Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030498E09Rik |
A |
T |
X: 38,047,315 (GRCm39) |
M119L |
probably benign |
Het |
Akap10 |
A |
T |
11: 61,768,179 (GRCm39) |
V646D |
probably damaging |
Het |
Aldh3a1 |
A |
G |
11: 61,105,548 (GRCm39) |
Y218C |
probably damaging |
Het |
Arfgef3 |
T |
A |
10: 18,540,660 (GRCm39) |
L174F |
probably damaging |
Het |
Arhgef6 |
T |
C |
X: 56,382,338 (GRCm39) |
K99E |
possibly damaging |
Het |
Atp9a |
T |
C |
2: 168,531,225 (GRCm39) |
K163E |
probably benign |
Het |
Birc6 |
C |
T |
17: 74,956,881 (GRCm39) |
A3605V |
probably benign |
Het |
C8b |
G |
A |
4: 104,637,888 (GRCm39) |
R120Q |
probably benign |
Het |
Ccr1l1 |
A |
C |
9: 123,778,444 (GRCm39) |
M1R |
probably null |
Het |
Clca3a2 |
A |
G |
3: 144,803,530 (GRCm39) |
S105P |
probably damaging |
Het |
Cntnap1 |
A |
G |
11: 101,072,508 (GRCm39) |
T502A |
possibly damaging |
Het |
Ddx10 |
C |
T |
9: 53,028,452 (GRCm39) |
|
probably null |
Het |
Dnah5 |
G |
A |
15: 28,233,441 (GRCm39) |
|
probably null |
Het |
Dock9 |
A |
T |
14: 121,879,035 (GRCm39) |
|
probably benign |
Het |
Gli2 |
A |
G |
1: 118,765,166 (GRCm39) |
V995A |
probably benign |
Het |
Gpr34 |
T |
C |
X: 13,505,788 (GRCm39) |
Y106H |
probably damaging |
Het |
Kmt2a |
A |
T |
9: 44,731,862 (GRCm39) |
|
probably benign |
Het |
Lamc1 |
C |
A |
1: 153,138,392 (GRCm39) |
R154L |
probably damaging |
Het |
Mat1a |
T |
A |
14: 40,827,561 (GRCm39) |
V5E |
probably benign |
Het |
Meioc |
A |
T |
11: 102,571,495 (GRCm39) |
E943V |
probably damaging |
Het |
Nav2 |
C |
T |
7: 49,141,205 (GRCm39) |
R917* |
probably null |
Het |
Or4f47 |
T |
C |
2: 111,972,518 (GRCm39) |
I76T |
probably benign |
Het |
Or7g32 |
T |
C |
9: 19,389,285 (GRCm39) |
N87S |
possibly damaging |
Het |
Pcsk9 |
T |
A |
4: 106,303,967 (GRCm39) |
I506L |
probably benign |
Het |
Phf14 |
T |
A |
6: 11,953,366 (GRCm39) |
D368E |
probably damaging |
Het |
Phka1 |
C |
A |
X: 101,580,819 (GRCm39) |
S964I |
probably damaging |
Het |
Pikfyve |
G |
A |
1: 65,286,226 (GRCm39) |
R1155Q |
probably damaging |
Het |
Plin2 |
C |
T |
4: 86,580,315 (GRCm39) |
V60M |
probably damaging |
Het |
Ptpn9 |
A |
G |
9: 56,934,671 (GRCm39) |
Q145R |
possibly damaging |
Het |
Sap30 |
A |
G |
8: 57,940,335 (GRCm39) |
I89T |
probably damaging |
Het |
Sec61a2 |
T |
C |
2: 5,881,276 (GRCm39) |
|
probably null |
Het |
Slc34a2 |
A |
C |
5: 53,221,340 (GRCm39) |
D262A |
probably benign |
Het |
Slc6a3 |
G |
A |
13: 73,705,300 (GRCm39) |
|
probably null |
Het |
Slfn4 |
A |
T |
11: 83,077,400 (GRCm39) |
T63S |
probably benign |
Het |
Tbx10 |
A |
T |
19: 4,048,571 (GRCm39) |
|
probably benign |
Het |
Tie1 |
A |
T |
4: 118,337,420 (GRCm39) |
N501K |
probably damaging |
Het |
Tmprss11f |
A |
T |
5: 86,685,966 (GRCm39) |
Y134N |
probably damaging |
Het |
Uevld |
A |
T |
7: 46,580,778 (GRCm39) |
D361E |
possibly damaging |
Het |
Ugt1a5 |
A |
C |
1: 88,094,537 (GRCm39) |
D255A |
probably damaging |
Het |
Vmn2r11 |
A |
G |
5: 109,201,935 (GRCm39) |
F190L |
probably benign |
Het |
Wfs1 |
G |
A |
5: 37,132,941 (GRCm39) |
R113C |
probably damaging |
Het |
Yipf5 |
T |
G |
18: 40,339,449 (GRCm39) |
M206L |
probably benign |
Het |
Zbtb10 |
A |
G |
3: 9,346,047 (GRCm39) |
D847G |
probably benign |
Het |
Zfp786 |
T |
A |
6: 47,798,258 (GRCm39) |
K227* |
probably null |
Het |
|
