Genes, Locations and Genetic Disorders on Chromosome 9

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ABL1 GDB:1196409q34.1-9q34.1 ABELSON MURINE LEUKEMIA VIRAL ONCOGENE HOMOLOG 1; ABL1
ABO GDB:1189569q34.1-9q34.2 ABO BLOOD GROUP; ABO
AK1 GDB:1196649q34.1-9q34.1 ADENYLATE KINASE-1; AK1
ALAD GDB:1196659q32-9q34 DELTA-AMINOLEVULINATE DEHYDRATASE; ALAD
ALDH1 GDB:1196679q21-9q21 ALDEHYDE DEHYDROGENASE-1; ALDH1
ALDOB GDB:1196699q22-9q22 9q22.3-9q22.3 9q22.3-9q31 FRUCTOSE INTOLERANCE, HEREDITARY
AMBP GDB:1206969q32-9q33 PROTEIN HC; HCP
AMCD1 GDB:4375199p22-9q22.3 ARTHROGRYPOSIS MULTIPLEX CONGENITA, DISTAL, TYPE 1; AMCD1
ASS GDB:1190109q34.1-9q34.1 CITRULLINEMIA
BDMF GDB:99544249p22-9p21 BONE DYSPLASIA WITH MEDULLARY FIBROSARCOMA
C5 GDB:1197349q33-9q33 9q34.1-9q34.1 COMPLEMENT COMPONENT-5, DEFICIENCY OF
CDKN2A GDB:3353629p21-9p21 MELANOMA, CUTANEOUS MALIGNANT, 2; CMM2
CYCLIN-DEPENDENT KINASE INHIBITOR 2A; CDKN2A
CHAC GDB:62684919q21-9q21 CHOREOACANTHOCYTOSIS; CHAC
CHH GDB:1382689p21-9p13 CARTILAGE-HAIR HYPOPLASIA; CHH
CMD1B GDB:6771479q13-9q22 CARDIOMYOPATHY, DILATED 1B; CMD1B
COL5A1 GDB:1314579q34.3-9q34.3 COLLAGEN, TYPE V, ALPHA-1 POLYPEPTIDE; COL5A1
CRAT GDB:3597599q34.1-9q34.1 CARNITINE ACETYLTRANSFERASE; CRAT
DBH GDB:1198369q34.3-9q34.3 DOPAMINE BETA-HYDROXYLASE, PLASMA; DBH
DFNB11 GDB:12201809q13-9q21 DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 7; DFNB7
DFNB7 GDB:6361789q13-9q21 DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 7; DFNB7
DYS GDB:1370859q31-9q33 9q31-9q31 9q31.2-9q31.3 DYSAUTONOMIA, FAMILIAL; DYS
DYT1 GDB:1198549q34-9q34 DYSTONIA 1, TORSION; DYT1
ENG GDB:1371939q34.1-9q34.1 ENDOGLIN; ENG
EPB72 GDB:1289939q34.1-9q34.1 ERYTHROCYTE SURFACE PROTEIN BAND 7.2; EPB72
STOMATOCYTOSIS I
FANCC GDB:1326729q22.3-9q22.3 FANCONI ANEMIA, COMPLEMENTATION GROUP C; FACC
FBP1 GDB:1415399q22.3-9q22.3 FRUCTOSE-1,6-BISPHOPHATASE 1; FBP1
FCMD GDB:2504129q31-9q31 FUKUYAMA-TYPE CONGENITAL MUSCULAR DYSTROPHY; FCMD
FRDA GDB:1199519q13-9q21.1 FRIEDREICH ATAXIA 1; FRDA1
GALT GDB:1199719p13-9p13 GALACTOSEMIA
GLDC GDB:1286119p24-9p23 9p22-9p22 HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE I; NKH1
GSM1 GDB:97842109q13-9q21 GENIOSPASM 1; GSM1
GSN GDB:1200199q33-9q33 9q34-9q34 AMYLOIDOSIS V
GELSOLIN; GSN
HDLDT1 GDB:98649259q31.1-9q31.1 ANALPHALIPOPROTEINEMIA
HSD17B3 GDB:3474879q22-9q22 PSEUDOHERMAPHRODITISM, MALE, WITH GYNECOMASTIA
HSN1 GDB:38536779q22.1-9q22.3 NEUROPATHY, HEREDITARY SENSORY, TYPE 1
IBM2 GDB:38014479p1-9q1 INCLUSION BODY MYOPATHY; IBM2
LALL GDB:99544269p22-9p21 LEUKEMIA, ACUTE, WITH LYMPHOMATOUS FEATURES; LALL
LCCS GDB:3861419q33-9q34 LETHAL CONGENITAL CONTRACTURE SYNDROME; LCCS
LGMD2H GDB:98622339q31-9q33 DYSTROPHY, HUTTERITE TYPE
MLLT3 GDB:1381729p22-9p22 MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 3; MLLT3
MROS GDB:99544309p11-9p11 MELKERSSON SYNDROME
MSSE GDB:1280199q22.2-9q22.3 EPITHELIOMA, SELF-HEALING SQUAMOUS
NOTCH1 GDB:1314009q34.3-9q34.3 NOTCH, DROSOPHILA, HOMOLOG OF, 1; NOTCH1
NPS1 GDB:1194559q34.1-9q34.1 NAIL-PATELLA SYNDROME; NPS1
ORM1 GDB:1202509q32-9q32 9q34.1-9q34.3 OROSOMUCOID 1; ORM1
PAPPA GDB:1347299q33.1-9q33.1 PREGNANCY-ASSOCIATED PLASMA PROTEIN A; PAPPA
PIP5K1B GDB:6862389q13-9q13 FRIEDREICH ATAXIA 1; FRDA1
PTCH GDB:1194479q22.1-9q22.3 9q22.3-9q22.3 BASAL CELL NEVUS SYNDROME; BCNS
PATCHED, DROSOPHILA, HOMOLOG OF; PTCH
PTGS1 GDB:1280709q32-9q33.3 PROSTAGLANDIN-ENDOPEROXIDASE SYNTHASE 1; PTGS1
RLN1 GDB:1195529pter-9q12 RELAXIN; RLN1
RLN2 GDB:1195539pter-9q12 RELAXIN, OVARIAN, OF PREGNANCY
RPD1 GDB:99544409q34-9q34 RETINITIS PIGMENTOSA-DEAFNESS SYNDROME 1, AUTOSOMAL DOMINANT
SARDH GDB:98351499q33-9q34 SARCOSINEMIA
TDFA GDB:99544209pter-9p22 FACTOR, AUTOSOMAL
TEK GDB:3441859p21-9p21 VENOUS MALFORMATIONS, MULTIPLE CUTANEOUS AND MUCOSAL; VMCM
TEK TYROSINE KINASE, ENDOTHELIAL; TEK
TSC1 GDB:1207359q34-9q34 TUBEROUS SCLEROSIS-1; TSC1
TYRP1 GDB:1263379p23-9p23 TYROSINASE-RELATED PROTEIN 1; TYRP1
ALBINISM III
XANTHISM
XPA GDB:1253639q22.3-9q22.3 9q34.1-9q34.1 XERODERMA PIGMENTOSUM I