Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrg7 |
T |
A |
16: 56,562,682 (GRCm39) |
I552L |
probably benign |
Het |
Ankrd11 |
A |
G |
8: 123,617,943 (GRCm39) |
|
probably benign |
Het |
Col12a1 |
T |
C |
9: 79,613,582 (GRCm39) |
T88A |
probably benign |
Het |
Col6a5 |
T |
G |
9: 105,811,444 (GRCm39) |
I692L |
unknown |
Het |
Cry2 |
T |
C |
2: 92,243,405 (GRCm39) |
I479V |
probably benign |
Het |
Ddx21 |
T |
C |
10: 62,423,318 (GRCm39) |
|
probably null |
Het |
Efcab12 |
T |
A |
6: 115,800,238 (GRCm39) |
I262F |
probably damaging |
Het |
Eif2ak2 |
T |
C |
17: 79,183,633 (GRCm39) |
D72G |
possibly damaging |
Het |
Fry |
T |
C |
5: 150,293,689 (GRCm39) |
F461L |
probably damaging |
Het |
Gm38706 |
G |
A |
6: 130,460,731 (GRCm39) |
|
noncoding transcript |
Het |
Gm9772 |
C |
T |
17: 22,226,107 (GRCm39) |
C59Y |
probably damaging |
Het |
Meig1 |
T |
C |
2: 3,410,263 (GRCm39) |
E79G |
probably damaging |
Het |
Mfng |
C |
T |
15: 78,648,588 (GRCm39) |
R163H |
probably benign |
Het |
Mfsd2b |
T |
A |
12: 4,915,908 (GRCm39) |
|
probably benign |
Het |
Nfatc2 |
A |
C |
2: 168,431,987 (GRCm39) |
I42S |
probably benign |
Het |
Nlgn3 |
G |
A |
X: 100,361,891 (GRCm39) |
V287I |
probably benign |
Het |
Npy6r |
C |
T |
18: 44,409,686 (GRCm39) |
T369I |
probably benign |
Het |
Or7a36 |
A |
G |
10: 78,820,143 (GRCm39) |
E173G |
probably benign |
Het |
Ptprb |
A |
G |
10: 116,179,820 (GRCm39) |
T1413A |
probably benign |
Het |
Ptprc |
A |
G |
1: 138,017,304 (GRCm39) |
S624P |
probably benign |
Het |
Pum3 |
A |
G |
19: 27,377,169 (GRCm39) |
V441A |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,315,860 (GRCm39) |
D2193E |
probably damaging |
Het |
Rbl1 |
A |
T |
2: 157,017,397 (GRCm39) |
|
probably benign |
Het |
Rnf167 |
T |
C |
11: 70,540,906 (GRCm39) |
|
probably benign |
Het |
Sdr9c7 |
T |
C |
10: 127,738,259 (GRCm39) |
V179A |
probably damaging |
Het |
Sema3c |
A |
G |
5: 17,932,615 (GRCm39) |
N706S |
possibly damaging |
Het |
Stt3a |
T |
C |
9: 36,646,762 (GRCm39) |
Y617C |
probably damaging |
Het |
Tdrd6 |
T |
A |
17: 43,936,966 (GRCm39) |
S1361C |
probably damaging |
Het |
Tha1 |
A |
C |
11: 117,760,502 (GRCm39) |
S241A |
probably damaging |
Het |
Tti1 |
G |
A |
2: 157,850,432 (GRCm39) |
A269V |
probably benign |
Het |
Ugt2a1 |
A |
G |
5: 87,633,886 (GRCm39) |
|
probably null |
Het |
Vmn2r10 |
T |
C |
5: 109,143,761 (GRCm39) |
T730A |
possibly 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 |
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 |
R7307:Adamts12
|
UTSW |
15 |
11,217,899 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
|