Other mutations in this stock |
Total: 102 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130230L23Rik |
A |
T |
5: 66,157,560 (GRCm39) |
M1K |
probably null |
Het |
Abca4 |
T |
A |
3: 121,899,010 (GRCm39) |
I664N |
probably damaging |
Het |
Acin1 |
T |
C |
14: 54,881,718 (GRCm39) |
D335G |
probably damaging |
Het |
Acoxl |
A |
G |
2: 127,719,707 (GRCm39) |
Y156C |
probably damaging |
Het |
Adamts20 |
A |
G |
15: 94,236,340 (GRCm39) |
F844L |
probably benign |
Het |
Ago1 |
A |
G |
4: 126,335,029 (GRCm39) |
Y398H |
probably damaging |
Het |
Aldob |
A |
G |
4: 49,543,835 (GRCm39) |
V49A |
possibly damaging |
Het |
Arhgap18 |
A |
G |
10: 26,722,026 (GRCm39) |
E71G |
probably damaging |
Het |
Asb12 |
G |
T |
X: 94,513,950 (GRCm39) |
H307N |
probably damaging |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
AY358078 |
T |
C |
14: 52,037,504 (GRCm39) |
M1T |
probably null |
Het |
Bcl2l15 |
A |
G |
3: 103,745,914 (GRCm39) |
|
probably null |
Het |
Brpf3 |
A |
G |
17: 29,026,342 (GRCm39) |
M472V |
probably benign |
Het |
Bsn |
A |
G |
9: 107,983,918 (GRCm39) |
S3379P |
unknown |
Het |
Cap2 |
T |
C |
13: 46,793,555 (GRCm39) |
V333A |
probably damaging |
Het |
Cd207 |
T |
A |
6: 83,652,635 (GRCm39) |
D165V |
probably damaging |
Het |
Cfap210 |
A |
T |
2: 69,612,181 (GRCm39) |
|
probably null |
Het |
Cmtr1 |
A |
G |
17: 29,893,148 (GRCm39) |
T496A |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Cstb |
A |
G |
10: 78,263,273 (GRCm39) |
*99W |
probably null |
Het |
Cstdc6 |
T |
G |
16: 36,142,148 (GRCm39) |
D76A |
possibly damaging |
Het |
Ddx11 |
G |
A |
17: 66,442,934 (GRCm39) |
|
probably null |
Het |
Dip2c |
T |
C |
13: 9,671,985 (GRCm39) |
M990T |
possibly damaging |
Het |
Epc2 |
A |
G |
2: 49,422,117 (GRCm39) |
Y337C |
probably damaging |
Het |
Fmn1 |
A |
G |
2: 113,539,783 (GRCm39) |
E1326G |
probably damaging |
Het |
Focad |
A |
T |
4: 88,096,326 (GRCm39) |
D236V |
probably damaging |
Het |
Fsd1 |
G |
A |
17: 56,298,254 (GRCm39) |
S193N |
probably benign |
Het |
Gm4922 |
T |
A |
10: 18,660,211 (GRCm39) |
R170S |
possibly damaging |
Het |
Gm5129 |
T |
C |
5: 29,940,654 (GRCm39) |
|
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Hspbap1 |
A |
T |
16: 35,621,934 (GRCm39) |
Y93F |
possibly damaging |
Het |
Iars2 |
A |
T |
1: 185,050,765 (GRCm39) |
D441E |
probably benign |
Het |
Il1rap |
A |
T |
16: 26,541,676 (GRCm39) |
H639L |
probably damaging |
Het |
Inhbc |
A |
T |
10: 127,193,416 (GRCm39) |
V200E |
probably benign |
Het |
Intu |
G |
T |
3: 40,618,765 (GRCm39) |
G257V |
probably damaging |
Het |
Kif23 |
C |
A |
9: 61,826,243 (GRCm39) |
A929S |
possibly damaging |
Het |
Kmt2b |
A |
T |
7: 30,274,083 (GRCm39) |
V2207E |
possibly damaging |
Het |
Ksr2 |
A |
C |
5: 117,643,594 (GRCm39) |
E121A |
probably benign |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lpl |
TGG |
TG |
8: 69,349,254 (GRCm39) |
|
probably null |
Het |
Mcmdc2 |
T |
C |
1: 10,001,030 (GRCm39) |
V435A |
probably damaging |
Het |
Mecom |
A |
G |
3: 30,563,577 (GRCm39) |
|
probably null |
Het |
Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
Mmp16 |
A |
T |
4: 18,116,013 (GRCm39) |
D539V |
probably benign |
Het |
Mpp1 |
A |
G |
X: 74,168,975 (GRCm39) |
|
probably null |
Het |
Mpp2 |
C |
T |
11: 101,955,493 (GRCm39) |
E86K |
