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Mcm3ap Gene Detail
Summary
  • Symbol
    Mcm3ap
  • Name
    minichromosome maintenance complex component 3 associated protein
  • Synonyms
    GANP, mKIAA0572
  • Feature Type
    protein coding gene
  • IDs
    MGI:1930089
    NCBI Gene: 54387
  • Alliance
  • Transcription Start Sites
    5 TSS
Location &
Maps
more
  • Sequence Map
    Chr10:76304761-76351691 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 10, 38.88 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    1218 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1930089
protein coding gene Chr10:76304736-76351693 (+)
129S1/SvImJ ENSMUSG00200041330
protein coding gene Chr10:72982916-73028830 (+)
A/J ENSMUSG00195047097
protein coding gene Chr10:73319537-73365451 (+)
AKR/J ENSMUSG00220038507
protein coding gene Chr10:72979252-73025163 (+)
BALB/cJ ENSMUSG00180047610
protein coding gene Chr10:73333985-73379903 (+)
C3H/HeJ ENSMUSG00175050197
protein coding gene Chr10:73205270-73251174 (+)
C57BL/6NJ ENSMUSG00215051513
protein coding gene Chr10:72942900-72988816 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0015469
protein coding gene Chr10:70515063-70561932 (+)
CAST/EiJ ENSTCUG00005049923
protein coding gene Chr10:72825546-72871218 (+)
CBA/J ENSMUSG00210049668
protein coding gene Chr10:73061468-73107378 (+)
DBA/2J ENSMUSG00185051974
protein coding gene Chr10:73403734-73449631 (+)
FVB/NJ ENSMUSG00205049444
protein coding gene Chr10:73096406-73142306 (+)
JF1/MsJ ENSUMUG00000041465
protein coding gene Chr10:74554028-74599570 (+)
LP/J ENSMUSG00230050096
protein coding gene Chr10:75173284-75219192 (+)
NOD/ShiLtJ ENSMUSG00190042365
protein coding gene Chr10:73381233-73427144 (+)
NZO/HlLtJ ENSMUSG00225046183
protein coding gene Chr10:79469982-79515888 (+)
PWK/PhJ ENSLUMG00010048945
protein coding gene Chr10:72944335-72990840 (+)
SPRET/EiJ ENSMSPG00010035141
protein coding gene Chr10:74737243-74782761 (+)
WSB/EiJ ENSIUOG00005047185
protein coding gene Chr10:72985901-73031842 (+)



Homology
more
  • Human Ortholog
    MCM3AP, minichromosome maintenance complex component 3 associated protein
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    MCM3AP, minichromosome maintenance complex component 3 associated protein
  • Synonyms
    GANP, MAP80, PNRIID, SAC3
  • Links
    NCBI Gene ID: 8888
    UniProt: O60318

  • Chr Location
    21q22.3; chr21:46235133-46286297 (-)  GRCh38

Human Diseases
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  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    8 phenotypes from 2 alleles in 2 genetic backgrounds
    48 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.
Mice homozygous for a null allele die by E12.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
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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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
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    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000001150 Ensembl Gene Model | MGI Sequence Detail 46931 C57BL/6J ±  kb
    transcript ENSMUST00000170795 Ensembl | MGI Sequence Detail 6427 Not Applicable  
    polypeptide ENSMUSP00000125960 Ensembl | MGI Sequence Detail 1971 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    • UniProt
      7 Sequences
    • Protein Ontology
      PR:000010244 germinal-center associated nuclear protein
    • EC
    • InterPro Domains
      IPR062097 GANP, MCM3AP C-terminal domain
      IPR031910 Germinal-centre associated nuclear protein, CID domain
      IPR031907 Germinal-centre associated nuclear protein, MCM3AP N-terminal domain
      IPR031908 Germinal-centre associated nuclear protein, nucleoporin homology domain
      IPR034265 MCM3AP, RNA recognition motif
      IPR000717 Proteasome component (PCI) domain
      IPR035979 RNA-binding domain superfamily
      IPR045107 SAC3/GANP/THP3
      IPR005062 SAC3/GANP/THP3, conserved domain
    • GlyGen
      Q9WUU9 9 sites, 1 N-linked glycan (1 site), 1 O-linked glycan (4 sites)
    Molecular
    Reagents
    less
    • All nucleic 126
      Genomic 1
      cDNA 122
      Primer pair 2
      Other 1

      Microarray probesets 3
    References
    more
    • Summaries
      All 89
      Developmental Gene Expression 5
      Diseases 2
      Gene Ontology 11
      Phenotypes 48
    • Earliest
      J:137335 Roderick TH, Chromosomal inversions in studies of mammalian mutagenesis. Genetics. 1979 May;92(1 Pt 1 Suppl):s121-6
    • Latest
      J:361105 Tateossian H, et al., DYRK1A kinase triplication is the major cause of Otitis Media in Down Syndrome. Elife. 2025;

    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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    last database update
    09/08/2026
    MGI 6.24
    The Jackson Laboratory