1,146 results for gkap1

Gkap1

(Rattus norvegicus)
Gene
Name: G kinase anchoring protein 1
Synonyms: LOC361202, G kinase-anchoring protein 1
Source: RGD:1306955
Biotype: protein coding gene
Symbol: Gkap1 (Rno)
Symbol: Gkap1
Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1); INTERACTS WITH 1-naphthyl isothiocyanate;
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Strict Orthology Symbols: gkap1

gkap1

(Danio rerio)
Gene
Name: G kinase anchoring protein 1
Synonyms: wu:fi16a08, zgc:66236, zgc:85804, zgc:110393
Source: ZFIN:ZDB-GENE-040426-2485
Biotype: protein coding gene
Symbol: gkap1 (Dre)
Symbol: gkap1
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Strict Orthology Symbols: gkap1

GKAP1

(Homo sapiens)
Gene
Name: G kinase anchoring protein 1
Synonyms: protein kinase anchoring protein GKAP42, FKSG21, GKAP42, cGMP-dependent protein kinase-anchoring protein of 42 kDa, FLJ25469, cGMP-dependent protein kinase anchoring protein 42kDa, G kinase-anchoring protein 1
Source: HGNC:17496
Biotype: protein coding gene
Symbol: GKAP1 (Hsa)
Symbol: GKAP1
Strict Orthology Symbols: gkap1

Gkap1

(Mus musculus)
Gene
Name: G kinase anchoring protein 1
Synonyms: Gkap42, D13Ertd340e, DNA segment, Chr 13, ERATO Doi 340, expressed, RIKEN cDNA 4933400B15 gene, 4933400B15Rik, 42kDa, cGMP-dependent protein kinase anchoring protein
Source: MGI:1891694
Biotype: protein coding gene
Symbol: Gkap1 (Mmu)
Symbol: Gkap1
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Strict Orthology Symbols: gkap1
Alleles: Gkap1 (Mmu)...Gkap1 (Mmu)...Gkap1 (Mmu)

gkap1

(Xenopus tropicalis)
Gene
Name: G kinase anchoring protein 1
Synonyms: gkap1-a, gkap1-b, gkap1, gkap42, G kinase anchoring protein 1, fksg21
Source: Xenbase:XB-GENE-1002568
Biotype: gene
Symbol: gkap1
Symbol: gkap1 (Xtr)
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Synonyms: gkap1...gkap1...gkap1
Strict Orthology Symbols: gkap1

gkap1.L

(Xenopus laevis)
Gene
Name: G kinase anchoring protein 1
Synonyms: gkap1-a, gkap1-b, gkap42, G kinase anchoring protein 1, gkap1.L, fksg21
Source: Xenbase:XB-GENE-1002576
Biotype: gene
Symbol: gkap1.L (Xla)
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Strict Orthology Symbols: gkap1
Symbol: gkap1.L

gkap1.S

(Xenopus laevis)
Gene
Name: G kinase anchoring protein 1
Synonyms: gkap1-a, gkap1-b, gkap1.S, gkap42, G kinase anchoring protein 1, fksg21
Source: Xenbase:XB-GENE-6254940
Biotype: gene
Symbol: gkap1.S (Xla)
Automated Gene Synopsis: Orthologous to human GKAP1 (G kinase anchoring protein 1).
Strict Orthology Symbols: gkap1
Symbol: gkap1.S

Gkap1tm2a(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5511599
Genes: Gkap1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Gkap1 (Mmu)
Genes: Gkap1 (Mmu)
Symbol: Gkap1tm2a(EUCOMM)Hmgu

Gkap1tm2b(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5614699
Genes: Gkap1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Gkap1 (Mmu)
Genes: Gkap1 (Mmu)
Symbol: Gkap1tm2b(EUCOMM)Hmgu

Id: MGI:6480463
Synonyms: Not Available
Symbol: Gkap1/Gkap1 [background:] C57BL/6N-Gkap1/BayMmucd
Genes: Gkap1 (Mmu)
Alleles: Gkap1 (Mmu)
Name: Gkap1/Gkap1 [background:] C57BL/6N-Gkap1/BayMmucd

Id: MGI:6470632
Synonyms: Not Available
Symbol: Gkap1/Gkap1 [background:] involves: C57BL/6 (Mmu)
Genes: Gkap1 (Mmu)
Alleles: Gkap1 (Mmu)
Name: Gkap1/Gkap1 [background:] involves: C57BL/6

Gkap1em1Feis

(Mus musculus)
Allele/Variant
Source: MGI:6470626
Genes: Gkap1 (Mmu)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Gkap1 (Mmu)
Genes: Gkap1 (Mmu)
Symbol: Gkap1em1Feis

Source: GO:0007199
Synonyms:
  • G protein signaling, coupled to cGMP nucleotide second messenger
  • G protein signalling, coupled to cGMP nucleotide second messenger
Branch: biological process
Genes: Gkap1 (Mmu)

