Version: 8.1.0Date: Fri Apr 18 2025
Category
inx-12
(Caenorhabditis elegans)Gene
Name: INneXin 12
Synonyms: opu-12, let-368, ZK770.3, CELE_ZK770.3
Source: WB:WBGene00002134
Biotype: protein coding gene
Symbol: inx-12 (Cel)
Symbol: inx-12
Gene Synopsis: inx-12 (innexin=invertebrate connexin analogue) encodes a protein of the innexin family; innexins are...sequence to the vertebrate connexins; innexins are the only known gap junction proteins in invertebrates; inx...-12 and inx-13 appear to be a tandom duplication; RNA interference of inx-12 results in an arrest at...with fluid filled dead rods; this phenotype and sequence homology to Drosophila innexins suggest that INX
Cross References: WB:inx-12...inx-12...inx-12
PANX1
(Homo sapiens)Gene
Name: pannexin 1
Synonyms: innexin, MGC21309, MRS1, PX1, pannexin-1, OZEMA7, UNQ2529, OOMD7
Source: HGNC:8599
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
ogre
(Drosophila melanogaster)Gene
Name: optic ganglion reduced
Synonyms: Optic ganglion reduced, innexin-1, cb-8, l(1)6Ec, Innexin 1, inx-1, contrast-blind-8, optic ganglia-reduced, Ogre, inx1, Dm-inx1, CG3039, innexin 1, l(1)ogre, l(1)jnL3, CB8, jnL3, Inx1, FBpp0070995
Source: FB:FBgn0004646
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
panx3
(Danio rerio)Gene
Name: pannexin 3
Synonyms: si:dkey-263o8.2
Source: ZFIN:ZDB-GENE-091204-114
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
Inx7
(Drosophila melanogaster)Gene
Name: Innexin 7
Synonyms: pas related protein 7, FBpp0070994, innexin7, inx7, inx-7, D-inx-7, Innexin7, Dm-inx7, prp7, CG32731, innexin 7, CG2977
Source: FB:FBgn0027106
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
Panx1
(Mus musculus)Gene
Name: pannexin 1
Synonyms: expressed sequence AI847747, px1, AI847747
Source: MGI:1860055
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
Inx2
(Drosophila melanogaster)Gene
Name: Innexin 2
Synonyms: Inx-2, l(1)G0035, Ix2, l(1)G0157, l(1)G0036, l(1)G0059, kropf, l(1)G0317, l(1)G0118, Dm-inx2, Dm-inx, prp33, INX-2, FBpp0291074, innexin2, Inx2, Innexin-2, pas related protein 33, l(1)G0364, D-inx-2, inx-2, l(1)G0043, Dm-Inx2, CG4590, inx2, Innexin2, innexin 2, Innexin
Source: FB:FBgn0027108
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
panx1a
(Danio rerio)Gene
Name: pannexin 1a
Synonyms: zgc:55631, panx1
Source: ZFIN:ZDB-GENE-040426-766
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
Inx3
(Drosophila melanogaster)Gene
Name: Innexin 3
Synonyms: Dm-Inx3, anon-EST:fe2B11, inx-3, Ix3, FBpp0084719, anon-fast-evolving-2B11, INX-3, inx3, innexin 3, innexin3, Dm-inx3, Innexin, CG1448, Innexin-3
Source: FB:FBgn0265274
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
shakB
(Drosophila melanogaster)Gene
Name: shaking B
Synonyms: ShakB, Pas, non-jumper-156, SHAK-B, l(1)W3, shakb, shB, FBpp0111481, shak-B, CG1321, inx8, CG32508, shakingB, nj-156, pas, shaking B, pass, section 6, 2, 3, R9-29, section 3, 6, W3, section 2, shaking-B, CG12678, passover-vital protein, Shak B, l(1)R-10-3, l(1)19Eb, l(1)TH73, l(1)R-10-7, Shak-B, Shaking-B, CG34358, l(1)R-9-29, passover, Passover, Inx8, nj156, lincRNA.1031, l(1)R-10-14, l(1)LB21, R-9-29, shkB, l(1)W3b, CG15451, Shaking B, E81
Source: FB:FBgn0085387
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
Panx3
(Mus musculus)Gene
Name: pannexin 3
Synonyms: 4833413G11Rik, RIKEN cDNA 4833413G11 gene
Source: MGI:1918881
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
zpg
(Drosophila melanogaster)Gene
Name: zero population growth
Synonyms: Innexin-4, inx4, Zpg, inx-4, CG10125, innexin 4, Inx4, FBpp0076692, Dm-inx4, innexin4, Innexin 4
Source: FB:FBgn0024177
Biotype: protein coding gene
Strict Orthology Symbols: inx-12
tm3279
(Caenorhabditis elegans)Allele/Variant
Source: WB:WBVar00252009
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: inx-12 (Cel)
KR428
(Caenorhabditis elegans)Model
Id: WB:WBStrain00023689
Synonyms: Not Available
Genes: inx-12 (Cel)
Source: GO:0110039
Synonyms: Not Available
Branch: biological process
Genes: inx-12 (Cel)
Gene Ontology
Source: GO:0055077
Synonyms:
- connexon channel activity
Branch: molecular function
Genes: inx-12 (Cel)
WBPaper00038232Ex14
(Caenorhabditis elegans)Allele/Variant
Source: WB:WBTransgene00018778
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Construct Regulatory Region: inx-12 (Cel)
Gene Ontology
Source: GO:0005921
Synonyms:
- communicating junction
- electrical synapse
Branch: cellular component
Genes: inx-12 (Cel)
Gene Ontology
Source: GO:0005243
Synonyms:
- connexin
- innexin
Branch: molecular function
Genes: inx-12 (Cel)
Disease
Source: DOID:1596
Definition: A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.
