Disease ID | Disease name | Source of annotation with DPP6 | OMIM link | Number of associated genes | genes |
---|---|---|---|---|---|
PS156200 | MENTAL RETARDATION, AUTOSOMAL DOMINANT | ClinVar, OMIM, HUMSAVAR | link to OMIM | 44 | EHMT1, KANSL1, AHDC1, SOX11, CDH15, KIRREL3, EEF1A2, KAT6A, ZMYND11, ARID1A, KMT2C, PPP2R5D, DYNC1H1, GRIN1, CTCF, SETD5, AUTS2, PACS1, DPP6, MBD5, DEAF1, KIF1A, SYNGAP1, PURA, POGZ, EPB41L1, PPP2R1A, NR1I3, CTNNB1, ARID1B, MYT1L, CACNG2, COL4A3BP, SMARCB1, MEF2C, SMARCE1, SMARCA4, ZBTB18, ADNP, GATAD2B, SETBP1, GRIN2B, CHAMP1, DYRK1A |
612956 | VENTRICULAR FIBRILLATION, PAROXYSMAL FAMILIAL, 2 | ClinVar, OMIM | link to OMIM | 1 | DPP6 |
Download the gene annotation in CSV format
GO term | GO ID | GO IC |
---|---|---|
aminopeptidase activity | GO:0004177 | 5.98 |
serine hydrolase activity | GO:0017171 | 4.26 |
hydrolase activity | GO:0016787 | 1.9 |
catalytic activity | GO:0003824 | 1.05 |
dipeptidyl-peptidase activity | GO:0008239 | 7.17 |
exopeptidase activity | GO:0008238 | 5.07 |
peptidase activity, acting on L-amino acid peptides | GO:0070011 | 3.26 |
channel regulator activity | GO:0016247 | 4.88 |
peptidase activity | GO:0008233 | 3.23 |
molecular function regulator | GO:0098772 | 2.51 |
potassium channel regulator activity | GO:0015459 | 5.93 |
serine-type peptidase activity | GO:0008236 | 4.27 |