Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adnp2 |
T |
C |
18: 80,174,205 (GRCm39) |
Y68C |
probably damaging |
Het |
Ahctf1 |
A |
T |
1: 179,591,038 (GRCm39) |
D1247E |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,606,192 (GRCm39) |
M2614K |
possibly damaging |
Het |
Alx3 |
A |
G |
3: 107,512,292 (GRCm39) |
H310R |
probably damaging |
Het |
Ambra1 |
C |
T |
2: 91,741,773 (GRCm39) |
T1016M |
probably damaging |
Het |
Ankrd35 |
A |
G |
3: 96,591,331 (GRCm39) |
E539G |
probably damaging |
Het |
Aptx |
A |
G |
4: 40,695,145 (GRCm39) |
|
probably benign |
Het |
Arsi |
C |
T |
18: 61,050,058 (GRCm39) |
R314C |
probably benign |
Het |
Atp1a3 |
T |
C |
7: 24,688,989 (GRCm39) |
|
probably benign |
Het |
Avl9 |
G |
T |
6: 56,713,468 (GRCm39) |
R242L |
probably benign |
Het |
Bicra |
G |
T |
7: 15,705,812 (GRCm39) |
T1543K |
probably benign |
Het |
Bltp2 |
T |
A |
11: 78,177,404 (GRCm39) |
V1903E |
possibly damaging |
Het |
Bzw2 |
A |
C |
12: 36,180,014 (GRCm39) |
I71S |
probably damaging |
Het |
Camk2a |
C |
T |
18: 61,093,079 (GRCm39) |
A302V |
probably damaging |
Het |
Ccdc12 |
A |
G |
9: 110,485,665 (GRCm39) |
E12G |
possibly damaging |
Het |
Cd300lb |
A |
T |
11: 114,819,164 (GRCm39) |
F19Y |
probably benign |
Het |
Clcn3 |
A |
T |
8: 61,380,330 (GRCm39) |
C535* |
probably null |
Het |
Cntnap5c |
A |
G |
17: 58,506,012 (GRCm39) |
T679A |
probably benign |
Het |
Cpsf7 |
G |
A |
19: 10,516,993 (GRCm39) |
S365N |
possibly damaging |
Het |
Cspg4b |
T |
A |
13: 113,505,310 (GRCm39) |
S2146R |
probably benign |
Het |
Cyp20a1 |
T |
C |
1: 60,426,285 (GRCm39) |
|
probably benign |
Het |
Decr2 |
A |
T |
17: 26,302,027 (GRCm39) |
N234K |
probably benign |
Het |
Def8 |
G |
A |
8: 124,183,234 (GRCm39) |
A278T |
probably damaging |
Het |
Dnah12 |
T |
C |
14: 26,494,601 (GRCm39) |
F1300L |
probably damaging |
Het |
Dock1 |
T |
C |
7: 134,331,793 (GRCm39) |
|
probably benign |
Het |
Dpy19l4 |
A |
T |
4: 11,267,619 (GRCm39) |
N440K |
probably damaging |
Het |
Eprs1 |
T |
C |
1: 185,146,588 (GRCm39) |
V1206A |
probably damaging |
Het |
Exoc6b |
A |
G |
6: 84,831,681 (GRCm39) |
|
probably null |
Het |
Fam184b |
A |
G |
5: 45,712,536 (GRCm39) |
|
probably benign |
Het |
Fcho1 |
A |
T |
8: 72,161,597 (GRCm39) |
S858T |
probably damaging |
Het |
Fgfr1 |
A |
G |
8: 26,058,214 (GRCm39) |
D430G |
possibly damaging |
Het |
Fmnl3 |
T |
C |
15: 99,219,013 (GRCm39) |
T807A |
probably damaging |
Het |
Gabra5 |
T |
C |
7: 57,063,476 (GRCm39) |
Y316C |
probably damaging |
Het |
Gh |
A |
G |
11: 106,192,346 (GRCm39) |
L16P |
probably damaging |
Het |
Glipr2 |
A |
T |
4: 43,970,532 (GRCm39) |
I87F |
probably damaging |
Het |
Glrb |
T |
A |
3: 80,763,221 (GRCm39) |
I259F |
probably damaging |
Het |
Gpr63 |
T |
C |
4: 25,007,651 (GRCm39) |
L125P |
probably damaging |
Het |
Grb2 |
A |
G |
11: 115,546,251 (GRCm39) |
Y37H |
probably damaging |
Het |
Haus2 |
G |
A |
2: 120,449,449 (GRCm39) |
|
probably benign |
Het |
