Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930111J21Rik1 |
A |
G |
11: 48,838,191 (GRCm39) |
Y799H |
probably damaging |
Het |
Akap5 |
G |
A |
12: 76,375,041 (GRCm39) |
A158T |
probably damaging |
Het |
Aox4 |
A |
G |
1: 58,286,434 (GRCm39) |
K689E |
probably benign |
Het |
Arid1b |
G |
A |
17: 5,046,423 (GRCm39) |
A404T |
unknown |
Het |
Bltp1 |
A |
G |
3: 37,065,885 (GRCm39) |
N53S |
|
Het |
Camk2b |
T |
A |
11: 5,929,711 (GRCm39) |
D396V |
probably damaging |
Het |
Cd53 |
T |
A |
3: 106,674,683 (GRCm39) |
D128V |
probably null |
Het |
Cdk15 |
G |
T |
1: 59,326,943 (GRCm39) |
R208L |
probably damaging |
Het |
Celsr1 |
T |
G |
15: 85,785,346 (GRCm39) |
K2963Q |
probably damaging |
Het |
Celsr2 |
A |
G |
3: 108,301,074 (GRCm39) |
S2740P |
probably damaging |
Het |
Clca4b |
A |
T |
3: 144,632,964 (GRCm39) |
L162H |
probably damaging |
Het |
Cntn1 |
A |
T |
15: 92,189,644 (GRCm39) |
T656S |
probably damaging |
Het |
Creb3l1 |
C |
T |
2: 91,822,231 (GRCm39) |
|
probably null |
Het |
Dpy19l2 |
A |
G |
9: 24,530,459 (GRCm39) |
Y507H |
probably damaging |
Het |
Dsc3 |
A |
T |
18: 20,122,752 (GRCm39) |
C57* |
probably null |
Het |
Gramd1b |
A |
G |
9: 40,217,689 (GRCm39) |
Y621H |
probably damaging |
Het |
Ifi207 |
A |
T |
1: 173,556,522 (GRCm39) |
C739S |
probably benign |
Het |
Il1rap |
T |
C |
16: 26,541,702 (GRCm39) |
S648P |
probably benign |
Het |
Ints5 |
C |
T |
19: 8,872,686 (GRCm39) |
T215I |
probably damaging |
Het |
Itm2c |
T |
C |
1: 85,834,255 (GRCm39) |
|
probably null |
Het |
Lmo7 |
T |
A |
14: 102,137,907 (GRCm39) |
S870T |
probably benign |
Het |
Lrpprc |
A |
T |
17: 85,015,548 (GRCm39) |
F1288I |
probably damaging |
Het |
Megf11 |
A |
T |
9: 64,547,376 (GRCm39) |
H209L |
probably damaging |
Het |
Mtss1 |
C |
T |
15: 58,926,869 (GRCm39) |
R69H |
probably damaging |
Het |
Nms |
A |
T |
1: 38,980,982 (GRCm39) |
H56L |
probably benign |
Het |
Or4f54 |
G |
A |
2: 111,122,736 (GRCm39) |
G41D |
probably damaging |
Het |
Or4k36 |
C |
T |
2: 111,146,288 (GRCm39) |
H155Y |
probably damaging |
Het |
Or56a5 |
A |
T |
7: 104,793,497 (GRCm39) |
M7K |
possibly damaging |
Het |
Or5t17 |
T |
C |
2: 86,833,140 (GRCm39) |
S276P |
probably benign |
Het |
Pds5a |
G |
A |
5: 65,792,747 (GRCm39) |
R729W |
probably damaging |
Het |
Pskh1 |
C |
T |
8: 106,639,598 (GRCm39) |
R93* |
probably null |
Het |
Rapgef2 |
G |
A |
3: 79,019,495 (GRCm39) |
L59F |
probably damaging |
Het |
Rtn4 |
G |
A |
11: 29,691,011 (GRCm39) |
V1101I |
probably damaging |
Het |
Sec31b |
C |
A |
19: 44,509,021 (GRCm39) |
V653F |
probably damaging |
Het |
Slc6a15 |
A |
G |
10: 103,229,277 (GRCm39) |
I105M |
probably benign |
Het |
Smurf1 |
A |
G |
5: 144,833,395 (GRCm39) |
V209A |
|
Het |
Snapc2 |
A |
G |
8: 4,304,591 (GRCm39) |
E115G |
probably damaging |
Het |
Sorcs2 |
T |
C |
5: 36,199,529 (GRCm39) |
E592G |
possibly damaging |
Het |
Spmip6 |
G |
A |
4: 41,508,614 (GRCm39) |
P17L |
|
Het |
Styxl2 |
T |
A |
1: 165,926,410 (GRCm39) |
K1067N |
probably damaging |
