Version: 8.0.0Date: Tue Jan 28 2025
Category
Ccdc63
(Rattus norvegicus)Gene
Name: coiled-coil domain containing 63
Synonyms: coiled-coil domain-containing protein 63, similar to hypothetical protein 4921511C16, LOC304484, MGC114454
Source: RGD:1562334
Biotype: protein coding gene
Symbol: Ccdc63 (Rno)
Symbol: Ccdc63
Gene Synopsis: Orthologous to human CCDC63 (coiled-coil domain containing 63); INTERACTS WITH bisphenol A; cadmium dichloride
Automated Gene Synopsis: Orthologous to human CCDC63 (coiled-coil domain containing 63).
Strict Orthology Symbols: CCDC63...Ccdc63
CCDC63
(Homo sapiens)Gene
Name: coiled-coil domain containing 63
Synonyms: coiled-coil domain-containing protein 63, outer row dynein assembly 5 homolog, FLJ35843, ODA5
Source: HGNC:26669
Biotype: protein coding gene
Symbol: CCDC63 (Hsa)
Symbol: CCDC63
Strict Orthology Symbols: ccdc63.L...Ccdc63
Ccdc63
(Mus musculus)Gene
Name: coiled-coil domain containing 63
Synonyms: RIKEN cDNA 4921511C16 gene, 4921511C16Rik
Source: MGI:3607777
Biotype: protein coding gene
Symbol: Ccdc63 (Mmu)
Symbol: Ccdc63
Automated Gene Synopsis: Orthologous to human CCDC63 (coiled-coil domain containing 63).
Strict Orthology Symbols: CCDC63...Ccdc63
Alleles: Ccdc63
ccdc63.L
(Xenopus laevis)Gene
Name: coiled-coil domain containing 63
Synonyms: coiled-coil domain containing 63, ccdc63.L
Source: Xenbase:XB-GENE-5873574
Biotype: gene
Symbol: ccdc63.L (Xla)
Automated Gene Synopsis: Orthologous to human CCDC63 (coiled-coil domain containing 63).
Strict Orthology Symbols: ccdc63
Symbol: ccdc63.L
ccdc63
(Xenopus tropicalis)Gene
Name: coiled-coil domain containing 63
Synonyms: coiled-coil domain containing 63, ccdc63
Source: Xenbase:XB-GENE-5873552
Biotype: gene
Symbol: ccdc63 (Xtr)
Symbol: ccdc63
Synonyms: ccdc63...ccdc63...ccdc63
Strict Orthology Symbols: ccdc63.L
Ccdc63em1Osb
(Mus musculus)Allele/Variant
Source: MGI:6343353
Genes: Ccdc63 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ccdc63
Genes: Ccdc63 (Mmu)
Symbol: Ccdc63em1Osb
Model
Id: MGI:6377564
Synonyms: Not Available
Symbol: Ccdc63/Ccdc63 [background:] involves: C57BL/6NJcl * DBA/2NJcl (Mmu)
Genes: Ccdc63 (Mmu)
Alleles: Ccdc63
Name: Ccdc63/Ccdc63 [background:] involves: C57BL/6NJcl * DBA/2NJcl
wam
(Drosophila melanogaster)Gene
Name: wampa
Synonyms: CG17083
Source: FB:FBgn0039070
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to human CCDC63 (coiled-coil domain containing 63).
Strict Orthology Symbols: ccdc63
Ccdc114
(Drosophila melanogaster)Gene
Name: Coiled-coil domain containing protein 114
Synonyms: CG14905
Source: FB:FBgn0038452
Biotype: protein coding gene
Automated Gene Synopsis: Orthologous to several human genes including CCDC63 (coiled-coil domain containing 63).
Strict Orthology Symbols: ccdc63
ODAD1
(Homo sapiens)Gene
Name: outer dynein arm docking complex subunit 1
Synonyms: CILD20, FLJ32926, outer dynein arm-docking complex subunit 1, CCDC114, coiled-coil domain containing 114, coiled-coil domain-containing protein 114
Source: HGNC:26560
Biotype: protein coding gene
Strict Orthology Symbols: ccdc63
odad1
(Danio rerio)Gene
Name: outer dynein arm docking complex subunit 1
Synonyms: ccdc114, zgc:101737, dynein intermediate chain
Source: ZFIN:ZDB-GENE-041114-110
Biotype: protein coding gene
Strict Orthology Symbols: ccdc63
Odad1
(Rattus norvegicus)Gene
Name: outer dynein arm docking complex subunit 1
Synonyms: LOC308594, similar to BC013491 protein, Ccdc114, outer dynein arm-docking complex subunit 1, coiled-coil domain containing 114, RGD1308141, coiled-coil domain-containing protein 114
Source: RGD:1308141
Biotype: protein coding gene
Strict Orthology Symbols: ccdc63
Odad1
(Mus musculus)Gene
Name: outer dynein arm docking complex subunit 1
Synonyms: cDNA sequence BC013491, Ccdc114, BC013491, coiled-coil domain containing 114, RGD1308141
Source: MGI:2446120
Biotype: protein coding gene
Strict Orthology Symbols: ccdc63
Source: DOID:0110625
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, infantile onset of chronic sinopulmonary infections, and variable occurence of laterality defects and has_material_basis_in homozygous or compound heterozygous mutation in the CCDC114 gene on chromosome 19q13.
