Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700113H08Rik |
T |
C |
10: 86,957,297 (GRCm39) |
V11A |
probably benign |
Het |
Abca12 |
A |
T |
1: 71,313,793 (GRCm39) |
|
probably null |
Het |
Abcc12 |
T |
A |
8: 87,234,568 (GRCm39) |
M1232L |
probably benign |
Het |
Adamts1 |
T |
C |
16: 85,597,117 (GRCm39) |
Y314C |
probably damaging |
Het |
Adgb |
A |
G |
10: 10,254,403 (GRCm39) |
|
probably null |
Het |
Ankrd12 |
T |
A |
17: 66,292,648 (GRCm39) |
K928N |
possibly damaging |
Het |
Ano5 |
A |
T |
7: 51,237,543 (GRCm39) |
K789I |
possibly damaging |
Het |
Cacna1d |
G |
T |
14: 29,833,026 (GRCm39) |
N938K |
probably damaging |
Het |
Camk1g |
T |
C |
1: 193,032,593 (GRCm39) |
R273G |
possibly damaging |
Het |
Caprin2 |
C |
A |
6: 148,744,528 (GRCm39) |
V966F |
probably damaging |
Het |
Card6 |
T |
C |
15: 5,128,954 (GRCm39) |
H814R |
probably benign |
Het |
Cenatac |
T |
C |
9: 44,324,215 (GRCm39) |
Q228R |
probably null |
Het |
Cflar |
A |
G |
1: 58,750,740 (GRCm39) |
|
probably benign |
Het |
Cftr |
T |
A |
6: 18,204,204 (GRCm39) |
N66K |
probably benign |
Het |
Clasrp |
C |
T |
7: 19,322,671 (GRCm39) |
|
probably null |
Het |
Clec4a4 |
T |
C |
6: 122,967,339 (GRCm39) |
I5T |
probably damaging |
Het |
Cmtr2 |
T |
C |
8: 110,948,251 (GRCm39) |
I187T |
possibly damaging |
Het |
Cnga1 |
A |
T |
5: 72,761,616 (GRCm39) |
F633I |
possibly damaging |
Het |
Col16a1 |
C |
T |
4: 129,967,057 (GRCm39) |
P909S |
unknown |
Het |
Csf1 |
C |
A |
3: 107,667,361 (GRCm39) |
A7S |
possibly damaging |
Het |
Cstpp1 |
T |
C |
2: 91,274,939 (GRCm39) |
|
probably benign |
Het |
Dhx30 |
A |
T |
9: 109,915,270 (GRCm39) |
V833D |
probably benign |
Het |
Dlg2 |
T |
G |
7: 92,080,263 (GRCm39) |
I712M |
probably benign |
Het |
Dmxl1 |
T |
A |
18: 50,011,382 (GRCm39) |
F1180I |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,896,631 (GRCm39) |
K2398* |
probably null |
Het |
Dus1l |
C |
T |
11: 120,680,262 (GRCm39) |
G471D |
possibly damaging |
Het |
Dync1h1 |
A |
T |
12: 110,621,893 (GRCm39) |
N3412I |
possibly damaging |
Het |
Dync1i2 |
T |
A |
2: 71,081,178 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,047,911 (GRCm39) |
S333P |
possibly damaging |
Het |
Eed |
A |
T |
7: 89,605,541 (GRCm39) |
N349K |
probably benign |
Het |
Eipr1 |
A |
T |
12: 28,816,769 (GRCm39) |
|
probably null |
Het |
Fbxw16 |
A |
C |
9: 109,277,222 (GRCm39) |
V40G |
probably damaging |
Het |
Fgfr4 |
A |
C |
13: 55,308,969 (GRCm39) |
R363S |
possibly damaging |
Het |
Fgl2 |
A |
T |
5: 21,578,229 (GRCm39) |
N172I |
possibly damaging |
Het |
Fhip1b |
G |
A |
7: 105,033,732 (GRCm39) |
R509C |
probably damaging |
Het |
Gabbr2 |
T |
A |
4: 46,875,744 (GRCm39) |
H126L |
possibly damaging |
Het |
Gcnt2 |
A |
T |
13: 41,014,338 (GRCm39) |
N170Y |
possibly damaging |
Het |
Gpt |
A |
G |
15: 76,583,093 (GRCm39) |
|
probably null |
Het |
Igsf10 |
A |
