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*619945 - FAMILY WITH SEQUENCE SIMILARITY 184, MEMBER B; FAM184B
Cytogenetic locations: 10574462
Gene summaries Genetic tests Medical literature
*170250 - LEUCINE AMINOPEPTIDASE 3; LAP3
*610605 - CYTOPLASMIC POLYADENYLATION ELEMENT-BINDING PROTEIN 2; CPEB2
Cytogenetic locations: 12672660
*607737 - FIBROBLAST GROWTH FACTOR-BINDING PROTEIN 1; FGFBP1
Cytogenetic locations: 11885605
*603450 - LIM DOMAIN-BINDING 2; LDB2
Cytogenetic locations: 4p16.3-p16.2
#612284 - MECKEL SYNDROME, TYPE 6; MKS6
Cytogenetic locations: 18513680
*605655 - F-BOX AND LEUCINE-RICH REPEAT PROTEIN 5; FBXL5
Cytogenetic locations: 4p16.3
#619111 - COACH SYNDROME 2; COACH2
Cytogenetic locations: 12929661
*607713 - FIBROBLAST GROWTH FACTOR-BINDING PROTEIN 2; FGFBP2
Cytogenetic locations: 11342666
*600387 - BONE MARROW STROMAL CELL ANTIGEN 1; BST1
Cytogenetic locations: Downstream
#612095 - RETINITIS PIGMENTOSA 41; RP41
Cytogenetic locations: 17605048
#616897 - OSTEOCHONDRODYSPLASIA, COMPLEX LETHAL, SYMOENS-BARNES-GISTELINCK TYPE; OCLSBG
Cytogenetic locations: 26365339
#619845 - RETINITIS PIGMENTOSA 93; RP93
Cytogenetic locations: 30267408
#608051 - MACULAR DYSTROPHY, RETINAL, 2; MCDR2
Cytogenetic locations: 18654668
*610311 - MEDIATOR COMPLEX SUBUNIT 28; MED28
Cytogenetic locations: 15467741
#619174 - DEAFNESS, AUTOSOMAL RECESSIVE 117; DFNB117
Cytogenetic locations: 4p16.2
#261630 - HYPERPHENYLALANINEMIA, BH4-DEFICIENT, C; HPABH4C
Cytogenetic locations: 142983
#612285 - JOUBERT SYNDROME 9; JBTS9
JOUBERT SYNDROME 9/15, DIGENIC, INCLUDED
Cytogenetic locations: 18387594
#612657 - CONE-ROD DYSTROPHY 12; CORD12
*612758 - TRANSMEMBRANE ANTERIOR POSTERIOR TRANSFORMATION 1; TAPT1
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