Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap13 |
T |
A |
7: 75,730,579 |
V500E |
possibly damaging |
Het |
Ankrd34b |
T |
C |
13: 92,439,462 |
S401P |
probably benign |
Het |
Arfgef2 |
T |
A |
2: 166,826,928 |
D41E |
probably benign |
Het |
Arid1a |
T |
C |
4: 133,753,568 |
N15S |
unknown |
Het |
Arsa |
A |
T |
15: 89,474,718 |
|
probably null |
Het |
B3gnt9 |
C |
A |
8: 105,254,432 |
C108F |
probably damaging |
Het |
Bbc3 |
C |
A |
7: 16,313,808 |
Y152* |
probably null |
Het |
Btbd1 |
T |
C |
7: 81,818,209 |
M188V |
probably benign |
Het |
Caln1 |
C |
T |
5: 130,822,997 |
T209I |
probably benign |
Het |
Casp12 |
C |
T |
9: 5,353,763 |
P266S |
possibly damaging |
Het |
Ccm2l |
A |
T |
2: 153,070,867 |
I109F |
probably damaging |
Het |
Chst15 |
A |
C |
7: 132,270,258 |
L98R |
probably damaging |
Het |
Ctsq |
A |
G |
13: 61,038,923 |
M89T |
probably benign |
Het |
Ddx39b |
T |
C |
17: 35,247,010 |
V169A |
probably benign |
Het |
Ddx58 |
A |
G |
4: 40,213,804 |
V618A |
probably benign |
Het |
Fam57b |
T |
C |
7: 126,827,495 |
F80S |
probably damaging |
Het |
Fhad1 |
T |
C |
4: 141,951,616 |
H583R |
probably benign |
Het |
Fndc1 |
T |
A |
17: 7,800,931 |
I139F |
probably damaging |
Het |
Gm5724 |
T |
A |
6: 141,773,778 |
M1L |
probably damaging |
Het |
Gm7145 |
C |
G |
1: 117,985,831 |
H148D |
probably benign |
Het |
Gpr62 |
C |
A |
9: 106,465,442 |
A96S |
probably damaging |
Het |
Gsap |
T |
A |
5: 21,270,620 |
|
probably null |
Het |
Hdhd5 |
T |
A |
6: 120,523,471 |
T89S |
probably damaging |
Het |
Kcna5 |
T |
A |
6: 126,533,629 |
Y512F |
probably damaging |
Het |
Krt84 |
C |
A |
15: 101,529,609 |
E304* |
probably null |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,189,077 |
|
probably benign |
Het |
Lrp6 |
C |
A |
6: 134,507,551 |
V370L |
probably benign |
Het |
Lrrc3c |
G |
A |
11: 98,599,318 |
G167D |
probably damaging |
Het |
Man2b1 |
C |
T |
8: 85,087,280 |
T291M |
probably benign |
Het |
Mapkbp1 |
A |
G |
2: 120,025,132 |
E1438G |
possibly damaging |
Het |
Med12l |
A |
G |
3: 59,276,017 |
T1947A |
probably benign |
Het |
Myh15 |
A |
T |
16: 49,061,574 |
T60S |
probably damaging |
Het |
Myo5a |
A |
T |
9: 75,171,563 |
I868F |
probably benign |
Het |
Myom3 |
A |
T |
4: 135,808,851 |
I1278F |
probably damaging |
Het |
Nbn |
G |
T |
4: 15,983,677 |
|
probably null |
Het |
Ncam2 |
G |
T |
16: 81,490,374 |
S392I |
probably damaging |
Het |
Nrg3 |
A |
C |
14: 38,370,735 |
L647* |
probably null |
Het |
Olfr1062 |
T |
A |
2: 86,423,612 |
|
probably null |
Het |
Olfr1393 |
A |
T |
11: 49,280,358 |
D70V |
probably damaging |
Het |
Olfr1406 |
A |
T |
1: 173,184,323 |
L37Q |
possibly damaging |
Het |
Olfr721-ps1 |
T |
C |
14: 14,407,251 |
S8P |
possibly damaging |
Het |
Pcdhb9 |
A |
G |
18: 37,401,492 |
N180D |
possibly damaging |
Het |
Pcdhga4 |
A |
G |
18: 37,686,919 |
N507S |
probably damaging |
Het |
Pdilt |
A |
G |
7: 119,487,951 |
V492A |
probably benign |
Het |
Phf12 |
A |
G |
11: 78,023,540 |
T603A |
possibly damaging |
Het |
Phox2b |
T |
A |
5: 67,097,585 |
I174F |
probably benign |
Het |
Polq |
A |
T |
16: 37,062,853 |
Q1793L |
possibly damaging |
Het |
Prmt9 |
T |
C |
8: 77,555,764 |
F97L |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,819,540 |
L280P |
probably damaging |
Het |
Pygl |
A |
T |
12: 70,197,406 |
M587K |
probably benign |
Het |
Rc3h2 |
T |
C |
2: 37,409,647 |
S124G |
probably benign |
Het |
Rdh5 |
A |
G |
10: 128,918,315 |
I83T |
possibly damaging |
Het |
Ryr2 |
T |
G |
13: 11,810,908 |
R561S |
probably damaging |
Het |
Scara3 |
A |
G |
14: 65,920,780 |
L593P |
probably damaging |
Het |
Scfd2 |
T |
C |
5: 74,531,343 |
I93V |
probably benign |
Het |
Sema4f |
C |
A |
6: 82,917,883 |
V444L |
possibly damaging |
Het |
Spata33 |
T |
C |
8: 123,214,395 |
L61P |
unknown |
Het |
Stard10 |
A |
T |
7: 101,343,136 |
|
probably null |
Het |
Stub1 |
T |
C |
17: 25,832,064 |
I115V |
probably benign |
Het |
Tmem247 |
C |
T |
17: 86,918,282 |
T50I |
probably benign |
Het |
Tnrc6b |
A |
G |
15: 80,887,022 |
M1103V |
possibly damaging |
Het |
Trim61 |
T |
C |
8: 65,013,874 |
Y245C |
probably benign |
Het |
Trip13 |
T |
C |
13: 73,920,011 |
I284V |
probably benign |
Het |
Trpm4 |
T |
C |
7: 45,327,268 |
|
probably null |
Het |
Ttn |
A |
G |
2: 76,730,574 |
L29161S |
probably damaging |
Het |
Ttn |
C |
A |
2: 76,909,748 |
L3528F |
unknown |
Het |
Ube2v2 |
G |
A |
16: 15,581,084 |
T47I |
probably benign |
Het |
Vwa5b1 |
C |
T |
4: 138,575,422 |
A921T |
possibly damaging |
Het |
Xylt1 |
T |
A |
7: 117,637,602 |
F526Y |
probably damaging |
Het |
|