Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
A |
C |
3: 137,771,183 (GRCm39) |
D124A |
probably benign |
Het |
Acd |
T |
C |
8: 106,425,514 (GRCm39) |
D273G |
probably damaging |
Het |
Acte1 |
G |
T |
7: 143,434,902 (GRCm39) |
|
probably null |
Het |
Adam15 |
T |
C |
3: 89,254,790 (GRCm39) |
D90G |
possibly damaging |
Het |
Adam2 |
A |
T |
14: 66,287,921 (GRCm39) |
C392S |
probably damaging |
Het |
Adam23 |
T |
A |
1: 63,576,131 (GRCm39) |
N304K |
probably damaging |
Het |
Adam34l |
A |
C |
8: 44,079,304 (GRCm39) |
F307V |
probably benign |
Het |
Aldh3b3 |
T |
C |
19: 4,013,882 (GRCm39) |
F28L |
probably damaging |
Het |
Bsn |
A |
G |
9: 107,992,993 (GRCm39) |
S920P |
probably benign |
Het |
Btc |
A |
G |
5: 91,550,515 (GRCm39) |
|
probably null |
Het |
Chchd2 |
A |
T |
5: 129,916,054 (GRCm39) |
V12E |
probably benign |
Het |
Chia1 |
A |
G |
3: 106,035,991 (GRCm39) |
|
probably benign |
Het |
Chil4 |
A |
T |
3: 106,111,382 (GRCm39) |
|
probably null |
Het |
Clock |
A |
G |
5: 76,364,671 (GRCm39) |
F815L |
unknown |
Het |
Cmtr2 |
C |
T |
8: 110,949,712 (GRCm39) |
T674M |
probably benign |
Het |
Cnbd1 |
A |
C |
4: 18,887,647 (GRCm39) |
I289R |
probably damaging |
Het |
Cog2 |
A |
T |
8: 125,253,837 (GRCm39) |
|
probably null |
Het |
Col13a1 |
T |
C |
10: 61,703,248 (GRCm39) |
I454V |
unknown |
Het |
Cyct |
T |
A |
2: 76,184,457 (GRCm39) |
Y98F |
probably benign |
Het |
Dcaf6 |
T |
C |
1: 165,227,236 (GRCm39) |
E297G |
possibly damaging |
Het |
Dgka |
T |
C |
10: 128,567,046 (GRCm39) |
H271R |
probably damaging |
Het |
Dnah9 |
T |
A |
11: 65,976,300 (GRCm39) |
I1250F |
probably benign |
Het |
Dock4 |
T |
C |
12: 40,686,155 (GRCm39) |
L130P |
probably damaging |
Het |
Dpyd |
G |
A |
3: 119,108,560 (GRCm39) |
V868I |
probably benign |
Het |
Dync1li1 |
T |
A |
9: 114,535,076 (GRCm39) |
D113E |
probably damaging |
Het |
Fat3 |
T |
C |
9: 15,932,719 (GRCm39) |
K1405E |
probably damaging |
Het |
Fbn2 |
A |
G |
18: 58,342,856 (GRCm39) |
C8R |
probably benign |
Het |
Frmd4a |
A |
G |
2: 4,609,044 (GRCm39) |
M971V |
probably benign |
Het |
Glyatl3 |
C |
T |
17: 41,223,553 (GRCm39) |
|
probably null |
Het |
Grip1 |
A |
T |
10: 119,821,454 (GRCm39) |
H373L |
probably benign |
Het |
Ins1 |
T |
C |
19: 52,253,258 (GRCm39) |
L66P |
possibly damaging |
Het |
Kif21b |
A |
T |
1: 136,101,800 (GRCm39) |
I1616L |
probably benign |
Het |
Map7d1 |
A |
G |
4: 126,128,024 (GRCm39) |
M637T |
unknown |
Het |
Mc2r |
A |
T |
18: 68,540,636 (GRCm39) |
M219K |
probably benign |
Het |
Mturn |
T |
C |
6: 54,676,541 (GRCm39) |
|
probably null |
Het |
Mutyh |
T |
A |
4: 116,674,074 (GRCm39) |
|
probably null |
Het |
Myh3 |
A |
G |
11: 66,984,397 (GRCm39) |
D1078G |
possibly damaging |
Het |
Or4d5 |
T |
C |
9: 40,012,451 (GRCm39) |
I112V |
probably benign |
Het |
Pcdha12 |
A |
G |
18: 37,153,874 (GRCm39) |
K198E |
probably damaging |
Het |
Pcf11 |
A |
T |
7: 92,306,534 (GRCm39) |
N1211K |
possibly damaging |
Het |
Piezo1 |
G |
A |
8: 123,213,832 (GRCm39) |
P1711S |
|
Het |
Pkd1 |
T |
A |
17: 24,769,451 (GRCm39) |
L72Q |
possibly damaging |
Het |
Pramel20 |
C |
A |
4: 143,299,314 (GRCm39) |
L326I |
probably damaging |
Het |
Prss12 |
A |
