Other mutations in this stock |
Total: 92 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930522L14Rik |
A |
G |
5: 109,884,926 (GRCm39) |
|
probably benign |
Het |
Abcd2 |
C |
T |
15: 91,043,327 (GRCm39) |
M620I |
probably benign |
Het |
Ada |
T |
A |
2: 163,572,271 (GRCm39) |
I243F |
probably benign |
Het |
Adam12 |
T |
C |
7: 133,576,145 (GRCm39) |
|
probably null |
Het |
Adarb2 |
A |
T |
13: 8,253,224 (GRCm39) |
|
probably benign |
Het |
Adk |
A |
C |
14: 21,473,604 (GRCm39) |
Q287P |
probably benign |
Het |
Ahnak |
A |
G |
19: 8,986,771 (GRCm39) |
|
probably benign |
Het |
Aoc3 |
C |
T |
11: 101,222,432 (GRCm39) |
R223W |
probably damaging |
Het |
Aqp11 |
T |
C |
7: 97,378,228 (GRCm39) |
D229G |
probably benign |
Het |
Arhgap28 |
A |
G |
17: 68,203,220 (GRCm39) |
S78P |
probably damaging |
Het |
Bfsp2 |
T |
A |
9: 103,303,854 (GRCm39) |
E383D |
possibly damaging |
Het |
Bmpr1b |
A |
T |
3: 141,563,191 (GRCm39) |
V251D |
possibly damaging |
Het |
Calhm1 |
C |
T |
19: 47,132,280 (GRCm39) |
V112I |
probably benign |
Het |
Catsperd |
A |
G |
17: 56,966,554 (GRCm39) |
D508G |
probably damaging |
Het |
Cfap54 |
A |
G |
10: 92,710,805 (GRCm39) |
|
probably null |
Het |
Cfap70 |
A |
T |
14: 20,498,631 (GRCm39) |
Y19N |
probably damaging |
Het |
Chga |
A |
T |
12: 102,529,210 (GRCm39) |
R396* |
probably null |
Het |
Cntnap3 |
T |
C |
13: 64,926,690 (GRCm39) |
E560G |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 15,971,759 (GRCm39) |
T3024A |
probably damaging |
Het |
Csrnp1 |
CCCTCCTCCTCCTCCTCCTC |
CCCTCCTCCTCCTCCTC |
9: 119,801,841 (GRCm39) |
|
probably benign |
Het |
Cysltr1 |
A |
G |
X: 105,622,261 (GRCm39) |
V75A |
possibly damaging |
Het |
Dnaaf11 |
T |
A |
15: 66,252,323 (GRCm39) |
M448L |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,313,952 (GRCm39) |
M4140K |
probably damaging |
Het |
Dph5 |
A |
G |
3: 115,722,352 (GRCm39) |
S277G |
probably benign |
Het |
Eftud2 |
A |
T |
11: 102,755,597 (GRCm39) |
D203E |
probably damaging |
Het |
Egf |
A |
G |
3: 129,499,882 (GRCm39) |
Y252H |
probably benign |
Het |
Egf |
A |
G |
3: 129,531,198 (GRCm39) |
S126P |
probably damaging |
Het |
Faf1 |
C |
T |
4: 109,748,138 (GRCm39) |
A481V |
probably benign |
Het |
Fat2 |
A |
T |
11: 55,153,655 (GRCm39) |
V3519D |
probably damaging |
Het |
Fbln7 |
C |
A |
2: 128,719,431 (GRCm39) |
A76E |
probably benign |
Het |
Galnt1 |
A |
T |
18: 24,387,582 (GRCm39) |
K49N |
probably benign |
Het |
Glb1 |
ACCC |
ACC |
9: 114,250,812 (GRCm39) |
|
probably null |
Het |
Grk1 |
T |
C |
8: 13,459,279 (GRCm39) |
Y277H |
probably damaging |
Het |
Hap1 |
A |
G |
11: 100,240,131 (GRCm39) |
L555P |
probably damaging |
Het |
Ier3 |
T |
C |
17: 36,133,000 (GRCm39) |
I94T |
possibly damaging |
Het |
Il11 |
T |
C |
7: 4,779,023 (GRCm39) |
T36A |
probably damaging |
Het |
Il5ra |
A |
T |
6: 106,708,851 (GRCm39) |
D296E |
probably damaging |
Het |
Itk |
A |
T |
11: 46,222,816 (GRCm39) |
V551E |
probably damaging |
Het |
Kcna2 |
T |
A |
3: 107,012,476 (GRCm39) |
D352E |
probably benign |
Het |
Kif5a |
A |
T |
10: 127,071,521 (GRCm39) |
S776T |
probably benign |
Het |
Klrb1c |
T |
C |
6: 128,757,366 (GRCm39) |
