Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acox1 |
T |
A |
11: 116,065,231 (GRCm39) |
D608V |
probably damaging |
Het |
Actg1 |
A |
T |
11: 120,239,013 (GRCm39) |
C26S |
unknown |
Het |
Ahnak |
T |
A |
19: 8,988,247 (GRCm39) |
V3177E |
possibly damaging |
Het |
Akap11 |
G |
A |
14: 78,750,938 (GRCm39) |
T483I |
|
Het |
Akr1cl |
A |
G |
1: 65,063,830 (GRCm39) |
S120P |
probably benign |
Het |
Ankle2 |
G |
A |
5: 110,400,610 (GRCm39) |
V649M |
possibly damaging |
Het |
Ankrd55 |
A |
T |
13: 112,504,570 (GRCm39) |
I439F |
probably damaging |
Het |
Asb8 |
A |
G |
15: 98,040,635 (GRCm39) |
M9T |
possibly damaging |
Het |
Ascc1 |
A |
T |
10: 59,843,645 (GRCm39) |
Y69F |
probably benign |
Het |
Atp9a |
A |
T |
2: 168,518,060 (GRCm39) |
|
probably null |
Het |
Cd8b1 |
T |
C |
6: 71,306,752 (GRCm39) |
F160L |
probably benign |
Het |
Cdh23 |
G |
A |
10: 60,143,306 (GRCm39) |
A3005V |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,818,350 (GRCm39) |
T842A |
probably benign |
Het |
Cgnl1 |
T |
A |
9: 71,630,847 (GRCm39) |
K552* |
probably null |
Het |
Cntnap4 |
C |
T |
8: 113,602,600 (GRCm39) |
T1227M |
possibly damaging |
Het |
Cobll1 |
C |
A |
2: 64,981,333 (GRCm39) |
V86F |
probably damaging |
Het |
Dchs2 |
A |
G |
3: 83,255,561 (GRCm39) |
N2419S |
probably damaging |
Het |
Dhx30 |
A |
T |
9: 109,914,494 (GRCm39) |
L1001* |
probably null |
Het |
Diaph1 |
C |
T |
18: 38,024,162 (GRCm39) |
V559M |
unknown |
Het |
Dis3l |
A |
T |
9: 64,217,731 (GRCm39) |
H783Q |
probably benign |
Het |
Dock7 |
T |
G |
4: 98,877,350 (GRCm39) |
T1063P |
unknown |
Het |
Dsc1 |
T |
C |
18: 20,232,214 (GRCm39) |
T265A |
possibly damaging |
Het |
Eif2ak4 |
A |
T |
2: 118,258,393 (GRCm39) |
Q581L |
probably damaging |
Het |
Eprs1 |
A |
T |
1: 185,106,334 (GRCm39) |
D183V |
possibly damaging |
Het |
Fads2 |
G |
C |
19: 10,069,183 (GRCm39) |
D80E |
probably benign |
Het |
Fam167b |
G |
A |
4: 129,470,875 (GRCm39) |
R158C |
probably damaging |
Het |
Flnb |
T |
A |
14: 7,892,976 (GRCm38) |
I682K |
possibly damaging |
Het |
Garin4 |
G |
A |
1: 190,894,900 (GRCm39) |
T581I |
possibly damaging |
Het |
Gpatch2l |
C |
T |
12: 86,291,152 (GRCm39) |
P112S |
probably benign |
Het |
Gpn1 |
T |
A |
5: 31,654,710 (GRCm39) |
H87Q |
unknown |
Het |
Greb1l |
T |
C |
18: 10,499,983 (GRCm39) |
V350A |
probably benign |
Het |
Grm5 |
A |
T |
7: 87,724,024 (GRCm39) |
K771N |
probably damaging |
Het |
H2bc8 |
A |
G |
13: 23,755,761 (GRCm39) |
D52G |
probably damaging |
Het |
Hcfc2 |
G |
T |
10: 82,535,041 (GRCm39) |
A22S |
probably benign |
Het |
Hnf4a |
A |
G |
2: 163,393,497 (GRCm39) |
D39G |
probably benign |
Het |
Il6st |
C |
T |
13: 112,635,340 (GRCm39) |
T584M |
probably damaging |
Het |
Irf3 |
T |
A |
7: 44,650,246 (GRCm39) |
V254E |
