Version: 8.0.0
Date: Tue Jan 28 2025
618 results for depdc7

Depdc7

(Rattus norvegicus)
Gene
Name: DEP domain containing 7
Synonyms: RGD1309720, DEP domain-containing protein 7, LOC295971, similar to Hypothetical protein MGC19163, MGC114389
Source: RGD:1309720
Biotype: protein coding gene
Symbol: Depdc7 (Rno)
Symbol: Depdc7
Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7); INTERACTS WITH 1-naphthyl isothiocyanate; 17beta-estradiol
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Strict Orthology Symbols: depdc7

DEPDC7

(Homo sapiens)
Gene
Name: DEP domain containing 7
Synonyms: dJ85M6.4 (novel 58.3 KDA protein), dJ85M6.4, TR2, DEP domain-containing protein 7, novel 58.3 KDA protein
Source: HGNC:29899
Biotype: protein coding gene
Symbol: DEPDC7 (Hsa)
Symbol: DEPDC7
Strict Orthology Symbols: depdc7

Depdc7

(Mus musculus)
Gene
Name: DEP domain containing 7
Synonyms: RGD1309720, MGC:19163, expressed sequence AV216087, AV216087
Source: MGI:2139258
Biotype: protein coding gene
Symbol: Depdc7 (Mmu)
Symbol: Depdc7
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Strict Orthology Symbols: depdc7
Alleles: Depdc7 (Mmu)...Depdc7 (Mmu)...Depdc7 (Mmu)...Depdc7 (Mmu)...Depdc7 (Mmu)

depdc7

(Xenopus tropicalis)
Gene
Name: DEP domain containing 7
Synonyms: depdc7, DEP domain containing 7, tr2, depdc7-a, depdc7-b
Source: Xenbase:XB-GENE-1010065
Biotype: gene
Symbol: depdc7 (Xtr)
Symbol: depdc7
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Synonyms: depdc7...depdc7...depdc7
Strict Orthology Symbols: DEPDC7...Depdc7...depdc7.S...depdc7b...depdc7a

depdc7b

(Danio rerio)
Gene
Name: DEP domain containing 7, paralog b
Synonyms: wu:fj82b07, si:ch211-11i22.4
Source: ZFIN:ZDB-GENE-030131-9492
Biotype: protein coding gene
Symbol: depdc7b (Dre)
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Strict Orthology Symbols: depdc7
Symbol: depdc7b

depdc7a

(Danio rerio)
Gene
Name: DEP domain containing 7, paralog a
Synonyms: depdc7, wu:fe36f02, zgc:136359
Source: ZFIN:ZDB-GENE-060512-176
Biotype: protein coding gene
Symbol: depdc7a (Dre)
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Synonyms: depdc7...depdc7...depdc7
Strict Orthology Symbols: depdc7
Symbol: depdc7a

depdc7.S

(Xenopus laevis)
Gene
Name: DEP domain containing 7
Synonyms: DEP domain containing 7, tr2, depdc7-a, depdc7.S, depdc7-b
Source: Xenbase:XB-GENE-6251452
Biotype: gene
Symbol: depdc7.S (Xla)
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Strict Orthology Symbols: depdc7
Symbol: depdc7.S

depdc7.L

(Xenopus laevis)
Gene
Name: DEP domain containing 7
Synonyms: DEP domain containing 7, depdc7-a, tr2, depdc7-b, depdc7.L
Source: Xenbase:XB-GENE-1010073
Biotype: gene
Symbol: depdc7.L (Xla)
Automated Gene Synopsis: Orthologous to human DEPDC7 (DEP domain containing 7).
Strict Orthology Symbols: depdc7
Symbol: depdc7.L

Depdc7em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7297939
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7em1Gpt

Depdc7tm1b(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5823223
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7tm1b(EUCOMM)Wtsi

Depdc7em2Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7750596
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7em2Smoc

Depdc7em1Smoc

(Mus musculus)
Allele/Variant
Source: MGI:7289315
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7em1Smoc

Depdc7em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7583365
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7em1Cya

