1,175 results for mcmdc2

MCMDC2

(Homo sapiens)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: minichromosome maintenance complex component-like, FLJ25692, MCM domain-containing protein C8orf45, uncharacterized protein C8orf45, minichromosome maintenance domain-containing protein 2, C8orf45, MCM domain-containing protein 2
Source: HGNC:26368
Biotype: protein coding gene
Symbol: MCMDC2 (Hsa)
Symbol: MCMDC2
Strict Orthology Symbols: mcmdc2

mcmdc2

(Danio rerio)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-030131-2568
Biotype: protein coding gene
Symbol: mcmdc2 (Dre)
Symbol: mcmdc2
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Strict Orthology Symbols: MCMDC2...Mcmdc2

Mcmdc2

(Mus musculus)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: 6030422M02Rik, RIKEN cDNA 6030422M02 gene
Source: MGI:3045334
Biotype: protein coding gene
Symbol: Mcmdc2 (Mmu)
Symbol: Mcmdc2
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Strict Orthology Symbols: mcmdc2
Alleles: Mcmdc2 (Mmu)...Mcmdc2 (Mmu)...Mcmdc2 (Mmu)...Mcmdc2 (Mmu)...Mcmdc2 (Mmu)

Mcmdc2

(Rattus norvegicus)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: minichromosome maintenance complex component-like, similar to hypothetical protein FLJ25692, uncharacterized protein C8orf45 homolog, minichromosome maintenance domain-containing protein 2, LOC500392, MCM domain-containing protein C8orf45 homolog, MCM domain-containing protein 2
Source: RGD:1561068
Biotype: protein coding gene
Symbol: Mcmdc2 (Rno)
Symbol: Mcmdc2
Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2); INTERACTS WITH (S)-nicotine
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Strict Orthology Symbols: mcmdc2

mcmdc2

(Xenopus tropicalis)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: mcmdc2, minichromosome maintenance domain containing 2
Source: Xenbase:XB-GENE-1012270
Biotype: gene
Symbol: mcmdc2 (Xtr)
Symbol: mcmdc2
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Synonyms: mcmdc2...mcmdc2...mcmdc2
Strict Orthology Symbols: mcmdc2.L...MCMDC2...Mcmdc2

mcmdc2.L

(Xenopus laevis)
Gene
Name: minichromosome maintenance domain containing 2
Synonyms: mcmdc2.L, minichromosome maintenance domain containing 2
Source: Xenbase:XB-GENE-6488408
Biotype: gene
Symbol: mcmdc2.L (Xla)
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Strict Orthology Symbols: mcmdc2
Symbol: mcmdc2.L

mcmdc2as

(Danio rerio)
Gene
Name: mcmdc2 antisense lncRNA
Synonyms: wu:fc11g08, wu:fc35f05, fc11g08, fc35f05
Source: ZFIN:ZDB-LINCRNAG-160518-1
Biotype: lincRNA gene
Symbol: mcmdc2as (Dre)
Symbol: mcmdc2as

Allele/Variant
Source: MGI:5892146
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm3c(EUCOMM)Hmgu

Allele/Variant
Source: MGI:5892148
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm4c(EUCOMM)Hmgu

Allele/Variant
Source: MGI:5511519
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm4a(EUCOMM)Hmgu

Allele/Variant
Source: MGI:5511194
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm3a(EUCOMM)Hmgu

Allele/Variant
Source: MGI:5892147
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm4b(EUCOMM)Hmgu

Allele/Variant
Source: MGI:5892145
Genes: Mcmdc2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Mcmdc2 (Mmu)
Genes: Mcmdc2 (Mmu)
Symbol: Mcmdc2tm3b(EUCOMM)Hmgu

Id: MGI:5898318
Synonyms: Not Available
Symbol: Mcmdc2/Mcmdc2 Spo11/Spo11 [background:] involves
Genes: Mcmdc2 (Mmu)
Alleles: Mcmdc2 (Mmu)
Name: Mcmdc2/Mcmdc2 Spo11/Spo11 [background:] involves

Id: MGI:5898300
Synonyms: Not Available
Symbol: Mcmdc2/Mcmdc2 [background:] involves: BALB/c * C57BL/6 * C57BL/6N
Genes: Mcmdc2 (Mmu)
Alleles: Mcmdc2 (Mmu)
Name: Mcmdc2/Mcmdc2 [background:] involves: BALB/c * C57BL/6 * C57BL/6N

mei-218

(Drosophila melanogaster)
Gene
Name: meiotic 218
Synonyms: CG8923, Mei-218, CG33067, transcript c
Source: FB:FBgn0002709
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human MCMDC2 (minichromosome maintenance domain containing 2).
Strict Orthology Symbols: mcmdc2

Source: GO:0007146
Synonyms: Not Available
Branch: biological process
Genes: MCMDC2 (Hsa)...Mcmdc2 (Mmu)...Mcmdc2 (Rno)

