ulnar deviation of the hand or of fingers of the hand Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0001193
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Genes

39 genes associated with the ulnar deviation of the hand or of fingers of the hand phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ASXL1 additional sex combs like transcriptional regulator 1
BCR breakpoint cluster region
BMP2 bone morphogenetic protein 2
BMPR1B bone morphogenetic protein receptor, type IB
CD96 CD96 molecule
COMP cartilage oligomeric matrix protein
CRKL v-crk avian sarcoma virus CT10 oncogene homolog-like
DHCR7 7-dehydrocholesterol reductase
DOK7 docking protein 7
FBN2 fibrillin 2
FLNA filamin A, alpha
GDF5 growth differentiation factor 5
HOXA13 homeobox A13
HOXD13 homeobox D13
HRAS Harvey rat sarcoma viral oncogene homolog
ICK intestinal cell (MAK-like) kinase
LBR lamin B receptor
LIFR leukemia inhibitory factor receptor alpha
MAFB v-maf avian musculoaponeurotic fibrosarcoma oncogene homolog B
MAPK1 mitogen-activated protein kinase 1
MYBPC1 myosin binding protein C, slow type
MYH3 myosin, heavy chain 3, skeletal muscle, embryonic
PAX3 paired box 3
PEX1 peroxisomal biogenesis factor 1
PIEZO2 piezo-type mechanosensitive ion channel component 2
RAB3GAP1 RAB3 GTPase activating protein subunit 1 (catalytic)
RAB3GAP2 RAB3 GTPase activating protein subunit 2 (non-catalytic)
RAPSN receptor-associated protein of the synapse
RBM28 RNA binding motif protein 28
SALL1 spalt-like transcription factor 1
SHOX short stature homeobox
SLC26A2 solute carrier family 26 (anion exchanger), member 2
SLCO5A1 solute carrier organic anion transporter family, member 5A1
SULF1 sulfatase 1
TBX22 T-box 22
TNNI2 troponin I type 2 (skeletal, fast)
TNNT3 troponin T type 3 (skeletal, fast)
TPM2 tropomyosin 2 (beta)
WNT7A wingless-type MMTV integration site family, member 7A