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Gm7694 Gene Detail
Summary
  • Symbol
    Gm7694
  • Name
    predicted gene 7694
Location &
Maps
more
  • Sequence Map
    Chr1:170125768-170133901 bp, - strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
    Ensembl | UCSC | NCBI
  • Genetic Map
    Chromosome 1, 76.84 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    401 from dbSNP Build 142
  • Strain Annotations
    17
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3649135
 protein coding gene Chr1:170125767-170133901 (-)
129S1/SvImJ ENSMUSG00200043257
 protein coding gene Chr1:167589739-167597822 (-)
A/J ENSMUSG00195045803
 protein coding gene Chr1:166909010-166917124 (-)
AKR/J ENSMUSG00220025651
 protein coding gene Chr1:166617441-166625566 (-)
BALB/cJ ENSMUSG00180043536
 protein coding gene Chr1:167185236-167193373 (-)
C3H/HeJ ENSMUSG00175046997
 protein coding gene Chr1:167245328-167253411 (-)
C57BL/6NJ ENSMUSG00215044507
 protein coding gene Chr1:167066534-167074669 (-)
CAROLI/EiJ MGP_CAROLIEiJ_G0014840
 protein coding gene Chr1:160553675-160561733 (-)
CAST/EiJ ENSTCUG00005045329
 protein coding gene Chr1:165575510-165583656 (-)
CBA/J ENSMUSG00210038180
 protein coding gene Chr1:167150314-167158451 (-)
DBA/2J ENSMUSG00185011706
 protein coding gene Chr1:171367116-171375251 (-)
FVB/NJ ENSMUSG00205025629
 protein coding gene Chr1:166107480-166115561 (-)
JF1/MsJ ENSUMUG00000004637
 protein coding gene Chr1:170510413-170518568 (-)
LP/J no annotation
NOD/ShiLtJ ENSMUSG00190028316
 protein coding gene Chr1:166908059-166916167 (-)
NZO/HlLtJ no annotation
PWK/PhJ ENSLUMG00010027396
 protein coding gene Chr1:165901350-165909479 (-)
SPRET/EiJ ENSMSPG00010045002
 protein coding gene Chr1:169454861-169462991 (-)
WSB/EiJ ENSIUOG00005035200
 protein coding gene Chr1:166316750-166324865 (-)



Homology
more
  • Human Ortholog
    C1orf226, chromosome 1 open reading frame 226
  • Vertebrate Orthologs
    1
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    C1orf226, chromosome 1 open reading frame 226
  • Links
    NCBI Gene ID: 400793
    UniProt: A1L170

  • Chr Location
    1q23.3; chr1:162378841-162386812 (+)  GRCh38
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    2 phenotypes from 1 allele in 1 genetic background
    7 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.
  • All Mutations and Alleles
    4
  • Chemically induced (other)
    2
  • Endonuclease-mediated
    1
  • Gene trapped
    1
  • Genomic Mutations
    2 involving Gm7694
  • Incidental Mutations
    APF
  • Find Mice (IMSR)
    13 strains or lines available
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
    597
Sequences &
Gene Models
less
Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000102752 Ensembl Gene Model | MGI Sequence Detail 8134 C57BL/6J ±  kb
transcript ENSMUST00000179801 Ensembl | MGI Sequence Detail 3827 Not Applicable  
polypeptide ENSMUSP00000136757 Ensembl | MGI Sequence Detail 270 Not Applicable  
For the selected sequence
Protein
Information
less
  • UniProt
    1 Sequence
  • InterPro Domains
    IPR027851 Protein of unknown function DUF4628
References
more
  • Summaries
    All 16
    Phenotypes 7
  • Earliest
    J:345621 Adams DJ, et al., Genetic determinants of micronucleus formation in vivo. Nature. 2024 Mar;627(8002):130-136
  • Latest
    J:375772 Buerger F, et al., Recessive variants in the intergenic NOS1AP-C1orf226 locus cause monogenic kidney disease responsive to anti-proteinuric treatment. Nat Commun. 2025 Nov 27;16(1):10654
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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Send questions and comments to User Support. 		last database update
09/08/2026
MGI 6.24 		The Jackson Laboratory