Other mutations in this stock |
Total: 41 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef28 |
A |
T |
13: 98,065,999 (GRCm39) |
V1618D |
probably benign |
Het |
Asic5 |
T |
A |
3: 81,911,791 (GRCm39) |
F129Y |
probably benign |
Het |
Cachd1 |
A |
C |
4: 100,831,276 (GRCm39) |
K689N |
probably damaging |
Het |
Cbfa2t2 |
A |
G |
2: 154,278,782 (GRCm39) |
|
probably benign |
Het |
Cdh26 |
T |
C |
2: 178,108,482 (GRCm39) |
V360A |
probably damaging |
Het |
Col9a3 |
C |
T |
2: 180,261,525 (GRCm39) |
A605V |
probably benign |
Het |
Csn3 |
A |
G |
5: 88,077,910 (GRCm39) |
T139A |
probably benign |
Het |
Ddx27 |
G |
T |
2: 166,859,806 (GRCm39) |
K79N |
possibly damaging |
Het |
Dhx29 |
G |
A |
13: 113,069,749 (GRCm39) |
D211N |
probably benign |
Het |
Dlg2 |
A |
G |
7: 91,646,532 (GRCm39) |
|
probably null |
Het |
Dse |
C |
A |
10: 34,028,678 (GRCm39) |
R804L |
probably benign |
Het |
Fgb |
T |
C |
3: 82,956,984 (GRCm39) |
|
probably null |
Het |
Gm11011 |
A |
T |
2: 169,429,392 (GRCm39) |
I31K |
unknown |
Het |
Hira |
A |
G |
16: 18,735,349 (GRCm39) |
T272A |
probably damaging |
Het |
Lcmt1 |
T |
A |
7: 123,000,686 (GRCm39) |
H117Q |
probably benign |
Het |
Mettl23 |
A |
G |
11: 116,734,437 (GRCm39) |
|
probably benign |
Het |
Mtmr2 |
T |
C |
9: 13,704,463 (GRCm39) |
Y197H |
probably benign |
Het |
Myo9a |
T |
G |
9: 59,778,284 (GRCm39) |
S1347A |
probably benign |
Het |
Myrfl |
A |
G |
10: 116,658,661 (GRCm39) |
V432A |
probably damaging |
Het |
Npdc1 |
G |
A |
2: 25,298,957 (GRCm39) |
D284N |
probably damaging |
Het |
Obscn |
G |
T |
11: 58,925,531 (GRCm39) |
H6347Q |
possibly damaging |
Het |
Or52r1b |
A |
T |
7: 102,691,547 (GRCm39) |
Y282F |
probably damaging |
Het |
Or8b53 |
T |
A |
9: 38,667,000 (GRCm39) |
N5K |
probably damaging |
Het |
Peg10 |
A |
G |
6: 4,755,913 (GRCm39) |
|
probably benign |
Het |
Pfkfb3 |
A |
G |
2: 11,506,483 (GRCm39) |
V10A |
probably benign |
Het |
Phf12 |
A |
G |
11: 77,915,871 (GRCm39) |
D175G |
probably damaging |
Het |
Plekhg6 |
T |
G |
6: 125,352,755 (GRCm39) |
I131L |
possibly damaging |
Het |
Ptbp3 |
A |
G |
4: 59,485,626 (GRCm39) |
V95A |
probably damaging |
Het |
Rbbp8 |
A |
G |
18: 11,855,664 (GRCm39) |
T604A |
probably benign |
Het |
Rbbp8nl |
G |
A |
2: 179,921,586 (GRCm39) |
P266L |
possibly damaging |
Het |
Ryr1 |
T |
C |
7: 28,715,148 (GRCm39) |
S4659G |
unknown |
Het |
Serpinb9d |
A |
G |
13: 33,380,423 (GRCm39) |
|
probably null |
Het |
Slc22a28 |
A |
C |
19: 8,048,462 (GRCm39) |
I395S |
possibly damaging |
Het |
Slco6c1 |
T |
A |
1: 97,055,656 (GRCm39) |
I82L |
probably benign |
Het |
Tdrd9 |
C |
T |
12: 111,964,336 (GRCm39) |
|
probably null |
Het |
Ube2v2 |
A |
G |
16: 15,374,343 (GRCm39) |
L77P |
possibly damaging |
Het |
Ugt3a1 |
T |
C |
15: 9,361,769 (GRCm39) |
S182P |
probably damaging |
Het |
Vwa5b1 |
T |
C |
4: 138,336,201 (GRCm39) |
E131G |
probably damaging |
Het |
Wdr18 |
C |
T |
10: 79,800,872 (GRCm39) |
A145V |
probably benign |
Het |
Xpnpep1 |
A |
G |
19: 52,993,253 (GRCm39) |
I358T |
probably damaging |
Het |
Zfp946 |
T |
A |
17: 22,673,676 (GRCm39) |
C143* |
probably null |
Het |
|
Other mutations in Sptan1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00668:Sptan1
|
APN |
2 |
29,883,968 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00932:Sptan1
|
APN |
2 |
29,905,622 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:Sptan1
|
APN |
2 |
29,890,083 (GRCm39) |
splice site |
probably benign |
|
IGL01070:Sptan1
|
APN |
2 |
29,904,185 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01625:Sptan1
|
APN |
2 |
29,916,126 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01657:Sptan1
|
APN |
2 |
29,908,491 (GRCm39) |
missense |
probably benign |
0.12 |
IGL01795:Sptan1
|
APN |
2 |
29,908,501 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01982:Sptan1