Genes: ccdc63 (Xtr)
Gene Ontology
Source: GO:0036158
Synonyms:
- ODA assembly
Branch: biological process
Genes: CCDC63 (Hsa)...Ccdc63 (Mmu)...Ccdc63 (Rno)
Gene Ontology
Source: GO:0003341
Synonyms:
- ciliary motility
- cilium beating
Branch: biological process
Genes: CCDC63 (Hsa)...Ccdc63 (Mmu)...Ccdc63 (Rno)
Gene Ontology
Source: GO:0007286
Synonyms:
- spermatid cell development
- spermiogenesis
Branch: biological process
Genes: CCDC63 (Hsa)...Ccdc63 (Mmu)...Ccdc63 (Rno)
Gene Ontology
Source: GO:0005930
Synonyms:
- ciliary axoneme
- cilium axoneme
Branch: cellular component
Genes: CCDC63 (Hsa)...Ccdc63 (Mmu)...Ccdc63 (Rno)
Gene Ontology
Source: GO:0007283
Synonyms:
- generation of spermatozoa
Branch: biological process
Genes: CCDC63 (Hsa)
Gene Ontology
Source: GO:0030154
Synonyms: Not Available
Branch: biological process
Genes: CCDC63 (Hsa)
Gene Ontology
Source: GO:0003674
Synonyms:
- molecular function
Branch: molecular function
Genes: Ccdc63 (Mmu)
(GRCh38)12:110853432G>T
(Homo sapiens)Allele/Variant
Source: rs114761668
Genes: CCDC63 (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)12:110853432G>T
(GRCh38)12:110858591A>C
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.110858591A>C
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110858591A>C
(GRCh38)12:110881145G>T
(Homo sapiens)Allele/Variant
Source: rs1163864985
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110881145G>T
(GRCh38)12:110858654C>T
(Homo sapiens)Allele/Variant
Source: rs200140147
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110858654C>T
(GRCh38)12:110898940T>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.110898940T>A
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110898940T>A
(GRCh38)12:110853535C>T
(Homo sapiens)Allele/Variant
Source: rs145250758
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110853535C>T
(GRCh38)12:110904611G>A
(Homo sapiens)Allele/Variant
Source: rs138877502
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904611G>A
(GRCh38)12:110884217G>C
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.110884217G>C
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884217G>C
(GRCh38)12:110893079G>A
(Homo sapiens)Allele/Variant
Source: rs143128187
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110893079G>A
(GRCh38)12:110904594T>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.110904594T>G
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904594T>G
(GRCh38)12:110873903C>T
(Homo sapiens)Allele/Variant
Source: rs766133465
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110873903C>T
(GRCh38)12:110884189C>T
(Homo sapiens)Allele/Variant
Source: rs778436400
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884189C>T
(GRCh38)12:110881153G>A
(Homo sapiens)Allele/Variant
Source: rs115904738
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110881153G>A
(GRCh38)12:110899099C>T
(Homo sapiens)Allele/Variant
Source: rs758287561
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110899099C>T
(GRCh38)12:110873914C>T
(Homo sapiens)Allele/Variant
Source: rs200569386
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110873914C>T
(GRCh38)12:110899075A>C
(Homo sapiens)Allele/Variant
Source: rs760224067
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110899075A>C
(GRCh38)12:110904746C>T
(Homo sapiens)Allele/Variant
Source: rs769568156
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904746C>T
(GRCh38)12:110879976T>A
(Homo sapiens)Allele/Variant
Source: rs1407251218
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110879976T>A
(GRCh38)12:110881144T>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.110881144T>G
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110881144T>G
(GRCh38)12:110904638C>T
(Homo sapiens)Allele/Variant
Source: rs762320804
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904638C>T
(GRCh38)12:110904657G>A
(Homo sapiens)Allele/Variant
Source: rs772838782
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904657G>A
(GRCh38)12:110904692C>A
(Homo sapiens)Allele/Variant
Source: rs372078813
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110904692C>A
(GRCh38)12:110853438C>T
(Homo sapiens)Allele/Variant
Source: rs1318861061
Genes: CCDC63 (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)12:110853438C>T
(GRCh38)12:110873915G>A
(Homo sapiens)Allele/Variant
Source: rs149075085
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110873915G>A
(GRCh38)12:110873960T>C
(Homo sapiens)Allele/Variant
Source: rs780746666
Genes: CCDC63 (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)12:110873960T>C
(GRCh38)12:110881152C>T
(Homo sapiens)Allele/Variant
Source: rs775890946
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110881152C>T
(GRCh38)12:110873948C>A
(Homo sapiens)Allele/Variant
Source: rs758717569
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110873948C>A
(GRCh38)12:110884198C>G
(Homo sapiens)Allele/Variant
Source: rs149841694
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884198C>G
(GRCh38)12:110884198C>T
(Homo sapiens)Allele/Variant
Source: rs149841694
Genes: CCDC63 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:110884198C>T