Other mutations in this stock |
Total: 101 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acot12 |
A |
G |
13: 91,932,510 (GRCm39) |
D502G |
probably benign |
Het |
Adrb1 |
T |
C |
19: 56,711,120 (GRCm39) |
V106A |
probably damaging |
Het |
Ahcyl2 |
G |
T |
6: 29,886,139 (GRCm39) |
G352W |
probably damaging |
Het |
Ahnak2 |
T |
G |
12: 112,745,851 (GRCm39) |
D446A |
|
Het |
Arhgap42 |
T |
C |
9: 9,035,532 (GRCm39) |
D270G |
probably benign |
Het |
Atp2a1 |
A |
G |
7: 126,058,828 (GRCm39) |
V129A |
possibly damaging |
Het |
B9d2 |
G |
A |
7: 25,380,784 (GRCm39) |
|
probably benign |
Het |
Bace1 |
A |
T |
9: 45,767,437 (GRCm39) |
I207F |
possibly damaging |
Het |
Blnk |
T |
A |
19: 40,940,834 (GRCm39) |
I190F |
possibly damaging |
Het |
Bmp7 |
C |
T |
2: 172,781,757 (GRCm39) |
E36K |
possibly damaging |
Het |
Brsk2 |
A |
G |
7: 141,554,597 (GRCm39) |
E654G |
probably benign |
Het |
Cacna2d3 |
T |
C |
14: 28,780,378 (GRCm39) |
H661R |
probably benign |
Het |
Cdh4 |
T |
C |
2: 179,532,695 (GRCm39) |
V719A |
probably benign |
Het |
Cdkn2d |
G |
T |
9: 21,200,540 (GRCm39) |
P77H |
probably damaging |
Het |
Chd3 |
A |
G |
11: 69,247,096 (GRCm39) |
V1024A |
probably damaging |
Het |
Chsy1 |
T |
A |
7: 65,820,992 (GRCm39) |
M409K |
possibly damaging |
Het |
Chsy1 |
T |
C |
7: 65,821,319 (GRCm39) |
L518P |
probably damaging |
Het |
Cic |
G |
A |
7: 24,972,278 (GRCm39) |
V670M |
probably damaging |
Het |
Clock |
A |
T |
5: 76,390,738 (GRCm39) |
|
probably null |
Het |
Coro1a |
C |
A |
7: 126,302,306 (GRCm39) |
V14L |
probably damaging |
Het |
Ctcfl |
C |
A |
2: 172,960,199 (GRCm39) |
C128F |
probably damaging |
Het |
Cyb5b |
A |
G |
8: 107,896,491 (GRCm39) |
T71A |
probably damaging |
Het |
Cyp2c40 |
C |
G |
19: 39,795,658 (GRCm39) |
V174L |
possibly damaging |
Het |
D630045J12Rik |
T |
A |
6: 38,173,562 (GRCm39) |
Q202L |
possibly damaging |
Het |
Dgkz |
T |
C |
2: 91,773,160 (GRCm39) |
|
probably benign |
Het |
Dlgap2 |
T |
C |
8: 14,872,697 (GRCm39) |
|
probably null |
Het |
Dnah1 |
T |
C |
14: 31,026,940 (GRCm39) |
I695V |
probably benign |
Het |
Dst |
T |
A |
1: 34,221,532 (GRCm39) |
S2445R |
possibly damaging |
Het |
Elob |
T |
C |
17: 24,043,950 (GRCm39) |
D83G |
probably benign |
Het |
Elp4 |
T |
A |
2: 105,624,933 (GRCm39) |
D320V |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Etfdh |
T |
C |
3: 79,530,886 (GRCm39) |
Y45C |
probably damaging |
Het |
Exph5 |
A |
G |
9: 53,287,073 (GRCm39) |
I1385V |
probably benign |
Het |
Fat3 |
A |
T |
9: 15,908,138 (GRCm39) |
D2621E |
probably damaging |
Het |
Fbxl6 |
G |
T |
15: 76,422,669 (GRCm39) |
A83D |
probably benign |
Het |
Fmo2 |
A |
G |
1: 162,716,318 (GRCm39) |
