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G |
Ace |
angiotensin I converting enzyme |
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ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:34906502 |
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NCBI chrNW_004624849:998,262...1,019,305
Ensembl chrNW_004624849:998,277...1,019,521
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G |
Actg1 |
actin gamma 1 |
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ISO |
ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:3351890 PMID:13680526 PMID:18414213 PMID:22366783 PMID:25052316 PMID:26188271 PMID:27625340 PMID:30143558 More...
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NCBI chrNW_004624801:10,496,876...10,499,737
Ensembl chrNW_004624801:10,496,718...10,499,637
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G |
Bicc1 |
BicC family RNA binding protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
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NCBI chrNW_004624791:4,732,581...5,057,912
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G |
Bmp4 |
bone morphogenetic protein 4 |
susceptibility |
ISO |
DNA:SNPs: :rs2071047,rs17563(human) |
RGD |
PMID:24131739 |
RGD:13442498 |
NCBI chrNW_004624731:15,262,480...15,269,196
Ensembl chrNW_004624731:15,263,274...15,269,743
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G |
Bmp7 |
bone morphogenetic protein 7 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:27657687 |
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NCBI chrNW_004624741:23,658,214...23,743,227
Ensembl chrNW_004624741:23,658,004...23,737,742
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G |
Cdc5l |
cell division cycle 5 like |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:27657687 |
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NCBI chrNW_004624754:15,477,188...15,517,656
Ensembl chrNW_004624754:15,477,193...15,517,636
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G |
Chd1l |
chromodomain helicase DNA binding protein 1 like |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:27657687 |
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NCBI chrNW_004624772:16,178,080...16,241,869
Ensembl chrNW_004624772:16,178,139...16,241,624
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G |
Col4a1 |
collagen type IV alpha 1 chain |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:31230195 |
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NCBI chrNW_004624793:2,325,104...2,426,814
Ensembl chrNW_004624793:2,325,128...2,426,817
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G |
Ctu2 |
cytosolic thiouridylase subunit 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:28492532 PMID:30143558 PMID:33057194 PMID:35982159 |
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NCBI chrNW_004624746:871,707...878,047
Ensembl chrNW_004624746:871,668...877,719
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G |
Dhx8 |
DEAH-box helicase 8 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:30143558 |
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NCBI chrNW_004624795:1,092,040...1,117,888
Ensembl chrNW_004624795:1,092,040...1,117,859
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G |
Dnase1 |
deoxyribonuclease 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624824:1,429,078...1,446,881
Ensembl chrNW_004624824:1,443,451...1,446,881
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G |
Emc1 |
ER membrane protein complex subunit 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:26572623 PMID:26942288 PMID:27657687 PMID:28492532 PMID:29271071 |
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NCBI chrNW_004624764:4,367,780...4,401,000
Ensembl chrNW_004624764:4,370,591...4,400,920
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G |
Etv4 |
ETS variant transcription factor 4 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:30143558 |
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NCBI chrNW_004624795:1,079,024...1,090,364
Ensembl chrNW_004624795:1,079,537...1,089,964
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G |
Fat4 |
FAT atypical cadherin 4 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:28878612 PMID:30143558 |
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NCBI chrNW_004624777:6,095,166...6,293,142
Ensembl chrNW_004624777:6,095,643...6,292,980
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G |
Foxc1 |
forkhead box C1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:30143558 PMID:32475988 |
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NCBI chrNW_004624756:23,060,065...23,062,407
Ensembl chrNW_004624756:23,060,751...23,062,343
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G |
Fras1 |
Fraser extracellular matrix complex subunit 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:12766769 PMID:16199547 PMID:18671281 PMID:25741868 PMID:28492532 PMID:28844315 PMID:30143558 PMID:34246755 More...
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NCBI chrNW_004624757:12,529,475...12,973,751
Ensembl chrNW_004624757:12,532,466...12,972,918
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G |
Frem1 |
FRAS1 related extracellular matrix 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 |
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NCBI chrNW_004624736:18,975,104...19,346,159
Ensembl chrNW_004624736:18,989,320...19,132,416
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G |
Frem2 |
FRAS1 related extracellular matrix 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:24700879 PMID:25741868 PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624920:1,683,342...1,908,602
Ensembl chrNW_004624920:1,683,351...1,904,557
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G |
Gata3 |
GATA binding protein 3 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
|
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NCBI chrNW_004624775:2,985,077...3,014,567
Ensembl chrNW_004624775:2,994,164...3,015,392
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G |
Gdf6 |
growth differentiation factor 6 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:18425797 PMID:19129173 PMID:23307924 PMID:23620759 PMID:24033266 PMID:25457163 PMID:25741868 PMID:28492532 PMID:30755392 PMID:32483926 PMID:32737436 PMID:38025229 More...
