Other mutations in this stock |
Total: 103 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Actn1 |
A |
G |
12: 80,230,393 (GRCm39) |
L287S |
probably damaging |
Het |
Adgrf1 |
A |
T |
17: 43,616,237 (GRCm39) |
Q292L |
possibly damaging |
Het |
Arhgap32 |
A |
G |
9: 32,172,026 (GRCm39) |
D1602G |
probably benign |
Het |
Atrnl1 |
C |
T |
19: 57,617,551 (GRCm39) |
P109S |
probably damaging |
Het |
Camsap1 |
G |
A |
2: 25,843,962 (GRCm39) |
H230Y |
probably benign |
Het |
Capns1 |
C |
T |
7: 29,891,612 (GRCm39) |
C144Y |
probably damaging |
Het |
Ccdc17 |
G |
A |
4: 116,455,994 (GRCm39) |
V341I |
possibly damaging |
Het |
Cd36 |
T |
C |
5: 18,002,033 (GRCm39) |
T323A |
probably damaging |
Het |
Cdc14a |
CGCTGCTGCTGCTGCTGCTG |
CGCTGCTGCTGCTGCTG |
3: 116,087,509 (GRCm39) |
|
probably benign |
Het |
Ckap2l |
G |
A |
2: 129,111,161 (GRCm39) |
Q679* |
probably null |
Het |
Clec4g |
T |
A |
8: 3,768,565 (GRCm39) |
N93I |
probably benign |
Het |
Cntnap2 |
T |
A |
6: 45,992,165 (GRCm39) |
L364Q |
probably damaging |
Het |
Cul9 |
A |
G |
17: 46,841,026 (GRCm39) |
M748T |
probably benign |
Het |
Dnah11 |
A |
T |
12: 118,150,711 (GRCm39) |
I349N |
probably damaging |
Het |
Dnajc14 |
T |
A |
10: 128,642,260 (GRCm39) |
Y61N |
probably benign |
Het |
Dock6 |
A |
T |
9: 21,713,802 (GRCm39) |
Y1909* |
probably null |
Het |
Dock8 |
T |
A |
19: 25,165,739 (GRCm39) |
D1874E |
probably benign |
Het |
Dpm1 |
A |
G |
2: 168,072,210 (GRCm39) |
S22P |
probably benign |
Het |
Dysf |
T |
C |
6: 84,128,885 (GRCm39) |
L1385P |
probably damaging |
Het |
Egf |
T |
C |
3: 129,491,421 (GRCm39) |
T859A |
probably benign |
Het |
Eif2b1 |
A |
T |
5: 124,711,867 (GRCm39) |
S162T |
probably benign |
Het |
Emilin1 |
T |
C |
5: 31,075,484 (GRCm39) |
L575P |
probably damaging |
Het |
Erp27 |
T |
A |
6: 136,886,550 (GRCm39) |
Q161L |
probably benign |
Het |
Fbxw10 |
C |
A |
11: 62,765,945 (GRCm39) |
D738E |
possibly damaging |
Het |
Fcgbp |
T |
G |
7: 27,790,937 (GRCm39) |
C733G |
probably damaging |
Het |
Fgb |
T |
A |
3: 82,957,122 (GRCm39) |
|
probably benign |
Het |
Gata3os |
A |
T |
2: 9,887,634 (GRCm39) |
T12S |
unknown |
Het |
Got1l1 |
G |
T |
8: 27,688,503 (GRCm39) |
Q283K |
probably benign |
Het |
Grk2 |
G |
A |
19: 4,340,871 (GRCm39) |
R226C |
probably damaging |
Het |
Hoxa10 |
T |
C |
6: 52,211,334 (GRCm39) |
D194G |
probably benign |
Het |
Ipcef1 |
G |
A |
10: 6,840,620 (GRCm39) |
T363I |
probably damaging |
Het |
Itga10 |
C |
A |
3: 96,564,273 (GRCm39) |
T922N |
probably damaging |
Het |
Itgad |
T |
C |
7: 127,777,552 (GRCm39) |
I144T |
probably benign |
Het |
Kat6b |
C |
A |
14: 21,567,564 (GRCm39) |
Q208K |
possibly damaging |
Het |
Kidins220 |
T |
G |
12: 25,088,383 (GRCm39) |
L1042R |
probably damaging |
Het |
Kmt2c |
T |
C |
5: 25,486,355 (GRCm39) |
S4733G |
probably damaging |
Het |
Lrig3 |
A |
G |
10: 125,850,736 (GRCm39) |
I1101V |
probably benign |
Het |
Lrp1 |
T |
A |
10: 127,431,229 (GRCm39) |
N311I |
probably damaging |
Het |
Man2a1 |
A |
T |
17: 64,958,310 (GRCm39) |
K275I |
probably benign |
Het |
Map3k10 |
T |
A |
7: 27,364,434 (GRCm39) |
N318I |
probably damaging |
Het |
Map3k8 |
G |
A |
18: 4,333,869 (GRCm39) |
R408W |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,873,593 (GRCm39) |
H1925R |
probably benign |
Het |
Med12l |
C |
T |
3: 58,984,207 (GRCm39) |
S461L |
probably damaging |
Het |
Mfap1a |
T |
C |
2: 121,333,237 (GRCm39) |
