Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932431P20Rik |
T |
A |
7: 29,536,525 |
|
noncoding transcript |
Het |
A2ml1 |
A |
T |
6: 128,547,305 |
N1121K |
probably null |
Het |
Actr10 |
A |
G |
12: 70,960,021 |
N351D |
probably damaging |
Het |
Adcy7 |
G |
A |
8: 88,317,978 |
A500T |
probably damaging |
Het |
Ankrd35 |
T |
C |
3: 96,679,248 |
I80T |
possibly damaging |
Het |
Arap2 |
G |
A |
5: 62,706,685 |
T532I |
probably damaging |
Het |
Bag3 |
AAAGG |
AAAGGAAGG |
7: 128,545,769 |
|
probably null |
Het |
C77080 |
A |
G |
4: 129,222,639 |
V732A |
probably benign |
Het |
Cc2d2a |
T |
C |
5: 43,684,033 |
|
probably benign |
Het |
Cep85l |
A |
T |
10: 53,348,731 |
M254K |
probably benign |
Het |
Clic4 |
A |
G |
4: 135,223,539 |
S114P |
probably damaging |
Het |
Ctsj |
T |
C |
13: 61,002,549 |
Y213C |
probably damaging |
Het |
Ddx28 |
A |
G |
8: 106,010,574 |
V284A |
probably damaging |
Het |
Dnase2b |
T |
A |
3: 146,584,688 |
D176V |
probably damaging |
Het |
Dsg2 |
T |
A |
18: 20,596,054 |
N663K |
probably damaging |
Het |
Dst |
T |
A |
1: 34,195,921 |
S3694T |
possibly damaging |
Het |
Emilin1 |
T |
C |
5: 30,915,692 |
S158P |
probably benign |
Het |
Eng |
T |
C |
2: 32,673,740 |
|
probably benign |
Het |
Fam160a2 |
T |
C |
7: 105,388,191 |
N395S |
probably damaging |
Het |
Fam189a1 |
T |
A |
7: 64,759,393 |
M418L |
probably benign |
Het |
Fdxr |
C |
A |
11: 115,270,382 |
V223L |
probably benign |
Het |
Frem2 |
T |
A |
3: 53,516,573 |
M3148L |
probably benign |
Het |
Hip1 |
A |
T |
5: 135,431,730 |
D114E |
probably benign |
Het |
Itga9 |
T |
C |
9: 118,877,115 |
|
probably benign |
Het |
Kcnt2 |
T |
A |
1: 140,509,441 |
N487K |
probably damaging |
Het |
Krt6a |
A |
G |
15: 101,693,171 |
F172L |
probably benign |
Het |
Megf8 |
C |
T |
7: 25,340,745 |
R1034W |
probably damaging |
Het |
Muc6 |
C |
T |
7: 141,649,810 |
D451N |
probably damaging |
Het |
Myo5a |
A |
G |
9: 75,217,943 |
T1838A |
possibly damaging |
Het |
N4bp2l2 |
A |
T |
5: 150,661,608 |
D302E |
probably damaging |
Het |
Nbeal2 |
T |
A |
9: 110,630,250 |
I1930F |
probably benign |
Het |
Npas4 |
A |
T |
19: 4,987,364 |
Y301N |
probably benign |
Het |
Nt5m |
A |
G |
11: 59,875,915 |
K211E |
probably benign |
Het |
Pfn4 |
A |
G |
12: 4,774,382 |
|
probably null |
Het |
Pfpl |
A |
C |
19: 12,430,479 |
D698A |
probably benign |
Het |
Pias1 |
G |
T |
9: 62,951,855 |
H124N |
possibly damaging |
Het |
Pja2 |
A |
T |
17: 64,311,167 |
|
probably benign |
Het |
Polr3e |
T |
C |
7: 120,932,242 |
Y185H |
probably benign |
Het |
Pomc |
T |
C |
12: 3,960,275 |
L172S |
probably benign |
Het |
Rapgef4 |
A |
G |
2: 72,045,189 |
T129A |
probably damaging |
Het |
Reep1 |
T |
C |
6: 71,773,294 |
S97P |
probably damaging |
Het |
Rttn |
T |
A |
18: 89,010,943 |
I595N |
possibly damaging |
Het |
Sap30 |
T |
C |
8: 57,485,472 |
|
probably null |
Het |
Slc1a7 |
T |
C |
4: 107,993,006 |
Y105H |
probably damaging |
Het |
Slc5a5 |
C |
T |
8: 70,892,458 |
M68I |
probably damaging |
Het |
Stab2 |
T |
A |
10: 86,940,639 |
Y791F |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,858,661 |
S911R |
probably benign |
Het |
Tdrd1 |
C |
A |
19: 56,858,662 |
H912N |
probably benign |
Het |
Tgm7 |
A |
T |
2: 121,098,581 |
F278Y |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,375,757 |
T310A |
probably damaging |
Het |
Tmem256 |
T |
C |
11: 69,839,445 |
I93T |
probably benign |
Het |
Trpm2 |
G |
A |
10: 77,920,471 |
Q1172* |
probably null |
Het |
Ttll8 |
A |
G |
15: 88,933,953 |
V173A |
possibly damaging |
Het |
Ubr5 |
T |
C |
15: 38,002,299 |
S1497G |
possibly damaging |
Het |
Ubr7 |
G |
A |
12: 102,761,505 |
|
probably null |
Het |
Vmn1r37 |
T |
A |
6: 66,731,894 |
M1K |
probably null |
Het |
Vmn2r14 |
A |
G |
5: 109,218,832 |
|
probably null |
Het |
Vps8 |
A |
G |
16: 21,576,757 |
R1266G |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,242,289 |
N192D |
probably damaging |
Het |
Zfp638 |
G |
C |
6: 83,929,518 |
D222H |
probably damaging |
Het |
Zscan29 |
A |
C |
2: 121,169,402 |
V106G |
probably damaging |
Het |
|