Version: 8.0.0Date: Tue Jan 28 2025
Category
odad2
(Danio rerio)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: armc4, sb:eu854, sb:eu579, sb:eu947
Source: ZFIN:ZDB-GENE-100316-7
Biotype: protein coding gene
Synonyms: armc4...armc4...armc4
odad2.S
(Xenopus laevis)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: armc4, outer dynein arm docking complex subunit 2, odad2.S
Source: Xenbase:XB-GENE-982932
Biotype: gene
Synonyms: armc4...armc4...armc4
odad2
(Xenopus tropicalis)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: armc4, outer dynein arm docking complex subunit 2, odad2
Source: Xenbase:XB-GENE-982927
Biotype: gene
Synonyms: armc4...armc4...armc4
ODAD2
(Homo sapiens)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: FLJ10817, DKFZp434P1735, armadillo repeat-containing protein 4, CILD23, FLJ10376, outer dynein arm-docking complex subunit 2, armadillo repeat containing 4, ARMC4, testis tissue sperm-binding protein Li 74n, RP11-691I13.1, FLJ32798, gudu
Source: HGNC:25583
Biotype: protein coding gene
Synonyms: ARMC4...ARMC4
Odad2
(Mus musculus)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: Armc4, ddx5-ps1, armadillo repeat containing 4, 4930463I21Rik, b2b643Clo, RIKEN cDNA 4930463I21 gene, b2b227.1Clo
Source: MGI:1922184
Biotype: protein coding gene
Synonyms: Armc4...Armc4
Odad2
(Rattus norvegicus)Gene
Name: outer dynein arm docking complex subunit 2
Synonyms: armadillo repeat-containing protein 4, Armc4, ddx5-ps1, outer dynein arm-docking complex subunit 2, armadillo repeat containing 4, LOC307036, ddx5-ps1 pseudogene
Source: RGD:1306933
Biotype: protein coding gene
Synonyms: Armc4...Armc4
zf3878
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-240814-2
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
Odad2em1(IMPC)Mbp
(Mus musculus)Allele/Variant
Source: MGI:6277027
Genes: Odad2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Armc4
Source: DOID:0110609
Definition: A primary ciliary dyskinesia that is characterized by autosomal recessive inheritance with outer dynein arm defect, respiratory distress and recurrent upper and lower airway infections, and variable occurence of situs inversus and has_material_basis_in homozygous or compound heterozygous mutation in the ARMC4 gene on chromosome 10p.
sa42032
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-161003-17199
Genes: odad2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: armc4
(GRCh38)10:27983938G>A
(Homo sapiens)Allele/Variant
Source: rs369669370
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983938G>A
Gene Synonyms: ARMC4
(GRCh38)10:27987521C>A
(Homo sapiens)Allele/Variant
Source: rs747965765
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987521C>A
Gene Synonyms: ARMC4
(GRCh38)10:27985220A>T
(Homo sapiens)Allele/Variant
Source: rs1193786815
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27985220A>T
Gene Synonyms: ARMC4
(GRCh38)10:27860823A>C
(Homo sapiens)Allele/Variant
Source: rs575075615
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860823A>C
Gene Synonyms: ARMC4
(GRCh38)10:27935219C>T
(Homo sapiens)Allele/Variant
Source: rs780112130
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27935219C>T
Gene Synonyms: ARMC4
(GRCh38)10:27971311T>C
(Homo sapiens)Allele/Variant
Source: rs766491818
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971311T>C
Gene Synonyms: ARMC4
(GRCh38)10:27983859C>A
(Homo sapiens)Allele/Variant
Source: rs372616728
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983859C>A
Gene Synonyms: ARMC4
(GRCh38)10:27985060C>A
(Homo sapiens)Allele/Variant
Source: rs550542420
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27985060C>A
Gene Synonyms: ARMC4
(GRCh38)10:27987508T>C
(Homo sapiens)Allele/Variant
Source: rs1465895645
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987508T>C
Gene Synonyms: ARMC4
(GRCh38)10:27984224T>C
(Homo sapiens)Allele/Variant
Source: rs1849734366
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27984224T>C
Gene Synonyms: ARMC4
(GRCh38)10:27936707A>T
(Homo sapiens)Allele/Variant
Source: rs2134099850
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27936707A>T
Gene Synonyms: ARMC4
(GRCh38)10:27983835T>G
(Homo sapiens)Allele/Variant
Source: rs1236480521
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983835T>G
Gene Synonyms: ARMC4
(GRCh38)10:27983882C>T
(Homo sapiens)Allele/Variant
Source: rs2133123588
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983882C>T
