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*616526 - SOLUTE CARRIER FAMILY 38 (AMINO ACID TRANSPORTER), MEMBER 11; SLC38A11
Cytogenetic locations: 18418736
Gene summaries Genetic tests Medical literature
*610318 - COBL-LIKE PROTEIN 1: COBLL1
Cytogenetic locations: 10231032
*603093 - BETA-3-GALACTOSYLTRANSFERASE 1; B3GALT1
*607648 - SERINE/THREONINE PROTEIN KINASE 39; STK39
Cytogenetic locations: 102720
%610155 - TYPE 1 DIABETES MELLITUS 19; T1D19
Cytogenetic locations: max
*609778 - XIN ACTIN-BINDING REPEAT-CONTAINING PROTEIN 2; XIRP2
Cytogenetic locations: 15454575
#613820 - NEPHRONOPHTHISIS 12; NPHP12
JOUBERT SYNDROME 11, INCLUDED; JBTS11, INCLUDED
Cytogenetic locations: 21258341
*609395 - SPC25, NDC80 KINETOCHORE COMPLEX COMPONENT; SPC25
Cytogenetic locations: IFIH1
*182392 - SODIUM VOLTAGE-GATED CHANNEL, ALPHA SUBUNIT 7; SCN7A
Cytogenetic locations: 11027237
*601524 - GROWTH FACTOR RECEPTOR-BOUND PROTEIN 14; GRB14
Cytogenetic locations: 601828
*615336 - CERAMIDE SYNTHASE 6; CERS6
Cytogenetic locations: 22013072
*607496 - NITRIC OXIDE SYNTHASE TRAFFICKER; NOSTRIN
Cytogenetic locations: 600403
#617938 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 62; DEE62
Cytogenetic locations: Gpd2
#609634 - MIGRAINE, FAMILIAL HEMIPLEGIC, 3; FHM3
Cytogenetic locations: 613334
#613819 - SHORT-RIB THORACIC DYSPLASIA 4 WITH OR WITHOUT POLYDACTYLY; SRTD4
Cytogenetic locations: 24183451
*620405 - CYSTEINE- AND SERINE-RICH NUCLEAR PROTEIN 3; CSRNP3
Cytogenetic locations: 17433858
*605295 - FIDGETIN; FIGN
Cytogenetic locations: Kcnj3
#617935 - EPILEPSY, FAMILIAL FOCAL, WITH VARIABLE FOCI 4; FFEVF4
#619317 - DEVELOPMENTAL AND EPILEPTIC ENCEPHALOPATHY 6B; DEE6B
#167400 - PAROXYSMAL EXTREME PAIN DISORDER; PEXPD
Cytogenetic locations: 2q24.2
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