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1,051 results for rufy2

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Rufy2

(Mus musculus)

Gene

Name: RUN and FYVE domain-containing 2

Synonyms: differentially expressed in normal and neoplastic cells, Denn, AI844453, expressed sequence AI844453, RIKEN cDNA 2610111M19 gene, LZ-FYVE, ZFYVE13, 2610111M19Rik

Source: MGI:1917682

Biotype: protein coding gene

Symbol: Rufy2 (Mmu)

Symbol: Rufy2

Automated Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2).

Strict Orthology Symbols: rufy2

Alleles: Rufy2 (Mmu)...Rufy2 (Mmu)...Rufy2 (Mmu)

RUFY2

(Homo sapiens)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: rab4-interacting protein related, FLJ10063, KIAA1537, RUN and FYVE domain-containing protein 2, RABIP4R, Run- and FYVE-domain containing protein, ZFYVE13, antigen MU-RMS-40.17, RUN and FYVE domain-containing 2

Source: HGNC:19761

Biotype: protein coding gene

Symbol: RUFY2 (Hsa)

Symbol: RUFY2

Strict Orthology Symbols: rufy2

Allele/Variant (22)

rufy2

(Danio rerio)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: wu:fj43e12, zgc:162300

Source: ZFIN:ZDB-GENE-070424-66

Biotype: protein coding gene

Symbol: rufy2 (Dre)

Symbol: rufy2

Automated Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2).

Strict Orthology Symbols: rufy2

Allele/Variant (2)

Rufy2

(Rattus norvegicus)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: RUN and FYVE domain-containing protein 2, LOC100910755, LOC690777, RUN and FYVE domain-containing protein 2-like, LOC361837, similar to RUN and FYVE domain-containing 2, RUN and FYVE domain-containing 2

Source: RGD:1592188

Biotype: protein coding gene

Symbol: Rufy2 (Rno)

Symbol: Rufy2

Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2); INTERACTS WITH acrylamide; bisphenol A

Automated Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2).

Strict Orthology Symbols: rufy2

Allele/Variant (19)

rufy2

(Xenopus tropicalis)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: rufy2, RUN and FYVE domain containing 2

Source: Xenbase:XB-GENE-1015917

Biotype: gene

Symbol: rufy2

Symbol: rufy2 (Xtr)

Automated Gene Synopsis: Orthologous to several human genes including RUFY2 (RUN and FYVE domain containing 2).

Synonyms: rufy2...rufy2...rufy2

Strict Orthology Symbols: rufy2

rufy2.L

(Xenopus laevis)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: RUN and FYVE domain containing 2, rufy2.L

Source: Xenbase:XB-GENE-17332852

Biotype: gene

Symbol: rufy2.L (Xla)

Automated Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2).

Strict Orthology Symbols: rufy2

Symbol: rufy2.L

rufy2.S

(Xenopus laevis)

Gene

Name: RUN and FYVE domain containing 2

Synonyms: RUN and FYVE domain containing 2, rufy2.S

Source: Xenbase:XB-GENE-6489285

Biotype: gene

Symbol: rufy2.S (Xla)

Automated Gene Synopsis: Orthologous to human RUFY2 (RUN and FYVE domain containing 2).

Strict Orthology Symbols: rufy2

Symbol: rufy2.S

Rufy2^em1Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7305670

Genes: Rufy2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Rufy2 (Mmu)

Genes: Rufy2 (Mmu)

Symbol: Rufy2^em1Gpt

Gene (1)

Rufy2^{tm1a(EUCOMM)Wtsi}

(Mus musculus)

Allele/Variant

Source: MGI:4434385

Genes: Rufy2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Rufy2 (Mmu)

Genes: Rufy2 (Mmu)

Symbol: Rufy2^{tm1a(EUCOMM)Wtsi}

Rufy2^em9Gpt

(Mus musculus)

Allele/Variant

Source: MGI:7305671

Genes: Rufy2 (Mmu)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Rufy2 (Mmu)

Genes: Rufy2 (Mmu)

Symbol: Rufy2^em9Gpt

Gene (1)

Rufy2^{tm1a(EUCOMM)Wtsi}/Rufy2^{tm1a(EUCOMM)Wtsi} [background:] C57BL/6N-Rufy2^{tm1a(EUCOMM)Wtsi}/Wtsi

