Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy8 |
T |
G |
15: 64,754,886 |
|
probably null |
Het |
Adgrv1 |
A |
G |
13: 81,557,081 |
F1537L |
probably damaging |
Het |
Aggf1 |
T |
C |
13: 95,364,723 |
S384G |
probably benign |
Het |
Anxa8 |
A |
T |
14: 34,094,765 |
D204V |
possibly damaging |
Het |
Asap3 |
A |
T |
4: 136,227,572 |
E71V |
possibly damaging |
Het |
BC024139 |
T |
C |
15: 76,119,746 |
*773W |
probably null |
Het |
Bckdhb |
T |
C |
9: 83,953,761 |
V106A |
possibly damaging |
Het |
Cep250 |
A |
G |
2: 155,981,459 |
D1010G |
probably benign |
Het |
Chrd |
T |
A |
16: 20,734,736 |
L243Q |
probably damaging |
Het |
Cib2 |
G |
T |
9: 54,549,891 |
L30I |
possibly damaging |
Het |
Cpsf7 |
T |
A |
19: 10,532,884 |
L113* |
probably null |
Het |
Cubn |
T |
A |
2: 13,445,029 |
I895L |
probably benign |
Het |
Cyp24a1 |
C |
A |
2: 170,487,979 |
R351I |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 27,034,156 |
D320V |
possibly damaging |
Het |
Dact1 |
C |
G |
12: 71,317,939 |
P498R |
probably benign |
Het |
Diaph1 |
T |
A |
18: 37,876,383 |
|
probably null |
Het |
Dopey2 |
A |
T |
16: 93,755,485 |
I271F |
possibly damaging |
Het |
Erich3 |
C |
A |
3: 154,727,437 |
F349L |
probably damaging |
Het |
Fam187b |
G |
C |
7: 30,989,290 |
V358L |
probably benign |
Het |
Fat4 |
T |
A |
3: 38,983,939 |
H3913Q |
probably benign |
Het |
Fbxw7 |
G |
C |
3: 84,958,627 |
E118D |
probably benign |
Het |
Fgf1 |
A |
G |
18: 38,847,108 |
I71T |
probably damaging |
Het |
Fryl |
A |
T |
5: 73,065,217 |
I2007K |
probably damaging |
Het |
Galnt2 |
C |
G |
8: 124,324,011 |
P130A |
probably benign |
Het |
H1fx |
G |
A |
6: 87,981,302 |
R19C |
probably damaging |
Het |
Hmga2 |
A |
C |
10: 120,476,024 |
S14A |
possibly damaging |
Het |
Hoxb4 |
C |
T |
11: 96,318,654 |
|
probably benign |
Het |
Hr |
A |
T |
14: 70,565,374 |
I756F |
probably damaging |
Het |
Hrasls5 |
A |
T |
19: 7,639,496 |
|
probably benign |
Het |
Hspa1b |
A |
T |
17: 34,958,185 |
S275T |
probably benign |
Het |
Ikbkap |
A |
G |
4: 56,787,939 |
Y331H |
probably damaging |
Het |
Kcnh1 |
T |
C |
1: 192,505,289 |
*99R |
probably null |
Het |
Kit |
C |
A |
5: 75,652,649 |
L864I |
probably benign |
Het |
Klk14 |
A |
T |
7: 43,694,456 |
K196* |
probably null |
Het |
Lmod1 |
A |
G |
1: 135,325,167 |
N53S |
probably damaging |
Het |
Myh13 |
T |
C |
11: 67,356,158 |
M1235T |
probably benign |
Het |
Neurl3 |
T |
A |
1: 36,268,704 |
K175* |
probably null |
Het |
Nlgn2 |
T |
A |
11: 69,825,924 |
K597M |
probably damaging |
Het |
Npdc1 |
T |
C |
2: 25,409,109 |
M306T |
probably damaging |
Het |
Obscn |
C |
T |
11: 59,067,943 |
|
probably null |
Het |
Olfr404-ps1 |
T |
C |
11: 74,239,696 |
L44P |
probably damaging |
Het |
