Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610318N02Rik |
G |
A |
16: 16,936,259 (GRCm39) |
P155L |
probably benign |
Het |
Ankrd6 |
A |
T |
4: 32,816,949 (GRCm39) |
Y393N |
possibly damaging |
Het |
Arhgap45 |
A |
G |
10: 79,865,016 (GRCm39) |
Q993R |
probably benign |
Het |
Arhgef33 |
G |
C |
17: 80,654,549 (GRCm39) |
|
probably null |
Het |
B4galnt3 |
T |
C |
6: 120,192,392 (GRCm39) |
D448G |
probably benign |
Het |
Capn1 |
C |
G |
19: 6,043,938 (GRCm39) |
E564D |
possibly damaging |
Het |
Ccdc85a |
A |
G |
11: 28,349,384 (GRCm39) |
S474P |
probably benign |
Het |
Cdk12 |
T |
A |
11: 98,140,626 (GRCm39) |
L1289* |
probably null |
Het |
Cramp1 |
A |
T |
17: 25,193,719 (GRCm39) |
N920K |
possibly damaging |
Het |
Cubn |
C |
T |
2: 13,345,143 (GRCm39) |
S2091N |
probably damaging |
Het |
Ddx1 |
A |
T |
12: 13,273,960 (GRCm39) |
I581N |
probably damaging |
Het |
Dnm2 |
A |
T |
9: 21,396,983 (GRCm39) |
N487Y |
probably damaging |
Het |
Enc1 |
A |
C |
13: 97,381,601 (GRCm39) |
N37T |
probably damaging |
Het |
Ephb3 |
T |
G |
16: 21,040,976 (GRCm39) |
I932S |
probably benign |
Het |
Frk |
T |
A |
10: 34,467,934 (GRCm39) |
M316K |
probably damaging |
Het |
Gdap2 |
C |
T |
3: 100,109,349 (GRCm39) |
R25C |
unknown |
Het |
Gpat2 |
T |
A |
2: 127,276,810 (GRCm39) |
D671E |
probably damaging |
Het |
Gpr179 |
C |
T |
11: 97,229,672 (GRCm39) |
E828K |
probably benign |
Het |
Greb1l |
T |
C |
18: 10,538,142 (GRCm39) |
Y1052H |
probably damaging |
Het |
Gtf2f1 |
C |
T |
17: 57,314,833 (GRCm39) |
S69N |
probably damaging |
Het |
Hid1 |
A |
C |
11: 115,239,308 (GRCm39) |
I785S |
probably damaging |
Het |
Hmcn2 |
T |
C |
2: 31,233,093 (GRCm39) |
I214T |
probably damaging |
Het |
Hsd3b5 |
G |
T |
3: 98,527,085 (GRCm39) |
F120L |
probably damaging |
Het |
Kif16b |
C |
T |
2: 142,554,851 (GRCm39) |
R649Q |
probably benign |
Het |
Kif17 |
A |
T |
4: 137,989,954 (GRCm39) |
E47D |
probably benign |
Het |
Kmt2b |
T |
C |
7: 30,279,896 (GRCm39) |
H1368R |
probably damaging |
Het |
Kmt2d |
A |
T |
15: 98,747,299 (GRCm39) |
S3342T |
unknown |
Het |
Krt82 |
A |
G |
15: 101,451,342 (GRCm39) |
C356R |
probably damaging |
Het |
Lrit2 |
A |
G |
14: 36,794,156 (GRCm39) |
K407E |
probably benign |
Het |
Malt1 |
T |
A |
18: 65,584,640 (GRCm39) |
H325Q |
possibly damaging |
Het |
Mccc2 |
T |
G |
13: 100,125,108 (GRCm39) |
D187A |
possibly damaging |
Het |
Mgll |
T |
A |
6: 88,791,103 (GRCm39) |
|
probably null |
Het |
Mindy2 |
T |
G |
9: 70,518,241 (GRCm39) |
E449A |
possibly damaging |
Het |
Muc5b |
G |
A |
7: 141,396,031 (GRCm39) |
V96M |
unknown |
Het |
Nlrp4e |
A |
G |
7: 23,020,953 (GRCm39) |
E480G |
probably benign |
Het |
Nup98 |
A |
G |
7: 101,784,002 (GRCm39) |
I1093T |
probably benign |
Het |
Or13a26 |
G |
A |
7: 140,285,060 (GRCm39) |
V299I |
probably benign |
Het |
Or1j4 |
G |
A |
2: 36,740,137 (GRCm39) |
M26I |
probably benign |
Het |
Or4g7 |
A |
T |
2: 111,309,105 (GRCm39) |
|
probably benign |
Het |
Or52a20 |
G |
T |
7: 103,366,173 (GRCm39) |
R124L |
probably damaging |
Het |
Pcdhb6 |
A |
T |
18: 37,468,531 (GRCm39) |
H484L |
probably benign |
Het |
Phldb1 |
T |
