Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
G |
T |
16: 20,218,739 (GRCm39) |
N214K |
probably benign |
Het |
Abcf1 |
A |
G |
17: 36,274,459 (GRCm39) |
|
probably null |
Het |
Agxt2 |
A |
T |
15: 10,409,623 (GRCm39) |
M508L |
probably benign |
Het |
Akr1c21 |
A |
T |
13: 4,626,318 (GRCm39) |
Y114F |
probably benign |
Het |
Amz1 |
T |
C |
5: 140,729,941 (GRCm39) |
|
probably null |
Het |
Ank1 |
G |
T |
8: 23,622,646 (GRCm39) |
A1732S |
probably benign |
Het |
Atg16l1 |
T |
C |
1: 87,687,805 (GRCm39) |
S50P |
possibly damaging |
Het |
AW551984 |
A |
G |
9: 39,509,236 (GRCm39) |
S302P |
probably damaging |
Het |
Ccn6 |
T |
A |
10: 39,034,296 (GRCm39) |
Y102F |
probably damaging |
Het |
Ces3a |
T |
A |
8: 105,780,322 (GRCm39) |
|
probably null |
Het |
Dedd |
C |
A |
1: 171,167,881 (GRCm39) |
P185Q |
probably benign |
Het |
Fam186a |
A |
T |
15: 99,845,395 (GRCm39) |
V283E |
unknown |
Het |
Fat2 |
C |
A |
11: 55,194,479 (GRCm39) |
V1187F |
probably benign |
Het |
Fbxw11 |
T |
C |
11: 32,661,999 (GRCm39) |
|
probably null |
Het |
Fcgbp |
C |
T |
7: 27,802,401 (GRCm39) |
T1443I |
probably damaging |
Het |
Foxj2 |
A |
G |
6: 122,814,801 (GRCm39) |
D279G |
probably benign |
Het |
Gbp5 |
A |
G |
3: 142,207,122 (GRCm39) |
D97G |
probably damaging |
Het |
Gm49368 |
A |
T |
7: 127,707,154 (GRCm39) |
T661S |
possibly damaging |
Het |
Gria4 |
T |
G |
9: 4,513,330 (GRCm39) |
T260P |
probably damaging |
Het |
Gtf2ird2 |
T |
A |
5: 134,230,267 (GRCm39) |
D195E |
possibly damaging |
Het |
Hectd4 |
T |
A |
5: 121,496,196 (GRCm39) |
|
probably null |
Het |
Ifngr2 |
G |
A |
16: 91,354,797 (GRCm39) |
C32Y |
unknown |
Het |
Ikzf5 |
A |
T |
7: 130,993,788 (GRCm39) |
C280S |
probably benign |
Het |
Ints9 |
G |
T |
14: 65,263,914 (GRCm39) |
E395D |
probably null |
Het |
Isoc2b |
T |
C |
7: 4,854,084 (GRCm39) |
D96G |
probably benign |
Het |
Jmjd1c |
T |
G |
10: 67,061,092 (GRCm39) |
S967R |
probably benign |
Het |
Kcnj3 |
A |
T |
2: 55,327,338 (GRCm39) |
K42N |
probably benign |
Het |
Kiz |
T |
C |
2: 146,733,006 (GRCm39) |
V394A |
possibly damaging |
Het |
Lmntd2 |
A |
G |
7: 140,790,602 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
C |
A |
18: 77,500,001 (GRCm39) |
D1690E |
possibly damaging |
Het |
Lrp1b |
T |
C |
2: 41,234,588 (GRCm39) |
D1121G |
|
Het |
Map3k2 |
T |
C |
18: 32,333,015 (GRCm39) |
V63A |
possibly damaging |
Het |
Mcc |
G |
T |
18: 44,609,303 (GRCm39) |
A499D |
probably damaging |
Het |
Mcpt9 |
T |
A |
14: 56,264,400 (GRCm39) |
I232F |
probably damaging |
Het |
Meltf |
A |
G |
16: 31,700,756 (GRCm39) |
K92R |
probably benign |
Het |
Mff |
T |
A |
1: 82,723,159 (GRCm39) |
|
probably null |
Het |
Mrgpra3 |
T |
A |
7: 47,239,695 (GRCm39) |
Y77F |
probably damaging |
Het |
Mylk |
G |
A |
16: 34,734,446 (GRCm39) |
|
probably null |
Het |
Ndufv2 |
A |
G |
17: 66,394,532 (GRCm39) |
V111A |
possibly damaging |
Het |
