Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700030K09Rik |
A |
G |
8: 73,208,959 (GRCm39) |
E363G |
probably benign |
Het |
Abcg2 |
T |
A |
6: 58,661,307 (GRCm39) |
|
probably null |
Het |
Adgrg7 |
T |
G |
16: 56,572,791 (GRCm39) |
I342L |
possibly damaging |
Het |
Akap6 |
A |
C |
12: 53,188,187 (GRCm39) |
D1867A |
probably benign |
Het |
Ankrd17 |
A |
T |
5: 90,381,918 (GRCm39) |
V2416D |
probably damaging |
Het |
Apaf1 |
A |
G |
10: 90,883,952 (GRCm39) |
V670A |
probably damaging |
Het |
Art5 |
A |
G |
7: 101,747,407 (GRCm39) |
L124P |
possibly damaging |
Het |
Atad5 |
T |
A |
11: 79,997,203 (GRCm39) |
D842E |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,694,229 (GRCm39) |
M1755V |
probably benign |
Het |
Capns1 |
A |
G |
7: 29,891,765 (GRCm39) |
L124P |
probably damaging |
Het |
Carmil1 |
A |
G |
13: 24,325,656 (GRCm39) |
S225P |
probably damaging |
Het |
Cars2 |
C |
T |
8: 11,580,299 (GRCm39) |
A247T |
possibly damaging |
Het |
Cd46 |
A |
G |
1: 194,744,721 (GRCm39) |
I339T |
probably benign |
Het |
Ceacam14 |
C |
A |
7: 17,548,153 (GRCm39) |
T81N |
probably benign |
Het |
Ceacam16 |
G |
A |
7: 19,595,066 (GRCm39) |
P4L |
probably benign |
Het |
Chek1 |
C |
A |
9: 36,635,279 (GRCm39) |
V35F |
probably damaging |
Het |
Cntnap5c |
A |
T |
17: 58,362,666 (GRCm39) |
I340L |
possibly damaging |
Het |
Col2a1 |
C |
A |
15: 97,885,461 (GRCm39) |
A461S |
unknown |
Het |
Comtd1 |
T |
C |
14: 21,898,340 (GRCm39) |
E27G |
possibly damaging |
Het |
Cyp2a12 |
A |
G |
7: 26,732,042 (GRCm39) |
N261S |
probably benign |
Het |
Dclk1 |
A |
G |
3: 55,154,633 (GRCm39) |
Y21C |
probably damaging |
Het |
Dis3l |
T |
A |
9: 64,214,545 (GRCm39) |
N981I |
probably benign |
Het |
Dlg5 |
A |
T |
14: 24,187,225 (GRCm39) |
I1819N |
probably damaging |
Het |
Elp1 |
T |
A |
4: 56,779,636 (GRCm39) |
|
probably null |
Het |
Enpep |
T |
C |
3: 129,074,231 (GRCm39) |
N772S |
probably damaging |
Het |
Erich1 |
T |
C |
8: 14,128,773 (GRCm39) |
T56A |
probably benign |
Het |
Ermp1 |
T |
C |
19: 29,614,798 (GRCm39) |
|
probably null |
Het |
Etl4 |
A |
G |
2: 20,803,545 (GRCm39) |
E807G |
probably benign |
Het |
Fat4 |
A |
T |
3: 39,037,544 (GRCm39) |
Y3732F |
probably damaging |
Het |
Fbxw18 |
T |
G |
9: 109,522,438 (GRCm39) |
T144P |
probably damaging |
Het |
Flywch1 |
A |
T |
17: 23,974,624 (GRCm39) |
I672K |
probably benign |
Het |
Foxk2 |
C |
A |
11: 121,151,213 (GRCm39) |
A86E |
probably benign |
Het |
Garem2 |
T |
C |
5: 30,313,297 (GRCm39) |
S54P |
probably damaging |
Het |
Gda |
A |
G |
19: 21,374,869 (GRCm39) |
|
probably null |
Het |
Gna15 |
T |
C |
10: 81,338,738 (GRCm39) |
Y367C |
probably damaging |
Het |
Golga3 |
A |
G |
5: 110,335,856 (GRCm39) |
|
probably null |
Het |
Greb1 |
T |
C |
12: 16,749,533 (GRCm39) |
S1098G |
probably damaging |
Het |
Hook3 |
C |
A |
8: 26,560,225 (GRCm39) |
L333F |
probably damaging |
Het |
Il6 |
C |
T |
5: 30,218,502 (GRCm39) |
Q33* |
probably null |
Het |
Iqgap1 |
T |
C |
7: 80,401,701 (GRCm39) |
E468G |
probably benign |
Het |
Iqgap1 |
A |
G |
7: 80,409,651 (GRCm39) |
I228T |
possibly damaging |
Het |
Kcnab1 |
A |
T |
3: 65,278,861 (GRCm39) |
I371F |
probably damaging |
Het |
Kcnj10 |
A |
T |
1: 172,197,455 (GRCm39) |
Y323F |
possibly damaging |
Het |
Klk1b5 |
T |
C |
7: 43,869,322 (GRCm39) |
|
probably null |
Het |
Lmo7 |
A |
G |
14: 102,157,951 (GRCm39) |
|
probably benign |
Het |
Loxhd1 |
A |
T |
18: 77,443,862 (GRCm39) |