G |
3: 59,235,489 (GRCm39) |
I1564T |
probably benign |
Het |
Il22ra1 |
C |
A |
4: 135,478,107 (GRCm39) |
Q393K |
possibly damaging |
Het |
Inpp5d |
A |
T |
1: 87,611,567 (GRCm39) |
K340* |
probably null |
Het |
Krt5 |
T |
A |
15: 101,617,453 (GRCm39) |
T427S |
probably benign |
Het |
Krt76 |
T |
C |
15: 101,798,929 (GRCm39) |
D252G |
probably damaging |
Het |
Krtap26-1 |
A |
G |
16: 88,444,198 (GRCm39) |
V141A |
not run |
Het |
Lce6a |
A |
T |
3: 92,527,642 (GRCm39) |
V55D |
probably benign |
Het |
Lpxn |
C |
T |
19: 12,802,185 (GRCm39) |
S170F |
possibly damaging |
Het |
Magi2 |
T |
C |
5: 20,670,838 (GRCm39) |
V394A |
probably benign |
Het |
Mbnl1 |
G |
A |
3: 60,522,242 (GRCm39) |
|
probably null |
Het |
Med16 |
T |
A |
10: 79,734,252 (GRCm39) |
K554M |
probably damaging |
Het |
Mettl14 |
T |
C |
3: 123,166,234 (GRCm39) |
D276G |
possibly damaging |
Het |
Mphosph9 |
T |
C |
5: 124,399,009 (GRCm39) |
D1002G |
probably damaging |
Het |
Mroh9 |
T |
C |
1: 162,866,678 (GRCm39) |
E686G |
probably damaging |
Het |
Nav1 |
T |
C |
1: 135,379,986 (GRCm39) |
Y1512C |
unknown |
Het |
Neb |
T |
C |
2: 52,082,035 (GRCm39) |
Y5712C |
probably damaging |
Het |
Nek7 |
T |
A |
1: 138,489,509 (GRCm39) |
|
probably benign |
Het |
Nptx1 |
T |
A |
11: 119,435,462 (GRCm39) |
I285F |
probably damaging |
Het |
Oas1d |
G |
T |
5: 121,053,034 (GRCm39) |
E30* |
probably null |
Het |
Or1p1b |
A |
T |
11: 74,130,725 (GRCm39) |
I112F |
probably damaging |
Het |
Or51g2 |
A |
G |
7: 102,622,317 (GRCm39) |
V294A |
possibly damaging |
Het |
Or6n1 |
C |
A |
1: 173,917,417 (GRCm39) |
Y270* |
probably null |
Het |
Parp4 |
T |
G |
14: 56,873,205 (GRCm39) |
S1150A |
possibly damaging |
Het |
Pinx1 |
A |
T |
14: 64,156,741 (GRCm39) |
K223* |
probably null |
Het |
Plekha5 |
T |
C |
6: 140,529,640 (GRCm39) |
L1034S |
probably damaging |
Het |
Ppp4r3a |
A |
G |
12: 101,019,755 (GRCm39) |
V400A |
possibly damaging |
Het |
Prtg |
A |
T |
9: 72,749,979 (GRCm39) |
I128F |
possibly damaging |
Het |
Rars1 |
T |
C |
11: 35,719,534 (GRCm39) |
E96G |
probably benign |
Het |
Rhpn1 |
T |
A |
15: 75,585,299 (GRCm39) |
S551T |
probably benign |
Het |
Selenow |
C |
T |
7: 15,656,176 (GRCm39) |
|
probably null |
Het |
Serpina9 |
A |
T |
12: 103,967,484 (GRCm39) |
|
probably null |
Het |
Shank3 |
A |
T |
15: 89,433,083 (GRCm39) |
D1276V |
probably damaging |
Het |
Slc27a6 |
A |
G |
18: 58,742,267 (GRCm39) |
T494A |
probably damaging |
Het |
Slc34a1 |
A |
C |
13: 24,003,317 (GRCm39) |
H285P |
probably damaging |
Het |
Slc6a21 |
A |
C |
7: 44,932,360 (GRCm39) |
T54P |
|
Het |
Syne2 |
A |
G |
12: 76,030,501 (GRCm39) |
|
probably null |
Het |
Tal1 |
T |
C |
4: 114,925,489 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
A |
G |
7: 65,302,009 (GRCm39) |
K178E |
probably benign |
Het |
Tex10 |
T |
A |
4: 48,459,984 (GRCm39) |
I456L |
probably benign |
Het |
