Other mutations in this stock |
Total: 123 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310009B15Rik |
T |
C |
1: 138,781,380 (GRCm39) |
T90A |
probably damaging |
Het |
A930011G23Rik |
T |
C |
5: 99,381,784 (GRCm39) |
D326G |
possibly damaging |
Het |
Abcc2 |
A |
T |
19: 43,795,581 (GRCm39) |
I446F |
probably damaging |
Het |
Adam34l |
T |
C |
8: 44,080,176 (GRCm39) |
K16R |
probably benign |
Het |
Adamts14 |
A |
G |
10: 61,034,439 (GRCm39) |
Y1150H |
probably benign |
Het |
Adgrl2 |
A |
G |
3: 148,522,880 (GRCm39) |
I217T |
possibly damaging |
Het |
Afap1l1 |
A |
T |
18: 61,874,842 (GRCm39) |
Y446* |
probably null |
Het |
Aimp2 |
G |
A |
5: 143,843,548 (GRCm39) |
A14V |
probably damaging |
Het |
Akap8 |
G |
A |
17: 32,535,586 (GRCm39) |
H143Y |
probably damaging |
Het |
Aldh2 |
A |
T |
5: 121,714,026 (GRCm39) |
V207E |
possibly damaging |
Het |
Aoc1l2 |
T |
A |
6: 48,907,703 (GRCm39) |
H234Q |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Arpp21 |
T |
C |
9: 111,986,861 (GRCm39) |
E230G |
probably damaging |
Het |
Arrdc3 |
G |
A |
13: 81,031,808 (GRCm39) |
D14N |
probably damaging |
Het |
Atn1 |
A |
G |
6: 124,722,291 (GRCm39) |
|
probably benign |
Het |
Atxn7l1 |
G |
A |
12: 33,408,743 (GRCm39) |
D302N |
probably damaging |
Het |
Bbs1 |
T |
A |
19: 4,941,736 (GRCm39) |
H518L |
probably benign |
Het |
Bltp1 |
A |
T |
3: 37,054,181 (GRCm39) |
H3100L |
probably benign |
Het |
Bmpr1a |
C |
A |
14: 34,147,050 (GRCm39) |
G241C |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Calcrl |
T |
C |
2: 84,200,855 (GRCm39) |
Y63C |
probably damaging |
Het |
Cand2 |
A |
G |
6: 115,762,093 (GRCm39) |
H173R |
possibly damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Card14 |
A |
T |
11: 119,212,647 (GRCm39) |
|
probably null |
Het |
Cd3d |
T |
A |
9: 44,896,299 (GRCm39) |
Y29* |
probably null |
Het |
Cd4 |
A |
G |
6: 124,844,651 (GRCm39) |
V378A |
possibly damaging |
Het |
Cluh |
A |
T |
11: 74,550,828 (GRCm39) |
H318L |
probably damaging |
Het |
Clvs1 |
T |
A |
4: 9,281,899 (GRCm39) |
D114E |
probably benign |
Het |
Cnot4 |
T |
A |
6: 35,000,344 (GRCm39) |
T548S |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crebbp |
A |
T |
16: 3,946,561 (GRCm39) |
|
probably null |
Het |
Dnah7a |
T |
G |
1: 53,621,835 (GRCm39) |
K1097Q |
possibly damaging |
Het |
Doc2a |
T |
A |
7: 126,450,979 (GRCm39) |
|
probably null |
Het |
Dpp10 |
A |
T |
1: 123,832,833 (GRCm39) |
V48E |
probably null |
Het |
Dsg2 |
A |
G |
18: 20,734,530 (GRCm39) |
K836R |
probably damaging |
Het |
Egr2 |
T |
C |
10: 67,375,857 (GRCm39) |
V164A |
probably damaging |
Het |
Erbin |
A |
T |
13: 103,970,221 (GRCm39) |
S1132T |
probably benign |
Het |
Espn |
T |
A |
4: 152,213,012 (GRCm39) |
|
probably null |
Het |
Fam83b |
A |
G |
9: 76,399,304 (GRCm39) |
S600P |
probably benign |
Het |
Fanca |
A |
T |
8: 124,024,551 (GRCm39) |
N425K |
possibly damaging |
Het |
Flot2 |
C |
T |
11: 77,949,445 (GRCm39) |
L294F |
probably damaging |
Het |
Frs2 |
A |
G |
10: 116,910,459 (GRCm39) |
V301A |
probably benign |
Het |
Fv1 |
T |
A |
4: 147,953,618 (GRCm39) |
N61K |
possibly damaging |
Het |
Fxr2 |
A |
G |