Het |
Tcl1b1 |
A |
T |
12: 105,130,823 (GRCm39) |
Q102L |
probably damaging |
Het |
Tmc1 |
T |
A |
19: 20,801,644 (GRCm39) |
N461Y |
probably benign |
Het |
Trim59 |
C |
A |
3: 68,945,134 (GRCm39) |
G69C |
probably damaging |
Het |
Tubg1 |
A |
G |
11: 101,017,003 (GRCm39) |
Y435C |
probably damaging |
Het |
Ucp3 |
A |
C |
7: 100,131,911 (GRCm39) |
H254P |
probably benign |
Het |
Vav2 |
T |
C |
2: 27,157,276 (GRCm39) |
D842G |
probably damaging |
Het |
Vmn1r203 |
T |
A |
13: 22,708,423 (GRCm39) |
L68H |
probably damaging |
Het |
Wee2 |
A |
G |
6: 40,421,057 (GRCm39) |
E49G |
probably benign |
Het |
Zfr |
A |
G |
15: 12,180,706 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Slc10a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00504:Slc10a2
|
APN |
8 |
5,141,667 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00504:Slc10a2
|
APN |
8 |
5,141,668 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00596:Slc10a2
|
APN |
8 |
5,141,680 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01472:Slc10a2
|
APN |
8 |
5,141,652 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Slc10a2
|
APN |
8 |
5,148,499 (GRCm39) |
missense |
probably damaging |
1.00 |
gall
|
UTSW |
8 |
5,141,621 (GRCm39) |
critical splice donor site |
probably null |
|
R0560:Slc10a2
|
UTSW |
8 |
5,139,092 (GRCm39) |
missense |
probably benign |
0.02 |
R0629:Slc10a2
|
UTSW |
8 |
5,148,562 (GRCm39) |
missense |
probably benign |
0.30 |
R0743:Slc10a2
|
UTSW |
8 |
5,139,132 (GRCm39) |
missense |
probably damaging |
0.99 |
R0970:Slc10a2
|
UTSW |
8 |
5,155,115 (GRCm39) |
missense |
probably benign |
0.00 |
R1033:Slc10a2
|
UTSW |
8 |
5,154,889 (GRCm39) |
missense |
probably damaging |
0.99 |
R1557:Slc10a2
|
UTSW |
8 |
5,141,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R1808:Slc10a2
|
UTSW |
8 |
5,154,856 (GRCm39) |
missense |
probably damaging |
0.96 |
R3620:Slc10a2
|
UTSW |
8 |
5,154,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R4084:Slc10a2
|
UTSW |
8 |
5,139,126 (GRCm39) |
missense |
possibly damaging |
0.71 |
R4112:Slc10a2
|
UTSW |
8 |
5,155,135 (GRCm39) |
missense |
probably benign |
|
R5693:Slc10a2
|
UTSW |
8 |
5,155,128 (GRCm39) |
missense |
probably damaging |
1.00 |
R6294:Slc10a2
|
UTSW |
8 |
5,141,621 (GRCm39) |
critical splice donor site |
probably null |
|
R6459:Slc10a2
|
UTSW |
8 |
5,148,581 (GRCm39) |
splice site |
probably null |
|
R7442:Slc10a2
|
UTSW |
8 |
5,139,086 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8479:Slc10a2
|
UTSW |
8 |
5,148,443 (GRCm39) |
splice site |
probably null |
|
R8822:Slc10a2
|
UTSW |
8 |
5,139,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R9075:Slc10a2
|
UTSW |
8 |
5,155,267 (GRCm39) |
start gained |
probably benign |
|
R9255:Slc10a2
|
UTSW |
8 |
5,148,565 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Slc10a2
|
UTSW |
8 |
5,148,448 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1188:Slc10a2
|
UTSW |
8 |
5,155,063 (GRCm39) |
missense |
probably damaging |
0.98 |
|