Other mutations in this stock |
Total: 105 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210408I21Rik |
T |
C |
13: 77,471,843 (GRCm39) |
W1083R |
possibly damaging |
Het |
Adamts10 |
T |
A |
17: 33,747,726 (GRCm39) |
L54Q |
probably damaging |
Het |
Ankrd24 |
A |
C |
10: 81,479,149 (GRCm39) |
|
probably benign |
Het |
Atg2b |
A |
G |
12: 105,618,888 (GRCm39) |
S813P |
probably benign |
Het |
Atp13a3 |
T |
A |
16: 30,160,058 (GRCm39) |
I716F |
probably damaging |
Het |
Atp6v1c1 |
T |
A |
15: 38,689,420 (GRCm39) |
W294R |
probably damaging |
Het |
Atrnl1 |
G |
T |
19: 58,030,793 (GRCm39) |
A1312S |
probably benign |
Het |
Bcl2 |
A |
T |
1: 106,640,338 (GRCm39) |
H91Q |
possibly damaging |
Het |
Cacna1c |
G |
A |
6: 118,607,263 (GRCm39) |
Q1214* |
probably null |
Het |
Cacna1g |
C |
A |
11: 94,324,673 (GRCm39) |
G1183W |
probably damaging |
Het |
Capsl |
A |
T |
15: 9,461,828 (GRCm39) |
M75L |
probably benign |
Het |
Ccdc122 |
T |
G |
14: 77,349,047 (GRCm39) |
|
probably benign |
Het |
Ccdc57 |
T |
G |
11: 120,772,683 (GRCm39) |
R645S |
possibly damaging |
Het |
Cdh8 |
T |
A |
8: 99,751,558 (GRCm39) |
R720* |
probably null |
Het |
Cenpx |
T |
G |
11: 120,602,610 (GRCm39) |
|
probably benign |
Het |
Clic3 |
T |
C |
2: 25,348,194 (GRCm39) |
S114P |
probably damaging |
Het |
Cracdl |
A |
T |
1: 37,664,046 (GRCm39) |
D617E |
probably benign |
Het |
Crtac1 |
A |
T |
19: 42,312,240 (GRCm39) |
W158R |
possibly damaging |
Het |
Dennd2b |
C |
T |
7: 109,156,240 (GRCm39) |
G170D |
probably damaging |
Het |
Dhrs11 |
T |
A |
11: 84,719,626 (GRCm39) |
Q33L |
probably benign |
Het |
Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
Dpp9 |
G |
T |
17: 56,498,016 (GRCm39) |
Q647K |
probably damaging |
Het |
Egf |
C |
T |
3: 129,510,327 (GRCm39) |
G64D |
probably damaging |
Het |
Eif2b4 |
C |
T |
5: 31,346,864 (GRCm39) |
|
probably benign |
Het |
Epas1 |
A |
G |
17: 87,113,267 (GRCm39) |
N151S |
probably benign |
Het |
Fastkd1 |
A |
T |
2: 69,521,651 (GRCm39) |
I707K |
probably benign |
Het |
Fbln2 |
A |
G |
6: 91,246,168 (GRCm39) |
T1005A |
probably benign |
Het |
Fgfrl1 |
T |
A |
5: 108,851,363 (GRCm39) |
Y93* |
probably null |
Het |
Fktn |
A |
G |
4: 53,744,637 (GRCm39) |
T306A |
probably benign |
Het |
Gabbr2 |
T |
G |
4: 46,991,139 (GRCm39) |
Y96S |
possibly damaging |
Het |
Gm16332 |
A |
T |
1: 139,819,396 (GRCm39) |
|
noncoding transcript |
Het |
Gm5145 |
G |
T |
17: 20,790,810 (GRCm39) |
V63F |
probably damaging |
Het |
Gm9970 |
G |
T |
5: 31,398,429 (GRCm39) |
|
probably benign |
Het |
Gpr158 |
A |
G |
2: 21,787,993 (GRCm39) |
T545A |
probably damaging |
Het |
Heatr1 |
G |
A |
13: 12,426,929 (GRCm39) |
E685K |
probably benign |
Het |
Herc6 |
A |
T |
6: 57,581,151 (GRCm39) |
I284F |
probably damaging |