11: 69,540,659 (GRCm39) |
E339G |
possibly damaging |
Het |
Gck |
T |
C |
11: 5,856,515 (GRCm39) |
Y214C |
probably damaging |
Het |
Golga3 |
C |
G |
5: 110,340,839 (GRCm39) |
T551R |
probably damaging |
Het |
Gorab |
A |
G |
1: 163,224,625 (GRCm39) |
S59P |
probably damaging |
Het |
Gsdme |
C |
T |
6: 50,185,102 (GRCm39) |
V451M |
probably damaging |
Het |
H2-T13 |
A |
C |
17: 36,391,938 (GRCm39) |
I216S |
probably damaging |
Het |
Herc4 |
T |
A |
10: 63,081,743 (GRCm39) |
V22E |
possibly damaging |
Het |
Hjurp |
GT |
GTT |
1: 88,194,246 (GRCm39) |
|
probably null |
Het |
Hoxa2 |
A |
T |
6: 52,141,576 (GRCm39) |
S17T |
probably damaging |
Het |
Hs3st5 |
A |
G |
10: 36,708,882 (GRCm39) |
Y139C |
probably damaging |
Het |
Ism1 |
G |
A |
2: 139,587,937 (GRCm39) |
V221I |
probably benign |
Het |
Kalrn |
T |
G |
16: 33,796,108 (GRCm39) |
L1222F |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,419,261 (GRCm39) |
N476S |
probably benign |
Het |
Kdm4c |
A |
G |
4: 74,261,631 (GRCm39) |
D602G |
possibly damaging |
Het |
Ktn1 |
A |
G |
14: 47,932,978 (GRCm39) |
K711E |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Macf1 |
A |
G |
4: 123,350,488 (GRCm39) |
S3792P |
probably damaging |
Het |
Maml3 |
C |
T |
3: 51,598,178 (GRCm39) |
M189I |
probably benign |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mep1a |
T |
G |
17: 43,813,573 (GRCm39) |
I13L |
probably benign |
Het |
Mkrn2 |
G |
T |
6: 115,586,562 (GRCm39) |
C16F |
probably damaging |
Het |
Mlh1 |
C |
T |
9: 111,057,631 (GRCm39) |
A727T |
probably damaging |
Het |
Muc21 |
A |
T |
17: 35,929,600 (GRCm39) |
S1529T |
probably benign |
Het |
Naa16 |
T |
C |
14: 79,593,931 (GRCm39) |
Y344C |
probably damaging |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nlrc4 |
T |
A |
17: 74,752,628 (GRCm39) |
Y585F |
probably benign |
Het |
Nrcam |
A |
G |
12: 44,587,753 (GRCm39) |
K149R |
probably damaging |
Het |
Nufip1 |
T |
A |
14: 76,372,287 (GRCm39) |
I467N |
probably damaging |
Het |
Nup133 |
A |
G |
8: 124,632,960 (GRCm39) |
I1057T |
possibly damaging |
Het |
Obscn |
A |
T |
11: 58,886,653 (GRCm39) |
|
probably benign |
Het |
Or10ag52 |
T |
A |
2: 87,043,588 (GRCm39) |
C117* |
probably null |
Het |
Or5k1 |
A |
G |
16: 58,617,309 (GRCm39) |
V300A |
probably benign |
Het |
Or5k14 |
A |
C |
16: 58,692,874 (GRCm39) |
I213R |
probably benign |
Het |
Pi4k2a |
A |
T |
19: 42,104,377 (GRCm39) |
I380F |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pik3cg |
A |
T |
12: 32,254,024 (GRCm39) |
D654E |
possibly damaging |
Het |
Poli |
G |
T |
18: 70,642,058 (GRCm39) |
P714Q |
probably damaging |
Het |
Polr3f |
A |
G |
2: 144,378,230 (GRCm39) |
N201D |
probably benign |
Het |
Prorp |
A |
G |
12: 55,384,991 (GRCm39) |
D89G |
probably damaging |
Het |
Ptprz1 |
A |
T |
6: 22,959,747 (GRCm39) |
K81N |
probably benign |
Het |
Rbm19 |
T |
C |
5: 120,271,948 (GRCm39) |
|
probably null |
Het |
Sec24a |
C |
T |
11: 51,627,190 (GRCm39) |
V241I |
probably benign |
Het |
Sgk3 |
A |
G |
1: 9,950,567 (GRCm39) |
T160A |
possibly damaging |
Het |
Slc1a4 |
A |
G |
11: 20,254,375 (GRCm39) |
I497T |
probably benign |
Het |
Slc26a9 |
A |
T |