C |
9: 44,605,344 (GRCm39) |
T604A |
possibly damaging |
Het |
Pitpnm3 |
G |
T |
11: 71,961,790 (GRCm39) |
A275D |
probably damaging |
Het |
Polr2a |
A |
T |
11: 69,638,118 (GRCm39) |
|
probably null |
Het |
Polr3a |
A |
G |
14: 24,510,055 (GRCm39) |
C960R |
probably benign |
Het |
Pou6f2 |
G |
A |
13: 18,414,298 (GRCm39) |
A159V |
|
Het |
Pramel11 |
A |
C |
4: 143,623,345 (GRCm39) |
Y276* |
probably null |
Het |
Pramel51 |
A |
C |
12: 88,148,519 (GRCm39) |
C32W |
probably damaging |
Het |
Psmc4 |
A |
G |
7: 27,742,085 (GRCm39) |
V303A |
probably benign |
Het |
Ptdss2 |
A |
G |
7: 140,731,645 (GRCm39) |
N151S |
possibly damaging |
Het |
Ptprk |
T |
A |
10: 28,465,004 (GRCm39) |
Y1295* |
probably null |
Het |
Rbm19 |
A |
G |
5: 120,324,283 (GRCm39) |
K881E |
possibly damaging |
Het |
Rcan2 |
T |
A |
17: 44,331,993 (GRCm39) |
Y183* |
probably null |
Het |
Rnd1 |
T |
C |
15: 98,568,680 (GRCm39) |
E166G |
probably damaging |
Het |
Rnf113a2 |
T |
A |
12: 84,464,953 (GRCm39) |
C282S |
probably damaging |
Het |
S100b |
G |
A |
10: 76,092,926 (GRCm39) |
G20R |
probably benign |
Het |
Sae1 |
G |
T |
7: 16,102,469 (GRCm39) |
Y168* |
probably null |
Het |
Samd9l |
C |
A |
6: 3,372,600 (GRCm39) |
G1554* |
probably null |
Het |
Samhd1 |
T |
C |
2: 156,976,940 (GRCm39) |
S55G |
probably benign |
Het |
Sgsm1 |
T |
C |
5: 113,421,512 (GRCm39) |
D525G |
probably benign |
Het |
Slc28a3 |
A |
T |
13: 58,710,986 (GRCm39) |
M512K |
probably damaging |
Het |
Slc9b2 |
T |
A |
3: 135,024,151 (GRCm39) |
N67K |
probably benign |
Het |
Smarca4 |
T |
A |
9: 21,550,096 (GRCm39) |
I402N |
probably damaging |
Het |
St7l |
T |
C |
3: 104,796,669 (GRCm39) |
F261L |
probably benign |
Het |
Syde2 |
T |
A |
3: 145,721,553 (GRCm39) |
V1140D |
probably damaging |
Het |
Syt6 |
T |
A |
3: 103,494,788 (GRCm39) |
I251N |
probably damaging |
Het |
Taok2 |
T |
C |
7: 126,465,990 (GRCm39) |
E916G |
probably damaging |
Het |
Tecta |
A |
G |
9: 42,289,288 (GRCm39) |
S426P |
probably damaging |
Het |
Thra |
T |
C |
11: 98,655,134 (GRCm39) |
I338T |
probably damaging |
Het |
Trub1 |
A |
T |
19: 57,461,135 (GRCm39) |
Y137F |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,841,691 (GRCm39) |
F2574L |
probably benign |
Het |
Ythdf3 |
T |
C |
3: 16,237,664 (GRCm39) |
S2P |
possibly damaging |
Het |
Zc3h13 |
T |
A |
14: 75,567,981 (GRCm39) |
D1091E |
probably damaging |
Het |
Zdhhc6 |
A |
G |
19: 55,301,682 (GRCm39) |
Y100H |
probably damaging |
Het |
|
Other mutations in Adamts12 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Adamts12
|
APN |
15 |
11,311,685 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00513:Adamts12
|
APN |
15 |
11,257,047 (GRCm39) |
missense |
probably benign |
0.28 |
IGL00579:Adamts12
|
APN |
15 |
11,152,100 (GRCm39) |
missense |
probably benign |
0.20 |
IGL00984:Adamts12
|
APN |
15 |
11,215,696 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01307:Adamts12
|
APN |
15 |
11,237,632 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL01314:Adamts12
|
APN |
15 |
11,071,939 (GRCm39) |
missense |
probably benign |
0.30 |
IGL01353:Adamts12
|
APN |
15 |