G |
3: 123,299,049 (GRCm39) |
D607G |
probably benign |
Het |
R3hdml |
T |
C |
2: 163,344,372 (GRCm39) |
*254R |
probably null |
Het |
Rasal3 |
TTGGACCTGAGTGGA |
TTGGA |
17: 32,612,502 (GRCm39) |
782 |
probably null |
Het |
Relch |
A |
T |
1: 105,615,077 (GRCm39) |
Y272F |
probably benign |
Het |
Rev3l |
C |
T |
10: 39,693,149 (GRCm39) |
P410S |
probably benign |
Het |
Sec14l2 |
A |
G |
11: 4,068,665 (GRCm39) |
V5A |
probably benign |
Het |
Slc12a3 |
A |
C |
8: 95,061,625 (GRCm39) |
I291L |
probably benign |
Het |
Slc4a10 |
T |
C |
2: 62,083,662 (GRCm39) |
F372L |
probably damaging |
Het |
Spta1 |
T |
C |
1: 174,035,978 (GRCm39) |
W1095R |
probably damaging |
Het |
Synj1 |
T |
C |
16: 90,785,095 (GRCm39) |
T254A |
probably damaging |
Het |
Taar2 |
T |
C |
10: 23,817,237 (GRCm39) |
F259S |
probably damaging |
Het |
Tns2 |
C |
A |
15: 102,018,996 (GRCm39) |
L396I |
probably damaging |
Het |
Tom1l1 |
TTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTG |
11: 90,540,648 (GRCm39) |
|
probably benign |
Het |
Traf5 |
T |
C |
1: 191,747,033 (GRCm39) |
D96G |
probably damaging |
Het |
Trgv3 |
A |
G |
13: 19,427,441 (GRCm39) |
E108G |
probably damaging |
Het |
Trpv6 |
A |
G |
6: 41,602,378 (GRCm39) |
V336A |
probably benign |
Het |
Usp45 |
A |
T |
4: 21,824,998 (GRCm39) |
L583F |
probably damaging |
Het |
Utrn |
T |
C |
10: 12,554,475 (GRCm39) |
D1538G |
probably benign |
Het |
Vmn1r209 |
T |
A |
13: 22,990,072 (GRCm39) |
H206L |
probably damaging |
Het |
Zfp51 |
T |
A |
17: 21,684,733 (GRCm39) |
H449Q |
probably benign |
Het |
Zfp653 |
G |
A |
9: 21,969,321 (GRCm39) |
S315F |
possibly damaging |
Het |
|
Other mutations in Mcpt1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0104:Mcpt1
|
UTSW |
14 |
56,256,888 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1458:Mcpt1
|
UTSW |
14 |
56,256,621 (GRCm39) |
splice site |
probably benign |
|
R1473:Mcpt1
|
UTSW |
14 |
56,256,990 (GRCm39) |
missense |
probably benign |
0.01 |
R1939:Mcpt1
|
UTSW |
14 |
56,256,546 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2907:Mcpt1
|
UTSW |
14 |
56,257,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R3966:Mcpt1
|
UTSW |
14 |
56,256,503 (GRCm39) |
missense |
probably benign |
0.14 |
R4235:Mcpt1
|
UTSW |
14 |
56,256,017 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4594:Mcpt1
|
UTSW |
14 |
56,256,109 (GRCm39) |
missense |
probably benign |
0.00 |
R4754:Mcpt1
|
UTSW |
14 |
56,256,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Mcpt1
|
UTSW |
14 |
56,257,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R5743:Mcpt1
|
UTSW |
14 |
56,256,072 (GRCm39) |
missense |
probably benign |
0.41 |
R5888:Mcpt1
|
UTSW |
14 |
56,256,969 (GRCm39) |
missense |
probably benign |
0.14 |
R6925:Mcpt1
|
UTSW |
14 |
56,256,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Mcpt1
|
UTSW |
14 |
56,256,609 (GRCm39) |
critical splice donor site |
probably null |
|
R8712:Mcpt1
|
UTSW |
14 |
56,256,170 (GRCm39) |
critical splice donor site |
probably benign |
|
R8885:Mcpt1
|
UTSW |
14 |
56,256,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R8903:Mcpt1
|
UTSW |
14 |
56,257,520 (GRCm39) |
missense |
probably benign |
0.14 |
|