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Tmt1a2 Gene Detail
Summary
  • Symbol
    Tmt1a2
  • Name
    thiol methyltransferase 1A2
  • Synonyms
    Mettl7a2, Ubie
Location &
Maps
more
  • Sequence Map
    Chr15:100251081-100259700 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 15, 56.27 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    436 from dbSNP Build 142
  • Strain Annotations
    12
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_3026615
protein coding gene Chr15:100251081-100259721 (+)
129S1/SvImJ ENSMUSG00200049944
protein coding gene Chr15:97456911-97465542 (+)
A/J ENSMUSG00195041706
protein coding gene Chr15:97334429-97343073 (+)
AKR/J ENSMUSG00220046265
protein coding gene Chr15:97327664-97336310 (+)
BALB/cJ ENSMUSG00180040506
protein coding gene Chr15:97232737-97241368 (+)
C3H/HeJ ENSMUSG00175040182
protein coding gene Chr15:97514414-97523056 (+)
C57BL/6NJ ENSMUSG00215049352
protein coding gene Chr15:97289507-97298149 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0020287
protein coding gene Chr15:94047054-94052469 (+)
CAST/EiJ no annotation
CBA/J ENSMUSG00210028120
protein coding gene Chr15:97289585-97298216 (+)
DBA/2J ENSMUSG00185038860
protein coding gene Chr15:97334022-97342662 (+)
FVB/NJ ENSMUSG00205021563
protein coding gene Chr15:97038523-97047163 (+)
JF1/MsJ no annotation
LP/J ENSMUSG00230039291
protein coding gene Chr15:100680255-100688886 (+)
NOD/ShiLtJ no annotation
NZO/HlLtJ no annotation
PWK/PhJ no annotation
SPRET/EiJ no annotation
WSB/EiJ no annotation



Homology
more
  • Human Ortholog
    TMT1A, thiol methyltransferase 1A
  • Vertebrate Orthologs
    5
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    TMT1A, thiol methyltransferase 1A
  • Synonyms
    AAM-B, AAMB, METTL7A
  • Links
    NCBI Gene ID: 25840
    UniProt: Q9H8H3

  • Chr Location
    12q13.12; chr12:50923472-50932510 (+)  GRCh38

Human Diseases
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  • References
    1 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    21 phenotype references
  • All Mutations and Alleles
    3
  • Chemically induced (other)
    1
  • Radiation induced
    2
  • Genomic Mutations
    3 involving Tmt1a2
  • Find Mice (IMSR)
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
  • cDNA Data
Sequences &
Gene Models
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Representative SequencesLengthStrain/SpeciesFlank
genomic 393082 NCBI Gene Model | MGI Sequence Detail 8620 C57BL/6J ±  kb
transcript NM_199477 RefSeq | MGI Sequence Detail 1808 Not Specified  
polypeptide NP_955771 RefSeq | MGI Sequence Detail 244 Not Specified  
For the selected sequence
Protein
Information
less
  • UniProt
    2 Sequences
Molecular
Reagents
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  • All nucleic 3
    cDNA 3

    Microarray probesets 1
Other
Accession IDs
less
MGI:7461485
References
more
  • Summaries
    All 33
    Diseases 1
    Phenotypes 21
  • Earliest
    J:7688 Lane PW, et al., Association of megacolon with a new dominant spotting gene (Dom) in the mouse. J Hered. 1984 Nov-Dec;75(6):435-9
  • Latest
    J:387680 Ahn B, et al., Disorganization of Transcriptional Regulation and Alteration of Keratin Family Gene Expression in Hairy Ear Mice. Genes (Basel). 2026 Jan 31;17(2)

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
09/15/2026
MGI 6.29
The Jackson Laboratory