T277S |
possibly damaging |
Het |
Lrp5 |
A |
T |
19: 3,664,339 (GRCm39) |
M796K |
probably benign |
Het |
Med15 |
A |
T |
16: 17,503,315 (GRCm39) |
|
probably null |
Het |
Mfn1 |
T |
A |
3: 32,596,975 (GRCm39) |
H144Q |
probably damaging |
Het |
Mmp25 |
T |
A |
17: 23,850,048 (GRCm39) |
Y504F |
probably damaging |
Het |
Nmi |
T |
C |
2: 51,842,555 (GRCm39) |
E179G |
probably damaging |
Het |
Nrxn2 |
T |
C |
19: 6,554,944 (GRCm39) |
I1141T |
probably damaging |
Het |
Olah |
T |
C |
2: 3,366,306 (GRCm39) |
S9G |
probably benign |
Het |
Or1m1 |
T |
C |
9: 18,666,391 (GRCm39) |
D180G |
probably damaging |
Het |
Or4c106 |
C |
A |
2: 88,683,128 (GRCm39) |
P278H |
probably damaging |
Het |
Or5b120 |
T |
G |
19: 13,479,852 (GRCm39) |
I48M |
probably damaging |
Het |
Or8b49 |
G |
T |
9: 38,505,707 (GRCm39) |
L63F |
probably damaging |
Het |
Or8k22 |
A |
C |
2: 86,162,872 (GRCm39) |
F276C |
probably damaging |
Het |
Otog |
T |
A |
7: 45,952,328 (GRCm39) |
C2591S |
probably damaging |
Het |
Pdgfrb |
G |
T |
18: 61,205,828 (GRCm39) |
V605F |
probably damaging |
Het |
Pik3cb |
T |
A |
9: 98,983,297 (GRCm39) |
K104* |
probably null |
Het |
Plb1 |
T |
A |
5: 32,471,433 (GRCm39) |
I580N |
probably damaging |
Het |
Plekha2 |
T |
C |
8: 25,578,413 (GRCm39) |
Y29C |
probably damaging |
Het |
Plekha7 |
T |
A |
7: 115,775,002 (GRCm39) |
Y213F |
probably damaging |
Het |
Plin5 |
T |
C |
17: 56,423,836 (GRCm39) |
D33G |
probably benign |
Het |
Pnpla2 |
C |
A |
7: 141,039,132 (GRCm39) |
Q371K |
probably damaging |
Het |
Ppm1n |
A |
G |
7: 19,012,110 (GRCm39) |
Y348H |
probably damaging |
Het |
Ppp2r1b |
T |
A |
9: 50,777,854 (GRCm39) |
D266E |
probably damaging |
Het |
Prss23 |
A |
G |
7: 89,159,119 (GRCm39) |
S317P |
probably damaging |
Het |
Prss33 |
C |
T |
17: 24,053,817 (GRCm39) |
V87M |
probably damaging |
Het |
Ptpn12 |
C |
A |
5: 21,207,466 (GRCm39) |
Q297H |
probably damaging |
Het |
Pum1 |
G |
T |
4: 130,478,802 (GRCm39) |
A571S |
probably damaging |
Het |
Rexo1 |
G |
T |
10: 80,379,943 (GRCm39) |
C13* |
probably null |
Het |
Rhpn1 |
A |
T |
15: 75,576,243 (GRCm39) |
M1L |
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Ripk2 |
A |
G |
4: 16,132,775 (GRCm39) |
|
probably null |
Het |
Rps6kc1 |
T |
C |
1: 190,530,920 (GRCm39) |
Y937C |
probably damaging |
Het |
Rrbp1 |
A |
G |
2: 143,796,118 (GRCm39) |
L1200P |
possibly damaging |
Het |
Ryr2 |
A |
G |
13: 11,592,759 (GRCm39) |
I4665T |
possibly damaging |
Het |
Sbno1 |
C |
A |
5: 124,516,606 (GRCm39) |
V1256F |
probably benign |
Het |
Senp5 |
T |
C |
16: 31,787,692 (GRCm39) |
I644V |
probably damaging |
Het |
Serpinb9e |
T |
A |
13: 33,436,961 (GRCm39) |
F94I |
probably damaging |
Het |
Sidt2 |
T |
C |
9: 45,856,638 (GRCm39) |
D477G |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,940,457 (GRCm39) |
H619Q |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
Sned1 |
T |
A |
1: 93,202,379 (GRCm39) |
D674E |
probably benign |
Het |
Sorl1 |
T |
C |
9: 41,895,788 (GRCm39) |
H1789R |
probably benign |
Het |
Sp2 |
T |
C |
11: 96,852,834 (GRCm39) |
D30G |
possibly damaging |
Het |
Stk33 |
T |
A |
7: 108,940,527 (GRCm39) |
N61I |
probably benign |
Het |
Stxbp1 |
T |
A |
2: 32,692,868 (GRCm39) |
I383F |
probably damaging |
Het |
Tbcd |
A |
G |
11: 121,494,457 (GRCm39) |
Q1006R |
possibly damaging |
Het |
Tln2 |
T |
C |
9: 67,209,842 (GRCm39) |
T432A |
probably damaging |
Het |
Tnfrsf21 |
A |
G |
17: 43,398,763 (GRCm39) |