E233G |
probably benign |
Het |
Kpna7 |
T |
C |
5: 144,944,804 (GRCm39) |
K12R |
possibly damaging |
Het |
Lhpp |
C |
T |
7: 132,212,406 (GRCm39) |
|
probably benign |
Het |
Lhx8 |
A |
T |
3: 154,033,808 (GRCm39) |
|
probably null |
Het |
Magel2 |
T |
A |
7: 62,027,778 (GRCm39) |
H227Q |
possibly damaging |
Het |
Man1a |
A |
G |
10: 53,950,594 (GRCm39) |
V176A |
probably damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,853,632 (GRCm39) |
M1152K |
probably benign |
Het |
Myof |
T |
C |
19: 37,904,952 (GRCm39) |
D1624G |
probably damaging |
Het |
Myom2 |
T |
C |
8: 15,154,123 (GRCm39) |
V687A |
probably benign |
Het |
Nav1 |
C |
A |
1: 135,379,945 (GRCm39) |
V1586F |
possibly damaging |
Het |
Ndufb8 |
T |
C |
19: 44,538,784 (GRCm39) |
E179G |
possibly damaging |
Het |
Nfam1 |
T |
C |
15: 82,885,684 (GRCm39) |
T223A |
probably damaging |
Het |
Nrcam |
T |
A |
12: 44,598,124 (GRCm39) |
V371E |
probably damaging |
Het |
Nup210l |
A |
G |
3: 90,087,518 (GRCm39) |
Q1097R |
probably null |
Het |
Obox5 |
T |
A |
7: 15,491,571 (GRCm39) |
M37K |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,952,356 (GRCm39) |
N4270K |
probably benign |
Het |
Or4d2 |
G |
A |
11: 87,784,022 (GRCm39) |
H243Y |
probably damaging |
Het |
Or5ak25 |
T |
A |
2: 85,268,630 (GRCm39) |
S291C |
probably damaging |
Het |
Or6c1 |
A |
G |
10: 129,517,708 (GRCm39) |
M300T |
probably benign |
Het |
Or8c15 |
G |
A |
9: 38,120,360 (GRCm39) |
A2T |
probably benign |
Het |
Or8k16 |
T |
C |
2: 85,520,183 (GRCm39) |
S137P |
possibly damaging |
Het |
Patj |
G |
A |
4: 98,562,545 (GRCm39) |
E1505K |
probably damaging |
Het |
Pnliprp1 |
T |
A |
19: 58,726,628 (GRCm39) |
Y328* |
probably null |
Het |
Ppp1r36 |
G |
A |
12: 76,465,741 (GRCm39) |
E43K |
probably damaging |
Het |
Ptch1 |
C |
T |
13: 63,668,121 (GRCm39) |
V939I |
probably damaging |
Het |
Rgs22 |
C |
A |
15: 36,093,084 (GRCm39) |
K396N |
probably damaging |
Het |
Rsrc1 |
A |
T |
3: 67,088,194 (GRCm39) |
H176L |
probably damaging |
Het |
Ryr3 |
A |
T |
2: 112,492,046 (GRCm39) |
F3743L |
probably damaging |
Het |
Scn7a |
C |
T |
2: 66,506,084 (GRCm39) |
G1602R |
probably benign |
Het |
Sftpc |
A |
T |
14: 70,760,110 (GRCm39) |
V49E |
probably damaging |
Het |
Slc16a10 |
A |
G |
10: 39,916,612 (GRCm39) |
V430A |
probably benign |
Het |
Slco4c1 |
A |
C |
1: 96,795,645 (GRCm39) |
S138A |
possibly damaging |
Het |
Snd1 |
T |
C |
6: 28,724,955 (GRCm39) |
I501T |
probably benign |
Het |
Stxbp2 |
T |
A |
8: 3,682,559 (GRCm39) |
D49E |
probably damaging |
Het |
Sytl4 |
A |
T |
X: 132,862,936 (GRCm39) |
D16E |
probably benign |
Het |
Tbc1d9b |
G |
A |
11: 50,035,894 (GRCm39) |
G130E |
probably benign |
Het |
Tdrd6 |
T |
A |
17: 43,936,452 (GRCm39) |
D1532V |
probably damaging |
Het |
Tekt1 |
T |
C |
11: 72,242,778 (GRCm39) |
D243G |
probably damaging |
Het |
Tet2 |
A |
G |
3: 133,192,427 (GRCm39) |
L669S |
possibly damaging |
Het |
Tnnt3 |
A |
G |
7: 142,066,072 (GRCm39) |
N201S |
probably benign |
Het |
Trdn |
A |
G |
10: 33,342,417 (GRCm39) |
|
probably null |
Het |
Trim36 |
T |
C |
18: 46,311,523 (GRCm39) |
E259G |
possibly damaging |
Het |
Trpm1 |
C |
T |