K65E |
probably damaging |
Het |
Mical1 |
T |
C |
10: 41,358,602 (GRCm39) |
S507P |
probably benign |
Het |
Miga2 |
T |
C |
2: 30,268,400 (GRCm39) |
V433A |
unknown |
Het |
Mpdz |
T |
C |
4: 81,274,653 (GRCm39) |
T848A |
probably benign |
Het |
Mycn |
A |
G |
12: 12,989,778 (GRCm39) |
V206A |
probably benign |
Het |
Ndst1 |
G |
A |
18: 60,838,220 (GRCm39) |
Q342* |
probably null |
Het |
Nectin1 |
A |
G |
9: 43,702,369 (GRCm39) |
M39V |
probably benign |
Het |
Nectin4 |
A |
T |
1: 171,210,209 (GRCm39) |
R234* |
probably null |
Het |
Ngb |
C |
G |
12: 87,145,317 (GRCm39) |
V113L |
possibly damaging |
Het |
Nphp3 |
T |
A |
9: 103,913,337 (GRCm39) |
Y990N |
probably damaging |
Het |
Nrdc |
T |
C |
4: 108,915,833 (GRCm39) |
|
probably null |
Het |
Or10a2 |
A |
T |
7: 106,673,739 (GRCm39) |
K235* |
probably null |
Het |
Or1e23 |
T |
A |
11: 73,407,351 (GRCm39) |
I225F |
probably damaging |
Het |
Or5p60 |
T |
A |
7: 107,723,801 (GRCm39) |
Y223F |
probably benign |
Het |
Osbpl6 |
A |
G |
2: 76,415,603 (GRCm39) |
Y655C |
probably damaging |
Het |
Pcdhgb4 |
A |
G |
18: 37,855,882 (GRCm39) |
Q759R |
probably benign |
Het |
Pcsk4 |
T |
C |
10: 80,161,800 (GRCm39) |
D164G |
probably damaging |
Het |
Pde4d |
T |
A |
13: 110,071,915 (GRCm39) |
I303N |
probably damaging |
Het |
Pdf |
T |
A |
8: 107,774,972 (GRCm39) |
M87L |
probably benign |
Het |
Pigb |
A |
G |
9: 72,941,840 (GRCm39) |
S140P |
probably damaging |
Het |
Plch1 |
T |
A |
3: 63,758,549 (GRCm39) |
|
probably benign |
Het |
Plxna1 |
G |
T |
6: 89,319,633 (GRCm39) |
D557E |
probably benign |
Het |
Polr2e |
C |
T |
10: 79,872,792 (GRCm39) |
V149M |
probably benign |
Het |
Polr3a |
A |
T |
14: 24,503,313 (GRCm39) |
C1174S |
probably benign |
Het |
Prb1c |
T |
A |
6: 132,338,891 (GRCm39) |
N109I |
unknown |
Het |
Psmd2 |
T |
A |
16: 20,474,369 (GRCm39) |
S308R |
probably benign |
Het |
Ptger1 |
T |
A |
8: 84,396,002 (GRCm39) |
V353E |
probably damaging |
Het |
Ptprc |
A |
G |
1: 137,996,111 (GRCm39) |
M940T |
probably benign |
Het |
Pus7l |
T |
C |
15: 94,425,781 (GRCm39) |
N540S |
probably damaging |
Het |
Rap1gds1 |
T |
A |
3: 138,756,317 (GRCm39) |
I13L |
probably benign |
Het |
Rasl10b |
A |
T |
11: 83,303,590 (GRCm39) |
N49I |
probably damaging |
Het |
Rftn1 |
A |
T |
17: 50,301,237 (GRCm39) |
N537K |
probably benign |
Het |
Rnase4 |
A |
G |
14: 51,342,645 (GRCm39) |
Y123C |
probably damaging |
Het |
Rnf181 |
A |
C |
6: 72,338,302 (GRCm39) |
N26K |
probably benign |
Het |
Rnf31 |
G |
A |
14: 55,836,269 (GRCm39) |
|
probably null |
Het |
Rpusd3 |
C |
G |
6: 113,393,200 (GRCm39) |
C304S |
unknown |
Het |
Rsf1 |
CGGC |
CGGCGGCGGGGGC |
7: 97,229,139 (GRCm39) |
|
probably benign |
Het |
Ryr3 |
C |
A |
2: 112,664,270 (GRCm39) |
V1694L |
probably benign |
Het |
Sanbr |
T |
C |
11: 23,559,098 (GRCm39) |
Y372C |
probably damaging |
Het |
Sephs2 |
T |
C |
7: 126,872,346 (GRCm39) |
D249G |
probably damaging |
Het |
Serpina10 |
A |
G |
12: 103,583,217 (GRCm39) |
I409T |
probably damaging |
Het |
Serpina5 |
C |
T |
12: 104,069,403 (GRCm39) |
A205V |
probably damaging |
Het |
Sfr1 |
T |
A |
19: 47,723,453 (GRCm39) |
V319E |
probably damaging |
Het |
Skil |
T |
A |
3: 31,171,639 (GRCm39) |
Y542N |
probably benign |
Het |
Slc15a5 |
T |
C |
6: 138,049,954 (GRCm39) |
T154A |
probably benign |
Het |
Slc27a2 |
T |
A |
2: 126,429,846 (GRCm39) |
L618Q |
probably damaging |
Het |
Slc6a6 |
A |
T |
