[object Object]

Category

3,392 results for EVI5

Page 2 of 68

GTPase activator activity

Gene Ontology

Source: GO:0005096

Synonyms:

ARF GAP activity
ARF GTPase activator activity

Branch: molecular function

Genes: Evi5l (Rno)...Evi5 (Rno)...EVI5 (Hsa)...Evi5 (Mmu)...Evi5 (Dme)

Genes Annotated with this GO Term (1201)

Scer\GAL4^{Evi5-CR02602-TG4.0}

(Drosophila melanogaster)

Allele/Variant

Source: FB:FBal0373448

Genes: Not Available

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Scer\GAL4<Evi5-CR02602-TG4.0>

small GTPase binding

Gene Ontology

Source: GO:0031267

Synonyms:

ADP-ribosylation factor binding
ARF binding

Branch: molecular function

Genes: Evi5l (Rno)...Evi5 (Rno)...EVI5 (Hsa)...Evi5 (Mmu)...Evi5 (Dme)

Genes Annotated with this GO Term (1241)

spindle

Gene Ontology

Source: GO:0005819

Synonyms: Not Available

Branch: cellular component

Genes: EVI5 (Hsa)...Evi5 (Mmu)

Genes Annotated with this GO Term (1742)

regulation of protein localization

Gene Ontology

Source: GO:0032880

Synonyms:

regulation of cellular protein localisation
regulation of cellular protein localization

Branch: biological process

Genes: Evi5 (Dme)

Genes Annotated with this GO Term (3535)

recycling endosome

Gene Ontology

Source: GO:0055037

Synonyms:

ERC
endosomal recycling compartment

Branch: cellular component

Genes: Evi5 (Dme)

Genes Annotated with this GO Term (803)

regulation of cell migration

Gene Ontology

Source: GO:0030334

Synonyms: Not Available

Branch: biological process

Genes: Evi5 (Dme)

Genes Annotated with this GO Term (3775)

vesicle

Gene Ontology

Source: GO:0031982

Synonyms:

membrane-bounded vesicle
membrane-enclosed vesicle

Branch: cellular component

Genes: Evi5 (Dme)

Genes Annotated with this GO Term (10000)

cell division

Gene Ontology

Source: GO:0051301

Synonyms: Not Available

Branch: biological process

Genes: EVI5 (Hsa)...Evi5 (Mmu)

Genes Annotated with this GO Term (2536)

sa15533

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130411-4099

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

sa17572

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-13676

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

sa17798

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-13874

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

sa19554

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-131217-14777

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

sa12742

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130411-2437

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

sa45254

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-181002-183

Genes: evi5b (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_region_variant, intron_variant

Diseases: Not Available

Variant Name: Not Available

Gene Synonyms: evi5

Genes: evi5b (Dre)

sa32739

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-160601-1891

Genes: evi5l (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: splice_donor_variant

Diseases: Not Available

Variant Name: Not Available

Genes: evi5l (Dre)

centrosome

Gene Ontology

Source: GO:0005813

Synonyms: Not Available

Branch: cellular component

Genes: EVI5 (Hsa)...Evi5 (Mmu)

Genes Annotated with this GO Term (2644)

(GRCh38)1:92607683C>T

(Homo sapiens)

Allele/Variant

Source: rs141343784

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: stop_retained_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92607683C>T

(GRCh38)1:92607727T>C

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.92607727T>C

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92607727T>C

(GRCh38)1:92693893G>C

(Homo sapiens)

Allele/Variant

Source: rs569327954

Genes: EVI5 (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)1:92693893G>C

(GRCh38)1:92736616G>C

(Homo sapiens)

Allele/Variant

Source: rs780400268

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92736616G>C

(GRCh38)1:92513797A>G

(Homo sapiens)

Allele/Variant

Source: rs6603979

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513797A>G

(GRCh38)1:92624334G>A

(Homo sapiens)

Allele/Variant

Source: rs142784307

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92624334G>A

(GRCh38)1:92695359G>A

(Homo sapiens)