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NCBI chrNW_004624763:3,473,047...3,490,346
Ensembl chrNW_004624763:3,474,671...3,490,297
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G |
Greb1l |
GREB1 like retinoic acid receptor coactivator |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:29100090 PMID:30143558 |
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NCBI chrNW_004624770:10,223,131...10,471,309
Ensembl chrNW_004624770:10,225,669...10,345,173
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G |
Hnf1b |
HNF1 homeobox B |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:15930087 PMID:16249435 PMID:16371430 PMID:17116179 PMID:18249217 PMID:18644064 PMID:20155289 PMID:21380624 PMID:21775974 PMID:23539225 PMID:24387224 PMID:24429398 PMID:24897035 PMID:24961278 PMID:25500806 PMID:25536396 PMID:25700310 PMID:25741868 PMID:26024028 PMID:26059258 PMID:26226118 PMID:26467025 PMID:28492532 PMID:30143558 PMID:31365591 PMID:31595705 PMID:31825128 PMID:32708349 PMID:33324081 PMID:33532864 PMID:33663443 More...
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NCBI chrNW_004624871:4,662,104...4,713,125
Ensembl chrNW_004624871:4,661,669...4,712,960
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G |
Hpse2 |
heparanase 2 (inactive) |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:19669792 PMID:20560210 PMID:25510506 PMID:27151922 PMID:28492532 PMID:30143558 More...
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NCBI chrNW_004624737:10,055,408...10,976,525
Ensembl chrNW_004624737:10,058,787...10,976,525
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G |
Jag1 |
jagged canonical Notch ligand 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 |
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NCBI chrNW_004624741:11,647,723...11,683,137
Ensembl chrNW_004624741:11,647,463...11,683,488
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G |
Kat6b |
lysine acetyltransferase 6B |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624754:8,204,266...8,391,328
Ensembl chrNW_004624754:8,204,943...8,392,724
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G |
Kmt2d |
lysine methyltransferase 2D |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
|
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NCBI chrNW_004624816:3,129,127...3,169,143
Ensembl chrNW_004624816:3,133,659...3,166,346
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G |
Lifr |
LIF receptor subunit alpha |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:26627873 PMID:28334964 PMID:28492532 PMID:34063511 PMID:34426522 More...
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NCBI chrNW_004624759:16,368,390...16,478,486
Ensembl chrNW_004624759:16,410,687...16,472,014
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G |
Notch2 |
notch receptor 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624772:15,572,350...15,726,312
Ensembl chrNW_004624772:15,571,998...15,726,426
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G |
Nphp1 |
nephrocystin 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:30143558 |
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NCBI chrNW_004624749:1,725,515...1,779,787
Ensembl chrNW_004624749:1,725,598...1,779,344
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G |
Nphp4 |
nephrocystin 4 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624818:5,325,946...5,432,290
Ensembl chrNW_004624818:5,327,038...5,432,901
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G |
Nrip1 |
nuclear receptor interacting protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:28381549 PMID:30143558 |
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NCBI chrNW_004624745:3,389,486...3,469,599
Ensembl chrNW_004624745:3,392,572...3,468,576
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G |
Ofd1 |
OFD1 centriole and centriolar satellite protein |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 |
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NCBI chrNW_004624882:376,447...417,066
Ensembl chrNW_004624882:376,556...416,509
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G |
Pax2 |
paired box 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:3377002 PMID:8589702 PMID:9106533 PMID:11093271 PMID:11241473 PMID:11461952 PMID:22213154 PMID:22350371 PMID:24429398 PMID:24676634 PMID:25741868 PMID:27226968 PMID:28492532 PMID:31001663 PMID:32203253 PMID:33532864 PMID:34696790 PMID:35444690 More...
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NCBI chrNW_004624831:375,851...453,968
Ensembl chrNW_004624831:375,866...453,930
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G |
Polr1c |
RNA polymerase I and III subunit C |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:27657687 |
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NCBI chrNW_004624754:16,125,322...16,129,339
Ensembl chrNW_004624754:16,122,935...16,136,395
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G |
Ret |
ret proto-oncogene |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:27657687 PMID:28492532 PMID:29641532 |
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NCBI chrNW_004624922:382,462...413,227
Ensembl chrNW_004624922:382,399...413,281
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G |
Robo1 |
roundabout guidance receptor 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:30692597 PMID:35227688 |
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NCBI chrNW_004624874:4,234,640...5,359,333
Ensembl chrNW_004624874:4,949,538...5,357,690
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G |
Robo2 |
roundabout guidance receptor 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:17357069 PMID:18235093 PMID:22995991 PMID:23536131 PMID:24429398 PMID:25741868 PMID:27657687 PMID:28492532 PMID:30143558 PMID:30586318 More...
