Version: 8.0.0
Date: Tue Jan 28 2025
4,436 results for arhgef33

Arhgef33

(Rattus norvegicus)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: LOC500608, RGD1560224, Rho guanine nucleotide exchange factor (GEF) 33
Source: RGD:1560224
Biotype: protein coding gene
Symbol: Arhgef33 (Rno)
Symbol: Arhgef33
Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33); INTERACTS WITH bisphenol A
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Strict Orthology Symbols: arhgef33

Arhgef33

(Mus musculus)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: LOC381112, RGD1560224, predicted gene 941, Gm941, gene model 941, (NCBI)
Source: MGI:2685787
Biotype: protein coding gene
Symbol: Arhgef33 (Mmu)
Symbol: Arhgef33
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Strict Orthology Symbols: arhgef33
Alleles: Arhgef33 (Mmu)

ARHGEF33

(Homo sapiens)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: DH and coiled-coil domain-containing protein ENSP00000381780, Rho guanine nucleotide exchange factor (GEF) 33, FLJ41381
Source: HGNC:37252
Biotype: protein coding gene
Symbol: ARHGEF33 (Hsa)
Symbol: ARHGEF33
Strict Orthology Symbols: arhgef33

arhgef33

(Danio rerio)
Gene
Name: Rho guanine nucleotide exchange factor (GEF) 33
Synonyms: si:ch211-15d5.10
Source: ZFIN:ZDB-GENE-131121-574
Biotype: protein coding gene
Symbol: arhgef33 (Dre)
Symbol: arhgef33
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Strict Orthology Symbols: arhgef33

arhgef33

(Xenopus tropicalis)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: arhgef33, Rho guanine nucleotide exchange factor 33
Source: Xenbase:XB-GENE-951465
Biotype: gene
Symbol: arhgef33
Symbol: arhgef33 (Xtr)
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Synonyms: arhgef33...arhgef33...arhgef33
Strict Orthology Symbols: arhgef33

arhgef33.S

(Xenopus laevis)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: Rho guanine nucleotide exchange factor 33, arhgef33.S
Source: Xenbase:XB-GENE-17341838
Biotype: gene
Symbol: arhgef33.S (Xla)
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Strict Orthology Symbols: arhgef33
Symbol: arhgef33.S

arhgef33.L

(Xenopus laevis)
Gene
Name: Rho guanine nucleotide exchange factor 33
Synonyms: arhgef33.L, Rho guanine nucleotide exchange factor 33
Source: Xenbase:XB-GENE-17341837
Biotype: gene
Symbol: arhgef33.L (Xla)
Automated Gene Synopsis: Orthologous to human ARHGEF33 (Rho guanine nucleotide exchange factor 33).
Strict Orthology Symbols: arhgef33
Symbol: arhgef33.L

Arhgef33em1(IMPC)Tcp

(Mus musculus)
Allele/Variant
Source: MGI:6388389
Genes: Arhgef33 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Arhgef33 (Mmu)
Genes: Arhgef33 (Mmu)
Symbol: Arhgef33em1(IMPC)Tcp

Arhgef33em1(IMPC)Tcp/Arhgef33em1(IMPC)Tcp [background:] C57BL/6N-Arhgef33em1(IMPC)Tcp/Cmmr

(Mus musculus)
Model
Id: MGI:7414782
Synonyms: Not Available
Symbol: Arhgef33/Arhgef33 [background:] C57BL/6N-Arhgef33/Cmmr (Mmu
Genes: Arhgef33 (Mmu)
Alleles: Arhgef33 (Mmu)
Name: Arhgef33/Arhgef33 [background:] C57BL/6N-Arhgef33/Cmmr

sa42936

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-8595
Genes: arhgef33 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: arhgef33 (Dre)

guanyl-nucleotide exchange factor activity

Gene Ontology
Source: GO:0005085
Synonyms:
  • ARF guanyl-nucleotide exchange factor activity
  • GDP-dissociation stimulator activity
Branch: molecular function
Genes: ARHGEF33 (Hsa)...Arhgef33 (Mmu)...Arhgef33 (Rno)...arhgef33 (Dre)

cellular_component

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: Arhgef33 (Mmu)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: Arhgef33 (Mmu)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: Arhgef33 (Mmu)

(GRCh38)2:38960517A>C

(Homo sapiens)
Allele/Variant
Source: rs1038870257
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960517A>C

(GRCh38)2:38929743C>A

(Homo sapiens)
Allele/Variant
Source: rs201883435
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38929743C>A

