Version: 8.0.0
Date: Tue Jan 28 2025
968 results for wdr34

dync2i2

(Danio rerio)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: dync2i1, zgc:171284, wdr34
Source: ZFIN:ZDB-GENE-070928-9
Biotype: protein coding gene
Synonyms: wdr34...wdr34...wdr34

dync2i2.L

(Xenopus laevis)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: dync2i2.L, dynein 2 intermediate chain 2, wdr34
Source: Xenbase:XB-GENE-953030
Biotype: gene
Synonyms: wdr34...wdr34...wdr34

dync2i2

(Xenopus tropicalis)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: dync2i2, dynein 2 intermediate chain 2, wdr34
Source: Xenbase:XB-GENE-953027
Biotype: gene
Synonyms: wdr34...wdr34...wdr34

DYNC2I2

(Homo sapiens)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: FAP133, WD repeat-containing protein 34, CFAP133, SRTD11, DIC5, cytoplasmic dynein 2 intermediate chain 2, MGC20486, WDR34, WD repeat domain 34, RP11-216B9.5, bA216B9.3
Source: HGNC:28296
Biotype: protein coding gene
Synonyms: WDR34...WDR34

Dync2i2

(Mus musculus)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: 3200002I06Rik, RIKEN cDNA 3200002I06 gene, WD repeat domain 34, Wdr34
Source: MGI:1919070
Biotype: protein coding gene
Synonyms: Wdr34...Wdr34

Dync2i2

(Rattus norvegicus)
Gene
Name: dynein 2 intermediate chain 2
Synonyms: WD repeat-containing protein 34, cytoplasmic dynein 2 intermediate chain 2, WD repeat domain 34, MGC95297, Wdr34
Source: RGD:1359465
Biotype: protein coding gene
Synonyms: Wdr34...Wdr34

Dync2i2em2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7583489
Genes: Dync2i2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Wdr34

Dync2i2Tn(pb-Act-RFP)1.1Zhu

(Mus musculus)
Allele/Variant
Source: MGI:7580877
Genes: Dync2i2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Wdr34

Dync2i2em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7298291
Genes: Dync2i2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Wdr34

Dync2i2tm1Blnw

(Mus musculus)
Allele/Variant
Source: MGI:6116689
Genes: Dync2i2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: Wdr34

short-rib thoracic dysplasia 11 with or without polydactyly

Disease
Source: DOID:0110095
Definition: An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the WDR34 gene on chromosome 9q34.

(GRCh38)9:128634002C>T

(Homo sapiens)
Allele/Variant
Source: rs201988969
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634002C>T
Gene Synonyms: WDR34

(GRCh38)9:128634213G>T

(Homo sapiens)
Allele/Variant
Source: rs754985227
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634213G>T
Gene Synonyms: WDR34

(GRCh38)9:128634691G>A

(Homo sapiens)
Allele/Variant
Source: rs1860335179
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634691G>A
Gene Synonyms: WDR34

(GRCh38)9:128634701G>A

(Homo sapiens)
Allele/Variant
Source: rs763634588
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634701G>A
Gene Synonyms: WDR34

(GRCh38)9:128635217C>T

(Homo sapiens)
Allele/Variant
Source: rs139569061
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128635217C>T
Gene Synonyms: WDR34

(GRCh38)9:128636962G>A

(Homo sapiens)
Allele/Variant
Source: rs1589430146
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128636962G>A
Gene Synonyms: WDR34

(GRCh38)9:128640841G>C

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128640841G>C
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128640841G>C
Gene Synonyms: WDR34

(GRCh38)9:128640851G>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128640851G>A
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128640851G>A
Gene Synonyms: WDR34

(GRCh38)9:128633996C>G

(Homo sapiens)
Allele/Variant
Source: rs1447465834
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633996C>G
Gene Synonyms: WDR34

(GRCh38)9:128633897G>A

(Homo sapiens)
Allele/Variant
Source: rs1467999563
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633897G>A
Gene Synonyms: WDR34

(GRCh38)9:128636307T>C

(Homo sapiens)
Allele/Variant
Source: rs139362186
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128636307T>C
Gene Synonyms: WDR34

(GRCh38)9:128636413G>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128636413G>A
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128636413G>A
Gene Synonyms: WDR34