|
APN |
2 |
29,909,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02040:Sptan1
|
APN |
2 |
29,903,725 (GRCm39) |
missense |
probably benign |
0.43 |
IGL02158:Sptan1
|
APN |
2 |
29,920,336 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02370:Sptan1
|
APN |
2 |
29,920,752 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02507:Sptan1
|
APN |
2 |
29,906,067 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02552:Sptan1
|
APN |
2 |
29,908,486 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02690:Sptan1
|
APN |
2 |
29,888,195 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02715:Sptan1
|
APN |
2 |
29,868,588 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02725:Sptan1
|
APN |
2 |
29,886,055 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03033:Sptan1
|
APN |
2 |
29,881,045 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03304:Sptan1
|
APN |
2 |
29,876,505 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03405:Sptan1
|
APN |
2 |
29,915,593 (GRCm39) |
missense |
probably damaging |
0.99 |
R0058:Sptan1
|
UTSW |
2 |
29,883,708 (GRCm39) |
splice site |
probably null |
|
R0058:Sptan1
|
UTSW |
2 |
29,883,708 (GRCm39) |
splice site |
probably null |
|
R0066:Sptan1
|
UTSW |
2 |
29,893,679 (GRCm39) |
splice site |
probably benign |
|
R0066:Sptan1
|
UTSW |
2 |
29,893,679 (GRCm39) |
splice site |
probably benign |
|
R0071:Sptan1
|
UTSW |
2 |
29,893,354 (GRCm39) |
nonsense |
probably null |
|
R0071:Sptan1
|
UTSW |
2 |
29,893,354 (GRCm39) |
nonsense |
probably null |
|
R0094:Sptan1
|
UTSW |
2 |
29,896,635 (GRCm39) |
missense |
probably benign |
0.37 |
R0230:Sptan1
|
UTSW |
2 |
29,900,704 (GRCm39) |
splice site |
probably benign |
|
R0242:Sptan1
|
UTSW |
2 |
29,908,413 (GRCm39) |
missense |
probably benign |
0.00 |
R0242:Sptan1
|
UTSW |
2 |
29,908,413 (GRCm39) |
missense |
probably benign |
0.00 |
R0366:Sptan1
|
UTSW |
2 |
29,882,764 (GRCm39) |
splice site |
probably null |
|
R0368:Sptan1
|
UTSW |
2 |
29,883,927 (GRCm39) |
missense |
probably benign |
0.29 |
R0396:Sptan1
|
UTSW |
2 |
29,881,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Sptan1
|
UTSW |
2 |
29,918,684 (GRCm39) |
missense |
probably null |
|
R0448:Sptan1
|
UTSW |
2 |
29,916,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Sptan1
|
UTSW |
2 |
29,903,860 (GRCm39) |
splice site |
probably benign |
|
R0580:Sptan1
|
UTSW |
2 |
29,897,587 (GRCm39) |
missense |
probably damaging |
0.99 |
R0739:Sptan1
|
UTSW |
2 |
29,903,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R0924:Sptan1
|
UTSW |
2 |
29,906,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R0930:Sptan1
|
UTSW |
2 |
29,906,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R0961:Sptan1
|
UTSW |
2 |
29,870,075 (GRCm39) |
splice site |
probably null |
|
R1352:Sptan1
|
UTSW |
2 |
29,911,199 (GRCm39) |
splice site |
probably benign |
|
R1456:Sptan1
|
UTSW |
2 |
29,870,215 (GRCm39) |
critical splice donor site |
probably null |
|
R1537:Sptan1
|
UTSW |
2 |
29,916,034 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1542:Sptan1
|
UTSW |
2 |
29,917,139 (GRCm39) |
missense |
probably damaging |
1.00 |
R1612:Sptan1
|
UTSW |
2 |
29,893,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R1623:Sptan1
|
UTSW |
2 |
29,876,432 (GRCm39) |
missense |
probably damaging |
0.96 |
R1834:Sptan1
|
UTSW |
2 |
29,882,013 (GRCm39) |
splice site |
probably benign |
|
R1879:Sptan1
|
UTSW |
2 |
29,885,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1893:Sptan1
|
UTSW |
2 |
29,910,472 (GRCm39) |
missense |
probably damaging |
0.98 |
R1914:Sptan1
|
UTSW |
2 |
29,901,048 (GRCm39) |
missense |
probably benign |
0.00 |
R1915:Sptan1
|
UTSW |
2 |
29,901,048 (GRCm39) |
missense |
probably benign |
0.00 |
R2022:Sptan1
|
UTSW |
2 |
