Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930426L09Rik |
T |
C |
2: 19,003,653 (GRCm39) |
|
probably benign |
Het |
4930590J08Rik |
T |
C |
6: 91,919,311 (GRCm39) |
S657P |
probably damaging |
Het |
Abca9 |
T |
C |
11: 110,025,080 (GRCm39) |
I988V |
probably benign |
Het |
Acte1 |
A |
G |
7: 143,425,524 (GRCm39) |
T58A |
probably benign |
Het |
Aox4 |
T |
A |
1: 58,270,662 (GRCm39) |
D280E |
probably benign |
Het |
Apob |
T |
A |
12: 8,055,060 (GRCm39) |
L1353* |
probably null |
Het |
Atp2b1 |
C |
T |
10: 98,858,691 (GRCm39) |
R222C |
probably damaging |
Het |
AW209491 |
T |
G |
13: 14,811,668 (GRCm39) |
S174A |
possibly damaging |
Het |
B930094E09Rik |
G |
C |
18: 31,742,911 (GRCm39) |
|
probably benign |
Het |
Cbln3 |
G |
T |
14: 56,121,517 (GRCm39) |
P43Q |
possibly damaging |
Het |
Ccdc181 |
A |
T |
1: 164,107,487 (GRCm39) |
T57S |
probably benign |
Het |
Ccr2 |
A |
C |
9: 123,906,008 (GRCm39) |
N96T |
probably damaging |
Het |
Cep131 |
T |
C |
11: 119,956,837 (GRCm39) |
I868V |
probably benign |
Het |
Chd2 |
A |
G |
7: 73,094,071 (GRCm39) |
I1535T |
probably damaging |
Het |
Chl1 |
A |
T |
6: 103,660,204 (GRCm39) |
T377S |
probably benign |
Het |
Cpeb3 |
A |
G |
19: 37,065,853 (GRCm39) |
F439L |
probably damaging |
Het |
Crb2 |
T |
C |
2: 37,680,269 (GRCm39) |
V399A |
probably damaging |
Het |
Cry2 |
C |
T |
2: 92,244,187 (GRCm39) |
G329R |
probably damaging |
Het |
Dock4 |
A |
G |
12: 40,781,868 (GRCm39) |
E691G |
probably benign |
Het |
Edil3 |
A |
T |
13: 88,970,108 (GRCm39) |
H3L |
probably benign |
Het |
Fpr3 |
G |
A |
17: 18,190,919 (GRCm39) |
W63* |
probably null |
Het |
Gtse1 |
T |
G |
15: 85,753,158 (GRCm39) |
N424K |
possibly damaging |
Het |
Kcnt1 |
G |
A |
2: 25,783,192 (GRCm39) |
V252M |
probably damaging |
Het |
Kifbp |
G |
A |
10: 62,399,029 (GRCm39) |
Q130* |
probably null |
Het |
Lmbrd2 |
T |
G |
15: 9,149,262 (GRCm39) |
I48M |
probably damaging |
Het |
Lrrc7 |
T |
G |
3: 158,059,069 (GRCm39) |
I13L |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,822,386 (GRCm39) |
S408P |
probably benign |
Het |
Mphosph10 |
A |
G |
7: 64,028,529 (GRCm39) |
V542A |
possibly damaging |
Het |
Msto1 |
C |
A |
3: 88,818,254 (GRCm39) |
R331L |
probably damaging |
Het |
Myh10 |
G |
A |
11: 68,692,979 (GRCm39) |
E1425K |
probably damaging |
Het |
Nup43 |
T |
C |
10: 7,554,437 (GRCm39) |
I340T |
probably benign |
Het |
Or1j4 |
T |
C |
2: 36,740,846 (GRCm39) |
S263P |
possibly damaging |
Het |
Pcm1 |
T |
A |
8: 41,736,669 (GRCm39) |
M884K |
probably damaging |
Het |
Phf20 |
T |
A |
2: 156,140,573 (GRCm39) |
L749H |
probably damaging |
Het |
Pigp |
T |
C |
16: 94,171,226 (GRCm39) |
R22G |
probably null |
Het |
Polr2b |
T |
C |
5: 77,468,824 (GRCm39) |
M200T |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,580,471 (GRCm39) |
D668E |
unknown |
Het |
Prss3 |
G |
A |
6: 41,352,060 (GRCm39) |
R68C |
probably benign |
Het |
Retreg3 |
G |
A |
11: 100,994,721 (GRCm39) |