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NCBI chrNW_004624745:800,963...2,121,445
Ensembl chrNW_004624745:804,797...1,390,551
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G |
Sall1 |
spalt like transcription factor 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624757:5,572,510...5,587,623
Ensembl chrNW_004624757:5,572,528...5,587,617
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G |
Six2 |
SIX homeobox 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:27657687 PMID:28492532 PMID:32164334 |
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NCBI chrNW_004624738:26,442,935...26,447,100
Ensembl chrNW_004624738:26,442,965...26,446,942
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G |
Slit2 |
slit guidance ligand 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:26026792 PMID:28492532 |
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NCBI chrNW_004624755:11,470,810...11,819,800
Ensembl chrNW_004624755:11,472,377...11,819,266
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G |
Srgap1 |
SLIT-ROBO Rho GTPase activating protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:26026792 PMID:30143558 |
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NCBI chrNW_004624802:4,164,969...4,472,491
Ensembl chrNW_004624802:4,165,054...4,472,293
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G |
Tbc1d1 |
TBC1 domain family member 1 |
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ISO |
ClinVar Annotator: match by term: Non-syndromic renal or urinary tract malformation |
ClinVar |
PMID:25741868 |
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NCBI chrNW_004624840:6,475,382...6,709,568
Ensembl chrNW_004624840:6,592,910...6,707,932
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G |
Tbx18 |
T-box transcription factor 18 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:26235987 PMID:30143558 |
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NCBI chrNW_004624799:9,694,167...9,721,468
Ensembl chrNW_004624799:9,694,374...9,719,385
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G |
Tbx6 |
T-box transcription factor 6 |
|
ISO |
CTD Direct Evidence: marker/mechanism |
CTD |
PMID:30578417 |
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NCBI chrNW_004624782:13,169,096...13,174,498
Ensembl chrNW_004624782:13,169,719...13,174,056
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G |
Tmem231 |
transmembrane protein 231 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:30143558 |
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NCBI chrNW_004624746:11,411,050...11,427,945
Ensembl chrNW_004624746:11,411,107...11,427,943
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G |
Trap1 |
TNF receptor associated protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624824:1,446,827...1,511,062
Ensembl chrNW_004624824:1,446,827...1,511,225
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G |
Trps1 |
transcriptional repressor GATA binding 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract |
ClinVar |
PMID:11112658 PMID:11950061 PMID:18946009 PMID:24502542 PMID:25792522 PMID:28492532 PMID:30143558 PMID:30541476 More...
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NCBI chrNW_004624763:13,792,649...14,035,120
Ensembl chrNW_004624763:13,798,113...14,035,138
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G |
Tshz3 |
teashirt zinc finger homeobox 3 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:39420202 |
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NCBI chrNW_004624794:6,279,964...6,351,026
Ensembl chrNW_004624794:6,280,513...6,350,727
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G |
Zmym2 |
zinc finger MYM-type containing 2 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract | ClinVar Annotator: match by term: Congenital anomalies of the kidney and urinary tract |
ClinVar |
PMID:25741868 PMID:32891193 |
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NCBI chrNW_004624776:17,631,511...17,744,153
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G |
Zng1a |
Zn regulated GTPase metalloprotein activator 1A |
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ISO |
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MouseDO |
|
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NCBI chrNW_004624736:4,878,241...4,934,000
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G |
Chrna3 |
cholinergic receptor nicotinic alpha 3 subunit |
|
ISO |
ClinVar Annotator: match by term: CHRNA3-related condition | ClinVar Annotator: match by term: Urinary bladder, atony of |
ClinVar OMIM |
PMID:25741868 PMID:28492532 PMID:31708116 |
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NCBI chrNW_004624894:2,324,480...2,357,389
Ensembl chrNW_004624894:2,324,501...2,357,723
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G |
Celsr3 |
cadherin EGF LAG seven-pass G-type receptor 3 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1 |
ClinVar |
|
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NCBI chrNW_004624730:2,650,096...2,675,930
Ensembl chrNW_004624730:2,651,756...2,675,923
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G |
Dnase1 |
deoxyribonuclease 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1 |
ClinVar |
PMID:24152966 PMID:28710113 PMID:35765067 |
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NCBI chrNW_004624824:1,429,078...1,446,881
Ensembl chrNW_004624824:1,443,451...1,446,881
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G |
Dstyk |
dual serine/threonine and tyrosine protein kinase |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1, susceptibility to |
OMIM ClinVar |
PMID:9536098 PMID:17273976 PMID:17576681 PMID:23862974 PMID:25741868 PMID:27657687 PMID:28492532 PMID:28566479 More...
