Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acad9 |
A |
T |
3: 36,136,324 (GRCm39) |
M370L |
probably benign |
Het |
Aimp1 |
A |
G |
3: 132,373,265 (GRCm39) |
M225T |
possibly damaging |
Het |
Atp8a1 |
T |
C |
5: 67,824,950 (GRCm39) |
I809V |
possibly damaging |
Het |
Bbs10 |
A |
G |
10: 111,135,622 (GRCm39) |
Y245C |
probably damaging |
Het |
Cabin1 |
A |
T |
10: 75,520,157 (GRCm39) |
F1572Y |
probably damaging |
Het |
Cd79a |
A |
G |
7: 24,598,772 (GRCm39) |
N107S |
possibly damaging |
Het |
Cdc7 |
G |
A |
5: 107,130,925 (GRCm39) |
A428T |
probably benign |
Het |
Cep290 |
A |
G |
10: 100,359,191 (GRCm39) |
T974A |
probably benign |
Het |
Cep350 |
A |
T |
1: 155,829,120 (GRCm39) |
N261K |
possibly damaging |
Het |
Cfap46 |
T |
A |
7: 139,241,001 (GRCm39) |
D8V |
probably damaging |
Het |
Col6a4 |
T |
C |
9: 105,952,185 (GRCm39) |
D571G |
probably damaging |
Het |
Cpe |
A |
C |
8: 65,070,645 (GRCm39) |
V200G |
probably benign |
Het |
Ctnnd1 |
C |
T |
2: 84,444,231 (GRCm39) |
|
probably null |
Het |
D5Ertd579e |
A |
C |
5: 36,772,921 (GRCm39) |
C491W |
probably damaging |
Het |
Dek |
A |
G |
13: 47,252,856 (GRCm39) |
I183T |
probably damaging |
Het |
Dennd1a |
A |
T |
2: 37,742,453 (GRCm39) |
H437Q |
possibly damaging |
Het |
Dido1 |
C |
T |
2: 180,302,940 (GRCm39) |
A1655T |
probably benign |
Het |
Eva1b |
A |
G |
4: 126,043,278 (GRCm39) |
D106G |
probably damaging |
Het |
Evc2 |
G |
T |
5: 37,581,923 (GRCm39) |
S1189I |
possibly damaging |
Het |
Faap100 |
A |
T |
11: 120,267,558 (GRCm39) |
L405Q |
probably damaging |
Het |
Fbxw15 |
T |
A |
9: 109,386,234 (GRCm39) |
M249L |
probably benign |
Het |
Gbp10 |
A |
T |
5: 105,366,326 (GRCm39) |
L526Q |
probably damaging |
Het |
Gm19402 |
A |
C |
10: 77,526,354 (GRCm39) |
|
probably benign |
Het |
Gm2244 |
A |
G |
14: 19,590,865 (GRCm39) |
Y141H |
probably damaging |
Het |
Gm4181 |
A |
T |
14: 51,870,666 (GRCm39) |
N98K |
probably damaging |
Het |
Golga4 |
C |
T |
9: 118,387,695 (GRCm39) |
R616* |
probably null |
Het |
Gpank1 |
T |
A |
17: 35,343,266 (GRCm39) |
S226T |
probably damaging |
Het |
Hipk3 |
T |
C |
2: 104,301,770 (GRCm39) |
M141V |
probably damaging |
Het |
Hoxc11 |
T |
C |
15: 102,863,178 (GRCm39) |
V73A |
probably benign |
Het |
Igf1r |
T |
G |
7: 67,653,885 (GRCm39) |
I141S |
possibly damaging |
Het |
Jak2 |
T |
A |
19: 29,273,059 (GRCm39) |
F628I |
probably benign |
Het |
Kcp |
C |
A |
6: 29,502,364 (GRCm39) |
V227L |
probably benign |
Het |
Larp6 |
A |
T |
9: 60,645,043 (GRCm39) |
R394S |
probably benign |
Het |
Lilra5 |
G |
A |
7: 4,245,114 (GRCm39) |
G253R |
probably damaging |
Het |
Map3k4 |
A |
G |
17: 12,482,945 (GRCm39) |
S591P |
probably damaging |
Het |
Mdfic2 |
T |
C |
6: 98,215,134 (GRCm39) |
D163G |
probably damaging |
Het |
Minar2 |
A |
G |
18: 59,205,296 (GRCm39) |
K28R |
probably benign |
Het |
Mrpl16 |
T |
A |
19: 11,750,332 (GRCm39) |
I72K |
probably damaging |
Het |
Nol11 |
C |
G |
11: 107,071,860 (GRCm39) |
R244S |
probably benign |
Het |
Nr2f1 |
T |
C |
13: 78,343,782 (GRCm39) |
T161A |
probably benign |
Het |
Nrdc |
G |
T |
4: 108,895,203 (GRCm39) |
V476F |
probably damaging |
Het |
Or10j7 |
G |
T |
1: 173,011,477 (GRCm39) |
H175N |
probably damaging |
Het |
Or10z1 |
A |
T |
1: 174,078,395 (GRCm39) |
S33T |
possibly damaging |
Het |
Or13a22 |
T |
A |
7: 140,072,626 (GRCm39) |
L25Q |
possibly damaging |
Het |
Or13m2-ps1 |
A |
T |
6: 42,777,843 (GRCm39) |
H56L |
probably benign |
Het |
P2rx1 |
A |
G |
11: 72,898,974 (GRCm39) |
I62V |
probably benign |
Het |
Pcdhgc5 |
A |
T |
18: 37,953,674 (GRCm39) |
Y316F |
probably benign |
Het |