|
probably benign |
Het |
Shank1 |
T |
C |
7: 44,006,630 (GRCm39) |
F2116L |
possibly damaging |
Het |
Spg21 |
T |
C |
9: 65,376,090 (GRCm39) |
S33P |
possibly damaging |
Het |
Spns3 |
A |
G |
11: 72,390,349 (GRCm39) |
S432P |
probably damaging |
Het |
Stra6 |
A |
G |
9: 58,042,452 (GRCm39) |
E27G |
probably damaging |
Het |
Tanc1 |
A |
G |
2: 59,673,320 (GRCm39) |
Q1468R |
probably benign |
Het |
Tbce |
T |
G |
13: 14,194,362 (GRCm39) |
E99A |
probably benign |
Het |
Tmem106b |
T |
C |
6: 13,084,252 (GRCm39) |
V252A |
probably damaging |
Het |
Trim10 |
A |
G |
17: 37,187,923 (GRCm39) |
T380A |
probably damaging |
Het |
Trim31 |
T |
A |
17: 37,220,501 (GRCm39) |
D472E |
probably damaging |
Het |
Vmn2r28 |
G |
A |
7: 5,491,003 (GRCm39) |
Q415* |
probably null |
Het |
Vwf |
G |
A |
6: 125,626,252 (GRCm39) |
C7Y |
unknown |
Het |
Yeats2 |
C |
T |
16: 20,033,225 (GRCm39) |
P1088L |
probably benign |
Het |
Zfp40 |
C |
A |
17: 23,397,354 (GRCm39) |
V48L |
possibly damaging |
Het |
|
Other mutations in Endod1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00472:Endod1
|
APN |
9 |
14,268,049 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01302:Endod1
|
APN |
9 |
14,268,535 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02895:Endod1
|
APN |
9 |
14,268,166 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02994:Endod1
|
APN |
9 |
14,268,183 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03120:Endod1
|
APN |
9 |
14,268,331 (GRCm39) |
missense |
probably damaging |
0.98 |
royal_gorge
|
UTSW |
9 |
14,268,166 (GRCm39) |
missense |
probably benign |
0.06 |
R0745:Endod1
|
UTSW |
9 |
14,268,413 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1087:Endod1
|
UTSW |
9 |
14,268,489 (GRCm39) |
missense |
possibly damaging |
0.69 |
R1829:Endod1
|
UTSW |
9 |
14,268,222 (GRCm39) |
missense |
probably damaging |
1.00 |
R1857:Endod1
|
UTSW |
9 |
14,268,405 (GRCm39) |
missense |
probably benign |
0.05 |
R2120:Endod1
|
UTSW |
9 |
14,268,949 (GRCm39) |
missense |
probably benign |
0.07 |
R3906:Endod1
|
UTSW |
9 |
14,292,151 (GRCm39) |
missense |
probably benign |
0.12 |
R4801:Endod1
|
UTSW |
9 |
14,268,319 (GRCm39) |
missense |
probably benign |
0.05 |
R4802:Endod1
|
UTSW |
9 |
14,268,319 (GRCm39) |
missense |
probably benign |
0.05 |
R5017:Endod1
|
UTSW |
9 |
14,268,187 (GRCm39) |
nonsense |
probably null |
|
R6027:Endod1
|
UTSW |
9 |
14,268,893 (GRCm39) |
nonsense |
probably null |
|
R6279:Endod1
|
UTSW |
9 |
14,268,166 (GRCm39) |
missense |
probably benign |
0.06 |
R6300:Endod1
|
UTSW |
9 |
14,268,166 (GRCm39) |
missense |
probably benign |
0.06 |
R6986:Endod1
|
UTSW |
9 |
14,268,606 (GRCm39) |
missense |
probably damaging |
1.00 |
R7314:Endod1
|
UTSW |
9 |
14,268,295 (GRCm39) |
missense |
probably benign |
0.07 |
R8921:Endod1
|
UTSW |
9 |
14,268,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Endod1
|
UTSW |
9 |
14,292,247 (GRCm39) |
missense |
probably damaging |
0.99 |
|