Overlapping Fingers Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A finger resting on the dorsal surface of an adjacent digit when the hand is at rest. (Human Phenotype Ontology, HP_0010557)
External Link https://www.disgenet.org/browser/0/1/0/C1446712
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Genes

27 genes associated with the disease Overlapping Fingers in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ATN1 atrophin 1
BICD2 bicaudal D homolog 2 (Drosophila)
CHST11 carbohydrate (chondroitin 4) sulfotransferase 11
CNTN1 contactin 1
COG7 component of oligomeric golgi complex 7
CTU2 cytosolic thiouridylase subunit 2 homolog (S. pombe)
EBP emopamil binding protein (sterol isomerase)
EVC Ellis van Creveld protein
EVC2 Ellis van Creveld syndrome 2
FLNA filamin A, alpha
KIAA0195 KIAA0195
KIAA1109 KIAA1109
MAGEL2 melanoma antigen family L2
MECOM MDS1 and EVI1 complex locus
MOGS mannosyl-oligosaccharide glucosidase
MYBPC1 myosin binding protein C, slow type
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
NALCN sodium leak channel, non selective
NEK9 NIMA-related kinase 9
PI4KA phosphatidylinositol 4-kinase, catalytic, alpha
RAD51C RAD51 paralog C
RLIM ring finger protein, LIM domain interacting
SAMD9 sterile alpha motif domain containing 9
SETBP1 SET binding protein 1
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)