probably benign |
Het |
Mtor |
T |
A |
4: 148,539,089 (GRCm39) |
F195L |
probably damaging |
Het |
Myo3a |
T |
C |
2: 22,404,657 (GRCm39) |
I663T |
probably benign |
Het |
Nlrp5 |
G |
A |
7: 23,123,407 (GRCm39) |
G756E |
possibly damaging |
Het |
Nudt18 |
T |
C |
14: 70,817,335 (GRCm39) |
L255P |
probably damaging |
Het |
Nup62 |
T |
A |
7: 44,478,472 (GRCm39) |
S162R |
possibly damaging |
Het |
Oosp2 |
C |
T |
19: 11,626,959 (GRCm39) |
|
probably null |
Het |
Or52n20 |
T |
A |
7: 104,320,524 (GRCm39) |
I205N |
possibly damaging |
Het |
Or6c66 |
A |
T |
10: 129,461,621 (GRCm39) |
I103K |
probably damaging |
Het |
Or7g20 |
G |
A |
9: 18,946,562 (GRCm39) |
A48T |
probably benign |
Het |
Or8h7 |
A |
G |
2: 86,720,956 (GRCm39) |
S188P |
probably damaging |
Het |
Pan2 |
A |
G |
10: 128,149,050 (GRCm39) |
D506G |
probably damaging |
Het |
Pcdh9 |
G |
A |
14: 94,125,471 (GRCm39) |
S233L |
probably damaging |
Het |
Pcdhgc5 |
T |
G |
18: 37,954,471 (GRCm39) |
S582A |
possibly damaging |
Het |
Pdik1l |
T |
C |
4: 134,006,222 (GRCm39) |
D70G |
probably damaging |
Het |
Peg12 |
T |
C |
7: 62,113,416 (GRCm39) |
H227R |
probably benign |
Het |
Pms1 |
C |
T |
1: 53,228,546 (GRCm39) |
V901I |
probably benign |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Pole |
A |
G |
5: 110,482,063 (GRCm39) |
E135G |
probably benign |
Het |
Ppp6r2 |
C |
A |
15: 89,166,141 (GRCm39) |
A715E |
probably benign |
Het |
Prickle4 |
T |
G |
17: 48,001,044 (GRCm39) |
H174P |
possibly damaging |
Het |
Prl2a1 |
T |
C |
13: 27,988,923 (GRCm39) |
L16P |
probably damaging |
Het |
Prss32 |
C |
T |
17: 24,072,868 (GRCm39) |
T33M |
probably benign |
Het |
Psmd13 |
C |
T |
7: 140,463,430 (GRCm39) |
T38I |
probably damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Rbbp6 |
T |
C |
7: 122,596,252 (GRCm39) |
V598A |
probably damaging |
Het |
Rbm34 |
C |
A |
8: 127,697,631 (GRCm39) |
A27S |
probably benign |
Het |
Rbm4b |
A |
G |
19: 4,812,331 (GRCm39) |
T247A |
probably benign |
Het |
Riiad1 |
G |
A |
3: 94,380,176 (GRCm39) |
P40S |
possibly damaging |
Het |
Sema4f |
T |
C |
6: 82,894,824 (GRCm39) |
D457G |
possibly damaging |
Het |
Sema6c |
A |
T |
3: 95,078,099 (GRCm39) |
I492F |
probably damaging |
Het |
Serpina3a |
A |
T |
12: 104,084,886 (GRCm39) |
I94L |
probably benign |
Het |
Skida1 |
TTGCTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGCTG |
2: 18,051,155 (GRCm39) |
|
probably benign |
Het |
Slc38a1 |
G |
A |
15: 96,485,016 (GRCm39) |
T221M |
probably damaging |
Het |
Slc6a17 |
T |
A |
3: 107,379,492 (GRCm39) |
M559L |
probably damaging |
Het |
Sntg2 |
T |
C |
12: 30,286,650 (GRCm39) |
N315D |
probably benign |
Het |
Snx10 |
T |
A |
6: 51,552,890 (GRCm39) |
V11E |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,047,405 (GRCm39) |
E1683G |
probably benign |
Het |
Ssc5d |
A |
T |
7: 4,931,506 (GRCm39) |
R238W |
probably damaging |
Het |
Ssh1 |
A |
T |
5: 114,081,512 (GRCm39) |
F617L |
probably damaging |
Het |
Taf1 |
T |
G |
X: 100,606,563 (GRCm39) |
M1254R |
probably damaging |
Het |
Tcirg1 |
A |
G |
19: 3,948,835 (GRCm39) |
L450P |
probably damaging |
Het |
Ticam1 |
C |
A |
17: 56,578,718 (GRCm39) |
A126S |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,890,821 (GRCm39) |
V388E |
probably damaging |
Het |
Tomm5 |
A |
G |
4: 45,107,939 (GRCm39) |
L32P |
