Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
0610040J01Rik |
T |
A |
5: 64,053,796 (GRCm39) |
M1K |
probably null |
Het |
Atoh8 |
A |
T |
6: 72,200,848 (GRCm39) |
L281M |
possibly damaging |
Het |
Bckdha |
A |
G |
7: 25,340,880 (GRCm39) |
|
probably null |
Het |
Chil6 |
A |
T |
3: 106,296,121 (GRCm39) |
Y371* |
probably null |
Het |
Cilk1 |
A |
T |
9: 78,048,520 (GRCm39) |
Q108L |
probably damaging |
Het |
Fbxw18 |
G |
T |
9: 109,522,376 (GRCm39) |
H164Q |
probably benign |
Het |
Gucd1 |
T |
G |
10: 75,345,650 (GRCm39) |
D135A |
probably benign |
Het |
Hacd1 |
A |
G |
2: 14,040,751 (GRCm39) |
I168T |
possibly damaging |
Het |
Hfm1 |
T |
C |
5: 107,021,896 (GRCm39) |
E1013G |
probably benign |
Het |
Hsf4 |
G |
A |
8: 105,999,217 (GRCm39) |
|
probably null |
Het |
Ift140 |
G |
T |
17: 25,264,151 (GRCm39) |
|
probably null |
Het |
Igsf3 |
A |
T |
3: 101,338,612 (GRCm39) |
I309F |
probably benign |
Het |
Imp4 |
T |
A |
1: 34,482,901 (GRCm39) |
L164Q |
probably damaging |
Het |
Jazf1 |
C |
T |
6: 52,747,311 (GRCm39) |
V204I |
probably benign |
Het |
Kmt2d |
T |
A |
15: 98,764,597 (GRCm39) |
D2V |
probably damaging |
Het |
Knl1 |
T |
C |
2: 118,899,910 (GRCm39) |
V537A |
probably benign |
Het |
Mep1b |
A |
T |
18: 21,208,720 (GRCm39) |
D32V |
possibly damaging |
Het |
Mki67 |
A |
G |
7: 135,306,066 (GRCm39) |
|
probably null |
Het |
Morn3 |
C |
T |
5: 123,175,822 (GRCm39) |
V189M |
probably damaging |
Het |
Mri1 |
C |
T |
8: 84,980,933 (GRCm39) |
C199Y |
possibly damaging |
Het |
Mtmr2 |
T |
C |
9: 13,713,293 (GRCm39) |
M490T |
probably benign |
Het |
Muc16 |
T |
C |
9: 18,548,066 (GRCm39) |
T6076A |
possibly damaging |
Het |
Myo1c |
A |
G |
11: 75,549,273 (GRCm39) |
E113G |
probably damaging |
Het |
Nat8f4 |
A |
T |
6: 85,878,052 (GRCm39) |
V157D |
probably damaging |
Het |
Nectin4 |
T |
C |
1: 171,214,192 (GRCm39) |
V449A |
probably damaging |
Het |
Ogdhl |
C |
T |
14: 32,061,909 (GRCm39) |
T528M |
probably damaging |
Het |
Ogfr |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
GGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGAGCCAGAGGACCCCAAAAGCCAGGTGGGGCCAGAGGACCCCCAAAGCCAGGTGG |
2: 180,237,059 (GRCm39) |
|
probably benign |
Het |
Or4c100 |
G |
A |
2: 88,356,835 (GRCm39) |
V303M |
probably benign |
Het |
Or52l1 |
A |
G |
7: 104,830,067 (GRCm39) |
V166A |
probably damaging |
Het |
Pcdhb12 |
AT |
A |
18: 37,570,393 (GRCm39) |
|
probably null |
Het |
Pigo |
T |
C |
4: 43,023,475 (GRCm39) |
D233G |
probably damaging |
Het |
Pkn2 |
A |
C |
3: 142,516,237 (GRCm39) |
V562G |
possibly damaging |
Het |
Plxna1 |
C |
A |
6: 89,333,817 (GRCm39) |
A271S |
probably benign |
Het |
Ppp1r3a |
C |
T |
6: 14,718,766 (GRCm39) |
S716N |
probably damaging |
Het |
Prss12 |
G |
A |
3: 123,271,762 (GRCm39) |
G256S |
probably benign |
Het |
Psg28 |
A |
T |
7: 18,164,331 (GRCm39) |
M127K |
probably benign |
Het |
Psmf1 |
T |
C |
2: 151,577,533 (GRCm39) |
D48G |
possibly damaging |
Het |
Rabggta |
T |
A |
14: 55,955,944 (GRCm39) |
M438L |
possibly damaging |
Het |
Rapgef3 |
T |
C |
15: 97,643,479 (GRCm39) |
I911V |
probably damaging |
Het |
Rbck1 |
T |
C |
2: 152,165,113 (GRCm39) |
E297G |
probably damaging |
Het |
Rras |
A |
T |
7: 44,669,945 (GRCm39) |
I126F |
probably damaging |
Het |
Slc22a28 |
T |
C |
19: 8,041,813 (GRCm39) |
R465G |
probably null |
Het |
Slc28a2b |
T |
A |
2: 122,352,338 (GRCm39) |
I365N |
probably damaging |
Het |
Snx19 |
A |
G |
9: 30,340,172 (GRCm39) |
T437A |
probably benign |
Het |
Son |
A |
T |
16: 91,444,838 (GRCm39) |
S15C |
probably damaging |
Het |
Spata31e1 |
C |
T |
13: 49,939,542 (GRCm39) |
V723M |
possibly damaging |
Het |
Tmtc2 |
T |
C |
10: 105,026,062 (GRCm39) |
Y802C |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,758,716 (GRCm39) |
M2181K |
probably damaging |
Het |
Ttc23l |
A |
G |
15: 10,530,767 (GRCm39) |
S282P |
probably damaging |
Het |
Zbtb7a |
G |
A |
10: 80,979,910 (GRCm39) |
D35N |
probably damaging |
Het |
Zc3h3 |
C |
A |
15: 75,681,489 (GRCm39) |
V531L |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,466,514 (GRCm39) |
D2249G |
probably benign |
Het |
Zfp87 |
T |
C |
13: 74,520,932 (GRCm39) |
K49E |
probably benign |
Het |
Zfp942 |
T |
C |
17: 22,147,463 (GRCm39) |
T389A |
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 |
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 |
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 |
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 |
|