Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610028H24Rik |
C |
T |
10: 76,285,115 (GRCm39) |
A8V |
probably benign |
Het |
Ago1 |
G |
A |
4: 126,357,628 (GRCm39) |
P16S |
probably benign |
Het |
Ak5 |
C |
T |
3: 152,187,306 (GRCm39) |
E394K |
probably benign |
Het |
Aldh7a1 |
T |
C |
18: 56,660,068 (GRCm39) |
Y498C |
probably damaging |
Het |
Alox12 |
T |
A |
11: 70,141,030 (GRCm39) |
D335V |
probably damaging |
Het |
Alx4 |
A |
T |
2: 93,498,904 (GRCm39) |
Y212F |
probably damaging |
Het |
Asb16 |
A |
G |
11: 102,167,303 (GRCm39) |
E223G |
probably damaging |
Het |
Atg9b |
C |
T |
5: 24,595,575 (GRCm39) |
V235M |
probably damaging |
Het |
BB014433 |
A |
G |
8: 15,092,304 (GRCm39) |
V183A |
probably benign |
Het |
Brca1 |
T |
A |
11: 101,414,367 (GRCm39) |
M1256L |
probably benign |
Het |
Bst1 |
A |
G |
5: 43,977,932 (GRCm39) |
I94V |
probably benign |
Het |
C3ar1 |
A |
G |
6: 122,827,599 (GRCm39) |
L206P |
probably benign |
Het |
Cabs1 |
T |
A |
5: 88,128,522 (GRCm39) |
M391K |
possibly damaging |
Het |
Cars1 |
C |
T |
7: 143,118,744 (GRCm39) |
R599Q |
probably damaging |
Het |
Ccdc190 |
T |
A |
1: 169,760,592 (GRCm39) |
Y73* |
probably null |
Het |
Cd177 |
A |
C |
7: 24,443,671 (GRCm39) |
L809W |
probably benign |
Het |
Cemip |
C |
A |
7: 83,600,805 (GRCm39) |
G939* |
probably null |
Het |
Clca3b |
T |
A |
3: 144,531,020 (GRCm39) |
I777F |
probably benign |
Het |
Cma2 |
T |
C |
14: 56,211,236 (GRCm39) |
I176T |
probably damaging |
Het |
Col12a1 |
T |
A |
9: 79,554,887 (GRCm39) |
T2064S |
probably damaging |
Het |
Csf1r |
A |
G |
18: 61,262,805 (GRCm39) |
N860S |
probably damaging |
Het |
Dab1 |
T |
A |
4: 104,369,461 (GRCm39) |
C3S |
probably benign |
Het |
Dennd4b |
A |
G |
3: 90,174,918 (GRCm39) |
E50G |
probably damaging |
Het |
Dis3l |
A |
T |
9: 64,214,795 (GRCm39) |
S925T |
probably benign |
Het |
Disp1 |
T |
C |
1: 182,868,076 (GRCm39) |
N1448S |
probably benign |
Het |
Dpp10 |
T |
C |
1: 123,264,580 (GRCm39) |
I747M |
probably damaging |
Het |
Enpp5 |
G |
A |
17: 44,396,155 (GRCm39) |
G356S |
probably damaging |
Het |
Ephx4 |
A |
T |
5: 107,551,522 (GRCm39) |
K36* |
probably null |
Het |
Fam135a |
C |
T |
1: 24,053,953 (GRCm39) |
V1195I |
probably damaging |
Het |
Fap |
A |
T |
2: 62,376,947 (GRCm39) |
Y234* |
probably null |
Het |
Fem1c |
A |
T |
18: 46,638,942 (GRCm39) |
N353K |
possibly damaging |
Het |
Furin |
C |
A |
7: 80,043,365 (GRCm39) |
R282L |
probably damaging |
Het |
Gm10549 |
C |
A |
18: 33,597,358 (GRCm39) |
|
probably benign |
Het |
Gm5930 |
A |
G |
14: 44,568,828 (GRCm39) |
*265Q |
probably null |
Het |
Hcrtr1 |
T |
A |
4: 130,031,379 (GRCm39) |
T15S |
probably benign |
Het |
Ifnar1 |
C |
T |
16: 91,296,425 (GRCm39) |
Q309* |
probably null |
Het |
Il18r1 |
A |
T |
1: 40,528,867 (GRCm39) |
I304L |
probably benign |
Het |
Ino80 |
A |
T |
2: 119,281,922 (GRCm39) |
Y185N |
probably damaging |
Het |
Itgb2 |
G |
A |
10: 77,395,507 (GRCm39) |
C536Y |
probably damaging |
Het |
Ivns1abp |
T |
C |
1: 151,236,744 (GRCm39) |
M435T |
probably benign |
Het |
Kcnh4 |
T |
C |
11: 100,647,911 (GRCm39) |
N151D |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,628,405 (GRCm39) |
M1499T |