Het |
Hook1 |
C |
G |
4: 95,890,794 (GRCm39) |
A301G |
possibly damaging |
Het |
Hpcal4 |
T |
A |
4: 123,084,491 (GRCm39) |
M140K |
possibly damaging |
Het |
Il11ra1 |
T |
C |
4: 41,766,096 (GRCm39) |
|
probably benign |
Het |
Ildr1 |
A |
T |
16: 36,542,917 (GRCm39) |
H439L |
possibly damaging |
Het |
Itga11 |
A |
G |
9: 62,684,009 (GRCm39) |
|
probably null |
Het |
Jag2 |
A |
T |
12: 112,880,252 (GRCm39) |
D337E |
probably benign |
Het |
Krt82 |
C |
T |
15: 101,458,923 (GRCm39) |
R39Q |
probably benign |
Het |
L3mbtl4 |
T |
A |
17: 68,666,475 (GRCm39) |
M1K |
probably null |
Het |
Lrrc32 |
T |
G |
7: 98,148,224 (GRCm39) |
F335V |
probably damaging |
Het |
Lurap1l |
T |
A |
4: 80,829,650 (GRCm39) |
V20E |
probably damaging |
Het |
Lyar |
T |
A |
5: 38,385,230 (GRCm39) |
V90D |
possibly damaging |
Het |
Man2c1 |
C |
T |
9: 57,048,469 (GRCm39) |
R778* |
probably null |
Het |
Mapk6 |
A |
G |
9: 75,295,714 (GRCm39) |
F595L |
probably benign |
Het |
Mccc1 |
A |
G |
3: 36,039,150 (GRCm39) |
I281T |
probably damaging |
Het |
Mier1 |
G |
A |
4: 102,988,195 (GRCm39) |
D40N |
probably damaging |
Het |
Mkx |
T |
C |
18: 7,002,432 (GRCm39) |
H38R |
probably benign |
Het |
Mroh4 |
A |
G |
15: 74,498,028 (GRCm39) |
L184P |
probably damaging |
Het |
Muc2 |
C |
A |
7: 141,307,877 (GRCm39) |
N834K |
probably benign |
Het |
Mycl |
A |
G |
4: 122,894,049 (GRCm39) |
D283G |
probably damaging |
Het |
Myh6 |
T |
C |
14: 55,190,750 (GRCm39) |
N975S |
probably damaging |
Het |
Myl12a |
A |
G |
17: 71,303,297 (GRCm39) |
|
probably benign |
Het |
Mysm1 |
T |
C |
4: 94,853,910 (GRCm39) |
T230A |
probably benign |
Het |
Naca |
A |
G |
10: 127,883,672 (GRCm39) |
K2099R |
probably null |
Het |
Nbeal1 |
T |
G |
1: 60,261,352 (GRCm39) |
|
probably null |
Het |
Nedd1 |
A |
G |
10: 92,534,772 (GRCm39) |
V246A |
probably benign |
Het |
Nid2 |
A |
G |
14: 19,839,829 (GRCm39) |
D806G |
probably benign |
Het |
Ninl |
G |
A |
2: 150,801,801 (GRCm39) |
R156* |
probably null |
Het |
Obscn |
T |
A |
11: 58,960,685 (GRCm39) |
I3418F |
probably damaging |
Het |
Or8g37 |
T |
A |
9: 39,731,193 (GRCm39) |
V86E |
probably benign |
Het |
Pappa2 |
T |
C |
1: 158,684,949 (GRCm39) |
N730S |
probably damaging |
Het |
Pcm1 |
G |
A |
8: 41,746,715 (GRCm39) |
D1305N |
probably damaging |
Het |
Pcsk4 |
A |
T |
10: 80,158,938 (GRCm39) |
I485N |
probably damaging |
Het |
Phldb2 |
T |
C |
16: 45,646,237 (GRCm39) |
R111G |
probably damaging |
Het |
Prdm10 |
T |
C |
9: 31,252,569 (GRCm39) |
F385S |
probably damaging |
Het |
Prkcsh |
C |
T |
9: 21,923,034 (GRCm39) |
P351L |
probably damaging |
Het |
Prrc2a |
G |
A |
17: 35,369,018 (GRCm39) |
P2006L |
probably damaging |
Het |
Rad51c |
T |
C |
11: 87,286,204 (GRCm39) |
D251G |
probably damaging |
Het |
Radil |
A |
