Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
G |
T |
16: 21,513,092 (GRCm39) |
L22M |
probably damaging |
Het |
Abca9 |
T |
C |
11: 109,998,384 (GRCm39) |
N1468S |
probably benign |
Het |
Abcc5 |
C |
T |
16: 20,163,446 (GRCm39) |
D1264N |
possibly damaging |
Het |
Abhd10 |
A |
G |
16: 45,553,099 (GRCm39) |
|
probably benign |
Het |
Acadvl |
G |
T |
11: 69,901,569 (GRCm39) |
A570E |
probably damaging |
Het |
Adgrb3 |
T |
A |
1: 25,586,629 (GRCm39) |
S355C |
probably damaging |
Het |
Adgrv1 |
A |
G |
13: 81,570,344 (GRCm39) |
V4953A |
possibly damaging |
Het |
Ano2 |
T |
A |
6: 125,992,536 (GRCm39) |
Y836* |
probably null |
Het |
Bach1 |
G |
A |
16: 87,516,179 (GRCm39) |
R240Q |
probably benign |
Het |
Ccdc8 |
T |
A |
7: 16,730,537 (GRCm39) |
D675E |
possibly damaging |
Het |
Ccnb2 |
A |
G |
9: 70,326,170 (GRCm39) |
V58A |
probably benign |
Het |
Cdcp3 |
T |
A |
7: 130,879,295 (GRCm39) |
|
probably null |
Het |
Cdh24 |
A |
T |
14: 54,875,547 (GRCm39) |
Y296N |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,198,266 (GRCm39) |
E2054G |
unknown |
Het |
Cnot1 |
A |
T |
8: 96,454,276 (GRCm39) |
F2067I |
probably damaging |
Het |
Csmd3 |
A |
G |
15: 47,813,334 (GRCm39) |
F329S |
|
Het |
Dact3 |
C |
A |
7: 16,619,840 (GRCm39) |
T445K |
unknown |
Het |
Dph6 |
C |
A |
2: 114,485,379 (GRCm39) |
|
probably benign |
Het |
Dst |
T |
A |
1: 34,209,517 (GRCm39) |
C1195S |
probably damaging |
Het |
Eeig1 |
A |
G |
2: 32,456,346 (GRCm39) |
D336G |
possibly damaging |
Het |
Fat3 |
T |
A |
9: 15,899,620 (GRCm39) |
N3138Y |
probably damaging |
Het |
Fbxw25 |
T |
C |
9: 109,483,651 (GRCm39) |
N187S |
|
Het |
Fuca1 |
A |
G |
4: 135,660,405 (GRCm39) |
I308V |
probably benign |
Het |
Galnt5 |
A |
G |
2: 57,907,222 (GRCm39) |
R562G |
probably damaging |
Het |
Gas8 |
G |
T |
8: 124,249,718 (GRCm39) |
R44S |
probably damaging |
Het |
Gja5 |
T |
C |
3: 96,958,071 (GRCm39) |
S43P |
possibly damaging |
Het |
Gm14403 |
A |
G |
2: 177,200,405 (GRCm39) |
D117G |
probably benign |
Het |
Gmpr2 |
G |
A |
14: 55,910,491 (GRCm39) |
V58M |
probably damaging |
Het |
Gtpbp6 |
T |
A |
5: 110,252,950 (GRCm39) |
I301F |
probably damaging |
Het |
H2bc22 |
T |
A |
13: 21,971,762 (GRCm39) |
D26E |
probably benign |
Het |
Hdhd5 |
T |
C |
6: 120,498,212 (GRCm39) |
Y129C |
probably damaging |
Het |
Hemgn |
A |
G |
4: 46,396,504 (GRCm39) |
M244T |
probably benign |
Het |
Hoxa1 |
T |
G |
6: 52,135,238 (GRCm39) |
|
probably null |
Het |
Iglc1 |
T |
A |
16: 18,880,551 (GRCm39) |
H90L |
|
Het |
Lamb2 |
C |
T |
9: 108,366,423 (GRCm39) |
S1545F |
possibly damaging |
Het |
Mc4r |
T |
C |
18: 66,992,580 (GRCm39) |
T178A |
probably benign |
Het |
Mcam |
T |
A |
9: 44,050,955 (GRCm39) |
S346T |
probably benign |
Het |
Mis18bp1 |
A |
G |
12: 65,195,626 (GRCm39) |
S713P |
probably benign |
Het |
Mybl2 |
A |
G |
2: 162,914,752 (GRCm39) |
Y290C |
probably damaging |
Het |
Or4k44 |
T |
C |
2: 111,368,281 (GRCm39) |
M118V |
probably damaging |
Het |
Or7e168 |
A |
T |
9: 19,720,225 (GRCm39) |
I204F |
possibly damaging |
Het |
Pak6 |
A |
G |
2: 118,525,068 (GRCm39) |
T565A |
probably damaging |
Het |
Pde5a |
A |
G |
3: 122,568,250 (GRCm39) |
T284A |
probably benign |
Het |
Pkd1l2 |
A |
T |
8: 117,756,384 (GRCm39) |
F1616Y |
probably damaging |
Het |
Pp2d1 |
T |
C |
17: 53,822,907 (GRCm39) |
E53G |
probably benign |
Het |
Ppp3cc |
A |
C |
14: 70,478,394 (GRCm39) |
S269R |
probably benign |
Het |
Ptprb |
A |
C |
10: 116,205,214 (GRCm39) |
D1856A |
possibly damaging |
Het |
Rgs22 |
A |
T |
15: 36,040,856 (GRCm39) |
V1001E |
