Other mutations in this stock |
Total: 110 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
A |
T |
6: 121,615,267 (GRCm39) |
H9L |
possibly damaging |
Het |
Aars1 |
T |
A |
8: 111,779,083 (GRCm39) |
I739K |
possibly damaging |
Het |
Abcb1b |
T |
A |
5: 8,875,661 (GRCm39) |
H611Q |
probably damaging |
Het |
Acod1 |
T |
A |
14: 103,292,643 (GRCm39) |
I389K |
possibly damaging |
Het |
Adgre1 |
T |
A |
17: 57,709,841 (GRCm39) |
L166* |
probably null |
Het |
Akap1 |
C |
A |
11: 88,730,450 (GRCm39) |
|
probably null |
Het |
Akna |
T |
A |
4: 63,312,872 (GRCm39) |
Q417L |
probably damaging |
Het |
Anxa7 |
T |
C |
14: 20,512,678 (GRCm39) |
D285G |
probably damaging |
Het |
Arhgap1 |
T |
C |
2: 91,500,514 (GRCm39) |
Y308H |
probably damaging |
Het |
Arhgef10 |
A |
C |
8: 15,004,446 (GRCm39) |
R360S |
probably damaging |
Het |
Arhgef11 |
T |
A |
3: 87,636,500 (GRCm39) |
|
probably null |
Het |
Arid3a |
A |
G |
10: 79,766,899 (GRCm39) |
T58A |
possibly damaging |
Het |
Atosb |
A |
T |
4: 43,036,441 (GRCm39) |
S97T |
probably benign |
Het |
Atp6v0a4 |
G |
A |
6: 38,059,016 (GRCm39) |
R256C |
probably damaging |
Het |
Camsap3 |
C |
A |
8: 3,648,772 (GRCm39) |
S163R |
probably benign |
Het |
Ccdc110 |
A |
T |
8: 46,395,663 (GRCm39) |
E518V |
probably damaging |
Het |
Ccdc180 |
G |
A |
4: 45,930,119 (GRCm39) |
|
probably null |
Het |
Ccnt1 |
T |
C |
15: 98,462,960 (GRCm39) |
M71V |
probably benign |
Het |
Celsr2 |
T |
A |
3: 108,304,570 (GRCm39) |
Y2263F |
probably benign |
Het |
Cfap36 |
A |
T |
11: 29,196,514 (GRCm39) |
|
probably null |
Het |
Cfap69 |
T |
C |
5: 5,663,734 (GRCm39) |
T498A |
probably benign |
Het |
Chadl |
T |
C |
15: 81,578,213 (GRCm39) |
D6G |
probably benign |
Het |
Clstn3 |
T |
A |
6: 124,436,812 (GRCm39) |
I132F |
possibly damaging |
Het |
Cnot4 |
A |
G |
6: 35,028,212 (GRCm39) |
V468A |
probably benign |
Het |
Crmp1 |
T |
G |
5: 37,422,617 (GRCm39) |
D141E |
possibly damaging |
Het |
Crtc1 |
A |
G |
8: 70,844,509 (GRCm39) |
|
probably null |
Het |
Cryz |
C |
A |
3: 154,317,189 (GRCm39) |
A136D |
probably damaging |
Het |
Dph6 |
A |
G |
2: 114,353,525 (GRCm39) |
V221A |
probably benign |
Het |
Dst |
A |
T |
1: 34,314,862 (GRCm39) |
N4267Y |
probably damaging |
Het |
Duox2 |
T |
A |
2: 122,127,167 (GRCm39) |
D170V |
possibly damaging |
Het |
Ecm2 |
A |
T |
13: 49,677,922 (GRCm39) |
K403* |
probably null |
Het |
Eif3d |
T |
C |
15: 77,843,924 (GRCm39) |
N474S |
probably benign |
Het |
Elf1 |
T |
C |
14: 79,802,965 (GRCm39) |
L106P |
probably damaging |
Het |
Exoc4 |
G |
C |
6: 33,273,857 (GRCm39) |
|
probably null |
Het |
F12 |
T |
C |
13: 55,574,130 (GRCm39) |
D34G |
probably benign |
Het |
Fam228b |
A |
T |
12: 4,798,117 (GRCm39) |
F200Y |
probably damaging |
Het |
Fgl2 |
T |
A |
5: 21,580,661 (GRCm39) |
D334E |
possibly damaging |
Het |
Fras1 |
T |
A |
5: 96,924,481 (GRCm39) |
F3641I |
probably benign |
Het |
Gabrb2 |
T |
G |
11: 42,484,674 (GRCm39) |
Y244D |
probably damaging |
Het |
Gcc1 |
A |
T |
6: 28,421,268 (GRCm39) |
D16E |
probably benign |
Het |
Gga3 |
C |
A |
11: 115,477,915 (GRCm39) |
G558* |
probably null |
Het |
Glt1d1 |
T |
C |
5: 127,740,391 (GRCm39) |
|
probably benign |
Het |
Gorasp2 |
T |
C |
2: 70,521,067 (GRCm39) |
S346P |
possibly damaging |
Het |
Hcn4 |
T |
C |
9: 58,767,582 (GRCm39) |
S1048P |
probably damaging |
Het |
Henmt1 |
T |
A |
3: 108,861,105 (GRCm39) |
|
probably benign |
Het |
Htt |
A |
C |
5: 35,066,006 (GRCm39) |
K3060N |
probably damaging |