Y90H |
probably damaging |
Het |
Fzd4 |
T |
A |
7: 89,056,761 (GRCm39) |
Y269* |
probably null |
Het |
Grik5 |
T |
A |
7: 24,757,951 (GRCm39) |
I377F |
probably damaging |
Het |
Havcr2 |
C |
A |
11: 46,349,889 (GRCm39) |
P137Q |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,392,405 (GRCm39) |
N223S |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,347,185 (GRCm39) |
S4792G |
probably benign |
Het |
Hps3 |
T |
G |
3: 20,084,616 (GRCm39) |
I191L |
probably benign |
Het |
Ica1l |
T |
A |
1: 60,049,369 (GRCm39) |
K195* |
probably null |
Het |
Idh2 |
TCCCAGGGCC |
TCC |
7: 79,748,079 (GRCm39) |
|
probably null |
Het |
Ift140 |
A |
G |
17: 25,311,315 (GRCm39) |
D1170G |
probably benign |
Het |
Igflr1 |
T |
C |
7: 30,266,776 (GRCm39) |
F208S |
possibly damaging |
Het |
Kcnma1 |
T |
C |
14: 23,580,310 (GRCm39) |
T313A |
probably benign |
Het |
Krt6a |
T |
A |
15: 101,598,994 (GRCm39) |
I524F |
unknown |
Het |
Lce1d |
G |
T |
3: 92,593,148 (GRCm39) |
H88Q |
unknown |
Het |
Lrmda |
A |
G |
14: 22,878,770 (GRCm39) |
E177G |
probably benign |
Het |
Lrrn3 |
T |
A |
12: 41,502,712 (GRCm39) |
N535I |
possibly damaging |
Het |
Map2k4 |
T |
A |
11: 65,666,583 (GRCm39) |
I40L |
unknown |
Het |
Map7d1 |
A |
G |
4: 126,130,429 (GRCm39) |
L459P |
probably damaging |
Het |
Mycn |
A |
C |
12: 12,990,292 (GRCm39) |
F35V |
probably benign |
Het |
Mzt2 |
A |
C |
16: 15,680,669 (GRCm39) |
M40R |
possibly damaging |
Het |
N4bp2 |
T |
G |
5: 65,948,458 (GRCm39) |
L363V |
probably damaging |
Het |
Nfat5 |
T |
A |
8: 108,097,221 (GRCm39) |
M1532K |
probably benign |
Het |
Notch1 |
G |
A |
2: 26,350,177 (GRCm39) |
T2321M |
probably benign |
Het |
Nr1h4 |
T |
C |
10: 89,334,123 (GRCm39) |
D89G |
probably benign |
Het |
Nsun4 |
G |
A |
4: 115,908,691 (GRCm39) |
T623I |
possibly damaging |
Het |
Nup155 |
T |
C |
15: 8,184,531 (GRCm39) |
S1309P |
probably benign |
Het |
Or4e1 |
T |
C |
14: 52,700,851 (GRCm39) |
N205S |
probably damaging |
Het |
Or51f5 |
T |
C |
7: 102,430,889 (GRCm39) |
S69P |
probably damaging |
Het |
Or8h10 |
T |
C |
2: 86,809,122 (GRCm39) |
Y6C |
probably benign |
Het |
Pcsk5 |
A |
G |
19: 17,814,336 (GRCm39) |
F61L |
probably benign |
Het |
Phrf1 |
A |
T |
7: 140,811,138 (GRCm39) |
|
probably null |
Het |
Pkd1 |
G |
A |
17: 24,792,605 (GRCm39) |
E1431K |
probably benign |
Het |
Pkd2 |
T |
A |
5: 104,628,219 (GRCm39) |
I431N |
probably damaging |
Het |
Plcb2 |
A |
G |
2: 118,546,124 (GRCm39) |
L557P |
probably damaging |
Het |
Poteg |
A |
G |
8: 27,984,988 (GRCm39) |
N449S |
probably benign |
Het |
Ppargc1b |
C |
A |
18: 61,445,281 (GRCm39) |
G192W |
probably damaging |
Het |
Rab13 |
T |
C |
3: 90,132,206 (GRCm39) |