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NCBI chrNW_004624807:5,942,610...5,993,049
Ensembl chrNW_004624807:5,942,799...5,993,049
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G |
Srgap1 |
SLIT-ROBO Rho GTPase activating protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1, susceptibility to |
ClinVar |
PMID:25741868 PMID:26026792 PMID:30143558 |
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NCBI chrNW_004624802:4,164,969...4,472,491
Ensembl chrNW_004624802:4,165,054...4,472,293
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G |
Trap1 |
TNF receptor associated protein 1 |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1 |
ClinVar |
PMID:24152966 PMID:28710113 PMID:35765067 |
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NCBI chrNW_004624824:1,446,827...1,511,062
Ensembl chrNW_004624824:1,446,827...1,511,225
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G |
Upk3a |
uroplakin 3A |
|
ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1 | ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 1, susceptibility to |
ClinVar |
PMID:15888565 PMID:16731295 PMID:25741868 |
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NCBI chrNW_004624752:4,354,415...4,361,250
Ensembl chrNW_004624752:4,351,164...4,361,235
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G |
Bmp4 |
bone morphogenetic protein 4 |
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ISO |
DNA:mutations:cds: c.485G> A (p.R162Q), c.1167T> C(human) |
RGD |
PMID:21927809 |
RGD:13446406 |
NCBI chrNW_004624731:15,262,480...15,269,196
Ensembl chrNW_004624731:15,263,274...15,269,743
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G |
Mmp9 |
matrix metallopeptidase 9 |
treatment |
ISO |
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RGD |
PMID:27448803 |
RGD:13204792 |
NCBI chrNW_004624790:8,584,399...8,591,763
Ensembl chrNW_004624790:8,583,457...8,591,713
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G |
Tbx18 |
T-box transcription factor 18 |
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ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 2 | ClinVar Annotator: match by term: Pelvi-ureteric junction obstruction | ClinVar Annotator: match by term: TBX18-related condition |
OMIM ClinVar |
PMID:25741868 PMID:25741890 PMID:26235987 PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624799:9,694,167...9,721,468
Ensembl chrNW_004624799:9,694,374...9,719,385
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G |
Timp1 |
TIMP metallopeptidase inhibitor 1 |
treatment |
ISO |
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RGD |
PMID:27448803 |
RGD:13204792 |
NCBI chrNW_004624978:120,723...125,006
Ensembl chrNW_004624978:121,803...124,912
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G |
Nrip1 |
nuclear receptor interacting protein 1 |
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ISO |
ClinVar Annotator: match by term: Congenital anomalies of kidney and urinary tract 3 | ClinVar Annotator: match by term: NRIP1-related condition |
OMIM ClinVar |
PMID:25741868 PMID:28381549 PMID:28492532 PMID:30143558 |
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NCBI chrNW_004624745:3,389,486...3,469,599
Ensembl chrNW_004624745:3,392,572...3,468,576
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G |
Hif1an |
hypoxia inducible factor 1 subunit alpha inhibitor |
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ISO |
ClinVar Annotator: match by term: Renal coloboma syndrome |
ClinVar |
PMID:11461952 PMID:24676634 PMID:28492532 |
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NCBI chrNW_004624831:206,856...226,876
Ensembl chrNW_004624831:206,414...216,592
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G |
Ndufb8 |
NADH:ubiquinone oxidoreductase subunit B8 |
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ISO |
ClinVar Annotator: match by term: Renal coloboma syndrome |
ClinVar |
PMID:11461952 PMID:24676634 PMID:28492532 |
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NCBI chrNW_004624831:195,552...200,458
Ensembl chrNW_004624831:191,625...200,860
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G |
Pax2 |
paired box 2 |
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ISO |
ClinVar Annotator: match by term: Papillorenal syndrome with macular abnormalities | ClinVar Annotator: match by term: Renal coloboma syndrome |
OMIM ClinVar |
PMID:2644560 PMID:3077329 PMID:3377002 PMID:7795640 PMID:8589702 PMID:8943028 PMID:9106533 PMID:9536098 PMID:9760197 PMID:10466411 PMID:10533062 PMID:11093271 PMID:11241473 PMID:11461952 PMID:15652857 PMID:16199547 PMID:17576681 PMID:20221250 PMID:20358591 PMID:21108633 PMID:21654726 PMID:22213154 PMID:22350371 PMID:23539225 PMID:24033266 PMID:24429398 PMID:24676634 PMID:25640679 PMID:25741868 PMID:27226968 PMID:27657687 PMID:28041643 PMID:28492532 PMID:28566479 PMID:29054766 PMID:29973660 PMID:30076350 PMID:30241513 PMID:30348286 PMID:30773290 PMID:31001663 PMID:31060108 PMID:31328266 PMID:31576025 PMID:31692565 PMID:32203253 PMID:32604935 PMID:32776440 PMID:33532864 PMID:34031707 PMID:34059960 PMID:34696790 PMID:34979951 PMID:35444690 PMID:35574290 PMID:36549658 More...
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NCBI chrNW_004624831:375,851...453,968
Ensembl chrNW_004624831:375,866...453,930
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