29,897,573 (GRCm39) |
missense |
probably damaging |
0.96 |
R2050:Sptan1
|
UTSW |
2 |
29,892,250 (GRCm39) |
missense |
probably benign |
|
R2103:Sptan1
|
UTSW |
2 |
29,920,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R2162:Sptan1
|
UTSW |
2 |
29,908,588 (GRCm39) |
splice site |
probably benign |
|
R2931:Sptan1
|
UTSW |
2 |
29,908,500 (GRCm39) |
missense |
probably benign |
|
R3726:Sptan1
|
UTSW |
2 |
29,908,431 (GRCm39) |
missense |
possibly damaging |
0.59 |
R4170:Sptan1
|
UTSW |
2 |
29,920,037 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4235:Sptan1
|
UTSW |
2 |
29,916,600 (GRCm39) |
missense |
probably damaging |
1.00 |
R4378:Sptan1
|
UTSW |
2 |
29,915,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R4424:Sptan1
|
UTSW |
2 |
29,919,721 (GRCm39) |
intron |
probably benign |
|
R4718:Sptan1
|
UTSW |
2 |
29,921,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R4777:Sptan1
|
UTSW |
2 |
29,886,447 (GRCm39) |
missense |
probably damaging |
0.98 |
R4849:Sptan1
|
UTSW |
2 |
29,901,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Sptan1
|
UTSW |
2 |
29,868,455 (GRCm39) |
missense |
probably damaging |
1.00 |
R5180:Sptan1
|
UTSW |
2 |
29,883,736 (GRCm39) |
intron |
probably benign |
|
R5181:Sptan1
|
UTSW |
2 |
29,883,736 (GRCm39) |
intron |
probably benign |
|
R5383:Sptan1
|
UTSW |
2 |
29,901,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R5592:Sptan1
|
UTSW |
2 |
29,876,731 (GRCm39) |
intron |
probably benign |
|
R5639:Sptan1
|
UTSW |
2 |
29,881,005 (GRCm39) |
nonsense |
probably null |
|
R5801:Sptan1
|
UTSW |
2 |
29,920,613 (GRCm39) |
splice site |
probably null |
|
R5947:Sptan1
|
UTSW |
2 |
29,884,379 (GRCm39) |
critical splice donor site |
probably null |
|
R6056:Sptan1
|
UTSW |
2 |
29,886,794 (GRCm39) |
missense |
probably benign |
0.36 |
R6090:Sptan1
|
UTSW |
2 |
29,883,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R6146:Sptan1
|
UTSW |
2 |
29,894,535 (GRCm39) |
missense |
probably benign |
0.01 |
R6254:Sptan1
|
UTSW |
2 |
29,897,561 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6366:Sptan1
|
UTSW |
2 |
29,910,467 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6378:Sptan1
|
UTSW |
2 |
29,908,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Sptan1
|
UTSW |
2 |
29,910,467 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6877:Sptan1
|
UTSW |
2 |
29,920,985 (GRCm39) |
missense |
probably damaging |
0.99 |
R7173:Sptan1
|
UTSW |
2 |
29,873,221 (GRCm39) |
missense |
probably benign |
0.02 |
R7248:Sptan1
|
UTSW |
2 |
29,892,311 (GRCm39) |
missense |
probably benign |
0.10 |
R7282:Sptan1
|
UTSW |
2 |
29,876,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R7527:Sptan1
|
UTSW |
2 |
29,870,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R7585:Sptan1
|
UTSW |
2 |
29,890,068 (GRCm39) |
missense |
probably benign |
0.06 |
R7779:Sptan1
|
UTSW |
2 |
29,911,319 (GRCm39) |
missense |
probably damaging |
1.00 |
R8051:Sptan1
|
UTSW |
2 |
29,920,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R8055:Sptan1
|
UTSW |
2 |
29,884,351 (GRCm39) |
missense |
probably benign |
0.22 |
R8103:Sptan1
|
UTSW |
2 |
29,910,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R8283:Sptan1
|
UTSW |
2 |
29,870,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R8507:Sptan1
|
UTSW |
2 |
29,916,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R8963:Sptan1
|
UTSW |
2 |
29,873,744 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9126:Sptan1
|
UTSW |
2 |
29,920,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R9206:Sptan1
|
UTSW |
2 |
29,920,724 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9273:Sptan1
|
UTSW |
2 |
29,880,977 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0028:Sptan1
|
UTSW |
2 |
29,910,042 (GRCm39) |
missense |
probably damaging |
1.00 |
|