Depdc7tm1a(EUCOMM)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5052484
Genes: Depdc7 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Depdc7 (Mmu)
Genes: Depdc7 (Mmu)
Symbol: Depdc7tm1a(EUCOMM)Wtsi

la020480Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-120806-11930
Genes: depdc7a (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: depdc7
Genes: depdc7a (Dre)

intracellular signal transduction

Gene Ontology
Source: GO:0035556
Synonyms:
  • intracellular signal transduction pathway
  • intracellular signaling cascade
Branch: biological process
Genes: depdc7a (Dre)...Depdc7 (Rno)...depdc7b (Dre)...Depdc7 (Mmu)...DEPDC7 (Hsa)

sa24599

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-20235
Genes: depdc7b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: depdc7b (Dre)

molecular_function

Gene Ontology
Source: GO:0003674
Synonyms:
  • molecular function
Branch: molecular function
Genes: DEPDC7 (Hsa)...Depdc7 (Mmu)...depdc7a (Dre)

cellular_component

Gene Ontology
Source: GO:0005575
Synonyms:
  • cell or subcellular entity
  • cellular component
Branch: cellular component
Genes: DEPDC7 (Hsa)...Depdc7 (Mmu)

biological_process

Gene Ontology
Source: GO:0008150
Synonyms:
  • biological process
  • physiological process
Branch: biological process
Genes: DEPDC7 (Hsa)

(GRCh38)11:33032957T>G

(Homo sapiens)
Allele/Variant
Source: rs185768707
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33032957T>G

(GRCh38)11:33025782T>G

(Homo sapiens)
Allele/Variant
Source: rs138325318
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33025782T>G

(GRCh38)11:33027687T>A

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33027687T>A
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33027687T>A

(GRCh38)11:33015992C>T

(Homo sapiens)
Allele/Variant
Source: NC_000011.10:g.33015992C>T
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33015992C>T

(GRCh38)11:33028773A>T

(Homo sapiens)
Allele/Variant
Source: rs201199439
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)11:33028773A>T

(GRCh38)11:33033398G>T

(Homo sapiens)
Allele/Variant
Source: rs367948856
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33033398G>T

(GRCh38)11:33025691A>G

(Homo sapiens)
Allele/Variant
Source: rs368794067
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33025691A>G

(GRCh38)11:33031460C>G

(Homo sapiens)
Allele/Variant
Source: rs765821983
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33031460C>G

(GRCh38)11:33032443G>A

(Homo sapiens)
Allele/Variant
Source: rs1373790305
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33032443G>A

(GRCh38)11:33025665G>A

(Homo sapiens)
Allele/Variant
Source: rs745587922
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33025665G>A

(GRCh38)11:33025904G>A

(Homo sapiens)
Allele/Variant
Source: rs1209438892
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33025904G>A

(GRCh38)11:33016019A>G

(Homo sapiens)
Allele/Variant
Source: rs1384944332
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33016019A>G

(GRCh38)11:33033369A>G

(Homo sapiens)
Allele/Variant
Source: rs1421692909
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33033369A>G

(GRCh38)11:33028606T>C

(Homo sapiens)
Allele/Variant
Source: rs144655252
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33028606T>C

(GRCh38)11:33031538C>T

(Homo sapiens)
Allele/Variant
Source: rs370596448
Genes: DEPDC7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)11:33031538C>T

(mRatBN7.2)3:91101825C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197157329
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91101825C>T

(mRatBN7.2)3:91116325T>C

(Rattus norvegicus)
Allele/Variant
Source: rs197418456
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91116325T>C

(mRatBN7.2)3:91110790T>A

(Rattus norvegicus)
Allele/Variant
Source: NC_051338.1:g.91110790T>A
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91110790T>A

(mRatBN7.2)3:91114196G>C

(Rattus norvegicus)
Allele/Variant
Source: rs197756622
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91114196G>C

(mRatBN7.2)3:91114882G>A

(Rattus norvegicus)
Allele/Variant
Source: rs198361266
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91114882G>A

(mRatBN7.2)3:91117001C>T

(Rattus norvegicus)
Allele/Variant
Source: rs197488416
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91117001C>T

(mRatBN7.2)3:91119929T>C

(Rattus norvegicus)
Allele/Variant
Source: rs198924027
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91119929T>C

(mRatBN7.2)3:91107813A>T

(Rattus norvegicus)
Allele/Variant
Source: rs198722577
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91107813A>T

(mRatBN7.2)3:91109156G>T

(Rattus norvegicus)
Allele/Variant
Source: rs198055359
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91109156G>T

(mRatBN7.2)3:91119241G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319964942
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91119241G>A

(mRatBN7.2)3:91100760G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319974735
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91100760G>A

(mRatBN7.2)3:91117317G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3319956201
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91117317G>A

(mRatBN7.2)3:91105281C>T

(Rattus norvegicus)
Allele/Variant
Source: rs198896833
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91105281C>T

(mRatBN7.2)3:91107522A>C

(Rattus norvegicus)
Allele/Variant
Source: rs199023016
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91107522A>C

(mRatBN7.2)3:91110047A>G

(Rattus norvegicus)
Allele/Variant
Source: rs199132416
Genes: Depdc7 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)3:91110047A>G