Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Atxn1l |
T |
C |
8: 110,459,312 (GRCm39) |
R317G |
probably benign |
Het |
B130006D01Rik |
T |
A |
11: 95,616,992 (GRCm39) |
|
probably benign |
Het |
Brinp2 |
T |
C |
1: 158,074,379 (GRCm39) |
T581A |
probably damaging |
Het |
Cacna1b |
A |
T |
2: 24,548,540 (GRCm39) |
I1179N |
probably damaging |
Het |
Cacnb3 |
A |
G |
15: 98,541,301 (GRCm39) |
D434G |
probably damaging |
Het |
Cdh19 |
T |
C |
1: 110,847,341 (GRCm39) |
T423A |
possibly damaging |
Het |
Chkb |
C |
T |
15: 89,311,986 (GRCm39) |
|
probably benign |
Het |
Cit |
T |
C |
5: 116,071,913 (GRCm39) |
Y623H |
probably benign |
Het |
Clstn3 |
G |
A |
6: 124,408,559 (GRCm39) |
R918C |
possibly damaging |
Het |
Dnah2 |
T |
A |
11: 69,406,906 (GRCm39) |
M200L |
probably benign |
Het |
Dnah9 |
T |
A |
11: 65,838,506 (GRCm39) |
H3097L |
probably benign |
Het |
Dst |
T |
A |
1: 34,314,401 (GRCm39) |
L4217H |
probably damaging |
Het |
Fam107b |
T |
A |
2: 3,779,565 (GRCm39) |
L80Q |
probably damaging |
Het |
Fgfr1 |
T |
A |
8: 26,045,595 (GRCm39) |
C55S |
probably damaging |
Het |
Igkv4-71 |
C |
A |
6: 69,220,264 (GRCm39) |
G78* |
probably null |
Het |
Igsf10 |
A |
G |
3: 59,237,452 (GRCm39) |
S910P |
probably benign |
Het |
Ikzf3 |
T |
C |
11: 98,407,718 (GRCm39) |
D41G |
probably damaging |
Het |
Larp1 |
T |
A |
11: 57,933,648 (GRCm39) |
I358N |
possibly damaging |
Het |
Marchf5 |
C |
T |
19: 37,188,067 (GRCm39) |
|
probably benign |
Het |
Myo1b |
A |
G |
1: 51,815,510 (GRCm39) |
V612A |
possibly damaging |
Het |
Nipbl |
T |
C |
15: 8,380,023 (GRCm39) |
D923G |
probably benign |
Het |
Nlrp4b |
T |
C |
7: 10,448,918 (GRCm39) |
F7L |
probably damaging |
Het |
Npas4 |
T |
C |
19: 5,037,355 (GRCm39) |
N313S |
possibly damaging |
Het |
Nynrin |
T |
A |
14: 56,109,502 (GRCm39) |
N1536K |
possibly damaging |
Het |
Or10d5 |
T |
A |
9: 39,861,921 (GRCm39) |
T49S |
probably benign |
Het |
Or13a22 |
A |
G |
7: 140,072,751 (GRCm39) |
N67D |
probably damaging |
Het |
Or4c107 |
T |
C |
2: 88,788,885 (GRCm39) |
V25A |
probably benign |
Het |
Pclo |
T |
C |
5: 14,589,647 (GRCm39) |
V649A |
unknown |
Het |
Pom121 |
A |
G |
5: 135,421,389 (GRCm39) |
|
probably benign |
Het |
Ptcd2 |
A |
T |
13: 99,466,521 (GRCm39) |
I224N |
possibly damaging |
Het |
Rsrp1 |
C |
T |
4: 134,651,290 (GRCm39) |
P18L |
unknown |
Het |
Sash1 |
A |
T |
10: 8,605,422 (GRCm39) |
N989K |
probably damaging |
Het |
Scn2a |
T |
A |
2: 65,546,219 (GRCm39) |
H927Q |
probably benign |
Het |
Selenoi |
G |
T |
5: 30,461,222 (GRCm39) |
V128F |
probably damaging |
Het |
Slc25a42 |
T |
C |
8: 70,642,092 (GRCm39) |
I117V |
probably benign |
Het |
Spata1 |
A |
G |
3: 146,195,558 (GRCm39) |
|
probably benign |
Het |
Sptlc3 |
A |
T |
2: 139,431,615 (GRCm39) |
Y379F |
possibly damaging |
Het |
Tent4a |
A |
T |
13: 69,648,678 (GRCm39) |
S693T |
probably benign |
Het |
Tinag |
C |
T |
9: 76,952,885 (GRCm39) |
R33K |
probably benign |
Het |
Trappc8 |
T |
C |
18: 20,968,061 (GRCm39) |
D1092G |
probably benign |
Het |
Xntrpc |
A |
G |
7: 101,722,401 (GRCm39) |
E22G |
probably damaging |
Het |
Zbtb7b |
A |
G |
3: 89,287,278 (GRCm39) |
M397T |
possibly damaging |
Het |
Zgpat |
A |
G |
2: 181,020,682 (GRCm39) |
D285G |
probably benign |
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 |
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 |
IGL02023:Mpdz
|
APN |
4 |
81,247,766 (GRCm39) |
missense |
probably damaging |
0.99 |
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 |
|