Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
A |
G |
1: 183,765,828 (GRCm39) |
V77A |
probably benign |
Het |
Actl7a |
G |
A |
4: 56,744,135 (GRCm39) |
V221M |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Arhgef10 |
C |
T |
8: 15,006,987 (GRCm39) |
|
probably benign |
Het |
Asgr2 |
T |
C |
11: 69,989,123 (GRCm39) |
L86P |
possibly damaging |
Het |
Atp12a |
A |
G |
14: 56,624,308 (GRCm39) |
R919G |
probably benign |
Het |
Atrn |
A |
G |
2: 130,836,971 (GRCm39) |
Y1145C |
probably damaging |
Het |
B3gnt5 |
T |
G |
16: 19,588,294 (GRCm39) |
L171R |
probably benign |
Het |
Bbof1 |
T |
A |
12: 84,457,859 (GRCm39) |
N41K |
possibly damaging |
Het |
Bdp1 |
A |
T |
13: 100,235,097 (GRCm39) |
W166R |
probably benign |
Het |
Bean1 |
A |
T |
8: 104,937,742 (GRCm39) |
H107L |
possibly damaging |
Het |
Brd4 |
T |
C |
17: 32,417,060 (GRCm39) |
|
probably benign |
Het |
Cadps |
T |
C |
14: 12,465,859 (GRCm38) |
K1017R |
possibly damaging |
Het |
Cep78 |
G |
A |
19: 15,951,715 (GRCm39) |
|
probably benign |
Het |
Cfap70 |
C |
T |
14: 20,445,020 (GRCm39) |
A1087T |
probably damaging |
Het |
Cideb |
A |
G |
14: 55,992,700 (GRCm39) |
V72A |
probably benign |
Het |
Cpz |
T |
C |
5: 35,675,012 (GRCm39) |
E79G |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,873,544 (GRCm39) |
L1188P |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,911,425 (GRCm39) |
P518L |
probably benign |
Het |
Cyp2j5 |
A |
T |
4: 96,551,491 (GRCm39) |
N77K |
probably damaging |
Het |
Cyp4f39 |
T |
G |
17: 32,702,265 (GRCm39) |
F254C |
probably benign |
Het |
Dkk1 |
C |
A |
19: 30,524,731 (GRCm39) |
V225L |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,226,639 (GRCm39) |
Y421C |
probably damaging |
Het |
Dll3 |
T |
C |
7: 27,998,348 (GRCm39) |
T206A |
probably benign |
Het |
Dnhd1 |
T |
C |
7: 105,362,614 (GRCm39) |
C3766R |
probably benign |
Het |
Dock9 |
G |
T |
14: 121,820,792 (GRCm39) |
S1534Y |
probably damaging |
Het |
Dst |
T |
C |
1: 34,200,110 (GRCm39) |
V96A |
probably damaging |
Het |
F2r |
A |
G |
13: 95,740,698 (GRCm39) |
F279S |
probably damaging |
Het |
Farp1 |
C |
A |
14: 121,492,908 (GRCm39) |
N503K |
probably benign |
Het |
Fbxw2 |
G |
A |
2: 34,712,776 (GRCm39) |
T95I |
probably damaging |
Het |
Fis1 |
A |
G |
5: 136,994,461 (GRCm39) |
T50A |
probably benign |
Het |
Frzb |
T |
G |
2: 80,276,772 (GRCm39) |
E138A |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,817,164 (GRCm39) |
D4299V |
probably benign |
Het |
Fyco1 |
C |
T |
9: 123,659,478 (GRCm39) |
D233N |
probably damaging |
Het |
Gmpr |
A |
G |
13: 45,667,997 (GRCm39) |
|
probably benign |
Het |
Hc |
C |
T |
2: 34,919,407 (GRCm39) |
|
probably benign |
Het |
Hnrnpa1 |
T |
C |
15: 103,150,699 (GRCm39) |
M186T |
possibly damaging |
Het |
Klhl42 |
A |
G |
6: 147,009,427 (GRCm39) |
N422S |
probably damaging |
Het |
Kmt2d |
C |
G |
15: 98,753,471 (GRCm39) |
K127N |
probably damaging |
Het |
Kmt2d |
T |
A |
15: 98,753,472 (GRCm39) |
K127M |
probably damaging |
Het |
Krt39 |
T |
A |
11: 99,405,461 (GRCm39) |
T480S |
probably benign |
Het |
Lims2 |
T |
A |
18: 32,088,395 (GRCm39) |
C198* |
probably null |
Het |
Mctp1 |
A |
G |
13: 76,532,729 (GRCm39) |
N26D |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,931,538 (GRCm39) |
S168P |
probably benign |
Het |
Myo3a |
A |
G |
2: 22,455,008 (GRCm39) |
Y71C |
probably benign |
Het |
Nlrp9c |
T |
A |
7: 26,084,319 (GRCm39) |
D420V |
probably damaging |
Het |
Ntf3 |
A |
T |
6: 126,079,485 (GRCm39) |
I7N |
possibly damaging |
Het |
Or10ag52 |
G |
A |
2: 87,043,721 (GRCm39) |
G162S |
probably benign |
Het |
Or13c25 |
G |
T |
4: 52,910,849 (GRCm39) |
T315K |
probably benign |
Het |
Or4c119 |
A |
G |
2: 88,986,925 (GRCm39) |
V198A |
probably benign |
Het |
Or8b38 |
T |
C |
9: 37,972,981 (GRCm39) |
Y122H |
probably damaging |
Het |
