Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcd4 |
T |
C |
12: 84,664,076 (GRCm39) |
T7A |
probably benign |
Het |
Adam33 |
T |
G |
2: 130,895,362 (GRCm39) |
D619A |
probably damaging |
Het |
Ajm1 |
T |
C |
2: 25,469,276 (GRCm39) |
T212A |
probably benign |
Het |
Aldh3b3 |
C |
T |
19: 4,018,522 (GRCm39) |
|
probably benign |
Het |
Arhgef15 |
G |
A |
11: 68,844,877 (GRCm39) |
P240L |
probably benign |
Het |
Arhgef40 |
C |
A |
14: 52,231,795 (GRCm39) |
T727K |
probably damaging |
Het |
Arrdc1 |
T |
C |
2: 24,817,840 (GRCm39) |
T43A |
probably benign |
Het |
Bcl2l15 |
A |
G |
3: 103,743,378 (GRCm39) |
N93S |
probably benign |
Het |
Cd5l |
G |
T |
3: 87,273,414 (GRCm39) |
E128* |
probably null |
Het |
Cep97 |
T |
C |
16: 55,735,946 (GRCm39) |
D284G |
probably benign |
Het |
Ckmt1 |
T |
A |
2: 121,191,073 (GRCm39) |
S162T |
probably damaging |
Het |
Clock |
G |
A |
5: 76,378,185 (GRCm39) |
P572S |
probably benign |
Het |
Cpeb4 |
A |
G |
11: 31,839,877 (GRCm39) |
D53G |
probably damaging |
Het |
Crocc2 |
T |
A |
1: 93,145,575 (GRCm39) |
S1485R |
probably damaging |
Het |
Dcaf5 |
G |
A |
12: 80,444,526 (GRCm39) |
A189V |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,111,936 (GRCm39) |
G1355S |
probably damaging |
Het |
Fam120b |
C |
T |
17: 15,623,344 (GRCm39) |
P441S |
probably benign |
Het |
Fbxo41 |
A |
G |
6: 85,461,486 (GRCm39) |
L74P |
probably damaging |
Het |
H2-DMa |
A |
G |
17: 34,356,975 (GRCm39) |
T158A |
probably benign |
Het |
Hcar2 |
T |
A |
5: 124,002,532 (GRCm39) |
T324S |
probably benign |
Het |
Hif3a |
T |
C |
7: 16,784,580 (GRCm39) |
I222V |
possibly damaging |
Het |
Ighv1-7 |
A |
G |
12: 114,502,501 (GRCm39) |
|
probably benign |
Het |
Il20 |
T |
C |
1: 130,835,165 (GRCm39) |
E151G |
probably benign |
Het |
Jarid2 |
A |
G |
13: 45,049,766 (GRCm39) |
E236G |
probably damaging |
Het |
Lamc2 |
T |
C |
1: 153,007,636 (GRCm39) |
Y846C |
probably damaging |
Het |
Lrp5 |
A |
G |
19: 3,672,512 (GRCm39) |
V599A |
probably benign |
Het |
Lrrc8b |
T |
A |
5: 105,628,163 (GRCm39) |
S170T |
possibly damaging |
Het |
Mex3d |
T |
C |
10: 80,218,428 (GRCm39) |
K263R |
probably damaging |
Het |
Mtor |
A |
G |
4: 148,553,463 (GRCm39) |
K784E |
possibly damaging |
Het |
Naip5 |
C |
A |
13: 100,367,170 (GRCm39) |
|
probably null |
Het |
Ncor1 |
T |
C |
11: 62,229,060 (GRCm39) |
T609A |
possibly damaging |
Het |
Ndufs1 |
C |
T |
1: 63,189,218 (GRCm39) |
A536T |
probably benign |
Het |
Neto1 |
A |
G |
18: 86,516,768 (GRCm39) |
I362V |
probably benign |
Het |
Nfatc3 |
T |
C |
8: 106,805,689 (GRCm39) |
L178P |
probably damaging |
Het |
Npdc1 |
G |
A |
2: 25,298,957 (GRCm39) |
D284N |
probably damaging |
Het |
Nsd3 |
C |
T |
8: 26,169,985 (GRCm39) |
T707M |
probably benign |
Het |
Or51f2 |
A |
C |
7: 102,527,004 (GRCm39) |
S226R |
probably benign |
Het |
Or5w1b |
A |
T |
2: 87,475,573 (GRCm39) |
V298E |
probably damaging |
Het |
Or9g19 |
T |
C |
2: 85,600,613 (GRCm39) |
V156A |
probably benign |
Het |
Pcnx1 |
T |
A |
12: 81,964,504 (GRCm39) |
S224T |
probably damaging |
Het |
Peak1 |
T |
C |
9: 56,165,058 (GRCm39) |
T957A |
probably damaging |
Het |
Pex7 |
A |
T |
10: 19,764,483 (GRCm39) |
D153E |
probably damaging |
Het |
Plscr1 |
A |
G |
9: 92,148,477 (GRCm39) |
E139G |
probably damaging |
Het |
Psmb8 |
T |
C |
17: 34,420,214 (GRCm39) |
Y269H |
probably benign |
Het |
Rmc1 |
T |
C |
18: 12,304,640 (GRCm39) |
F72L |
possibly damaging |
Het |
Secisbp2l |
C |
T |
2: 125,582,657 (GRCm39) |
G933D |
possibly damaging |
Het |
Sft2d2 |
T |
C |
1: 165,012,657 (GRCm39) |
T80A |
probably damaging |
Het |
Slc12a5 |
A |
G |
2: 164,829,141 (GRCm39) |
I583M |
possibly damaging |
Het |
Slc23a4 |
T |
C |
6: 34,933,957 (GRCm39) |
M49V |
probably benign |
Het |
Smarcb1 |
G |
A |
10: 75,740,252 (GRCm39) |
Q309* |
probably null |
Het |
Sphkap |
A |
T |
1: 83,256,006 (GRCm39) |
V294E |
probably benign |
Het |
Stoml1 |
C |
A |
9: 58,160,653 (GRCm39) |
P35Q |
probably damaging |
Het |
Timm10b |
G |
C |
7: 105,290,329 (GRCm39) |
R42P |
probably damaging |
Het |
Tnfrsf8 |
A |
T |
4: 145,019,203 (GRCm39) |
S211T |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,536,164 (GRCm39) |
T26738A |
probably damaging |
Het |
Vps13d |
A |
T |
4: 144,801,452 (GRCm39) |
Y474N |
probably damaging |
Het |
Wdr81 |
A |
T |
11: 75,336,732 (GRCm39) |
F1552L |
probably damaging |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Wnt7a |
A |
C |
6: 91,371,637 (GRCm39) |
Y108* |
probably null |
Het |
Zfp512b |
C |
T |
2: 181,227,461 (GRCm39) |
R56K |
probably benign |
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 |
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 |
R6285:Knl1
|
UTSW |
2 |
118,902,422 (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 |
|