Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4932414N04Rik |
A |
T |
2: 68,574,624 (GRCm39) |
H618L |
possibly damaging |
Het |
Aacs |
T |
C |
5: 125,593,323 (GRCm39) |
V642A |
probably benign |
Het |
Alms1 |
A |
G |
6: 85,587,796 (GRCm39) |
|
probably null |
Het |
Arhgap39 |
A |
G |
15: 76,636,152 (GRCm39) |
|
probably benign |
Het |
Bard1 |
C |
T |
1: 71,085,921 (GRCm39) |
V595I |
probably benign |
Het |
Bptf |
T |
C |
11: 106,937,953 (GRCm39) |
K2713E |
probably damaging |
Het |
Calhm1 |
C |
T |
19: 47,129,742 (GRCm39) |
G260D |
possibly damaging |
Het |
Ccdc154 |
A |
C |
17: 25,390,779 (GRCm39) |
K643T |
probably benign |
Het |
Ccl4 |
T |
A |
11: 83,554,383 (GRCm39) |
S59T |
probably damaging |
Het |
Cntd1 |
T |
C |
11: 101,174,259 (GRCm39) |
S73P |
probably benign |
Het |
Colgalt2 |
A |
T |
1: 152,348,859 (GRCm39) |
D168V |
probably damaging |
Het |
Fam117a |
T |
C |
11: 95,266,452 (GRCm39) |
|
probably benign |
Het |
Fat1 |
A |
G |
8: 45,476,827 (GRCm39) |
T1935A |
probably benign |
Het |
Fbxw21 |
T |
A |
9: 108,975,653 (GRCm39) |
I248F |
possibly damaging |
Het |
Fhod3 |
A |
T |
18: 25,246,657 (GRCm39) |
M1288L |
probably benign |
Het |
Gm5114 |
T |
G |
7: 39,057,885 (GRCm39) |
K578T |
probably damaging |
Het |
Gxylt2 |
A |
T |
6: 100,727,496 (GRCm39) |
|
probably benign |
Het |
Helz |
G |
T |
11: 107,495,174 (GRCm39) |
A383S |
probably benign |
Het |
Ift172 |
C |
A |
5: 31,421,195 (GRCm39) |
E968* |
probably null |
Het |
Itpripl1 |
T |
C |
2: 126,983,924 (GRCm39) |
N66S |
possibly damaging |
Het |
Kcnma1 |
A |
G |
14: 23,423,265 (GRCm39) |
Y686H |
probably damaging |
Het |
Ndrg1 |
C |
A |
15: 66,815,008 (GRCm39) |
|
probably benign |
Het |
Ogdh |
T |
C |
11: 6,297,216 (GRCm39) |
V545A |
probably benign |
Het |
Or10al5 |
A |
G |
17: 38,063,284 (GRCm39) |
I180V |
possibly damaging |
Het |
P3h3 |
G |
A |
6: 124,831,269 (GRCm39) |
|
probably benign |
Het |
Ppme1 |
A |
T |
7: 99,983,182 (GRCm39) |
|
probably null |
Het |
Prkag1 |
T |
G |
15: 98,713,563 (GRCm39) |
D44A |
probably damaging |
Het |
Prpf39 |
T |
C |
12: 65,090,145 (GRCm39) |
|
probably benign |
Het |
Rabep1 |
C |
A |
11: 70,810,033 (GRCm39) |
R489S |
probably damaging |
Het |
Scn10a |
A |
G |
9: 119,523,168 (GRCm39) |
V75A |
possibly damaging |
Het |
Sema3d |
T |
C |
5: 12,498,042 (GRCm39) |
L16P |
possibly damaging |
Het |
Skida1 |
T |
C |
2: 18,051,997 (GRCm39) |
|
probably benign |
Het |
Syne1 |
A |
G |
10: 5,298,945 (GRCm39) |
I1047T |
possibly damaging |
Het |
Syt17 |
A |
G |
7: 117,981,216 (GRCm39) |
Y369H |
probably benign |
Het |
Tmem131l |
C |
T |
3: 83,829,238 (GRCm39) |
|
probably benign |
Het |
Traf3ip2 |
A |
T |
10: 39,510,669 (GRCm39) |
D314V |
probably damaging |
Het |
Ttc28 |
T |
G |
5: 111,431,933 (GRCm39) |
|
probably benign |
Het |
Ush1c |
A |
C |
7: 45,874,872 (GRCm39) |
|
probably benign |
Het |
Utp20 |
A |
T |
10: 88,602,969 (GRCm39) |
Y1884N |
possibly damaging |
Het |
Vmn2r112 |
T |
A |
17: 22,824,251 (GRCm39) |
I502K |
probably benign |
Het |
Vmn2r60 |
T |
C |
7: 41,791,744 (GRCm39) |
|
probably benign |
Het |
