Gene: KIF1B ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 Biomarker disease BEFREE Four loci for autosomal dominant hereditary motor and sensory neuropathy type II (HMSN II) or Charcot-Marie-Tooth disease type 2 (CMT2) have been localized on chromosomes 1p35-p36 (CMT2A), 3q13-q22 (CMT2B), 7p14 (CMT2D), and 3p (HMSN-P). 10520946 1999
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 Biomarker disease BEFREE Linkage to 1p35-p36 (CMT2A), 3q (CMT2B), and 7p (CMT2D) chromosomes has been reported in the disease; however, most HMSN II families do not link to any of the reported loci. 9595994 1998
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 GeneticVariation disease BEFREE A CMT2 family was examined for linkage to the CMT2A, CMT2B, and CMT2D loci using short tandem repeat polymorphisms. 9219740 1997
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 GeneticVariation disease BEFREE Linkage mapping of the gene for Charcot-Marie-Tooth disease type 2 to chromosome 1p (CMT2A) and the clinical features of CMT2A. 9409358 1997
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 GeneticVariation disease BEFREE Localization of a gene (CMT2A) for autosomal dominant Charcot-Marie-Tooth disease type 2 to chromosome 1p and evidence of genetic heterogeneity. 8406488 1993
Entrez Id: 23095
Gene Symbol: KIF1B
KIF1B 		0.060 Biomarker disease BEFREE The distal HMN shows similarities with the hereditary motor and sensory neuropathies type I and II (HMSN I and HMSN II) or Charcot-Marie-Tooth disease type 1 and 2 (CMT 1 and CMT 2) and with some proximal HMN or spinal muscular atrophies (SMA). 1517763 1992