Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3425401B19Rik |
A |
G |
14: 32,385,788 (GRCm39) |
V59A |
probably benign |
Het |
Aatk |
A |
T |
11: 119,902,565 (GRCm39) |
H610Q |
probably benign |
Het |
Acox1 |
G |
A |
11: 116,071,867 (GRCm39) |
A187V |
probably damaging |
Het |
Acsbg3 |
A |
G |
17: 57,189,177 (GRCm39) |
Y195C |
probably benign |
Het |
AI661453 |
C |
T |
17: 47,757,570 (GRCm39) |
R76W |
probably damaging |
Het |
Anapc1 |
C |
T |
2: 128,500,221 (GRCm39) |
R808Q |
probably damaging |
Het |
Ankrd26 |
T |
C |
6: 118,500,067 (GRCm39) |
T1135A |
possibly damaging |
Het |
Arhgap17 |
A |
G |
7: 122,921,148 (GRCm39) |
V113A |
probably benign |
Het |
Art3 |
T |
C |
5: 92,562,138 (GRCm39) |
C379R |
unknown |
Het |
Bltp3a |
T |
C |
17: 28,105,799 (GRCm39) |
L775P |
probably damaging |
Het |
Bmp5 |
A |
G |
9: 75,800,982 (GRCm39) |
I371V |
probably damaging |
Het |
Ccdc88b |
T |
A |
19: 6,833,096 (GRCm39) |
E281V |
probably damaging |
Het |
Ces1e |
A |
T |
8: 93,946,031 (GRCm39) |
Y171N |
probably damaging |
Het |
Cib3 |
A |
T |
8: 72,961,034 (GRCm39) |
F68I |
possibly damaging |
Het |
Crtac1 |
A |
T |
19: 42,402,557 (GRCm39) |
L17Q |
possibly damaging |
Het |
Crybg3 |
A |
T |
16: 59,376,207 (GRCm39) |
S1682R |
probably benign |
Het |
Ddx60 |
G |
A |
8: 62,465,312 (GRCm39) |
G1323D |
probably damaging |
Het |
Dock3 |
A |
C |
9: 106,788,483 (GRCm39) |
D161E |
probably benign |
Het |
Dpep3 |
A |
C |
8: 106,705,369 (GRCm39) |
L127R |
probably damaging |
Het |
Dus2 |
A |
G |
8: 106,772,568 (GRCm39) |
D226G |
probably damaging |
Het |
Ebna1bp2 |
T |
C |
4: 118,480,821 (GRCm39) |
V184A |
possibly damaging |
Het |
Edem1 |
T |
A |
6: 108,823,648 (GRCm39) |
I348N |
probably damaging |
Het |
Efcab8 |
A |
T |
2: 153,656,362 (GRCm39) |
M599L |
unknown |
Het |
Eif2ak4 |
A |
T |
2: 118,261,313 (GRCm39) |
K618* |
probably null |
Het |
Fbxw27 |
T |
C |
9: 109,602,215 (GRCm39) |
K253E |
possibly damaging |
Het |
Fgf5 |
A |
G |
5: 98,423,113 (GRCm39) |
E166G |
possibly damaging |
Het |
Flot1 |
G |
T |
17: 36,141,555 (GRCm39) |
E321* |
probably null |
Het |
Gm14443 |
T |
C |
2: 175,012,248 (GRCm39) |
E66G |
probably benign |
Het |
Gprc6a |
G |
A |
10: 51,491,884 (GRCm39) |
P622S |
probably damaging |
Het |
Gsta2 |
A |
T |
9: 78,244,876 (GRCm39) |
Y79* |
probably null |
Het |
Hecw2 |
A |
G |
1: 53,904,287 (GRCm39) |
S1154P |
probably damaging |
Het |
Hrob |
A |
T |
11: 102,146,586 (GRCm39) |
Q287H |
possibly damaging |
Het |
Kcnd2 |
T |
C |
6: 21,216,367 (GRCm39) |
S24P |
probably benign |
Het |
L1td1 |
T |
C |
4: 98,624,753 (GRCm39) |
I316T |
probably benign |
Het |
Lrsam1 |
G |
T |
2: 32,818,077 (GRCm39) |
Q660K |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,548,153 (GRCm39) |
T6047S |
probably benign |
Het |
Muc16 |
T |
A |
9: 18,552,383 (GRCm39) |
T4637S |
probably benign |
Het |
Myo5a |
T |
C |
9: 75,078,914 (GRCm39) |
Y891H |
probably damaging |
Het |
Nkd2 |
G |
T |
13: 73,995,131 (GRCm39) |
D22E |
possibly damaging |
Het |
Patl2 |
A |
T |
2: 121,954,212 (GRCm39) |
V453E |
probably damaging |
Het |
Pcnx2 |
A |
G |
8: 126,488,313 (GRCm39) |
Y1744H |
probably damaging |
Het |
Phf8-ps |
T |
G |
17: 33,285,647 (GRCm39) |
N385T |
probably damaging |
Het |
Pira2 |
T |
A |
7: 3,845,517 (GRCm39) |
H289L |
possibly damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,158,117 (GRCm39) |
I569T |
probably benign |
Het |
Ppp4r4 |
T |
C |
12: 103,562,735 (GRCm39) |
V568A |
probably benign |
Het |
Ptf1a |
G |
A |
2: 19,451,062 (GRCm39) |
G131S |
probably benign |
Het |
Rasgrf2 |
G |
T |
13: 92,160,188 (GRCm39) |
H396N |
probably damaging |
Het |
Rfx1 |
C |
T |
8: 84,814,376 (GRCm39) |
T315M |
probably damaging |
Het |
Rnf207 |
C |
A |
4: 152,400,402 (GRCm39) |
R148L |
probably damaging |
Het |
Scn11a |
T |
G |
9: 119,584,181 (GRCm39) |
N1478T |
probably damaging |
Het |
Sdr39u1 |
C |
T |
14: 56,135,194 (GRCm39) |
V250I |
probably benign |
Het |
Serinc3 |
T |
C |
2: 163,471,095 (GRCm39) |
T276A |
probably damaging |
Het |
Speer4a3 |
AACT |
A |
5: 26,155,849 (GRCm39) |
|
probably benign |
Het |
Stambp |
C |
A |
6: 83,534,469 (GRCm39) |
A273S |
probably benign |
Het |
Taf2 |
T |
C |
15: 54,910,881 (GRCm39) |
|
probably null |
Het |
Tex26 |
A |
T |
5: 149,386,642 (GRCm39) |
Y232F |
probably damaging |
Het |
Tmem258 |
T |
C |
19: 10,184,578 (GRCm39) |
L55P |
probably damaging |
Het |
Trappc8 |
A |
G |
18: 20,979,630 (GRCm39) |
I755T |
possibly damaging |
Het |
Ubr4 |
T |
C |
4: 139,194,595 (GRCm39) |
Y1163H |
unknown |
Het |
Usp14 |
G |
A |
18: 10,005,630 (GRCm39) |
T254I |
probably benign |
Het |
Vcan |
A |
G |
13: 89,839,247 (GRCm39) |
L2099P |
probably benign |
Het |
Wdfy3 |
C |
T |
5: 102,042,866 (GRCm39) |
V1962I |
possibly damaging |
Het |
Zfp407 |
T |
C |
18: 84,577,574 (GRCm39) |
T1180A |
probably benign |
Het |
Zfp644 |
C |
A |
5: 106,784,691 (GRCm39) |
G619C |
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 |
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 |
R9782:Knl1
|
UTSW |
2 |
118,899,910 (GRCm39) |
missense |
probably benign |
0.02 |
|