Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef4 |
T |
C |
1: 34,762,162 (GRCm39) |
S473P |
unknown |
Het |
Azin1 |
A |
T |
15: 38,493,849 (GRCm39) |
I258N |
probably benign |
Het |
Bod1l |
G |
A |
5: 41,989,574 (GRCm39) |
A383V |
probably benign |
Het |
Carmil3 |
GGACGA |
GGA |
14: 55,736,933 (GRCm39) |
|
probably benign |
Het |
Cd200r3 |
T |
A |
16: 44,774,552 (GRCm39) |
D188E |
probably benign |
Het |
Cd4 |
A |
T |
6: 124,847,414 (GRCm39) |
F250Y |
probably benign |
Het |
Clcn4 |
T |
A |
7: 7,290,813 (GRCm39) |
Y662F |
probably benign |
Het |
Cpa2 |
T |
C |
6: 30,552,020 (GRCm39) |
V249A |
probably benign |
Het |
Depdc5 |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
CTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCT |
5: 33,067,751 (GRCm39) |
|
probably benign |
Het |
Dhx57 |
A |
G |
17: 80,582,511 (GRCm39) |
Y365H |
probably damaging |
Het |
Dsg1c |
A |
G |
18: 20,408,322 (GRCm39) |
E457G |
probably benign |
Het |
Eef2k |
T |
A |
7: 120,457,822 (GRCm39) |
Y60* |
probably null |
Het |
Efcc1 |
A |
G |
6: 87,730,133 (GRCm39) |
D482G |
probably null |
Het |
Exoc4 |
C |
T |
6: 33,254,179 (GRCm39) |
R112C |
probably damaging |
Het |
Fam178b |
A |
T |
1: 36,639,606 (GRCm39) |
D293E |
probably benign |
Het |
Fbxl21 |
G |
A |
13: 56,674,873 (GRCm39) |
V49I |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,667,953 (GRCm39) |
V91A |
probably damaging |
Het |
H2-M10.4 |
T |
C |
17: 36,772,736 (GRCm39) |
E82G |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,439,531 (GRCm39) |
I5434T |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,492,452 (GRCm39) |
V343A |
probably benign |
Het |
Incenp |
T |
C |
19: 9,861,303 (GRCm39) |
N450S |
unknown |
Het |
Iqsec3 |
T |
C |
6: 121,356,977 (GRCm39) |
K1035E |
possibly damaging |
Het |
Ltn1 |
A |
T |
16: 87,223,174 (GRCm39) |
V102D |
probably damaging |
Het |
Mcur1 |
T |
C |
13: 43,698,016 (GRCm39) |
T295A |
probably damaging |
Het |
Pals1 |
A |
T |
12: 78,871,611 (GRCm39) |
D397V |
possibly damaging |
Het |
Pcdha3 |
T |
C |
18: 37,081,013 (GRCm39) |
V585A |
probably damaging |
Het |
Plcd4 |
A |
G |
1: 74,602,627 (GRCm39) |
T594A |
probably damaging |
Het |
Ppp1r3c |
T |
C |
19: 36,711,522 (GRCm39) |
K83E |
probably damaging |
Het |
Sesn3 |
C |
A |
9: 14,233,954 (GRCm39) |
T309K |
probably benign |
Het |
Slc38a3 |
T |
C |
9: 107,533,405 (GRCm39) |
N251S |
probably benign |
Het |
Srsf4 |
A |
G |
4: 131,601,175 (GRCm39) |
K34R |
probably damaging |
Het |
Tfpi2 |
T |
C |
6: 3,968,044 (GRCm39) |
N32S |
possibly damaging |
Het |
Ttll2 |
A |
T |
17: 7,619,120 (GRCm39) |
I269N |
probably benign |
Het |
Utp3 |
T |
C |
5: 88,703,458 (GRCm39) |
V329A |
probably benign |
Het |
Vmn2r102 |
A |
G |
17: 19,914,975 (GRCm39) |
T847A |
probably benign |
Het |
Vmn2r70 |
A |
T |
7: 85,214,541 (GRCm39) |
W204R |
probably damaging |
Het |
Xrcc3 |
A |
G |
12: 111,770,966 (GRCm39) |
L321P |
probably damaging |
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 |
R0328:Sptbn4
|
UTSW |
7 |
27,063,595 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|