(Mus musculus)

Model

Id: MGI:6461622

Synonyms: Not Available

Symbol: Rufy2/Rufy2 [background:] C57BL/6N-Rufy2/Wtsi

Genes: Rufy2 (Mmu)

Alleles: Rufy2 (Mmu)

Name: Rufy2/Rufy2 [background:] C57BL/6N-Rufy2/Wtsi

Gene (1)

RUFY1

(Homo sapiens)

Gene

Name: RUN and FYVE domain containing 1

Synonyms: la-binding protein 1, FLJ22251, rab4-interacting protein, RUN and FYVE domain-containing protein 1, FYVE-finger protein EIP1, zinc finger FYVE domain-containing protein 12, RABIP4, RUN and FYVE domain-containing 1, ZFYVE12

Source: HGNC:19760

Biotype: protein coding gene

Strict Orthology Symbols: rufy2

Allele/Variant (44)

CG31064

(Drosophila melanogaster)

Gene

Name: Not Available

Synonyms: RUFY1, CG14261, CG6001

Source: FB:FBgn0051064

Biotype: protein coding gene

Strict Orthology Symbols: rufy2

Allele/Variant (424)

Rufy1

(Rattus norvegicus)

Gene

Name: RUN and FYVE domain containing 1

Synonyms: LOC360521, RUN and FYVE domain-containing protein 1

Source: RGD:1305099

Biotype: protein coding gene

Strict Orthology Symbols: rufy2

Allele/Variant (379)

Rufy1

(Mus musculus)

Gene

Name: RUN and FYVE domain containing 1

Synonyms: 3000002E04Rik, Rabip4, RIKEN cDNA 3000002E04 gene, ZFYVE12

Source: MGI:2429762

Biotype: protein coding gene

Strict Orthology Symbols: rufy2

la027406Tg

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-130129-2233

Genes: rufy2 (Dre)

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Genes: rufy2 (Dre)

Gene (1)

Hsap\RUFY2^UAS.Tag:HA

(Drosophila melanogaster)

Allele/Variant

Source: FB:FBal0388519

Genes: Not Available

Synonyms: Not Available

Variant Type: unreported

Molecular Consequence: Not Available

Diseases: Not Available

Variant Name: Not Available

Symbol: Hsap\RUFY2

Construct Expressed Component: RUFY2 (Hsa)

SH3 domain binding

Gene Ontology

Source: GO:0017124

Synonyms: Not Available

Branch: molecular function

Genes: Rufy2 (Rno)...RUFY2 (Hsa)...Rufy2 (Mmu)

Genes Annotated with this GO Term (394)

regulation of endocytosis

Gene Ontology

Source: GO:0030100

Synonyms: Not Available

Branch: biological process

Genes: RUFY2 (Hsa)

Genes Annotated with this GO Term (1272)

endosome

Gene Ontology

Source: GO:0005768

Synonyms: Not Available

Branch: cellular component

Genes: RUFY2 (Hsa)

Genes Annotated with this GO Term (4269)

sa6296

(Danio rerio)

Allele/Variant

Source: ZFIN:ZDB-ALT-161003-18141

Genes: rufy2 (Dre)

Synonyms: Not Available

Variant Type: point_mutation

Molecular Consequence: stop_gained

Diseases: Not Available

Variant Name: Not Available

Genes: rufy2 (Dre)

metal ion binding

Gene Ontology

Source: GO:0046872

Synonyms:

heavy metal binding
metal binding

Branch: molecular function

Genes: RUFY2 (Hsa)...rufy2 (Dre)...Rufy2 (Rno)...Rufy2 (Mmu)

Genes Annotated with this GO Term (10000)

cytoplasm

Gene Ontology

Source: GO:0005737

Synonyms: Not Available

Branch: cellular component

Genes: rufy2 (Dre)...Rufy2 (Mmu)...RUFY2 (Hsa)...Rufy2 (Rno)

Genes Annotated with this GO Term (10000)

nucleus

Gene Ontology

Source: GO:0005634

Synonyms:

cell nucleus
horsetail nucleus

Branch: cellular component

Genes: Rufy2 (Mmu)...RUFY2 (Hsa)

Genes Annotated with this GO Term (10000)

protein binding

Gene Ontology

Source: GO:0005515

Synonyms:

glycoprotein binding
protein amino acid binding

Branch: molecular function

Genes: RUFY2 (Hsa)

