TTLL5, tubulin tyrosine ligase like 5, 23093

N. diseases: 34; N. variants: 24
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267606822
rs267606822
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome). 20206334 2010
dbSNP: rs267606822
rs267606822
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy. 20690116 2010
dbSNP: rs267606822
rs267606822
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing. 20518025 2010
dbSNP: rs267606824
rs267606824
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome). 20206334 2010
dbSNP: rs267606824
rs267606824
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy. 20690116 2010
dbSNP: rs267606824
rs267606824
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing. 20518025 2010
dbSNP: rs267606825
rs267606825
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT High-throughput sequencing of a 4.1 Mb linkage interval reveals FLVCR2 deletions and mutations in lethal cerebral vasculopathy. 20690116 2010
dbSNP: rs267606825
rs267606825
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Mutations in FLVCR2 are associated with proliferative vasculopathy and hydranencephaly-hydrocephaly syndrome (Fowler syndrome). 20206334 2010
dbSNP: rs267606825
rs267606825
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		0.800 GeneticVariation UNIPROT Unexpected allelic heterogeneity and spectrum of mutations in Fowler syndrome revealed by next-generation exome sequencing. 20518025 2010
dbSNP: rs199882533
rs199882533
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C4014501
Disease:
CONE-ROD DYSTROPHY 19 		T 0.800 CausalMutation CLINVAR
dbSNP: rs199882533
rs199882533
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C4014501
Disease:
CONE-ROD DYSTROPHY 19 		0.800 GeneticVariation UNIPROT
dbSNP: rs199882533
rs199882533
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C4014501
Disease:
CONE-ROD DYSTROPHY 19 		A 0.800 CausalMutation CLINVAR
dbSNP: rs267606822
rs267606822
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		G 0.800 CausalMutation CLINVAR
dbSNP: rs267606824
rs267606824
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		T 0.800 CausalMutation CLINVAR
dbSNP: rs267606825
rs267606825
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		G 0.800 CausalMutation CLINVAR
dbSNP: rs267606825
rs267606825
Entrez Id: 23093;55640
Gene Symbol: TTLL5;FLVCR2
TTLL5;FLVCR2
CUI: C1856972
Disease:
Encephaloclastic Proliferative Vasculopathy 		T 0.800 CausalMutation CLINVAR
dbSNP: rs72725608
rs72725608
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0007286
Disease:
Carpal Tunnel Syndrome 		C 0.700 GeneticVariation GWASCAT A genome-wide association analysis identifies 16 novel susceptibility loci for carpal tunnel syndrome. 30833571 2019
dbSNP: rs11159152
rs11159152
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17103681
rs17103681
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17183738
rs17183738
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs175886
rs175886
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs175888
rs175888
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17783198
rs17783198
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17783198
rs17783198
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1863036
rs1863036
Entrez Id: 23093
Gene Symbol: TTLL5
TTLL5
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017