Het |
Ibsp |
C |
T |
5: 104,450,024 (GRCm39) |
L8F |
probably damaging |
Het |
Kif27 |
A |
T |
13: 58,451,378 (GRCm39) |
D983E |
probably damaging |
Het |
Kif3a |
T |
A |
11: 53,481,560 (GRCm39) |
|
probably benign |
Het |
Kif3c |
A |
C |
12: 3,417,090 (GRCm39) |
K370N |
possibly damaging |
Het |
Loxhd1 |
T |
C |
18: 77,468,256 (GRCm39) |
|
probably benign |
Het |
Maz |
A |
T |
7: 126,623,758 (GRCm39) |
D74E |
probably damaging |
Het |
Med21 |
T |
C |
6: 146,551,732 (GRCm39) |
S128P |
probably damaging |
Het |
Mms19 |
A |
C |
19: 41,943,607 (GRCm39) |
M374R |
probably damaging |
Het |
Mprip |
T |
C |
11: 59,657,571 (GRCm39) |
V801A |
probably damaging |
Het |
Mrpl3 |
T |
C |
9: 104,932,872 (GRCm39) |
V111A |
probably benign |
Het |
Mtfr2 |
T |
A |
10: 20,224,158 (GRCm39) |
Y31N |
probably damaging |
Het |
Myh3 |
C |
T |
11: 66,990,498 (GRCm39) |
R1677C |
probably damaging |
Het |
Mynn |
T |
A |
3: 30,661,230 (GRCm39) |
*61K |
probably null |
Het |
Neb |
A |
C |
2: 52,060,479 (GRCm39) |
M2286R |
possibly damaging |
Het |
Ngf |
A |
T |
3: 102,427,661 (GRCm39) |
R137* |
probably null |
Het |
Nr1i3 |
T |
A |
1: 171,041,982 (GRCm39) |
V22E |
probably damaging |
Het |
Nxpe5 |
T |
C |
5: 138,249,566 (GRCm39) |
V452A |
probably damaging |
Het |
Oas1e |
C |
A |
5: 120,933,395 (GRCm39) |
A57S |
probably benign |
Het |
Or11g27 |
A |
T |
14: 50,771,151 (GRCm39) |
K94M |
probably damaging |
Het |
Or14j10 |
T |
A |
17: 37,935,024 (GRCm39) |
R167S |
probably benign |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Pax3 |
A |
G |
1: 78,080,141 (GRCm39) |
L415P |
probably damaging |
Het |
Pcnt |
G |
T |
10: 76,205,655 (GRCm39) |
|
probably benign |
Het |
Peg3 |
G |
T |
7: 6,714,672 (GRCm39) |
D183E |
possibly damaging |
Het |
Pglyrp1 |
G |
T |
7: 18,623,313 (GRCm39) |
G120V |
probably damaging |
Het |
Pnp2 |
T |
A |
14: 51,196,990 (GRCm39) |
Y25* |
probably null |
Het |
Pomt1 |
T |
A |
2: 32,142,023 (GRCm39) |
H584Q |
possibly damaging |
Het |
Ppp1r12a |
A |
G |
10: 108,089,193 (GRCm39) |
N611D |
possibly damaging |
Het |
Prkcq |
G |
A |
2: 11,288,643 (GRCm39) |
G532E |
probably benign |
Het |
Prl6a1 |
A |
T |
13: 27,501,980 (GRCm39) |
I116F |
probably damaging |
Het |
Pwp1 |
A |
G |
10: 85,721,480 (GRCm39) |
T361A |
possibly damaging |
Het |
Rab4a |
A |
T |
8: 124,554,081 (GRCm39) |
H5L |
probably damaging |
Het |
Raet1e |
C |
A |
10: 22,056,761 (GRCm39) |
H112Q |
possibly damaging |
Het |
Ramp1 |
T |
C |
1: 91,124,592 (GRCm39) |
I51T |
possibly damaging |
Het |
Raph1 |
G |
T |
1: 60,565,058 (GRCm39) |
T143K |
probably benign |
Het |
Rhpn1 |
A |
G |
15: 75,581,088 (GRCm39) |
E110G |
possibly damaging |
Het |
Rnf168 |
A |
T |
16: 32,117,287 (GRCm39) |
T283S |
possibly damaging |
Het |
Ros1 |
T |
A |
10: 51,977,857 (GRCm39) |
Y1463F |
possibly damaging |
Het |
Rtn4ip1 |
A |
G |
10: 43,797,430 (GRCm39) |
Q223R |
probably null |
Het |
Rtp4 |
G |
T |
16: 23,431,679 (GRCm39) |
M70I |
probably benign |
Het |
Sag |
C |
A |
1: 87,762,340 (GRCm39) |
T335K |
probably damaging |
Het |
Satb1 |
T |
A |
17: 52,047,374 (GRCm39) |
Q647L |
probably benign |
Het |
Sec31b |
T |
C |
19: 44,508,847 (GRCm39) |
|
probably benign |
Het |
Sgo1 |
C |
T |
17: 53,986,691 (GRCm39) |
D167N |
probably damaging |
Het |
Slco1a8 |
T |
C |
6: 141,936,147 (GRCm39) |
T313A |
probably benign |
Het |
Smchd1 |
T |
C |
17: 71,738,231 (GRCm39) |
I545V |
probably benign |
Het |
St6gal1 |
G |
T |
16: 23,139,891 (GRCm39) |