6: 91,726,808 (GRCm39) |
Y483F |
probably benign |
Het |
Sprr1b |
T |
C |
3: 92,344,443 (GRCm39) |
I144M |
probably benign |
Het |
Stat5a |
T |
A |
11: 100,771,161 (GRCm39) |
V580E |
|
Het |
Tnk1 |
C |
T |
11: 69,746,011 (GRCm39) |
D305N |
probably damaging |
Het |
Tox2 |
A |
G |
2: 163,164,930 (GRCm39) |
*523W |
probably null |
Het |
Trav12-2 |
A |
G |
14: 53,854,085 (GRCm39) |
N20D |
probably benign |
Het |
Trav16 |
T |
A |
14: 53,981,046 (GRCm39) |
N78K |
probably damaging |
Het |
Trf |
C |
T |
9: 103,104,130 (GRCm39) |
A78T |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,711,543 (GRCm39) |
|
probably benign |
Het |
Vmn2r67 |
T |
A |
7: 84,785,834 (GRCm39) |
M724L |
probably benign |
Het |
Vmn2r94 |
A |
T |
17: 18,477,261 (GRCm39) |
F383L |
probably benign |
Het |
Vwa2 |
T |
C |
19: 56,895,208 (GRCm39) |
S461P |
probably benign |
Het |
Zfp991 |
G |
A |
4: 147,264,327 (GRCm39) |
G568E |
probably damaging |
Het |
Zfpl1 |
A |
G |
19: 6,134,440 (GRCm39) |
F15S |
probably damaging |
Het |
|
Other mutations in Mast1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01395:Mast1
|
APN |
8 |
85,639,444 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01862:Mast1
|
APN |
8 |
85,639,875 (GRCm39) |
splice site |
probably null |
|
IGL01918:Mast1
|
APN |
8 |
85,647,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02212:Mast1
|
APN |
8 |
85,648,026 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02221:Mast1
|
APN |
8 |
85,645,384 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02370:Mast1
|
APN |
8 |
85,638,883 (GRCm39) |
missense |
probably benign |
|
IGL02470:Mast1
|
APN |
8 |
85,647,841 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02596:Mast1
|
APN |
8 |
85,644,400 (GRCm39) |
missense |
probably benign |
|
IGL02716:Mast1
|
APN |
8 |
85,662,352 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02987:Mast1
|
APN |
8 |
85,652,348 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL03287:Mast1
|
APN |
8 |
85,639,982 (GRCm39) |
missense |
probably benign |
0.01 |
R0255:Mast1
|
UTSW |
8 |
85,638,650 (GRCm39) |
missense |
probably benign |
|
R0388:Mast1
|
UTSW |
8 |
85,642,166 (GRCm39) |
missense |
probably benign |
0.13 |
R0480:Mast1
|
UTSW |
8 |
85,639,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R0727:Mast1
|
UTSW |
8 |
85,648,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R1175:Mast1
|
UTSW |
8 |
85,651,956 (GRCm39) |
missense |
probably benign |
0.29 |
R1297:Mast1
|
UTSW |
8 |
85,639,345 (GRCm39) |
missense |
probably benign |
0.05 |
R1328:Mast1
|
UTSW |
8 |
85,644,617 (GRCm39) |
intron |
probably benign |
|
R1454:Mast1
|
UTSW |
8 |
85,647,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Mast1
|
UTSW |
8 |
85,655,238 (GRCm39) |
nonsense |
probably null |
|
R1752:Mast1
|
UTSW |
8 |
85,651,965 (GRCm39) |
missense |
probably benign |
|
R1777:Mast1
|
UTSW |
8 |
85,638,697 (GRCm39) |
missense |
probably benign |
|
R1905:Mast1
|
UTSW |
8 |
85,642,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1906:Mast1
|
UTSW |
8 |
85,642,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R1907:Mast1
|
UTSW |
8 |
85,642,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R2056:Mast1
|
UTSW |
8 |
85,646,995 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2071:Mast1
|
UTSW |
8 |
85,647,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R2145:Mast1
|
UTSW |
8 |
85,648,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R2318:Mast1
