Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700014D04Rik |
T |
C |
13: 59,742,620 |
E44G |
probably benign |
Het |
Anxa7 |
A |
G |
14: 20,471,467 |
Y54H |
unknown |
Het |
Arhgef3 |
A |
G |
14: 27,397,605 |
T331A |
probably benign |
Het |
Arhgef40 |
G |
T |
14: 51,989,930 |
C477F |
possibly damaging |
Het |
Arsi |
G |
A |
18: 60,916,651 |
G202E |
probably benign |
Het |
Atp13a5 |
C |
A |
16: 29,321,709 |
R343L |
probably damaging |
Het |
Brdt |
ACAGCAGCAGCAGCAGC |
ACAGCAGCAGCAGC |
5: 107,359,853 |
|
probably benign |
Het |
Btbd2 |
G |
T |
10: 80,643,913 |
D426E |
probably damaging |
Het |
Cabin1 |
A |
C |
10: 75,725,745 |
I974R |
possibly damaging |
Het |
Cacna1i |
G |
A |
15: 80,389,122 |
V1670M |
probably damaging |
Het |
Cc2d2a |
C |
A |
5: 43,688,252 |
Q288K |
probably damaging |
Het |
Ccl20 |
T |
A |
1: 83,117,829 |
I37K |
possibly damaging |
Het |
Cdcp1 |
A |
G |
9: 123,190,094 |
V40A |
probably benign |
Het |
Cdcp1 |
T |
C |
9: 123,215,831 |
T27A |
probably benign |
Het |
Cdh4 |
C |
T |
2: 179,886,842 |
T581I |
probably damaging |
Het |
Cgn |
A |
G |
3: 94,762,557 |
|
probably null |
Het |
Col7a1 |
G |
A |
9: 108,965,928 |
G1493D |
unknown |
Het |
Creb3 |
A |
G |
4: 43,563,302 |
E133G |
probably benign |
Het |
Dchs1 |
T |
C |
7: 105,771,720 |
T498A |
probably benign |
Het |
Dis3l |
A |
C |
9: 64,317,776 |
V413G |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,024,958 |
E3865G |
probably damaging |
Het |
Fam219b |
A |
G |
9: 57,539,281 |
Y139C |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,997,136 |
Y2523* |
probably null |
Het |
Fat3 |
A |
T |
9: 15,997,138 |
Y2523N |
probably benign |
Het |
Fmnl1 |
T |
C |
11: 103,197,147 |
S40P |
probably benign |
Het |
Gm17727 |
T |
A |
9: 35,777,122 |
I56F |
probably benign |
Het |
Gm4792 |
T |
C |
10: 94,298,490 |
D6G |
unknown |
Het |
Hhat |
G |
T |
1: 192,693,906 |
Y306* |
probably null |
Het |
Hmcn1 |
A |
G |
1: 150,598,285 |
I4802T |
probably benign |
Het |
Hmcn1 |
G |
A |
1: 150,627,152 |
T3908I |
probably damaging |
Het |
Hsph1 |
A |
T |
5: 149,630,773 |
N79K |
probably damaging |
Het |
Ikbke |
T |
A |
1: 131,259,218 |
Y579F |
probably damaging |
Het |
Jak2 |
A |
G |
19: 29,299,557 |
D838G |
probably benign |
Het |
Klhdc7b |
T |
C |
15: 89,387,020 |
S702P |
probably benign |
Het |
Lingo3 |
C |
A |
10: 80,835,598 |
R166L |
probably benign |
Het |
Lins1 |
T |
C |
7: 66,711,909 |
F436S |
probably damaging |
Het |
Lman1 |
T |
C |
18: 65,991,684 |
D328G |
probably benign |
Het |
Lox |
A |
G |
18: 52,528,307 |
C232R |
probably damaging |
Het |
Lrrc59 |
T |
C |
11: 94,638,595 |
V165A |
probably benign |
Het |
Map9 |
A |
G |
3: 82,380,221 |
D50G |
probably damaging |
Het |
March1 |
T |
A |
8: 66,386,942 |
Y126N |
possibly damaging |
Het |
Mcf2l |
T |
C |
8: 12,915,982 |
F3L |
probably benign |
Het |
Nin |
G |
A |
12: 70,043,795 |
Q949* |
probably null |
Het |
Nlgn3 |
A |
G |
X: 101,320,033 |
H636R |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,099,547 |
D411G |
possibly damaging |
Het |
Olfr1263 |
A |
G |
2: 90,015,020 |
Y30C |
probably damaging |
Het |
Olfr1449 |
G |
C |
19: 12,934,968 |
A77P |
probably damaging |
Het |
Plekha7 |
A |
G |
7: 116,140,681 |
V579A |
probably damaging |
Het |
Prrc2c |
T |
C |
1: 162,705,959 |
|
probably benign |
Het |
Rab7b |
T |
C |
1: 131,697,068 |
|
probably null |
Het |
Reg3b |
G |
T |
6: 78,372,214 |
|
probably null |
Het |
Rgs20 |
A |
G |
1: 4,910,572 |
Y177H |
probably damaging |
Het |
Ripk3 |
G |
T |
14: 55,785,329 |
N379K |
probably benign |
Het |
Rnf220 |
G |
T |
4: 117,307,568 |
Q7K |
probably benign |
Het |
Ros1 |
T |
A |
10: 52,124,103 |
K1109* |
probably null |
Het |
Slc22a7 |
T |
G |
17: 46,433,153 |
R460S |
probably damaging |
Het |
Slc4a2 |
A |
G |
5: 24,439,328 |
M975V |
probably damaging |
Het |
Slc4a3 |
A |
T |
1: 75,557,308 |
I1100F |
probably damaging |
Het |
Smco1 |
A |
G |
16: 32,274,132 |
E207G |
probably benign |
Het |
Snrnp200 |
A |
G |
2: 127,216,736 |
E369G |
probably benign |
Het |
Tcf4 |
T |
A |
18: 69,657,853 |
M178K |
probably benign |
Het |
Tex2 |
T |
C |
11: 106,567,902 |
|
probably benign |
Het |
Tjp1 |
A |
T |
7: 65,323,129 |
I521N |
probably damaging |
Het |
Tmem203 |
A |
G |
2: 25,255,994 |
T109A |
probably benign |
Het |
Tmem50b |
T |
C |
16: 91,578,029 |
I126V |
probably benign |
Het |
Ugcg |
C |
T |
4: 59,207,798 |
P46S |
probably benign |
Het |
Ush2a |
T |
C |
1: 188,862,809 |
F3813L |
probably benign |
Het |
Vmn1r203 |
C |
T |
13: 22,524,351 |
R101W |
probably damaging |
Het |
Vmn2r79 |
G |
A |
7: 87,001,413 |
V136I |
probably benign |
Het |
Wdr38 |
A |
G |
2: 39,000,729 |
Y205C |
probably damaging |
Het |
Zfp248 |
A |
G |
6: 118,429,303 |
F442L |
probably damaging |
Het |
Znrf4 |
A |
G |
17: 56,511,599 |
I236T |
probably damaging |
Het |
|