possibly damaging |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Kank4 |
T |
A |
4: 98,668,289 (GRCm39) |
K53* |
probably null |
Het |
Kcnj11 |
A |
T |
7: 45,748,176 (GRCm39) |
F382L |
possibly damaging |
Het |
Kcnq3 |
T |
C |
15: 65,867,510 (GRCm39) |
Y711C |
probably damaging |
Het |
Kctd3 |
A |
G |
1: 188,704,636 (GRCm39) |
S712P |
possibly damaging |
Het |
Krt20 |
A |
G |
11: 99,323,087 (GRCm39) |
I245T |
possibly damaging |
Het |
Larp1b |
T |
C |
3: 40,925,039 (GRCm39) |
I219T |
probably damaging |
Het |
Lman2l |
A |
G |
1: 36,478,771 (GRCm39) |
F114L |
probably damaging |
Het |
Loxl2 |
T |
A |
14: 69,929,859 (GRCm39) |
Y746N |
possibly damaging |
Het |
Lrrc43 |
T |
C |
5: 123,646,109 (GRCm39) |
S628P |
probably benign |
Het |
Mroh8 |
A |
C |
2: 157,111,545 (GRCm39) |
D136E |
probably damaging |
Het |
Nek8 |
T |
A |
11: 78,063,342 (GRCm39) |
M141L |
probably benign |
Het |
Nr2e1 |
C |
A |
10: 42,454,268 (GRCm39) |
R22L |
probably damaging |
Het |
Nr6a1 |
C |
T |
2: 38,816,129 (GRCm39) |
|
probably null |
Het |
Onecut2 |
A |
G |
18: 64,473,890 (GRCm39) |
Y147C |
probably damaging |
Het |
Or1ad1 |
T |
A |
11: 50,876,166 (GRCm39) |
C213S |
probably damaging |
Het |
Or1j1 |
T |
A |
2: 36,702,214 (GRCm39) |
M297L |
possibly damaging |
Het |
Or5d37 |
A |
G |
2: 87,924,194 (GRCm39) |
F29L |
probably damaging |
Het |
Or5d39 |
T |
C |
2: 87,979,908 (GRCm39) |
M152V |
probably benign |
Het |
Pcdhac2 |
T |
C |
18: 37,277,316 (GRCm39) |
F99L |
probably benign |
Het |
Pcdhga2 |
T |
G |
18: 37,802,795 (GRCm39) |
V213G |
possibly damaging |
Het |
Pgap1 |
A |
T |
1: 54,519,908 (GRCm39) |
V909E |
probably benign |
Het |
Pik3r4 |
A |
T |
9: 105,547,038 (GRCm39) |
T939S |
probably benign |
Het |
Pip4k2c |
T |
C |
10: 127,035,246 (GRCm39) |
D374G |
possibly damaging |
Het |
Plxdc1 |
A |
T |
11: 97,844,788 (GRCm39) |
D252E |
probably benign |
Het |
Pm20d1 |
A |
C |
1: 131,730,115 (GRCm39) |
D218A |
probably damaging |
Het |
Polq |
C |
A |
16: 36,865,265 (GRCm39) |
Q706K |
probably damaging |
Het |
Pram1 |
A |
T |
17: 33,860,131 (GRCm39) |
I233F |
probably benign |
Het |
Prr27 |
C |
A |
5: 87,990,994 (GRCm39) |
P202Q |
probably benign |
Het |
Prss41 |
A |
T |
17: 24,061,361 (GRCm39) |
H143Q |
probably damaging |
Het |
Ptpn21 |
A |
G |
12: 98,655,261 (GRCm39) |
Y569H |
probably damaging |
Het |
Rad17 |
T |
C |
13: 100,773,564 (GRCm39) |
K142E |
probably damaging |
Het |
Rcan3 |
T |
C |
4: 135,152,607 (GRCm39) |
E38G |
probably benign |
Het |
Rgl3 |
C |
A |
9: 21,885,356 (GRCm39) |
R658L |
possibly damaging |
Het |
Rnf125 |
T |
A |
18: 21,116,240 (GRCm39) |
*141K |
probably null |
Het |
Ros1 |
G |
T |
10: 52,019,502 (GRCm39) |
N711K |
probably damaging |
Het |
Rsph10b |
T |
A |
5: 143,896,504 (GRCm39) |
Y421N |
probably benign |
Het |
Ryr1 |
C |
T |
7: 28,776,471 (GRCm39) |
V2222I |
