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*609896 - EUKARYOTIC TRANSLATION INITIATION FACTOR 4E FAMILY, MEMBER 3; EIF4E3
Cytogenetic locations: 15153109
Gene summaries Genetic tests Medical literature
*613322 - GLUCOSIDE XYLOSYLTRANSFERASE 2; GXYLT2
Cytogenetic locations: 604299
*609729 - PDZ DOMAIN-CONTAINING RING FINGER PROTEIN 3; PDZRN3
Cytogenetic locations: 10470851
*613250 - ENDOGENOUS BORNA-LIKE N ELEMENT-CONTAINING PROTEIN 2; EBLN2
Cytogenetic locations: 20054395
*616895 - SURVIVAL-ASSOCIATED MITOCHONDRIAL MELANOMA-SPECIFIC ONCOGENIC NONCODING RNA; SAMMSON
Cytogenetic locations: 27008969
*607535 - RING1- AND YY1-BINDING PROTEIN; RYBP
Cytogenetic locations: 11953439
#617306 - COLOBOMA, OSTEOPETROSIS, MICROPHTHALMIA, MACROCEPHALY, ALBINISM, AND DEAFNESS; COMMAD
Cytogenetic locations: 27889061
#619921 - DYSTONIA 35, CHILDHOOD-ONSET; DYT35
Cytogenetic locations: 34542157
*613822 - PROTEIN PHOSPHATASE 4, REGULATORY SUBUNIT 2; PPP4R2
Cytogenetic locations: 20154705
*605187 - G PROTEIN-COUPLED RECEPTOR 27; GPR27
Cytogenetic locations: 10833454
#614456 - MELANOMA, CUTANEOUS MALIGNANT, SUSCEPTIBILITY TO, 8; CMM8
Cytogenetic locations: 22080950
#103500 - TIETZ ALBINISM-DEAFNESS SYNDROME; TADS
Cytogenetic locations: 13985019
#610628 - HYPOGONADOTROPIC HYPOGONADISM 4 WITH OR WITHOUT ANOSMIA; HH4
Cytogenetic locations: 17761590
#619922 - NEURODEVELOPMENTAL DISORDER WITH DYSTONIA AND SEIZURES; NEDDS
*613663 - SHQ1, H/ACA RIBONUCLEOPROTEIN ASSEMBLY FACTOR; SHQ1
#193510 - WAARDENBURG SYNDROME, TYPE 2A; WS2A
Cytogenetic locations: 28490648
#613670 - INTELLECTUAL DEVELOPMENTAL DISORDER WITH LANGUAGE IMPAIRMENT AND WITH OR WITHOUT AUTISTIC FEATURES; IDDLA
Cytogenetic locations: 25131622
*605515 - FORKHEAD BOX P1; FOXP1
Cytogenetic locations: 12692134
*607002 - PROKINETICIN 2; PROK2
Cytogenetic locations: 18064003
*156845 - MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF
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