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*609553 - RETBINDIN
Cytogenetic locations: 12107411
Gene summaries Genetic tests Medical literature
*314990 - ZINC FINGER PROTEIN 711; ZNF711
Cytogenetic locations: 10398247
*313475 - SYNAPTOPHYSIN; SYP
Cytogenetic locations: 19377476
#304340 - PETTIGREW SYNDROME; PGS
Cytogenetic locations: 11822699
#300963 - RITSCHER-SCHINZEL SYNDROME 2; RTSC2
Cytogenetic locations: 21826058
#300953 - TRICHOTHIODYSTROPHY 5, NONPHOTOSENSITIVE; TTD5
Cytogenetic locations: 31793730
#300919 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 99; XLID99
*300859 - COILED-COIL DOMAIN-CONTAINING PROTEIN 22; CCDC22
#300831 - CK SYNDROME; CKS
#300803 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 97; XLID97
#300802 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 96; XLID96
#300676 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC 14; MRXS14
Cytogenetic locations: 22957832
#300659 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED 93; XLID93
Cytogenetic locations: 30628072
*300646 - ZINC FINGER DHHC DOMAIN-CONTAINING PROTEIN 9; ZDHHC9
Cytogenetic locations: 25649377
*300629 - ADAPTOR-RELATED PROTEIN COMPLEX 1, SIGMA-2 SUBUNIT; AP1S2
Cytogenetic locations: 12599187
*300621 - SPINDLIN FAMILY, MEMBER 2A; SPIN2A
Cytogenetic locations: 300858
*300553 - BROMODOMAIN- AND WD REPEAT-CONTAINING PROTEIN 3; BRWD3
*300517 - SPINDLIN FAMILY, MEMBER 2B; SPIN2B
Cytogenetic locations: 12145692
#300422 - FG SYNDROME 4; FGS4
INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, WITH OR WITHOUT NYSTAGMUS, INCLUDED
#300354 - INTELLECTUAL DEVELOPMENTAL DISORDER, X-LINKED, SYNDROMIC, CABEZAS TYPE; MRXSC
Cytogenetic locations: 300188
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