Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700017N19Rik |
T |
A |
10: 100,612,829 |
Y335* |
probably null |
Het |
Alpk1 |
A |
T |
3: 127,672,494 |
L1121Q |
probably damaging |
Het |
Alpk1 |
A |
G |
3: 127,695,733 |
I99T |
probably damaging |
Het |
Ap2a2 |
T |
A |
7: 141,626,136 |
F717I |
probably damaging |
Het |
Arhgap33 |
C |
T |
7: 30,523,052 |
D1152N |
probably benign |
Het |
Arvcf |
A |
G |
16: 18,401,600 |
D642G |
probably benign |
Het |
Astn1 |
T |
G |
1: 158,502,349 |
M258R |
probably damaging |
Het |
Brinp3 |
C |
G |
1: 146,902,010 |
L732V |
possibly damaging |
Het |
Carmil1 |
T |
C |
13: 24,098,810 |
D547G |
possibly damaging |
Het |
Ccdc177 |
A |
G |
12: 80,759,018 |
F161L |
possibly damaging |
Het |
Cfap57 |
C |
T |
4: 118,614,931 |
V84I |
probably benign |
Het |
Cnot10 |
A |
G |
9: 114,625,903 |
Y221H |
probably damaging |
Het |
Col6a3 |
T |
A |
1: 90,828,133 |
I145F |
probably damaging |
Het |
Crybg2 |
A |
G |
4: 134,074,123 |
T865A |
probably benign |
Het |
Cyp4f37 |
A |
G |
17: 32,629,844 |
S229G |
possibly damaging |
Het |
Ddx56 |
G |
A |
11: 6,261,720 |
T462I |
probably damaging |
Het |
Dhx30 |
T |
C |
9: 110,092,898 |
M239V |
probably benign |
Het |
Dusp9 |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
TAAAGCGGAGGCCAAAGCGGAGGCCAAAGCGGAGGCTAAAGCGGAGGCCAAAGCGGAGGCCAAAG |
X: 73,640,611 |
|
probably benign |
Het |
Enpp5 |
G |
A |
17: 44,085,264 |
G356S |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,620,239 |
K994E |
probably damaging |
Het |
Fam83a |
A |
C |
15: 57,986,425 |
T122P |
probably benign |
Het |
Fbxo24 |
C |
A |
5: 137,619,623 |
C293F |
possibly damaging |
Het |
Fech |
A |
T |
18: 64,458,184 |
S390T |
probably benign |
Het |
Fras1 |
A |
G |
5: 96,614,889 |
H750R |
probably benign |
Het |
Frmpd2 |
A |
G |
14: 33,571,969 |
D1364G |
probably benign |
Het |
Ganab |
T |
C |
19: 8,912,528 |
I652T |
probably benign |
Het |
Gm21103 |
T |
A |
14: 6,301,955 |
T153S |
probably benign |
Het |
Gm21886 |
GGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGTTAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG |
GGGCCTGCAGACAGTAGGTACTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGGCCTGCAGACAGTAGGTGCTCACTGAGACCTGCAGACAGTAGGTGCTCACTGAG |
18: 80,089,752 |
|
probably benign |
Het |
Gm5799 |
A |
G |
14: 43,544,538 |
I56V |
possibly damaging |
Het |
Gm7276 |
T |
C |
18: 77,185,487 |
R184G |
unknown |
Het |
Gmip |
T |
G |
8: 69,820,499 |
D845E |
probably benign |
Het |
Hspa9 |
T |
C |
18: 34,949,029 |
K175E |
probably damaging |
Het |
Ipo13 |
A |
G |
4: 117,894,871 |
F890L |
probably benign |
Het |
Klrb1f |
C |
T |
6: 129,056,345 |
R179* |
probably null |