D623G |
probably damaging |
Het |
Trib2 |
A |
G |
12: 15,843,830 (GRCm39) |
F271L |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,810,477 (GRCm39) |
V17A |
probably benign |
Het |
Ubqlnl |
A |
T |
7: 103,797,890 (GRCm39) |
C536S |
probably benign |
Het |
Vmn1r230 |
T |
A |
17: 21,067,063 (GRCm39) |
M84K |
probably damaging |
Het |
Vmn2r97 |
A |
T |
17: 19,167,584 (GRCm39) |
R613* |
probably null |
Het |
Yeats2 |
T |
A |
16: 19,972,916 (GRCm39) |
D23E |
probably damaging |
Het |
Zan |
T |
A |
5: 137,434,662 (GRCm39) |
I2214F |
unknown |
Het |
Zbtb40 |
T |
C |
4: 136,718,946 (GRCm39) |
D917G |
probably damaging |
Het |
Zcchc2 |
C |
A |
1: 105,949,453 (GRCm39) |
|
probably null |
Het |
Zdhhc23 |
G |
T |
16: 43,794,282 (GRCm39) |
Q131K |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,578 (GRCm39) |
T320A |
probably benign |
Het |
Zfp532 |
A |
G |
18: 65,757,998 (GRCm39) |
T644A |
possibly damaging |
Het |
|
Other mutations in Kat6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00264:Kat6b
|
APN |
14 |
21,718,627 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01128:Kat6b
|
APN |
14 |
21,710,928 (GRCm39) |
missense |
probably benign |
|
IGL02272:Kat6b
|
APN |
14 |
21,676,846 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02349:Kat6b
|
APN |
14 |
21,687,661 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02402:Kat6b
|
APN |
14 |
21,681,415 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02474:Kat6b
|
APN |
14 |
21,719,107 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02516:Kat6b
|
APN |
14 |
21,659,936 (GRCm39) |
splice site |
probably benign |
|
IGL02666:Kat6b
|
APN |
14 |
21,678,938 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02971:Kat6b
|
APN |
14 |
21,719,826 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Kat6b
|
APN |
14 |
21,711,638 (GRCm39) |
nonsense |
probably null |
|
IGL03274:Kat6b
|
APN |
14 |
21,659,831 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03308:Kat6b
|
APN |
14 |
21,674,902 (GRCm39) |
missense |
probably damaging |
0.99 |
R0118:Kat6b
|
UTSW |
14 |
21,720,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R0383:Kat6b
|
UTSW |
14 |
21,719,149 (GRCm39) |
missense |
probably benign |
0.02 |
R0441:Kat6b
|
UTSW |
14 |
21,720,301 (GRCm39) |
missense |
probably damaging |
1.00 |
R0457:Kat6b
|
UTSW |
14 |
21,720,598 (GRCm39) |
missense |
probably damaging |
0.96 |
R0558:Kat6b
|
UTSW |
14 |
21,719,489 (GRCm39) |
missense |
probably benign |
0.03 |
R0662:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R0684:Kat6b
|
UTSW |
14 |
21,718,849 (GRCm39) |
missense |
probably benign |
|
R0755:Kat6b
|
UTSW |
14 |
21,687,661 (GRCm39) |
missense |
probably damaging |
0.99 |
R1216:Kat6b
|
UTSW |
14 |
21,672,108 (GRCm39) |
nonsense |
probably null |
|
R1479:Kat6b
|
UTSW |
14 |
21,669,024 (GRCm39) |
missense |
probably benign |
0.19 |
R1873:Kat6b
|
UTSW |
14 |
21,567,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R1957:Kat6b
|
UTSW |
14 |
21,678,947 (GRCm39) |
missense |
probably damaging |
1.00 |
R2151:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2152:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2154:Kat6b
|
UTSW |
14 |
21,718,735 (GRCm39) |
missense |
probably benign |
0.02 |
R2399:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R3740:Kat6b
|
UTSW |
14 |
21,720,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R3771:Kat6b
|
UTSW |
14 |