Papln |
C |
A |
12: 83,836,028 (GRCm39) |
Y1222* |
probably null |
Het |
Pgm3 |
T |
G |
9: 86,440,531 (GRCm39) |
I387L |
possibly damaging |
Het |
Pira12 |
G |
C |
7: 3,900,871 (GRCm39) |
P20R |
probably damaging |
Het |
Pkd1 |
C |
A |
17: 24,814,131 (GRCm39) |
P4167Q |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,854,947 (GRCm39) |
V1174E |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,943,031 (GRCm39) |
N9D |
probably benign |
Het |
Prkaa2 |
G |
A |
4: 104,893,950 (GRCm39) |
Q456* |
probably null |
Het |
Ptch2 |
G |
T |
4: 116,965,858 (GRCm39) |
V425L |
probably benign |
Het |
Ptprh |
A |
T |
7: 4,552,394 (GRCm39) |
S957T |
probably benign |
Het |
Riok1 |
A |
G |
13: 38,241,177 (GRCm39) |
D444G |
probably benign |
Het |
Rrbp1 |
A |
T |
2: 143,830,211 (GRCm39) |
V652E |
probably benign |
Het |
Rrp36 |
C |
T |
17: 46,983,671 (GRCm39) |
R47Q |
possibly damaging |
Het |
Sec24c |
T |
C |
14: 20,736,955 (GRCm39) |
S304P |
probably damaging |
Het |
Serpinb6b |
A |
T |
13: 33,158,991 (GRCm39) |
D64V |
possibly damaging |
Het |
Serpinb9b |
A |
T |
13: 33,223,531 (GRCm39) |
|
probably null |
Het |
Six6 |
T |
A |
12: 72,988,538 (GRCm39) |
I237N |
probably damaging |
Het |
Slc25a36 |
A |
T |
9: 96,975,135 (GRCm39) |
M127K |
probably benign |
Het |
Slc2a10 |
A |
G |
2: 165,356,550 (GRCm39) |
D70G |
probably damaging |
Het |
Slc2a3 |
T |
A |
6: 122,713,700 (GRCm39) |
I171F |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,940,401 (GRCm39) |
T1087A |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,391,779 (GRCm39) |
Y242C |
probably damaging |
Het |
St14 |
A |
G |
9: 31,001,166 (GRCm39) |
V855A |
possibly damaging |
Het |
Stx2 |
G |
A |
5: 129,065,903 (GRCm39) |
T251M |
probably damaging |
Het |
Svs3b |
A |
T |
2: 164,097,848 (GRCm39) |
S158T |
probably benign |
Het |
Synpo |
C |
T |
18: 60,736,661 (GRCm39) |
M428I |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,626,612 (GRCm39) |
Y1113N |
possibly damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,775,760 (GRCm39) |
R17H |
probably damaging |
Het |
Tbl3 |
G |
A |
17: 24,923,477 (GRCm39) |
T284I |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,971,927 (GRCm39) |
T127A |
possibly damaging |
Het |
Tgoln1 |
T |
C |
6: 72,593,084 (GRCm39) |
E132G |
probably benign |
Het |
Timeless |
T |
C |
10: 128,077,583 (GRCm39) |
I221T |
probably damaging |
Het |
Tmem176b |
C |
T |
6: 48,815,138 (GRCm39) |
A52T |
possibly damaging |
Het |
Tmem192 |
C |
T |
8: 65,418,235 (GRCm39) |
L207F |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,176,996 (GRCm39) |
|
probably null |
Het |
Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
Tubb5 |
T |
C |
17: 36,146,190 (GRCm39) |
Y340C |
probably benign |
Het |
Ubr1 |
G |
A |
2: 120,761,449 (GRCm39) |
T576I |
probably benign |
Het |
Vcan |
T |
C |
13: 89,841,134 (GRCm39) |
E1470G |
probably damaging |
Het |
Vmn1r200 |
T |
A |
13: 22,579,663 (GRCm39) |
N146K |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,839 (GRCm39) |
I317F |
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,949,710 (GRCm39) |
I710T |
possibly damaging |
Het |
Wipf1 |
T |
A |
2: 73,270,499 (GRCm39) |
K61N |
probably benign |
Het |
Zfp112 |
T |
C |
7: 23,824,662 (GRCm39) |
V210A |
probably benign |
Het |
Zfp612 |
G |
A |
8: 110,815,095 (GRCm39) |
V101M |
probably benign |
Het |
Zfp637 |
A |
G |
6: 117,822,681 (GRCm39) |
R270G |
probably damaging |
Het |
Zfp652 |
A |
G |
11: 95,654,851 (GRCm39) |
E418G |
possibly damaging |
Het |
Zfp97 |
A |
G |
17: 17,365,265 (GRCm39) |
I255V |
probably benign |
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 |
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 |
R9026:Kl
|
UTSW |
5 |
150,876,491 (GRCm39) |
missense |
probably benign |
0.23 |
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 |
|
|