Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
A |
17: 24,387,562 |
I797N |
possibly damaging |
Het |
Actbl2 |
A |
G |
13: 111,255,944 |
E271G |
probably damaging |
Het |
Aplp2 |
T |
C |
9: 31,157,788 |
N526D |
probably benign |
Het |
Cacna1e |
A |
C |
1: 154,479,305 |
N389K |
probably damaging |
Het |
Ccdc18 |
T |
C |
5: 108,174,954 |
I640T |
possibly damaging |
Het |
Ccdc39 |
T |
A |
3: 33,814,367 |
T857S |
probably benign |
Het |
Ccser1 |
T |
A |
6: 61,311,168 |
L105* |
probably null |
Het |
Efhc1 |
T |
A |
1: 20,972,940 |
M361K |
probably benign |
Het |
Fgfr2 |
C |
A |
7: 130,167,745 |
L637F |
probably damaging |
Het |
Fmo9 |
A |
G |
1: 166,664,595 |
|
probably null |
Het |
Gm4302 |
A |
G |
10: 100,341,396 |
T181A |
probably benign |
Het |
Gpat2 |
G |
C |
2: 127,431,918 |
G294R |
possibly damaging |
Het |
Hoxb4 |
A |
G |
11: 96,320,327 |
*251W |
probably null |
Het |
Il1r1 |
T |
A |
1: 40,294,890 |
Y207N |
probably damaging |
Het |
Kcnc2 |
C |
T |
10: 112,463,189 |
T622M |
possibly damaging |
Het |
Kcnk9 |
C |
T |
15: 72,546,243 |
A13T |
probably benign |
Het |
Kdm4c |
C |
T |
4: 74,330,715 |
P69S |
probably damaging |
Het |
Kmt2e |
T |
C |
5: 23,499,519 |
S1237P |
probably benign |
Het |
Lrrc37a |
G |
A |
11: 103,501,089 |
T1170I |
probably benign |
Het |
Lyn |
T |
A |
4: 3,745,527 |
F109I |
probably damaging |
Het |
Lynx1 |
T |
C |
15: 74,751,319 |
Y88C |
probably damaging |
Het |
Mon1b |
T |
A |
8: 113,638,077 |
I162N |
probably damaging |
Het |
Muc4 |
A |
G |
16: 32,736,243 |
|
probably benign |
Het |
Nbn |
T |
A |
4: 15,979,327 |
F437L |
probably benign |
Het |
Neil3 |
T |
C |
8: 53,587,276 |
K564E |
possibly damaging |
Het |
Nfe2l1 |
A |
T |
11: 96,820,051 |
S293T |
probably damaging |
Het |
Olfr121 |
T |
A |
17: 37,752,099 |
S82T |
probably benign |
Het |
Olfr292 |
C |
T |
7: 86,695,059 |
A201V |
probably benign |
Het |
Olfr577 |
T |
C |
7: 102,973,753 |
T80A |
probably damaging |
Het |
Olfr706 |
C |
A |
7: 106,886,014 |
A268S |
probably benign |
Het |
Pcdhb22 |
A |
T |
18: 37,518,304 |
|
probably benign |
Het |
Pcdhgb6 |
A |
G |
18: 37,742,625 |
N129D |
probably damaging |
Het |
Pias2 |
C |
T |
18: 77,152,670 |
T574M |
possibly damaging |
Het |
Plec |
G |
A |
15: 76,177,640 |
T2564I |
probably damaging |
Het |
Qrich2 |
A |
G |
11: 116,458,228 |
|
probably benign |
Het |
Scgb1b12 |
T |
A |
7: 32,334,459 |
V48E |
probably damaging |
Het |
Scn5a |
A |
T |
9: 119,543,356 |
L224Q |
probably damaging |
Het |
Snx3 |
T |
A |
10: 42,534,731 |
Y132* |
probably null |
Het |
Stk39 |
T |
A |
2: 68,392,238 |
I161F |
probably benign |
Het |
Tcaf2 |
A |
C |
6: 42,626,178 |
L816R |
probably damaging |
Het |
Thap4 |
C |
A |
1: 93,725,156 |
|
probably null |
Het |
Tmc5 |
T |
A |
7: 118,656,814 |
V704E |
probably damaging |
Het |
Tmem39a |
A |
G |
16: 38,585,237 |
T59A |
probably benign |
Het |
Tshz2 |
A |
G |
2: 169,886,019 |
N376S |
probably damaging |
Het |
Vmn1r60 |
T |
C |
7: 5,545,018 |
N28D |
probably damaging |
Het |
Zfp637 |
C |
T |
6: 117,845,324 |
R138W |
probably damaging |
Het |
|