Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
C |
T |
13: 81,727,713 (GRCm39) |
W309* |
probably null |
Het |
Aox1 |
G |
A |
1: 58,124,620 (GRCm39) |
V954I |
probably benign |
Het |
Asnsd1 |
A |
C |
1: 53,387,187 (GRCm39) |
|
probably null |
Het |
Aste1 |
A |
G |
9: 105,274,056 (GRCm39) |
K38E |
probably damaging |
Het |
Catsperg1 |
A |
G |
7: 28,899,664 (GRCm39) |
V339A |
probably damaging |
Het |
Ccdc13 |
A |
G |
9: 121,627,975 (GRCm39) |
|
probably benign |
Het |
Cd79b |
C |
A |
11: 106,203,267 (GRCm39) |
|
probably null |
Het |
Cemip2 |
C |
A |
19: 21,789,751 (GRCm39) |
N650K |
probably benign |
Het |
Chd3 |
A |
G |
11: 69,247,380 (GRCm39) |
L981P |
probably damaging |
Het |
Chia1 |
T |
C |
3: 106,029,761 (GRCm39) |
F132L |
probably damaging |
Het |
Dhx9 |
G |
A |
1: 153,348,209 (GRCm39) |
P336S |
probably damaging |
Het |
Dido1 |
T |
C |
2: 180,303,945 (GRCm39) |
K1320E |
probably damaging |
Het |
Dmbt1 |
G |
T |
7: 130,668,463 (GRCm39) |
C573F |
possibly damaging |
Het |
Dmtn |
A |
G |
14: 70,850,776 (GRCm39) |
I205T |
probably benign |
Het |
Efnb3 |
C |
A |
11: 69,447,591 (GRCm39) |
V181L |
probably benign |
Het |
Flg2 |
G |
T |
3: 93,109,166 (GRCm39) |
C398F |
possibly damaging |
Het |
Gabbr1 |
A |
G |
17: 37,380,257 (GRCm39) |
D604G |
probably damaging |
Het |
Glis2 |
T |
A |
16: 4,428,197 (GRCm39) |
L83* |
probably null |
Het |
Gm10719 |
T |
A |
9: 3,019,040 (GRCm39) |
|
probably null |
Homo |
Hipk3 |
T |
C |
2: 104,264,086 (GRCm39) |
D804G |
probably damaging |
Het |
Kcnd1 |
G |
C |
X: 7,690,148 (GRCm39) |
A23P |
probably damaging |
Homo |
Kcnj13 |
A |
G |
1: 87,314,256 (GRCm39) |
V322A |
probably benign |
Het |
Nav3 |
A |
G |
10: 109,688,426 (GRCm39) |
L617P |
probably damaging |
Het |
Npc1 |
ACAGCAGCAGCAGCAGCAG |
ACAGCAGCAGCAGCAG |
18: 12,369,249 (GRCm39) |
|
probably benign |
Het |
Or8b3b |
A |
G |
9: 38,584,510 (GRCm39) |
S90P |
probably benign |
Het |
Osgin1 |
G |
A |
8: 120,172,183 (GRCm39) |
V326I |
probably benign |
Het |
Pcsk7 |
A |
C |
9: 45,821,674 (GRCm39) |
N156T |
possibly damaging |
Het |
Pde4d |
C |
T |
13: 110,085,967 (GRCm39) |
S515L |
probably damaging |
Het |
Peg10 |
GC |
GCCCC |
6: 4,756,452 (GRCm39) |
|
probably benign |
Het |
Ppp2r5a |
T |
A |
1: 191,094,447 (GRCm39) |
Q191L |
probably benign |
Het |
Prom2 |
A |
G |
2: 127,381,695 (GRCm39) |
|
probably null |
Het |
Rsf1 |
CG |
CGACGGCGGTG |
7: 97,229,115 (GRCm39) |
|
probably benign |
Het |
Sart3 |
C |
T |
5: 113,881,267 (GRCm39) |
A938T |
probably benign |
Het |
Scn3a |
T |
C |
2: 65,325,380 (GRCm39) |
I1046V |
probably benign |
Het |
Sh3glb2 |
T |
C |
2: 30,235,805 (GRCm39) |
E313G |
possibly damaging |
Het |
Slc13a1 |
A |
T |
6: 24,090,795 (GRCm39) |
Y541* |
probably null |
Het |
Spata31h1 |
T |
A |
10: 82,126,946 (GRCm39) |
K2021N |
probably benign |
Het |
Speer1d |
C |
T |
5: 11,307,197 (GRCm39) |
T25I |
probably damaging |
Het |
Tm6sf2 |
T |
C |
8: 70,525,724 (GRCm39) |
V27A |
possibly damaging |
Het |
Tmem116 |
C |
T |
5: 121,629,171 (GRCm39) |
T188M |
probably benign |
Het |
Trim21 |
A |
G |
7: 102,208,646 (GRCm39) |
S358P |
probably damaging |
Het |
Ttc21a |
A |
G |
9: 119,795,838 (GRCm39) |
Y1224C |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,710,552 (GRCm39) |
|
probably benign |
Het |
Vmn2r99 |
A |
G |
17: 19,602,820 (GRCm39) |
Q525R |
probably benign |
Het |
|
Other mutations in Smtnl2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Smtnl2
|
APN |
11 |
72,294,085 (GRCm39) |
splice site |
probably benign |
|
IGL00948:Smtnl2
|
APN |
11 |
72,302,067 (GRCm39) |
splice site |
probably null |
|
IGL01310:Smtnl2
|
APN |
11 |
72,292,171 (GRCm39) |
splice site |
probably null |
|
IGL02277:Smtnl2
|
APN |
11 |
72,282,199 (GRCm39) |
missense |
probably damaging |
0.99 |
R0508:Smtnl2
|
UTSW |
11 |
72,293,962 (GRCm39) |
missense |
probably damaging |
1.00 |
R0784:Smtnl2
|
UTSW |
11 |
72,290,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Smtnl2
|
UTSW |
11 |
72,292,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R1971:Smtnl2
|
UTSW |
11 |
72,302,183 (GRCm39) |
missense |
probably benign |
0.00 |
R5094:Smtnl2
|
UTSW |
11 |
72,291,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R5270:Smtnl2
|
UTSW |
11 |
72,290,743 (GRCm39) |
missense |
probably benign |
0.00 |
R5518:Smtnl2
|
UTSW |
11 |
72,292,342 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5965:Smtnl2
|
UTSW |
11 |
72,291,279 (GRCm39) |
splice site |
probably null |
|
R6213:Smtnl2
|
UTSW |
11 |
72,292,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6255:Smtnl2
|
UTSW |
11 |
72,292,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6257:Smtnl2
|
UTSW |
11 |
72,292,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R6580:Smtnl2
|
UTSW |
11 |
72,293,859 (GRCm39) |
missense |
probably benign |
0.12 |
R7996:Smtnl2
|
UTSW |
11 |
72,291,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Smtnl2
|
UTSW |
11 |
72,293,993 (GRCm39) |
missense |
probably benign |
|
R9140:Smtnl2
|
UTSW |
11 |
72,290,793 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Smtnl2
|
UTSW |
11 |
72,293,835 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Smtnl2
|
UTSW |
11 |
72,302,537 (GRCm39) |
utr 5 prime |
probably benign |
|
Z1177:Smtnl2
|
UTSW |
11 |
72,292,307 (GRCm39) |
missense |
probably damaging |
1.00 |
|