Vmn2r63 |
T |
C |
7: 42,552,699 (GRCm39) |
I852M |
probably benign |
Het |
Vmn2r9 |
T |
A |
5: 108,995,405 (GRCm39) |
E414D |
probably benign |
Het |
Wnt4 |
A |
G |
4: 137,022,754 (GRCm39) |
T106A |
probably damaging |
Het |
Zbtb26 |
A |
T |
2: 37,326,807 (GRCm39) |
N76K |
possibly damaging |
Het |
Zfhx2 |
T |
C |
14: 55,309,445 (GRCm39) |
T885A |
probably benign |
Het |
|
Other mutations in Sptbn4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Sptbn4
|
APN |
7 |
27,068,859 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00468:Sptbn4
|
APN |
7 |
27,117,390 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01396:Sptbn4
|
APN |
7 |
27,114,196 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01700:Sptbn4
|
APN |
7 |
27,103,693 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01878:Sptbn4
|
APN |
7 |
27,063,571 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02066:Sptbn4
|
APN |
7 |
27,063,940 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL02116:Sptbn4
|
APN |
7 |
27,063,782 (GRCm39) |
missense |
probably benign |
|
IGL02226:Sptbn4
|
APN |
7 |
27,065,132 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02333:Sptbn4
|
APN |
7 |
27,063,724 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02337:Sptbn4
|
APN |
7 |
27,127,672 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02451:Sptbn4
|
APN |
7 |
27,065,014 (GRCm39) |
missense |
probably null |
0.15 |
IGL02487:Sptbn4
|
APN |
7 |
27,118,522 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02530:Sptbn4
|
APN |
7 |
27,090,976 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02724:Sptbn4
|
APN |
7 |
27,067,104 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02850:Sptbn4
|
APN |
7 |
27,126,258 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02851:Sptbn4
|
APN |
7 |
27,126,258 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02869:Sptbn4
|
APN |
7 |
27,093,573 (GRCm39) |
splice site |
probably benign |
|
IGL02961:Sptbn4
|
APN |
7 |
27,097,392 (GRCm39) |
missense |
probably damaging |
1.00 |
ANU22:Sptbn4
|
UTSW |
7 |
27,056,812 (GRCm39) |
nonsense |
probably null |
|
R0194:Sptbn4
|
UTSW |
7 |
27,104,336 (GRCm39) |
missense |
probably benign |
0.00 |
R0379:Sptbn4
|
UTSW |
7 |
27,059,161 (GRCm39) |
splice site |
probably benign |
|
R0510:Sptbn4
|
UTSW |
7 |
27,060,991 (GRCm39) |
critical splice donor site |
probably null |
|
R0550:Sptbn4
|
UTSW |
7 |
27,063,803 (GRCm39) |
missense |
probably benign |
0.16 |
R0557:Sptbn4
|
UTSW |
7 |
27,107,753 (GRCm39) |
nonsense |
probably null |
|
R1336:Sptbn4
|
UTSW |
7 |
27,117,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R1494:Sptbn4
|
UTSW |
7 |
27,133,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R1630:Sptbn4
|
UTSW |
7 |
27,118,164 (GRCm39) |
missense |
probably benign |
0.09 |
R1803:Sptbn4
|
UTSW |
7 |
27,118,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1834:Sptbn4
|
UTSW |
7 |
27,066,071 (GRCm39) |
missense |
probably null |
0.96 |
R1906:Sptbn4
|
UTSW |
7 |
27,090,856 (GRCm39) |
critical splice donor site |
probably null |
|
R1924:Sptbn4