probably damaging |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp28 |
T |
G |
9: 48,920,494 (GRCm39) |
D240E |
probably benign |
Het |
Usp34 |
T |
C |
11: 23,311,593 (GRCm39) |
Y462H |
possibly damaging |
Het |
Utp14b |
C |
A |
1: 78,643,148 (GRCm39) |
Q349K |
probably damaging |
Het |
Utp20 |
G |
T |
10: 88,585,305 (GRCm39) |
D2586E |
probably benign |
Het |
Vmn1r173 |
A |
G |
7: 23,402,660 (GRCm39) |
I298M |
unknown |
Het |
Vmn1r37 |
T |
A |
6: 66,708,461 (GRCm39) |
I29K |
probably benign |
Het |
Vmn2r23 |
G |
A |
6: 123,679,874 (GRCm39) |
G32D |
probably damaging |
Het |
Xpo7 |
A |
T |
14: 70,931,431 (GRCm39) |
F296I |
probably damaging |
Het |
Zfhx4 |
A |
G |
3: 5,477,774 (GRCm39) |
E3463G |
probably damaging |
Het |
Zfp455 |
G |
T |
13: 67,355,509 (GRCm39) |
R194L |
probably benign |
Het |
Zfp663 |
T |
C |
2: 165,194,651 (GRCm39) |
T523A |
possibly damaging |
Het |
|
Other mutations in Ints8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01390:Ints8
|
APN |
4 |
11,218,679 (GRCm39) |
splice site |
probably benign |
|
IGL01925:Ints8
|
APN |
4 |
11,235,617 (GRCm39) |
splice site |
probably benign |
|
IGL02195:Ints8
|
APN |
4 |
11,221,222 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02215:Ints8
|
APN |
4 |
11,209,244 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02429:Ints8
|
APN |
4 |
11,231,720 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02484:Ints8
|
APN |
4 |
11,208,834 (GRCm39) |
nonsense |
probably null |
|
IGL02558:Ints8
|
APN |
4 |
11,218,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02725:Ints8
|
APN |
4 |
11,239,406 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02742:Ints8
|
APN |
4 |
11,241,627 (GRCm39) |
missense |
possibly damaging |
0.75 |
IGL02831:Ints8
|
APN |
4 |
11,245,896 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL03140:Ints8
|
APN |
4 |
11,235,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03171:Ints8
|
APN |
4 |
11,231,702 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03335:Ints8
|
APN |
4 |
11,216,460 (GRCm39) |
missense |
probably damaging |
1.00 |
G1Funyon:Ints8
|
UTSW |
4 |
11,246,120 (GRCm39) |
missense |
probably damaging |
1.00 |
P0026:Ints8
|
UTSW |
4 |
11,225,788 (GRCm39) |
nonsense |
probably null |
|
R0054:Ints8
|
UTSW |
4 |
11,204,595 (GRCm39) |
utr 3 prime |
probably benign |
|
R0063:Ints8
|
UTSW |
4 |
11,252,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0063:Ints8
|
UTSW |
4 |
11,252,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R0184:Ints8
|
UTSW |
4 |
11,218,637 (GRCm39) |
missense |
probably benign |
0.03 |
R0299:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R0499:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R0540:Ints8
|
UTSW |
4 |
11,252,926 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0657:Ints8
|
UTSW |
4 |
11,246,097 (GRCm39) |
missense |
probably benign |
0.04 |
R1232:Ints8
|
UTSW |
4 |
11,234,587 (GRCm39) |
missense |
possibly damaging |
0.81 |
R1296:Ints8
|
UTSW |
4 |
11,221,204 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1390:Ints8
|
UTSW |
4 |
11,239,461 (GRCm39) |
missense |
probably benign |
0.22 |
R1503:Ints8
|
UTSW |
4 |
11,245,842 (GRCm39) |
missense |
probably damaging |
0.97 |
R1587:Ints8
|
UTSW |
4 |
11,245,722 (GRCm39) |
critical splice donor site |