Genes Annotated with this GO Term (10000)

(GRCh38)10:68404730T>C

(Homo sapiens)

Allele/Variant

Source: rs772732981

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68404730T>C

(GRCh38)10:68386127T>G

(Homo sapiens)

Allele/Variant

Source: rs996731103

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

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

Diseases: Not Available

Variant Name: (GRCh38)10:68386127T>G

(GRCh38)10:68363653T>A

(Homo sapiens)

Allele/Variant

Source: NC_000010.11:g.68363653T>A

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68363653T>A

(GRCh38)10:68406780C>A

(Homo sapiens)

Allele/Variant

Source: rs762065487

Genes: RUFY2 (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)10:68406780C>A

(GRCh38)10:68396849C>T

(Homo sapiens)

Allele/Variant

Source: rs267602554

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68396849C>T

(GRCh38)10:68401668G>A

(Homo sapiens)

Allele/Variant

Source: NC_000010.11:g.68401668G>A

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68401668G>A

(GRCh38)10:68406766G>A

(Homo sapiens)

Allele/Variant

Source: rs200501110

Genes: RUFY2 (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)10:68406766G>A

(GRCh38)10:68364090T>G

(Homo sapiens)

Allele/Variant

Source: rs370795568

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68364090T>G

(GRCh38)10:68383874T>C

(Homo sapiens)

Allele/Variant

Source: rs2049280309

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68383874T>C

(GRCh38)10:68379478C>T

(Homo sapiens)

Allele/Variant

Source: rs202078546

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68379478C>T

(GRCh38)10:68383841T>C

(Homo sapiens)

Allele/Variant

Source: rs1044281127

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68383841T>C

(GRCh38)10:68401638C>T

(Homo sapiens)

Allele/Variant

Source: rs774388674

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68401638C>T

(GRCh38)10:68406841A>C

(Homo sapiens)

Allele/Variant

Source: rs769215045

Genes: RUFY2 (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)10:68406841A>C

(GRCh38)10:68383905C>T

(Homo sapiens)

Allele/Variant

Source: rs371028948

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68383905C>T

(GRCh38)10:68394089A>C

(Homo sapiens)

Allele/Variant

Source: rs770342069

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68394089A>C

(GRCh38)10:68346059T>G

(Homo sapiens)

Allele/Variant

Source: rs369778216

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68346059T>G

(GRCh38)10:68401657C>G

(Homo sapiens)

Allele/Variant

Source: rs752288965

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68401657C>G

(GRCh38)10:68376946A>C

(Homo sapiens)

Allele/Variant

Source: rs758709452

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68376946A>C

(GRCh38)10:68379494T>C

(Homo sapiens)

Allele/Variant

Source: NC_000010.11:g.68379494T>C

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68379494T>C

(GRCh38)10:68341629G>A

(Homo sapiens)

Allele/Variant

Source: rs150055889

Genes: HNRNPH3 (Hsa), RUFY2 (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)10:68341629G>A

(GRCh38)10:68383812A>G

(Homo sapiens)

Allele/Variant

Source: rs769858718

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68383812A>G

(GRCh38)10:68383859C>T

(Homo sapiens)

Allele/Variant

Source: rs760366895

Genes: RUFY2 (Hsa)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: missense_variant, non_coding_transcript_exon_variant

Diseases: Not Available

Variant Name: (GRCh38)10:68383859C>T

(mRatBN7.2)20:25635843T>A

(Rattus norvegicus)

Allele/Variant

Source: NC_051355.1:g.25635843T>A

Genes: Rufy2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)20:25635843T>A

(mRatBN7.2)20:25655812C>T

(Rattus norvegicus)

Allele/Variant

Source: rs104902362

Genes: Rufy2 (Rno)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: intron_variant

Diseases: Not Available

Variant Name: (mRatBN7.2)20:25655812C>T

(GRCm39)10:62850214T>C

(Mus musculus)

Allele/Variant

Source: rs223355751

Genes: Rufy2 (Mmu)

Synonyms: Not Available

Variant Type: SNP

Molecular Consequence: 3_prime_UTR_variant, intron_variant

Diseases: Not Available

Variant Name: (GRCm39)10:62850214T>C

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