Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alkal1 |
T |
A |
1: 6,459,728 (GRCm39) |
D101E |
probably benign |
Het |
Ank2 |
C |
T |
3: 126,741,271 (GRCm39) |
A1538T |
|
Het |
Arhgap21 |
A |
G |
2: 20,854,290 (GRCm39) |
S1701P |
probably damaging |
Het |
Arhgap21 |
A |
G |
2: 20,855,169 (GRCm39) |
Y1408H |
probably damaging |
Het |
Armc3 |
A |
T |
2: 19,293,761 (GRCm39) |
L517F |
probably damaging |
Het |
Cep57l1 |
T |
A |
10: 41,616,842 (GRCm39) |
E148D |
probably damaging |
Het |
Clstn1 |
A |
C |
4: 149,719,811 (GRCm39) |
Q452P |
probably damaging |
Het |
Csmd1 |
C |
A |
8: 16,151,004 (GRCm39) |
R1437L |
probably damaging |
Het |
Dcbld1 |
C |
T |
10: 52,188,922 (GRCm39) |
T249I |
possibly damaging |
Het |
Dsp |
A |
G |
13: 38,369,151 (GRCm39) |
E749G |
probably damaging |
Het |
Enox1 |
A |
C |
14: 77,815,220 (GRCm39) |
N126T |
probably damaging |
Het |
Fgfr1 |
T |
A |
8: 26,048,201 (GRCm39) |
L99Q |
probably damaging |
Het |
Fscn3 |
G |
A |
6: 28,434,445 (GRCm39) |
R340Q |
probably benign |
Het |
Glrb |
C |
T |
3: 80,767,491 (GRCm39) |
C243Y |
probably damaging |
Het |
Gpld1 |
A |
T |
13: 25,146,305 (GRCm39) |
Y183F |
probably damaging |
Het |
Has2 |
T |
C |
15: 56,531,108 (GRCm39) |
K536E |
possibly damaging |
Het |
Igtp |
A |
G |
11: 58,097,906 (GRCm39) |
E359G |
probably benign |
Het |
Kat14 |
A |
G |
2: 144,236,162 (GRCm39) |
D509G |
probably damaging |
Het |
Kbtbd2 |
C |
A |
6: 56,756,722 (GRCm39) |
S338I |
possibly damaging |
Het |
Ncoa3 |
C |
T |
2: 165,891,987 (GRCm39) |
A121V |
probably damaging |
Het |
Nfatc4 |
A |
G |
14: 56,069,414 (GRCm39) |
T647A |
possibly damaging |
Het |
Nip7 |
T |
C |
8: 107,783,997 (GRCm39) |
F79S |
probably damaging |
Het |
Nrxn3 |
A |
C |
12: 88,817,074 (GRCm39) |
E251D |
possibly damaging |
Het |
Olig2 |
T |
C |
16: 91,024,048 (GRCm39) |
I254T |
unknown |
Het |
Or55b4 |
C |
A |
7: 102,133,818 (GRCm39) |
V170F |
probably damaging |
Het |
Or5ac16 |
G |
A |
16: 59,022,318 (GRCm39) |
A157V |
probably benign |
Het |
Ostf1 |
A |
T |
19: 18,562,065 (GRCm39) |
L177* |
probably null |
Het |
Pabpc2 |
A |
T |
18: 39,907,319 (GRCm39) |
I195F |
possibly damaging |
Het |
Pacs1 |
A |
T |
19: 5,202,378 (GRCm39) |
M404K |
probably benign |
Het |
Pcdh1 |
A |
G |
18: 38,330,529 (GRCm39) |
S964P |
probably benign |
Het |
Pcdhb3 |
T |
A |
18: 37,436,012 (GRCm39) |
N659K |
probably benign |
Het |
Pla2g6 |
A |
T |
15: 79,181,633 (GRCm39) |
Y537* |
probably null |
Het |
Plekhn1 |
G |
A |
4: 156,316,691 (GRCm39) |
T330M |
probably damaging |
Het |
Proc |
G |
A |
18: 32,260,532 (GRCm39) |
R198* |
probably null |
Het |
Rfx8 |
G |
T |
1: 39,722,091 (GRCm39) |
T298K |
probably damaging |
Het |
S1pr4 |
A |
C |
10: 81,334,341 (GRCm39) |
S378A |
probably benign |
Het |
Saxo5 |
T |
C |
8: 3,533,525 (GRCm39) |
F277S |
probably damaging |
Het |
Slfn2 |
T |
A |
11: 82,960,799 (GRCm39) |
F259L |
probably damaging |
Het |
Snx14 |
T |
C |
9: 88,289,527 (GRCm39) |
T242A |
probably benign |
Het |
Sptbn2 |
A |
G |
19: 4,774,153 (GRCm39) |
N68S |
probably damaging |
Het |
Tmem44 |
A |
T |
16: 30,362,228 (GRCm39) |
S201T |
probably benign |
Het |
Ttc3 |
A |
T |
16: 94,188,241 (GRCm39) |
I177L |
probably benign |
Het |
Vmn1r177 |
T |
C |
7: 23,565,559 (GRCm39) |
T106A |
probably damaging |
Het |
Vmn1r28 |
T |
C |
6: 58,243,039 (GRCm39) |
M294T |
probably benign |
Het |
Zfp518b |
G |
A |
5: 38,829,530 (GRCm39) |
T825I |
probably benign |
Het |
Zfp729b |
A |
T |
13: 67,740,194 (GRCm39) |
N690K |
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 |
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 |
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 |
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 |
|