Version: 8.1.0Date: Fri Apr 18 2025
Category
Cnnm3
(Mus musculus)Gene
Name: cyclin M3
Synonyms: Acdp3, ancient conserved domain protein 3
Source: MGI:2151055
Biotype: protein coding gene
Symbol: Cnnm3 (Mmu)
Symbol: Cnnm3
Automated Gene Synopsis: Orthologous to human CNNM3 (cyclin and CBS domain divalent metal cation transport mediator 3).
Strict Orthology Symbols: cnnm3
Alleles: Cnnm3
Cnnm3
(Rattus norvegicus)Gene
Name: cyclin and CBS domain divalent metal cation transport mediator 3
Synonyms: cyclin M3, LOC301345, metal transporter CNNM3
Source: RGD:1307926
Biotype: protein coding gene
Symbol: Cnnm3 (Rno)
Symbol: Cnnm3
Gene Synopsis: Orthologous to human CNNM3 (cyclin and CBS domain divalent metal cation transport mediator 3); INTERACTS
Automated Gene Synopsis: Orthologous to human CNNM3 (cyclin and CBS domain divalent metal cation transport mediator 3).
Synonyms: metal transporter CNNM3
Strict Orthology Symbols: cnnm3
CNNM3
(Homo sapiens)Gene
Name: cyclin and CBS domain divalent metal cation transport mediator 3
Synonyms: cyclin M3, ACDP3, metal transporter CNNM3, ancient conserved domain-containing protein 3, DKFZp434I1016, SLC70A3, FLJ20018, cyclin-M3, ancient conserved domain protein 3
Source: HGNC:104
Biotype: protein coding gene
Symbol: CNNM3 (Hsa)
Symbol: CNNM3
Synonyms: metal transporter CNNM3
Strict Orthology Symbols: cnnm3
cnnm3
(Xenopus tropicalis)Gene
Name: cyclin and CBS domain divalent metal cation transport mediator 3
Synonyms: cyclin and CBS domain divalent metal cation transport mediator 3, LOC121402134, cnnm3
Source: Xenbase:XB-GENE-981953
Biotype: gene
Symbol: cnnm3 (Xtr)
Symbol: cnnm3
Automated Gene Synopsis: Orthologous to human CNNM3 (cyclin and CBS domain divalent metal cation transport mediator 3).
Synonyms: cnnm3...cnnm3...cnnm3
Strict Orthology Symbols: cnnm3.L...Cnnm3...CNNM3
CNNM3-DT
(Homo sapiens)Gene
Name: CNNM3 divergent transcript
Synonyms: Not Available
Source: HGNC:53592
Biotype: ncRNA gene
Symbol: CNNM3-DT (Hsa)
Symbol: CNNM3-DT
cnnm3.L
(Xenopus laevis)Gene
Name: cyclin and CBS domain divalent metal cation transport mediator 3
Synonyms: cyclin and CBS domain divalent metal cation transport mediator 3, cnnm3.L, LOC121402134
Source: Xenbase:XB-GENE-6485590
Biotype: gene
Symbol: cnnm3.L (Xla)
Automated Gene Synopsis: Orthologous to human CNNM3 (cyclin and CBS domain divalent metal cation transport mediator 3).
Strict Orthology Symbols: cnnm3
Symbol: cnnm3.L
Cnnm3em1(IMPC)Bay
(Mus musculus)Allele/Variant
Source: MGI:7425597
Genes: Cnnm3 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Cnnm3
Genes: Cnnm3 (Mmu)
Symbol: Cnnm3em1(IMPC)Bay
cnnm-1
(Caenorhabditis elegans)Gene
Name: vertebrate CNNM family homolog 1
Synonyms: CELE_C52D10.12, C52D10.12
Source: WB:WBGene00016879
Biotype: protein coding gene
Automated Gene Synopsis: transport mediator 1); CNNM2 (cyclin and CBS domain divalent metal cation transport mediator 2); and CNNM3
Strict Orthology Symbols: cnnm3
MAM3
(Saccharomyces cerevisiae)Gene
Name: Not Available
Synonyms: YOL060C
Source: SGD:S000005421
Biotype: protein coding gene
Automated Gene Synopsis: transport mediator 1); CNNM2 (cyclin and CBS domain divalent metal cation transport mediator 2); and CNNM3
Strict Orthology Symbols: cnnm3
cnnm-2
(Caenorhabditis elegans)Gene
Name: vertebrate CNNM family homolog 2
Synonyms: CELE_R04E5.2, R04E5.2
Source: WB:WBGene00019869
Biotype: protein coding gene
Automated Gene Synopsis: transport mediator 1); CNNM2 (cyclin and CBS domain divalent metal cation transport mediator 2); and CNNM3
Strict Orthology Symbols: cnnm3
cnnm-3
(Caenorhabditis elegans)Gene
Name: vertebrate CNNM family homolog 3
Synonyms: CELE_C33D12.2, C33D12.2
Source: WB:WBGene00016343
Biotype: protein coding gene
Automated Gene Synopsis: transport mediator 1); CNNM2 (cyclin and CBS domain divalent metal cation transport mediator 2); and CNNM3
Strict Orthology Symbols: CNNM3
uex
(Drosophila melanogaster)Gene
Name: unextended
Synonyms: l(2)IR3, GroupIII, CR41594, Uex, IR3, l(2Rh)IR3, CG40084, CG42595, l(2R)EMS45-73, EMS45-73, l(2)41Ad, 41Ad, l(2R)A', l(2)EMS34-7, lethal (2) IR3
Source: FB:FBgn0262124
Biotype: protein coding gene
Strict Orthology Symbols: cnnm3
Gene Ontology
Source: GO:0010960
Synonyms: Not Available
Branch: biological process
Genes: Cnnm3 (Rno)...CNNM3 (Hsa)...Cnnm3 (Mmu)
Gene Ontology
Source: GO:0022857
Synonyms:
- substrate-specific transmembrane transporter activity
- substrate-specific transporter activity
Branch: molecular function
Genes: CNNM3 (Hsa)...Cnnm3 (Rno)...Cnnm3 (Mmu)
Gene Ontology
Source: GO:0006811
Synonyms:
- ion transport
Branch: biological process
Genes: CNNM3 (Hsa)...Cnnm3 (Rno)...Cnnm3 (Mmu)
Gene Ontology
Source: GO:0055085
Synonyms:
- ATP hydrolysis coupled transmembrane transport
- membrane transport
Branch: biological process
Genes: CNNM3 (Hsa)...Cnnm3 (Rno)
(GRCh38)2:96817029T>C
(Homo sapiens)Allele/Variant
Source: rs1348979992
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817029T>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816882C>G
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.96816882C>G
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816882C>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816956G>A
(Homo sapiens)Allele/Variant
Source: rs1247412393
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816956G>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817076C>G
(Homo sapiens)Allele/Variant
Source: rs1015625758
