Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8a |
T |
C |
11: 109,953,942 (GRCm39) |
K833E |
probably benign |
Het |
Adam29 |
T |
C |
8: 56,325,519 (GRCm39) |
I312V |
probably benign |
Het |
Adcy8 |
T |
A |
15: 64,694,069 (GRCm39) |
I403F |
probably damaging |
Het |
Ahcyl1 |
A |
T |
3: 107,575,010 (GRCm39) |
N444K |
probably damaging |
Het |
Ang4 |
T |
C |
14: 52,001,511 (GRCm39) |
|
probably benign |
Het |
Atf6b |
T |
C |
17: 34,870,841 (GRCm39) |
V401A |
possibly damaging |
Het |
Atp7a |
A |
T |
X: 105,138,588 (GRCm39) |
I604F |
probably damaging |
Het |
Cd151 |
T |
C |
7: 141,050,370 (GRCm39) |
Y202H |
probably damaging |
Het |
Cd99l2 |
A |
T |
X: 70,493,552 (GRCm39) |
N64K |
possibly damaging |
Het |
Cog7 |
C |
T |
7: 121,543,000 (GRCm39) |
|
probably null |
Het |
Decr2 |
A |
T |
17: 26,306,354 (GRCm39) |
M94K |
probably benign |
Het |
Dock11 |
A |
T |
X: 35,232,422 (GRCm39) |
H188L |
probably benign |
Het |
Dscam |
T |
C |
16: 96,602,397 (GRCm39) |
S682G |
probably benign |
Het |
Efcab3 |
A |
T |
11: 104,612,258 (GRCm39) |
|
probably benign |
Het |
Gja3 |
G |
T |
14: 57,273,136 (GRCm39) |
P412Q |
probably damaging |
Het |
Glrb |
T |
C |
3: 80,758,262 (GRCm39) |
N333D |
probably benign |
Het |
Gpr65 |
T |
A |
12: 98,242,127 (GRCm39) |
V260D |
probably benign |
Het |
Hormad1 |
A |
G |
3: 95,485,604 (GRCm39) |
E264G |
possibly damaging |
Het |
Hsph1 |
T |
C |
5: 149,557,324 (GRCm39) |
R46G |
probably damaging |
Het |
Hycc2 |
G |
A |
1: 58,569,274 (GRCm39) |
A435V |
possibly damaging |
Het |
Iars1 |
A |
G |
13: 49,841,725 (GRCm39) |
Y71C |
probably damaging |
Het |
Lsg1 |
T |
C |
16: 30,404,494 (GRCm39) |
H35R |
probably damaging |
Het |
Mfge8 |
C |
T |
7: 78,794,985 (GRCm39) |
|
probably benign |
Het |
Mgat4c |
T |
A |
10: 102,214,045 (GRCm39) |
Y9* |
probably null |
Het |
Muc19 |
T |
C |
15: 91,772,453 (GRCm39) |
|
noncoding transcript |
Het |
Nbea |
A |
T |
3: 55,588,437 (GRCm39) |
M2434K |
probably damaging |
Het |
Ncoa2 |
A |
G |
1: 13,245,078 (GRCm39) |
L540P |
probably damaging |
Het |
Nhsl2 |
A |
G |
X: 101,121,858 (GRCm39) |
R554G |
probably damaging |
Het |
Npdc1 |
T |
A |
2: 25,298,032 (GRCm39) |
|
probably benign |
Het |
Or2aj6 |
A |
T |
16: 19,443,158 (GRCm39) |
S231T |
probably benign |
Het |
Osbpl10 |
T |
A |
9: 115,055,790 (GRCm39) |
V654D |
probably damaging |
Het |
Plxna1 |
C |
A |
6: 89,334,314 (GRCm39) |
G105V |
possibly damaging |
Het |
Pnma8b |
T |
C |
7: 16,679,616 (GRCm39) |
V200A |
probably damaging |
Het |
Ppard |
A |
G |
17: 28,517,871 (GRCm39) |
H313R |
probably benign |
Het |
Rasgrp4 |
T |
C |
7: 28,838,335 (GRCm39) |
L103P |
probably damaging |
Het |
Rigi |
A |
G |
4: 40,216,487 (GRCm39) |
Y504H |
possibly damaging |
Het |
Ripk4 |
A |
T |
16: 97,556,431 (GRCm39) |
L104Q |
probably damaging |
Het |
Setd2 |
T |
C |
9: 110,423,704 (GRCm39) |
V2253A |
probably benign |
Het |
Setdb2 |
A |
G |
14: 59,668,607 (GRCm39) |
S43P |
probably damaging |
Het |
Stab2 |
C |
A |
10: 86,707,695 (GRCm39) |
G1742V |
possibly damaging |
Het |
Timm23 |
A |
G |
14: 31,915,804 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,615,999 (GRCm39) |
N14902S |
possibly damaging |
Het |
Ush2a |
A |
G |
1: 188,465,711 (GRCm39) |
T2760A |
probably benign |
Het |
Vmn2r25 |
T |
C |
6: 123,816,388 (GRCm39) |
N398D |
probably damaging |
Het |
|
Other mutations in Mpdz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Mpdz
|
APN |
4 |
81,228,461 (GRCm39) |
nonsense |
probably null |
|
IGL00325:Mpdz
|
APN |
4 |
81,235,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00497:Mpdz
|
APN |
4 |
81,253,979 (GRCm39) |
missense |
probably benign |
0.30 |
IGL00502:Mpdz
|
APN |
4 |
81,287,960 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00539:Mpdz
|
APN |
4 |
81,279,588 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL00938:Mpdz