Allele/Variant

Source: rs200758588

Genes: EVI5 (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)1:92695359G>A

(GRCh38)1:92625911C>A

(Homo sapiens)

Allele/Variant

Source: rs1655569406

Genes: EVI5 (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)1:92625911C>A

(GRCh38)1:92694369C>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.92694369C>A

Genes: EVI5 (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)1:92694369C>A

(GRCh38)1:92697972T>G

(Homo sapiens)

Allele/Variant

Source: rs200747400

Genes: EVI5 (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)1:92697972T>G

(GRCh38)1:92607702C>T

(Homo sapiens)

Allele/Variant

Source: rs781351466

Genes: EVI5 (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)1:92607702C>T

(GRCh38)1:92624246C>T

(Homo sapiens)

Allele/Variant

Source: rs201719783

Genes: EVI5 (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)1:92624246C>T

(GRCh38)1:92695397C>A

(Homo sapiens)

Allele/Variant

Source: rs367754544

Genes: EVI5 (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)1:92695397C>A

(GRCh38)1:92697879T>C

(Homo sapiens)

Allele/Variant

Source: rs781444194

Genes: EVI5 (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)1:92697879T>C

(GRCh38)1:92607671C>A

(Homo sapiens)

Allele/Variant

Source: rs11808092

Genes: EVI5 (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)1:92607671C>A

(GRCh38)1:92792383G>C

(Homo sapiens)

Allele/Variant

Source: rs370949072

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92792383G>C

(GRCh38)1:92792384T>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.92792384T>A

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92792384T>A

(GRCh38)1:92513963C>T

(Homo sapiens)

Allele/Variant

Source: rs1283685554

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513963C>T

(GRCh38)1:92513910T>C

(Homo sapiens)

Allele/Variant

Source: rs747893888

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513910T>C

(GRCh38)1:92624266T>C

(Homo sapiens)

Allele/Variant

Source: rs7514716

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92624266T>C

(GRCh38)1:92736503G>A

(Homo sapiens)

Allele/Variant

Source: rs756848081

Genes: EVI5 (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)1:92736503G>A

(GRCh38)1:92792383G>T

(Homo sapiens)

Allele/Variant

Source: rs370949072

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92792383G>T

(GRCh38)1:92607606C>T

(Homo sapiens)

Allele/Variant

Source: rs770316787

Genes: EVI5 (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)1:92607606C>T

(GRCh38)1:92665959G>A

(Homo sapiens)

Allele/Variant

Source: rs200507358

Genes: EVI5 (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)1:92665959G>A

(GRCh38)1:92513741C>T

(Homo sapiens)

Allele/Variant

Source: rs1659409038

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513741C>T

(GRCh38)1:92624305C>G

(Homo sapiens)

Allele/Variant

Source: rs377644327

Genes: EVI5 (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)1:92624305C>G

(GRCh38)1:92704727C>T

(Homo sapiens)

Allele/Variant

Source: rs1489130472

Genes: EVI5 (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)1:92704727C>T

(GRCh38)1:92624321C>G

(Homo sapiens)

Allele/Variant

Source: rs201423013

Genes: EVI5 (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)1:92624321C>G

(GRCh38)1:92513722C>T

(Homo sapiens)

Allele/Variant

Source: rs144597007

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513722C>T

(GRCh38)1:92513759T>A

(Homo sapiens)

Allele/Variant

Source: NC_000001.11:g.92513759T>A

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, stop_lost, 3_prime_UTR_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92513759T>A

(GRCh38)1:92563658G>A

(Homo sapiens)

Allele/Variant

Source: rs771112779

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, stop_gained

Diseases: Not Available

Variant Name: (GRCh38)1:92563658G>A

(GRCh38)1:92607696G>A

(Homo sapiens)

Allele/Variant

Source: rs1650748304

Genes: EVI5 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, non_coding_transcript_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)1:92607696G>A

(GRCh38)1:92703495T>C

(Homo sapiens)

Allele/Variant

Source: rs141479784

Genes: EVI5 (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)1:92703495T>C

Page 2 of 68