(GRCh38)9:128634207C>T

(Homo sapiens)
Allele/Variant
Source: rs1453654191
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634207C>T
Gene Synonyms: WDR34

(GRCh38)9:128634323G>A

(Homo sapiens)
Allele/Variant
Source: rs200101013
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634323G>A
Gene Synonyms: WDR34

(GRCh38)9:128634389C>T

(Homo sapiens)
Allele/Variant
Source: rs374616949
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634389C>T
Gene Synonyms: WDR34

(GRCh38)9:128634702A>G

(Homo sapiens)
Allele/Variant
Source: rs1860335863
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634702A>G
Gene Synonyms: WDR34

(GRCh38)9:128634732G>C

(Homo sapiens)
Allele/Variant
Source: rs537004785
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634732G>C
Gene Synonyms: WDR34

(GRCh38)9:128635267A>G

(Homo sapiens)
Allele/Variant
Source: rs1441872910
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128635267A>G
Gene Synonyms: WDR34

(GRCh38)9:128635665A>G

(Homo sapiens)
Allele/Variant
Source: rs754488103
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128635665A>G
Gene Synonyms: WDR34

(GRCh38)9:128633960G>A

(Homo sapiens)
Allele/Variant
Source: rs1177862092
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633960G>A
Gene Synonyms: WDR34

(GRCh38)9:128634258C>T

(Homo sapiens)
Allele/Variant
Source: rs587777094
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634258C>T
Gene Synonyms: WDR34

(GRCh38)9:128633906G>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128633906G>A
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633906G>A
Gene Synonyms: WDR34

(GRCh38)9:128634291T>C

(Homo sapiens)
Allele/Variant
Source: rs587777098
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634291T>C
Gene Synonyms: WDR34

(GRCh38)9:128634352G>A

(Homo sapiens)
Allele/Variant
Source: rs371747861
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634352G>A
Gene Synonyms: WDR34

(GRCh38)9:128634734G>C

(Homo sapiens)
Allele/Variant
Source: rs999307682
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634734G>C
Gene Synonyms: WDR34

(GRCh38)9:128634804C>T

(Homo sapiens)
Allele/Variant
Source: rs1344384758
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634804C>T
Gene Synonyms: WDR34

(GRCh38)9:128634805A>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128634805A>G
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634805A>G
Gene Synonyms: WDR34

(GRCh38)9:128633785C>T

(Homo sapiens)
Allele/Variant
Source: rs752702804
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633785C>T
Gene Synonyms: WDR34

(GRCh38)9:128633786T>C

(Homo sapiens)
Allele/Variant
Source: rs777478835
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633786T>C
Gene Synonyms: WDR34

(GRCh38)9:128633898T>C

(Homo sapiens)
Allele/Variant
Source: rs1564336534
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633898T>C
Gene Synonyms: WDR34

(GRCh38)9:128634236G>A

(Homo sapiens)
Allele/Variant
Source: rs1240843143
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634236G>A
Gene Synonyms: WDR34

(GRCh38)9:128634238C>T

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128634238C>T
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634238C>T
Gene Synonyms: WDR34

(GRCh38)9:128634253A>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.128634253A>G
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634253A>G
Gene Synonyms: WDR34

(GRCh38)9:128634266G>A

(Homo sapiens)
Allele/Variant
Source: rs376351607
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634266G>A
Gene Synonyms: WDR34

(GRCh38)9:128635197G>A

(Homo sapiens)
Allele/Variant
Source: rs558962462
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128635197G>A
Gene Synonyms: WDR34

(GRCh38)9:128634757G>A

(Homo sapiens)
Allele/Variant
Source: rs762641265
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634757G>A
Gene Synonyms: WDR34

(GRCh38)9:128634772G>A

(Homo sapiens)
Allele/Variant
Source: rs149225851
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634772G>A
Gene Synonyms: WDR34

(GRCh38)9:128634788G>A

(Homo sapiens)
Allele/Variant
Source: rs772143102
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128634788G>A
Gene Synonyms: WDR34

(GRCh38)9:128633791G>A

(Homo sapiens)
Allele/Variant
Source: rs368864898
Genes: DYNC2I2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:128633791G>A
Gene Synonyms: WDR34