probably benign |
Het |
Rnf8 |
T |
A |
17: 29,847,980 (GRCm39) |
V344E |
probably benign |
Het |
Rpn1 |
T |
C |
6: 88,061,550 (GRCm39) |
L13P |
possibly damaging |
Het |
Rsbn1 |
A |
T |
3: 103,822,326 (GRCm39) |
H187L |
probably benign |
Het |
Sdr16c6 |
T |
A |
4: 4,058,801 (GRCm39) |
I262F |
not run |
Het |
Sec22a |
A |
G |
16: 35,149,894 (GRCm39) |
F211L |
probably benign |
Het |
Slc16a4 |
G |
A |
3: 107,205,297 (GRCm39) |
A42T |
possibly damaging |
Het |
Smap1 |
T |
A |
1: 23,887,376 (GRCm39) |
Q386L |
probably benign |
Het |
Sos1 |
A |
T |
17: 80,787,323 (GRCm39) |
F10L |
probably benign |
Het |
Stab1 |
C |
A |
14: 30,862,578 (GRCm39) |
V2282L |
probably benign |
Het |
Tex55 |
C |
T |
16: 38,648,453 (GRCm39) |
D219N |
possibly damaging |
Het |
Tmprss11f |
C |
T |
5: 86,672,019 (GRCm39) |
G391D |
probably damaging |
Het |
Tnfaip2 |
A |
G |
12: 111,412,072 (GRCm39) |
S158G |
probably damaging |
Het |
Trav6d-5 |
A |
G |
14: 53,032,843 (GRCm39) |
T31A |
probably benign |
Het |
Tst |
G |
A |
15: 78,289,903 (GRCm39) |
A44V |
probably damaging |
Het |
Vmn1r210 |
A |
T |
13: 23,011,405 (GRCm39) |
F294I |
probably benign |
Het |
Vwc2 |
T |
C |
11: 11,066,415 (GRCm39) |
F168L |
probably damaging |
Het |
Wdr25 |
G |
A |
12: 108,958,819 (GRCm39) |
G344S |
possibly damaging |
Het |
Zfp605 |
A |
G |
5: 110,275,386 (GRCm39) |
Y168C |
probably benign |
Het |
Zfp790 |
T |
A |
7: 29,525,130 (GRCm39) |
Y49* |
probably null |
Het |
Zfp93 |
T |
C |
7: 23,975,794 (GRCm39) |
F593S |
probably damaging |
Het |
Zfr |
C |
T |
15: 12,160,614 (GRCm39) |
T729I |
possibly damaging |
Het |
|
Other mutations in Sptbn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00421:Sptbn2
|
APN |
19 |
4,774,733 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00688:Sptbn2
|
APN |
19 |
4,775,966 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01339:Sptbn2
|
APN |
19 |
4,796,000 (GRCm39) |
nonsense |
probably null |
|
IGL01373:Sptbn2
|
APN |
19 |
4,796,000 (GRCm39) |
nonsense |
probably null |
|
IGL01420:Sptbn2
|
APN |
19 |
4,784,153 (GRCm39) |
missense |
probably benign |
|
IGL01456:Sptbn2
|
APN |
19 |
4,796,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01953:Sptbn2
|
APN |
19 |
4,799,721 (GRCm39) |
missense |
probably benign |
|
IGL03026:Sptbn2
|
APN |
19 |
4,774,261 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03275:Sptbn2
|
APN |
19 |
4,782,689 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL03286:Sptbn2
|
APN |
19 |
4,797,860 (GRCm39) |
missense |
probably damaging |
0.97 |
F5770:Sptbn2
|
UTSW |
19 |
4,800,660 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4696001:Sptbn2
|
UTSW |
19 |
4,795,605 (GRCm39) |
missense |
probably benign |
0.00 |
R0046:Sptbn2
|
UTSW |
19 |
4,795,405 (GRCm39) |
intron |
probably benign |
|
R0046:Sptbn2
|
UTSW |
19 |
4,795,405 (GRCm39) |
intron |
probably benign |
|
R0121:Sptbn2
|
UTSW |
19 |
4,795,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R0127:Sptbn2
|
UTSW |
19 |
4,774,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R0212:Sptbn2
|
UTSW |
19 |
4,796,970 (GRCm39) |
critical splice donor site |
probably null |
|
R0277:Sptbn2
|
UTSW |
19 |
4,795,173 (GRCm39) |
missense |
probably benign |
0.28 |
R0417:Sptbn2
|
UTSW |
19 |
4,787,954 (GRCm39) |
missense |
probably benign |
0.01 |
R0457:Sptbn2
|
UTSW |
19 |
4,795,966 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0536:Sptbn2
|
UTSW |
19 |
4,776,718 (GRCm39) |
missense |
probably damaging |
0.99 |
R0631:Sptbn2
|
UTSW |
19 |
4,790,014 (GRCm39) |
missense |
probably benign |
0.01 |
