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*606882 - ATPase, Cu(2+)-TRANSPORTING, BETA POLYPEPTIDE; ATP7B
Cytogenetic locations: 12544487
Gene summaries Genetic tests Medical literature
#620009 - KERATODERMA-ICHTHYOSIS-DEAFNESS SYNDROME, AUTOSOMAL RECESSIVE; KDIDAR
Cytogenetic locations: 28017832
*614758 - DYNACTIN 4; DCTN4
Cytogenetic locations: 16554302
#614482 - HUPPKE-BRENDEL SYNDROME; HPBDS
Cytogenetic locations: 35999711
*610232 - ATPase 13A3; ATP13A3
Cytogenetic locations: 34493544
*608552 - VPS33B LATE ENDOSOME AND LYSOSOME ASSOCIATED; VPS33B
Cytogenetic locations: 26463206
*607238 - COMM DOMAIN-CONTAINING PROTEIN 1; COMMD1
Cytogenetic locations: 19949209
*606682 - HPS4 BIOGENESIS OF LYSOSOMAL ORGANELLES COMPLEX 3, SUBUNIT 2; HPS4
Cytogenetic locations: Lss
*603864 - COPPER CHAPERONE FOR SUPEROXIDE DISMUTASE; CCS
Cytogenetic locations: Majin
*603580 - PROTOCADHERIN 8; PCDH8
Cytogenetic locations: 11549318
*603085 - SOLUTE CARRIER FAMILY 31 (COPPER TRANSPORTER), MEMBER 1; SLC31A1
Cytogenetic locations: 9q31.1
*602270 - ANTIOXIDANT PROTEIN 1; ATOX1
Cytogenetic locations: distal
#309400 - MENKES DISEASE; MNK
Cytogenetic locations: 14222346
*300011 - ATPase, Cu(2+)-TRANSPORTING, ALPHA POLYPEPTIDE; ATP7A
Cytogenetic locations: 24002164
#277900 - WILSON DISEASE; WND
Cytogenetic locations: 18432554
*156350 - METALLOTHIONEIN 1A; MT1A
#128101 - DYSTONIA 4, TORSION, AUTOSOMAL DOMINANT; DYT4
Cytogenetic locations: 19p13.3
*117700 - CERULOPLASMIN; CP
Cytogenetic locations: 3q23
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