Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9930012K11Rik |
T |
C |
14: 70,394,969 (GRCm39) |
R62G |
probably benign |
Het |
Abcb9 |
A |
G |
5: 124,215,308 (GRCm39) |
F478L |
probably benign |
Het |
Abcc9 |
A |
T |
6: 142,621,257 (GRCm39) |
N494K |
probably damaging |
Het |
Atp11a |
T |
G |
8: 12,911,973 (GRCm39) |
M124R |
|
Het |
C1ra |
G |
A |
6: 124,494,684 (GRCm39) |
E316K |
probably benign |
Het |
Ccdc110 |
T |
A |
8: 46,395,130 (GRCm39) |
H340Q |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,915,801 (GRCm39) |
L724P |
probably damaging |
Het |
Cfap74 |
A |
G |
4: 155,539,489 (GRCm39) |
N938S |
unknown |
Het |
Chil3 |
T |
G |
3: 106,055,984 (GRCm39) |
D363A |
probably damaging |
Het |
Ciart |
G |
A |
3: 95,788,656 (GRCm39) |
P61L |
probably damaging |
Het |
Cpne3 |
A |
G |
4: 19,525,169 (GRCm39) |
V442A |
possibly damaging |
Het |
Ctsh |
T |
C |
9: 89,946,300 (GRCm39) |
V130A |
probably damaging |
Het |
Cyp3a44 |
T |
C |
5: 145,725,212 (GRCm39) |
K330E |
probably benign |
Het |
Dgcr2 |
A |
T |
16: 17,667,633 (GRCm39) |
D275E |
probably damaging |
Het |
Dnah1 |
A |
T |
14: 31,024,321 (GRCm39) |
D919E |
probably benign |
Het |
Ell3 |
TCTCCTC |
TCTC |
2: 121,269,937 (GRCm39) |
|
probably benign |
Het |
Entrep3 |
T |
C |
3: 89,091,250 (GRCm39) |
F74L |
probably damaging |
Het |
Epb41l3 |
T |
A |
17: 69,554,683 (GRCm39) |
F261Y |
possibly damaging |
Het |
Fbxo3 |
A |
C |
2: 103,885,280 (GRCm39) |
H383P |
probably damaging |
Het |
Foxp1 |
C |
T |
6: 98,922,510 (GRCm39) |
V441M |
unknown |
Het |
Gm29106 |
C |
T |
1: 118,126,521 (GRCm39) |
S71F |
probably benign |
Het |
Golga3 |
T |
A |
5: 110,336,573 (GRCm39) |
L364* |
probably null |
Het |
H1f1 |
C |
T |
13: 23,947,832 (GRCm39) |
L45F |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,279,422 (GRCm39) |
L110H |
probably damaging |
Het |
Igkv4-53 |
A |
T |
6: 69,625,898 (GRCm39) |
S90T |
possibly damaging |
Het |
Kctd17 |
CAGCTGGAGGAGC |
CAGC |
15: 78,321,113 (GRCm39) |
|
probably benign |
Het |
Kti12 |
G |
T |
4: 108,705,571 (GRCm39) |
G162W |
probably damaging |
Het |
Lama3 |
T |
A |
18: 12,667,120 (GRCm39) |
I763N |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,369,922 (GRCm39) |
I1613K |
probably benign |
Het |
Mkrn1 |
T |
C |
6: 39,387,031 (GRCm39) |
D102G |
probably benign |
Het |
Muc2 |
T |
A |
7: 141,299,175 (GRCm39) |
|
probably null |
Het |
Nr1h2 |
T |
C |
7: 44,199,746 (GRCm39) |
Y391C |
possibly damaging |
Het |
Odam |
T |
C |
5: 88,040,299 (GRCm39) |
I255T |
possibly damaging |
Het |
Or11m3 |
A |
G |
15: 98,395,694 (GRCm39) |
M114V |
probably benign |
Het |
Or6c35 |
T |
A |
10: 129,168,996 (GRCm39) |
I82K |
probably damaging |
Het |
Or9m1 |
T |
A |
2: 87,733,852 (GRCm39) |
H56L |
probably damaging |
Het |
Per3 |
A |
T |
4: 151,097,014 (GRCm39) |
M837K |
possibly damaging |
Het |
Pitpnm3 |
T |
A |
11: 71,961,144 (GRCm39) |
H357L |
possibly damaging |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Plcb1 |
T |
C |
2: 135,093,654 (GRCm39) |
Y156H |
possibly damaging |
Het |
Ppm1d |
C |
T |
11: 85,230,492 (GRCm39) |
P370L |
possibly damaging |
Het |
Prrc2b |
T |
C |
2: 32,098,686 (GRCm39) |
V666A |
probably benign |
Het |
Ptpn3 |
A |
T |
4: 57,204,985 (GRCm39) |
C725* |
probably null |
Het |
Rapgefl1 |
T |
C |
11: 98,738,209 (GRCm39) |
W437R |
probably damaging |
Het |
Sema4g |
T |
C |
19: 44,980,967 (GRCm39) |
L5P |
probably damaging |
Het |
Sipa1l1 |
C |
T |
12: 82,480,600 (GRCm39) |
P1529L |
probably benign |
Het |
Slc12a2 |
T |
C |
18: 58,032,464 (GRCm39) |