probably benign |
Het |
Lamb1 |
A |
T |
12: 31,373,461 (GRCm39) |
T1397S |
possibly damaging |
Het |
Leng1 |
G |
A |
7: 3,664,211 (GRCm39) |
R239* |
probably null |
Het |
Map2k4 |
A |
T |
11: 65,584,355 (GRCm39) |
N309K |
possibly damaging |
Het |
Mcm3 |
A |
G |
1: 20,873,768 (GRCm39) |
F784S |
probably damaging |
Het |
Mrgpra9 |
T |
A |
7: 46,884,884 (GRCm39) |
N260I |
probably benign |
Het |
Mrnip |
C |
A |
11: 50,090,679 (GRCm39) |
T281N |
possibly damaging |
Het |
Myo9b |
A |
G |
8: 71,808,501 (GRCm39) |
T1715A |
possibly damaging |
Het |
Nectin3 |
A |
G |
16: 46,269,184 (GRCm39) |
I406T |
possibly damaging |
Het |
Neto1 |
A |
G |
18: 86,516,699 (GRCm39) |
T339A |
possibly damaging |
Het |
Ntn1 |
T |
C |
11: 68,104,025 (GRCm39) |
D541G |
probably damaging |
Het |
Nuak2 |
C |
A |
1: 132,244,132 (GRCm39) |
H55Q |
probably damaging |
Het |
Nufip2 |
A |
G |
11: 77,582,439 (GRCm39) |
T118A |
probably benign |
Het |
Or11i1 |
T |
G |
3: 106,729,638 (GRCm39) |
N79T |
possibly damaging |
Het |
Or12e7 |
T |
A |
2: 87,288,271 (GRCm39) |
V254E |
probably damaging |
Het |
Or51af1 |
T |
A |
7: 103,141,858 (GRCm39) |
T76S |
probably damaging |
Het |
Or52e19 |
C |
A |
7: 102,959,000 (GRCm39) |
A24D |
probably benign |
Het |
Or5d16 |
A |
T |
2: 87,773,518 (GRCm39) |
Y151* |
probably null |
Het |
Or5p59 |
T |
C |
7: 107,702,774 (GRCm39) |
V86A |
probably benign |
Het |
Or6d13 |
C |
T |
6: 116,517,561 (GRCm39) |
T49M |
probably benign |
Het |
Or7a40 |
A |
T |
16: 16,491,784 (GRCm39) |
D20E |
probably benign |
Het |
Or7g29 |
T |
C |
9: 19,286,237 (GRCm39) |
*313W |
probably null |
Het |
Pcdhb5 |
T |
A |
18: 37,453,933 (GRCm39) |
H104Q |
probably benign |
Het |
Phf11a |
T |
C |
14: 59,514,986 (GRCm39) |
R232G |
probably damaging |
Het |
Pik3r5 |
C |
T |
11: 68,383,615 (GRCm39) |
T478I |
probably benign |
Het |
Prkacb |
T |
A |
3: 146,438,401 (GRCm39) |
E380V |
probably damaging |
Het |
Prl7c1 |
G |
T |
13: 27,957,776 (GRCm39) |
D221E |
probably damaging |
Het |
Prr11 |
T |
A |
11: 86,996,950 (GRCm39) |
K5* |
probably null |
Het |
Prrc2b |
G |
A |
2: 32,112,332 (GRCm39) |
G1932D |
probably damaging |
Het |
Rexo1 |
A |
T |
10: 80,378,845 (GRCm39) |
Y1064N |
possibly damaging |
Het |
Rnf182 |
C |
T |
13: 43,822,147 (GRCm39) |
Q233* |
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Sash1 |
C |
G |
10: 8,605,291 (GRCm39) |
G1033A |
probably benign |
Het |
Sncaip |
C |
A |
18: 53,039,609 (GRCm39) |
S189* |
probably null |
Het |
Sorl1 |
T |
C |
9: 41,982,530 (GRCm39) |
Y350C |
probably damaging |
Het |
Speg |
T |
C |
1: 75,383,328 (GRCm39) |
V1141A |
possibly damaging |
Het |
Speg |
C |
A |
1: 75,406,167 (GRCm39) |
D3091E |
possibly damaging |
Het |
Sucnr1 |
A |
T |
3: 59,994,144 (GRCm39) |
D224V |
probably benign |
Het |
Tg |
G |
A |
15: 66,631,407 (GRCm39) |
A559T |
probably damaging |
Het |
Tmem132d |
A |
G |
5: 127,861,502 (GRCm39) |
I873T |
probably benign |
Het |
Tmem229a |
C |
T |
6: 24,954,920 (GRCm39) |
C278Y |
probably damaging |
Het |
Togaram1 |
T |
C |
12: 65,013,364 (GRCm39) |
I205T |
possibly damaging |
Het |
Usp19 |
T |
A |
9: 108,374,082 (GRCm39) |
L713Q |
probably damaging |
Het |
Vsig10 |
A |
G |
5: 117,489,824 (GRCm39) |
