Array based characterization of a terminal deletion involving chromosome subband 15q26.2: an emerging syndrome associated with growth retardation, cardiac defects and developmental delay

Table 2 USCS known genes in 93.86–100.30 Mb on chr 15 based on RefSeq, Uniprot annotation, and Genbank mRNA

Gene	Uniprot accession number	Basepair position on chr 15	Size in basepairs
IGF1R	P08069	97010288–97319034	308746
TTC23	Q5W5X9	97494052–97607246	113194
MEF2A	Q59GX4	97956185–98071524	115354
ADAMTS17	Q8TE56	98331993–98699650	367657
LINS1	Q9NVQ3	98926957–98959902	32945
ASB7	Q6GSJ6	98960358–99007174	46816
ALDH1A3	Q96GT2	99237584–99274352	36768
LRRK1	Q6NYC0	99276983–99427840	150857
CHSY1	Q86X52	99533455–99609649	76194
SELS	Q6GYA4	99628737–99635223	6486
SNRPA1	P09661	99639238–99652983	13745
TM2D3	Q9BRN9	99999572–100010117	10545
TARSL2	Q6B0A1	100011478–100082168	70690
OR4F4	Q96R69	100279868–100280785	917

ISSN: 1471-2350