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*620119 - LONG NONCODING RNA CRYBG3
Cytogenetic locations: -
Gene summaries Genetic tests Medical literature
*618668 - GAMMA-AMINOBUTYRIC ACID RECEPTOR, RH0-3; GABRR3
Cytogenetic locations: 15258161
*600066 - EPHRIN RECEPTOR EphA6; EPHA6
%114200 - CAMPTODACTYLY 1; CAMPD1
STREBLODACTYLY, INCLUDED
Cytogenetic locations: 15963204
*601166 - G PROTEIN-COUPLED RECEPTOR 15; GPR15
Cytogenetic locations: 3p14.1
*616588 - DIHYDROFOLATE REDUCTASE-LIKE 1; DHFRL1
Cytogenetic locations: 21876184
*620146 - CRYSTALLIN BETA-GAMMA DOMAIN-CONTAINING PROTEIN 3; CRYBG3
Cytogenetic locations: 608868
#613575 - RETINITIS PIGMENTOSA 55; RP55
Cytogenetic locations: 31736247
#619012 - COMBINED OXIDATIVE PHOSPHORYLATION DEFICIENCY 48; COXPD48
Cytogenetic locations: 608501
*612049 - RIBOSOMAL OXYGENASE 2; RIOX2
Cytogenetic locations: 15897898
#618892 - HARDEROPORPHYRIA; HARPO
Cytogenetic locations: 16159891
*619677 - CLAUDIN DOMAIN-CONTAINING PROTEIN 1; CLDND1
Cytogenetic locations: 33037622
*617491 - NOP2/SUN RNA METHYLTRANSFERASE FAMILY, MEMBER 3; NSUN3
#600151 - BARDET-BIEDL SYNDROME 3; BBS3
Cytogenetic locations: 19714014
#121300 - COPROPORPHYRIA, HEREDITARY; HCP
Cytogenetic locations: 12181641
*608845 - ADP-RIBOSYLATION FACTOR-LIKE GTPase 6; ARL6
*612732 - COPROPORPHYRINOGEN OXIDASE; CPOX
#209900 - BARDET-BIEDL SYNDROME 1; BBS1
Cytogenetic locations: 1p36, 1p36, 1p36
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