Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Apobr |
A |
C |
7: 126,588,024 |
D89A |
probably damaging |
Het |
Bhlhe41 |
C |
T |
6: 145,862,968 |
|
probably benign |
Het |
Cacna1s |
G |
A |
1: 136,095,785 |
V674M |
probably benign |
Het |
Cavin2 |
T |
C |
1: 51,289,870 |
|
probably null |
Het |
Cd300lb |
T |
C |
11: 114,924,937 |
S106G |
possibly damaging |
Het |
Ceacam15 |
A |
G |
7: 16,673,196 |
V132A |
probably benign |
Het |
Ddi2 |
G |
T |
4: 141,684,765 |
Q279K |
probably benign |
Het |
Dnah11 |
A |
G |
12: 117,883,416 |
V4304A |
probably damaging |
Het |
Dnah2 |
C |
T |
11: 69,458,920 |
R2399Q |
probably benign |
Het |
Dnase1l1 |
C |
T |
X: 74,277,038 |
|
probably null |
Het |
Epsti1 |
T |
A |
14: 77,904,650 |
H55Q |
probably benign |
Het |
Flad1 |
T |
C |
3: 89,411,196 |
T17A |
probably damaging |
Het |
Fzd2 |
C |
T |
11: 102,606,155 |
T475M |
probably damaging |
Het |
Gemin5 |
C |
A |
11: 58,130,061 |
W1099L |
probably damaging |
Het |
Gm9892 |
T |
C |
8: 52,196,929 |
|
noncoding transcript |
Het |
Gmeb2 |
A |
G |
2: 181,255,986 |
|
probably benign |
Het |
Grip1 |
A |
G |
10: 119,929,928 |
E55G |
probably damaging |
Het |
Hltf |
T |
C |
3: 20,108,112 |
S825P |
probably damaging |
Het |
Kcnh3 |
A |
T |
15: 99,241,939 |
Q902L |
probably null |
Het |
Kcnt2 |
C |
T |
1: 140,609,615 |
P1037L |
probably damaging |
Het |
Klhl18 |
G |
C |
9: 110,436,127 |
N335K |
possibly damaging |
Het |
Lama5 |
A |
C |
2: 180,193,801 |
L1253R |
probably damaging |
Het |
Lancl2 |
T |
G |
6: 57,724,582 |
S230A |
probably benign |
Het |
Lmcd1 |
A |
G |
6: 112,315,588 |
M134V |
probably damaging |
Het |
Lrrc23 |
C |
A |
6: 124,774,482 |
A205S |
probably damaging |
Het |
Mfsd13b |
T |
A |
7: 120,991,738 |
I234N |
probably damaging |
Het |
Mroh3 |
A |
G |
1: 136,196,323 |
S386P |
probably damaging |
Het |
Mylk3 |
A |
C |
8: 85,355,431 |
F313V |
possibly damaging |
Het |
Myo9b |
A |
T |
8: 71,333,388 |
Q643L |
possibly damaging |
Het |
Nacad |
T |
C |
11: 6,605,745 |
S2G |
unknown |
Het |
Olfr1269 |
A |
T |
2: 90,118,699 |
W300R |
probably damaging |
Het |
Olfr136 |
C |
T |
17: 38,335,456 |
Q100* |
probably null |
Het |
Olfr419 |
G |
T |
1: 174,250,756 |
T57K |
possibly damaging |
Het |
Olfr908 |
T |
C |
9: 38,516,116 |
F28S |
probably damaging |
Het |
Pkd1 |
T |
C |
17: 24,576,074 |
V2245A |
probably damaging |
Het |
Pkdrej |
G |
A |
15: 85,817,118 |
T1539I |
possibly damaging |
Het |
Plch2 |
G |
T |
4: 154,989,999 |
|
probably null |
Het |
Pygm |
G |
A |
19: 6,384,579 |
R34H |
probably damaging |
Het |
Rgs12 |
T |
C |
5: 35,021,104 |
|
probably benign |
Het |
Ruvbl1 |
T |
C |
6: 88,485,908 |
I338T |
probably damaging |
Het |
Sapcd1 |
T |
A |
17: 35,026,731 |
Q104L |
probably damaging |
Het |
Satb2 |
T |
C |
1: 56,796,907 |
E575G |
probably damaging |
Het |
Sema6b |
T |
A |
17: 56,127,091 |
|
probably null |
Het |
Slc25a11 |
T |
C |
11: 70,646,185 |
N15D |
probably damaging |
Het |
Slc26a6 |
C |
T |
9: 108,860,646 |
T526M |
probably damaging |
Het |
Tcaf3 |
G |
T |
6: 42,587,510 |
T906K |
possibly damaging |
Het |
Thbd |
A |
T |
2: 148,406,983 |
C322S |
probably damaging |
Het |
Traf2 |
A |
G |
2: 25,520,440 |
L399P |
probably damaging |
Het |
Troap |
T |
A |
15: 99,078,817 |
V274D |
probably damaging |
Het |
Utrn |
G |
A |
10: 12,401,355 |
T3406M |
probably damaging |
Het |
Uts2 |
G |
T |
4: 150,999,051 |
A40S |
possibly damaging |
Het |
Vmn2r109 |
T |
A |
17: 20,554,341 |
I251F |
possibly damaging |
Het |
Vmn2r67 |
A |
G |
7: 85,137,022 |
S592P |
probably damaging |
Het |
Vps13b |
T |
G |
15: 35,876,413 |
W2797G |
probably damaging |
Het |
Ythdf1 |
A |
T |
2: 180,912,188 |
M51K |
probably damaging |
Het |
Zfp60 |
T |
A |
7: 27,738,530 |
|
probably benign |
Het |
Zfp882 |
T |
A |
8: 71,914,360 |
F344I |
probably damaging |
Het |
|