From: Function-informed transcriptome analysis of Drosophila renal tubule
Gene | Affymetrix signal | Enrichment | Blast probability | OMIM reference | Human disease | Available fly stocks |
---|---|---|---|---|---|---|
CG10226 | 290 ± 25 | 28.3 | 1.00E-184 | 171050 | Colchicine resistance |  |
CG7402 | 99 ± 4 | 26.9 | 2.00E-40 | 253000 | Mucopolysaccharidosis IVA |  |
Ir | 1,302 ± 112 | 14.2 | 1.00E-76 | 600359 | Bartter syndrome, antenatal, 601678 |  |
ry | 655 ± 44 | 13.0 | 1.00E-184 | 607633 | Xanthinuria, type I, 278300 |  |
Ptx1 | 183 ± 8 | 12.7 | 6.00E-38 | 602669 | Anterior segment mesenchymal dysgenesis and cataract, 107250 |  |
Fmo-1 | 131 ± 11 | 12.0 | 9.00E-27 | 136132 | [Fish-odor syndrome], 602079 |  |
CG4484 | 504 ± 50 | 12.0 | 1.00E-49 | 606202 | Oculocutaneous albinism, type IV, 606574 |  |
DS00004.14 | 759 ± 54 | 10.6 | 1.00E-123 | 603470 | Citrullinemia, 215700 |  |
CG9455 | 355 ± 40 | 9.0 | 1.00E-42 | 107400 | Emphysema; emphysema-cirrhosis, hemorrhagic diathesis due to |  |
CG5582 | 825 ± 49 | 8.5 | 1.00E-69 | 607042 | Ceroid-lipofuscinosis, neuronal-3, juvenile, 204200 |  |
Cyp4d2 | 1,008 ± 70 | 8.3 | 1.00E-27 | 107910 | Gynecomastia, familial, due to increased aromatase activity |  |
CG7433 | 1,364 ± 50 | 7.4 | 1.00E-153 | 137150 | GABA-transaminase deficiency |  |
CG1140 | 894 ± 26 | 7.3 | 1.00E-176 | 245050 | Ketoacidosis due to SCOT deficiency |  |
CG9547 | 860 ± 34 | 7.0 | 1.00E-164 | 231670 | Glutaricaciduria, type I |  |
PhKgamma | 2,665 ± 152 | 6.9 | 1.00E-111 | 172471 | Glycogenosis, hepatic, autosomal |  |
CG4623 | 382 ± 37 | 6.8 | 4.00E-28 | 606598 | Charcot-Marie-Tooth disease, mixed axonal and demyelinating | l(3)j7B3 |
CG12370 | 203 ± 17 | 6.7 | 5.00E-40 | 138033 |  |  |
CG15556 | 221 ± 12 | 6.4 | 6.00E-12 | 602851 | Convulsions, familial febrile, 4, 604352 |  |
KCNQ | 101 ± 0 | 6.4 | 1.00E-108 | 602235 | Epilepsy, benign, neonatal, type 1, 121200; myokymia with neonatal |  |
CG17119 | 852 ± 28 | 5.7 | 6.00E-74 | 606272 | Cystinosis, atypical nephropathic; cystinosis, late-onset juvenile |  |
CG7408 | 168 ± 6 | 5.6 | 3.00E-27 | 300180 | Chondrodysplasia punctata, X-linked recessive, 302950 |  |
Spat | 724 ± 39 | 5.1 | 2.00E-88 | 604285 | Hyperoxaluria, primary, type 1, 259900 | EP(x)1365 |
CG8743 | 1,001 ± 44 | 4.9 | 1.00E-100 | 605248 | Mucolipidosis IV, 252650 |  |
CG14593 | 59 ± 13 | 4.9 | 2.00E-33 | 131244 | ABCD syndrome, 600501; Hirschsprung disease-2, 600155 |  |
CG1673 | 911 ± 142 | 4.8 | 1.00E-100 | 113530 | Hypervalinemia or hyperleucine-isoleucinemia (?) |  |
Ndae1 | 531 ± 34 | 4.7 | 1.00E-184 | 603345 | Renal tubular acidosis, proximal, with ocular abnormalities, 604278 |  |
CG7834 | 3441 ± 106 | 4.3 | 8.00E-80 | 130410 | Glutaricaciduria, type IIB, 231680 | EP(2)2553, l(2)k00405 |
Pvr | 294 ± 26 | 4.2 | 6.00E-69 | 164770 | Myeloid malignancy, predisposition to |  |
CG12030 | 887 ± 51 | 4.1 | 1.00E-124 | 606953 | Galactose epimerase deficiency, 230350 |  |
Mdr49 | 239 ± 25 | 4.0 | 1.00E-184 | 171060 | Cholestasis, familial intrahepatic, of pregnancy, 147480 | l(2)k05224 |
CG4685 | 563 ± 19 | 4.0 | 1.00E-129 | 271980 | Succinic semialdehyde dehydrogenase deficiency | EP(2)2545, l(2)k08713 |
CG12338 | 774 ± 16 | 3.9 | 4.00E-40 | 124050 |  |  |
CG12582 | 183 ± 14 | 3.8 | 1.00E-142 | 248510 | Mannosidosis, beta- | l(2)k10108 |
Reg-3 | 463 ± 24 | 3.8 | 1.00E-184 | 274270 | Thymine-uraciluria |  |
Cyp12c1 | 73 ± 5 | 3.8 | 2.00E-34 | 124080 | Aldosterone to renin ratio raised; hypoaldosteronism, congenital, |  |
Fur1 | 724 ± 29 | 3.7 | 1.00E-163 | 162150 | Obesity with impaired prohormone processing, 600955 |  |
Cyp9c1 | 258 ± 14 | 3.7 | 7.00E-53 | 274180 | Thromboxane synthase deficiency | l(3)05545 |
Drip | 318 ± 16 | 3.6 | 1.00E-37 | 154050 | Cataract, polymorphic and lamellar, 604219 |  |
CG8654 | 274 ± 29 | 3.6 | 2.00E-62 | 607096 | Hypouricemia, renal, 220150 |  |
Cyp9f2 | 1,700 ± 60 | 3.6 | 1.00E-69 | 124010 | CYP3A4 promoter polymorphism; CYP3A4-V |  |
ERR | 239 ± 21 | 3.5 | 5.00E-29 | 313700 | Androgen insensitivity, 300068; breast cancer, male | EP(3)3340 |
CG3603 | 94 ± 7 | 3.4 | 5.00E-20 | 222745 | DECR deficiency (2) (?) |  |
CG9232 | 877 ± 20 | 3.4 | 1.00E-118 | 606999 | Galactosemia, 230400 |  |
CG8417 | 502 ± 31 | 3.2 | 3.00E-71 | 154550 | Carbohydrate-deficient glycoprotein syndrome, type Ib, 602579 | EP(2)0844, EP(2)2192, EP(2)2358, l(2)05428, l(2)k06503 |
CG4663 | 439 ± 14 | 3.2 | 2.00E-29 | 601789 | Adrenoleukodystrophy, neonatal, 202370; Zellweger syndrome, 214100 |  |
Cat | 4,316 ± 88 | 3.2 | 1.00E-184 | 115500 | Acatalasemia |  |
Prominin-like | 308 ± 24 | 3.0 | 1.00E-20 | 604365 | Retinal degeneration, autosomal recessive, prominin-related | EP(2)0740 |