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*614681 - AMINOGLYCOSIDE PHOSPHOTRANSFERASE DOMAIN-CONTAINING PROTEIN 1; AGPHD1
Cytogenetic locations: 15q22.2
Gene summaries Genetic tests Medical literature
*176846 - PROTEASOME SUBUNIT, ALPHA-TYPE, 4; PSMA4
Cytogenetic locations: 12025653
*617944 - ABHYDROLASE DOMAIN-CONTAINING PROTEIN 17C, DEPALMITOYLASE; ABHD17C
Cytogenetic locations: mutation
*609540 - SKI8 SUBUNIT OF SUPERKILLER COMPLEX; SKIC8
Cytogenetic locations: 151740
%607728 - POROKERATOSIS 4, DISSEMINATED SUPERFICIAL ACTINIC TYPE; POROK4
Cytogenetic locations: 22983302
*607050 - START DOMAIN-CONTAINING PROTEIN 5; STARD5
Cytogenetic locations: 611766
*606600 - RAS PROTEIN-SPECIFIC GUANINE NUCLEOTIDE-RELEASING FACTOR 1; RASGRF1
Cytogenetic locations: 11753386
*617196 - TRANSMEMBRANE CHANNEL-LIKE PROTEIN 3; TMC3
Cytogenetic locations: 608181
*620437 - TRANSMEMBRANE p24 TRAFFICKING PROTEIN 3; TMED3
Cytogenetic locations: 35748162
*615466 - TALIN ROD DOMAIN-CONTAINING PROTEIN 1; TLNRD1
Cytogenetic locations: 11247670
#609439 - DEAFNESS, AUTOSOMAL RECESSIVE 48; DFNB48
Cytogenetic locations: 23023331
*610183 - ZINC FINGER AN1 DOMAIN-CONTAINING PROTEIN 6; ZFAND6
Cytogenetic locations: 11054541
*608366 - CELL MIGRATION-INDUCING HYALURONIDASE 1; CEMIP
Cytogenetic locations: 604152
#614869 - USHER SYNDROME, TYPE IJ; USH1J
*116820 - CATHEPSIN H; CTSH
Cytogenetic locations: 22849458
#618367 - NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION; NEDMEHM
Cytogenetic locations: 30031689
*618054 - MEMBRANE INTEGRAL NOTCH2-ASSOCIATED RECEPTOR 1; MINAR1
Cytogenetic locations: 30080879
*180230 - RETINOIC ACID-BINDING PROTEIN, CELLULAR, TYPE I; CRABP1
Cytogenetic locations: 12825608
*603035 - INTERLEUKIN 16; IL16
Cytogenetic locations: 14607889
*607303 - MORTALITY FACTOR 4-LIKE PROTEIN 1; MORF4L1
Cytogenetic locations: 603263
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