Het |
Mrvi1 |
A |
T |
7: 110,923,756 |
V160D |
probably benign |
Het |
Nasp |
A |
G |
4: 116,610,588 |
V400A |
possibly damaging |
Het |
Ncoa7 |
T |
A |
10: 30,722,851 |
K25N |
possibly damaging |
Het |
Ndrg1 |
A |
C |
15: 66,960,533 |
M1R |
probably null |
Het |
Nf1 |
G |
A |
11: 79,473,414 |
A1557T |
probably damaging |
Het |
Nrde2 |
G |
A |
12: 100,142,250 |
Q361* |
probably null |
Het |
Olfr1330 |
A |
T |
4: 118,893,130 |
I16F |
possibly damaging |
Het |
Olfr150 |
T |
C |
9: 39,737,126 |
F104L |
probably benign |
Het |
Olfr221 |
A |
T |
14: 52,035,853 |
L86* |
probably null |
Het |
Olfr350 |
T |
C |
2: 36,850,466 |
L140P |
probably benign |
Het |
Olfr366 |
C |
T |
2: 37,219,762 |
T91I |
possibly damaging |
Het |
Olfr829 |
A |
T |
9: 18,856,789 |
I46F |
possibly damaging |
Het |
Opn1sw |
A |
T |
6: 29,379,857 |
L126Q |
probably damaging |
Het |
Osmr |
A |
G |
15: 6,823,567 |
Y616H |
probably damaging |
Het |
Pagr1a |
T |
C |
7: 127,016,564 |
T120A |
probably benign |
Het |
Patj |
A |
G |
4: 98,411,139 |
E166G |
probably damaging |
Het |
Plk4 |
G |
A |
3: 40,812,178 |
V764I |
probably benign |
Het |
Polr3h |
G |
A |
15: 81,916,401 |
|
probably null |
Het |
Ptprb |
T |
A |
10: 116,341,138 |
D989E |
probably benign |
Het |
Sdk2 |
A |
T |
11: 113,868,083 |
|
probably null |
Het |
Setd1b |
C |
A |
5: 123,152,576 |
R869S |
unknown |
Het |
Sgcz |
T |
C |
8: 37,523,411 |
I263V |
probably benign |
Het |
Skint8 |
G |
A |
4: 111,928,561 |
G68D |
probably benign |
Het |
Slc22a7 |
A |
T |
17: 46,434,627 |
V326E |
probably benign |
Het |
Slc39a1 |
T |
G |
3: 90,249,089 |
L38R |
probably damaging |
Het |
Slc4a4 |
A |
G |
5: 89,214,647 |
|
probably null |
Het |
Sptlc3 |
A |
G |
2: 139,589,617 |
E353G |
possibly damaging |
Het |
Ssh2 |
G |
T |
11: 77,450,108 |
L695F |
probably damaging |
Het |
Tacr2 |
C |
A |
10: 62,261,648 |
Y302* |
probably null |
Het |
Tas2r117 |
T |
C |
6: 132,803,229 |
L110P |
probably damaging |
Het |
Tex9 |
A |
T |
9: 72,486,778 |
|
probably null |
Het |
Tmem17 |
A |
T |
11: 22,518,645 |
T195S |
probably benign |
Het |
Trcg1 |
T |
A |
9: 57,241,483 |
S113T |
probably benign |
Het |
Trpa1 |
A |
T |
1: 14,884,198 |
F826I |
probably benign |
Het |
Usp17lc |
A |
G |
7: 103,418,368 |
Y290C |
probably damaging |
Het |
Vmn2r32 |
T |
A |
7: 7,474,213 |
D393V |
possibly damaging |
Het |
Wdfy4 |
A |
G |
14: 33,149,584 |
L290P |
|
Het |
Xpnpep1 |
G |
C |
19: 53,006,291 |
A302G |
probably benign |
Het |
Zgrf1 |
A |
G |
3: 127,563,071 |
S649G |
probably benign |
Het |
Zscan4b |
C |
T |
7: 10,900,864 |
C484Y |
probably damaging |
Het |
Zscan4b |
T |
C |
7: 10,901,893 |
D169G |
probably benign |
Het |
|