Source: GO:0046628
Synonyms:
  • activation of insulin receptor signaling pathway
  • positive regulation of insulin receptor signalling pathway
Branch: biological process
Genes: Gkap1 (Rno)...Gkap1 (Mmu)...GKAP1 (Hsa)

Gene Ontology
Source: GO:0005794
Synonyms:
  • Golgi
  • Golgi complex
Branch: cellular component
Genes: gkap1 (Dre)...Gkap1 (Rno)...GKAP1 (Hsa)...Gkap1 (Mmu)

Gene Ontology
Source: GO:0007165
Synonyms:
  • signaling cascade
  • signaling pathway
Branch: biological process
Genes: gkap1 (Dre)...Gkap1 (Rno)...GKAP1 (Hsa)...Gkap1 (Mmu)

Gene Ontology
Source: GO:0016301
Synonyms:
  • phosphokinase activity
Branch: molecular function
Genes: GKAP1 (Hsa)

Source: GO:0042802
Synonyms:
  • isoform-specific homophilic binding
  • protein homopolymerization
Branch: molecular function
Genes: Gkap1 (Rno)...GKAP1 (Hsa)...Gkap1 (Mmu)

sa7621

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-19121
Genes: gkap1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: Not Available
Genes: gkap1 (Dre)

sa34498

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3165
Genes: gkap1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: gkap1 (Dre)

sa34497

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3164
Genes: gkap1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gkap1 (Dre)

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: Gkap1 (Mmu)...GKAP1 (Hsa)

(GRCh38)9:83799271C>T

(Homo sapiens)
Allele/Variant
Source: rs745867590
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83799271C>T

(GRCh38)9:83741959T>C

(Homo sapiens)
Allele/Variant
Source: rs145631053
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83741959T>C

(GRCh38)9:83742535T>G

(Homo sapiens)
Allele/Variant
Source: rs775706002
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83742535T>G

(GRCh38)9:83768828T>A

(Homo sapiens)
Allele/Variant
Source: rs137996136
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768828T>A

(GRCh38)9:83784758T>A

(Homo sapiens)
Allele/Variant
Source: rs779573874
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83784758T>A

(GRCh38)9:83768895G>A

(Homo sapiens)
Allele/Variant
Source: rs1174517387
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768895G>A

(GRCh38)9:83806366G>A

(Homo sapiens)
Allele/Variant
Source: rs1381555343
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83806366G>A

(GRCh38)9:83748356A>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.83748356A>G
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83748356A>G

(GRCh38)9:83784723T>C

(Homo sapiens)
Allele/Variant
Source: rs764047918
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83784723T>C

(GRCh38)9:83806370T>A

(Homo sapiens)
Allele/Variant
Source: rs779809540
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83806370T>A

(GRCh38)9:83768855T>A

(Homo sapiens)
Allele/Variant
Source: rs768669281
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768855T>A

(GRCh38)9:83768822T>C

(Homo sapiens)
Allele/Variant
Source: rs148840512
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768822T>C

(GRCh38)9:83768925T>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.83768925T>G
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768925T>G

(GRCh38)9:83806367T>C

(Homo sapiens)
Allele/Variant
Source: rs1417333607
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83806367T>C

(GRCh38)9:83768906A>T

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.83768906A>T
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83768906A>T

(GRCh38)9:83780393T>C

(Homo sapiens)
Allele/Variant
Source: rs761882263
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83780393T>C

(GRCh38)9:83780397A>C

(Homo sapiens)
Allele/Variant
Source: rs1182067918
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83780397A>C

(GRCh38)9:83799237T>C

(Homo sapiens)
Allele/Variant
Source: rs150602176
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83799237T>C

(GRCh38)9:83806493C>G

(Homo sapiens)
Allele/Variant
Source: rs147325367
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83806493C>G

(GRCh38)9:83799256G>C

(Homo sapiens)
Allele/Variant
Source: rs781224571
Genes: GKAP1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:83799256G>C

(mRatBN7.2)17:6386979C>T

(Rattus norvegicus)
Allele/Variant
Source: rs105037128
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6386979C>T

(mRatBN7.2)17:6419187A>G

(Rattus norvegicus)
Allele/Variant
Source: NC_051352.1:g.6419187A>G
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6419187A>G

(mRatBN7.2)17:6420003C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197898573
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6420003C>T

(mRatBN7.2)17:6398080C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323052812
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6398080C>T

(mRatBN7.2)17:6398901G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3323051130
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6398901G>T

(mRatBN7.2)17:6414553G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3323004133
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6414553G>A

(mRatBN7.2)17:6392065A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323113248
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6392065A>G

(mRatBN7.2)17:6401297A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3323076320
Genes: Gkap1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)17:6401297A>G