Pecam1 |
T |
C |
11: 106,576,065 (GRCm39) |
D490G |
probably benign |
Het |
Pfkfb2 |
A |
T |
1: 130,635,299 (GRCm39) |
Y87* |
probably null |
Het |
Poldip2 |
A |
G |
11: 78,408,458 (GRCm39) |
|
probably null |
Het |
Ppp2r5b |
T |
A |
19: 6,280,566 (GRCm39) |
Q304L |
probably benign |
Het |
Pramel26 |
A |
G |
4: 143,542,609 (GRCm39) |
C4R |
probably damaging |
Het |
Psg26 |
A |
G |
7: 18,216,753 (GRCm39) |
F29L |
probably benign |
Het |
Ptk6 |
A |
T |
2: 180,838,886 (GRCm39) |
L289Q |
probably null |
Het |
Ptprt |
A |
T |
2: 161,743,417 (GRCm39) |
I508N |
possibly damaging |
Het |
Rasgrp4 |
T |
C |
7: 28,847,808 (GRCm39) |
F406S |
probably damaging |
Het |
Rspo3 |
A |
G |
10: 29,375,926 (GRCm39) |
|
probably null |
Het |
Septin8 |
G |
T |
11: 53,425,594 (GRCm39) |
|
probably null |
Het |
Sirt2 |
A |
C |
7: 28,487,471 (GRCm39) |
T345P |
probably benign |
Het |
Slc6a20b |
T |
C |
9: 123,438,161 (GRCm39) |
E205G |
possibly damaging |
Het |
Sqstm1 |
G |
A |
11: 50,093,418 (GRCm39) |
Q327* |
probably null |
Het |
Susd3 |
T |
A |
13: 49,390,997 (GRCm39) |
S98C |
probably damaging |
Het |
Tada2b |
G |
A |
5: 36,634,186 (GRCm39) |
R56W |
probably damaging |
Het |
Tbc1d2 |
A |
T |
4: 46,615,045 (GRCm39) |
V546E |
possibly damaging |
Het |
Tbx6 |
A |
G |
7: 126,380,740 (GRCm39) |
Q21R |
possibly damaging |
Het |
Usp24 |
T |
G |
4: 106,231,297 (GRCm39) |
|
probably null |
Het |
Vinac1 |
T |
G |
2: 128,879,719 (GRCm39) |
T736P |
possibly damaging |
Het |
Vmn2r103 |
A |
G |
17: 20,032,406 (GRCm39) |
T727A |
probably benign |
Het |
Wdr48 |
C |
T |
9: 119,749,676 (GRCm39) |
T531M |
probably damaging |
Het |
|
Other mutations in Knl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Knl1
|
APN |
2 |
118,894,564 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00582:Knl1
|
APN |
2 |
118,932,980 (GRCm39) |
missense |
probably benign |
0.19 |
IGL00666:Knl1
|
APN |
2 |
118,900,945 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01062:Knl1
|
APN |
2 |
118,907,461 (GRCm39) |
missense |
probably benign |
0.33 |
IGL01395:Knl1
|
APN |
2 |
118,902,047 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01604:Knl1
|
APN |
2 |
118,900,482 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01996:Knl1
|
APN |
2 |
118,934,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02086:Knl1
|
APN |
2 |
118,931,255 (GRCm39) |
missense |
probably benign |
0.40 |
IGL02105:Knl1
|
APN |
2 |
118,902,289 (GRCm39) |
missense |
probably benign |
|
IGL02106:Knl1
|
APN |
2 |
118,902,489 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02201:Knl1
|
APN |
2 |
118,899,633 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02252:Knl1
|
APN |
2 |
118,903,021 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02414:Knl1
|
APN |
2 |
118,900,804 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL02655:Knl1
|
APN |
2 |
118,901,473 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02682:Knl1
|
APN |
2 |
118,908,450 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02710:Knl1
|
APN |
2 |
118,901,411 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02877:Knl1
|
APN |
2 |
118,919,312 (GRCm39) |
missense |
probably benign |
0.08 |
IGL03100:Knl1
|
APN |
2 |
118,931,251 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03210:Knl1
|
APN |
2 |
118,901,098 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03138:Knl1
|
UTSW |
2 |
118,902,840 (GRCm39) |
missense |
probably damaging |
0.96 |
R0023:Knl1
|
UTSW |
2 |
118,933,030 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0064:Knl1
|
UTSW |
2 |
118,906,724 (GRCm39) |
missense |
probably benign |
