Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afg3l2 |
A |
G |
18: 67,540,529 (GRCm39) |
I660T |
probably damaging |
Het |
Amtn |
T |
A |
5: 88,532,944 (GRCm39) |
Y186* |
probably null |
Het |
Atosa |
A |
G |
9: 74,917,399 (GRCm39) |
E666G |
probably benign |
Het |
Atrip |
A |
G |
9: 108,894,569 (GRCm39) |
S453P |
possibly damaging |
Het |
Bahcc1 |
T |
C |
11: 120,164,813 (GRCm39) |
L840P |
probably damaging |
Het |
Capn2 |
T |
C |
1: 182,306,165 (GRCm39) |
E527G |
possibly damaging |
Het |
Caprin2 |
A |
T |
6: 148,779,316 (GRCm39) |
Y164N |
possibly damaging |
Het |
Ccnh |
T |
A |
13: 85,344,446 (GRCm39) |
|
probably null |
Het |
Cdon |
G |
T |
9: 35,403,162 (GRCm39) |
V1091F |
possibly damaging |
Het |
Ceacam14 |
A |
G |
7: 17,548,267 (GRCm39) |
Y119C |
probably damaging |
Het |
Ces2h |
A |
G |
8: 105,745,611 (GRCm39) |
K445E |
possibly damaging |
Het |
Cfap46 |
A |
G |
7: 139,191,947 (GRCm39) |
S2357P |
probably damaging |
Het |
Commd4 |
A |
T |
9: 57,063,499 (GRCm39) |
S86R |
possibly damaging |
Het |
Cpsf6 |
A |
T |
10: 117,196,934 (GRCm39) |
|
probably benign |
Het |
Dag1 |
A |
T |
9: 108,086,646 (GRCm39) |
V165E |
probably benign |
Het |
Dmxl1 |
A |
T |
18: 50,065,008 (GRCm39) |
K2618* |
probably null |
Het |
Dnah17 |
A |
G |
11: 117,991,882 (GRCm39) |
Y1229H |
probably benign |
Het |
Endov |
T |
A |
11: 119,382,625 (GRCm39) |
L24Q |
probably damaging |
Het |
Fap |
C |
T |
2: 62,332,803 (GRCm39) |
V717M |
probably damaging |
Het |
Fbxl2 |
A |
G |
9: 113,815,546 (GRCm39) |
L239P |
probably damaging |
Het |
Fbxl5 |
A |
T |
5: 43,916,182 (GRCm39) |
V367D |
possibly damaging |
Het |
Fkbp10 |
G |
T |
11: 100,314,352 (GRCm39) |
W384L |
probably damaging |
Het |
Gbp8 |
C |
T |
5: 105,166,682 (GRCm39) |
V216I |
possibly damaging |
Het |
Gclm |
G |
A |
3: 122,059,936 (GRCm39) |
A239T |
probably benign |
Het |
Gm11569 |
C |
T |
11: 99,689,556 (GRCm39) |
|
probably benign |
Het |
Gnas |
C |
A |
2: 174,141,468 (GRCm39) |
|
probably benign |
Het |
Grb10 |
T |
A |
11: 11,883,566 (GRCm39) |
N508I |
probably benign |
Het |
Gykl1 |
T |
G |
18: 52,827,267 (GRCm39) |
I158M |
probably benign |
Het |
Ide |
G |
A |
19: 37,295,420 (GRCm39) |
T214M |
unknown |
Het |
Il12rb2 |
T |
A |
6: 67,272,262 (GRCm39) |
Q341H |
possibly damaging |
Het |
Ints1 |
T |
C |
5: 139,740,744 (GRCm39) |
E1946G |
probably benign |
Het |
Kdelr3 |
T |
C |
15: 79,410,100 (GRCm39) |
|
probably null |
Het |
Kif1b |
A |
C |
4: 149,358,306 (GRCm39) |
|
probably null |
Het |
Kri1 |
A |
G |
9: 21,191,533 (GRCm39) |
I320T |
probably damaging |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lin9 |
T |
C |
1: 180,486,646 (GRCm39) |
S111P |
probably benign |
Het |
Lpcat2b |
C |
A |
5: 107,580,773 (GRCm39) |
P34Q |
probably damaging |
Het |
Ltk |
T |
A |
2: 119,590,080 (GRCm39) |
T49S |
probably benign |
Het |
Map3k9 |
A |
T |
12: 81,780,896 (GRCm39) |
H421Q |
probably benign |
Het |
Mapkbp1 |
T |
A |
2: 119,852,201 (GRCm39) |
|
probably null |
