Version: 8.0.0
Date: Tue Jan 28 2025
6,487 results for cgnl1

CGNL1

(Homo sapiens)
Gene
Name: cingulin like 1
Synonyms: cingulin-like 1, MGC138254, cingulin-like protein 1, paracingulin, junction-associated coiled-coil protein, PCING, FLJ14957, KIAA1749, JACOP
Source: HGNC:25931
Biotype: protein coding gene
Symbol: CGNL1 (Hsa)
Symbol: CGNL1
Strict Orthology Symbols: cgnl1

Cgnl1

(Rattus norvegicus)
Gene
Name: cingulin-like 1
Synonyms: RGD1304623, cingulin-like protein 1, similar to KIAA1749 protein, LOC315795
Source: RGD:1304623
Biotype: protein coding gene
Symbol: Cgnl1 (Rno)
Symbol: Cgnl1
Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1); INTERACTS WITH (+)-schisandrin B; 2,3,7,8-tetrachlorodibenzodioxine
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Strict Orthology Symbols: cgnl1
Alleles: Cgnl1 (Rno)...Cgnl1 (Rno)

cgnl1

(Danio rerio)
Gene
Name: cingulin-like 1
Synonyms: Not Available
Source: ZFIN:ZDB-GENE-071009-2
Biotype: protein coding gene
Symbol: cgnl1 (Dre)
Symbol: cgnl1
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Strict Orthology Symbols: cgnl1

Cgnl1

(Mus musculus)
Gene
Name: cingulin-like 1
Synonyms: 9930020M10Rik, RGD1304623, RIKEN cDNA 9930020M10 gene, AI503810, RIKEN cDNA 4933421H10 gene, expressed sequence AI503810, Jacop, 4933421H10Rik
Source: MGI:1915428
Biotype: protein coding gene
Symbol: Cgnl1 (Mmu)
Symbol: Cgnl1
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Strict Orthology Symbols: cgnl1
Alleles: Cgnl1 (Mmu)

cgnl1

(Xenopus tropicalis)
Gene
Name: cingulin-like 1
Synonyms: cingulin-like 1, cgnl1
Source: Xenbase:XB-GENE-5754486
Biotype: gene
Symbol: cgnl1
Symbol: cgnl1 (Xtr)
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Synonyms: cgnl1...cgnl1...cgnl1
Strict Orthology Symbols: cgnl1

cgnl1.L

(Xenopus laevis)
Gene
Name: cingulin-like 1
Synonyms: cgnl1.L, cingulin-like 1
Source: Xenbase:XB-GENE-5754563
Biotype: gene
Symbol: cgnl1.L (Xla)
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Strict Orthology Symbols: cgnl1
Symbol: cgnl1.L

cgnl1.S

(Xenopus laevis)
Gene
Name: cingulin-like 1
Synonyms: cingulin-like 1, cgnl1.S
Source: Xenbase:XB-GENE-17338686
Biotype: gene
Symbol: cgnl1.S (Xla)
Automated Gene Synopsis: Orthologous to human CGNL1 (cingulin like 1).
Strict Orthology Symbols: cgnl1
Symbol: cgnl1.S

Cgnl1em1(IMPC)Mbp

(Mus musculus)
Allele/Variant
Source: MGI:6152430
Genes: Cgnl1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Cgnl1 (Mmu)
Genes: Cgnl1 (Mmu)
Symbol: Cgnl1em1(IMPC)Mbp

Cgnl1em2Mcwi

(Rattus norvegicus)
Allele/Variant
Source: RGD:13799349
Genes: Cgnl1 (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Cgnl1 (Rno)
Genes: Cgnl1 (Rno)
Symbol: Cgnl1em2Mcwi

Cgnl1em1Mcwi

(Rattus norvegicus)
Allele/Variant
Source: RGD:13799347
Genes: Cgnl1 (Rno)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Cgnl1 (Rno)
Genes: Cgnl1 (Rno)
Symbol: Cgnl1em1Mcwi

Cgnl1em1(IMPC)Mbp/Cgnl1em1(IMPC)Mbp [background:] C57BL/6NCrl-Cgnl1em1(IMPC)Mbp/Mmucd

(Mus musculus)
Model
Id: MGI:6288392
Synonyms: Not Available
Symbol: Cgnl1/Cgnl1 [background:] C57BL/6NCrl-Cgnl1/Mmucd (Mmu)
Genes: Cgnl1 (Mmu)
Alleles: Cgnl1 (Mmu)
Name: Cgnl1/Cgnl1 [background:] C57BL/6NCrl-Cgnl1/Mmucd

unc-15

(Caenorhabditis elegans)
Gene
Name: UNCoordinated 15
Synonyms: CELE_F07A5.7, F07A5.7
Source: WB:WBGene00006754
Biotype: protein coding gene
Strict Orthology Symbols: Cgnl1

SS-Cgnl1em1Mcwi

(Rattus norvegicus)
Model
Id: RGD:13799346
Synonyms: Not Available
Genes: Cgnl1 (Rno)
Alleles: Cgnl1 (Rno)
Name: SS-<Cgnl1>

protein localization to cell-cell junction

Gene Ontology
Source: GO:0150105
Synonyms: Not Available
Branch: biological process
Genes: CGNL1 (Hsa)...cgnl1 (Dre)...Cgnl1 (Mmu)...Cgnl1 (Rno)