Olfr553 |
G |
A |
7: 102,614,486 |
L168F |
probably damaging |
Het |
Olfr913 |
T |
C |
9: 38,594,905 |
I228T |
possibly damaging |
Het |
Pbrm1 |
A |
T |
14: 31,084,790 |
Y1042F |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,677,907 |
|
probably benign |
Het |
Peg10 |
CATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAGGATC |
CATC |
6: 4,756,431 |
|
probably benign |
Het |
Phf12 |
C |
T |
11: 78,022,511 |
Q430* |
probably null |
Het |
Pld3 |
C |
T |
7: 27,535,897 |
R302H |
probably damaging |
Het |
Plekha5 |
T |
C |
6: 140,525,858 |
S112P |
probably benign |
Het |
Pmfbp1 |
T |
A |
8: 109,530,307 |
S548T |
possibly damaging |
Het |
Ppa1 |
A |
T |
10: 61,667,603 |
I220F |
probably damaging |
Het |
Ppp2r3d |
A |
G |
9: 124,439,078 |
|
probably benign |
Het |
Psmg2 |
A |
T |
18: 67,648,857 |
E164D |
possibly damaging |
Het |
Rarb |
T |
C |
14: 16,443,824 |
R155G |
probably damaging |
Het |
Rnf215 |
T |
C |
11: 4,136,609 |
L162S |
probably damaging |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,579,906 |
|
probably benign |
Het |
Rtkn2 |
G |
A |
10: 68,026,632 |
V330M |
probably damaging |
Het |
Slc16a4 |
A |
T |
3: 107,311,498 |
I472F |
probably benign |
Het |
Snx14 |
T |
C |
9: 88,394,382 |
N617D |
possibly damaging |
Het |
Spire2 |
T |
C |
8: 123,356,727 |
V150A |
probably damaging |
Het |
Sptbn1 |
C |
A |
11: 30,114,787 |
R1904M |
probably damaging |
Het |
Swap70 |
A |
G |
7: 110,281,303 |
E575G |
possibly damaging |
Het |
Tbxas1 |
A |
T |
6: 38,919,153 |
M1L |
possibly damaging |
Het |
Tenm3 |
A |
T |
8: 48,256,837 |
V1688D |
probably damaging |
Het |
Tgfbr3 |
A |
T |
5: 107,149,914 |
S207T |
probably damaging |
Het |
Timm44 |
A |
G |
8: 4,267,282 |
F248L |
probably damaging |
Het |
Tmem161a |
T |
C |
8: 70,181,199 |
L170P |
probably damaging |
Het |
Tmem63a |
A |
T |
1: 180,960,470 |
Y263F |
possibly damaging |
Het |
Tnfsf9 |
C |
A |
17: 57,105,513 |
L28I |
probably benign |
Het |
Tph2 |
T |
A |
10: 115,174,106 |
N183I |
probably benign |
Het |
Ttyh1 |
T |
C |
7: 4,122,529 |
I60T |
probably damaging |
Het |
Ubn1 |
T |
G |
16: 5,064,547 |
S48A |
probably damaging |
Het |
Ubr5 |
T |
C |
15: 37,989,598 |
N2019S |
probably benign |
Het |
Wbp2 |
T |
C |
11: 116,086,910 |
N6D |
probably benign |
Het |
Wdr59 |
T |
A |
8: 111,459,040 |
E810V |
possibly damaging |
Het |
Wiz |
T |
C |
17: 32,360,421 |
D220G |
probably damaging |
Het |
Yipf7 |
A |
G |
5: 69,517,070 |
L244P |
probably damaging |
Het |
Zdhhc17 |
T |
C |
10: 110,955,111 |
T366A |
possibly damaging |
Het |
Zfp169 |
A |
T |
13: 48,490,996 |
|
probably benign |
Het |
Zfp707 |
C |
T |
15: 75,969,723 |
|
probably benign |
Het |
Zfp788 |
A |
G |
7: 41,649,560 |
H540R |
probably damaging |
Het |
|