Version: 8.1.0
Date: Fri Apr 18 2025
1,992 results for dennd2c

Dennd2c

(Rattus norvegicus)
Gene
Name: DENN domain containing 2C
Synonyms: DENN/MADD domain containing 2C, DENN domain-containing protein 2C, LOC295333, similar to A930010I20 protein, RGD1308197
Source: RGD:1308197
Biotype: protein coding gene
Symbol: Dennd2c (Rno)
Symbol: Dennd2c
Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C); INTERACTS WITH (+)-schisandrin B; acetamide
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Strict Orthology Symbols: dennd2c

Dennd2c

(Mus musculus)
Gene
Name: DENN domain containing 2C
Synonyms: RIKEN cDNA A930010I20 gene, A930010I20Rik, RGD1308197
Source: MGI:3036254
Biotype: protein coding gene
Symbol: Dennd2c (Mmu)
Symbol: Dennd2c
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Strict Orthology Symbols: dennd2c
Alleles: Dennd2c (Mmu)...Dennd2c (Mmu)...Dennd2c (Mmu)...Dennd2c (Mmu)

DENND2C

(Homo sapiens)
Gene
Name: DENN domain containing 2C
Synonyms: DENN/MADD domain containing 2C, FLJ37099, DKFZp686G0351, dJ1156J9.1, DENN domain-containing protein 2C, RP5-1156J9.1, DKFZp686N1631, DKFZp779P1149
Source: HGNC:24748
Biotype: protein coding gene
Symbol: DENND2C (Hsa)
Symbol: DENND2C
Strict Orthology Symbols: dennd2c

dennd2c

(Danio rerio)
Gene
Name: DENN/MADD domain containing 2C
Synonyms: si:dkeyp-31a2.2, si:dkeyp-46c9.6, si:dkeyp-31a2.1
Source: ZFIN:ZDB-GENE-081105-71
Biotype: protein coding gene
Symbol: dennd2c (Dre)
Symbol: dennd2c
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Strict Orthology Symbols: DENND2C...Dennd2c

dennd2c

(Xenopus tropicalis)
Gene
Name: DENN/MADD domain containing 2C
Synonyms: DENN/MADD domain containing 2C, dennd2c
Source: Xenbase:XB-GENE-5955506
Biotype: gene
Symbol: dennd2c (Xtr)
Symbol: dennd2c
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Synonyms: dennd2c...dennd2c...dennd2c
Strict Orthology Symbols: DENND2C...dennd2c.S...Dennd2c...dennd2c.L

dennd2c.L

(Xenopus laevis)
Gene
Name: DENN/MADD domain containing 2C
Synonyms: DENN/MADD domain containing 2C, dennd2c.L
Source: Xenbase:XB-GENE-6485628
Biotype: gene
Symbol: dennd2c.L (Xla)
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Strict Orthology Symbols: dennd2c
Symbol: dennd2c.L

dennd2c.S

(Xenopus laevis)
Gene
Name: DENN/MADD domain containing 2C
Synonyms: DENN/MADD domain containing 2C, dennd2c.S
Source: Xenbase:XB-GENE-6488480
Biotype: gene
Symbol: dennd2c.S (Xla)
Automated Gene Synopsis: Orthologous to human DENND2C (DENN domain containing 2C).
Strict Orthology Symbols: dennd2c
Symbol: dennd2c.S

Dennd2ctm1e(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4419463
Genes: Dennd2c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Dennd2c (Mmu)
Genes: Dennd2c (Mmu)
Symbol: Dennd2ctm1e(KOMP)Wtsi

Dennd2ctm1b(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:5708259
Genes: Dennd2c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Dennd2c (Mmu)
Genes: Dennd2c (Mmu)
Symbol: Dennd2ctm1b(KOMP)Wtsi

Dennd2ctm1e.1(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:6274704
Genes: Dennd2c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Dennd2c (Mmu)
Genes: Dennd2c (Mmu)
Symbol: Dennd2ctm1e.1(KOMP)Wtsi

Dennd2ctm1a(KOMP)Wtsi

(Mus musculus)
Allele/Variant
Source: MGI:4419317
Genes: Dennd2c (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Dennd2c (Mmu)
Genes: Dennd2c (Mmu)
Symbol: Dennd2ctm1a(KOMP)Wtsi

Dennd2ctm1b(KOMP)Wtsi/Dennd2ctm1b(KOMP)Wtsi [background:] C57BL/6N-Dennd2ctm1b(KOMP)Wtsi/Ucd

