Other mutations in this stock |
Total: 29 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
G |
T |
8: 87,251,459 (GRCm39) |
|
probably null |
Het |
Ace |
T |
A |
11: 105,864,705 (GRCm39) |
|
probably null |
Het |
Bax |
T |
C |
7: 45,116,195 (GRCm39) |
D2G |
probably damaging |
Het |
Clec16a |
G |
A |
16: 10,549,543 (GRCm39) |
C872Y |
probably damaging |
Het |
Cmya5 |
T |
A |
13: 93,232,703 (GRCm39) |
Y795F |
probably damaging |
Het |
Coro2b |
T |
C |
9: 62,336,512 (GRCm39) |
D254G |
probably damaging |
Het |
Crhbp |
G |
T |
13: 95,572,963 (GRCm39) |
P261H |
probably damaging |
Het |
Cyp4f14 |
T |
C |
17: 33,125,065 (GRCm39) |
D452G |
probably benign |
Het |
Gm8444 |
T |
C |
15: 81,727,902 (GRCm39) |
|
probably benign |
Het |
Gria1 |
T |
A |
11: 57,218,447 (GRCm39) |
M900K |
possibly damaging |
Het |
Kcnj3 |
A |
G |
2: 55,327,559 (GRCm39) |
H116R |
probably damaging |
Het |
Lin9 |
T |
A |
1: 180,496,763 (GRCm39) |
L351I |
probably benign |
Het |
Map3k2 |
A |
G |
18: 32,340,509 (GRCm39) |
D172G |
probably damaging |
Het |
Mmp1b |
T |
C |
9: 7,384,897 (GRCm39) |
I251V |
possibly damaging |
Het |
Mpdz |
A |
C |
4: 81,210,817 (GRCm39) |
H1689Q |
probably damaging |
Het |
Mybpc3 |
C |
T |
2: 90,953,283 (GRCm39) |
A176V |
probably damaging |
Het |
Or5b124 |
A |
T |
19: 13,610,729 (GRCm39) |
T85S |
possibly damaging |
Het |
Otud7a |
T |
A |
7: 63,385,574 (GRCm39) |
I352N |
probably damaging |
Het |
Ptrh1 |
T |
C |
2: 32,666,758 (GRCm39) |
V109A |
probably damaging |
Het |
Pxn |
A |
G |
5: 115,682,428 (GRCm39) |
T14A |
probably damaging |
Het |
Rtn4 |
T |
A |
11: 29,683,645 (GRCm39) |
L173Q |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,733,038 (GRCm39) |
S603P |
probably damaging |
Het |
Scara5 |
CG |
C |
14: 65,997,111 (GRCm39) |
|
probably null |
Het |
Scgb2b19 |
T |
C |
7: 32,978,006 (GRCm39) |
N97S |
probably benign |
Het |
Shank2 |
T |
A |
7: 143,965,029 (GRCm39) |
I872N |
possibly damaging |
Het |
Ush2a |
A |
G |
1: 188,083,276 (GRCm39) |
Y273C |
probably damaging |
Het |
Vmn2r121 |
T |
C |
X: 123,043,272 (GRCm39) |
T120A |
probably benign |
Het |
Vmn2r52 |
T |
A |
7: 9,903,052 (GRCm39) |
I459L |
probably benign |
Het |
Zfp974 |
A |
C |
7: 27,625,715 (GRCm39) |
S52A |
probably benign |
Het |
|
Other mutations in Spink5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Spink5
|
APN |
18 |
44,120,938 (GRCm39) |
splice site |
probably benign |
|
IGL00332:Spink5
|
APN |
18 |
44,100,111 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00501:Spink5
|
APN |
18 |
44,110,806 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL00772:Spink5
|
APN |
18 |
44,139,487 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00920:Spink5
|
APN |
18 |
44,136,276 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00980:Spink5
|
APN |
18 |
44,140,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01016:Spink5
|
APN |
18 |
44,140,711 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01155:Spink5
|
APN |
18 |
44,114,214 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01374:Spink5
|
APN |
18 |
44,122,471 (GRCm39) |
missense |
possibly damaging |
0.74 |
IGL01629:Spink5
|
APN |
18 |
44,129,677 (GRCm39) |
splice site |
probably benign |
|
IGL01907:Spink5
|
APN |
18 |
44,129,743 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01931:Spink5
|
APN |
18 |
44,148,705 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02237:Spink5
|
APN |
18 |
44,145,934 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02306:Spink5
|
APN |
18 |
44,097,511 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02402:Spink5
|
APN |
18 |
44,100,171 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Spink5
|
APN |
18 |
44,123,811 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02552:Spink5
|
APN |
18 |
44,125,235 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL02554:Spink5
|
APN |
18 |
44,148,661 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03066:Spink5
|
APN |
18 |
44,149,457 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03288:Spink5
|
APN |
18 |
44,147,827 (GRCm39) |
missense |
possibly damaging |
0.59 |
crusty2
|
UTSW |
18 |
44,133,001 (GRCm39) |
splice site |
probably benign |
|
R0079:Spink5
|
UTSW |
18 |
44,110,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Spink5
|
UTSW |
18 |
44,136,265 (GRCm39) |
missense |
probably benign |
0.00 |
R0452:Spink5
|
UTSW |
18 |
44,096,385 (GRCm39) |
missense |
possibly damaging |
0.74 |
R0569:Spink5
|
UTSW |
18 |
44,122,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R0639:Spink5
|
UTSW |
18 |
44,146,042 (GRCm39) |
splice site |
probably null |
|
R0648:Spink5
|
UTSW |
18 |
44,132,864 (GRCm39) |
splice site |
