Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,902,047 (GRCm39) |
E726G |
probably benign |
Het |
Cdyl2 |
T |
A |
8: 117,321,928 (GRCm39) |
|
probably benign |
Het |
Cep41 |
T |
C |
6: 30,660,966 (GRCm39) |
T109A |
probably benign |
Het |
Clca3b |
C |
T |
3: 144,552,972 (GRCm39) |
W84* |
probably null |
Het |
Cyp27b1 |
A |
G |
10: 126,885,551 (GRCm39) |
D130G |
probably benign |
Het |
Cyp2f2 |
T |
C |
7: 26,829,242 (GRCm39) |
V249A |
possibly damaging |
Het |
Cyth3 |
G |
A |
5: 143,692,920 (GRCm39) |
|
probably null |
Het |
Dnah8 |
G |
T |
17: 30,925,431 (GRCm39) |
E1289* |
probably null |
Het |
Fam171a1 |
A |
T |
2: 3,179,327 (GRCm39) |
D51V |
possibly damaging |
Het |
Farp2 |
A |
G |
1: 93,488,896 (GRCm39) |
R107G |
possibly damaging |
Het |
Gemin6 |
T |
C |
17: 80,535,294 (GRCm39) |
F85L |
possibly damaging |
Het |
Hivep3 |
A |
C |
4: 119,955,571 (GRCm39) |
T1296P |
probably damaging |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Htt |
T |
A |
5: 34,976,021 (GRCm39) |
S670T |
probably benign |
Het |
Klhl24 |
A |
T |
16: 19,941,717 (GRCm39) |
N555I |
possibly damaging |
Het |
Limd1 |
T |
A |
9: 123,308,948 (GRCm39) |
S216T |
probably benign |
Het |
Lmf2 |
A |
T |
15: 89,238,102 (GRCm39) |
I234N |
probably damaging |
Het |
Mrpl4 |
C |
A |
9: 20,919,863 (GRCm39) |
D271E |
probably benign |
Het |
Mydgf |
C |
T |
17: 56,486,407 (GRCm39) |
G75R |
probably damaging |
Het |
Nat1 |
A |
G |
8: 67,943,630 (GRCm39) |
D5G |
possibly damaging |
Het |
Or2t46 |
T |
C |
11: 58,472,636 (GRCm39) |
V322A |
probably benign |
Het |
Or5h22 |
A |
T |
16: 58,895,052 (GRCm39) |
Y130* |
probably null |
Het |
Or5k15 |
A |
C |
16: 58,710,048 (GRCm39) |
H178Q |
probably damaging |
Het |
Pla2g4c |
T |
A |
7: 13,077,951 (GRCm39) |
M363K |
probably benign |
Het |
Prex1 |
A |
G |
2: 166,480,329 (GRCm39) |
F137S |
probably damaging |
Het |
Rbm12b1 |
A |
G |
4: 12,146,038 (GRCm39) |
D670G |
probably damaging |
Het |
Rrp12 |
C |
A |
19: 41,860,231 (GRCm39) |
M997I |
possibly damaging |
Het |
Scn3a |
A |
G |
2: 65,327,736 (GRCm39) |
V918A |
probably benign |
Het |
Slit1 |
A |
T |
19: 41,590,739 (GRCm39) |
I1311N |
probably damaging |
Het |
Ube2j2 |
C |
T |
4: 156,030,834 (GRCm39) |
|
probably benign |
Het |
Ucp2 |
A |
G |
7: 100,147,629 (GRCm39) |
T203A |
probably benign |
Het |
Upk1b |
C |
T |
16: 38,600,347 (GRCm39) |
G211D |
possibly damaging |
Het |
Vmn1r220 |
A |
T |
13: 23,367,935 (GRCm39) |
F254I |
probably benign |
Het |
Zcchc4 |
T |
C |
5: 52,965,638 (GRCm39) |
F314S |
probably damaging |
Het |
|
Other mutations in Slc35g2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03264:Slc35g2
|
APN |
9 |
100,434,699 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0127:Slc35g2
|
UTSW |
9 |
100,435,170 (GRCm39) |
missense |
probably benign |
0.12 |
R0626:Slc35g2
|
UTSW |
9 |
100,435,495 (GRCm39) |
missense |
probably benign |
0.00 |
R1123:Slc35g2
|
UTSW |
9 |
100,435,047 (GRCm39) |
missense |
probably damaging |
0.98 |
R2012:Slc35g2
|
UTSW |
9 |
100,435,120 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2057:Slc35g2
|
UTSW |
9 |
100,435,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R3922:Slc35g2
|
UTSW |
9 |
100,434,780 (GRCm39) |
missense |
probably benign |
0.20 |
R3924:Slc35g2
|
UTSW |
9 |
100,434,780 (GRCm39) |
missense |
probably benign |
0.20 |
R4561:Slc35g2
|
UTSW |
9 |
100,435,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Slc35g2
|
UTSW |
9 |
100,434,555 (GRCm39) |
missense |
probably benign |
0.20 |
R4732:Slc35g2
|
UTSW |
9 |
100,434,555 (GRCm39) |
missense |
probably benign |
0.20 |
R4733:Slc35g2
|
UTSW |
9 |
100,434,555 (GRCm39) |
missense |
probably benign |
0.20 |
R4760:Slc35g2
|
UTSW |
9 |
100,435,549 (GRCm39) |
missense |
probably benign |
0.22 |
R8310:Slc35g2
|
UTSW |
9 |
100,434,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R8420:Slc35g2
|
UTSW |
9 |
100,435,224 (GRCm39) |
missense |
probably benign |
|
X0020:Slc35g2
|
UTSW |
9 |
100,435,069 (GRCm39) |
missense |
probably benign |
0.30 |
Z1176:Slc35g2
|
UTSW |
9 |
100,434,582 (GRCm39) |
missense |
probably damaging |
1.00 |
|