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Gm11437 Gene Detail
Summary
  • Symbol
    Gm11437
  • Name
    predicted gene 11437
  • Feature Type
    protein coding gene
  • IDs
    MGI:3650287
    NCBI Gene: 628813
  • Alliance
  • Transcription Start Sites
    2 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:84039187-84058302 bp, - strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 11, 51.29 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    175 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3650287
protein coding gene Chr11:84039177-84058302 (-)
129S1/SvImJ MGP_129S1SvImJ_G0018868
protein coding gene Chr11:85550062-85569956 (-)
A/J MGP_AJ_G0018835
protein coding gene Chr11:82300225-82320379 (-)
AKR/J MGP_AKRJ_G0018805
protein coding gene Chr11:84722447-84750833 (-)
BALB/cJ MGP_BALBcJ_G0018808
protein coding gene Chr11:82686829-82706503 (-)
C3H/HeJ MGP_C3HHeJ_G0018622
protein coding gene Chr11:84775460-84794997 (-)
C57BL/6NJ MGP_C57BL6NJ_G0019260
protein coding gene Chr11:88140994-88175018 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0016893
protein coding gene Chr11:79390536-79410926 (-)
CAST/EiJ MGP_CASTEiJ_G0018177
protein coding gene Chr11:85414103-85448362 (-)
CBA/J MGP_CBAJ_G0018593
protein coding gene Chr11:91907790-91933688 (-)
DBA/2J MGP_DBA2J_G0018701
protein coding gene Chr11:81877791-81896914 (-)
FVB/NJ MGP_FVBNJ_G0018690
protein coding gene Chr11:81349358-81369310 (-)
LP/J MGP_LPJ_G0018771
protein coding gene Chr11:86081821-86105495 (-)
NOD/ShiLtJ MGP_NODShiLtJ_G0018717
protein coding gene Chr11:92069574-92090588 (-)
NZO/HlLtJ MGP_NZOHlLtJ_G0019300
protein coding gene Chr11:85009139-85034326 (-)
PWK/PhJ MGP_PWKPhJ_G0017946
protein coding gene Chr11:82637423-82670635 (-)
SPRET/EiJ MGP_SPRETEiJ_G0017738
protein coding gene Chr11:84548644-84567524 (-)
WSB/EiJ MGP_WSBEiJ_G0018228
protein coding gene Chr11:84853162-84874038 (-)



Homology
more
  • Human Ortholog
    C17orf78, chromosome 17 open reading frame 78
  • Vertebrate Orthologs
    2
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C17orf78, chromosome 17 open reading frame 78
  • Links
    NCBI Gene ID: 284099
    neXtProt AC: NX_Q8N4C9
    UniProt: Q8N4C9

  • Chr Location
    17q12; chr17:37375985-37392708 (+)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    11 phenotype references
Gene Ontology
(GO)
Classifications
less
  • All GO Annotations
  • GO References
Molecular Function

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

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

Click cells to view annotations.
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
  • cDNA Data
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic 628813 NCBI Gene Model | MGI Sequence Detail 19116 C57BL/6J ±  kb
transcript NM_001037932 RefSeq | MGI Sequence Detail 1229 C57BL/6  
polypeptide Q5QR91 UniProt | EBI | MGI Sequence Detail 290 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 2
    cDNA 2

    Microarray probesets 2
Other
Accession IDs
less
MGI:2144184
References
more
  • Summaries
    All 27
    Gene Ontology 1
    Phenotypes 11
  • Earliest
    J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
  • Latest
    J:334297 Warren EB, et al., 17q12 deletion syndrome mouse model shows defects in craniofacial, brain and kidney development, and glucose homeostasis. Dis Model Mech. 2022 Dec 1;15(12):dmm049752

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
03/19/2024
MGI 6.23
The Jackson Laboratory