Gene Synonyms: ARMC4
(GRCh38)10:27983945C>T
(Homo sapiens)Allele/Variant
Source: rs150780082
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27983945C>T
Gene Synonyms: ARMC4
(GRCh38)10:27984433A>C
(Homo sapiens)Allele/Variant
Source: rs55716902
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27984433A>C
Gene Synonyms: ARMC4
(GRCh38)10:27987616T>C
(Homo sapiens)Allele/Variant
Source: rs146689340
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27987616T>C
Gene Synonyms: ARMC4
(GRCh38)10:27994951C>T
(Homo sapiens)Allele/Variant
Source: rs760968744
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27994951C>T
Gene Synonyms: ARMC4
(GRCh38)10:27995046C>A
(Homo sapiens)Allele/Variant
Source: rs752348839
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained
Diseases: Not Available
Variant Name: (GRCh38)10:27995046C>A
Gene Synonyms: ARMC4
(GRCh38)10:27860633C>T
(Homo sapiens)Allele/Variant
Source: rs1167723751
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860633C>T
Gene Synonyms: ARMC4
(GRCh38)10:27860646C>T
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27860646C>T
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860646C>T
Gene Synonyms: ARMC4
(GRCh38)10:27812526C>A
(Homo sapiens)Allele/Variant
Source: rs3737184
Genes: ODAD2 (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)10:27812526C>A
Gene Synonyms: ARMC4
(GRCh38)10:27862558G>T
(Homo sapiens)Allele/Variant
Source: rs587777049
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27862558G>T
Gene Synonyms: ARMC4
(GRCh38)10:27862603C>T
(Homo sapiens)Allele/Variant
Source: rs376143899
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27862603C>T
Gene Synonyms: ARMC4
(GRCh38)10:27939983C>T
(Homo sapiens)Allele/Variant
Source: rs1060503678
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27939983C>T
Gene Synonyms: ARMC4
(GRCh38)10:27944889T>A
(Homo sapiens)Allele/Variant
Source: rs773452157
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944889T>A
Gene Synonyms: ARMC4
(GRCh38)10:27940580G>A
(Homo sapiens)Allele/Variant
Source: rs868755574
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27940580G>A
Gene Synonyms: ARMC4
(GRCh38)10:27944820C>T
(Homo sapiens)Allele/Variant
Source: rs1472984153
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944820C>T
Gene Synonyms: ARMC4
(GRCh38)10:27937154C>T
(Homo sapiens)Allele/Variant
Source: rs58502831
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27937154C>T
Gene Synonyms: ARMC4
(GRCh38)10:27971148C>G
(Homo sapiens)Allele/Variant
Source: rs775228185
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971148C>G
Gene Synonyms: ARMC4
(GRCh38)10:27939877G>A
(Homo sapiens)Allele/Variant
Source: rs764297273
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27939877G>A
Gene Synonyms: ARMC4
(GRCh38)10:27860762G>A
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27860762G>A
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27860762G>A
Gene Synonyms: ARMC4
(GRCh38)10:27940804A>T
(Homo sapiens)Allele/Variant
Source: rs1245635112
Genes: ODAD2 (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)10:27940804A>T
Gene Synonyms: ARMC4
(GRCh38)10:27936816C>T
(Homo sapiens)Allele/Variant
Source: rs762544821
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27936816C>T
Gene Synonyms: ARMC4
(GRCh38)10:27944966C>T
(Homo sapiens)Allele/Variant
Source: rs1590099355
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944966C>T
Gene Synonyms: ARMC4
(GRCh38)10:27907763A>G
(Homo sapiens)Allele/Variant
Source: NC_000010.11:g.27907763A>G
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27907763A>G
Gene Synonyms: ARMC4
(GRCh38)10:27961549T>C
(Homo sapiens)Allele/Variant
Source: rs1388906763
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27961549T>C
Gene Synonyms: ARMC4
(GRCh38)10:27944351T>C
(Homo sapiens)Allele/Variant
Source: rs920398574
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944351T>C
Gene Synonyms: ARMC4
(GRCh38)10:27961564T>C
(Homo sapiens)Allele/Variant
Source: rs199776339
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27961564T>C
Gene Synonyms: ARMC4
(GRCh38)10:27944373A>C
(Homo sapiens)Allele/Variant
Source: rs370164015
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27944373A>C
Gene Synonyms: ARMC4
(GRCh38)10:27971274G>C
(Homo sapiens)Allele/Variant
Source: rs1032612529
Genes: ODAD2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)10:27971274G>C
Gene Synonyms: ARMC4