Version: 8.2.0Date: Wed Aug 27 2025
Category
Mat2b
(Rattus norvegicus)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit
Synonyms: MGC94725, MAT II beta, methionine adenosyltransferase 2 subunit beta, similar to methionine adenosyltransferase II, beta, methionine adenosyltransferase II, beta, methionine adenosyltransferase 2 beta subunit, LOC689330, methionine adenosyltransferase 2B
Source: RGD:1593534
Biotype: protein coding gene
Symbol: Mat2b (Rno)
Symbol: Mat2b
Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit); PARTICIPATES
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Strict Orthology Symbols: Mat2b
Mat2b
(Mus musculus)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit methionine
Synonyms: MATIIbeta, RIKEN cDNA 2410018D16 gene, AI182287, expressed sequence AU022853, RIKEN cDNA 1110064C04 gene, AU022853, 1110064C04Rik, expressed sequence AI182287, 2410018D16Rik
Source: MGI:1913667
Biotype: protein coding gene
Symbol: Mat2b (Mmu)
Symbol: Mat2b
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Strict Orthology Symbols: Mat2b
Alleles: Mat2b
MAT2B
(Homo sapiens)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit
Synonyms: MATIIbeta, short chain dehydrogenase/reductase family 23E, member 1, MAT II beta, dTDP-4-keto-6-deoxy-D-glucose 4-reductase, SDR23E1, testicular tissue protein Li 118, methionine adenosyltransferase II, beta, MAT-II, putative protein product of Nbla02999, methionine adenosyltransferase 2 subunit beta, beta regulatory subunit of methionine adenosyltransferase, TGR, Nbla02999, putative dTDP-4-keto-6-deoxy-D-glucose 4-reductase, methionine adenosyltransferase 2B, MGC12237
Source: HGNC:6905
Biotype: protein coding gene
Symbol: MAT2B (Hsa)
Symbol: MAT2B
Strict Orthology Symbols: Mat2b
mat2b
(Danio rerio)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit methionine
Synonyms: wu:fb48h02, wu:fc55d01, zgc:110308, fc55d01
Source: ZFIN:ZDB-GENE-030131-786
Biotype: protein coding gene
Symbol: mat2b (Dre)
Symbol: mat2b
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Strict Orthology Symbols: Mat2b
mat2b
(Xenopus tropicalis)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit
Synonyms: methionine adenosyltransferase 2 non-catalytic beta subunit, mat2b
Source: Xenbase:XB-GENE-972023
Biotype: gene
Symbol: mat2b (Xtr)
Symbol: mat2b
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Synonyms: mat2b...mat2b
Strict Orthology Symbols: Mat2b
mat2b.L
(Xenopus laevis)Gene
Name: methionine adenosyltransferase 2 non-catalytic beta subunit
Synonyms: methionine adenosyltransferase 2 non-catalytic beta subunit, mat2b.L
Source: Xenbase:XB-GENE-972027
Biotype: gene
Symbol: mat2b.L (Xla)
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Strict Orthology Symbols: MAT2B...mat2b
Symbol: mat2b.L
Mat2bem16Gpt
(Mus musculus)Allele/Variant
Source: MGI:7302049
Genes: Mat2b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mat2b
Genes: Mat2b (Mmu)
Symbol: Mat2bem16Gpt
Mat2bem1Gpt
(Mus musculus)Allele/Variant
Source: MGI:7302050
Genes: Mat2b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mat2b
Genes: Mat2b (Mmu)
Symbol: Mat2bem1Gpt
CG5854
(Drosophila melanogaster)Gene
Name: Not Available
Synonyms: anon-WO0118547.306
Source: FB:FBgn0039130
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human MAT2B (methionine adenosyltransferase 2 non-catalytic beta subunit).