D530G |
possibly damaging |
Het |
Zfp106 |
A |
G |
2: 120,364,983 (GRCm39) |
S475P |
probably damaging |
Het |
|
Other mutations in 1700010I14Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00988:1700010I14Rik
|
APN |
17 |
9,215,937 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01569:1700010I14Rik
|
APN |
17 |
9,215,827 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03024:1700010I14Rik
|
APN |
17 |
9,212,464 (GRCm39) |
missense |
probably benign |
0.33 |
IGL03410:1700010I14Rik
|
APN |
17 |
9,220,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0017:1700010I14Rik
|
UTSW |
17 |
9,226,938 (GRCm39) |
utr 3 prime |
probably benign |
|
R0324:1700010I14Rik
|
UTSW |
17 |
9,219,989 (GRCm39) |
missense |
probably benign |
0.33 |
R0361:1700010I14Rik
|
UTSW |
17 |
9,211,378 (GRCm39) |
missense |
probably benign |
0.39 |
R0482:1700010I14Rik
|
UTSW |
17 |
9,207,255 (GRCm39) |
critical splice donor site |
probably null |
|
R0529:1700010I14Rik
|
UTSW |
17 |
9,211,228 (GRCm39) |
missense |
probably benign |
0.32 |
R1102:1700010I14Rik
|
UTSW |
17 |
9,211,460 (GRCm39) |
missense |
probably damaging |
1.00 |
R1964:1700010I14Rik
|
UTSW |
17 |
9,211,324 (GRCm39) |
missense |
probably damaging |
0.99 |
R3620:1700010I14Rik
|
UTSW |
17 |
9,226,864 (GRCm39) |
missense |
probably benign |
0.15 |
R4259:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4261:1700010I14Rik
|
UTSW |
17 |
9,214,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R4687:1700010I14Rik
|
UTSW |
17 |
9,210,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R4707:1700010I14Rik
|
UTSW |
17 |
9,224,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:1700010I14Rik
|
UTSW |
17 |
9,226,845 (GRCm39) |
missense |
probably benign |
0.41 |
R4979:1700010I14Rik
|
UTSW |
17 |
9,220,643 (GRCm39) |
missense |
probably damaging |
1.00 |
R5225:1700010I14Rik
|
UTSW |
17 |
9,226,839 (GRCm39) |
nonsense |
probably null |
|
R5383:1700010I14Rik
|
UTSW |
17 |
9,211,532 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6031:1700010I14Rik
|
UTSW |
17 |
9,214,084 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6736:1700010I14Rik
|
UTSW |
17 |
9,211,100 (GRCm39) |
missense |
probably benign |
0.01 |
R7089:1700010I14Rik
|
UTSW |
17 |
9,226,927 (GRCm39) |
missense |
probably benign |
0.00 |
R7097:1700010I14Rik
|
UTSW |
17 |
9,224,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R7292:1700010I14Rik
|
UTSW |
17 |
9,215,861 (GRCm39) |
nonsense |
probably null |
|
R7405:1700010I14Rik
|
UTSW |
17 |
9,220,649 (GRCm39) |
missense |
probably damaging |
0.99 |
R7567:1700010I14Rik
|
UTSW |
17 |
9,226,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R7877:1700010I14Rik
|
UTSW |
17 |
9,220,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R8794:1700010I14Rik
|
UTSW |
17 |
9,226,939 (GRCm39) |
missense |
unknown |
|
R8805:1700010I14Rik
|
UTSW |
17 |
9,226,737 (GRCm39) |
nonsense |
probably null |
|
R9007:1700010I14Rik
|
UTSW |
17 |
9,226,935 (GRCm39) |
missense |
probably benign |
0.01 |
R9308:1700010I14Rik
|
UTSW |
17 |
9,220,667 (GRCm39) |
nonsense |
probably null |
|
R9400:1700010I14Rik
|
UTSW |
17 |
9,211,118 (GRCm39) |
missense |
probably benign |
0.01 |
|