S178P |
probably benign |
Het |
Ralgds |
A |
G |
2: 28,437,607 (GRCm39) |
D571G |
probably damaging |
Het |
Ror2 |
A |
G |
13: 53,264,849 (GRCm39) |
S748P |
probably benign |
Het |
Sart1 |
A |
T |
19: 5,434,905 (GRCm39) |
L167Q |
probably damaging |
Het |
Septin12 |
A |
G |
16: 4,810,055 (GRCm39) |
V160A |
possibly damaging |
Het |
Sgo1 |
T |
C |
17: 53,986,295 (GRCm39) |
S299G |
probably benign |
Het |
Shoc1 |
T |
C |
4: 59,076,140 (GRCm39) |
N601S |
possibly damaging |
Het |
Slc35b4 |
T |
A |
6: 34,140,296 (GRCm39) |
D152V |
probably benign |
Het |
Spata31h1 |
T |
C |
10: 82,120,449 (GRCm39) |
Y4187C |
probably damaging |
Het |
Specc1 |
T |
A |
11: 62,019,235 (GRCm39) |
|
probably null |
Het |
Synj1 |
G |
A |
16: 90,737,371 (GRCm39) |
T1308I |
probably benign |
Het |
Thap12 |
T |
G |
7: 98,359,438 (GRCm39) |
L106V |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,057,916 (GRCm39) |
M1501T |
possibly damaging |
Het |
Top2a |
G |
T |
11: 98,891,663 (GRCm39) |
N1153K |
probably benign |
Het |
Trpm5 |
A |
G |
7: 142,634,723 (GRCm39) |
L658P |
probably damaging |
Het |
Ttc21b |
G |
A |
2: 66,047,548 (GRCm39) |
A849V |
possibly damaging |
Het |
Vcf1 |
C |
T |
11: 113,554,215 (GRCm39) |
G160D |
probably damaging |
Het |
Vmn1r80 |
A |
T |
7: 11,927,750 (GRCm39) |
I287F |
probably damaging |
Het |
Vmn1r87 |
T |
C |
7: 12,865,745 (GRCm39) |
S181G |
probably damaging |
Het |
Vmn2r71 |
A |
T |
7: 85,273,115 (GRCm39) |
H643L |
probably benign |
Het |
Washc5 |
G |
A |
15: 59,238,041 (GRCm39) |
R228C |
probably damaging |
Het |
Wdr72 |
T |
C |
9: 74,117,408 (GRCm39) |
S719P |
probably damaging |
Het |
Xrcc3 |
G |
T |
12: 111,774,336 (GRCm39) |
D164E |
probably benign |
Het |
Zc2hc1b |
G |
A |
10: 13,044,529 (GRCm39) |
R45C |
probably damaging |
Het |
Zfp335 |
A |
G |
2: 164,737,912 (GRCm39) |
Y900H |
probably damaging |
Het |
Zfp512b |
G |
A |
2: 181,228,875 (GRCm39) |
R697C |
probably damaging |
Het |
Zfp60 |
T |
C |
7: 27,448,561 (GRCm39) |
Y410H |
probably damaging |
Het |
Zfp60 |
T |
A |
7: 27,448,696 (GRCm39) |
C455S |
probably damaging |
Het |
Zfp605 |
C |
T |
5: 110,275,157 (GRCm39) |
Q92* |
probably null |
Het |
Zfp64 |
C |
T |
2: 168,767,585 (GRCm39) |
D676N |
probably damaging |
Het |
|
Other mutations in Mipol1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00719:Mipol1
|
APN |
12 |
57,354,139 (GRCm39) |
splice site |
probably benign |
|
IGL01139:Mipol1
|
APN |
12 |
57,352,821 (GRCm39) |
nonsense |
probably null |
|
IGL02679:Mipol1
|
APN |
12 |
57,352,829 (GRCm39) |
missense |
possibly damaging |
0.84 |
IGL03109:Mipol1
|
APN |
12 |
57,411,010 (GRCm39) |
missense |
probably benign |
0.20 |
R0001:Mipol1