Strict Orthology Symbols: MAT2B
Gene Ontology
Source: GO:0048269
Synonyms:
- MAT complex
Branch: cellular component
Genes: MAT2B (Hsa)...mat2b (Dre)...Mat2b (Mmu)...Mat2b (Rno)
Gene Ontology
Source: GO:0006556
Synonyms:
- S-adenosyl methionine biosynthesis
- S-adenosyl methionine biosynthetic process
Branch: biological process
Genes: MAT2B (Hsa)...Mat2b (Rno)...mat2b (Dre)...Mat2b (Mmu)
Gene Ontology
Source: GO:0048270
Synonyms:
- MAT regulator activity
Branch: molecular function
Genes: MAT2B (Hsa)...mat2b (Dre)...Mat2b (Mmu)...Mat2b (Rno)
Gene Ontology
Source: GO:0006730
Synonyms:
- one carbon metabolic process
- one carbon metabolism
Branch: biological process
Genes: Mat2b (Rno)...mat2b (Dre)...Mat2b (Mmu)...MAT2B (Hsa)
Gene Ontology
Source: GO:0030234
Synonyms:
- catalytic regulator activity
- enzyme modulator
Branch: molecular function
Genes: Mat2b (Rno)...Mat2b (Mmu)
Hsap\MAT2BUAS.Tag:HA
(Drosophila melanogaster)Allele/Variant
Source: FB:FBal0370170
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Hsap\MAT2B
Construct Expressed Component: MAT2B (Hsa)
Gene Ontology
Source: GO:0019899
Synonyms: Not Available
Branch: molecular function
Genes: Mat2b (Rno)...Mat2b (Mmu)...MAT2B (Hsa)
Gene Ontology
Source: GO:0070062
Synonyms:
- exosome
- extracellular vesicular exosome
Branch: cellular component
Genes: MAT2B (Hsa)
sa43679
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-9187
Genes: mat2b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: mat2b (Dre)
Gene Ontology
Source: GO:0005739
Synonyms:
- mitochondria
Branch: cellular component
Genes: Mat2b (Mmu)
Gene Ontology
Source: GO:0016740
Synonyms: Not Available
Branch: molecular function
Genes: MAT2B (Hsa)
Gene Ontology
Source: GO:0005634
Synonyms:
- cell nucleus
- horsetail nucleus
Branch: cellular component
Genes: Mat2b (Rno)...Mat2b (Mmu)...MAT2B (Hsa)
Gene Ontology
Source: GO:0008150
Synonyms:
- biological process
- physiological process
Branch: biological process
Genes: Mat2b (Rno)
Gene Ontology
Source: GO:0005829
Synonyms: Not Available
Branch: cellular component
Genes: MAT2B (Hsa)
Gene Ontology
Source: GO:0005515
Synonyms:
- glycoprotein binding
- protein amino acid binding
Branch: molecular function
Genes: MAT2B (Hsa)
(GRCh38)5:163518263C>T
(Homo sapiens)Allele/Variant
Source: rs80145956
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163518263C>T
(GRCh38)5:163512099A>T
(Homo sapiens)Allele/Variant
Source: rs369618222
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163512099A>T
(GRCh38)5:163512101G>A
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.163512101G>A
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163512101G>A
(GRCh38)5:163517591T>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.163517591T>G
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163517591T>G
(GRCh38)5:163518329T>C
(Homo sapiens)Allele/Variant
Source: rs192771488
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163518329T>C
(GRCh38)5:163516542T>C
(Homo sapiens)Allele/Variant
Source: rs763480646
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163516542T>C
(GRCh38)5:163513564A>G
(Homo sapiens)Allele/Variant
Source: rs1207048090
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163513564A>G
(GRCh38)5:163517598A>G
(Homo sapiens)Allele/Variant
Source: rs140996665
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163517598A>G
(GRCh38)5:163517635T>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.163517635T>G
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163517635T>G
(GRCh38)5:163518293G>A
(Homo sapiens)Allele/Variant
Source: rs768283411
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163518293G>A
(GRCh38)5:163512112T>G
(Homo sapiens)Allele/Variant
Source: rs1374990714
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163512112T>G
(GRCh38)5:163512104G>T
(Homo sapiens)Allele/Variant
Source: rs767834890
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163512104G>T
(GRCh38)5:163513950A>G
(Homo sapiens)Allele/Variant
Source: rs1471363674
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163513950A>G
(GRCh38)5:163516577G>C
(Homo sapiens)Allele/Variant
Source: rs201528924
Genes: MAT2B (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:163516577G>C
(mRatBN7.2)10:25110811T>C
(Rattus norvegicus)Allele/Variant
Source: rs197031542
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25110811T>C
(mRatBN7.2)10:25111604A>G
(Rattus norvegicus)Allele/Variant
Source: rs3321800273
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25111604A>G
(mRatBN7.2)10:25112098C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321814868
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25112098C>T
(mRatBN7.2)10:25112444G>A
(Rattus norvegicus)Allele/Variant
Source: rs3321824074
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25112444G>A
(mRatBN7.2)10:25118672A>T
(Rattus norvegicus)Allele/Variant
Source: rs3321517712
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25118672A>T
(mRatBN7.2)10:25119340T>C
(Rattus norvegicus)Allele/Variant
Source: rs3321517679
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25119340T>C
(mRatBN7.2)10:25119484C>A
(Rattus norvegicus)Allele/Variant
Source: rs3321833586
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25119484C>A
(mRatBN7.2)10:25121082C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321800341
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25121082C>T
(mRatBN7.2)10:25118551T>C
(Rattus norvegicus)Allele/Variant
Source: rs3321657134
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25118551T>C
(mRatBN7.2)10:25121343C>T
(Rattus norvegicus)Allele/Variant
Source: rs3321776045
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25121343C>T
(mRatBN7.2)10:25112979A>G
(Rattus norvegicus)Allele/Variant
Source: rs3321517684
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25112979A>G
(mRatBN7.2)10:25108046G>C
(Rattus norvegicus)Allele/Variant
Source: rs197292257
Genes: Mat2b (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)10:25108046G>C