abnormality of the vocal cords Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormality of the vocal cord. (Human Phenotype Ontology, HP_0008777)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0008777
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Genes

14 genes associated with the abnormality of the vocal cords phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
DCTN1 dynactin 1
GDAP1 ganglioside induced differentiation associated protein 1
MATR3 matrin 3
MFN2 mitofusin 2
MYCN v-myc avian myelocytomatosis viral oncogene neuroblastoma derived homolog
PMP22 peripheral myelin protein 22
PRX periaxin
RHBDF2 rhomboid 5 homolog 2 (Drosophila)
SDHAF2 succinate dehydrogenase complex assembly factor 2
SDHC succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
SDHD succinate dehydrogenase complex, subunit D, integral membrane protein
SLC52A3 solute carrier family 52 (riboflavin transporter), member 3
SLC5A7 solute carrier family 5 (sodium/choline cotransporter), member 7
TRPV4 transient receptor potential cation channel, subfamily V, member 4