SS-Cgnl1em2Mcwi

(Rattus norvegicus)
Model
Id: RGD:13799348
Synonyms: Not Available
Genes: Cgnl1 (Rno)
Alleles: Cgnl1 (Rno)
Name: SS-<Cgnl1>

negative regulation of small GTPase mediated signal transduction

Gene Ontology
Source: GO:0051058
Synonyms:
  • down regulation of small GTPase mediated signal transduction
  • down-regulation of small GTPase mediated signal transduction
Branch: biological process
Genes: CGNL1 (Hsa)...Cgnl1 (Rno)...Cgnl1 (Mmu)

negative regulation of stress fiber assembly

Gene Ontology
Source: GO:0051497
Synonyms:
  • down regulation of stress fiber formation
  • down-regulation of stress fiber formation
Branch: biological process
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...Cgnl1 (Mmu)

apical junction complex

Gene Ontology
Source: GO:0043296
Synonyms:
  • apical cell junction complex
  • apical junction
Branch: cellular component
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...Cgnl1 (Mmu)

myosin complex

Gene Ontology
Source: GO:0016459
Synonyms: Not Available
Branch: cellular component
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...cgnl1 (Dre)...Cgnl1 (Mmu)

bicellular tight junction

Gene Ontology
Source: GO:0005923
Synonyms:
  • zonula occludens
Branch: cellular component
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...cgnl1 (Dre)...Cgnl1 (Mmu)

actin filament organization

Gene Ontology
Source: GO:0007015
Synonyms:
  • actin filament organisation
  • regulation of actin filament localization
Branch: biological process
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...Cgnl1 (Mmu)

actin cytoskeleton

Gene Ontology
Source: GO:0015629
Synonyms: Not Available
Branch: cellular component
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...Cgnl1 (Mmu)

sa21073

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15694
Genes: cgnl1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: cgnl1 (Dre)

sa41023

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-17036
Genes: cgnl1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: cgnl1 (Dre)

sa15287

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-3881
Genes: cgnl1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: cgnl1 (Dre)

sa11664

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-1476
Genes: cgnl1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: cgnl1 (Dre)

sa41022

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-17035
Genes: cgnl1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: cgnl1 (Dre)

protein-containing complex

Gene Ontology
Source: GO:0032991
Synonyms:
  • macromolecular complex
  • macromolecule complex
Branch: cellular component
Genes: Cgnl1 (Rno)...CGNL1 (Hsa)...Cgnl1 (Mmu)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Cgnl1 (Mmu)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: CGNL1 (Hsa)

(GRCh38)15:57438096C>A

(Homo sapiens)
Allele/Variant
Source: rs552662762
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57438096C>A

(GRCh38)15:57438715G>C

(Homo sapiens)
Allele/Variant
Source: rs773600425
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57438715G>C

(GRCh38)15:57439365T>C

(Homo sapiens)
Allele/Variant
Source: rs1457014035
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57439365T>C

(GRCh38)15:57439530A>G

(Homo sapiens)
Allele/Variant
Source: rs1280396
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57439530A>G

(GRCh38)15:57439469G>C

(Homo sapiens)
Allele/Variant
Source: rs758390323
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57439469G>C

(GRCh38)15:57440456A>G

(Homo sapiens)
Allele/Variant
Source: rs371292908
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57440456A>G

(GRCh38)15:57451596G>A

(Homo sapiens)
Allele/Variant
Source: rs780724057
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57451596G>A

(GRCh38)15:57547480G>A

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.57547480G>A
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57547480G>A

(GRCh38)15:57545684C>G

(Homo sapiens)
Allele/Variant
Source: rs140907780
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57545684C>G

(GRCh38)15:57516918C>T

(Homo sapiens)
Allele/Variant
Source: rs139813604
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57516918C>T

(GRCh38)15:57438110A>G

(Homo sapiens)
Allele/Variant
Source: rs566024340
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57438110A>G

(GRCh38)15:57452217A>G

(Homo sapiens)
Allele/Variant
Source: rs56726484
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57452217A>G

(GRCh38)15:57453762G>A

(Homo sapiens)
Allele/Variant
Source: rs149480547
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57453762G>A

(GRCh38)15:57453812G>A

(Homo sapiens)
Allele/Variant
Source: rs142690387
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57453812G>A

(GRCh38)15:57440464A>G

(Homo sapiens)
Allele/Variant
Source: rs766576603
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57440464A>G

(GRCh38)15:57451538A>C

(Homo sapiens)
Allele/Variant
Source: rs531526050
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57451538A>C

(GRCh38)15:57451597T>G

(Homo sapiens)
Allele/Variant
Source: rs747655307
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57451597T>G

(GRCh38)15:57546184A>G

(Homo sapiens)
Allele/Variant
Source: rs773909069
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57546184A>G

(GRCh38)15:57547459C>T

(Homo sapiens)
Allele/Variant
Source: rs1210430383
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57547459C>T

(GRCh38)15:57438393C>G

(Homo sapiens)
Allele/Variant
Source: rs375993774
Genes: CGNL1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:57438393C>G