Het |
Mcm4 |
A |
G |
16: 15,443,434 (GRCm39) |
S830P |
probably damaging |
Het |
Nek10 |
T |
A |
14: 14,860,736 (GRCm38) |
|
probably null |
Het |
Nlrp9b |
A |
T |
7: 19,758,417 (GRCm39) |
R551S |
probably benign |
Het |
Nol4l |
T |
C |
2: 153,260,026 (GRCm39) |
T143A |
probably damaging |
Het |
Or1r1 |
T |
C |
11: 73,875,362 (GRCm39) |
H24R |
possibly damaging |
Het |
Or51g1 |
T |
A |
7: 102,633,748 (GRCm39) |
T208S |
probably benign |
Het |
Or6z5 |
T |
C |
7: 6,477,742 (GRCm39) |
|
probably null |
Het |
Or7a39 |
A |
T |
10: 78,715,919 (GRCm39) |
R304S |
probably benign |
Het |
Pde4dip |
G |
T |
3: 97,616,806 (GRCm39) |
A1812D |
probably damaging |
Het |
Plekhb1 |
C |
A |
7: 100,305,960 (GRCm39) |
G26C |
probably damaging |
Het |
Polr1a |
T |
A |
6: 71,906,410 (GRCm39) |
F409I |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,702,625 (GRCm39) |
M1197K |
probably benign |
Het |
Qrich2 |
T |
C |
11: 116,335,828 (GRCm39) |
I2114V |
probably damaging |
Het |
Rbm27 |
T |
C |
18: 42,450,731 (GRCm39) |
Y449H |
probably damaging |
Het |
Rp1l1 |
A |
G |
14: 64,267,195 (GRCm39) |
D927G |
probably damaging |
Het |
Secisbp2 |
C |
A |
13: 51,833,857 (GRCm39) |
Q666K |
probably damaging |
Het |
Slc45a2 |
T |
C |
15: 11,001,219 (GRCm39) |
I106T |
probably damaging |
Het |
Slx4 |
G |
T |
16: 3,797,831 (GRCm39) |
Q1518K |
probably damaging |
Het |
Smim10l1 |
T |
C |
6: 133,082,489 (GRCm39) |
F12S |
probably damaging |
Het |
Son |
T |
C |
16: 91,468,301 (GRCm39) |
V306A |
possibly damaging |
Het |
Stab1 |
A |
G |
14: 30,882,178 (GRCm39) |
S506P |
probably benign |
Het |
Syne2 |
A |
C |
12: 76,040,919 (GRCm39) |
D3859A |
probably benign |
Het |
Tab1 |
T |
A |
15: 80,032,930 (GRCm39) |
Y71* |
probably null |
Het |
Tarbp1 |
A |
C |
8: 127,174,079 (GRCm39) |
M909R |
probably damaging |
Het |
Tex15 |
T |
G |
8: 34,063,220 (GRCm39) |
S1157R |
probably benign |
Het |
Tnni3 |
G |
A |
7: 4,523,453 (GRCm39) |
T120I |
probably benign |
Het |
Ttn |
T |
C |
2: 76,747,888 (GRCm39) |
E4387G |
probably benign |
Het |
Ugt3a1 |
G |
A |
15: 9,361,534 (GRCm39) |
|
silent |
Het |
Unc5d |
T |
C |
8: 29,156,870 (GRCm39) |
I783V |
probably benign |
Het |
Usp40 |
T |
C |
1: 87,923,474 (GRCm39) |
T266A |
probably benign |
Het |
Vmn2r59 |
C |
T |
7: 41,695,468 (GRCm39) |
V315I |
probably benign |
Het |
Zbtb48 |
G |
T |
4: 152,105,067 (GRCm39) |
H532N |
probably damaging |
Het |
Zfp1005 |
C |
T |
2: 150,111,394 (GRCm39) |
H695Y |
possibly damaging |
Het |
|
Other mutations in Adam8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00781:Adam8
|
APN |
7 |
139,567,158 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02044:Adam8
|
APN |
7 |
139,562,735 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL02228:Adam8
|
APN |
7 |
139,568,719 (GRCm39) |
splice site |
probably null |
|
IGL02257:Adam8
|
APN |
7 |
139,567,561 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL03101:Adam8
|
APN |
7 |