|
UTSW |
8 |
85,647,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R2842:Mast1
|
UTSW |
8 |
85,650,537 (GRCm39) |
missense |
probably damaging |
1.00 |
R3870:Mast1
|
UTSW |
8 |
85,645,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R3895:Mast1
|
UTSW |
8 |
85,662,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R3973:Mast1
|
UTSW |
8 |
85,645,393 (GRCm39) |
missense |
probably damaging |
1.00 |
R4405:Mast1
|
UTSW |
8 |
85,647,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4533:Mast1
|
UTSW |
8 |
85,647,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R4725:Mast1
|
UTSW |
8 |
85,655,635 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4770:Mast1
|
UTSW |
8 |
85,655,875 (GRCm39) |
missense |
probably benign |
0.02 |
R4776:Mast1
|
UTSW |
8 |
85,663,822 (GRCm39) |
critical splice donor site |
probably null |
|
R4835:Mast1
|
UTSW |
8 |
85,650,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R4871:Mast1
|
UTSW |
8 |
85,647,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Mast1
|
UTSW |
8 |
85,645,357 (GRCm39) |
missense |
probably damaging |
0.99 |
R4960:Mast1
|
UTSW |
8 |
85,644,500 (GRCm39) |
missense |
probably benign |
|
R4978:Mast1
|
UTSW |
8 |
85,662,416 (GRCm39) |
missense |
probably damaging |
0.98 |
R5164:Mast1
|
UTSW |
8 |
85,640,147 (GRCm39) |
unclassified |
probably benign |
|
R5235:Mast1
|
UTSW |
8 |
85,640,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R5297:Mast1
|
UTSW |
8 |
85,639,947 (GRCm39) |
critical splice donor site |
probably null |
|
R5463:Mast1
|
UTSW |
8 |
85,652,136 (GRCm39) |
missense |
probably damaging |
1.00 |
R5546:Mast1
|
UTSW |
8 |
85,642,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5651:Mast1
|
UTSW |
8 |
85,655,597 (GRCm39) |
nonsense |
probably null |
|
R6124:Mast1
|
UTSW |
8 |
85,651,936 (GRCm39) |
missense |
probably benign |
0.01 |
R6213:Mast1
|
UTSW |
8 |
85,642,198 (GRCm39) |
missense |
probably damaging |
1.00 |
R6717:Mast1
|
UTSW |
8 |
85,644,383 (GRCm39) |
missense |
probably benign |
|
R7000:Mast1
|
UTSW |
8 |
85,655,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R7011:Mast1
|
UTSW |
8 |
85,638,574 (GRCm39) |
nonsense |
probably null |
|
R7164:Mast1
|
UTSW |
8 |
85,661,933 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7695:Mast1
|
UTSW |
8 |
85,647,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R7845:Mast1
|
UTSW |
8 |
85,651,954 (GRCm39) |
nonsense |
probably null |
|
R7882:Mast1
|
UTSW |
8 |
85,639,947 (GRCm39) |
critical splice donor site |
probably null |
|
R8167:Mast1
|
UTSW |
8 |
85,647,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R8197:Mast1
|
UTSW |
8 |
85,639,450 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8773:Mast1
|
UTSW |
8 |
85,642,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R9477:Mast1
|
UTSW |
8 |
85,638,779 (GRCm39) |
missense |
probably benign |
0.18 |
R9557:Mast1
|
UTSW |
8 |
85,657,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R9655:Mast1
|
UTSW |
8 |
85,650,660 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Mast1
|
UTSW |
8 |
85,647,507 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mast1
|
UTSW |
8 |
85,645,310 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Mast1
|
UTSW |
8 |
85,639,088 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Mast1
|
UTSW |
8 |
85,647,075 (GRCm39) |
missense |
probably benign |
0.09 |
|