Other mutations in Mtcl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00092:Mtcl1
|
APN |
17 |
66,651,314 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01774:Mtcl1
|
APN |
17 |
66,692,880 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01918:Mtcl1
|
APN |
17 |
66,675,263 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02000:Mtcl1
|
APN |
17 |
66,661,185 (GRCm39) |
missense |
probably benign |
0.19 |
IGL02074:Mtcl1
|
APN |
17 |
66,673,463 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02338:Mtcl1
|
APN |
17 |
66,686,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02597:Mtcl1
|
APN |
17 |
66,645,016 (GRCm39) |
missense |
probably benign |
|
IGL03034:Mtcl1
|
APN |
17 |
66,651,193 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03120:Mtcl1
|
APN |
17 |
66,686,378 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03184:Mtcl1
|
APN |
17 |
66,661,209 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03240:Mtcl1
|
APN |
17 |
66,645,014 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03332:Mtcl1
|
APN |
17 |
66,645,014 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4378001:Mtcl1
|
UTSW |
17 |
66,745,274 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4520001:Mtcl1
|
UTSW |
17 |
66,692,907 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0110:Mtcl1
|
UTSW |
17 |
66,665,109 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0113:Mtcl1
|
UTSW |
17 |
66,661,237 (GRCm39) |
missense |
possibly damaging |
0.52 |
R0321:Mtcl1
|
UTSW |
17 |
66,686,426 (GRCm39) |
missense |
probably damaging |
1.00 |
R0366:Mtcl1
|
UTSW |
17 |
66,645,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R0629:Mtcl1
|
UTSW |
17 |
66,645,137 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1466:Mtcl1
|
UTSW |
17 |
66,687,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1466:Mtcl1
|
UTSW |
17 |
66,687,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Mtcl1
|
UTSW |
17 |
66,755,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Mtcl1
|
UTSW |
17 |
66,755,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R1471:Mtcl1
|
UTSW |
17 |
66,686,143 (GRCm39) |
missense |
probably damaging |
0.96 |
R1650:Mtcl1
|
UTSW |
17 |
66,692,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Mtcl1
|
UTSW |
17 |
66,687,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R1855:Mtcl1
|
UTSW |
17 |
66,686,509 (GRCm39) |
missense |
probably benign |
|
R1882:Mtcl1
|
UTSW |
17 |
66,686,315 (GRCm39) |
missense |
probably benign |
0.01 |
R1935:Mtcl1
|
UTSW |
17 |
66,686,409 (GRCm39) |
missense |
probably benign |
0.10 |
R2063:Mtcl1
|
UTSW |
17 |
66,653,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R2132:Mtcl1
|
UTSW |
17 |
66,650,618 (GRCm39) |
missense |
probably benign |
0.04 |
R2197:Mtcl1
|
UTSW |
17 |
66,673,427 (GRCm39) |
missense |
probably benign |
|
R3196:Mtcl1
|
UTSW |
17 |
66,650,829 (GRCm39) |
missense |
probably benign |
0.07 |
R3877:Mtcl1
|
UTSW |
17 |
66,649,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R4116:Mtcl1
|
UTSW |
17 |
66,673,476 (GRCm39) |
missense |
probably benign |
|
R4204:Mtcl1
|
UTSW |
17 |
66,745,256 (GRCm39) |
missense |
probably damaging |
1.00 |
R4373:Mtcl1
|
UTSW |
17 |
66,687,074 (GRCm39) |
missense |
probably benign |
0.05 |
R4396:Mtcl1
|
UTSW |
17 |
66,651,220 (GRCm39) |
missense |
