Other mutations in this stock |
Total: 90 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931429L15Rik |
A |
G |
9: 46,221,552 (GRCm39) |
|
probably benign |
Het |
4933411K16Rik |
T |
C |
19: 42,041,489 (GRCm39) |
Y207H |
probably damaging |
Het |
Abcc1 |
T |
A |
16: 14,266,298 (GRCm39) |
L832Q |
probably damaging |
Het |
Acan |
T |
A |
7: 78,750,552 (GRCm39) |
H1774Q |
probably benign |
Het |
Adss2 |
T |
C |
1: 177,599,760 (GRCm39) |
T275A |
probably benign |
Het |
Ano5 |
G |
A |
7: 51,233,523 (GRCm39) |
R595H |
probably damaging |
Het |
Araf |
G |
T |
X: 20,725,943 (GRCm39) |
R522L |
probably damaging |
Het |
Arhgef28 |
C |
T |
13: 98,102,054 (GRCm39) |
V807I |
possibly damaging |
Het |
Bin1 |
T |
C |
18: 32,545,757 (GRCm39) |
I103T |
probably damaging |
Het |
C4b |
C |
T |
17: 34,958,995 (GRCm39) |
R478Q |
probably benign |
Het |
Cacna1b |
G |
A |
2: 24,568,047 (GRCm39) |
P1015S |
probably benign |
Het |
Capn1 |
A |
G |
19: 6,057,528 (GRCm39) |
|
probably null |
Het |
Cep290 |
A |
G |
10: 100,374,828 (GRCm39) |
Q1358R |
probably damaging |
Het |
Cfap126 |
T |
C |
1: 170,953,386 (GRCm39) |
|
probably benign |
Het |
Chn1 |
T |
C |
2: 73,509,951 (GRCm39) |
|
probably benign |
Het |
Cldn8 |
T |
C |
16: 88,359,289 (GRCm39) |
E212G |
probably benign |
Het |
Cxcr6 |
A |
T |
9: 123,639,412 (GRCm39) |
I138F |
probably benign |
Het |
Dab2ip |
G |
A |
2: 35,608,803 (GRCm39) |
R579H |
probably damaging |
Het |
Dcaf8 |
T |
C |
1: 172,021,422 (GRCm39) |
M538T |
probably benign |
Het |
Dhrs4 |
T |
G |
14: 55,725,107 (GRCm39) |
L201V |
probably damaging |
Het |
Dnah12 |
C |
T |
14: 26,431,403 (GRCm39) |
A407V |
probably benign |
Het |
Elavl3 |
T |
A |
9: 21,937,461 (GRCm39) |
|
probably benign |
Het |
Elp4 |
T |
C |
2: 105,662,506 (GRCm39) |
H88R |
probably benign |
Het |
Ercc3 |
T |
C |
18: 32,394,350 (GRCm39) |
|
probably benign |
Het |
Eri1 |
A |
G |
8: 35,936,335 (GRCm39) |
S329P |
possibly damaging |
Het |
Erich2 |
A |
T |
2: 70,343,117 (GRCm39) |
|
probably benign |
Het |
Esyt1 |
A |
G |
10: 128,348,297 (GRCm39) |
S864P |
possibly damaging |
Het |
Fam170b |
A |
G |
14: 32,557,588 (GRCm39) |
E141G |
probably damaging |
Het |
Fat1 |
A |
G |
8: 45,486,427 (GRCm39) |
Y3304C |
probably damaging |
Het |
Fbn1 |
T |
C |
2: 125,151,415 (GRCm39) |
T2531A |
probably benign |
Het |
Fgfr3 |
T |
C |
5: 33,887,094 (GRCm39) |
V166A |
probably damaging |
Het |
Glt8d2 |
T |
C |
10: 82,495,372 (GRCm39) |
D194G |
probably damaging |
Het |
Gpr89 |
A |
G |
3: 96,812,526 (GRCm39) |
I5T |
probably benign |
Het |
Gpx6 |
A |
T |
13: 21,503,090 (GRCm39) |
H168L |
probably benign |
Het |
Gusb |
T |
C |
5: 130,027,385 (GRCm39) |
T307A |
probably benign |
Het |
Hjurp |
A |
T |
1: 88,202,772 (GRCm39) |
Y71N |
possibly damaging |
Het |
Ifngr1 |
A |
G |
10: 19,477,193 (GRCm39) |
D118G |
probably benign |
Het |
Ipcef1 |
A |
T |
10: 6,885,173 (GRCm39) |
|
probably null |
Het |
Kbtbd3 |
A |
T |
9: 4,330,276 (GRCm39) |
T217S |
probably benign |
Het |
Kmt5a |
GAA |
GA |
5: 124,597,948 (GRCm39) |
|
probably null |
Het |
Lrp1 |
T |
C |
10: 127,374,880 (GRCm39) |
D4526G |
probably damaging |
Het |
Lrp1b |
A |
T |
2: 42,213,674 (GRCm39) |
V46D |
probably damaging |
Het |
Lsm8 |
T |
A |
6: 18,849,658 (GRCm39) |
M22K |
probably benign |
Het |
Map1lc3b |
C |
T |
8: 122,323,339 (GRCm39) |
R70C |
possibly damaging |
Het |
Meiob |
T |
A |
17: 25,032,026 (GRCm39) |
S14T |
possibly damaging |
Het |
Mkx |
G |
T |
18: 6,992,330 (GRCm39) |
