Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ago1 |
T |
A |
4: 126,342,601 (GRCm39) |
Q514L |
probably benign |
Het |
Alpi |
G |
C |
1: 87,027,184 (GRCm39) |
T365S |
probably damaging |
Het |
Cbx4 |
A |
T |
11: 118,971,908 (GRCm39) |
V489E |
probably damaging |
Het |
Ccdc162 |
T |
C |
10: 41,503,145 (GRCm39) |
D999G |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,457,740 (GRCm39) |
E88G |
probably damaging |
Het |
D6Ertd527e |
C |
G |
6: 87,088,506 (GRCm39) |
T223S |
unknown |
Het |
Ddx1 |
A |
T |
12: 13,295,721 (GRCm39) |
I33N |
probably damaging |
Het |
Diaph3 |
G |
A |
14: 87,103,922 (GRCm39) |
L821F |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,126,851 (GRCm39) |
M221I |
probably benign |
Het |
Gm3233 |
G |
T |
10: 77,595,249 (GRCm39) |
|
probably benign |
Het |
Heg1 |
A |
C |
16: 33,587,145 (GRCm39) |
I1327L |
probably damaging |
Het |
Ifnar1 |
G |
A |
16: 91,302,303 (GRCm39) |
|
probably null |
Het |
Itpr1 |
C |
T |
6: 108,482,864 (GRCm39) |
L2310F |
probably damaging |
Het |
Or5b98 |
T |
C |
19: 12,931,681 (GRCm39) |
S243P |
probably damaging |
Het |
Pcdhb7 |
A |
G |
18: 37,476,487 (GRCm39) |
N541S |
possibly damaging |
Het |
Prelp |
A |
G |
1: 133,842,479 (GRCm39) |
L222P |
probably damaging |
Het |
Prl8a8 |
A |
G |
13: 27,692,412 (GRCm39) |
I193T |
probably damaging |
Het |
Prpf4b |
G |
T |
13: 35,084,354 (GRCm39) |
R914L |
probably damaging |
Het |
Ptbp2 |
G |
C |
3: 119,514,484 (GRCm39) |
Q448E |
probably benign |
Het |
Rsf1 |
GCG |
GCGACGGCGACG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
Slc9a9 |
A |
T |
9: 94,552,280 (GRCm39) |
M56L |
probably benign |
Het |
Slfn4 |
A |
G |
11: 83,078,000 (GRCm39) |
I263V |
possibly damaging |
Het |
Taar2 |
A |
G |
10: 23,817,177 (GRCm39) |
N239S |
probably benign |
Het |
Trrap |
T |
A |
5: 144,727,680 (GRCm39) |
I467N |
possibly damaging |
Het |
Ttc28 |
T |
C |
5: 111,424,142 (GRCm39) |
Y1439H |
probably damaging |
Het |
Usp34 |
A |
G |
11: 23,438,666 (GRCm39) |
I3409M |
probably benign |
Het |
Zbbx |
G |
T |
3: 74,985,872 (GRCm39) |
N388K |
probably damaging |
Het |
Znhit2 |
A |
G |
19: 6,112,287 (GRCm39) |
N344S |
probably damaging |
Het |
|
Other mutations in Gm15130 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Gm15130
|
APN |
2 |
110,969,322 (GRCm39) |
missense |
unknown |
|
IGL03176:Gm15130
|
APN |
2 |
110,978,846 (GRCm39) |
missense |
unknown |
|
R0066:Gm15130
|
UTSW |
2 |
110,969,284 (GRCm39) |
splice site |
probably benign |
|
R0066:Gm15130
|
UTSW |
2 |
110,969,284 (GRCm39) |
splice site |
probably benign |
|
R4716:Gm15130
|
UTSW |
2 |
110,964,560 (GRCm39) |
nonsense |
probably null |
|
R4754:Gm15130
|
UTSW |
2 |
110,973,207 (GRCm39) |
missense |
unknown |
|
R4816:Gm15130
|
UTSW |
2 |
110,965,714 (GRCm39) |
splice site |
probably benign |
|
R5283:Gm15130
|
UTSW |
2 |
110,965,754 (GRCm39) |
missense |
unknown |
|
R5973:Gm15130
|
UTSW |
2 |
110,965,714 (GRCm39) |
splice site |
probably benign |
|
R6152:Gm15130
|
UTSW |
2 |
110,974,950 (GRCm39) |
missense |
unknown |
|
R7708:Gm15130
|
UTSW |
2 |
110,974,962 (GRCm39) |
missense |
|
|
R7813:Gm15130
|
UTSW |
2 |
110,969,320 (GRCm39) |
missense |
|
|
R7934:Gm15130
|
UTSW |
2 |
110,964,582 (GRCm39) |
missense |
|
|
R8490:Gm15130
|
UTSW |
2 |
110,983,230 (GRCm39) |
critical splice donor site |
probably null |
|
Z1176:Gm15130
|
UTSW |
2 |
110,974,932 (GRCm39) |
critical splice donor site |
probably null |
|
|