139,568,456 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0320:Adam8
|
UTSW |
7 |
139,566,355 (GRCm39) |
missense |
probably damaging |
1.00 |
R0384:Adam8
|
UTSW |
7 |
139,566,725 (GRCm39) |
unclassified |
probably benign |
|
R1169:Adam8
|
UTSW |
7 |
139,563,842 (GRCm39) |
missense |
probably benign |
0.11 |
R1340:Adam8
|
UTSW |
7 |
139,571,290 (GRCm39) |
missense |
probably damaging |
0.99 |
R1699:Adam8
|
UTSW |
7 |
139,563,224 (GRCm39) |
missense |
possibly damaging |
0.72 |
R3725:Adam8
|
UTSW |
7 |
139,563,781 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3874:Adam8
|
UTSW |
7 |
139,567,520 (GRCm39) |
missense |
probably damaging |
1.00 |
R4716:Adam8
|
UTSW |
7 |
139,563,851 (GRCm39) |
missense |
probably benign |
0.31 |
R4754:Adam8
|
UTSW |
7 |
139,564,693 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4907:Adam8
|
UTSW |
7 |
139,569,286 (GRCm39) |
missense |
probably benign |
0.03 |
R5345:Adam8
|
UTSW |
7 |
139,567,552 (GRCm39) |
missense |
probably benign |
0.03 |
R5579:Adam8
|
UTSW |
7 |
139,568,897 (GRCm39) |
missense |
probably benign |
0.03 |
R5805:Adam8
|
UTSW |
7 |
139,565,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5948:Adam8
|
UTSW |
7 |
139,567,797 (GRCm39) |
missense |
probably benign |
0.07 |
R5991:Adam8
|
UTSW |
7 |
139,570,200 (GRCm39) |
missense |
probably damaging |
1.00 |
R6280:Adam8
|
UTSW |
7 |
139,564,720 (GRCm39) |
missense |
probably damaging |
0.99 |
R6456:Adam8
|
UTSW |
7 |
139,566,701 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7098:Adam8
|
UTSW |
7 |
139,559,412 (GRCm39) |
missense |
possibly damaging |
0.53 |
R7105:Adam8
|
UTSW |
7 |
139,569,968 (GRCm39) |
missense |
probably benign |
0.00 |
R7334:Adam8
|
UTSW |
7 |
139,568,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R7342:Adam8
|
UTSW |
7 |
139,566,304 (GRCm39) |
missense |
probably benign |
0.00 |
R7382:Adam8
|
UTSW |
7 |
139,570,020 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7425:Adam8
|
UTSW |
7 |
139,572,394 (GRCm39) |
unclassified |
probably benign |
|
R7507:Adam8
|
UTSW |
7 |
139,567,091 (GRCm39) |
critical splice donor site |
probably null |
|
R7637:Adam8
|
UTSW |
7 |
139,565,343 (GRCm39) |
missense |
probably damaging |
0.98 |
R7904:Adam8
|
UTSW |
7 |
139,567,591 (GRCm39) |
missense |
probably benign |
0.17 |
R8024:Adam8
|
UTSW |
7 |
139,567,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R8176:Adam8
|
UTSW |
7 |
139,568,786 (GRCm39) |
missense |
probably benign |
0.03 |
R8438:Adam8
|
UTSW |
7 |
139,565,249 (GRCm39) |
critical splice donor site |
probably null |
|
R8439:Adam8
|
UTSW |
7 |
139,567,762 (GRCm39) |
missense |
probably benign |
0.25 |
R9077:Adam8
|
UTSW |
7 |
139,567,552 (GRCm39) |
missense |
probably benign |
0.03 |
R9312:Adam8
|
UTSW |
7 |
139,565,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R9346:Adam8
|
UTSW |
7 |
139,567,634 (GRCm39) |
missense |
probably benign |
0.00 |
R9566:Adam8
|
UTSW |
7 |
139,565,285 (GRCm39) |
missense |
probably benign |
|
|