Tfcp2 |
A |
G |
15: 100,420,310 (GRCm39) |
F175S |
probably damaging |
Het |
Timp2 |
C |
T |
11: 118,194,626 (GRCm39) |
A188T |
probably damaging |
Het |
Tmc5 |
T |
A |
7: 118,268,440 (GRCm39) |
I836N |
probably damaging |
Het |
Tmem100 |
T |
A |
11: 89,926,302 (GRCm39) |
M43K |
probably benign |
Het |
Ulk2 |
A |
G |
11: 61,745,378 (GRCm39) |
Y9H |
probably damaging |
Het |
Usp7 |
T |
C |
16: 8,523,027 (GRCm39) |
K311E |
probably damaging |
Het |
Vmn1r238 |
G |
A |
18: 3,123,033 (GRCm39) |
T127I |
probably benign |
Het |
Vmn2r28 |
T |
C |
7: 5,496,678 (GRCm39) |
Y58C |
probably damaging |
Het |
Wdr55 |
G |
A |
18: 36,893,469 (GRCm39) |
G44S |
probably benign |
Het |
Zfp677 |
C |
A |
17: 21,617,647 (GRCm39) |
H235N |
probably damaging |
Het |
Zfp869 |
T |
A |
8: 70,159,636 (GRCm39) |
R312S |
probably damaging |
Het |
|
Other mutations in Jcad |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00650:Jcad
|
APN |
18 |
4,675,692 (GRCm39) |
missense |
probably benign |
0.14 |
IGL00672:Jcad
|
APN |
18 |
4,674,835 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL00782:Jcad
|
APN |
18 |
4,675,073 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00825:Jcad
|
APN |
18 |
4,673,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01522:Jcad
|
APN |
18 |
4,673,312 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01796:Jcad
|
APN |
18 |
4,672,855 (GRCm39) |
nonsense |
probably null |
|
IGL01973:Jcad
|
APN |
18 |
4,675,514 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02083:Jcad
|
APN |
18 |
4,680,266 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02625:Jcad
|
APN |
18 |
4,674,422 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03002:Jcad
|
APN |
18 |
4,675,153 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03325:Jcad
|
APN |
18 |
4,673,902 (GRCm39) |
missense |
probably benign |
|
R0304:Jcad
|
UTSW |
18 |
4,673,325 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0487:Jcad
|
UTSW |
18 |
4,673,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R0519:Jcad
|
UTSW |
18 |
4,649,122 (GRCm39) |
start gained |
probably benign |
|
R0664:Jcad
|
UTSW |
18 |
4,676,063 (GRCm39) |
missense |
probably damaging |
0.97 |
R1649:Jcad
|
UTSW |
18 |
4,673,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R1710:Jcad
|
UTSW |
18 |
4,674,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R1734:Jcad
|
UTSW |
18 |
4,674,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Jcad
|
UTSW |
18 |
4,675,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R1824:Jcad
|
UTSW |
18 |
4,649,293 (GRCm39) |
missense |
probably benign |
|
R1850:Jcad
|
UTSW |
18 |
4,675,730 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1872:Jcad
|
UTSW |
18 |
4,673,048 (GRCm39) |
missense |
probably benign |
|
R1878:Jcad
|
UTSW |
18 |
4,673,857 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1918:Jcad
|
UTSW |
18 |