Y183* |
probably null |
Het |
Mrs2 |
T |
C |
13: 25,189,017 (GRCm39) |
Y99C |
probably benign |
Het |
Mycbpap |
T |
C |
11: 94,396,387 (GRCm39) |
K151R |
probably benign |
Het |
Neb |
T |
G |
2: 52,218,746 (GRCm39) |
Q88P |
probably damaging |
Het |
Noc4l |
T |
A |
5: 110,797,944 (GRCm39) |
H319L |
probably damaging |
Het |
Nt5c2 |
G |
A |
19: 46,893,417 (GRCm39) |
T122I |
probably damaging |
Het |
Nuggc |
A |
T |
14: 65,861,582 (GRCm39) |
N476I |
probably damaging |
Het |
Obscn |
T |
A |
11: 58,921,862 (GRCm39) |
H5978L |
probably benign |
Het |
Oc90 |
G |
T |
15: 65,748,370 (GRCm39) |
A412D |
probably damaging |
Het |
Or2l13b |
T |
A |
16: 19,349,133 (GRCm39) |
D179V |
possibly damaging |
Het |
Or3a4 |
A |
G |
11: 73,944,650 (GRCm39) |
*312Q |
probably null |
Het |
Or4a76 |
A |
G |
2: 89,460,358 (GRCm39) |
S295P |
possibly damaging |
Het |
Or5w18 |
T |
G |
2: 87,633,212 (GRCm39) |
S160A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,682 (GRCm39) |
S214R |
probably benign |
Het |
Or8k33 |
A |
T |
2: 86,384,096 (GRCm39) |
V124E |
probably damaging |
Het |
Pdzrn3 |
A |
T |
6: 101,127,930 (GRCm39) |
V912E |
probably benign |
Het |
Phactr1 |
T |
A |
13: 43,248,466 (GRCm39) |
Y387N |
probably damaging |
Het |
Picalm |
T |
A |
7: 89,779,859 (GRCm39) |
C27S |
probably benign |
Het |
Pkd1l1 |
T |
A |
11: 8,891,077 (GRCm39) |
I314F |
possibly damaging |
Het |
Pold2 |
T |
C |
11: 5,824,175 (GRCm39) |
E210G |
possibly damaging |
Het |
Ptprz1 |
C |
T |
6: 23,049,523 (GRCm39) |
|
probably benign |
Het |
Rac1 |
G |
T |
5: 143,493,093 (GRCm39) |
A165E |
probably damaging |
Het |
Rpap3 |
G |
T |
15: 97,584,364 (GRCm39) |
T360K |
possibly damaging |
Het |
Scn9a |
G |
A |
2: 66,357,232 (GRCm39) |
T1012I |
probably benign |
Het |
Sdad1 |
A |
G |
5: 92,457,682 (GRCm39) |
I20T |
possibly damaging |
Het |
Setbp1 |
T |
G |
18: 78,903,127 (GRCm39) |
K180T |
probably damaging |
Het |
Sgpl1 |
T |
C |
10: 60,938,368 (GRCm39) |
N475S |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,090,693 (GRCm39) |
S1148P |
possibly damaging |
Het |
Sin3a |
T |
A |
9: 57,026,442 (GRCm39) |
H1119Q |
possibly damaging |
Het |
Slc26a7 |
T |
A |
4: 14,506,489 (GRCm39) |
Y620F |
probably benign |
Het |
Slc4a1 |
T |
C |
11: 102,251,997 (GRCm39) |
I36V |
probably benign |
Het |
Smarca2 |
C |
G |
19: 26,608,501 (GRCm39) |
P263A |
possibly damaging |
Het |
Sp100 |
T |
C |
1: 85,591,242 (GRCm39) |
|
probably benign |
Het |
Spag6l |
A |
G |
16: 16,598,478 (GRCm39) |
|
probably benign |
Het |
Sptbn1 |
T |
C |
11: 30,071,498 (GRCm39) |
N1491S |
probably damaging |
Het |
Tbl1xr1 |
T |
G |
3: 22,245,115 (GRCm39) |
V155G |
possibly damaging |
Het |
Tmc1 |
A |
G |
19: 20,845,719 (GRCm39) |
I168T |
probably damaging |
Het |
Tmem87b |
G |
A |
2: 128,668,313 (GRCm39) |
|
probably null |
Het |
Tnfrsf9 |
T |
A |
4: 151,017,561 (GRCm39) |
|
probably null |
Het |
Tnni3k |
T |
C |
3: 154,645,295 (GRCm39) |
D530G |
probably damaging |
Het |
Vmn1r209 |
G |
A |
13: 22,989,934 (GRCm39) |
S252F |
probably damaging |
Het |
Zbtb3 |
A |
T |
19: 8,780,714 (GRCm39) |
N109I |
probably damaging |
Het |
Zdhhc17 |
T |
G |
10: 110,782,071 (GRCm39) |
H541P |
probably damaging |
Het |
Zfp84 |
A |
G |
7: 29,476,039 (GRCm39) |
I244V |
possibly damaging |
Het |
Zyx |
A |
G |
6: 42,333,246 (GRCm39) |
Y393C |
probably damaging |
Het |
|
Other mutations in Cpb1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00896:Cpb1
|
APN |
3 |