Nkd2 |
T |
C |
13: 73,973,861 (GRCm39) |
E99G |
probably damaging |
Het |
Nlk |
C |
A |
11: 78,474,225 (GRCm39) |
G358V |
probably damaging |
Het |
Nnmt |
A |
T |
9: 48,503,532 (GRCm39) |
C165S |
probably damaging |
Het |
Nxpe4 |
T |
A |
9: 48,304,640 (GRCm39) |
C242* |
probably null |
Het |
Oas1b |
A |
T |
5: 120,955,705 (GRCm39) |
N162I |
probably damaging |
Het |
Or4s2 |
A |
G |
2: 88,473,554 (GRCm39) |
I148V |
probably benign |
Het |
Otog |
A |
G |
7: 45,916,700 (GRCm39) |
N879S |
probably damaging |
Het |
Pcsk7 |
T |
A |
9: 45,838,923 (GRCm39) |
Y612N |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Pgbd5 |
T |
C |
8: 125,160,750 (GRCm39) |
D39G |
probably benign |
Het |
Pkhd1l1 |
C |
T |
15: 44,368,581 (GRCm39) |
Q800* |
probably null |
Het |
Pkn3 |
T |
C |
2: 29,977,122 (GRCm39) |
S621P |
probably benign |
Het |
Polr3c |
T |
C |
3: 96,622,501 (GRCm39) |
I385V |
probably benign |
Het |
Ppp1r21 |
G |
T |
17: 88,863,031 (GRCm39) |
G257W |
probably benign |
Het |
Prkn |
A |
G |
17: 11,653,501 (GRCm39) |
D199G |
probably benign |
Het |
Pxylp1 |
C |
T |
9: 96,738,420 (GRCm39) |
|
probably null |
Het |
Rasgrp1 |
T |
C |
2: 117,116,589 (GRCm39) |
T613A |
probably benign |
Het |
Robo3 |
C |
T |
9: 37,336,674 (GRCm39) |
V387I |
probably benign |
Het |
Rxfp2 |
T |
A |
5: 149,973,046 (GRCm39) |
Y174N |
possibly damaging |
Het |
Sec24a |
T |
C |
11: 51,604,379 (GRCm39) |
M746V |
probably damaging |
Het |
Sema4f |
T |
A |
6: 82,891,355 (GRCm39) |
E571D |
possibly damaging |
Het |
Septin3 |
T |
C |
15: 82,170,657 (GRCm39) |
V217A |
probably benign |
Het |
Serpinb1b |
A |
C |
13: 33,277,548 (GRCm39) |
K260N |
probably benign |
Het |
Sin3b |
A |
G |
8: 73,476,500 (GRCm39) |
T645A |
possibly damaging |
Het |
Sobp |
C |
T |
10: 42,897,830 (GRCm39) |
R585Q |
probably damaging |
Het |
Specc1l |
T |
A |
10: 75,082,281 (GRCm39) |
L559Q |
possibly damaging |
Het |
Srxn1 |
C |
T |
2: 151,947,573 (GRCm39) |
|
probably benign |
Het |
Sspo |
G |
A |
6: 48,432,794 (GRCm39) |
R890Q |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,518,591 (GRCm39) |
D505G |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,972,087 (GRCm39) |
I653K |
probably damaging |
Het |
Tnks |
C |
T |
8: 35,298,866 (GRCm39) |
E1296K |
probably damaging |
Het |
Ttbk2 |
A |
T |
2: 120,579,121 (GRCm39) |
I667N |
probably benign |
Het |
Usp24 |
T |
C |
4: 106,199,550 (GRCm39) |
S165P |
possibly damaging |
Het |
Usp46 |
T |
A |
5: 74,189,598 (GRCm39) |
K109* |
probably null |
Het |
Vmn1r191 |
A |
G |
13: 22,362,942 (GRCm39) |
C271R |
probably benign |
Het |
Zfp592 |
T |
C |
7: 80,673,200 (GRCm39) |
S55P |
probably damaging |
Het |
Zmynd15 |
T |
C |
11: 70,351,867 (GRCm39) |
S158P |
probably benign |
Het |
Zscan22 |
T |
G |
7: 12,640,664 (GRCm39) |
C303G |
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 |
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 |
|