probably damaging |
Het |
Samsn1 |
C |
T |
16: 75,656,449 (GRCm39) |
C333Y |
probably damaging |
Het |
Slc9a2 |
G |
A |
1: 40,794,944 (GRCm39) |
E502K |
probably benign |
Het |
Stard9 |
A |
T |
2: 120,533,500 (GRCm39) |
E3252D |
possibly damaging |
Het |
Syne1 |
C |
A |
10: 5,123,008 (GRCm39) |
R309S |
probably damaging |
Het |
Syne1 |
T |
C |
10: 5,172,289 (GRCm39) |
I5051V |
probably benign |
Het |
Syngap1 |
A |
G |
17: 27,183,948 (GRCm39) |
S1241G |
probably damaging |
Het |
Tbpl2 |
T |
C |
2: 23,966,030 (GRCm39) |
K321R |
probably damaging |
Het |
Tnrc18 |
C |
T |
5: 142,717,107 (GRCm39) |
G2449E |
probably damaging |
Het |
Trim25 |
A |
G |
11: 88,901,731 (GRCm39) |
D342G |
probably benign |
Het |
Tssk4 |
T |
A |
14: 55,887,904 (GRCm39) |
H33Q |
probably benign |
Het |
Ttc3 |
G |
A |
16: 94,268,831 (GRCm39) |
G1971D |
possibly damaging |
Het |
Tufm |
C |
T |
7: 126,088,849 (GRCm39) |
Q347* |
probably null |
Het |
Ubxn10 |
G |
A |
4: 138,448,133 (GRCm39) |
S181F |
possibly damaging |
Het |
Ushbp1 |
T |
C |
8: 71,841,539 (GRCm39) |
E430G |
probably benign |
Het |
Vmn1r33 |
T |
C |
6: 66,588,716 (GRCm39) |
I279M |
possibly damaging |
Het |
Vmn2r115 |
T |
C |
17: 23,564,784 (GRCm39) |
F224L |
probably damaging |
Het |
Vmn2r23 |
A |
T |
6: 123,681,323 (GRCm39) |
H77L |
probably benign |
Het |
Vps13a |
T |
C |
19: 16,663,961 (GRCm39) |
I1481V |
probably benign |
Het |
Vps35 |
T |
C |
8: 86,007,898 (GRCm39) |
N294S |
possibly damaging |
Het |
Washc3 |
A |
T |
10: 88,051,916 (GRCm39) |
T102S |
probably benign |
Het |
Zfp27 |
T |
A |
7: 29,595,359 (GRCm39) |
E202V |
possibly damaging |
Het |
Zfp58 |
T |
C |
13: 67,640,035 (GRCm39) |
H152R |
possibly damaging |
Het |
Zfr2 |
T |
C |
10: 81,080,496 (GRCm39) |
V390A |
probably damaging |
Het |
|
Other mutations in Gucy2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00849:Gucy2c
|
APN |
6 |
136,742,612 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01081:Gucy2c
|
APN |
6 |
136,679,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01285:Gucy2c
|
APN |
6 |
136,686,739 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01395:Gucy2c
|
APN |
6 |
136,675,027 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01408:Gucy2c
|
APN |
6 |
136,675,009 (GRCm39) |
missense |
probably benign |
0.19 |
IGL01752:Gucy2c
|
APN |
6 |
136,747,106 (GRCm39) |
missense |
probably benign |
0.10 |
IGL01766:Gucy2c
|
APN |
6 |
136,692,971 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02245:Gucy2c
|
APN |
6 |
136,706,201 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02648:Gucy2c
|
APN |
6 |
136,706,211 (GRCm39) |
nonsense |
probably null |
|
IGL02794:Gucy2c
|
APN |
6 |
136,690,146 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03023:Gucy2c
|
APN |
6 |
136,679,794 (GRCm39) |
splice site |