probably benign |
|
R0705:Spink5
|
UTSW |
18 |
44,125,341 (GRCm39) |
missense |
probably benign |
0.01 |
R1170:Spink5
|
UTSW |
18 |
44,116,630 (GRCm39) |
missense |
probably benign |
0.07 |
R1290:Spink5
|
UTSW |
18 |
44,140,778 (GRCm39) |
missense |
probably damaging |
0.99 |
R1345:Spink5
|
UTSW |
18 |
44,123,749 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1458:Spink5
|
UTSW |
18 |
44,140,786 (GRCm39) |
missense |
probably benign |
0.01 |
R1530:Spink5
|
UTSW |
18 |
44,148,738 (GRCm39) |
missense |
probably damaging |
0.96 |
R1570:Spink5
|
UTSW |
18 |
44,100,174 (GRCm39) |
missense |
probably benign |
0.00 |
R1820:Spink5
|
UTSW |
18 |
44,122,486 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1843:Spink5
|
UTSW |
18 |
44,132,958 (GRCm39) |
missense |
probably benign |
0.03 |
R1968:Spink5
|
UTSW |
18 |
44,123,775 (GRCm39) |
missense |
probably benign |
0.06 |
R2050:Spink5
|
UTSW |
18 |
44,140,825 (GRCm39) |
critical splice donor site |
probably null |
|
R2252:Spink5
|
UTSW |
18 |
44,153,891 (GRCm39) |
nonsense |
probably null |
|
R2278:Spink5
|
UTSW |
18 |
44,119,396 (GRCm39) |
missense |
probably benign |
0.07 |
R2279:Spink5
|
UTSW |
18 |
44,119,396 (GRCm39) |
missense |
probably benign |
0.07 |
R2696:Spink5
|
UTSW |
18 |
44,115,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2992:Spink5
|
UTSW |
18 |
44,129,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R3422:Spink5
|
UTSW |
18 |
44,143,311 (GRCm39) |
missense |
probably benign |
0.01 |
R3934:Spink5
|
UTSW |
18 |
44,149,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R4179:Spink5
|
UTSW |
18 |
44,120,934 (GRCm39) |
missense |
probably benign |
|
R4854:Spink5
|
UTSW |
18 |
44,153,908 (GRCm39) |
makesense |
probably null |
|
R5011:Spink5
|
UTSW |
18 |
44,139,479 (GRCm39) |
missense |
probably damaging |
0.97 |
R5133:Spink5
|
UTSW |
18 |
44,119,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R5163:Spink5
|
UTSW |
18 |
44,132,924 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5185:Spink5
|
UTSW |
18 |
44,148,711 (GRCm39) |
missense |
probably damaging |
0.97 |
R5187:Spink5
|
UTSW |
18 |
44,122,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R5292:Spink5
|
UTSW |
18 |
44,139,521 (GRCm39) |
missense |
probably benign |
|
R5600:Spink5
|
UTSW |
18 |
44,151,778 (GRCm39) |
missense |
probably damaging |
0.96 |
R6267:Spink5
|
UTSW |
18 |
44,147,824 (GRCm39) |
missense |
probably damaging |
0.99 |
R6296:Spink5
|
UTSW |
18 |
44,147,824 (GRCm39) |
missense |
probably damaging |
0.99 |
R6373:Spink5
|
UTSW |
18 |
44,123,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Spink5
|
UTSW |
18 |
44,143,109 (GRCm39) |
splice site |
probably null |
|
R6982:Spink5
|
UTSW |
18 |
44,110,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R7332:Spink5
|
UTSW |
18 |
44,115,317 (GRCm39) |
missense |
probably damaging |
0.96 |
R7396:Spink5
|
UTSW |
18 |
44,110,722 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7643:Spink5
|
UTSW |
18 |
44,143,319 (GRCm39) |
missense |
probably benign |
0.37 |
R7726:Spink5
|
UTSW |
18 |
44,096,419 (GRCm39) |
missense |
probably damaging |
1.00 |
R7828:Spink5
|
UTSW |
18 |
44,143,296 (GRCm39) |
missense |
probably benign |
0.15 |
R7836:Spink5
|
UTSW |
18 |
44,132,888 (GRCm39) |
missense |
probably benign |
0.00 |
R7880:Spink5
|
UTSW |
18 |
44,119,393 (GRCm39) |
missense |
probably benign |
0.40 |
R8031:Spink5
|
UTSW |
18 |
44,143,303 (GRCm39) |
missense |
probably benign |
0.07 |
R8198:Spink5
|
UTSW |
18 |
44,125,947 (GRCm39) |
missense |
probably benign |
0.17 |
R8361:Spink5
|
UTSW |
18 |
44,122,529 (GRCm39) |
missense |
probably damaging |
1.00 |
R8375:Spink5
|
UTSW |
18 |
44,123,786 (GRCm39) |
missense |
probably benign |
0.01 |
R8684:Spink5
|
UTSW |
18 |
44,143,305 (GRCm39) |
missense |
probably benign |
0.02 |
R8749:Spink5
|
UTSW |
18 |
44,122,425 (GRCm39) |
nonsense |
probably null |
|
R8918:Spink5
|
UTSW |
18 |
44,100,087 (GRCm39) |
missense |
probably damaging |
0.98 |
R9064:Spink5
|
UTSW |
18 |
44,100,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R9161:Spink5
|
UTSW |
18 |
44,147,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R9221:Spink5
|
UTSW |
18 |
44,119,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R9292:Spink5
|
UTSW |
18 |
44,148,075 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9545:Spink5
|
UTSW |
18 |
44,136,262 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9784:Spink5
|
UTSW |
18 |
44,119,490 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Spink5
|
UTSW |
18 |
44,129,764 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Spink5
|
UTSW |
18 |
44,129,702 (GRCm39) |
missense |
probably damaging |
0.97 |
|