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Category

148 results for inx-18

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inx-18

(Caenorhabditis elegans)

Gene

Name: INneXin 18

Synonyms: C18H7.2, opu-18, CELE_C18H7.2

Source: WB:WBGene00002140

Biotype: protein coding gene

Symbol: inx-18 (Cel)

Symbol: inx-18

Gene Synopsis: inx-18 encodes a predicted member of the innexin family.

Cross References: inx-18...WB:inx-18...inx-18

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-18

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-18

Allele/Variant (538)

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-18

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-18

Allele/Variant (90)

Panx1

(Mus musculus)

Gene

Name: pannexin 1

Synonyms: expressed sequence AI847747, px1, AI847747

Source: MGI:1860055

Biotype: protein coding gene

Strict Orthology Symbols: inx-18

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-18

Allele/Variant (114)

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-18

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-18

Allele/Variant (167)

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-18

Allele/Variant (3573)

Panx3

(Mus musculus)

Gene

Name: pannexin 3

Synonyms: 4833413G11Rik, RIKEN cDNA 4833413G11 gene

Source: MGI:1918881

Biotype: protein coding gene

Strict Orthology Symbols: inx-18

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-18

Allele/Variant (88)

gap junction channel activity

Gene Ontology

Source: GO:0005243

Synonyms:

connexin
innexin

Branch: molecular function

Genes: inx-18 (Cel)

Genes Annotated with this GO Term (144)

gap junction

Gene Ontology

Source: GO:0005921

Synonyms:

communicating junction
electrical synapse

Branch: cellular component

Genes: inx-18 (Cel)

Genes Annotated with this GO Term (178)

depressive disorder

Disease

Source: DOID:1596

Definition: A mood disorder characterized by persistent sadness, emptiness, or irritability and decreased ability to function.

Genes: inx-18 (Cel)

monoatomic ion transmembrane transport

Gene Ontology

Source: GO:0034220

Synonyms:

ATP hydrolysis coupled ion transmembrane transport
ion membrane transport

Branch: biological process

Genes: inx-18 (Cel)

Genes Annotated with this GO Term (4268)

(WBcel235)IV:611305T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.611305T>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:611305T>A

Gene Cross References: inx-18

(WBcel235)IV:614009A>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.614009A>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:614009A>G

Gene Cross References: inx-18

(WBcel235)IV:609104A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.609104A>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:609104A>T

Gene Cross References: inx-18

(WBcel235)IV:610136T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610136T>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610136T>A

Gene Cross References: inx-18

(WBcel235)IV:610328C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610328C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610328C>T

Gene Cross References: inx-18

(WBcel235)IV:611439A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.611439A>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:611439A>T

Gene Cross References: inx-18

(WBcel235)IV:606738G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.606738G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:606738G>A

Gene Cross References: inx-18

(WBcel235)IV:613961G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.613961G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:613961G>A

Gene Cross References: inx-18

(WBcel235)IV:610211T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610211T>C

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610211T>C

Gene Cross References: inx-18

(WBcel235)IV:610370C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610370C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610370C>T

Gene Cross References: inx-18

(WBcel235)IV:606912G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.606912G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:606912G>A

Gene Cross References: inx-18

(WBcel235)IV:613503T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.613503T>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:613503T>A

Gene Cross References: inx-18

(WBcel235)IV:612163G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.612163G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: synonymous_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:612163G>A

Gene Cross References: inx-18

(WBcel235)IV:606824G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.606824G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:606824G>A

Gene Cross References: inx-18

(WBcel235)IV:613361C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.613361C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:613361C>T

Gene Cross References: inx-18

(WBcel235)IV:610153T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610153T>C

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610153T>C

Gene Cross References: inx-18

(WBcel235)IV:607253A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.607253A>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:607253A>T

Gene Cross References: inx-18

(WBcel235)IV:607794A>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.607794A>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:607794A>G

Gene Cross References: inx-18

(WBcel235)IV:612845G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.612845G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:612845G>A

Gene Cross References: inx-18

(WBcel235)IV:608595C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.608595C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:608595C>T

Gene Cross References: inx-18

(WBcel235)IV:607252A>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.607252A>C

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:607252A>C

Gene Cross References: inx-18

(WBcel235)IV:607510C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.607510C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:607510C>T

Gene Cross References: inx-18

(WBcel235)IV:609966A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.609966A>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:609966A>T

Gene Cross References: inx-18

(WBcel235)IV:610499A>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610499A>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610499A>G

Gene Cross References: inx-18

(WBcel235)IV:610740G>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610740G>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610740G>A

Gene Cross References: inx-18

(WBcel235)IV:610818A>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610818A>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610818A>T

Gene Cross References: inx-18

(WBcel235)IV:609478T>C

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.609478T>C

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:609478T>C

Gene Cross References: inx-18

(WBcel235)IV:609586A>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.609586A>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:609586A>G

Gene Cross References: inx-18

(WBcel235)IV:610807T>A

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.610807T>A

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:610807T>A

Gene Cross References: inx-18

(WBcel235)IV:612902C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.612902C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:612902C>T

Gene Cross References: inx-18

(WBcel235)IV:612589A>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.612589A>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:612589A>G

Gene Cross References: inx-18

(WBcel235)IV:608256C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.608256C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:608256C>T

Gene Cross References: inx-18

(WBcel235)IV:608389C>T

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.608389C>T

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:608389C>T

Gene Cross References: inx-18

(WBcel235)IV:608491T>G

(Caenorhabditis elegans)

Allele/Variant

Source: NC_003282.8:g.608491T>G

Genes: inx-18 (Cel)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (WBcel235)IV:608491T>G

Gene Cross References: inx-18

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