probably null |
|
IGL03178:Gucy2c
|
APN |
6 |
136,706,237 (GRCm39) |
splice site |
probably benign |
|
IGL03310:Gucy2c
|
APN |
6 |
136,728,044 (GRCm39) |
missense |
probably benign |
|
IGL03374:Gucy2c
|
APN |
6 |
136,742,628 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03393:Gucy2c
|
APN |
6 |
136,696,665 (GRCm39) |
missense |
probably benign |
0.04 |
BB001:Gucy2c
|
UTSW |
6 |
136,740,053 (GRCm39) |
missense |
probably benign |
0.35 |
BB011:Gucy2c
|
UTSW |
6 |
136,740,053 (GRCm39) |
missense |
probably benign |
0.35 |
R0031:Gucy2c
|
UTSW |
6 |
136,674,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R0128:Gucy2c
|
UTSW |
6 |
136,681,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Gucy2c
|
UTSW |
6 |
136,727,915 (GRCm39) |
critical splice donor site |
probably null |
|
R0593:Gucy2c
|
UTSW |
6 |
136,705,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R0613:Gucy2c
|
UTSW |
6 |
136,737,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Gucy2c
|
UTSW |
6 |
136,704,799 (GRCm39) |
splice site |
probably null |
|
R0828:Gucy2c
|
UTSW |
6 |
136,686,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R0837:Gucy2c
|
UTSW |
6 |
136,699,418 (GRCm39) |
missense |
probably damaging |
0.99 |
R0880:Gucy2c
|
UTSW |
6 |
136,686,830 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1350:Gucy2c
|
UTSW |
6 |
136,720,912 (GRCm39) |
critical splice donor site |
probably null |
|
R1487:Gucy2c
|
UTSW |
6 |
136,725,824 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1680:Gucy2c
|
UTSW |
6 |
136,699,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Gucy2c
|
UTSW |
6 |
136,725,773 (GRCm39) |
splice site |
probably benign |
|
R1791:Gucy2c
|
UTSW |
6 |
136,721,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R1953:Gucy2c
|
UTSW |
6 |
136,681,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R2135:Gucy2c
|
UTSW |
6 |
136,700,726 (GRCm39) |
missense |
probably damaging |
1.00 |
R2227:Gucy2c
|
UTSW |
6 |
136,679,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R2350:Gucy2c
|
UTSW |
6 |
136,740,072 (GRCm39) |
missense |
probably damaging |
0.98 |
R2906:Gucy2c
|
UTSW |
6 |
136,685,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R2907:Gucy2c
|
UTSW |
6 |
136,685,385 (GRCm39) |
missense |
probably damaging |
1.00 |
R3699:Gucy2c
|
UTSW |
6 |
136,747,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R3972:Gucy2c
|
UTSW |
6 |
136,685,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Gucy2c
|
UTSW |
6 |
136,685,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Gucy2c
|
UTSW |
6 |
136,744,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Gucy2c
|
UTSW |
6 |
136,744,150 (GRCm39) |
missense |
probably damaging |
1.00 |
R4776:Gucy2c
|
UTSW |
6 |
136,699,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5087:Gucy2c