20,306,193 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01061:Cpb1
|
APN |
3 |
20,320,680 (GRCm39) |
missense |
probably benign |
0.06 |
IGL01376:Cpb1
|
APN |
3 |
20,324,488 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01409:Cpb1
|
APN |
3 |
20,303,969 (GRCm39) |
missense |
possibly damaging |
0.51 |
IGL01505:Cpb1
|
APN |
3 |
20,320,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01599:Cpb1
|
APN |
3 |
20,306,118 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01672:Cpb1
|
APN |
3 |
20,329,585 (GRCm39) |
missense |
probably null |
0.34 |
IGL02421:Cpb1
|
APN |
3 |
20,306,148 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Cpb1
|
APN |
3 |
20,319,520 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02825:Cpb1
|
APN |
3 |
20,303,889 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02929:Cpb1
|
APN |
3 |
20,329,630 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03229:Cpb1
|
APN |
3 |
20,304,001 (GRCm39) |
nonsense |
probably null |
|
R0106:Cpb1
|
UTSW |
3 |
20,320,697 (GRCm39) |
splice site |
probably null |
|
R0106:Cpb1
|
UTSW |
3 |
20,320,697 (GRCm39) |
splice site |
probably null |
|
R0485:Cpb1
|
UTSW |
3 |
20,329,792 (GRCm39) |
missense |
unknown |
|
R0609:Cpb1
|
UTSW |
3 |
20,316,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R0622:Cpb1
|
UTSW |
3 |
20,303,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R0676:Cpb1
|
UTSW |
3 |
20,320,697 (GRCm39) |
splice site |
probably null |
|
R0829:Cpb1
|
UTSW |
3 |
20,306,107 (GRCm39) |
splice site |
probably benign |
|
R0981:Cpb1
|
UTSW |
3 |
20,329,654 (GRCm39) |
missense |
probably benign |
0.29 |
R1535:Cpb1
|
UTSW |
3 |
20,320,451 (GRCm39) |
missense |
probably benign |
0.19 |
R1607:Cpb1
|
UTSW |
3 |
20,317,946 (GRCm39) |
missense |
probably benign |
0.03 |
R1707:Cpb1
|
UTSW |
3 |
20,329,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R1753:Cpb1
|
UTSW |
3 |
20,320,405 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1866:Cpb1
|
UTSW |
3 |
20,317,920 (GRCm39) |
missense |
probably benign |
0.00 |
R2177:Cpb1
|
UTSW |
3 |
20,320,611 (GRCm39) |
missense |
probably benign |
0.41 |
R2234:Cpb1
|
UTSW |
3 |
20,329,629 (GRCm39) |
missense |
probably benign |
0.04 |
R3110:Cpb1
|
UTSW |
3 |
20,319,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R3112:Cpb1
|
UTSW |
3 |
20,319,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R4353:Cpb1
|
UTSW |
3 |
20,316,708 (GRCm39) |
missense |
probably benign |
0.07 |
R4405:Cpb1
|
UTSW |
3 |
20,317,733 (GRCm39) |
missense |
probably benign |
0.00 |
R4485:Cpb1
|
UTSW |
3 |
20,303,865 (GRCm39) |
missense |
probably benign |
0.00 |
R4734:Cpb1
|
UTSW |
3 |
20,317,876 (GRCm39) |
missense |
probably benign |
0.43 |
R4984:Cpb1
|
UTSW |
3 |
20,324,516 (GRCm39) |
frame shift |
probably null |
|
R5807:Cpb1
|
UTSW |
3 |
20,317,906 (GRCm39) |
missense |
probably damaging |
0.98 |
R6377:Cpb1
|
UTSW |
3 |
20,329,748 (GRCm39) |
critical splice donor site |
probably null |
|
R6441:Cpb1
|
UTSW |
3 |
20,303,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R7175:Cpb1
|
UTSW |
3 |
20,317,927 (GRCm39) |
missense |
probably benign |
0.00 |
R7488:Cpb1
|
UTSW |
3 |
20,324,488 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8288:Cpb1
|
UTSW |
3 |
20,319,531 (GRCm39) |
nonsense |
probably null |
|
R9260:Cpb1
|
UTSW |
3 |
20,316,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R9568:Cpb1
|
UTSW |
3 |
20,320,697 (GRCm39) |
splice site |
probably null |
|
|