3HHeJ_G0022746
protein coding gene Chr16:88995294-88995452 (+)
C57BL/6NJ MGP_C57BL6NJ_G0023432
protein coding gene Chr16:92902577-92902735 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0020935
protein coding gene Chr16:83610175-83610330 (+)
CAST/EiJ MGP_CASTEiJ_G0022266
protein coding gene Chr16:89467577-89467735 (+)
CBA/J MGP_CBAJ_G0022715
protein coding gene Chr16:96880679-96880837 (+)
DBA/2J MGP_DBA2J_G0022849
protein coding gene Chr16:85771301-85771447 (+)
FVB/NJ no annotation
LP/J MGP_LPJ_G0022919
protein coding gene Chr16:89707583-89707729 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0022844
protein coding gene Chr16:101470484-101470642 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0023450
protein coding gene Chr16:88939886-88940044 (+)
PWK/PhJ MGP_PWKPhJ_G0022010
protein coding gene Chr16:85912641-85912787 (+)
SPRET/EiJ MGP_SPRETEiJ_G0021841
protein coding gene Chr16:88482034-88482192 (+)
WSB/EiJ MGP_WSBEiJ_G0022317
protein coding gene Chr16:89172208-89172366 (+)



Homology
less
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    4 phenotype references
Expression
less
Sequences &
Gene Models
less
  • All Sequences
  • RefSeq
  • UniProt
Representative SequencesLengthStrain/SpeciesFlank
genomic 102637417 NCBI Gene Model | MGI Sequence Detail 159 C57BL/6J ±  kb
transcript XM_006523124 RefSeq | MGI Sequence Detail 159 C57BL/6J  
polypeptide D3YX18 UniProt | EBI | MGI Sequence Detail 52 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR021743 Keratin-associated protein, type6/8/16/19/20/21
Molecular
Reagents
less

  • Microarray probesets 1
References
more
  • Summaries
    All 11
    Phenotypes 4
  • Earliest
    J:185269 Raveau M, et al., The app-runx1 region is critical for birth defects and electrocardiographic dysfunctions observed in a down syndrome mouse model. PLoS Genet. 2012 May;8(5):e1002724
  • Latest
    J:262380 Watson-Scales S, et al., Analysis of motor dysfunction in Down Syndrome reveals motor neuron degeneration. PLoS Genet. 2018 May;14(5):e1007383

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
10/08/2019
MGI 6.14
The Jackson Laboratory