|
UTSW |
7 |
27,106,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R1951:Sptbn4
|
UTSW |
7 |
27,065,868 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1989:Sptbn4
|
UTSW |
7 |
27,067,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R1990:Sptbn4
|
UTSW |
7 |
27,123,235 (GRCm39) |
missense |
probably benign |
0.19 |
R2005:Sptbn4
|
UTSW |
7 |
27,065,844 (GRCm39) |
nonsense |
probably null |
|
R2083:Sptbn4
|
UTSW |
7 |
27,127,681 (GRCm39) |
missense |
probably benign |
0.29 |
R2176:Sptbn4
|
UTSW |
7 |
27,063,587 (GRCm39) |
missense |
probably benign |
0.21 |
R2211:Sptbn4
|
UTSW |
7 |
27,067,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R2262:Sptbn4
|
UTSW |
7 |
27,133,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R2263:Sptbn4
|
UTSW |
7 |
27,133,782 (GRCm39) |
missense |
probably damaging |
1.00 |
R2374:Sptbn4
|
UTSW |
7 |
27,059,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R2407:Sptbn4
|
UTSW |
7 |
27,117,523 (GRCm39) |
nonsense |
probably null |
|
R4115:Sptbn4
|
UTSW |
7 |
27,090,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R4116:Sptbn4
|
UTSW |
7 |
27,090,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R4392:Sptbn4
|
UTSW |
7 |
27,117,896 (GRCm39) |
missense |
probably damaging |
0.97 |
R4426:Sptbn4
|
UTSW |
7 |
27,123,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R4535:Sptbn4
|
UTSW |
7 |
27,067,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R4684:Sptbn4
|
UTSW |
7 |
27,066,160 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4684:Sptbn4
|
UTSW |
7 |
27,063,844 (GRCm39) |
missense |
probably damaging |
0.96 |
R4707:Sptbn4
|
UTSW |
7 |
27,116,431 (GRCm39) |
missense |
probably benign |
0.12 |
R4876:Sptbn4
|
UTSW |
7 |
27,071,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Sptbn4
|
UTSW |
7 |
27,068,816 (GRCm39) |
missense |
probably damaging |
1.00 |
R5371:Sptbn4
|
UTSW |
7 |
27,059,166 (GRCm39) |
critical splice donor site |
probably null |
|
R5790:Sptbn4
|
UTSW |
7 |
27,065,853 (GRCm39) |
missense |
probably damaging |
0.99 |
R5857:Sptbn4
|
UTSW |
7 |
27,118,138 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5908:Sptbn4
|
UTSW |
7 |
27,103,678 (GRCm39) |
missense |
probably benign |
0.00 |
R5980:Sptbn4
|
UTSW |
7 |
27,071,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R6005:Sptbn4
|
UTSW |
7 |
27,118,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6013:Sptbn4
|
UTSW |
7 |
27,063,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R6037:Sptbn4
|
UTSW |
7 |
27,063,595 (GRCm39) |
missense |
probably damaging |
0.97 |
R6037:Sptbn4
|
UTSW |
7 |
27,063,595 (GRCm39) |
missense |
probably damaging |
0.97 |
R6129:Sptbn4
|
UTSW |
7 |
27,059,513 (GRCm39) |
missense |
probably damaging |
0.98 |
R6146:Sptbn4
|
UTSW |
7 |
27,064,012 (GRCm39) |
nonsense |
probably null |
|
R6762:Sptbn4
|
UTSW |
7 |
27,093,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Sptbn4
|
UTSW |
7 |
27,071,375 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7178:Sptbn4
|
UTSW |
7 |
27,117,481 (GRCm39) |
missense |
probably damaging |
1.00 |
R7212:Sptbn4