11,292,091 (GRCm39) |
splice site |
probably benign |
|
IGL01373:Adamts12
|
APN |
15 |
11,310,816 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01522:Adamts12
|
APN |
15 |
11,065,245 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01589:Adamts12
|
APN |
15 |
11,311,323 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01715:Adamts12
|
APN |
15 |
11,258,182 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL01966:Adamts12
|
APN |
15 |
11,258,269 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01994:Adamts12
|
APN |
15 |
11,345,680 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Adamts12
|
APN |
15 |
11,215,696 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02216:Adamts12
|
APN |
15 |
11,241,571 (GRCm39) |
missense |
possibly damaging |
0.63 |
IGL02252:Adamts12
|
APN |
15 |
11,311,101 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02336:Adamts12
|
APN |
15 |
11,311,331 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02445:Adamts12
|
APN |
15 |
11,286,798 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03115:Adamts12
|
APN |
15 |
11,263,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03131:Adamts12
|
APN |
15 |
11,345,650 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03161:Adamts12
|
APN |
15 |
11,292,168 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03403:Adamts12
|
APN |
15 |
11,241,574 (GRCm39) |
missense |
probably damaging |
1.00 |
I2289:Adamts12
|
UTSW |
15 |
11,071,894 (GRCm39) |
missense |
probably benign |
0.13 |
PIT4677001:Adamts12
|
UTSW |
15 |
11,286,896 (GRCm39) |
missense |
probably benign |
0.33 |
R0016:Adamts12
|
UTSW |
15 |
11,217,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0016:Adamts12
|
UTSW |
15 |
11,217,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Adamts12
|
UTSW |
15 |
11,285,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0027:Adamts12
|
UTSW |
15 |
11,285,959 (GRCm39) |
missense |
probably damaging |
0.99 |
R0028:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Adamts12
|
UTSW |
15 |
11,311,184 (GRCm39) |
missense |
probably benign |
0.08 |
R0108:Adamts12
|
UTSW |
15 |
11,311,184 (GRCm39) |
missense |
probably benign |
0.08 |
R0122:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0196:Adamts12
|
UTSW |
15 |
11,071,594 (GRCm39) |
missense |
probably benign |
0.11 |
R0308:Adamts12
|
UTSW |
15 |
11,311,646 (GRCm39) |
missense |
probably damaging |
0.98 |
R0335:Adamts12
|
UTSW |
15 |
11,311,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0667:Adamts12
|
UTSW |
15 |
11,215,710 (GRCm39) |
missense |
probably damaging |
1.00 |
R0729:Adamts12
|
UTSW |
15 |
11,255,769 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1162:Adamts12
|
UTSW |
15 |
11,277,544 (GRCm39) |
critical splice donor site |
probably null |
|
R1173:Adamts12
|
UTSW |
15 |
11,071,843 (GRCm39) |
missense |
probably benign |
|
R1174:Adamts12
|
UTSW |
15 |
11,071,843 (GRCm39) |
missense |
probably benign |
|
R1319:Adamts12
|
UTSW |
15 |
11,286,877 (GRCm39) |
missense |
probably benign |
0.02 |
R1344:Adamts12
|
UTSW |
15 |
11,286,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1367:Adamts12