0.00 |
R0064:Knl1
|
UTSW |
2 |
118,906,724 (GRCm39) |
missense |
probably benign |
0.00 |
R0078:Knl1
|
UTSW |
2 |
118,900,373 (GRCm39) |
missense |
probably benign |
0.16 |
R0178:Knl1
|
UTSW |
2 |
118,888,886 (GRCm39) |
splice site |
probably benign |
|
R0295:Knl1
|
UTSW |
2 |
118,919,320 (GRCm39) |
missense |
probably damaging |
1.00 |
R0433:Knl1
|
UTSW |
2 |
118,934,542 (GRCm39) |
missense |
probably damaging |
0.96 |
R0453:Knl1
|
UTSW |
2 |
118,898,869 (GRCm39) |
missense |
probably damaging |
1.00 |
R0569:Knl1
|
UTSW |
2 |
118,927,916 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0827:Knl1
|
UTSW |
2 |
118,919,382 (GRCm39) |
splice site |
probably benign |
|
R0920:Knl1
|
UTSW |
2 |
118,900,309 (GRCm39) |
missense |
probably benign |
0.00 |
R1120:Knl1
|
UTSW |
2 |
118,892,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R1155:Knl1
|
UTSW |
2 |
118,901,635 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1204:Knl1
|
UTSW |
2 |
118,901,670 (GRCm39) |
missense |
probably benign |
0.00 |
R1241:Knl1
|
UTSW |
2 |
118,903,054 (GRCm39) |
missense |
probably benign |
0.03 |
R1387:Knl1
|
UTSW |
2 |
118,901,211 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1448:Knl1
|
UTSW |
2 |
118,898,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1469:Knl1
|
UTSW |
2 |
118,901,827 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1469:Knl1
|
UTSW |
2 |
118,901,827 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1719:Knl1
|
UTSW |
2 |
118,902,219 (GRCm39) |
missense |
probably benign |
0.01 |
R1721:Knl1
|
UTSW |
2 |
118,906,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R2128:Knl1
|
UTSW |
2 |
118,902,300 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2170:Knl1
|
UTSW |
2 |
118,918,075 (GRCm39) |
critical splice donor site |
probably null |
|
R2227:Knl1
|
UTSW |
2 |
118,902,481 (GRCm39) |
missense |
probably damaging |
0.97 |
R2246:Knl1
|
UTSW |
2 |
118,902,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R2275:Knl1
|
UTSW |
2 |
118,902,762 (GRCm39) |
missense |
probably damaging |
0.99 |
R2508:Knl1
|
UTSW |
2 |
118,888,849 (GRCm39) |
nonsense |
probably null |
|
R3115:Knl1
|
UTSW |
2 |
118,900,872 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3122:Knl1
|
UTSW |
2 |
118,899,425 (GRCm39) |
missense |
probably benign |
0.32 |
R3431:Knl1
|
UTSW |
2 |
118,892,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R3755:Knl1
|
UTSW |
2 |
118,933,060 (GRCm39) |
missense |
probably damaging |
1.00 |
R4461:Knl1
|
UTSW |
2 |
118,890,080 (GRCm39) |
missense |
probably benign |
0.00 |
R4600:Knl1
|
UTSW |
2 |
118,901,025 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4713:Knl1
|
UTSW |
2 |
118,899,618 (GRCm39) |
nonsense |
probably null |
|
R4758:Knl1
|
UTSW |
2 |
118,902,213 (GRCm39) |
frame shift |
probably null |
|
R4762:Knl1
|
UTSW |
2 |
118,902,417 (GRCm39) |
missense |
probably benign |
0.01 |
R4869:Knl1
|
UTSW |
2 |
118,902,832 (GRCm39) |
missense |
possibly damaging |
0.73 |
R4870:Knl1
|
UTSW |
2 |
118,911,994 (GRCm39) |
missense |
probably benign |
0.22 |
R4935:Knl1
|
UTSW |
2 |
118,899,438 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5167:Knl1
|
UTSW |
2 |
118,900,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5184:Knl1
|
UTSW |
2 |
118,899,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R5293:Knl1
|
UTSW |
2 |
118,900,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R5326:Knl1
|
UTSW |
2 |
118,898,829 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5331:Knl1
|
UTSW |
2 |
118,900,736 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5353:Knl1
|
UTSW |
2 |
