Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700049A03Rik |
G |
T |
12: 71,211,320 (GRCm39) |
E685* |
probably null |
Het |
2700049A03Rik |
A |
T |
12: 71,211,321 (GRCm39) |
E685V |
possibly damaging |
Het |
3425401B19Rik |
T |
C |
14: 32,385,650 (GRCm39) |
Y105C |
possibly damaging |
Het |
Aoc1l3 |
C |
T |
6: 48,964,928 (GRCm39) |
P312L |
possibly damaging |
Het |
Apol7e |
A |
T |
15: 77,602,262 (GRCm39) |
T287S |
probably benign |
Het |
Arhgap12 |
A |
T |
18: 6,037,057 (GRCm39) |
N561K |
probably benign |
Het |
Armc3 |
G |
T |
2: 19,305,476 (GRCm39) |
A757S |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,799,240 (GRCm39) |
S295T |
probably benign |
Het |
Brd4 |
T |
A |
17: 32,430,244 (GRCm39) |
K686N |
possibly damaging |
Het |
Btnl6 |
T |
C |
17: 34,727,202 (GRCm39) |
T443A |
probably benign |
Het |
Cacna1g |
T |
C |
11: 94,306,922 (GRCm39) |
T1801A |
probably damaging |
Het |
Celsr2 |
G |
A |
3: 108,310,555 (GRCm39) |
T1509I |
possibly damaging |
Het |
Cers1 |
A |
G |
8: 70,782,660 (GRCm39) |
D10G |
possibly damaging |
Het |
Cntnap3 |
A |
G |
13: 64,929,618 (GRCm39) |
V527A |
probably damaging |
Het |
Cog1 |
G |
T |
11: 113,545,836 (GRCm39) |
M370I |
probably benign |
Het |
Col6a6 |
C |
G |
9: 105,657,891 (GRCm39) |
V774L |
probably damaging |
Het |
Csf1r |
T |
A |
18: 61,245,836 (GRCm39) |
S264R |
probably benign |
Het |
Ctnna2 |
A |
T |
6: 76,931,740 (GRCm39) |
V620D |
probably damaging |
Het |
Eif2b4 |
A |
G |
5: 31,348,512 (GRCm39) |
S88P |
possibly damaging |
Het |
Frmd4b |
G |
A |
6: 97,300,690 (GRCm39) |
L214F |
possibly damaging |
Het |
Fstl1 |
T |
A |
16: 37,647,113 (GRCm39) |
L161Q |
probably damaging |
Het |
Hdac1 |
A |
G |
4: 129,418,113 (GRCm39) |
F94S |
probably damaging |
Het |
Hlf |
T |
C |
11: 90,278,929 (GRCm39) |
D45G |
probably benign |
Het |
Hps3 |
A |
T |
3: 20,072,976 (GRCm39) |
M501K |
probably damaging |
Het |
Ighv14-4 |
A |
G |
12: 114,140,174 (GRCm39) |
Y79H |
probably damaging |
Het |
Ip6k1 |
T |
A |
9: 107,923,086 (GRCm39) |
V406D |
probably damaging |
Het |
Iqcf1 |
T |
C |
9: 106,379,077 (GRCm39) |
S29P |
probably benign |
Het |
Itga11 |
A |
G |
9: 62,678,664 (GRCm39) |
T944A |
probably benign |
Het |
Kcnj12 |
A |
G |
11: 60,961,103 (GRCm39) |
N467S |
probably benign |
Het |
Klhdc3 |
T |
A |
17: 46,988,858 (GRCm39) |
N111Y |
possibly damaging |
Het |
Kmt2c |
T |
C |
5: 25,614,136 (GRCm39) |
R195G |
possibly damaging |
Het |
Lin9 |
A |
G |
1: 180,486,676 (GRCm39) |
I81V |
probably null |
Het |
Lrp2 |
T |
C |
2: 69,331,892 (GRCm39) |
D1621G |
probably damaging |
Het |
Neb |
A |
G |
2: 52,146,801 (GRCm39) |
I2821T |
possibly damaging |
Het |
Or14j6 |
T |
C |
17: 38,214,464 (GRCm39) |
V9A |
probably benign |
Het |
Or2a25 |
A |
T |
6: 42,889,271 (GRCm39) |
K271N |
probably damaging |
Het |
Or4c112 |
G |
T |
2: 88,853,770 (GRCm39) |
H192Q |
probably benign |
Het |
Or56b1 |
A |
T |
7: 104,285,540 (GRCm39) |
I220L |
possibly damaging |
Het |
Or8b3b |
C |
T |
9: 38,584,159 (GRCm39) |
V207I |
probably benign |
Het |
Paxip1 |
A |
G |
5: 27,977,027 (GRCm39) |
|
probably benign |
Het |
Pfas |
T |
C |
11: 68,880,779 (GRCm39) |
|
probably benign |
Het |
Pfdn1 |
C |
T |
18: 36,584,145 (GRCm39) |
G63D |
probably damaging |
Het |
Pgghg |
T |
C |
7: 140,525,208 (GRCm39) |
F405L |
probably damaging |
Het |
Plcd3 |
T |
C |
11: 102,992,209 (GRCm39) |
M50V |
probably null |
Het |
Plekha8 |
C |
A |
6: 54,596,334 (GRCm39) |
S198R |
probably benign |
Het |
Ppp4c |
C |
T |
7: 126,386,499 (GRCm39) |
G166D |
probably damaging |
Het |
Rassf2 |
T |
C |
2: 131,840,180 (GRCm39) |
|
probably null |
Het |
Rnf217 |
T |
A |
10: 31,379,804 (GRCm39) |
I473F |
possibly damaging |
Het |
Sec16a |
G |