1: 131,690,532 (GRCm39) |
D512V |
probably damaging |
Het |
Slc43a3 |
C |
T |
2: 84,788,084 (GRCm39) |
R489C |
probably damaging |
Het |
Slc5a12 |
T |
A |
2: 110,452,089 (GRCm39) |
F327L |
probably benign |
Het |
Slitrk3 |
A |
G |
3: 72,957,104 (GRCm39) |
V556A |
possibly damaging |
Het |
Spata6l |
A |
G |
19: 28,926,024 (GRCm39) |
F130L |
probably damaging |
Het |
Spib |
T |
C |
7: 44,178,281 (GRCm39) |
E180G |
probably benign |
Het |
Spint2 |
T |
A |
7: 28,958,833 (GRCm39) |
N128Y |
probably damaging |
Het |
Spx |
G |
A |
6: 142,364,245 (GRCm39) |
G102E |
probably benign |
Het |
Spz1 |
T |
A |
13: 92,712,166 (GRCm39) |
E103D |
possibly damaging |
Het |
Sstr2 |
T |
C |
11: 113,515,495 (GRCm39) |
I138T |
probably benign |
Het |
Sytl3 |
T |
A |
17: 7,000,448 (GRCm39) |
I206N |
possibly damaging |
Het |
Tcaf2 |
T |
C |
6: 42,606,791 (GRCm39) |
T388A |
probably benign |
Het |
Tdpoz8 |
G |
T |
3: 92,981,344 (GRCm39) |
A121S |
probably benign |
Het |
Thap12 |
T |
C |
7: 98,365,572 (GRCm39) |
V580A |
possibly damaging |
Het |
Tlr5 |
T |
A |
1: 182,801,912 (GRCm39) |
D405E |
probably damaging |
Het |
Tnxb |
T |
C |
17: 34,890,878 (GRCm39) |
V407A |
probably damaging |
Het |
Trim43a |
T |
G |
9: 88,466,312 (GRCm39) |
L211R |
probably damaging |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Ttll8 |
T |
C |
15: 88,798,654 (GRCm39) |
T694A |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Ube3a |
C |
T |
7: 58,953,535 (GRCm39) |
A823V |
probably damaging |
Het |
Ubqln5 |
C |
A |
7: 103,778,741 (GRCm39) |
V28F |
probably damaging |
Het |
Ulk1 |
T |
A |
5: 110,935,017 (GRCm39) |
Q972L |
probably damaging |
Het |
Unc93b1 |
T |
C |
19: 3,994,062 (GRCm39) |
Y398H |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,822,531 (GRCm39) |
D615G |
probably benign |
Het |
Utp15 |
A |
G |
13: 98,387,420 (GRCm39) |
C385R |
probably benign |
Het |
Vmn2r91 |
T |
A |
17: 18,356,142 (GRCm39) |
V603D |
probably damaging |
Het |
Whamm |
C |
T |
7: 81,241,519 (GRCm39) |
R277* |
probably null |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Yjefn3 |
A |
T |
8: 70,341,645 (GRCm39) |
|
probably null |
Het |
Ywhab |
A |
T |
2: 163,853,807 (GRCm39) |
I95F |
probably damaging |
Het |
Zfp143 |
C |
T |
7: 109,660,489 (GRCm39) |
|
probably benign |
Het |
Zfp607b |
C |
G |
7: 27,401,949 (GRCm39) |
T135R |
possibly damaging |
Het |
Zfp970 |
A |
G |
2: 177,166,663 (GRCm39) |
Q79R |
possibly damaging |
Het |
|
Other mutations in Tpx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01348:Tpx2
|
APN |
2 |
152,735,511 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01810:Tpx2
|
APN |
2 |
152,726,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:Tpx2
|
APN |
2 |
152,726,096 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02184:Tpx2
|
APN |
2 |
152,724,240 (GRCm39) |
nonsense |
probably null |
|
IGL02422:Tpx2
|
APN |
2 |
152,715,064 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02441:Tpx2
|
APN |
2 |
152,724,207 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7952_Tpx2_601
|
UTSW |
2 |
152,735,514 (GRCm39) |
missense |
probably damaging |
1.00 |
reddened
|
UTSW |
2 |
