Source: ALL

Gene Gene Full Name DSI g DPI g pLI Disease Type Score gda EL gda EI gda N. PMIDs N. SNPs gda First Ref. Last Ref.
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1863732
Disease: Spondyloepimetaphyseal dysplasia with multiple dislocations
Spondyloepimetaphyseal dysplasia with multiple dislocations 		disease 0.730 None 1.000 5 3 2011 2015
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0878659
Disease: Disproportionate short stature
Disproportionate short stature 		phenotype 0.300 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0410528
Disease: Skeletal dysplasia
Skeletal dysplasia 		disease 0.110 None 1.000 1 0 2011 2011
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0432211
Disease: Spondyloepimetaphyseal disorder
Spondyloepimetaphyseal disorder 		disease 0.110 None 1.000 1 0 2016 2016
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0029422
Disease: Osteochondrodysplasias
Osteochondrodysplasias 		group 0.110 None 1.000 1 0 2011 2011
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0027651
Disease: Neoplasms
Neoplasms 		group 0.100 None 1.000 18 0 2004 2020
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0006826
Disease: Malignant Neoplasms
Malignant Neoplasms 		group 0.100 None 0.900 10 0 2005 2018
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0086437
Disease: Joint laxity
Joint laxity 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1850630
Disease: Broad distal phalanx of finger
Broad distal phalanx of finger 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1853242
Disease: Midface retrusion
Midface retrusion 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0239234
Disease: Low set ears
Low set ears 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1854114
Disease: Short nose
Short nose 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1968592
Disease: Abnormal calcification of the carpal bones
Abnormal calcification of the carpal bones 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0221355
Disease: Macrocephaly
Macrocephaly 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0221354
Disease: Frontal bossing
Frontal bossing 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1858085
Disease: Malar flattening
Malar flattening 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1858120
Disease: Generalized hypotonia
Generalized hypotonia 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1863749
Disease: Carpal bone hypoplasia
Carpal bone hypoplasia 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0080178
Disease: Spina Bifida
Spina Bifida 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1863734
Disease: Caudal interpedicular narrowing
Caudal interpedicular narrowing 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1863739
Disease: Narrow femoral neck
Narrow femoral neck 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C0265563
Disease: Congenital dislocation of radial head
Congenital dislocation of radial head 		disease 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1850196
Disease: Posterior scalloping of vertebral bodies
Posterior scalloping of vertebral bodies 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1850135
Disease: Flared metaphysis
Flared metaphysis 		phenotype 0.100 None 0 0
Entrez Id: 3835
Gene Symbol: KIF22
KIF22 		kinesin family member 22 0.552 0.654 9.2E-10
CUI: C1836542
Disease: Depressed nasal bridge
Depressed nasal bridge 		phenotype 0.100 None 0 0