(Mus musculus)
Model
Id: MGI:5797473
Synonyms: Not Available
Symbol: Dennd2c/Dennd2c [background:] C57BL/6N-Dennd2c/Ucd (
Genes: Dennd2c (Mmu)
Alleles: Dennd2c (Mmu)
Name: Dennd2c/Dennd2c [background:] C57BL/6N-Dennd2c/Ucd

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: DENND2C (Hsa)...Dennd2c (Mmu)...dennd2c (Dre)...Dennd2c (Rno)

sa34321

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-15038
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa34324

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3023
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa34322

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3021
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa34325

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3024
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa34323

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-3022
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa9597

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-5205
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa15429

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-4005
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

sa16106

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-4620
Genes: dennd2c (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_region_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: dennd2c (Dre)

nucleoplasm

Gene Ontology
Source: GO:0005654
Synonyms: Not Available
Branch: cellular component
Genes: DENND2C (Hsa)...Dennd2c (Rno)...Dennd2c (Mmu)

protein binding

Gene Ontology
Source: GO:0005515
Synonyms:
  • glycoprotein binding
  • protein amino acid binding
Branch: molecular function
Genes: DENND2C (Hsa)

(GRCh38)1:114608804C>T

(Homo sapiens)
Allele/Variant
Source: rs576899104
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114608804C>T

(GRCh38)1:114600336C>T

(Homo sapiens)
Allele/Variant
Source: rs142352302
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600336C>T

(GRCh38)1:114608735G>A

(Homo sapiens)
Allele/Variant
Source: rs150852312
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114608735G>A

(GRCh38)1:114618439T>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114618439T>A
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114618439T>A

(GRCh38)1:114625322G>A

(Homo sapiens)
Allele/Variant
Source: rs139285200
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625322G>A

(GRCh38)1:114625815C>T

(Homo sapiens)
Allele/Variant
Source: rs1002740270
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625815C>T

(GRCh38)1:114625962G>A

(Homo sapiens)
Allele/Variant
Source: rs767850733
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625962G>A

(GRCh38)1:114608736G>T

(Homo sapiens)
Allele/Variant
Source: rs751813811
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114608736G>T

(GRCh38)1:114618421T>C

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114618421T>C
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114618421T>C

(GRCh38)1:114625187T>G

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114625187T>G
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625187T>G

(GRCh38)1:114625682T>G

(Homo sapiens)
Allele/Variant
Source: rs148237625
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625682T>G

(GRCh38)1:114594511C>T

(Homo sapiens)
Allele/Variant
Source: rs768969571
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114594511C>T

(GRCh38)1:114594523A>T

(Homo sapiens)
Allele/Variant
Source: rs773075931
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114594523A>T

(GRCh38)1:114600307C>T

(Homo sapiens)
Allele/Variant
Source: rs1443718069
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600307C>T

(GRCh38)1:114600351G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114600351G>A
Genes: DENND2C (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)1:114600351G>A

(GRCh38)1:114600876G>A

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114600876G>A
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600876G>A

(GRCh38)1:114600877G>A

(Homo sapiens)
Allele/Variant
Source: rs141493549
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600877G>A

(GRCh38)1:114618449T>C

(Homo sapiens)
Allele/Variant
Source: rs745845534
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114618449T>C

(GRCh38)1:114625893C>T

(Homo sapiens)
Allele/Variant
Source: rs267597930
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625893C>T

(GRCh38)1:114600845C>T

(Homo sapiens)
Allele/Variant
Source: rs769328707
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600845C>T

(GRCh38)1:114595834C>G

(Homo sapiens)
Allele/Variant
Source: NC_000001.11:g.114595834C>G
Genes: DENND2C (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)1:114595834C>G

(GRCh38)1:114595865T>C

(Homo sapiens)
Allele/Variant
Source: rs1655328737
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114595865T>C

(GRCh38)1:114625464T>G

(Homo sapiens)
Allele/Variant
Source: rs1035921997
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114625464T>G

(GRCh38)1:114600863C>T

(Homo sapiens)
Allele/Variant
Source: rs766659862
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114600863C>T

(GRCh38)1:114601521T>C

(Homo sapiens)
Allele/Variant
Source: rs202049154
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114601521T>C

(GRCh38)1:114608695G>C

(Homo sapiens)
Allele/Variant
Source: rs200263613
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114608695G>C

(GRCh38)1:114611101G>A

(Homo sapiens)
Allele/Variant
Source: rs146250607
Genes: DENND2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:114611101G>A