A21S |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,530,300 (GRCm39) |
L2186I |
probably damaging |
Het |
Sun2 |
T |
A |
15: 79,611,810 (GRCm39) |
|
probably benign |
Het |
Taf4 |
G |
A |
2: 179,565,884 (GRCm39) |
T849M |
probably damaging |
Het |
Tdrd5 |
A |
T |
1: 156,129,473 (GRCm39) |
I79N |
probably damaging |
Het |
Tdrd7 |
A |
G |
4: 45,987,582 (GRCm39) |
I72V |
probably damaging |
Het |
Tnxb |
T |
A |
17: 34,928,542 (GRCm39) |
V2652E |
possibly damaging |
Het |
Trim30a |
C |
T |
7: 104,078,559 (GRCm39) |
|
probably null |
Het |
Tshz3 |
A |
G |
7: 36,469,534 (GRCm39) |
T508A |
probably damaging |
Het |
Ttc21b |
A |
G |
2: 66,053,908 (GRCm39) |
L757P |
probably damaging |
Het |
Ubtd2 |
A |
C |
11: 32,449,223 (GRCm39) |
|
probably null |
Het |
Ubtd2 |
G |
T |
11: 32,449,224 (GRCm39) |
|
probably null |
Het |
Vmn1r218 |
C |
T |
13: 23,321,225 (GRCm39) |
Q111* |
probably null |
Het |
Vmn2r75 |
G |
A |
7: 85,797,309 (GRCm39) |
Q835* |
probably null |
Het |
Vwa8 |
T |
A |
14: 79,331,179 (GRCm39) |
M1229K |
probably benign |
Het |
Wdr76 |
C |
T |
2: 121,349,932 (GRCm39) |
R111C |
probably damaging |
Het |
Xcr1 |
T |
A |
9: 123,684,940 (GRCm39) |
D274V |
possibly damaging |
Het |
Ypel5 |
C |
T |
17: 73,153,332 (GRCm39) |
T12I |
probably benign |
Het |
|
Other mutations in Ptprh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01766:Ptprh
|
APN |
7 |
4,583,915 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02420:Ptprh
|
APN |
7 |
4,583,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02619:Ptprh
|
APN |
7 |
4,552,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02729:Ptprh
|
APN |
7 |
4,583,873 (GRCm39) |
missense |
probably damaging |
0.99 |
BB008:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
BB018:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R0018:Ptprh
|
UTSW |
7 |
4,604,845 (GRCm39) |
critical splice donor site |
probably null |
|
R0449:Ptprh
|
UTSW |
7 |
4,601,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Ptprh
|
UTSW |
7 |
4,600,997 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0626:Ptprh
|
UTSW |
7 |
4,567,271 (GRCm39) |
missense |
probably benign |
0.00 |
R0741:Ptprh
|
UTSW |
7 |
4,557,172 (GRCm39) |
critical splice donor site |
probably null |
|
R1068:Ptprh
|
UTSW |
7 |
4,552,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1226:Ptprh
|
UTSW |
7 |
4,606,091 (GRCm39) |
nonsense |
probably null |
|
R1487:Ptprh
|
UTSW |
7 |
4,555,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Ptprh
|
UTSW |
7 |
4,583,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1537:Ptprh
|
UTSW |
7 |
4,552,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Ptprh
|
UTSW |
7 |
4,555,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Ptprh
|
UTSW |
7 |
4,604,912 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Ptprh
|
UTSW |
7 |
4,552,394 (GRCm39) |
missense |
probably benign |
0.25 |
R2082:Ptprh
|
UTSW |
7 |
4,553,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptprh
|
UTSW |
7 |
4,604,867 (GRCm39) |
missense |
probably benign |
0.26 |
R2214:Ptprh
|
UTSW |
7 |
4,555,921 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2245:Ptprh
|
UTSW |
7 |
4,576,345 (GRCm39) |
missense |
probably benign |
0.09 |
R2271:Ptprh
|
UTSW |
7 |
4,606,132 (GRCm39) |
start gained |
probably benign |
|
R3693:Ptprh
|
UTSW |
7 |
4,557,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R3713:Ptprh
|
UTSW |
7 |
4,574,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4081:Ptprh
