Version: 8.1.0Date: Fri Apr 18 2025
Category
CSM2
(Saccharomyces cerevisiae)Gene
Name: Chromosome Segregation in Meiosis
Synonyms: YIL132C
Source: SGD:S000001394
Biotype: protein coding gene
Symbol: CSM2 (Sce)
Symbol: CSM2
Alleles: csm2-Δ (Sce)...csm2-F46A (Sce)
csm2-F46A
(Saccharomyces cerevisiae)Allele/Variant
Source: SGD:S000287570
Genes: CSM2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: csm2-F46A (Sce)
Genes: CSM2 (Sce)
Symbol: csm2-F46A
csm2-Δ
(Saccharomyces cerevisiae)Allele/Variant
Source: SGD:S000280405
Genes: CSM2 (Sce)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: csm2-Δ (Sce)
Genes: CSM2 (Sce)
Symbol: csm2-Δ
DES
(Homo sapiens)Gene
Name: desmin
Synonyms: CDCD3, ARVD7, ARVC7, cardiomyopathy, dilated 1I, CMD1I, CSM2, CSM1, SCPNK, LGMD2R, FLJ39719, FLJ12025, intermediate filament protein, FLJ41793, FLJ41013, LGMD1D, MFM1, cardiomyopathy, dilated 1F (autosomal dominant), LGMD1E, CMD1F, mutant desmin p.K241E
Source: HGNC:2770
Biotype: protein coding gene
Synonyms: CSM2...CSM2...CSM2
des.S
(Xenopus laevis)Gene
Name: desmin, gene 1
Synonyms: desmin, gene 1, des.1, desm, des.S, des.1-b, csm1, des.1-a, csm2
Source: Xenbase:XB-GENE-6254678
Biotype: gene
Synonyms: csm2...csm2
des.L
(Xenopus laevis)Gene
Name: desmin, gene 1
Synonyms: des.L, desmin, gene 1, desm, des.1, des.1-b, csm1, des.1-a, csm2
Source: Xenbase:XB-GENE-494935
Biotype: gene
Synonyms: csm2...csm2
des
(Xenopus tropicalis)Gene
Name: desmin, gene 1
Synonyms: des, desmin, gene 1, desm, des.1, des.1-b, csm1, csm2, des.1-a
Source: Xenbase:XB-GENE-494931
Biotype: gene
Synonyms: csm2...csm2
Gene Ontology
Source: GO:0097196
Synonyms: Not Available
Branch: cellular component
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0043007
Synonyms:
- rDNA maintenance
- ribosomal DNA maintenance
Branch: biological process
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0000730
Synonyms:
- Rad51 nucleoprotein filament formation
Branch: biological process
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0000725
Synonyms: Not Available
Branch: biological process
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0045132
Synonyms: Not Available
Branch: biological process
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0035861
Synonyms:
- DNA damage foci
- DNA damage focus
Branch: cellular component
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0051321
Synonyms:
- meiosis
Branch: biological process
Genes: CSM2 (Sce)
Gene Ontology
Source: GO:0006281
Synonyms: Not Available
Branch: biological process
Genes: CSM2 (Sce)
(GRCh38)2:219418499T>C
(Homo sapiens)Allele/Variant
Source: rs1954359599
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418499T>C
Gene Synonyms: CSM2
(GRCh38)2:219418537A>T
(Homo sapiens)Allele/Variant
Source: rs1318299
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418537A>T
Gene Synonyms: CSM2
(GRCh38)2:219418820G>C
(Homo sapiens)Allele/Variant
Source: rs794728996
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418820G>C
Gene Synonyms: CSM2
(GRCh38)2:219418821C>A
(Homo sapiens)Allele/Variant
Source: rs1954373010
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418821C>A
Gene Synonyms: CSM2
(GRCh38)2:219420910A>C
(Homo sapiens)Allele/Variant
Source: rs397516700
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420910A>C
Gene Synonyms: CSM2
(GRCh38)2:219420925C>A
(Homo sapiens)Allele/Variant
Source: rs368453327
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420925C>A
Gene Synonyms: CSM2
(GRCh38)2:219420929C>T
(Homo sapiens)Allele/Variant
Source: rs1157722667
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420929C>T
Gene Synonyms: CSM2
(GRCh38)2:219420930G>A
(Homo sapiens)Allele/Variant
Source: rs1227068284
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420930G>A
Gene Synonyms: CSM2
(GRCh38)2:219420584G>A
(Homo sapiens)Allele/Variant
Source: rs369144706
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420584G>A
Gene Synonyms: CSM2
(GRCh38)2:219418655G>A
(Homo sapiens)Allele/Variant
Source: rs397516692
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418655G>A