Genes: inx-12 (Cel)
Gene Ontology
Source: GO:0034220
Synonyms:
- ATP hydrolysis coupled ion transmembrane transport
- ion membrane transport
Branch: biological process
Genes: inx-12 (Cel)
h121
(Caenorhabditis elegans)Allele/Variant
Source: WB:WBVar00146441
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: inx-12 (Cel)
(WBcel235)I:3755602A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755602A>G
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755602A>G
Gene Cross References: inx-12
(WBcel235)I:3758336G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758336G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758336G>A
Gene Cross References: inx-12
(WBcel235)I:3755997C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755997C>T
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755997C>T
Gene Cross References: inx-12
(WBcel235)I:3758447G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758447G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758447G>A
Gene Cross References: inx-12
(WBcel235)I:3758957G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758957G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758957G>A
Gene Cross References: inx-12
(WBcel235)I:3758304G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758304G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758304G>A
Gene Cross References: inx-12
(WBcel235)I:3758599G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758599G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758599G>A
Gene Cross References: inx-12
(WBcel235)I:3756900G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756900G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756900G>A
Gene Cross References: inx-12
(WBcel235)I:3758798G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758798G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758798G>A
Gene Cross References: inx-12
(WBcel235)I:3757514G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757514G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757514G>A
Gene Cross References: inx-12
(WBcel235)I:3756111C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756111C>T
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756111C>T
Gene Cross References: inx-12
(WBcel235)I:3756487G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756487G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756487G>A
Gene Cross References: inx-12
(WBcel235)I:3758708C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758708C>T
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758708C>T
Gene Cross References: inx-12
(WBcel235)I:3755504T>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755504T>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755504T>A
Gene Cross References: inx-12
(WBcel235)I:3756357T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756357T>C
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756357T>C
Gene Cross References: inx-12
(WBcel235)I:3758702T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758702T>C
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758702T>C
Gene Cross References: inx-12
(WBcel235)I:3755528T>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755528T>C
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755528T>C
Gene Cross References: inx-12
(WBcel235)I:3757137G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757137G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757137G>A
Gene Cross References: inx-12
(WBcel235)I:3755642T>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755642T>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755642T>A
Gene Cross References: inx-12
(WBcel235)I:3756632G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756632G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756632G>A
Gene Cross References: inx-12
(WBcel235)I:3755812G>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3755812G>T
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3755812G>T
Gene Cross References: inx-12
(WBcel235)I:3757389A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757389A>G
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757389A>G
Gene Cross References: inx-12
(WBcel235)I:3757512G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757512G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757512G>A
Gene Cross References: inx-12
(WBcel235)I:3757739A>C
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757739A>C
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757739A>C
Gene Cross References: inx-12
(WBcel235)I:3758364G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758364G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758364G>A
Gene Cross References: inx-12
(WBcel235)I:3757715G>A
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3757715G>A
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3757715G>A
Gene Cross References: inx-12
(WBcel235)I:3758964C>T
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3758964C>T
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3758964C>T
Gene Cross References: inx-12
(WBcel235)I:3756062A>G
(Caenorhabditis elegans)Allele/Variant
Source: NC_003279.8:g.3756062A>G
Genes: inx-12 (Cel)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (WBcel235)I:3756062A>G
Gene Cross References: inx-12