Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
A |
3: 137,770,909 (GRCm39) |
Q33K |
possibly damaging |
Het |
Acap2 |
A |
G |
16: 30,925,906 (GRCm39) |
L550P |
probably damaging |
Het |
Acsm3 |
A |
T |
7: 119,373,845 (GRCm39) |
S244C |
probably benign |
Het |
Adam28 |
T |
A |
14: 68,846,593 (GRCm39) |
D740V |
probably benign |
Het |
Adcy4 |
C |
A |
14: 56,016,426 (GRCm39) |
V342L |
probably damaging |
Het |
Adcyap1r1 |
A |
G |
6: 55,458,107 (GRCm39) |
T303A |
probably benign |
Het |
Agr2 |
T |
C |
12: 36,046,091 (GRCm39) |
V74A |
probably benign |
Het |
Akp3 |
A |
T |
1: 87,054,786 (GRCm39) |
T374S |
possibly damaging |
Het |
Ankrd36 |
A |
T |
11: 5,610,696 (GRCm39) |
I1181L |
probably benign |
Het |
Arhgap11a |
A |
T |
2: 113,664,411 (GRCm39) |
V624E |
probably benign |
Het |
Arhgap30 |
A |
T |
1: 171,228,258 (GRCm39) |
D112V |
probably damaging |
Het |
Atp8b4 |
A |
G |
2: 126,184,883 (GRCm39) |
F927L |
probably benign |
Het |
Bend4 |
C |
A |
5: 67,584,475 (GRCm39) |
G150C |
unknown |
Het |
Cd300lg |
T |
A |
11: 101,944,998 (GRCm39) |
S403T |
probably damaging |
Het |
Cep57l1 |
T |
A |
10: 41,607,086 (GRCm39) |
Q159L |
probably damaging |
Het |
Cipc |
C |
T |
12: 86,999,634 (GRCm39) |
T57M |
probably damaging |
Het |
Def8 |
T |
C |
8: 124,186,391 (GRCm39) |
C377R |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,720,746 (GRCm39) |
D1285G |
probably damaging |
Het |
Efcab10 |
A |
G |
12: 33,448,398 (GRCm39) |
D77G |
probably damaging |
Het |
Eml4 |
C |
T |
17: 83,764,479 (GRCm39) |
T663M |
probably damaging |
Het |
Ercc8 |
A |
G |
13: 108,320,389 (GRCm39) |
E325G |
possibly damaging |
Het |
Ermap |
C |
A |
4: 119,035,240 (GRCm39) |
A583S |
probably damaging |
Het |
F13a1 |
C |
T |
13: 37,102,506 (GRCm39) |
G406S |
probably null |
Het |
Faap20 |
T |
A |
4: 155,335,426 (GRCm39) |
C141S |
probably benign |
Het |
Fam193a |
A |
G |
5: 34,616,536 (GRCm39) |
T904A |
possibly damaging |
Het |
Garin2 |
T |
C |
12: 78,757,097 (GRCm39) |
F18S |
probably benign |
Het |
Gas8 |
A |
G |
8: 124,260,134 (GRCm39) |
D455G |
probably benign |
Het |
Gm21863 |
T |
C |
12: 20,004,521 (GRCm39) |
S6P |
probably damaging |
Het |
Gm4841 |
A |
T |
18: 60,403,988 (GRCm39) |
I35N |
probably damaging |
Het |
Grk4 |
T |
A |
5: 34,877,084 (GRCm39) |
C260S |
probably damaging |
Het |
Huwe1 |
G |
A |
X: 150,716,084 (GRCm39) |
R4331Q |
unknown |
Het |
Ighv5-6 |
A |
G |
12: 113,589,247 (GRCm39) |
Y78H |
probably benign |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Lyve1 |
C |
A |
7: 110,453,182 (GRCm39) |
C138F |
probably damaging |
Het |
Med27 |
G |
A |
2: 29,399,446 (GRCm39) |
W92* |
probably null |
Het |
Mical3 |
A |
T |
6: 120,986,848 (GRCm39) |
|
probably benign |
Het |
Mrgpra4 |
C |
A |
7: 47,631,208 (GRCm39) |
R131L |
possibly damaging |
Het |
Myf5 |
T |
C |
10: 107,321,308 (GRCm39) |
N162S |
probably benign |
Het |
Myh15 |
G |
A |
16: 49,007,433 (GRCm39) |
E1835K |
probably damaging |
Het |
Myo9a |
T |
A |
9: 59,716,757 (GRCm39) |
Y486N |
probably damaging |
Het |
Ncapg |
T |
A |
5: 45,853,115 (GRCm39) |
N860K |
probably benign |
Het |
Nr4a3 |
T |
C |
4: 48,052,194 (GRCm39) |
F316S |
possibly damaging |
Het |
Nsd3 |
T |
A |
8: 26,172,576 (GRCm39) |
S778R |
probably benign |
Het |
Or2r2 |
A |
G |
6: 42,463,795 (GRCm39) |
F111L |
probably damaging |
Het |
Or4c119 |
A |
T |
2: 88,986,988 (GRCm39) |
V177E |
probably benign |
Het |
Or4c31 |
A |
G |
2: 88,292,196 (GRCm39) |
I190V |
probably damaging |
Het |
Or5p6 |