|
UTSW |
12 |
57,507,625 (GRCm39) |
splice site |
probably benign |
|
R0220:Mipol1
|
UTSW |
12 |
57,503,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R0271:Mipol1
|
UTSW |
12 |
57,507,740 (GRCm39) |
unclassified |
probably benign |
|
R0284:Mipol1
|
UTSW |
12 |
57,503,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R0496:Mipol1
|
UTSW |
12 |
57,503,963 (GRCm39) |
missense |
probably damaging |
0.99 |
R0538:Mipol1
|
UTSW |
12 |
57,461,197 (GRCm39) |
critical splice donor site |
probably null |
|
R1082:Mipol1
|
UTSW |
12 |
57,372,402 (GRCm39) |
missense |
probably damaging |
0.98 |
R1552:Mipol1
|
UTSW |
12 |
57,352,874 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1558:Mipol1
|
UTSW |
12 |
57,379,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Mipol1
|
UTSW |
12 |
57,379,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R2104:Mipol1
|
UTSW |
12 |
57,352,842 (GRCm39) |
splice site |
probably null |
|
R2495:Mipol1
|
UTSW |
12 |
57,507,776 (GRCm39) |
splice site |
probably benign |
|
R3723:Mipol1
|
UTSW |
12 |
57,503,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4431:Mipol1
|
UTSW |
12 |
57,350,310 (GRCm39) |
missense |
possibly damaging |
0.58 |
R4447:Mipol1
|
UTSW |
12 |
57,399,534 (GRCm39) |
intron |
probably benign |
|
R4654:Mipol1
|
UTSW |
12 |
57,352,918 (GRCm39) |
missense |
probably benign |
0.22 |
R4847:Mipol1
|
UTSW |
12 |
57,350,282 (GRCm39) |
missense |
probably damaging |
0.99 |
R4851:Mipol1
|
UTSW |
12 |
57,379,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R5113:Mipol1
|
UTSW |
12 |
57,543,285 (GRCm39) |
missense |
probably benign |
0.36 |
R5668:Mipol1
|
UTSW |
12 |
57,372,346 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6535:Mipol1
|
UTSW |
12 |
57,352,886 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7172:Mipol1
|
UTSW |
12 |
57,372,321 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7191:Mipol1
|
UTSW |
12 |
57,503,852 (GRCm39) |
missense |
probably benign |
0.01 |
R8508:Mipol1
|
UTSW |
12 |
57,352,874 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8752:Mipol1
|
UTSW |
12 |
57,372,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R8772:Mipol1
|
UTSW |
12 |
57,372,418 (GRCm39) |
missense |
probably benign |
0.23 |
R8861:Mipol1
|
UTSW |
12 |
57,352,802 (GRCm39) |
missense |
probably benign |
0.00 |
R8928:Mipol1
|
UTSW |
12 |
57,507,651 (GRCm39) |
missense |
probably benign |
0.00 |
R9011:Mipol1
|
UTSW |
12 |
57,503,865 (GRCm39) |
missense |
probably benign |
0.03 |
R9250:Mipol1
|
UTSW |
12 |
57,461,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R9383:Mipol1
|
UTSW |
12 |
57,352,820 (GRCm39) |
missense |
probably benign |
0.00 |
|