|
APN |
4 |
81,210,749 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00990:Mpdz
|
APN |
4 |
81,221,821 (GRCm39) |
splice site |
probably benign |
|
IGL01394:Mpdz
|
APN |
4 |
81,210,728 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL01537:Mpdz
|
APN |
4 |
81,287,895 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01558:Mpdz
|
APN |
4 |
81,213,767 (GRCm39) |
nonsense |
probably null |
|
IGL01561:Mpdz
|
APN |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01649:Mpdz
|
APN |
4 |
81,221,870 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01743:Mpdz
|
APN |
4 |
81,235,919 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01941:Mpdz
|
APN |
4 |
81,204,624 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01969:Mpdz
|
APN |
4 |
81,276,961 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02081:Mpdz
|
APN |
4 |
81,254,106 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02304:Mpdz
|
APN |
4 |
81,215,796 (GRCm39) |
splice site |
probably benign |
|
IGL02304:Mpdz
|
APN |
4 |
81,228,394 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02410:Mpdz
|
APN |
4 |
81,215,730 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02449:Mpdz
|
APN |
4 |
81,247,659 (GRCm39) |
splice site |
probably null |
|
IGL02671:Mpdz
|
APN |
4 |
81,208,510 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02708:Mpdz
|
APN |
4 |
81,202,808 (GRCm39) |
splice site |
probably null |
|
IGL02718:Mpdz
|
APN |
4 |
81,303,439 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03065:Mpdz
|
APN |
4 |
81,210,802 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03378:Mpdz
|
APN |
4 |
81,337,285 (GRCm39) |
splice site |
probably benign |
|
PIT4458001:Mpdz
|
UTSW |
4 |
81,337,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0108:Mpdz
|
UTSW |
4 |
81,300,042 (GRCm39) |
missense |
probably damaging |
1.00 |
R0119:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0402:Mpdz
|
UTSW |
4 |
81,279,677 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0499:Mpdz
|
UTSW |
4 |
81,210,768 (GRCm39) |
missense |
probably benign |
0.44 |
R0718:Mpdz
|
UTSW |
4 |
81,210,710 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0844:Mpdz
|
UTSW |
4 |
81,339,431 (GRCm39) |
start gained |
probably benign |
|
R0883:Mpdz
|
UTSW |
4 |
81,278,228 (GRCm39) |
splice site |
probably benign |
|
R0885:Mpdz
|
UTSW |
4 |
81,287,829 (GRCm39) |
missense |
probably benign |
0.04 |
R1344:Mpdz
|
UTSW |
4 |
81,226,556 (GRCm39) |
missense |
probably benign |
0.01 |
R1432:Mpdz
|
UTSW |
4 |
81,210,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R1488:Mpdz
|
UTSW |
4 |
81,266,945 (GRCm39) |
nonsense |
probably null |
|
R1589:Mpdz
|
UTSW |
4 |
81,339,413 (GRCm39) |
missense |
probably benign |
0.00 |
R1756:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1940:Mpdz
|
UTSW |
4 |
81,279,680 (GRCm39) |
missense |
probably benign |
0.01 |
R2068:Mpdz
|
UTSW |
4 |
81,254,067 (GRCm39) |
missense |
probably null |
1.00 |
R2182:Mpdz
|
UTSW |
4 |
81,266,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R2213:Mpdz
|
UTSW |
4 |
81,228,409 (GRCm39) |
missense |
probably damaging |
0.99 |
R2265:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2268:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R2269:Mpdz
|
UTSW |
4 |
81,301,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Mpdz
|
UTSW |
4 |
81,203,695 (GRCm39) |
splice site |
probably benign |
|
R3746:Mpdz
|
UTSW |
4 |
81,281,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R3902:Mpdz
|
UTSW |
4 |
81,225,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R4095:Mpdz
|
UTSW |
4 |
81,302,060 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4097:Mpdz
|
UTSW |
4 |
81,253,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R4206:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
