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Morc2a Gene Detail
Summary
  • Symbol
    Morc2a
  • Name
    microrchidia 2A
  • Synonyms
    8430403M08Rik, Zcwcc1
  • Feature Type
    protein coding gene
  • IDs
    MGI:1921772
    NCBI Gene: 74522
  • Alliance
  • Transcription Start Sites
    3 TSS
Location &
Maps
more
  • Sequence Map
    Chr11:3599191-3640477 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 11, 2.56 cM
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    719 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1921772
protein coding gene Chr11:3599132-3640477 (+)
129S1/SvImJ MGP_129S1SvImJ_G0017962
protein coding gene Chr11:537265-581023 (+)
A/J MGP_AJ_G0017935
protein coding gene Chr11:574370-618654 (+)
AKR/J MGP_AKRJ_G0017899
protein coding gene Chr11:595499-636446 (+)
BALB/cJ MGP_BALBcJ_G0017903
protein coding gene Chr11:541713-582693 (+)
C3H/HeJ MGP_C3HHeJ_G0017716
protein coding gene Chr11:526909-568542 (+)
C57BL/6NJ MGP_C57BL6NJ_G0018356
protein coding gene Chr11:612955-653849 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0016015
protein coding gene Chr11:477226-518854 (+)
CAST/EiJ MGP_CASTEiJ_G0017278
protein coding gene Chr11:491686-536318 (+)
CBA/J MGP_CBAJ_G0017691
protein coding gene Chr11:785734-826736 (+)
DBA/2J MGP_DBA2J_G0017802
protein coding gene Chr11:487898-528871 (+)
FVB/NJ MGP_FVBNJ_G0017793
protein coding gene Chr11:518591-560596 (+)
LP/J MGP_LPJ_G0017872
protein coding gene Chr11:626015-669211 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0017819
protein coding gene Chr11:533732-576190 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0018395
protein coding gene Chr11:609612-653319 (+)
PWK/PhJ MGP_PWKPhJ_G0017059
protein coding gene Chr11:474874-517465 (+)
SPRET/EiJ MGP_SPRETEiJ_G0016855
protein coding gene Chr11:564886-609957 (+)
WSB/EiJ MGP_WSBEiJ_G0017332
protein coding gene Chr11:485425-527440 (+)



Homology
more
  • Human Ortholog
    MORC2, MORC family CW-type zinc finger 2
  • Vertebrate Orthologs
    3
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    MORC2, MORC family CW-type zinc finger 2
  • Synonyms
    CMT2Z, DIGFAN, ZCW3, ZCWCC1
  • Links
    NCBI Gene ID: 22880
    neXtProt AC: NX_Q9Y6X9
    UniProt: Q9Y6X9

  • Chr Location
    22q12.2; chr22:30925130-30968774 (-)  GRCh38

Human Diseases
more
  • Diseases
    1 with Morc2a mouse models; 1 with human MORC2 associations

Human Disease Mouse Models
      
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    1 with disease annotations
  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
less
  • Phenotype Summary
    170 phenotypes from 5 alleles in 5 genetic backgrounds
    5 phenotypes from multigenic genotypes
    16 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 exhibit embryonic lethality around E13.5 and decreased embryo size. Mice homozygous for a null allele activated in neurons exhibit increased brain size, altered brain architecture, and behavioral changes. Heterozygosity for the p.S87L mutation is partially prenatal lethal and leads to Charcot-Marie-Tooth disease-like neuropathies.
Gene Ontology
(GO)
Classifications
less
  • 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
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
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic ENSMUSG00000034543 Ensembl Gene Model | MGI Sequence Detail 41287 C57BL/6J ±  kb
    transcript ENSMUST00000096441 Ensembl | MGI Sequence Detail 5656 Not Applicable  
    polypeptide ENSMUSP00000094176 Ensembl | MGI Sequence Detail 1030 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    Molecular
    Reagents
    less
    • All nucleic 8
      cDNA 7
      Primer pair 1

      Microarray probesets 3
    References
    more
    • Summaries
      All 46
      Developmental Gene Expression 6
      Diseases 1
      Gene Ontology 8
      Phenotypes 16
    • Earliest
      J:65060 Kawai J, et al., Functional annotation of a full-length mouse cDNA collection. Nature. 2001 Feb 8;409(6821):685-90
    • Latest
      J:350444 Martinez-Mayer J, et al., Knockout mice with pituitary malformations help identify human cases of hypopituitarism. Genome Med. 2024 May 31;16(1):75

    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
    12/10/2024
    MGI 6.24
    The Jackson Laboratory