Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap42 |
T |
A |
9: 9,115,709 (GRCm39) |
E122D |
probably damaging |
Het |
Asb3 |
G |
A |
11: 30,979,067 (GRCm39) |
|
probably null |
Het |
Avl9 |
T |
C |
6: 56,713,536 (GRCm39) |
S265P |
probably benign |
Het |
Cep44 |
C |
T |
8: 57,000,459 (GRCm39) |
R18Q |
probably damaging |
Het |
Clec10a |
T |
C |
11: 70,060,554 (GRCm39) |
|
probably benign |
Het |
Cog4 |
A |
G |
8: 111,579,065 (GRCm39) |
I115V |
probably benign |
Het |
Coq3 |
C |
T |
4: 21,900,430 (GRCm39) |
A219V |
probably benign |
Het |
Cry2 |
G |
A |
2: 92,243,462 (GRCm39) |
R460* |
probably null |
Het |
Ddx39b |
A |
G |
17: 35,472,337 (GRCm39) |
|
probably benign |
Het |
Dhx40 |
G |
A |
11: 86,662,755 (GRCm39) |
R646C |
probably damaging |
Het |
Ears2 |
G |
A |
7: 121,662,284 (GRCm39) |
R55C |
probably damaging |
Het |
Eif3m |
C |
T |
2: 104,845,214 (GRCm39) |
G26R |
probably damaging |
Het |
Exo5 |
A |
G |
4: 120,779,742 (GRCm39) |
L41P |
probably benign |
Het |
Fut10 |
A |
G |
8: 31,749,965 (GRCm39) |
H417R |
probably damaging |
Het |
Gars1 |
T |
A |
6: 55,037,929 (GRCm39) |
L296Q |
probably damaging |
Het |
Gpr143 |
A |
T |
X: 151,576,439 (GRCm39) |
|
probably benign |
Het |
Htr1b |
C |
A |
9: 81,513,689 (GRCm39) |
R306L |
probably damaging |
Het |
Lama3 |
G |
A |
18: 12,661,858 (GRCm39) |
A2185T |
probably damaging |
Het |
Mbd5 |
C |
A |
2: 49,169,460 (GRCm39) |
Q1544K |
possibly damaging |
Het |
Mccc1 |
T |
C |
3: 36,014,178 (GRCm39) |
E713G |
possibly damaging |
Het |
Mttp |
A |
G |
3: 137,817,505 (GRCm39) |
F415S |
probably benign |
Het |
Mug1 |
A |
G |
6: 121,864,386 (GRCm39) |
T1428A |
probably benign |
Het |
Mup6 |
A |
C |
4: 60,006,009 (GRCm39) |
D159A |
probably damaging |
Het |
Nsd2 |
T |
C |
5: 34,037,472 (GRCm39) |
L698P |
probably damaging |
Het |
Or2w6 |
A |
T |
13: 21,843,001 (GRCm39) |
M164K |
probably damaging |
Het |
Or4p22 |
G |
T |
2: 88,317,519 (GRCm39) |
V148F |
probably benign |
Het |
Or5p70 |
A |
G |
7: 107,994,720 (GRCm39) |
N131S |
probably benign |
Het |
Or6c217 |
A |
T |
10: 129,738,287 (GRCm39) |
C97* |
probably null |
Het |
Osgepl1 |
G |
A |
1: 53,360,675 (GRCm39) |
R372H |
probably benign |
Het |
Pias2 |
C |
T |
18: 77,232,799 (GRCm39) |
H537Y |
probably damaging |
Het |
Smn1 |
A |
G |
13: 100,264,472 (GRCm39) |
T68A |
probably benign |
Het |
Syde2 |
A |
G |
3: 145,707,231 (GRCm39) |
K657R |
possibly damaging |
Het |
Tdrd5 |
A |
T |
1: 156,098,190 (GRCm39) |
H625Q |
possibly damaging |
Het |
Tead3 |
T |
C |
17: 28,560,325 (GRCm39) |
Y2C |
probably damaging |
Het |
Tmem255a |
T |
A |
X: 37,296,940 (GRCm39) |
T280S |
probably benign |
Het |
Ttpa |
A |
G |
4: 20,021,215 (GRCm39) |
T128A |
possibly damaging |
Het |
Wdhd1 |
A |
G |
14: 47,509,591 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Slc38a7 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00514:Slc38a7
|
APN |
8 |
96,567,105 (GRCm39) |
unclassified |
probably benign |
|
IGL00816:Slc38a7
|
APN |
8 |
96,570,748 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01781:Slc38a7
|
APN |
8 |
96,570,386 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01990:Slc38a7
|
APN |
8 |
96,571,590 (GRCm39) |
nonsense |
probably null |
|
IGL02424:Slc38a7
|
APN |
8 |
96,568,200 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03277:Slc38a7
|
APN |
8 |
96,575,104 (GRCm39) |
missense |
probably damaging |
1.00 |
R0082:Slc38a7
|
UTSW |
8 |
96,567,109 (GRCm39) |
unclassified |
probably benign |
|
R0271:Slc38a7
|
UTSW |
8 |
96,572,506 (GRCm39) |
missense |
probably damaging |
0.98 |
R1479:Slc38a7
|
UTSW |
8 |
96,575,122 (GRCm39) |
missense |
probably benign |
|
R2246:Slc38a7
|
UTSW |
8 |
96,570,468 (GRCm39) |
missense |
probably damaging |
0.97 |
R2897:Slc38a7
|
UTSW |
8 |
96,572,424 (GRCm39) |
splice site |
probably benign |
|
R2920:Slc38a7
|
UTSW |
8 |
96,572,571 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3746:Slc38a7
|
UTSW |
8 |
96,570,380 (GRCm39) |
splice site |
probably benign |
|
R3884:Slc38a7
|
UTSW |
8 |
96,572,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Slc38a7
|
UTSW |
8 |
96,575,230 (GRCm39) |
missense |
probably benign |
|
R5073:Slc38a7
|
UTSW |
8 |
96,568,278 (GRCm39) |
missense |
probably damaging |
1.00 |
R6249:Slc38a7
|
UTSW |
8 |
96,564,302 (GRCm39) |
splice site |
probably null |
|
R6379:Slc38a7
|
UTSW |
8 |
96,575,155 (GRCm39) |
missense |
probably benign |
|
R6821:Slc38a7
|
UTSW |
8 |
96,571,548 (GRCm39) |
missense |
probably benign |
0.25 |
R7735:Slc38a7
|
UTSW |
8 |
96,568,295 (GRCm39) |
missense |
probably benign |
0.00 |
R9668:Slc38a7
|
UTSW |
8 |
96,570,772 (GRCm39) |
missense |
probably benign |
0.00 |
|