A |
G |
7: 107,631,286 (GRCm39) |
F88S |
probably damaging |
Het |
Or7e173 |
T |
C |
9: 19,938,344 (GRCm39) |
N297D |
|
Het |
Or8b37 |
T |
A |
9: 37,958,885 (GRCm39) |
Y122* |
probably null |
Het |
Or8w1 |
A |
T |
2: 87,465,369 (GRCm39) |
C241S |
probably damaging |
Het |
Or9m2 |
A |
G |
2: 87,820,568 (GRCm39) |
T38A |
probably damaging |
Het |
Pdlim4 |
C |
T |
11: 53,946,280 (GRCm39) |
G231S |
probably benign |
Het |
Pknox2 |
C |
T |
9: 36,821,044 (GRCm39) |
V273I |
possibly damaging |
Het |
Pm20d1 |
A |
G |
1: 131,739,822 (GRCm39) |
H390R |
probably benign |
Het |
Prkg2 |
A |
T |
5: 99,114,386 (GRCm39) |
D587E |
probably benign |
Het |
Prps1l1 |
T |
A |
12: 35,035,546 (GRCm39) |
D220E |
possibly damaging |
Het |
Prss3l |
A |
G |
6: 41,422,990 (GRCm39) |
F4L |
probably benign |
Het |
Ptchd3 |
T |
C |
11: 121,721,682 (GRCm39) |
V185A |
possibly damaging |
Het |
Rag2 |
A |
T |
2: 101,460,494 (GRCm39) |
N268I |
possibly damaging |
Het |
Rarres2 |
A |
G |
6: 48,549,020 (GRCm39) |
|
probably null |
Het |
Rrp12 |
T |
C |
19: 41,860,223 (GRCm39) |
H1000R |
probably benign |
Het |
S100a2 |
A |
T |
3: 90,498,811 (GRCm39) |
Y104F |
unknown |
Het |
Sell |
A |
G |
1: 163,893,042 (GRCm39) |
Y86C |
probably damaging |
Het |
Serpinb6d |
A |
T |
13: 33,851,656 (GRCm39) |
T138S |
possibly damaging |
Het |
Slamf7 |
T |
A |
1: 171,466,312 (GRCm39) |
I228F |
probably benign |
Het |
Slc11a1 |
G |
A |
1: 74,416,325 (GRCm39) |
V92M |
probably damaging |
Het |
Spi1 |
A |
G |
2: 90,912,862 (GRCm39) |
N5S |
unknown |
Het |
Stard9 |
G |
T |
2: 120,536,283 (GRCm39) |
D4151Y |
probably damaging |
Het |
Stmnd1 |
A |
G |
13: 46,452,983 (GRCm39) |
T220A |
probably benign |
Het |
Tacc2 |
G |
T |
7: 130,225,266 (GRCm39) |
W650C |
probably damaging |
Het |
Tmc5 |
A |
G |
7: 118,241,594 (GRCm39) |
N429S |
possibly damaging |
Het |
Tmem201 |
A |
C |
4: 149,812,627 (GRCm39) |
L230V |
probably benign |
Het |
Tmem222 |
T |
C |
4: 132,997,119 (GRCm39) |
E94G |
possibly damaging |
Het |
Trappc4 |
A |
G |
9: 44,315,655 (GRCm39) |
F186S |
probably damaging |
Het |
Trim17 |
A |
G |
11: 58,862,273 (GRCm39) |
N435S |
probably benign |
Het |
Trim68 |
A |
T |
7: 102,329,447 (GRCm39) |
L227Q |
probably damaging |
Het |
Tuba3b |
T |
G |
6: 145,563,996 (GRCm39) |
V14G |
possibly damaging |
Het |
Ubr2 |
G |
T |
17: 47,245,041 (GRCm39) |
H1662N |
probably damaging |
Het |
Vps13c |
T |
A |
9: 67,861,863 (GRCm39) |
V2915E |
probably damaging |
Het |
Vsig10 |
C |
T |
5: 117,476,323 (GRCm39) |
T259I |
probably benign |
Het |
Zfp267 |
A |
G |
3: 36,219,066 (GRCm39) |
Y363C |
possibly damaging |
Het |
|
Other mutations in Kl |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00800:Kl
|
APN |
5 |
150,904,233 (GRCm39) |
nonsense |
probably null |
|
IGL00815:Kl
|
APN |
5 |
150,904,315 (GRCm39) |
missense |
possibly damaging |
0.55 |
IGL00840:Kl
|
APN |
5 |
150,904,252 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL01347:Kl
|
APN |
5 |
150,904,130 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01642:Kl
|
APN |
5 |
150,904,334 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL01774:Kl
|
APN |
5 |
150,911,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01937:Kl
|
APN |
5 |
150,912,402 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01945:Kl
|
APN |
5 |
150,912,402 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02510:Kl
|
APN |
5 |
150,912,466 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02696:Kl
|
APN |
5 |