probably damaging |
1.00 |
R4591:Mtcl1
|
UTSW |
17 |
66,655,506 (GRCm39) |
missense |
probably benign |
0.07 |
R4610:Mtcl1
|
UTSW |
17 |
66,684,882 (GRCm39) |
missense |
probably benign |
0.04 |
R4681:Mtcl1
|
UTSW |
17 |
66,756,139 (GRCm39) |
missense |
unknown |
|
R4922:Mtcl1
|
UTSW |
17 |
66,655,474 (GRCm39) |
missense |
probably benign |
0.29 |
R4992:Mtcl1
|
UTSW |
17 |
66,649,834 (GRCm39) |
missense |
probably damaging |
0.99 |
R5169:Mtcl1
|
UTSW |
17 |
66,650,818 (GRCm39) |
missense |
probably benign |
0.00 |
R5542:Mtcl1
|
UTSW |
17 |
66,691,354 (GRCm39) |
intron |
probably benign |
|
R5804:Mtcl1
|
UTSW |
17 |
66,650,132 (GRCm39) |
missense |
probably benign |
0.03 |
R5998:Mtcl1
|
UTSW |
17 |
66,675,275 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Mtcl1
|
UTSW |
17 |
66,686,326 (GRCm39) |
missense |
probably benign |
0.10 |
R6191:Mtcl1
|
UTSW |
17 |
66,650,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R6254:Mtcl1
|
UTSW |
17 |
66,665,129 (GRCm39) |
missense |
probably benign |
0.02 |
R6260:Mtcl1
|
UTSW |
17 |
66,650,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R6524:Mtcl1
|
UTSW |
17 |
66,655,280 (GRCm39) |
missense |
probably benign |
0.15 |
R6884:Mtcl1
|
UTSW |
17 |
66,745,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R7199:Mtcl1
|
UTSW |
17 |
66,647,534 (GRCm39) |
missense |
probably benign |
0.13 |
R7431:Mtcl1
|
UTSW |
17 |
66,649,901 (GRCm39) |
nonsense |
probably null |
|
R7479:Mtcl1
|
UTSW |
17 |
66,686,485 (GRCm39) |
missense |
probably benign |
|
R7564:Mtcl1
|
UTSW |
17 |
66,678,322 (GRCm39) |
missense |
probably benign |
|
R7608:Mtcl1
|
UTSW |
17 |
66,650,300 (GRCm39) |
missense |
probably damaging |
0.96 |
R7691:Mtcl1
|
UTSW |
17 |
66,687,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R7847:Mtcl1
|
UTSW |
17 |
66,651,328 (GRCm39) |
missense |
probably damaging |
0.96 |
R7908:Mtcl1
|
UTSW |
17 |
66,678,325 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8262:Mtcl1
|
UTSW |
17 |
66,650,653 (GRCm39) |
missense |
probably damaging |
0.99 |
R8324:Mtcl1
|
UTSW |
17 |
66,743,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8477:Mtcl1
|
UTSW |
17 |
66,684,942 (GRCm39) |
missense |
probably benign |
0.10 |
R8927:Mtcl1
|
UTSW |
17 |
66,755,628 (GRCm39) |
missense |
probably benign |
0.00 |
R8928:Mtcl1
|
UTSW |
17 |
66,755,628 (GRCm39) |
missense |
probably benign |
0.00 |
R9016:Mtcl1
|
UTSW |
17 |
66,651,062 (GRCm39) |
missense |
probably damaging |
1.00 |
R9048:Mtcl1
|
UTSW |
17 |
66,678,331 (GRCm39) |
missense |
probably benign |
0.01 |
R9059:Mtcl1
|
UTSW |
17 |
66,650,606 (GRCm39) |
missense |
probably benign |
0.04 |
R9221:Mtcl1
|
UTSW |
17 |
66,650,879 (GRCm39) |
missense |
probably benign |
0.00 |
R9327:Mtcl1
|
UTSW |
17 |
66,645,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R9398:Mtcl1
|
UTSW |
17 |
66,755,462 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9762:Mtcl1
|
UTSW |
17 |
66,673,347 (GRCm39) |
missense |
probably benign |
0.00 |
X0065:Mtcl1
|
UTSW |
17 |
66,686,602 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Mtcl1
|
UTSW |
17 |
66,650,723 (GRCm39) |
missense |
probably benign |
0.20 |
Z1176:Mtcl1
|
UTSW |
17 |
66,686,455 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Mtcl1
|
UTSW |
17 |
66,651,290 (GRCm39) |
missense |
probably damaging |
1.00 |
|