|
UTSW |
7 |
4,583,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Ptprh
|
UTSW |
7 |
4,600,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R4689:Ptprh
|
UTSW |
7 |
4,600,996 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4782:Ptprh
|
UTSW |
7 |
4,572,576 (GRCm39) |
missense |
probably benign |
0.08 |
R4838:Ptprh
|
UTSW |
7 |
4,576,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4974:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R5218:Ptprh
|
UTSW |
7 |
4,600,919 (GRCm39) |
missense |
probably benign |
0.05 |
R5430:Ptprh
|
UTSW |
7 |
4,554,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Ptprh
|
UTSW |
7 |
4,552,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5544:Ptprh
|
UTSW |
7 |
4,583,909 (GRCm39) |
nonsense |
probably null |
|
R5547:Ptprh
|
UTSW |
7 |
4,557,221 (GRCm39) |
nonsense |
probably null |
|
R5869:Ptprh
|
UTSW |
7 |
4,604,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Ptprh
|
UTSW |
7 |
4,576,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Ptprh
|
UTSW |
7 |
4,576,361 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6112:Ptprh
|
UTSW |
7 |
4,600,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6493:Ptprh
|
UTSW |
7 |
4,583,989 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6733:Ptprh
|
UTSW |
7 |
4,606,043 (GRCm39) |
splice site |
probably null |
|
R6836:Ptprh
|
UTSW |
7 |
4,554,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Ptprh
|
UTSW |
7 |
4,552,370 (GRCm39) |
nonsense |
probably null |
|
R6868:Ptprh
|
UTSW |
7 |
4,604,864 (GRCm39) |
missense |
probably benign |
|
R7015:Ptprh
|
UTSW |
7 |
4,555,626 (GRCm39) |
critical splice donor site |
probably null |
|
R7092:Ptprh
|
UTSW |
7 |
4,583,860 (GRCm39) |
critical splice donor site |
probably null |
|
R7147:Ptprh
|
UTSW |
7 |
4,553,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Ptprh
|
UTSW |
7 |
4,572,480 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7358:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R7436:Ptprh
|
UTSW |
7 |
4,555,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Ptprh
|
UTSW |
7 |
4,574,780 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7863:Ptprh
|
UTSW |
7 |
4,606,097 (GRCm39) |
start codon destroyed |
probably benign |
0.31 |
R7931:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R7973:Ptprh
|
UTSW |
7 |
4,583,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8239:Ptprh
|
UTSW |
7 |
4,584,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8331:Ptprh
|
UTSW |
7 |
4,552,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Ptprh
|
UTSW |
7 |
4,554,022 (GRCm39) |
missense |
probably benign |
0.03 |
R8700:Ptprh
|
UTSW |
7 |
4,567,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Ptprh
|
UTSW |
7 |
4,567,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Ptprh
|
UTSW |
7 |
4,583,944 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9119:Ptprh
|
UTSW |
7 |
4,555,712 (GRCm39) |
missense |
probably benign |
0.25 |
R9203:Ptprh
|
UTSW |
7 |
4,574,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Ptprh
|
UTSW |
7 |
4,583,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R9250:Ptprh
|
UTSW |
7 |
4,576,289 (GRCm39) |
missense |
probably benign |
0.03 |
RF022:Ptprh
|
UTSW |
7 |
4,552,367 (GRCm39) |
missense |
probably benign |
|
Z1177:Ptprh
|
UTSW |
7 |
4,601,117 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ptprh
|
UTSW |
7 |
4,600,970 (GRCm39) |
missense |
probably damaging |
0.99 |
|