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Map7d2 Gene Detail
Summary
  • Symbol
    Map7d2
  • Name
    MAP7 domain containing 2
  • Synonyms
    1600028E09Rik, 2900002G04Rik, 5330432J06Rik, C030036K04Rik, Mtap7d2
  • Feature Type
    protein coding gene
  • IDs
    MGI:1917474
    NCBI Gene: 78283
  • Alliance
  • Transcription Start Sites
    14 TSS
Location &
Maps
more
  • Sequence Map
    ChrX:158197568-158281753 bp, + strand
    From Ensembl annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome X, 73.45 cM, cytoband F4
  • Mapping Data
    2 experiments
Strain
Comparison
more
  • SNPs within 2kb
    209 from dbSNP Build 142
  • Strain Annotations
    18
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_1917474
protein coding gene ChrX:158197488-158281954 (+)
129S1/SvImJ MGP_129S1SvImJ_G0036225
protein coding gene ChrX:157310098-157397621 (+)
A/J MGP_AJ_G0036195
protein coding gene ChrX:156590187-156679956 (+)
AKR/J MGP_AKRJ_G0036123
protein coding gene ChrX:161561065-161655085 (+)
BALB/cJ MGP_BALBcJ_G0036188
protein coding gene ChrX:154667121-154764128 (+)
C3H/HeJ MGP_C3HHeJ_G0035894
protein coding gene ChrX:157702310-157796024 (+)
C57BL/6NJ MGP_C57BL6NJ_G0036710
protein coding gene ChrX:162000179-162088730 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0033532
protein coding gene ChrX:147867212-147947459 (+)
CAST/EiJ MGP_CASTEiJ_G0035183
protein coding gene ChrX:136743758-136836209 (+)
CBA/J MGP_CBAJ_G0035869
protein coding gene ChrX:166616250-166708927 (+)
DBA/2J MGP_DBA2J_G0036035
protein coding gene ChrX:155575312-155663110 (+)
FVB/NJ MGP_FVBNJ_G0035966
protein coding gene ChrX:154703102-154783590 (+)
LP/J MGP_LPJ_G0036120
protein coding gene ChrX:158473108-158559636 (+)
NOD/ShiLtJ MGP_NODShiLtJ_G0035998
protein coding gene ChrX:175300883-175399265 (+)
NZO/HlLtJ MGP_NZOHlLtJ_G0036751
protein coding gene ChrX:156854676-156944784 (+)
PWK/PhJ MGP_PWKPhJ_G0034881
protein coding gene ChrX:133624193-133709687 (+)
SPRET/EiJ MGP_SPRETEiJ_G0034702
protein coding gene ChrX:137170187-137258891 (+)
WSB/EiJ MGP_WSBEiJ_G0035318
protein coding gene ChrX:154824038-154911738 (+)



Homology
more
  • Human Ortholog
    MAP7D2, MAP7 domain containing 2
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    MAP7D2, MAP7 domain containing 2
  • Links
    NCBI Gene ID: 256714
    neXtProt AC: NX_Q96T17
    UniProt: Q96T17

  • Chr Location
    Xp22.12; chrX:20006713-20116907 (-)  GRCh38

Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    1 phenotype from 1 allele in 1 genetic background
    11 images
    8 phenotype references
  • All Mutations and Alleles
    6
  • Endonuclease-mediated
    1
  • Gene trapped
    3
  • Radiation induced
    1
  • Spontaneous
    1
  • Genomic Mutations
    2 involving Map7d2
  • Find Mice (IMSR)
Male chimeras hemizygous for a gene trapped allele appear normal at E9.5.
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
non-membrane-bounded 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
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic ENSMUSG00000041020 Ensembl Gene Model | MGI Sequence Detail 84186 C57BL/6J ±  kb
transcript ENSMUST00000112471 Ensembl | MGI Sequence Detail 3670 Not Applicable  
polypeptide ENSMUSP00000108090 Ensembl | MGI Sequence Detail 781 Not Applicable  
For the selected sequence
Protein
Information
less
Molecular
Reagents
less
  • All nucleic 26
    Genomic 2
    cDNA 24

    Microarray probesets 4
Other
Accession IDs
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MGI:1920503, MGI:1924891, MGI:1925533
References
more
  • Summaries
    All 29
    Developmental Gene Expression 1
    Gene Ontology 1
    Phenotypes 8
  • Earliest
    J:46359 Blair HJ, et al., Mouse mutants carrying deletions that remove the genes mutated in Coffin-Lowry syndrome and lactic acidosis. Hum Mol Genet. 1998 Mar;7(3):549-55
  • Latest
    J:326541 Cyagen Biosciences Inc., Cyagen Biosciences Website. 2022;

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
04/09/2024
MGI 6.23
The Jackson Laboratory