gene / OMIM reference
ATP7B / Wilsons Disease / 13q14.3-q21.1 / AL162377
AL138821 / 606882
BMIQ2 / Quantitative trait for body mass index / 13q14 / Not cloned / 606643
BRCA2 / Breast cancer 2,early onset / 13q12.3 / AL442512
AL137247 / 600185
BRCA3 / Breast cancer 3 / 13q21 / Not cloned / 605365
CLN5 / Ceroid-lipofuscinosis, Neuronal-5 / 13q21.1-
q32 / AL355879 / 608102
BRCD1 / Breast cancer, ductal / 13 / Not cloned / 211410
D13S25 / B-cell chronic lymphocytic leukaemia / 13q14 / Not cloned / 109543
DDX26 / Non small cell lung cancer / 13q14.12-
q14.2 / AL137780
AL354820 / 604331
EDNRB / Hirschsprung Disease / 13q22 / AL139002 / 131244
ENUR1 / Nocturnal Enuresis / 13q13-q14.3 / Not cloned / 600631
ERCC5 / Xeroderma pigmentosum / 13q33 / AL157769 / 133530
F10 / Factor X deficiency / 13q34 / AL137002 / 227600
F7 / Factor VII deficiency / 13q34 / AL137002 / 227500
FGF14 / Fibroblast growth factor 14 / 13q34 / AL160153 / 601515
FLT3 / Decreased survival in Acute myeloid leukaemia / 13q12 / AL356575
AL445262
AL356915 / 136351
FOXO1A / Alveolar
rhabdomyosarcoma / 13q14.1 / AL133318
AL355132 / 136533
DAOA / Schizophrenia / 13q34 / AL359751 / 607408
GER / Gastroesophageal reflux / 13q14 / Not cloned / 109350
GJA3 / Cataract, zonular
pulverulent-3 / 13q11 / AL138688 / 121015
GJB2 / Deafness, autosomal
recessive-1 / 13q11 / AL138688 / 121011
GJB6 / Deafness, autosomal
dominant-3 / 13q12 / AL355984 / 604418
HTR2A / Psycotic illness / 13q14-q21 / AL136958
AL160397 / 182135
ING1 / Squamous cell carcinoma,
head and neck / 13q34 / AL157820 / 601566
IPF1 / Pancreatic aqenesis,
maturity-onset diabetes / 13q12.1 / AL353195 / 600733
IRS2 / Noninsulin-dependent
diabetes mellitus / 13q34 / AL162497 / 600797
ITM2B / Dementia / 13q14 / AL139322 / 603904
LDLR / Cholesterol lowering factor / 13q / Not cloned / 604595
LIG4 / LIG4 syndrome / 13q22-q34 / AL157762 / 601837
MBS1 / Moebius syndrome / 13q12.2-q13 / Not cloned / 157900
MCOR / Congenital microcoria / 13q31-32 / Not cloned / 156600
PAPA2 / Postaxial polydactyl,
TypeA2 / 13q21-q32 / Not cloned / 602085
PCCA / Propioninacidemia / 13q32 / AL356575
AL355338
AL136526
AL353697 / 232000
PHF11 / Asthma,atopic hypersensitivity / 13q14.1 / AL139321 / 607796
RB1 / Retinoblastoma / 13q14.1-
q14.2 / AL136960
AL392048 / 180200
RFXAP / Bare lymphocyte syndrome / 13q14 / AL159973 / 601861
RHOK / Oguchi disease-2 / 13q34 / Partialy Contained in BX537316 / 180381
RIEG2 / Rieger syndrome / 13q14 / Not cloned / 601499
RNF6 / Esophageal carcinoma / 13q12.11 / AL138966 / 604242
SACS / Spastic Ataxia / 13q12 / AL157766 / 604490
SCA8 / Spinocerebellar ataxia 8 / 13q21 / Not cloned / 603680
SCG3 / Muscular dystrophy, limb-girdle, type2C / 13q12 / AL157766
AL160256
AL356287 / 253700
SLC10A2 / Bile acid malabsorption / 13q33 / AL161771 / 601295
SLC25A15 / Hyperornithinemia-Hyperammonemia-Homocitrulline syndrome / 13q14 / AL161614 / 603861
SPG20 / Troyer Syndrome / 13q12.3 / AL139377 / 607111
SPG24 / Spastic paraplegia 24 / 13q14 / Not cloned / 607584
STQTL13 / Stature QTL 13 / 13q32-33 / Not cloned / 606258
ZIC2 / Holoprosencephaly-5 / 13q32 / AL355338 / 603073
ZNF198 / Stem cell leukaemia
syndrome / 13q11-q12 / AL137119
AL138688 / 602221
Supplementary Table S8 –Disease genes on chromosome 13. This information was taken from the Genecards database (http://bioinfo.weizmann.ac.il/cards/)