probably null |
|
R1701:Ints8
|
UTSW |
4 |
11,231,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R1721:Ints8
|
UTSW |
4 |
11,241,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R1757:Ints8
|
UTSW |
4 |
11,254,109 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R1777:Ints8
|
UTSW |
4 |
11,225,600 (GRCm39) |
critical splice donor site |
probably null |
|
R1868:Ints8
|
UTSW |
4 |
11,241,684 (GRCm39) |
missense |
probably damaging |
0.97 |
R1952:Ints8
|
UTSW |
4 |
11,221,150 (GRCm39) |
missense |
probably benign |
0.21 |
R2084:Ints8
|
UTSW |
4 |
11,230,377 (GRCm39) |
missense |
probably benign |
0.31 |
R2108:Ints8
|
UTSW |
4 |
11,235,552 (GRCm39) |
missense |
probably damaging |
0.99 |
R2202:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2203:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2205:Ints8
|
UTSW |
4 |
11,225,712 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2439:Ints8
|
UTSW |
4 |
11,225,725 (GRCm39) |
missense |
probably benign |
0.29 |
R2504:Ints8
|
UTSW |
4 |
11,241,642 (GRCm39) |
missense |
probably benign |
0.03 |
R3824:Ints8
|
UTSW |
4 |
11,225,621 (GRCm39) |
nonsense |
probably null |
|
R4664:Ints8
|
UTSW |
4 |
11,227,152 (GRCm39) |
missense |
probably benign |
0.04 |
R4703:Ints8
|
UTSW |
4 |
11,223,785 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4895:Ints8
|
UTSW |
4 |
11,230,367 (GRCm39) |
nonsense |
probably null |
|
R5206:Ints8
|
UTSW |
4 |
11,216,477 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5262:Ints8
|
UTSW |
4 |
11,211,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R5505:Ints8
|
UTSW |
4 |
11,221,143 (GRCm39) |
missense |
probably benign |
0.18 |
R5513:Ints8
|
UTSW |
4 |
11,248,303 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5750:Ints8
|
UTSW |
4 |
11,241,654 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5892:Ints8
|
UTSW |
4 |
11,223,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6007:Ints8
|
UTSW |
4 |
11,208,845 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6229:Ints8
|
UTSW |
4 |
11,252,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R6466:Ints8
|
UTSW |
4 |
11,252,878 (GRCm39) |
missense |
probably damaging |
0.99 |
R6709:Ints8
|
UTSW |
4 |
11,221,117 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6986:Ints8
|
UTSW |
4 |
11,204,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R6998:Ints8
|
UTSW |
4 |
11,204,537 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7074:Ints8
|
UTSW |
4 |
11,204,574 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7221:Ints8
|
UTSW |
4 |
11,225,613 (GRCm39) |
missense |
probably benign |
0.01 |
R7772:Ints8
|
UTSW |
4 |
11,227,190 (GRCm39) |
missense |
probably damaging |
0.97 |
R7872:Ints8
|
UTSW |
4 |
11,254,062 (GRCm39) |
missense |
probably benign |
0.00 |
R7953:Ints8
|
UTSW |
4 |
11,227,128 (GRCm39) |
missense |
probably benign |
|
R8184:Ints8
|
UTSW |
4 |
11,204,534 (GRCm39) |
missense |
probably damaging |
1.00 |
R8301:Ints8
|
UTSW |
4 |
11,246,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Ints8
|
UTSW |
4 |
11,208,824 (GRCm39) |
critical splice donor site |
probably null |
|
R8868:Ints8
|
UTSW |
4 |
11,230,488 (GRCm39) |
missense |
probably benign |
|
R9245:Ints8
|
UTSW |
4 |
11,213,811 (GRCm39) |
critical splice acceptor site |
probably null |
|
|