G |
5: 142,470,918 (GRCm39) |
F1088L |
probably benign |
Het |
Rere |
C |
A |
4: 150,699,624 (GRCm39) |
|
probably benign |
Het |
Rnf167 |
T |
A |
11: 70,540,961 (GRCm39) |
C196S |
probably benign |
Het |
Robo2 |
T |
A |
16: 74,149,633 (GRCm39) |
Y65F |
probably damaging |
Het |
Scarf2 |
G |
A |
16: 17,621,371 (GRCm39) |
C319Y |
probably damaging |
Het |
Sec24c |
A |
G |
14: 20,743,780 (GRCm39) |
D995G |
probably damaging |
Het |
Selenbp1 |
T |
C |
3: 94,851,211 (GRCm39) |
L369S |
probably benign |
Het |
Sgpl1 |
A |
T |
10: 60,959,123 (GRCm39) |
I53K |
possibly damaging |
Het |
Sh3bp5 |
C |
A |
14: 31,099,452 (GRCm39) |
R265L |
probably benign |
Het |
Slc1a6 |
A |
T |
10: 78,635,952 (GRCm39) |
Y339F |
probably damaging |
Het |
Smchd1 |
G |
T |
17: 71,667,048 (GRCm39) |
Y1781* |
probably null |
Het |
Smg1 |
T |
C |
7: 117,779,697 (GRCm39) |
S1233G |
probably benign |
Het |
Snap91 |
A |
T |
9: 86,665,507 (GRCm39) |
|
probably benign |
Het |
Snx29 |
T |
A |
16: 11,238,600 (GRCm39) |
L112Q |
probably damaging |
Het |
Sptbn5 |
T |
C |
2: 119,889,622 (GRCm39) |
|
probably benign |
Het |
Srl |
A |
T |
16: 4,310,222 (GRCm39) |
H502Q |
possibly damaging |
Het |
St8sia3 |
A |
G |
18: 64,404,820 (GRCm39) |
M366V |
probably benign |
Het |
Stk19 |
A |
T |
17: 35,041,485 (GRCm39) |
|
probably benign |
Het |
Syngap1 |
G |
A |
17: 27,180,423 (GRCm39) |
A611T |
probably benign |
Het |
Tas2r113 |
A |
G |
6: 132,870,670 (GRCm39) |
T233A |
possibly damaging |
Het |
Tbcc |
G |
A |
17: 47,202,145 (GRCm39) |
W177* |
probably null |
Het |
Tcstv3 |
T |
A |
13: 120,779,618 (GRCm39) |
|
probably null |
Het |
Trav13-5 |
T |
A |
14: 54,033,408 (GRCm39) |
C106S |
probably damaging |
Het |
Trmt61a |
G |
A |
12: 111,645,147 (GRCm39) |
V28M |
possibly damaging |
Het |
Ubap2l |
G |
A |
3: 89,928,210 (GRCm39) |
T553M |
probably damaging |
Het |
Urb1 |
T |
C |
16: 90,554,715 (GRCm39) |
N1839S |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,475,742 (GRCm39) |
L2893P |
probably damaging |
Het |
Usp24 |
G |
A |
4: 106,217,359 (GRCm39) |
V421M |
possibly damaging |
Het |
Vmn1r43 |
T |
C |
6: 89,846,892 (GRCm39) |
E198G |
probably benign |
Het |
Vps13d |
A |
C |
4: 144,904,626 (GRCm39) |
S130A |
probably damaging |
Het |
Zfp426 |
T |
A |
9: 20,382,310 (GRCm39) |
I211F |
probably benign |
Het |
Znfx1 |
T |
C |
2: 166,880,489 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mep1b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00392:Mep1b
|
APN |
18 |
21,217,243 (GRCm39) |
nonsense |
probably null |
|
IGL01470:Mep1b
|
APN |
18 |
21,230,524 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01866:Mep1b
|
APN |
18 |
21,228,050 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02865:Mep1b
|
APN |
18 |