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817076C>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816660C>T
(Homo sapiens)Allele/Variant
Source: rs561303055
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816660C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96826967C>T
(Homo sapiens)Allele/Variant
Source: rs948665847
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96826967C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816701G>A
(Homo sapiens)Allele/Variant
Source: rs1409682427
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816701G>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96828636C>T
(Homo sapiens)Allele/Variant
Source: rs148563074
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96828636C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96828648C>T
(Homo sapiens)Allele/Variant
Source: rs148219000
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96828648C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817158C>G
(Homo sapiens)Allele/Variant
Source: rs778887659
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817158C>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816291T>C
(Homo sapiens)Allele/Variant
Source: rs775001414
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816291T>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816842C>T
(Homo sapiens)Allele/Variant
Source: rs865847530
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816842C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816858C>A
(Homo sapiens)Allele/Variant
Source: rs1437458093
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816858C>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817014G>T
(Homo sapiens)Allele/Variant
Source: rs1311694187
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817014G>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96825165A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.96825165A>C
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96825165A>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96832609G>A
(Homo sapiens)Allele/Variant
Source: rs2079622985
Genes: CNNM3 (Hsa), ANKRD23 (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)2:96832609G>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816353G>A
(Homo sapiens)Allele/Variant
Source: rs780987233
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816353G>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96827754C>T
(Homo sapiens)Allele/Variant
Source: rs140550487
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96827754C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817393T>G
(Homo sapiens)Allele/Variant
Source: rs763919255
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817393T>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816680T>C
(Homo sapiens)Allele/Variant
Source: rs905088464
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816680T>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816305C>T
(Homo sapiens)Allele/Variant
Source: rs373318478
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816305C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816363C>T
(Homo sapiens)Allele/Variant
Source: rs1378760263
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816363C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816824C>T
(Homo sapiens)Allele/Variant
Source: rs1191059096
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816824C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96828120G>A
(Homo sapiens)Allele/Variant
Source: rs1360606313
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96828120G>A
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817277G>C
(Homo sapiens)Allele/Variant
Source: rs760811058
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817277G>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817437A>G
(Homo sapiens)Allele/Variant
Source: rs144557284
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817437A>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96827764A>G
(Homo sapiens)Allele/Variant
Source: rs921809362
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96827764A>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816372G>C
(Homo sapiens)Allele/Variant
Source: rs1348867850
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816372G>C
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96817032C>T
(Homo sapiens)Allele/Variant
Source: rs764705972
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96817032C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816305C>G
(Homo sapiens)Allele/Variant
Source: rs373318478
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816305C>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96816653G>T
(Homo sapiens)Allele/Variant
Source: rs1036231967
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:96816653G>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96828157C>T
(Homo sapiens)Allele/Variant
Source: rs145950088
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96828157C>T
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96829035C>G
(Homo sapiens)Allele/Variant
Source: rs140443890
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96829035C>G
Gene Synonyms: metal transporter CNNM3
(GRCh38)2:96829117A>C
(Homo sapiens)Allele/Variant
Source: rs760570294
Genes: CNNM3-DT (Hsa), CNNM3 (Hsa), ANKRD23 (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)2:96829117A>C
Gene Synonyms: metal transporter CNNM3