0.13 |
R4675:Mpdz
|
UTSW |
4 |
81,302,049 (GRCm39) |
missense |
probably damaging |
0.98 |
R4884:Mpdz
|
UTSW |
4 |
81,279,713 (GRCm39) |
missense |
probably damaging |
0.97 |
R5044:Mpdz
|
UTSW |
4 |
81,299,934 (GRCm39) |
missense |
probably benign |
0.16 |
R5050:Mpdz
|
UTSW |
4 |
81,213,685 (GRCm39) |
missense |
probably benign |
0.00 |
R5243:Mpdz
|
UTSW |
4 |
81,225,116 (GRCm39) |
missense |
probably damaging |
1.00 |
R5332:Mpdz
|
UTSW |
4 |
81,210,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R5435:Mpdz
|
UTSW |
4 |
81,201,724 (GRCm39) |
intron |
probably benign |
|
R5720:Mpdz
|
UTSW |
4 |
81,205,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R5743:Mpdz
|
UTSW |
4 |
81,339,425 (GRCm39) |
start codon destroyed |
probably null |
0.30 |
R5764:Mpdz
|
UTSW |
4 |
81,274,683 (GRCm39) |
missense |
probably benign |
0.13 |
R5876:Mpdz
|
UTSW |
4 |
81,203,711 (GRCm39) |
nonsense |
probably null |
|
R5938:Mpdz
|
UTSW |
4 |
81,202,851 (GRCm39) |
missense |
probably damaging |
1.00 |
R5988:Mpdz
|
UTSW |
4 |
81,202,812 (GRCm39) |
critical splice donor site |
probably null |
|
R6125:Mpdz
|
UTSW |
4 |
81,215,764 (GRCm39) |
missense |
probably benign |
0.00 |
R6178:Mpdz
|
UTSW |
4 |
81,226,602 (GRCm39) |
missense |
probably damaging |
1.00 |
R6235:Mpdz
|
UTSW |
4 |
81,303,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6293:Mpdz
|
UTSW |
4 |
81,278,293 (GRCm39) |
missense |
probably damaging |
1.00 |
R6387:Mpdz
|
UTSW |
4 |
81,299,946 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6488:Mpdz
|
UTSW |
4 |
81,205,970 (GRCm39) |
missense |
probably benign |
0.11 |
R6536:Mpdz
|
UTSW |
4 |
81,301,654 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Mpdz
|
UTSW |
4 |
81,274,667 (GRCm39) |
missense |
probably benign |
0.11 |
R6879:Mpdz
|
UTSW |
4 |
81,266,893 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7180:Mpdz
|
UTSW |
4 |
81,253,988 (GRCm39) |
missense |
probably damaging |
0.98 |
R7199:Mpdz
|
UTSW |
4 |
81,215,570 (GRCm39) |
missense |
probably damaging |
0.98 |
R7209:Mpdz
|
UTSW |
4 |
81,225,114 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7309:Mpdz
|
UTSW |
4 |
81,300,195 (GRCm39) |
splice site |
probably null |
|
R7359:Mpdz
|
UTSW |
4 |
81,274,632 (GRCm39) |
missense |
probably benign |
0.01 |
R7561:Mpdz
|
UTSW |
4 |
81,225,388 (GRCm39) |
missense |
probably damaging |
0.99 |
R7565:Mpdz
|
UTSW |
4 |
81,221,891 (GRCm39) |
missense |
probably benign |
0.01 |
R7738:Mpdz
|
UTSW |
4 |
81,253,986 (GRCm39) |
missense |
probably benign |
0.01 |
R7941:Mpdz
|
UTSW |
4 |
81,200,987 (GRCm39) |
missense |
probably benign |
0.04 |
R8074:Mpdz
|
UTSW |
4 |
81,267,324 (GRCm39) |
missense |
probably benign |
0.00 |
R8957:Mpdz
|
UTSW |
4 |
81,251,216 (GRCm39) |
nonsense |
probably null |
|
R8998:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R8999:Mpdz
|
UTSW |
4 |
81,202,882 (GRCm39) |
nonsense |
probably null |
|
R9001:Mpdz
|
UTSW |
4 |
81,299,999 (GRCm39) |
missense |
probably benign |
|
R9223:Mpdz
|
UTSW |
4 |
81,202,867 (GRCm39) |
missense |
probably damaging |
1.00 |
R9415:Mpdz
|
UTSW |
4 |
81,235,905 (GRCm39) |
nonsense |
probably null |
|
R9486:Mpdz
|
UTSW |
4 |
81,254,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R9520:Mpdz
|
UTSW |
4 |
81,304,555 (GRCm39) |
missense |
probably benign |
|
R9526:Mpdz
|
UTSW |
4 |
81,274,653 (GRCm39) |
missense |
probably benign |
|
R9556:Mpdz
|
UTSW |
4 |
81,278,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R9722:Mpdz
|
UTSW |
4 |
81,304,504 (GRCm39) |
missense |
probably damaging |
0.97 |
RF013:Mpdz
|
UTSW |
4 |
81,211,829 (GRCm39) |
missense |
possibly damaging |
0.60 |
X0011:Mpdz
|
UTSW |
4 |
81,210,996 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Mpdz
|
UTSW |
4 |
81,238,727 (GRCm39) |
missense |
probably damaging |
0.99 |
|