21,567,166 (GRCm39) |
missense |
probably damaging |
1.00 |
R4178:Kat6b
|
UTSW |
14 |
21,668,972 (GRCm39) |
nonsense |
probably null |
|
R4261:Kat6b
|
UTSW |
14 |
21,719,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R4551:Kat6b
|
UTSW |
14 |
21,711,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R4724:Kat6b
|
UTSW |
14 |
21,711,030 (GRCm39) |
missense |
probably benign |
|
R5055:Kat6b
|
UTSW |
14 |
21,567,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R5098:Kat6b
|
UTSW |
14 |
21,669,083 (GRCm39) |
splice site |
probably benign |
|
R5121:Kat6b
|
UTSW |
14 |
21,669,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R5158:Kat6b
|
UTSW |
14 |
21,720,054 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5488:Kat6b
|
UTSW |
14 |
21,719,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5489:Kat6b
|
UTSW |
14 |
21,719,332 (GRCm39) |
missense |
probably damaging |
1.00 |
R5653:Kat6b
|
UTSW |
14 |
21,719,440 (GRCm39) |
missense |
probably benign |
0.10 |
R5742:Kat6b
|
UTSW |
14 |
21,718,503 (GRCm39) |
missense |
probably damaging |
0.99 |
R5868:Kat6b
|
UTSW |
14 |
21,684,547 (GRCm39) |
missense |
probably damaging |
1.00 |
R5969:Kat6b
|
UTSW |
14 |
21,720,860 (GRCm39) |
missense |
probably damaging |
0.97 |
R6110:Kat6b
|
UTSW |
14 |
21,720,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6427:Kat6b
|
UTSW |
14 |
21,567,480 (GRCm39) |
missense |
probably benign |
0.24 |
R6457:Kat6b
|
UTSW |
14 |
21,720,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R6639:Kat6b
|
UTSW |
14 |
21,567,562 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6891:Kat6b
|
UTSW |
14 |
21,719,104 (GRCm39) |
missense |
probably benign |
0.01 |
R7784:Kat6b
|
UTSW |
14 |
21,710,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R7916:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R7977:Kat6b
|
UTSW |
14 |
21,719,931 (GRCm39) |
missense |
probably benign |
0.00 |
R7987:Kat6b
|
UTSW |
14 |
21,719,931 (GRCm39) |
missense |
probably benign |
0.00 |
R8167:Kat6b
|
UTSW |
14 |
21,719,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R8266:Kat6b
|
UTSW |
14 |
21,566,913 (GRCm39) |
start gained |
probably benign |
|
R8483:Kat6b
|
UTSW |
14 |
21,719,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Kat6b
|
UTSW |
14 |
21,719,629 (GRCm39) |
missense |
probably benign |
0.30 |
R8909:Kat6b
|
UTSW |
14 |
21,719,214 (GRCm39) |
missense |
probably benign |
|
R8931:Kat6b
|
UTSW |
14 |
21,674,995 (GRCm39) |
missense |
probably damaging |
0.98 |
R9112:Kat6b
|
UTSW |
14 |
21,675,256 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9182:Kat6b
|
UTSW |
14 |
21,567,187 (GRCm39) |
missense |
probably benign |
0.20 |
R9224:Kat6b
|
UTSW |
14 |
21,720,031 (GRCm39) |
missense |
probably benign |
0.14 |
R9273:Kat6b
|
UTSW |
14 |
21,711,551 (GRCm39) |
missense |
probably benign |
0.07 |
R9332:Kat6b
|
UTSW |
14 |
21,720,093 (GRCm39) |
missense |
probably benign |
0.00 |
R9380:Kat6b
|
UTSW |
14 |
21,678,926 (GRCm39) |
missense |
probably damaging |
1.00 |
R9397:Kat6b
|
UTSW |
14 |
21,675,244 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9400:Kat6b
|
UTSW |
14 |
21,659,826 (GRCm39) |
missense |
probably damaging |
0.99 |
R9432:Kat6b
|
UTSW |
14 |
21,672,077 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Kat6b
|
UTSW |
14 |
21,712,417 (GRCm39) |
small deletion |
probably benign |
|
R9526:Kat6b
|
UTSW |
14 |
21,567,564 (GRCm39) |
missense |
possibly damaging |
0.94 |
|