R0734:Sptbn2
|
UTSW |
19 |
4,798,151 (GRCm39) |
nonsense |
probably null |
|
R0742:Sptbn2
|
UTSW |
19 |
4,769,011 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1195:Sptbn2
|
UTSW |
19 |
4,795,921 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1195:Sptbn2
|
UTSW |
19 |
4,795,921 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1195:Sptbn2
|
UTSW |
19 |
4,795,921 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1364:Sptbn2
|
UTSW |
19 |
4,782,693 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Sptbn2
|
UTSW |
19 |
4,769,004 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1498:Sptbn2
|
UTSW |
19 |
4,794,274 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1606:Sptbn2
|
UTSW |
19 |
4,800,270 (GRCm39) |
critical splice donor site |
probably null |
|
R1678:Sptbn2
|
UTSW |
19 |
4,800,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R1746:Sptbn2
|
UTSW |
19 |
4,795,992 (GRCm39) |
nonsense |
probably null |
|
R1820:Sptbn2
|
UTSW |
19 |
4,776,624 (GRCm39) |
missense |
probably damaging |
0.98 |
R1830:Sptbn2
|
UTSW |
19 |
4,782,569 (GRCm39) |
missense |
probably benign |
0.09 |
R1863:Sptbn2
|
UTSW |
19 |
4,782,713 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1967:Sptbn2
|
UTSW |
19 |
4,795,327 (GRCm39) |
missense |
probably benign |
0.00 |
R2085:Sptbn2
|
UTSW |
19 |
4,788,587 (GRCm39) |
missense |
probably benign |
0.09 |
R2301:Sptbn2
|
UTSW |
19 |
4,784,166 (GRCm39) |
missense |
probably benign |
0.00 |
R2310:Sptbn2
|
UTSW |
19 |
4,768,963 (GRCm39) |
missense |
probably benign |
0.19 |
R2888:Sptbn2
|
UTSW |
19 |
4,798,664 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3788:Sptbn2
|
UTSW |
19 |
4,795,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4429:Sptbn2
|
UTSW |
19 |
4,788,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R4536:Sptbn2
|
UTSW |
19 |
4,782,630 (GRCm39) |
missense |
probably damaging |
1.00 |
R4662:Sptbn2
|
UTSW |
19 |
4,789,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Sptbn2
|
UTSW |
19 |
4,782,524 (GRCm39) |
missense |
probably benign |
0.25 |
R4731:Sptbn2
|
UTSW |
19 |
4,792,508 (GRCm39) |
missense |
probably damaging |
0.96 |
R4747:Sptbn2
|
UTSW |
19 |
4,798,182 (GRCm39) |
missense |
probably benign |
0.27 |
R4889:Sptbn2
|
UTSW |
19 |
4,779,458 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4891:Sptbn2
|
UTSW |
19 |
4,788,497 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Sptbn2
|
UTSW |
19 |
4,779,337 (GRCm39) |
missense |
probably benign |
0.13 |
R4968:Sptbn2
|
UTSW |
19 |
4,779,230 (GRCm39) |
splice site |
probably null |
|
R4981:Sptbn2
|
UTSW |
19 |
4,801,686 (GRCm39) |
missense |
probably benign |
0.22 |
R5159:Sptbn2
|
UTSW |
19 |
4,787,885 (GRCm39) |
missense |
probably benign |
0.12 |
R5202:Sptbn2
|
UTSW |
19 |
4,774,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R5253:Sptbn2
|
UTSW |
19 |
4,800,110 (GRCm39) |
missense |
probably benign |
0.01 |
R5294:Sptbn2
|
UTSW |
19 |
4,768,936 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5465:Sptbn2
|
UTSW |
19 |
4,800,133 (GRCm39) |
missense |
probably benign |
0.00 |
R5546:Sptbn2
|
UTSW |
19 |
4,775,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R5593:Sptbn2
|
UTSW |
19 |
4,798,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R5780:Sptbn2
|
UTSW |
19 |
4,774,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:Sptbn2
|
UTSW |
19 |
4,788,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R6008:Sptbn2
|
UTSW |
19 |
4,789,306 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6108:Sptbn2
|
UTSW |
19 |