4,674,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Jcad
|
UTSW |
18 |
4,675,162 (GRCm39) |
missense |
probably benign |
0.07 |
R2420:Jcad
|
UTSW |
18 |
4,675,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R2504:Jcad
|
UTSW |
18 |
4,674,026 (GRCm39) |
missense |
probably damaging |
0.99 |
R2936:Jcad
|
UTSW |
18 |
4,675,153 (GRCm39) |
missense |
probably benign |
0.00 |
R4420:Jcad
|
UTSW |
18 |
4,676,032 (GRCm39) |
missense |
probably benign |
0.00 |
R4668:Jcad
|
UTSW |
18 |
4,680,221 (GRCm39) |
splice site |
probably null |
|
R4670:Jcad
|
UTSW |
18 |
4,674,175 (GRCm39) |
missense |
probably benign |
0.03 |
R4671:Jcad
|
UTSW |
18 |
4,674,175 (GRCm39) |
missense |
probably benign |
0.03 |
R4707:Jcad
|
UTSW |
18 |
4,649,338 (GRCm39) |
nonsense |
probably null |
|
R4720:Jcad
|
UTSW |
18 |
4,674,055 (GRCm39) |
missense |
probably benign |
0.03 |
R4815:Jcad
|
UTSW |
18 |
4,675,223 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4906:Jcad
|
UTSW |
18 |
4,673,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R5214:Jcad
|
UTSW |
18 |
4,674,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R5439:Jcad
|
UTSW |
18 |
4,675,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R5563:Jcad
|
UTSW |
18 |
4,673,944 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5721:Jcad
|
UTSW |
18 |
4,676,044 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5825:Jcad
|
UTSW |
18 |
4,674,896 (GRCm39) |
missense |
probably benign |
0.00 |
R5952:Jcad
|
UTSW |
18 |
4,674,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R6661:Jcad
|
UTSW |
18 |
4,675,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R6928:Jcad
|
UTSW |
18 |
4,673,372 (GRCm39) |
missense |
probably benign |
0.00 |
R7426:Jcad
|
UTSW |
18 |
4,675,529 (GRCm39) |
missense |
probably benign |
0.11 |
R7943:Jcad
|
UTSW |
18 |
4,672,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8010:Jcad
|
UTSW |
18 |
4,674,581 (GRCm39) |
missense |
probably benign |
|
R8080:Jcad
|
UTSW |
18 |
4,649,270 (GRCm39) |
missense |
probably benign |
0.01 |
R8133:Jcad
|
UTSW |
18 |
4,649,384 (GRCm39) |
missense |
probably benign |
0.03 |
R8168:Jcad
|
UTSW |
18 |
4,675,094 (GRCm39) |
missense |
probably benign |
0.00 |
R8232:Jcad
|
UTSW |
18 |
4,674,862 (GRCm39) |
missense |
probably benign |
0.23 |
R8276:Jcad
|
UTSW |
18 |
4,674,318 (GRCm39) |
missense |
probably damaging |
1.00 |
R8408:Jcad
|
UTSW |
18 |
4,649,402 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9173:Jcad
|
UTSW |
18 |
4,675,820 (GRCm39) |
missense |
probably benign |
0.42 |
R9415:Jcad
|
UTSW |
18 |
4,673,912 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Jcad
|
UTSW |
18 |
4,673,252 (GRCm39) |
nonsense |
probably null |
|
T0722:Jcad
|
UTSW |
18 |
4,675,531 (GRCm39) |
missense |
probably benign |
0.25 |
X0017:Jcad
|
UTSW |
18 |
4,676,044 (GRCm39) |
missense |
probably benign |
0.01 |
|