|
UTSW |
6 |
136,744,033 (GRCm39) |
missense |
possibly damaging |
0.69 |
R5284:Gucy2c
|
UTSW |
6 |
136,740,041 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5366:Gucy2c
|
UTSW |
6 |
136,697,739 (GRCm39) |
missense |
probably damaging |
0.99 |
R5466:Gucy2c
|
UTSW |
6 |
136,758,463 (GRCm39) |
nonsense |
probably null |
|
R5911:Gucy2c
|
UTSW |
6 |
136,699,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R6160:Gucy2c
|
UTSW |
6 |
136,717,684 (GRCm39) |
nonsense |
probably null |
|
R6367:Gucy2c
|
UTSW |
6 |
136,686,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6441:Gucy2c
|
UTSW |
6 |
136,700,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R6812:Gucy2c
|
UTSW |
6 |
136,674,993 (GRCm39) |
missense |
probably benign |
|
R6865:Gucy2c
|
UTSW |
6 |
136,747,127 (GRCm39) |
missense |
probably benign |
0.13 |
R7065:Gucy2c
|
UTSW |
6 |
136,697,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Gucy2c
|
UTSW |
6 |
136,674,937 (GRCm39) |
missense |
probably benign |
0.19 |
R7096:Gucy2c
|
UTSW |
6 |
136,705,339 (GRCm39) |
missense |
probably benign |
0.11 |
R7138:Gucy2c
|
UTSW |
6 |
136,705,342 (GRCm39) |
missense |
probably damaging |
1.00 |
R7343:Gucy2c
|
UTSW |
6 |
136,679,746 (GRCm39) |
missense |
probably damaging |
1.00 |
R7538:Gucy2c
|
UTSW |
6 |
136,686,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7587:Gucy2c
|
UTSW |
6 |
136,681,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R7666:Gucy2c
|
UTSW |
6 |
136,674,966 (GRCm39) |
missense |
probably benign |
|
R7675:Gucy2c
|
UTSW |
6 |
136,693,030 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7822:Gucy2c
|
UTSW |
6 |
136,685,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Gucy2c
|
UTSW |
6 |
136,746,814 (GRCm39) |
splice site |
probably null |
|
R7924:Gucy2c
|
UTSW |
6 |
136,740,053 (GRCm39) |
missense |
probably benign |
0.35 |
R8078:Gucy2c
|
UTSW |
6 |
136,674,919 (GRCm39) |
missense |
probably damaging |
1.00 |
R8094:Gucy2c
|
UTSW |
6 |
136,714,446 (GRCm39) |
missense |
probably benign |
0.33 |
R8391:Gucy2c
|
UTSW |
6 |
136,681,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R8428:Gucy2c
|
UTSW |
6 |
136,704,892 (GRCm39) |
missense |
probably damaging |
0.96 |
R9188:Gucy2c
|
UTSW |
6 |
136,700,756 (GRCm39) |
missense |
probably benign |
0.44 |
R9325:Gucy2c
|
UTSW |
6 |
136,743,992 (GRCm39) |
nonsense |
probably null |
|
R9361:Gucy2c
|
UTSW |
6 |
136,714,429 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9413:Gucy2c
|
UTSW |
6 |
136,700,771 (GRCm39) |
missense |
possibly damaging |
0.94 |
Z1088:Gucy2c
|
UTSW |
6 |
136,720,979 (GRCm39) |
missense |
probably benign |
|
Z1177:Gucy2c
|
UTSW |
6 |
136,744,194 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Gucy2c
|
UTSW |
6 |
136,696,685 (GRCm39) |
missense |
probably damaging |
1.00 |
|