chromosome	gene symbol	phenotype
16p12.1	ATP2A1 ATPase, Ca++ transporting, fast twitch 1	Brody myopathy -ATP2A1
16p13.1	ABCC9 ATP-binding cassette, sub-family C (member 9)	Cardiomyopathy, dilated, 1O -CMD1O
16p13.3-p12	LITAF lipopolysaccharide-induced TNF factor	Hereditary motor and sensory, type 1C -CMT1C
16q12	FUS fusion (involved in t(12;16) in malignant liposarcoma)	Amyotrophic lateral sclerosis -ALS6
16q21	BEAN Brain expressed, associated with Nedd42	Spinocerebellar ataxia 28 - spinocerebellar ataxia-31 -SCA31
16q21-q23.1	FA2H fatty acid 2-hydroxylase	Spastic paraplegia 35, autosomal recessive -SPG35 Dysmyelinating leukodystrophy -FAHN
16q22	?	atrial fibillation, familial, 8 -ATFB8
16q22-q23	TK2 Thymidine kinase 2, mitochondrial	Mitochondrial dna depletion syndrome, myopathic form -MTDPS3
16q22.1	?	Spinocerebellar ataxia 4 -SCA4
16q22.1	AARS alanyl-tRNA synthetase	Charcot-Marie-Tooth disease, axonal, type 2N -CMT2N
16q24	TUBB3 tubulin, beta 3	Fibrosis of extraocular muscles, congenital, 3 -CFEOM3
16q24.1	GAN gigaxonin	Giant axonal neuropathy-1 -GAN1
16q24.3	SPG7 paraplegin	Spastic paraplegia 7 -SPG7