|
UTSW |
15 |
11,256,980 (GRCm39) |
splice site |
probably benign |
|
R1396:Adamts12
|
UTSW |
15 |
11,311,558 (GRCm39) |
missense |
probably benign |
0.01 |
R1418:Adamts12
|
UTSW |
15 |
11,286,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R1447:Adamts12
|
UTSW |
15 |
11,263,447 (GRCm39) |
missense |
probably benign |
0.42 |
R1466:Adamts12
|
UTSW |
15 |
11,311,445 (GRCm39) |
missense |
probably benign |
|
R1466:Adamts12
|
UTSW |
15 |
11,311,445 (GRCm39) |
missense |
probably benign |
|
R1599:Adamts12
|
UTSW |
15 |
11,071,797 (GRCm39) |
missense |
probably damaging |
0.99 |
R1700:Adamts12
|
UTSW |
15 |
11,152,143 (GRCm39) |
missense |
probably benign |
0.00 |
R1748:Adamts12
|
UTSW |
15 |
11,241,548 (GRCm39) |
missense |
probably damaging |
0.99 |
R1826:Adamts12
|
UTSW |
15 |
11,071,606 (GRCm39) |
missense |
probably benign |
0.06 |
R1870:Adamts12
|
UTSW |
15 |
11,311,240 (GRCm39) |
missense |
probably benign |
0.06 |
R1871:Adamts12
|
UTSW |
15 |
11,311,240 (GRCm39) |
missense |
probably benign |
0.06 |
R1872:Adamts12
|
UTSW |
15 |
11,217,966 (GRCm39) |
nonsense |
probably null |
|
R1931:Adamts12
|
UTSW |
15 |
11,270,685 (GRCm39) |
missense |
probably benign |
0.00 |
R2041:Adamts12
|
UTSW |
15 |
11,215,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R2119:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Adamts12
|
UTSW |
15 |
11,310,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R2161:Adamts12
|
UTSW |
15 |
11,215,821 (GRCm39) |
missense |
probably damaging |
0.99 |
R2655:Adamts12
|
UTSW |
15 |
11,065,174 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4010:Adamts12
|
UTSW |
15 |
11,286,169 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4208:Adamts12
|
UTSW |
15 |
11,071,840 (GRCm39) |
missense |
probably benign |
|
R4666:Adamts12
|
UTSW |
15 |
11,311,578 (GRCm39) |
missense |
probably benign |
0.08 |
R4731:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Adamts12
|
UTSW |
15 |
11,270,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Adamts12
|
UTSW |
15 |
11,285,987 (GRCm39) |
missense |
probably benign |
0.03 |
R4877:Adamts12
|
UTSW |
15 |
11,327,787 (GRCm39) |
missense |
probably damaging |
1.00 |
R4929:Adamts12
|
UTSW |
15 |
11,259,108 (GRCm39) |
missense |
probably damaging |
0.96 |
R5060:Adamts12
|
UTSW |
15 |
11,300,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5145:Adamts12
|
UTSW |
15 |
11,285,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R5191:Adamts12
|
UTSW |
15 |
11,327,843 (GRCm39) |
missense |
probably benign |
0.18 |
R5492:Adamts12
|
UTSW |
15 |
11,336,384 (GRCm39) |
missense |
probably benign |
0.05 |
R5580:Adamts12
|
UTSW |
15 |
11,152,086 (GRCm39) |
missense |
probably benign |
0.14 |
R5645:Adamts12
|
UTSW |
15 |
11,277,506 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5724:Adamts12
|
UTSW |
15 |
11,286,836 (GRCm39) |
missense |
probably benign |
0.15 |
R6240:Adamts12
|
UTSW |
15 |
11,286,044 (GRCm39) |
missense |
probably benign |
0.44 |
R6331:Adamts12
|
UTSW |
15 |
11,241,519 (GRCm39) |
missense |
probably damaging |
1.00 |
R6381:Adamts12
|
UTSW |
15 |
