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*300764 - MELANOMA ANTIGEN, FAMILY A, 9B; MAGEA9B
Gene summaries Genetic tests Medical literature
*618039 - TBC1 DOMAIN FAMILY, MEMBER 9B; TBC1D9B
Cytogenetic locations: 19734811
*615666 - PUTATIVE tRNA METHYLTRANSFERASE 9B; TRMT9B
Cytogenetic locations: 10819331
*300285 - RAS-ASSOCIATED PROTEIN 9B; RAB9B
Cytogenetic locations: associated
*613773 - IMMUNOGLOBULIN SUPERFAMILY, MEMBER 9B; IGSF9B
Cytogenetic locations: 10470851
*614446 - ATPase, CLASS II, TYPE 9B; ATP9B
Cytogenetic locations: 21914794
*614148 - C1q- AND TUMOR NECROSIS FACTOR-RELATED PROTEIN 9B; C1QTNF9B
Cytogenetic locations: 19666007
#616586 - SPASTIC PARAPLEGIA 9B, AUTOSOMAL RECESSIVE; SPG9B
Cytogenetic locations: Interstitial
*602864 - WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER 9B; WNT9B
Cytogenetic locations: 12573259
*604852 - CHEMOKINE, CXC MOTIF, LIGAND 11; CXCL11
Cytogenetic locations: Histatin-3
*603325 - PROTEIN PHOSPHATASE 1, REGULATORY SUBUNIT 9B; PPP1R9B
Cytogenetic locations: 108728
#618823 - CONGENITAL MYOPATHY 9B, PROXIMAL, WITH MINICORE LESIONS; CMYO9B
Cytogenetic locations: 35393337
*612205 - AUTOPHAGY-RELATED 9B; ATG9B
SONE, INCLUDED
Cytogenetic locations: 15755735
#620887 - MULTIPLE MITOCHONDRIAL DYSFUNCTIONS SYNDROME 9B; MMDS9B
#614879 - PEROXISOME BIOGENESIS DISORDER 9B; PBD9B
PEROXISOME BIOGENESIS DISORDER, COMPLEMENTATION GROUP 11, INCLUDED; CG11, INCLUDED
Cytogenetic locations: 23352163
*300247 - BONE MORPHOGENETIC PROTEIN 15; BMP15
Cytogenetic locations: 300629
*103270 - FERREDOXIN REDUCTASE; FDXR
Cytogenetic locations: 28747430
*601757 - PEROXISOME BIOGENESIS FACTOR 7; PEX7
Cytogenetic locations: 17535304
*600819 - FMR1 AUTOSOMAL HOMOLOG 1; FXR1
Cytogenetic locations: Butyrylcholinesterase
*138250 - ALDEHYDE DEHYDROGENASE 18 FAMILY, MEMBER A1; ALDH18A1
Cytogenetic locations: 24767728
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