7: 63,870,002 (GRCm39) |
P436S |
probably benign |
Het |
Vmn1r183 |
T |
A |
7: 23,754,926 (GRCm39) |
L243Q |
probably damaging |
Het |
Vps13b |
T |
C |
15: 35,597,555 (GRCm39) |
S1032P |
probably damaging |
Het |
Vps37d |
T |
C |
5: 135,105,395 (GRCm39) |
E76G |
probably damaging |
Het |
Vps72 |
A |
G |
3: 95,028,615 (GRCm39) |
H202R |
probably benign |
Het |
Wdr75 |
T |
C |
1: 45,858,762 (GRCm39) |
S644P |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,770,843 (GRCm39) |
E697V |
possibly damaging |
Het |
Xirp2 |
A |
G |
2: 67,345,262 (GRCm39) |
D2501G |
probably benign |
Het |
Zfp472 |
T |
C |
17: 33,194,936 (GRCm39) |
W24R |
probably damaging |
Het |
Zmym6 |
T |
C |
4: 127,016,565 (GRCm39) |
V782A |
probably damaging |
Het |
|
Other mutations in Mcoln3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00508:Mcoln3
|
APN |
3 |
145,839,683 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01106:Mcoln3
|
APN |
3 |
145,843,019 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01712:Mcoln3
|
APN |
3 |
145,834,019 (GRCm39) |
unclassified |
probably benign |
|
IGL02115:Mcoln3
|
APN |
3 |
145,843,056 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02116:Mcoln3
|
APN |
3 |
145,839,664 (GRCm39) |
missense |
probably benign |
0.29 |
P4717OSA:Mcoln3
|
UTSW |
3 |
145,830,504 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Mcoln3
|
UTSW |
3 |
145,846,345 (GRCm39) |
nonsense |
probably null |
|
R2056:Mcoln3
|
UTSW |
3 |
145,833,979 (GRCm39) |
missense |
probably benign |
0.01 |
R3000:Mcoln3
|
UTSW |
3 |
145,839,662 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4366:Mcoln3
|
UTSW |
3 |
145,846,247 (GRCm39) |
missense |
possibly damaging |
0.76 |
R4667:Mcoln3
|
UTSW |
3 |
145,836,959 (GRCm39) |
missense |
probably benign |
0.01 |
R4950:Mcoln3
|
UTSW |
3 |
145,845,274 (GRCm39) |
missense |
probably damaging |
0.96 |
R5457:Mcoln3
|
UTSW |
3 |
145,833,877 (GRCm39) |
missense |
probably benign |
0.00 |
R6302:Mcoln3
|
UTSW |
3 |
145,830,527 (GRCm39) |
missense |
probably benign |
0.00 |
R6353:Mcoln3
|
UTSW |
3 |
145,836,909 (GRCm39) |
missense |
probably damaging |
0.99 |
R6632:Mcoln3
|
UTSW |
3 |
145,833,942 (GRCm39) |
missense |
probably benign |
|
R6915:Mcoln3
|
UTSW |
3 |
145,843,011 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7790:Mcoln3
|
UTSW |
3 |
145,845,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R7838:Mcoln3
|
UTSW |
3 |
145,845,230 (GRCm39) |
missense |
probably damaging |
1.00 |
R7861:Mcoln3
|
UTSW |
3 |
145,830,546 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8348:Mcoln3
|
UTSW |
3 |
145,836,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R8509:Mcoln3
|
UTSW |
3 |
145,830,647 (GRCm39) |
missense |
probably benign |
0.00 |
R8708:Mcoln3
|
UTSW |
3 |
145,846,276 (GRCm39) |
nonsense |
probably null |
|
R8838:Mcoln3
|
UTSW |
3 |
145,845,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R8861:Mcoln3
|
UTSW |
3 |
145,845,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R8981:Mcoln3
|
UTSW |
3 |
145,827,554 (GRCm39) |
missense |
probably benign |
|
Z1176:Mcoln3
|
UTSW |
3 |
145,846,221 (GRCm39) |
missense |
probably benign |
0.00 |
|