(GRCh38)2:38929821T>C

(Homo sapiens)
Allele/Variant
Source: rs1379916593
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38929821T>C

(GRCh38)2:38937386C>T

(Homo sapiens)
Allele/Variant
Source: rs377504175
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38937386C>T

(GRCh38)2:38960430C>A

(Homo sapiens)
Allele/Variant
Source: rs915516796
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960430C>A

(GRCh38)2:38944025G>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38944025G>T
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38944025G>T

(GRCh38)2:38937401C>T

(Homo sapiens)
Allele/Variant
Source: rs756321032
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38937401C>T

(GRCh38)2:38953177T>C

(Homo sapiens)
Allele/Variant
Source: rs139196444
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38953177T>C

(GRCh38)2:38954404C>A

(Homo sapiens)
Allele/Variant
Source: rs1201933128
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38954404C>A

(GRCh38)2:38937487G>C

(Homo sapiens)
Allele/Variant
Source: rs548940033
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38937487G>C

(GRCh38)2:38943949A>G

(Homo sapiens)
Allele/Variant
Source: rs912862244
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38943949A>G

(GRCh38)2:38943954A>G

(Homo sapiens)
Allele/Variant
Source: rs1164517386
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38943954A>G

(GRCh38)2:38960339G>C

(Homo sapiens)
Allele/Variant
Source: rs921632785
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960339G>C

(GRCh38)2:38960475C>A

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38960475C>A
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960475C>A

(GRCh38)2:38960344C>G

(Homo sapiens)
Allele/Variant
Source: rs1351990929
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960344C>G

(GRCh38)2:38960005C>T

(Homo sapiens)
Allele/Variant
Source: rs772939186
Genes: ARHGEF33 (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)2:38960005C>T

(GRCh38)2:38959933G>A

(Homo sapiens)
Allele/Variant
Source: rs998668435
Genes: ARHGEF33 (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)2:38959933G>A

(GRCh38)2:38944027G>A

(Homo sapiens)
Allele/Variant
Source: rs986731308
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38944027G>A

(GRCh38)2:38956965C>T

(Homo sapiens)
Allele/Variant
Source: rs1238557267
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38956965C>T

(GRCh38)2:38959892G>C

(Homo sapiens)
Allele/Variant
Source: rs768699856
Genes: ARHGEF33 (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)2:38959892G>C

(GRCh38)2:38960130G>A

(Homo sapiens)
Allele/Variant
Source: rs1377077056
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960130G>A

(GRCh38)2:38931114C>T

(Homo sapiens)
Allele/Variant
Source: rs1558431903
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38931114C>T

(GRCh38)2:38931222A>G

(Homo sapiens)
Allele/Variant
Source: rs773170064
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38931222A>G

(GRCh38)2:38935823T>A

(Homo sapiens)
Allele/Variant
Source: rs1219582557
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38935823T>A

(GRCh38)2:38960425G>A

(Homo sapiens)
Allele/Variant
Source: rs1273753905
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960425G>A

(GRCh38)2:38957031C>T

(Homo sapiens)
Allele/Variant
Source: rs781162421
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38957031C>T

(GRCh38)2:38960470C>T

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38960470C>T
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960470C>T

(GRCh38)2:38959936G>A

(Homo sapiens)
Allele/Variant
Source: rs191433768
Genes: ARHGEF33 (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)2:38959936G>A

(GRCh38)2:38960502G>A

(Homo sapiens)
Allele/Variant
Source: rs911623465
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960502G>A

(GRCh38)2:38958065G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38958065G>C
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38958065G>C

(GRCh38)2:38937458G>C

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38937458G>C
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38937458G>C

(GRCh38)2:38958102C>G

(Homo sapiens)
Allele/Variant
Source: rs1036847460
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38958102C>G

(GRCh38)2:38959926C>G

(Homo sapiens)
Allele/Variant
Source: rs1042820924
Genes: ARHGEF33 (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)2:38959926C>G

(GRCh38)2:38960267C>G

(Homo sapiens)
Allele/Variant
Source: NC_000002.12:g.38960267C>G
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38960267C>G

(GRCh38)2:38953238T>C

(Homo sapiens)
Allele/Variant
Source: rs375426166
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38953238T>C

(GRCh38)2:38954448C>T

(Homo sapiens)
Allele/Variant
Source: rs368877445
Genes: ARHGEF33 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:38954448C>T