150,904,450 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03028:Kl
|
APN |
5 |
150,915,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03149:Kl
|
APN |
5 |
150,906,200 (GRCm39) |
nonsense |
probably null |
|
anatolia
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
ararat
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
Turkic
|
UTSW |
5 |
150,876,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R0480:Kl
|
UTSW |
5 |
150,876,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R0565:Kl
|
UTSW |
5 |
150,904,409 (GRCm39) |
missense |
possibly damaging |
0.76 |
R0723:Kl
|
UTSW |
5 |
150,876,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R1052:Kl
|
UTSW |
5 |
150,905,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R1205:Kl
|
UTSW |
5 |
150,904,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Kl
|
UTSW |
5 |
150,912,062 (GRCm39) |
missense |
probably benign |
0.00 |
R1529:Kl
|
UTSW |
5 |
150,912,406 (GRCm39) |
missense |
probably benign |
|
R1588:Kl
|
UTSW |
5 |
150,906,097 (GRCm39) |
missense |
probably benign |
0.20 |
R1714:Kl
|
UTSW |
5 |
150,876,798 (GRCm39) |
missense |
probably benign |
0.05 |
R1748:Kl
|
UTSW |
5 |
150,904,450 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1885:Kl
|
UTSW |
5 |
150,876,959 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1920:Kl
|
UTSW |
5 |
150,906,132 (GRCm39) |
missense |
probably benign |
0.15 |
R2156:Kl
|
UTSW |
5 |
150,912,425 (GRCm39) |
missense |
probably benign |
0.41 |
R2926:Kl
|
UTSW |
5 |
150,876,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R4837:Kl
|
UTSW |
5 |
150,904,312 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5221:Kl
|
UTSW |
5 |
150,912,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R5687:Kl
|
UTSW |
5 |
150,911,931 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5726:Kl
|
UTSW |
5 |
150,915,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5727:Kl
|
UTSW |
5 |
150,915,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5735:Kl
|
UTSW |
5 |
150,915,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5797:Kl
|
UTSW |
5 |
150,915,003 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5933:Kl
|
UTSW |
5 |
150,912,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R6075:Kl
|
UTSW |
5 |
150,876,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6076:Kl
|
UTSW |
5 |
150,876,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6077:Kl
|
UTSW |
5 |
150,876,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6149:Kl
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6150:Kl
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6151:Kl
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6158:Kl
|
UTSW |
5 |
150,912,318 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6236:Kl
|
UTSW |
5 |
150,876,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R6609:Kl
|
UTSW |
5 |
150,912,427 (GRCm39) |
missense |
probably benign |
0.00 |
R7489:Kl
|
UTSW |
5 |
150,876,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R8406:Kl
|
UTSW |
5 |
150,906,229 (GRCm39) |
missense |
probably benign |
0.01 |
R9087:Kl
|
UTSW |
5 |
150,911,957 (GRCm39) |
missense |
probably benign |
0.19 |
R9380:Kl
|
UTSW |
5 |
150,912,342 (GRCm39) |
missense |
possibly damaging |
0.50 |
RF005:Kl
|
UTSW |
5 |
150,876,885 (GRCm39) |
missense |
probably benign |
0.07 |
RF024:Kl
|
UTSW |
5 |
150,876,885 (GRCm39) |
missense |
probably benign |
0.07 |
X0066:Kl
|
UTSW |
5 |
150,915,080 (GRCm39) |
nonsense |
probably null |
|
|