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*300508 - UTP14A SMALL SUBUNIT PROCESSOME COMPONENT; UTP14A
Cytogenetic locations: 300117
Gene summaries Genetic tests Medical literature
*300513 - G PROTEIN-COUPLED RECEPTOR 119; GPR119
Cytogenetic locations: 12044878
*300333 - RAS-ASSOCIATED PROTEIN RAB33A; RAB33A
Cytogenetic locations: #9116044
*300282 - ECTO-NOX DISULFIDE-THIOL EXCHANGER 2; ENOX2
Cytogenetic locations: mutation
*300242 - SOLUTE CARRIER FAMILY 25 (MITOCHONDRIAL CARRIER, BRAIN), MEMBER 14; SLC25A14
Cytogenetic locations: #9852133
#300496 - AUTISM, SUSCEPTIBILITY TO, X-LINKED 3; AUTSX3
Cytogenetic locations: Xq26.1
#300555 - DENT DISEASE 2; DENT2
Cytogenetic locations: 27625794
*300937 - RHO GTPase-ACTIVATING PROTEIN 36; ARHGAP36
Cytogenetic locations: 25024229
#301029 - SHUKLA-VERNON SYNDROME; SHUVER
Cytogenetic locations: max
#300614 - DEAFNESS, X-LINKED 5, WITH PERIPHERAL NEUROPATHY; DFNX5
Cytogenetic locations: 25986071
*300297 - APELIN; APLN
Cytogenetic locations: 11384769
#300909 - ANGIOEDEMA INDUCED BY ACE INHIBITORS, SUSCEPTIBILITY TO; AEACEI
Cytogenetic locations: 300348
*300688 - BCL6 COREPRESSOR-LIKE 1; BCORL1
#300673 - ENCEPHALOPATHY, NEONATAL SEVERE, DUE TO MECP2 MUTATIONS
#300799 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, RAYMOND TYPE; MRXSR
Cytogenetic locations: 25649377
#301082 - IMMUNODEFICIENCY 102; IMD102
Cytogenetic locations: 300411
#301074 - AUTOINFLAMMATORY SYNDROME, FAMILIAL, X-LINKED, BEHCET-LIKE 2; AIFBL2
Cytogenetic locations: 34326534
*300145 - X-PROLYL AMINOPEPTIDASE 2; XPNPEP2
*300441 - SAM- AND SH3 DOMAIN-CONTAINING PROTEIN 3; SASH3
#300816 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 6; COXPD6
Cytogenetic locations: 25583628
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