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Table 1 ResSeq genes within the deleted region (chr10:105,001–12,815,001)

From: Clinical report of a neonate carrying a large deletion in the 10p15.3p13 region and review of the literature

ResSeq genes

OMIM phenotype

MIM number

ZMYND11

Mental retardation, autosomal dominant

#616,083

IL2RA

Immunodeficiency with lymphoproliferation and autoimmunity

#601,942

GATA3

Hypoparathyroidism, sensorineural deafness, and renal dysplasia

#146,255

DHTKD1

2-aminoadipic 2-oxoadipic aciduria

Charcot-Marie-Tooth disease, axonal, type 2Q

#204,750

KLF6

Gastric cancer, somatic #613,659

Prostate cancer, somatic

#613,659

AKR1C2

46, XY sex reversal

#614,279

AKR1C4

46, XY sex reversal

#614,279