152,711,644 (GRCm39) |
missense |
probably benign |
0.00 |
Shamed
|
UTSW |
2 |
152,715,024 (GRCm39) |
missense |
probably benign |
|
R0063:Tpx2
|
UTSW |
2 |
152,722,043 (GRCm39) |
missense |
probably damaging |
0.99 |
R0076:Tpx2
|
UTSW |
2 |
152,735,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R0271:Tpx2
|
UTSW |
2 |
152,709,287 (GRCm39) |
splice site |
probably benign |
|
R0311:Tpx2
|
UTSW |
2 |
152,732,412 (GRCm39) |
missense |
probably damaging |
0.98 |
R0617:Tpx2
|
UTSW |
2 |
152,715,058 (GRCm39) |
missense |
probably benign |
0.01 |
R1871:Tpx2
|
UTSW |
2 |
152,735,523 (GRCm39) |
missense |
probably damaging |
1.00 |
R1882:Tpx2
|
UTSW |
2 |
152,711,611 (GRCm39) |
missense |
probably benign |
|
R1990:Tpx2
|
UTSW |
2 |
152,732,544 (GRCm39) |
missense |
probably benign |
|
R1991:Tpx2
|
UTSW |
2 |
152,732,544 (GRCm39) |
missense |
probably benign |
|
R4686:Tpx2
|
UTSW |
2 |
152,731,103 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4712:Tpx2
|
UTSW |
2 |
152,726,958 (GRCm39) |
missense |
probably damaging |
1.00 |
R4792:Tpx2
|
UTSW |
2 |
152,727,016 (GRCm39) |
missense |
probably damaging |
0.98 |
R4873:Tpx2
|
UTSW |
2 |
152,735,535 (GRCm39) |
missense |
probably benign |
0.00 |
R4875:Tpx2
|
UTSW |
2 |
152,735,535 (GRCm39) |
missense |
probably benign |
0.00 |
R4991:Tpx2
|
UTSW |
2 |
152,711,644 (GRCm39) |
missense |
probably benign |
0.00 |
R5178:Tpx2
|
UTSW |
2 |
152,717,469 (GRCm39) |
missense |
probably benign |
0.01 |
R5757:Tpx2
|
UTSW |
2 |
152,727,151 (GRCm39) |
splice site |
probably null |
|
R6158:Tpx2
|
UTSW |
2 |
152,715,024 (GRCm39) |
missense |
probably benign |
|
R6225:Tpx2
|
UTSW |
2 |
152,718,548 (GRCm39) |
missense |
probably benign |
|
R6539:Tpx2
|
UTSW |
2 |
152,718,518 (GRCm39) |
nonsense |
probably null |
|
R6633:Tpx2
|
UTSW |
2 |
152,709,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R7358:Tpx2
|
UTSW |
2 |
152,718,550 (GRCm39) |
missense |
probably benign |
|
R7741:Tpx2
|
UTSW |
2 |
152,709,263 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7952:Tpx2
|
UTSW |
2 |
152,735,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8433:Tpx2
|
UTSW |
2 |
152,722,056 (GRCm39) |
missense |
probably damaging |
0.99 |
R8888:Tpx2
|
UTSW |
2 |
152,724,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8895:Tpx2
|
UTSW |
2 |
152,724,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R8920:Tpx2
|
UTSW |
2 |
152,726,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R9191:Tpx2
|
UTSW |
2 |
152,727,124 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9267:Tpx2
|
UTSW |
2 |
152,732,517 (GRCm39) |
missense |
probably damaging |
0.99 |
R9486:Tpx2
|
UTSW |
2 |
152,726,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R9610:Tpx2
|
UTSW |
2 |
152,715,124 (GRCm39) |
missense |
probably benign |
0.05 |
R9611:Tpx2
|
UTSW |
2 |
152,715,124 (GRCm39) |
missense |
probably benign |
0.05 |
R9679:Tpx2
|
UTSW |
2 |
152,711,618 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9722:Tpx2
|
UTSW |
2 |
152,733,476 (GRCm39) |
critical splice donor site |
probably null |
|
X0023:Tpx2
|
UTSW |
2 |
152,726,948 (GRCm39) |
missense |
probably benign |
0.05 |
|