|
UTSW |
7 |
27,116,210 (GRCm39) |
missense |
probably benign |
0.44 |
R7465:Sptbn4
|
UTSW |
7 |
27,066,114 (GRCm39) |
missense |
probably benign |
0.00 |
R7471:Sptbn4
|
UTSW |
7 |
27,108,439 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7510:Sptbn4
|
UTSW |
7 |
27,127,693 (GRCm39) |
missense |
probably benign |
0.13 |
R7527:Sptbn4
|
UTSW |
7 |
27,075,015 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7528:Sptbn4
|
UTSW |
7 |
27,141,960 (GRCm39) |
missense |
probably benign |
0.00 |
R7572:Sptbn4
|
UTSW |
7 |
27,071,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R7649:Sptbn4
|
UTSW |
7 |
27,061,002 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7714:Sptbn4
|
UTSW |
7 |
27,063,761 (GRCm39) |
missense |
probably benign |
0.02 |
R7780:Sptbn4
|
UTSW |
7 |
27,061,059 (GRCm39) |
missense |
possibly damaging |
0.70 |
R7854:Sptbn4
|
UTSW |
7 |
27,061,835 (GRCm39) |
missense |
probably benign |
|
R8002:Sptbn4
|
UTSW |
7 |
27,117,417 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8058:Sptbn4
|
UTSW |
7 |
27,063,694 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8181:Sptbn4
|
UTSW |
7 |
27,074,808 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8195:Sptbn4
|
UTSW |
7 |
27,108,314 (GRCm39) |
nonsense |
probably null |
|
R8353:Sptbn4
|
UTSW |
7 |
27,103,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8392:Sptbn4
|
UTSW |
7 |
27,071,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Sptbn4
|
UTSW |
7 |
27,103,663 (GRCm39) |
missense |
probably damaging |
1.00 |
R8815:Sptbn4
|
UTSW |
7 |
27,106,657 (GRCm39) |
nonsense |
probably null |
|
R8818:Sptbn4
|
UTSW |
7 |
27,063,592 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9171:Sptbn4
|
UTSW |
7 |
27,141,844 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9259:Sptbn4
|
UTSW |
7 |
27,067,124 (GRCm39) |
missense |
possibly damaging |
0.74 |
R9477:Sptbn4
|
UTSW |
7 |
27,132,624 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9564:Sptbn4
|
UTSW |
7 |
27,117,504 (GRCm39) |
missense |
probably damaging |
0.98 |
R9572:Sptbn4
|
UTSW |
7 |
27,066,095 (GRCm39) |
missense |
probably benign |
0.16 |
R9623:Sptbn4
|
UTSW |
7 |
27,107,807 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Sptbn4
|
UTSW |
7 |
27,091,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R9782:Sptbn4
|
UTSW |
7 |
27,107,993 (GRCm39) |
missense |
probably benign |
0.02 |
R9790:Sptbn4
|
UTSW |
7 |
27,071,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R9791:Sptbn4
|
UTSW |
7 |
27,071,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R9798:Sptbn4
|
UTSW |
7 |
27,056,717 (GRCm39) |
makesense |
probably null |
|
X0020:Sptbn4
|
UTSW |
7 |
27,102,159 (GRCm39) |
critical splice donor site |
probably null |
|
X0066:Sptbn4
|
UTSW |
7 |
27,056,736 (GRCm39) |
unclassified |
probably benign |
|
Z1176:Sptbn4
|
UTSW |
7 |
27,059,450 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Sptbn4
|
UTSW |
7 |
27,108,527 (GRCm39) |
missense |
probably benign |
0.41 |
Z1177:Sptbn4
|
UTSW |
7 |
27,104,007 (GRCm39) |
missense |
probably damaging |
1.00 |
|