Gene Synonyms: CSM2
(GRCh38)2:219418461C>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219418461C>T
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418461C>T
Gene Synonyms: CSM2
(GRCh38)2:219418470A>G
(Homo sapiens)Allele/Variant
Source: rs1954358286
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418470A>G
Gene Synonyms: CSM2
(GRCh38)2:219418490C>A
(Homo sapiens)Allele/Variant
Source: rs1196125127
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418490C>A
Gene Synonyms: CSM2
(GRCh38)2:219418508C>A
(Homo sapiens)Allele/Variant
Source: rs60798368
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418508C>A
Gene Synonyms: CSM2
(GRCh38)2:219418520G>A
(Homo sapiens)Allele/Variant
Source: rs759306707
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418520G>A
Gene Synonyms: CSM2
(GRCh38)2:219418523G>A
(Homo sapiens)Allele/Variant
Source: rs749447320
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418523G>A
Gene Synonyms: CSM2
(GRCh38)2:219420866C>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219420866C>A
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420866C>A
Gene Synonyms: CSM2
(GRCh38)2:219420874G>A
(Homo sapiens)Allele/Variant
Source: rs771455648
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420874G>A
Gene Synonyms: CSM2
(GRCh38)2:219420886A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219420886A>C
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420886A>C
Gene Synonyms: CSM2
(GRCh38)2:219420109T>C
(Homo sapiens)Allele/Variant
Source: rs773271116
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219420109T>C
Gene Synonyms: CSM2
(GRCh38)2:219425667C>T
(Homo sapiens)Allele/Variant
Source: rs2125171932
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219425667C>T
Gene Synonyms: CSM2
(GRCh38)2:219418712G>A
(Homo sapiens)Allele/Variant
Source: rs200545412
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418712G>A
Gene Synonyms: CSM2
(GRCh38)2:219419005C>T
(Homo sapiens)Allele/Variant
Source: rs1954382613
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219419005C>T
Gene Synonyms: CSM2
(GRCh38)2:219421442C>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219421442C>G
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219421442C>G
Gene Synonyms: CSM2
(GRCh38)2:219425956G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219425956G>A
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219425956G>A
Gene Synonyms: CSM2
(GRCh38)2:219418618C>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219418618C>T
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418618C>T
Gene Synonyms: CSM2
(GRCh38)2:219421446T>C
(Homo sapiens)Allele/Variant
Source: rs1432061016
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219421446T>C
Gene Synonyms: CSM2
(GRCh38)2:219421357G>A
(Homo sapiens)Allele/Variant
Source: rs2125168616
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219421357G>A
Gene Synonyms: CSM2
(GRCh38)2:219418648G>T
(Homo sapiens)Allele/Variant
Source: rs1276880158
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418648G>T
Gene Synonyms: CSM2
(GRCh38)2:219421462C>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.219421462C>T
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219421462C>T
Gene Synonyms: CSM2
(GRCh38)2:219418492C>T
(Homo sapiens)Allele/Variant
Source: rs886042179
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418492C>T
Gene Synonyms: CSM2
(GRCh38)2:219418502T>C
(Homo sapiens)Allele/Variant
Source: rs750819338
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418502T>C
Gene Synonyms: CSM2
(GRCh38)2:219418508C>T
(Homo sapiens)Allele/Variant
Source: rs60798368
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418508C>T
Gene Synonyms: CSM2
(GRCh38)2:219418524C>A
(Homo sapiens)Allele/Variant
Source: rs755107287
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418524C>A
Gene Synonyms: CSM2
(GRCh38)2:219418545C>T
(Homo sapiens)Allele/Variant
Source: rs1954361986
Genes: DES (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:219418545C>T
Gene Synonyms: CSM2