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AW209491 Gene Detail
Summary
  • Symbol
    AW209491
  • Name
    expressed sequence AW209491
  • Feature Type
    protein coding gene
  • IDs
    MGI:2145422
    NCBI Gene: 105351
  • Alliance
  • Transcription Start Sites
    1 TSS
Location &
Maps
more
  • Sequence Map
    Chr13:14804830-14812787 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 13, 5.36 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    307 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_2145422
protein coding gene Chr13:14804739-14813681 (+)
129S1/SvImJ MGP_129S1SvImJ_G0020246
protein coding gene Chr13:11618506-11626473 (+)
A/J MGP_AJ_G0020204
protein coding gene Chr13:11527739-11535695 (+)
AKR/J MGP_AKRJ_G0020178
protein coding gene Chr13:11674521-11682463 (+)
BALB/cJ MGP_BALBcJ_G0020190
protein coding gene Chr13:11498168-11506137 (+)
C3H/HeJ MGP_C3HHeJ_G0019994
protein coding gene Chr13:11813542-11821550 (+)
C57BL/6NJ MGP_C57BL6NJ_G0020634
protein coding gene Chr13:12246273-12254234 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0018240
protein coding gene Chr13:10219752-10227878 (+)
CAST/EiJ MGP_CASTEiJ_G0019527
protein coding gene Chr13:11480552-11488240 (+)
CBA/J MGP_CBAJ_G0019958
protein coding gene Chr13:12603243-12611226 (+)
DBA/2J MGP_DBA2J_G0020077
protein coding gene Chr13:11174754-11183092 (+)
FVB/NJ MGP_FVBNJ_G0020058
protein coding gene Chr13:10936996-10944984 (+)
LP/J MGP_LPJ_G0020147
protein coding gene Chr13:11830030-11839295 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0020095
protein coding gene Chr13:12772386-12780515 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0020661
protein coding gene Chr13:11481385-11493293 (+)
PWK/PhJ MGP_PWKPhJ_G0019291
protein coding gene Chr13:11254945-11263136 (+)
SPRET/EiJ MGP_SPRETEiJ_G0019098
protein coding gene Chr13:10630144-10642434 (+)
WSB/EiJ MGP_WSBEiJ_G0019589
protein coding gene Chr13:11486676-11495784 (+)



Homology
more
  • Human Ortholog
    C7orf25, chromosome 7 open reading frame 25
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C7orf25, chromosome 7 open reading frame 25
  • Links
    NCBI Gene ID: 79020
    UniProt: Q9BPX7

  • Chr Location
    7p14.1; chr7:42909273-42912305 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 1 allele in 1 genetic background
    6 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Gene Ontology
(GO)
Classifications
less
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

No experimental evidence to support Cellular Component annotation, following literature review. See J:73796.
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
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 105351 NCBI Gene Model | MGI Sequence Detail 7958 C57BL/6J ±  kb
    transcript NM_134067 RefSeq | MGI Sequence Detail 2010 C57BL/6  
    polypeptide Q91WD4 UniProt | EBI | MGI Sequence Detail 421 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 11
      cDNA 11

      Microarray probesets 3
    References
    more
    • Summaries
      All 23
      Phenotypes 6
    • Earliest
      J:86696 Zambrowicz BP, et al., Wnk1 kinase deficiency lowers blood pressure in mice: a gene-trap screen to identify potential targets for therapeutic intervention. Proc Natl Acad Sci U S A. 2003 Nov 25;100(24):14109-14
    • Latest
      J:142754 Hansen GM, et al., Large-scale gene trapping in C57BL/6N mouse embryonic stem cells. Genome Res. 2008 Oct;18(10):1670-9

    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
    03/18/2025
    MGI 6.24
    The Jackson Laboratory