11,257,080 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6393:Adamts12
|
UTSW |
15 |
11,255,721 (GRCm39) |
missense |
probably damaging |
0.97 |
R6419:Adamts12
|
UTSW |
15 |
11,215,759 (GRCm39) |
missense |
possibly damaging |
0.72 |
R6571:Adamts12
|
UTSW |
15 |
11,065,187 (GRCm39) |
missense |
probably benign |
0.00 |
R6821:Adamts12
|
UTSW |
15 |
11,152,134 (GRCm39) |
missense |
probably benign |
0.14 |
R6913:Adamts12
|
UTSW |
15 |
11,215,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R6973:Adamts12
|
UTSW |
15 |
11,331,866 (GRCm39) |
nonsense |
probably null |
|
R7188:Adamts12
|
UTSW |
15 |
11,336,411 (GRCm39) |
nonsense |
probably null |
|
R7290:Adamts12
|
UTSW |
15 |
11,277,452 (GRCm39) |
missense |
probably benign |
0.08 |
R7376:Adamts12
|
UTSW |
15 |
11,277,425 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7419:Adamts12
|
UTSW |
15 |
11,317,365 (GRCm39) |
missense |
probably benign |
0.00 |
R7484:Adamts12
|
UTSW |
15 |
11,345,734 (GRCm39) |
missense |
probably benign |
0.25 |
R7562:Adamts12
|
UTSW |
15 |
11,270,697 (GRCm39) |
missense |
probably benign |
0.01 |
R7653:Adamts12
|
UTSW |
15 |
11,257,115 (GRCm39) |
missense |
probably benign |
0.28 |
R7696:Adamts12
|
UTSW |
15 |
11,258,224 (GRCm39) |
missense |
probably damaging |
1.00 |
R7957:Adamts12
|
UTSW |
15 |
11,317,298 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7980:Adamts12
|
UTSW |
15 |
11,263,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R7992:Adamts12
|
UTSW |
15 |
11,310,904 (GRCm39) |
missense |
probably benign |
|
R8032:Adamts12
|
UTSW |
15 |
11,259,189 (GRCm39) |
critical splice donor site |
probably null |
|
R8109:Adamts12
|
UTSW |
15 |
11,331,877 (GRCm39) |
missense |
probably benign |
0.02 |
R8402:Adamts12
|
UTSW |
15 |
11,263,376 (GRCm39) |
missense |
probably damaging |
0.96 |
R8751:Adamts12
|
UTSW |
15 |
11,215,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Adamts12
|
UTSW |
15 |
11,237,678 (GRCm39) |
missense |
probably damaging |
1.00 |
R8934:Adamts12
|
UTSW |
15 |
11,300,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R8952:Adamts12
|
UTSW |
15 |
11,286,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Adamts12
|
UTSW |
15 |
11,317,443 (GRCm39) |
critical splice donor site |
probably null |
|
R9042:Adamts12
|
UTSW |
15 |
11,152,134 (GRCm39) |
missense |
probably benign |
0.08 |
R9162:Adamts12
|
UTSW |
15 |
11,311,721 (GRCm39) |
missense |
probably benign |
0.29 |
R9190:Adamts12
|
UTSW |
15 |
11,336,446 (GRCm39) |
missense |
probably benign |
0.02 |
R9700:Adamts12
|
UTSW |
15 |
11,311,442 (GRCm39) |
missense |
probably benign |
0.04 |
R9748:Adamts12
|
UTSW |
15 |
11,310,628 (GRCm39) |
missense |
probably damaging |
0.99 |
V1662:Adamts12
|
UTSW |
15 |
11,071,894 (GRCm39) |
missense |
probably benign |
0.13 |
X0022:Adamts12
|
UTSW |
15 |
11,277,534 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Adamts12
|
UTSW |
15 |
11,336,469 (GRCm39) |
missense |
not run |
|
Z1177:Adamts12
|
UTSW |
15 |
11,336,469 (GRCm39) |
missense |
not run |
|
Z1177:Adamts12
|
UTSW |
15 |
11,317,410 (GRCm39) |
missense |
probably damaging |
1.00 |
|