21,226,441 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03093:Mep1b
|
APN |
18 |
21,226,710 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03126:Mep1b
|
APN |
18 |
21,221,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03196:Mep1b
|
APN |
18 |
21,228,121 (GRCm39) |
missense |
probably benign |
0.01 |
P0022:Mep1b
|
UTSW |
18 |
21,221,598 (GRCm39) |
splice site |
probably benign |
|
R0143:Mep1b
|
UTSW |
18 |
21,228,164 (GRCm39) |
splice site |
probably benign |
|
R0743:Mep1b
|
UTSW |
18 |
21,213,515 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0961:Mep1b
|
UTSW |
18 |
21,221,786 (GRCm39) |
nonsense |
probably null |
|
R1913:Mep1b
|
UTSW |
18 |
21,226,286 (GRCm39) |
missense |
probably benign |
0.21 |
R2162:Mep1b
|
UTSW |
18 |
21,219,296 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2307:Mep1b
|
UTSW |
18 |
21,221,632 (GRCm39) |
missense |
probably damaging |
1.00 |
R3000:Mep1b
|
UTSW |
18 |
21,226,361 (GRCm39) |
missense |
probably damaging |
0.96 |
R3833:Mep1b
|
UTSW |
18 |
21,219,296 (GRCm39) |
missense |
possibly damaging |
0.82 |
R3862:Mep1b
|
UTSW |
18 |
21,217,226 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3863:Mep1b
|
UTSW |
18 |
21,217,226 (GRCm39) |
missense |
possibly damaging |
0.56 |
R3864:Mep1b
|
UTSW |
18 |
21,217,226 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4171:Mep1b
|
UTSW |
18 |
21,228,163 (GRCm39) |
splice site |
probably null |
|
R4774:Mep1b
|
UTSW |
18 |
21,219,241 (GRCm39) |
missense |
probably benign |
0.24 |
R5411:Mep1b
|
UTSW |
18 |
21,219,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R6952:Mep1b
|
UTSW |
18 |
21,221,727 (GRCm39) |
missense |
probably benign |
0.00 |
R7056:Mep1b
|
UTSW |
18 |
21,224,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Mep1b
|
UTSW |
18 |
21,233,108 (GRCm39) |
missense |
probably benign |
0.35 |
R7217:Mep1b
|
UTSW |
18 |
21,226,600 (GRCm39) |
missense |
probably benign |
0.01 |
R7641:Mep1b
|
UTSW |
18 |
21,228,034 (GRCm39) |
missense |
possibly damaging |
0.47 |
R7843:Mep1b
|
UTSW |
18 |
21,228,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Mep1b
|
UTSW |
18 |
21,222,442 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8794:Mep1b
|
UTSW |
18 |
21,224,325 (GRCm39) |
missense |
probably damaging |
0.96 |
R8845:Mep1b
|
UTSW |
18 |
21,230,379 (GRCm39) |
nonsense |
probably null |
|
R8877:Mep1b
|
UTSW |
18 |
21,221,630 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8975:Mep1b
|
UTSW |
18 |
21,208,714 (GRCm39) |
missense |
probably benign |
0.17 |
R9352:Mep1b
|
UTSW |
18 |
21,209,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R9448:Mep1b
|
UTSW |
18 |
21,217,199 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Mep1b
|
UTSW |
18 |
21,208,720 (GRCm39) |
missense |
possibly damaging |
0.75 |
|