118,901,464 (GRCm39) |
missense |
probably benign |
0.01 |
R5493:Knl1
|
UTSW |
2 |
118,899,211 (GRCm39) |
missense |
probably damaging |
0.98 |
R5542:Knl1
|
UTSW |
2 |
118,898,829 (GRCm39) |
missense |
possibly damaging |
0.66 |
R5632:Knl1
|
UTSW |
2 |
118,900,833 (GRCm39) |
missense |
probably damaging |
1.00 |
R5650:Knl1
|
UTSW |
2 |
118,912,031 (GRCm39) |
nonsense |
probably null |
|
R5854:Knl1
|
UTSW |
2 |
118,900,884 (GRCm39) |
missense |
probably benign |
0.02 |
R5979:Knl1
|
UTSW |
2 |
118,899,841 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6086:Knl1
|
UTSW |
2 |
118,924,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Knl1
|
UTSW |
2 |
118,900,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R6313:Knl1
|
UTSW |
2 |
118,899,799 (GRCm39) |
missense |
probably damaging |
1.00 |
R6419:Knl1
|
UTSW |
2 |
118,899,484 (GRCm39) |
missense |
probably benign |
0.02 |
R6608:Knl1
|
UTSW |
2 |
118,917,093 (GRCm39) |
missense |
probably damaging |
0.99 |
R6881:Knl1
|
UTSW |
2 |
118,925,665 (GRCm39) |
missense |
possibly damaging |
0.67 |
R7161:Knl1
|
UTSW |
2 |
118,901,266 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7206:Knl1
|
UTSW |
2 |
118,899,780 (GRCm39) |
missense |
probably benign |
0.35 |
R7270:Knl1
|
UTSW |
2 |
118,933,003 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7276:Knl1
|
UTSW |
2 |
118,902,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R7358:Knl1
|
UTSW |
2 |
118,901,040 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7402:Knl1
|
UTSW |
2 |
118,925,707 (GRCm39) |
nonsense |
probably null |
|
R7408:Knl1
|
UTSW |
2 |
118,901,073 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7475:Knl1
|
UTSW |
2 |
118,918,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R7516:Knl1
|
UTSW |
2 |
118,901,179 (GRCm39) |
missense |
probably damaging |
0.99 |
R7524:Knl1
|
UTSW |
2 |
118,896,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R7559:Knl1
|
UTSW |
2 |
118,924,487 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7607:Knl1
|
UTSW |
2 |
118,925,614 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7745:Knl1
|
UTSW |
2 |
118,902,037 (GRCm39) |
missense |
probably benign |
0.13 |
R7847:Knl1
|
UTSW |
2 |
118,901,457 (GRCm39) |
missense |
probably benign |
0.02 |
R8423:Knl1
|
UTSW |
2 |
118,900,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Knl1
|
UTSW |
2 |
118,899,524 (GRCm39) |
missense |
probably benign |
0.34 |
R8727:Knl1
|
UTSW |
2 |
118,899,524 (GRCm39) |
missense |
probably benign |
0.34 |
R8995:Knl1
|
UTSW |
2 |
118,902,990 (GRCm39) |
missense |
probably benign |
0.11 |
R9023:Knl1
|
UTSW |
2 |
118,900,761 (GRCm39) |
missense |
probably benign |
0.27 |
R9100:Knl1
|
UTSW |
2 |
118,899,469 (GRCm39) |
missense |
probably benign |
0.02 |
R9102:Knl1
|
UTSW |
2 |
118,917,973 (GRCm39) |
missense |
probably benign |
0.22 |
R9303:Knl1
|
UTSW |
2 |
118,898,829 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9400:Knl1
|
UTSW |
2 |
118,931,224 (GRCm39) |
missense |
probably damaging |
0.98 |
R9426:Knl1
|
UTSW |
2 |
118,899,979 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9583:Knl1
|
UTSW |
2 |
118,887,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Knl1
|
UTSW |
2 |
118,907,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R9616:Knl1
|
UTSW |
2 |
118,899,994 (GRCm39) |
missense |
probably benign |
0.02 |
R9671:Knl1
|
UTSW |
2 |
118,901,089 (GRCm39) |
missense |
probably damaging |
1.00 |
R9766:Knl1
|
UTSW |
2 |
118,900,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Knl1
|
UTSW |
2 |
118,899,910 (GRCm39) |
missense |
probably benign |
0.02 |
|