Source: GO:0042140
Synonyms: Not Available
Branch: biological process
Genes: MCMDC2 (Hsa)...Mcmdc2 (Mmu)...Mcmdc2 (Rno)

Source: GO:1990918
Synonyms: Not Available
Branch: biological process
Genes: Mcmdc2 (Mmu)...Mcmdc2 (Rno)...MCMDC2 (Hsa)

Source: GO:0000727
Synonyms: Not Available
Branch: biological process
Genes: Mcmdc2 (Mmu)...Mcmdc2 (Rno)...MCMDC2 (Hsa)

Source: GO:0007130
Synonyms:
  • synaptonemal complex formation
Branch: biological process
Genes: Mcmdc2 (Mmu)...Mcmdc2 (Rno)...MCMDC2 (Hsa)

Gene Ontology
Source: GO:0048477
Synonyms:
  • ovum development
Branch: biological process
Genes: Mcmdc2 (Mmu)...Mcmdc2 (Rno)...MCMDC2 (Hsa)

Source: GO:0032508
Synonyms:
  • DNA unwinding
  • duplex DNA melting
Branch: biological process
Genes: Mcmdc2 (Rno)...MCMDC2 (Hsa)...Mcmdc2 (Mmu)

Gene Ontology
Source: GO:0007283
Synonyms:
  • generation of spermatozoa
Branch: biological process
Genes: MCMDC2 (Hsa)...Mcmdc2 (Mmu)...Mcmdc2 (Rno)

Gene Ontology
Source: GO:0051321
Synonyms:
  • meiosis
Branch: biological process
Genes: MCMDC2 (Hsa)

Gene Ontology
Source: GO:0005524
Synonyms:
  • Mg-ATP binding
  • MgATP binding
Branch: molecular function
Genes: Mcmdc2 (Rno)...MCMDC2 (Hsa)...Mcmdc2 (Mmu)

Gene Ontology
Source: GO:0005634
Synonyms:
  • cell nucleus
  • horsetail nucleus
Branch: cellular component
Genes: Mcmdc2 (Mmu)...MCMDC2 (Hsa)...Mcmdc2 (Rno)

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: MCMDC2 (Hsa)

(GRCh38)8:66890892C>A

(Homo sapiens)
Allele/Variant
Source: rs112645348
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890892C>A

(GRCh38)8:66877506G>C

(Homo sapiens)
Allele/Variant
Source: rs145983403
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66877506G>C

(GRCh38)8:66883856A>T

(Homo sapiens)
Allele/Variant
Source: rs369758604
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883856A>T

(GRCh38)8:66890974A>G

(Homo sapiens)
Allele/Variant
Source: rs561670232
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890974A>G

(GRCh38)8:66880905A>T

(Homo sapiens)
Allele/Variant
Source: rs760279097
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66880905A>T

(GRCh38)8:66878585A>T

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.66878585A>T
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878585A>T

(GRCh38)8:66878928A>G

(Homo sapiens)
Allele/Variant
Source: rs181029958
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878928A>G

(GRCh38)8:66883865C>G

(Homo sapiens)
Allele/Variant
Source: rs765329862
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883865C>G

(GRCh38)8:66890906G>A

(Homo sapiens)
Allele/Variant
Source: rs373658749
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890906G>A

(GRCh38)8:66874171C>T

(Homo sapiens)
Allele/Variant
Source: rs1811159019
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874171C>T

(GRCh38)8:66877433T>G

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.66877433T>G
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66877433T>G

(GRCh38)8:66878673A>G

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.66878673A>G
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878673A>G

(GRCh38)8:66874571G>T

(Homo sapiens)
Allele/Variant
Source: rs781559154
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874571G>T

(GRCh38)8:66883796C>G

(Homo sapiens)
Allele/Variant
Source: rs377744254
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883796C>G

(GRCh38)8:66883928G>A

(Homo sapiens)
Allele/Variant
Source: rs140963222
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883928G>A

(GRCh38)8:66878865G>A

(Homo sapiens)
Allele/Variant
Source: rs753555437
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66878865G>A

(GRCh38)8:66874223A>G

(Homo sapiens)
Allele/Variant
Source: rs1811161564
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66874223A>G

(GRCh38)8:66883909C>G

(Homo sapiens)
Allele/Variant
Source: rs144829606
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883909C>G

(GRCh38)8:66877397G>A

(Homo sapiens)
Allele/Variant
Source: rs367891525
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66877397G>A

(GRCh38)8:66883834C>T

(Homo sapiens)
Allele/Variant
Source: rs773320366
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66883834C>T

(GRCh38)8:66890897G>A

(Homo sapiens)
Allele/Variant
Source: rs779816268
Genes: MCMDC2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:66890897G>A

Gene Ontology
Source: GO:0006281
Synonyms: Not Available
Branch: biological process
Genes: MCMDC2 (Hsa)