L388P |
probably damaging |
Het |
Sltm |
T |
A |
9: 70,493,360 (GRCm39) |
S786T |
probably damaging |
Het |
Srsf1 |
T |
C |
11: 87,940,082 (GRCm39) |
I198T |
probably benign |
Het |
Ssh2 |
C |
T |
11: 77,345,755 (GRCm39) |
R1247* |
probably null |
Het |
Ssu2 |
T |
C |
6: 112,353,438 (GRCm39) |
T229A |
probably benign |
Het |
Stra6 |
T |
A |
9: 58,059,777 (GRCm39) |
H579Q |
probably damaging |
Het |
Tanc2 |
T |
A |
11: 105,754,833 (GRCm39) |
V559E |
probably benign |
Het |
Trp53bp1 |
A |
G |
2: 121,030,230 (GRCm39) |
Y1762H |
probably damaging |
Het |
Usp15 |
T |
C |
10: 122,982,826 (GRCm39) |
Y263C |
possibly damaging |
Het |
Usp17ld |
A |
T |
7: 102,899,495 (GRCm39) |
V479E |
probably damaging |
Het |
Vmn2r15 |
A |
T |
5: 109,441,185 (GRCm39) |
S224R |
possibly damaging |
Het |
Vmn2r8 |
A |
T |
5: 108,949,700 (GRCm39) |
N382K |
probably benign |
Het |
Vmn2r94 |
T |
C |
17: 18,477,659 (GRCm39) |
I251V |
probably benign |
Het |
Wnt2b |
A |
T |
3: 104,854,408 (GRCm39) |
V350D |
possibly damaging |
Het |
|
Other mutations in Nipal4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02531:Nipal4
|
APN |
11 |
46,042,152 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03203:Nipal4
|
APN |
11 |
46,041,123 (GRCm39) |
missense |
probably damaging |
1.00 |
H8786:Nipal4
|
UTSW |
11 |
46,041,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Nipal4
|
UTSW |
11 |
46,041,268 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0239:Nipal4
|
UTSW |
11 |
46,041,268 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0331:Nipal4
|
UTSW |
11 |
46,041,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0414:Nipal4
|
UTSW |
11 |
46,052,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R0613:Nipal4
|
UTSW |
11 |
46,041,211 (GRCm39) |
missense |
probably benign |
0.31 |
R0940:Nipal4
|
UTSW |
11 |
46,041,139 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1797:Nipal4
|
UTSW |
11 |
46,042,160 (GRCm39) |
missense |
probably benign |
0.06 |
R1889:Nipal4
|
UTSW |
11 |
46,041,560 (GRCm39) |
missense |
probably damaging |
0.99 |
R1899:Nipal4
|
UTSW |
11 |
46,041,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R1974:Nipal4
|
UTSW |
11 |
46,042,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R2066:Nipal4
|
UTSW |
11 |
46,047,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R3705:Nipal4
|
UTSW |
11 |
46,052,678 (GRCm39) |
splice site |
probably benign |
|
R3941:Nipal4
|
UTSW |
11 |
46,041,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R4597:Nipal4
|
UTSW |
11 |
46,042,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Nipal4
|
UTSW |
11 |
46,052,837 (GRCm39) |
missense |
possibly damaging |
0.68 |
R5888:Nipal4
|
UTSW |
11 |
46,042,166 (GRCm39) |
missense |
probably damaging |
0.98 |
R6533:Nipal4
|
UTSW |
11 |
46,041,234 (GRCm39) |
nonsense |
probably null |
|
R7444:Nipal4
|
UTSW |
11 |
46,057,062 (GRCm39) |
missense |
probably benign |
0.27 |
R8203:Nipal4
|
UTSW |
11 |
46,041,147 (GRCm39) |
missense |
probably damaging |
1.00 |
R8825:Nipal4
|
UTSW |
11 |
46,052,873 (GRCm39) |
missense |
probably benign |
0.01 |
R8826:Nipal4
|
UTSW |
11 |
46,045,470 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8881:Nipal4
|
UTSW |
11 |
46,042,177 (GRCm39) |
missense |
probably benign |
0.00 |
R9514:Nipal4
|
UTSW |
11 |
46,052,922 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9768:Nipal4
|
UTSW |
11 |
46,041,473 (GRCm39) |
missense |
probably damaging |
1.00 |
X0018:Nipal4
|
UTSW |
11 |
46,052,873 (GRCm39) |
missense |
probably benign |
0.01 |
|