Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
A |
G |
5: 113,183,226 |
S1041P |
probably benign |
Het |
Aatf |
ACACACACACACACACACACACACACACACACACACACACACACACACAC |
ACACACACACACACACACACACACACACACACACACACACACACACACACAC |
11: 84,471,038 |
|
probably null |
Het |
Arpin |
A |
T |
7: 79,927,715 |
W195R |
probably damaging |
Het |
Asap1 |
A |
G |
15: 64,092,076 |
V1091A |
probably damaging |
Het |
Bmp7 |
C |
A |
2: 172,939,991 |
A27S |
probably benign |
Het |
Ccnh |
T |
A |
13: 85,211,872 |
Y297* |
probably null |
Het |
Ccno |
C |
A |
13: 112,988,113 |
D72E |
probably benign |
Het |
Cd70 |
T |
G |
17: 57,148,770 |
T67P |
probably damaging |
Het |
Chml |
CTGTTTG |
CTG |
1: 175,687,400 |
|
probably null |
Het |
Chst4 |
A |
G |
8: 110,030,913 |
F106S |
probably damaging |
Het |
Cntnap3 |
A |
C |
13: 64,903,773 |
L23R |
probably benign |
Het |
Crybg2 |
T |
A |
4: 134,087,599 |
L1288H |
probably damaging |
Het |
Cse1l |
T |
A |
2: 166,935,671 |
|
probably null |
Het |
Cyfip2 |
T |
C |
11: 46,242,350 |
H841R |
probably damaging |
Het |
Cyp2c39 |
T |
C |
19: 39,560,961 |
Y308H |
possibly damaging |
Het |
Cyp4f18 |
G |
A |
8: 71,988,643 |
P498S |
possibly damaging |
Het |
Dennd1b |
G |
A |
1: 139,062,873 |
E192K |
probably damaging |
Het |
Dnah3 |
T |
A |
7: 119,967,552 |
I97F |
|
Het |
Entpd3 |
A |
G |
9: 120,560,586 |
R313G |
possibly damaging |
Het |
Erg28 |
G |
A |
12: 85,819,479 |
T75I |
probably damaging |
Het |
Fam171a1 |
A |
G |
2: 3,225,384 |
H518R |
probably benign |
Het |
Fam50b |
G |
A |
13: 34,747,101 |
E187K |
possibly damaging |
Het |
Galntl6 |
T |
C |
8: 57,837,188 |
E457G |
probably damaging |
Het |
Glt8d1 |
A |
T |
14: 31,010,339 |
H192L |
probably damaging |
Het |
Gm15446 |
T |
A |
5: 109,943,299 |
C472* |
probably null |
Het |
Gm28363 |
A |
T |
1: 117,697,498 |
M1L |
unknown |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 142,240,817 |
|
probably benign |
Het |
Gstp3 |
T |
A |
19: 4,058,746 |
K45* |
probably null |
Het |
Hsd17b13 |
A |
G |
5: 103,965,815 |
F258L |
possibly damaging |
Het |
Htt |
T |
C |
5: 34,864,649 |
S1646P |
probably benign |
Het |
Ipo11 |
T |
C |
13: 106,892,468 |
M326V |
probably benign |
Het |
Itpr3 |
T |
A |
17: 27,117,179 |
I2293N |
probably damaging |
Het |
Klk8 |
A |
G |
7: 43,799,326 |
|
probably null |
Het |
Kntc1 |
T |
A |
5: 123,784,227 |
L963H |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,636,052 |
L769* |
probably null |
Het |
Map3k13 |
A |
G |
16: 21,921,596 |
S558G |
probably benign |
Het |
Mbd1 |
G |
A |
18: 74,274,057 |
|
probably null |
Het |
Mep1a |
T |
C |
17: 43,479,235 |
N408D |
probably benign |
Het |
Mtrf1 |
A |
G |
14: 79,406,938 |
T229A |
probably benign |
Het |
Muc4 |
C |
T |
16: 32,754,935 |
S1603L |
unknown |
Het |
Myo1b |
A |
C |
1: 51,779,580 |
I512S |
possibly damaging |
Het |
N4bp2 |
A |
G |
5: 65,807,103 |
I832V |
probably benign |
Het |
Nadsyn1 |
T |
A |
7: 143,798,496 |
K618* |
probably null |
Het |
Ncstn |
T |
C |
1: 172,075,456 |
D87G |
probably benign |
Het |
Neurl4 |
T |
C |
11: 69,903,186 |
V156A |
probably benign |
Het |
Nfasc |
C |
A |
1: 132,600,013 |
G885V |
not run |
Het |
Nox4 |
A |
T |
7: 87,314,127 |
Y180F |
possibly damaging |
Het |
Nuggc |
A |
G |
14: 65,623,251 |
T449A |
probably benign |
Het |
Olfr799 |
A |
G |
10: 129,647,412 |
I95V |
probably benign |
Het |
Pik3r4 |
T |
C |
9: 105,663,117 |
S735P |
probably damaging |
Het |
Ppp1r9b |
T |
C |
11: 95,001,909 |
I645T |
probably damaging |
Het |
Rras2 |
G |
A |
7: 114,117,548 |
|
probably benign |
Het |
Rtel1 |
T |
C |
2: 181,321,029 |
M25T |
probably damaging |
Het |
Serpinb3c |
T |
A |
1: 107,273,153 |
Y178F |
possibly damaging |
Het |
Sh3bp2 |
A |
G |
5: 34,559,085 |
H280R |
not run |
Het |
Six4 |
CT |
C |
12: 73,104,239 |
|
probably benign |
Het |
Skor1 |
T |
C |
9: 63,146,501 |
E62G |
probably damaging |
Het |
Slc22a22 |
T |
A |
15: 57,263,355 |
N106I |
possibly damaging |
Het |
Slc44a4 |
T |
A |
17: 34,923,852 |
|
probably null |
Het |
Sppl2c |
A |
G |
11: 104,188,516 |
|
probably null |
Het |
Sptbn2 |
C |
G |
19: 4,749,012 |
R2037G |
probably benign |
Het |
Stx5a |
T |
A |
19: 8,755,118 |
W384R |
unknown |
Het |
Topaz1 |
A |
G |
9: 122,780,700 |
Y1111C |
possibly damaging |
Het |
Ttbk1 |
T |
A |
17: 46,446,238 |
M1157L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,717,215 |
T32204A |
probably benign |
Het |
Ttn |
T |
C |
2: 76,748,145 |
T24135A |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,965,137 |
E632G |
unknown |
Het |
Vmn2r109 |
T |
C |
17: 20,540,520 |
I858M |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,623,661 |
Q561L |
possibly damaging |
Het |
Yme1l1 |
A |
G |
2: 23,181,065 |
D271G |
probably damaging |
Het |
Zfp629 |
A |
G |
7: 127,611,995 |
F214S |
probably damaging |
Het |
Zfp709 |
A |
G |
8: 71,889,464 |
I246V |
probably benign |
Het |
|