C |
2: 26,331,825 (GRCm39) |
N63K |
possibly damaging |
Het |
Sik3 |
A |
G |
9: 46,130,784 (GRCm39) |
D1240G |
probably benign |
Het |
Slamf1 |
A |
G |
1: 171,625,745 (GRCm39) |
D307G |
probably null |
Het |
Slc2a3 |
A |
G |
6: 122,709,388 (GRCm39) |
I337T |
probably benign |
Het |
Tent4a |
A |
G |
13: 69,661,115 (GRCm39) |
V51A |
probably damaging |
Het |
Tinag |
C |
T |
9: 76,859,187 (GRCm39) |
D474N |
probably benign |
Het |
Ublcp1 |
A |
G |
11: 44,349,109 (GRCm39) |
F242L |
probably benign |
Het |
Ucp1 |
C |
A |
8: 84,017,270 (GRCm39) |
A20D |
probably damaging |
Het |
Ugt1a7c |
C |
T |
1: 88,023,104 (GRCm39) |
R88W |
possibly damaging |
Het |
Wipf3 |
A |
G |
6: 54,458,780 (GRCm39) |
D45G |
probably damaging |
Het |
Zfp592 |
G |
A |
7: 80,674,280 (GRCm39) |
A415T |
probably benign |
Het |
|
Other mutations in Med15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00235:Med15
|
APN |
16 |
17,498,590 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL00780:Med15
|
APN |
16 |
17,471,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02365:Med15
|
APN |
16 |
17,489,470 (GRCm39) |
intron |
probably benign |
|
R0324:Med15
|
UTSW |
16 |
17,515,476 (GRCm39) |
missense |
probably damaging |
0.98 |
R1225:Med15
|
UTSW |
16 |
17,540,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Med15
|
UTSW |
16 |
17,540,644 (GRCm39) |
missense |
probably damaging |
0.96 |
R1745:Med15
|
UTSW |
16 |
17,473,570 (GRCm39) |
unclassified |
probably benign |
|
R1801:Med15
|
UTSW |
16 |
17,498,599 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1838:Med15
|
UTSW |
16 |
17,471,426 (GRCm39) |
missense |
probably benign |
0.11 |
R1901:Med15
|
UTSW |
16 |
17,491,018 (GRCm39) |
unclassified |
probably benign |
|
R2153:Med15
|
UTSW |
16 |
17,503,315 (GRCm39) |
critical splice donor site |
probably null |
|
R2974:Med15
|
UTSW |
16 |
17,470,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R3808:Med15
|
UTSW |
16 |
17,473,598 (GRCm39) |
unclassified |
probably benign |
|
R4240:Med15
|
UTSW |
16 |
17,473,358 (GRCm39) |
missense |
probably damaging |
1.00 |
R4483:Med15
|
UTSW |
16 |
17,489,428 (GRCm39) |
intron |
probably benign |
|
R4484:Med15
|
UTSW |
16 |
17,489,428 (GRCm39) |
intron |
probably benign |
|
R4577:Med15
|
UTSW |
16 |
17,492,379 (GRCm39) |
nonsense |
probably null |
|
R5652:Med15
|
UTSW |
16 |
17,473,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R6244:Med15
|
UTSW |
16 |
17,470,609 (GRCm39) |
nonsense |
probably null |
|
R6701:Med15
|
UTSW |
16 |
17,489,447 (GRCm39) |
intron |
probably benign |
|
R6793:Med15
|
UTSW |
16 |
17,470,567 (GRCm39) |
unclassified |
probably benign |
|
R7036:Med15
|
UTSW |
16 |
17,516,019 (GRCm39) |
start codon destroyed |
probably null |
|
R7038:Med15
|
UTSW |
16 |
17,470,591 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7211:Med15
|
UTSW |
16 |
17,515,977 (GRCm39) |
missense |
unknown |
|
R7317:Med15
|
UTSW |
16 |
17,489,507 (GRCm39) |
missense |
unknown |
|
R7390:Med15
|
UTSW |
16 |
17,540,626 (GRCm39) |
missense |
unknown |
|
R7471:Med15
|
UTSW |
16 |
17,540,729 (GRCm39) |
missense |
probably benign |
0.03 |
R7726:Med15
|
UTSW |
16 |
17,473,038 (GRCm39) |
missense |
possibly damaging |
0.87 |
R8872:Med15
|
UTSW |
16 |
17,470,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R9043:Med15
|
UTSW |
16 |
17,470,582 (GRCm39) |
missense |
probably benign |
0.07 |
R9084:Med15
|
UTSW |
16 |
17,471,072 (GRCm39) |
missense |
probably damaging |
0.99 |
R9089:Med15
|
UTSW |
16 |
17,473,421 (GRCm39) |
missense |
unknown |
|
R9363:Med15
|
UTSW |
16 |
17,489,414 (GRCm39) |
missense |
unknown |
|
Z1177:Med15
|
UTSW |
16 |
17,471,096 (GRCm39) |
missense |
possibly damaging |
0.81 |
|