Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700014D04Rik |
T |
C |
13: 59,742,198 |
T603A |
probably benign |
Het |
Aars |
A |
G |
8: 111,054,153 |
D850G |
probably benign |
Het |
Abcc9 |
T |
A |
6: 142,598,110 |
T1480S |
possibly damaging |
Het |
Adgrb3 |
C |
A |
1: 25,553,702 |
V335F |
probably damaging |
Het |
Agfg1 |
C |
A |
1: 82,882,237 |
A275D |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,678,019 |
C2713* |
probably null |
Het |
Atp8a1 |
G |
A |
5: 67,749,149 |
A474V |
|
Het |
Baz1a |
C |
A |
12: 54,916,554 |
S918I |
probably damaging |
Het |
Bcl2l12 |
G |
T |
7: 44,994,250 |
T120K |
possibly damaging |
Het |
Bcl6 |
G |
T |
16: 23,972,357 |
Q416K |
possibly damaging |
Het |
Cdhr1 |
T |
A |
14: 37,098,098 |
I16F |
probably benign |
Het |
Celsr1 |
G |
T |
15: 86,033,085 |
S229* |
probably null |
Het |
Cilp |
T |
C |
9: 65,278,099 |
V492A |
probably damaging |
Het |
Crim1 |
CCGC |
CC |
17: 78,350,865 |
|
probably null |
Het |
Ctcfl |
T |
G |
2: 173,106,088 |
T479P |
probably damaging |
Het |
Dlx6 |
A |
C |
6: 6,863,581 |
M68L |
probably benign |
Het |
Dpy19l4 |
A |
G |
4: 11,265,806 |
V714A |
probably benign |
Het |
Elovl7 |
T |
A |
13: 108,282,654 |
N273K |
probably benign |
Het |
Fbxo22 |
A |
G |
9: 55,223,344 |
K299R |
probably benign |
Het |
Fig4 |
A |
G |
10: 41,267,737 |
V242A |
probably benign |
Het |
Fmo9 |
A |
T |
1: 166,677,620 |
M68K |
probably damaging |
Het |
Fry |
T |
A |
5: 150,378,938 |
Y537N |
probably damaging |
Het |
Fryl |
C |
T |
5: 73,065,220 |
W2006* |
probably null |
Het |
Fzd8 |
T |
A |
18: 9,213,205 |
C96S |
possibly damaging |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 142,240,713 |
|
probably benign |
Het |
Gm4450 |
T |
G |
3: 98,456,503 |
T9P |
probably damaging |
Het |
Gspt1 |
T |
C |
16: 11,232,671 |
D272G |
possibly damaging |
Het |
Gzmf |
A |
T |
14: 56,211,356 |
M1K |
probably null |
Het |
Hipk1 |
T |
C |
3: 103,777,979 |
T107A |
probably benign |
Het |
Ighe |
C |
T |
12: 113,269,487 |
C438Y |
|
Het |
Igkv4-50 |
T |
A |
6: 69,700,983 |
R46W |
|
Het |
Igsf3 |
T |
A |
3: 101,425,759 |
Y118N |
probably damaging |
Het |
Ispd |
T |
C |
12: 36,502,074 |
V309A |
probably benign |
Het |
Itsn1 |
T |
A |
16: 91,815,520 |
Y266N |
probably damaging |
Het |
Jph3 |
A |
G |
8: 121,785,115 |
E614G |
probably damaging |
Het |
Klk1b8 |
T |
A |
7: 43,954,250 |
D170E |
probably benign |
Het |
Ly6e |
A |
T |
15: 74,958,304 |
K36* |
probably null |
Het |
Map3k6 |
C |
A |
4: 133,241,156 |
A23E |
probably damaging |
Het |
Med13l |
T |
A |
5: 118,745,024 |
M1316K |
probably benign |
Het |
Olfr1038-ps |
A |
T |
2: 86,122,024 |
I34F |
possibly damaging |
Het |
Olfr368 |
T |
C |
2: 37,332,281 |
V178A |
possibly damaging |
Het |
Olfr813 |
A |
G |
10: 129,857,429 |
R304G |
probably benign |
Het |
Pih1d2 |
T |
A |
9: 50,618,605 |
C45S |
probably damaging |
Het |
Pik3r2 |
G |
A |
8: 70,771,093 |
S318L |
possibly damaging |
Het |
Pknox1 |
T |
C |
17: 31,583,778 |
I9T |
probably benign |
Het |
Pknox2 |
T |
C |
9: 36,923,745 |
I143V |
probably damaging |
Het |
Polr1d |
A |
G |
5: 147,078,678 |
Y57C |
probably damaging |
Het |
Pum3 |
A |
T |
19: 27,398,936 |
D527E |
probably benign |
Het |
Rars2 |
T |
A |
4: 34,654,819 |
H374Q |
probably damaging |
Het |
Rassf9 |
G |
A |
10: 102,512,508 |
|
probably benign |
Het |
Rbl1 |
T |
A |
2: 157,174,822 |
H619L |
possibly damaging |
Het |
Scamp4 |
T |
C |
10: 80,612,404 |
V153A |
probably benign |
Het |
Sec23b |
T |
G |
2: 144,578,366 |
I450S |
probably benign |
Het |
Slc35b2 |
A |
G |
17: 45,566,984 |
I297V |
probably benign |
Het |
Slc4a4 |
C |
T |
5: 89,179,666 |
T654I |
probably damaging |
Het |
Slc6a5 |
T |
A |
7: 49,951,437 |
M662K |
probably damaging |
Het |
Smarcad1 |
T |
C |
6: 65,094,337 |
Y589H |
probably benign |
Het |
Stab1 |
A |
T |
14: 31,161,112 |
F374I |
probably benign |
Het |
Stat5a |
C |
T |
11: 100,865,428 |
T158M |
possibly damaging |
Het |
Trpc3 |
A |
T |
3: 36,621,354 |
Y878* |
probably null |
Het |
Ubr1 |
T |
A |
2: 120,935,284 |
T491S |
probably benign |
Het |
Uggt1 |
C |
T |
1: 36,216,131 |
|
probably null |
Het |
Ugt1a6a |
T |
A |
1: 88,139,160 |
Y229* |
probably null |
Het |
Vmn1r225 |
G |
A |
17: 20,502,649 |
W117* |
probably null |
Het |
Vmn1r225 |
A |
C |
17: 20,502,650 |
K118Q |
probably damaging |
Het |
Vmn1r43 |
G |
A |
6: 89,869,895 |
T203M |
probably damaging |
Het |
Vmn2r116 |
T |
C |
17: 23,401,592 |
S767P |
probably damaging |
Het |
Wdr90 |
AGAC |
AGACGAC |
17: 25,845,776 |
|
probably benign |
Het |
Ythdf3 |
C |
T |
3: 16,204,495 |
P280S |
probably damaging |
Het |
Zbbx |
A |
G |
3: 75,112,083 |
S107P |
probably benign |
Het |
Zdhhc7 |
A |
T |
8: 120,086,686 |
V128E |
probably benign |
Het |
Zfp235 |
A |
G |
7: 24,142,126 |
S657G |
probably damaging |
Het |
Zfp442 |
T |
A |
2: 150,409,695 |
I96F |
possibly damaging |
Het |
Zfp84 |
G |
A |
7: 29,776,872 |
E330K |
probably damaging |
Het |
|