4,781,420 (GRCm39) |
critical splice donor site |
probably null |
|
R6236:Sptbn2
|
UTSW |
19 |
4,798,166 (GRCm39) |
missense |
probably benign |
0.01 |
R6307:Sptbn2
|
UTSW |
19 |
4,774,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R6383:Sptbn2
|
UTSW |
19 |
4,782,524 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6397:Sptbn2
|
UTSW |
19 |
4,792,446 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6453:Sptbn2
|
UTSW |
19 |
4,794,208 (GRCm39) |
missense |
possibly damaging |
0.67 |
R6561:Sptbn2
|
UTSW |
19 |
4,797,954 (GRCm39) |
missense |
probably benign |
0.39 |
R6564:Sptbn2
|
UTSW |
19 |
4,782,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R6644:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R6703:Sptbn2
|
UTSW |
19 |
4,799,843 (GRCm39) |
missense |
probably benign |
|
R6703:Sptbn2
|
UTSW |
19 |
4,799,842 (GRCm39) |
missense |
probably benign |
|
R6753:Sptbn2
|
UTSW |
19 |
4,797,813 (GRCm39) |
missense |
probably benign |
0.01 |
R7007:Sptbn2
|
UTSW |
19 |
4,794,173 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7131:Sptbn2
|
UTSW |
19 |
4,799,488 (GRCm39) |
missense |
probably null |
|
R7219:Sptbn2
|
UTSW |
19 |
4,774,201 (GRCm39) |
missense |
probably damaging |
1.00 |
R7285:Sptbn2
|
UTSW |
19 |
4,787,471 (GRCm39) |
missense |
probably benign |
0.00 |
R7308:Sptbn2
|
UTSW |
19 |
4,801,602 (GRCm39) |
missense |
probably benign |
|
R7469:Sptbn2
|
UTSW |
19 |
4,795,146 (GRCm39) |
missense |
probably benign |
0.00 |
R7502:Sptbn2
|
UTSW |
19 |
4,798,110 (GRCm39) |
missense |
probably benign |
0.02 |
R7635:Sptbn2
|
UTSW |
19 |
4,794,235 (GRCm39) |
missense |
probably damaging |
1.00 |
R7733:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7738:Sptbn2
|
UTSW |
19 |
4,774,153 (GRCm39) |
missense |
probably damaging |
1.00 |
R7742:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7767:Sptbn2
|
UTSW |
19 |
4,784,171 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7795:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7796:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7871:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7877:Sptbn2
|
UTSW |
19 |
4,794,290 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7920:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7921:Sptbn2
|
UTSW |
19 |
4,799,040 (GRCm39) |
missense |
probably benign |
0.05 |
R7923:Sptbn2
|
UTSW |
19 |
4,796,827 (GRCm39) |
missense |
probably benign |
0.01 |
R8137:Sptbn2
|
UTSW |
19 |
4,787,431 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8305:Sptbn2
|
UTSW |
19 |
4,779,158 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8695:Sptbn2
|
UTSW |
19 |
4,796,724 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8790:Sptbn2
|
UTSW |
19 |
4,782,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R9125:Sptbn2
|
UTSW |
19 |
4,784,241 (GRCm39) |
missense |
probably benign |
0.04 |
R9483:Sptbn2
|
UTSW |
19 |
4,789,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R9620:Sptbn2
|
UTSW |
19 |
4,800,535 (GRCm39) |
missense |
probably damaging |
0.99 |
R9631:Sptbn2
|
UTSW |
19 |
4,788,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9646:Sptbn2
|
UTSW |
19 |
4,795,341 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Sptbn2
|
UTSW |
19 |
4,800,535 (GRCm39) |
missense |
probably damaging |
0.99 |
V7580:Sptbn2
|
UTSW |
19 |
4,800,660 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Sptbn2
|
UTSW |
19 |
4,795,219 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Sptbn2
|
UTSW |
19 |
4,788,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|