Hmgcr |
T |
C |
13: 96,788,653 (GRCm39) |
N749S |
probably damaging |
Het |
Igf1r |
T |
C |
7: 67,814,990 (GRCm39) |
V297A |
probably damaging |
Het |
Il12rb2 |
G |
T |
6: 67,293,270 (GRCm39) |
P69H |
probably damaging |
Het |
Ints3 |
C |
A |
3: 90,315,818 (GRCm39) |
M315I |
probably benign |
Het |
Izumo2 |
C |
T |
7: 44,364,833 (GRCm39) |
T116I |
probably benign |
Het |
Kctd19 |
A |
C |
8: 106,121,993 (GRCm39) |
Y185D |
probably damaging |
Het |
Lama4 |
A |
G |
10: 38,936,218 (GRCm39) |
N631S |
possibly damaging |
Het |
Lama5 |
T |
G |
2: 179,819,872 (GRCm39) |
|
probably null |
Het |
Lamc1 |
A |
C |
1: 153,138,185 (GRCm39) |
L223R |
probably damaging |
Het |
Lgr4 |
G |
A |
2: 109,828,010 (GRCm39) |
|
probably null |
Het |
Loxhd1 |
T |
C |
18: 77,427,196 (GRCm39) |
L398P |
probably damaging |
Het |
Mapk9 |
T |
A |
11: 49,757,866 (GRCm39) |
D103E |
possibly damaging |
Het |
Marchf6 |
T |
C |
15: 31,469,678 (GRCm39) |
|
probably benign |
Het |
Mlxipl |
G |
A |
5: 135,162,043 (GRCm39) |
|
probably benign |
Het |
Mrgbp |
C |
A |
2: 180,225,231 (GRCm39) |
D62E |
probably benign |
Het |
Mtap |
A |
T |
4: 89,070,235 (GRCm39) |
|
probably benign |
Het |
Myt1 |
G |
A |
2: 181,443,664 (GRCm39) |
G497S |
probably damaging |
Het |
Naa25 |
T |
G |
5: 121,545,247 (GRCm39) |
|
probably benign |
Het |
Nfat5 |
C |
T |
8: 108,065,707 (GRCm39) |
R156W |
probably damaging |
Het |
Nkpd1 |
T |
C |
7: 19,253,852 (GRCm39) |
C73R |
probably benign |
Het |
Nup210l |
T |
C |
3: 90,027,218 (GRCm39) |
I200T |
probably damaging |
Het |
Nvl |
C |
A |
1: 180,941,698 (GRCm39) |
D581Y |
probably damaging |
Het |
Or51a6 |
T |
C |
7: 102,604,185 (GRCm39) |
M208V |
probably benign |
Het |
Or51f2 |
T |
C |
7: 102,527,068 (GRCm39) |
V247A |
probably benign |
Het |
Or5t17 |
T |
A |
2: 86,832,710 (GRCm39) |
Y132* |
probably null |
Het |
Or8b1c |
A |
G |
9: 38,384,612 (GRCm39) |
T190A |
probably benign |
Het |
Or9q1 |
T |
C |
19: 13,805,050 (GRCm39) |
T237A |
probably damaging |
Het |
Pcdh7 |
G |
T |
5: 58,070,590 (GRCm39) |
E1089D |
probably benign |
Het |
Pik3cd |
A |
G |
4: 149,740,836 (GRCm39) |
|
probably null |
Het |
Plekhh2 |
A |
T |
17: 84,864,820 (GRCm39) |
K69N |
probably damaging |
Het |
Ptgdr2 |
G |
A |
19: 10,917,792 (GRCm39) |
C103Y |
probably damaging |
Het |
Rrad |
A |
C |
8: 105,355,299 (GRCm39) |
H236Q |
probably benign |
Het |
Rslcan18 |
C |
T |
13: 67,246,533 (GRCm39) |
A236T |
probably benign |
Het |
Ryr2 |
C |
A |
13: 11,839,265 (GRCm39) |
D503Y |
probably damaging |
Het |
Siglec1 |
T |
C |
2: 130,916,980 (GRCm39) |
T1092A |
probably benign |
Het |
Siglecf |
A |
G |
7: 43,005,350 (GRCm39) |
T437A |
probably benign |
Het |
Spta1 |
A |
T |
1: 174,032,839 (GRCm39) |
Q965H |
probably damaging |
Het |
Stk10 |
A |
T |
11: 32,539,460 (GRCm39) |
E280V |
probably benign |
Het |
Tfg |
T |
C |
16: 56,511,351 (GRCm39) |
Y326C |
possibly damaging |
Het |
Tpp2 |
T |
A |
1: 43,999,299 (GRCm39) |
S358T |
possibly damaging |
Het |
Trim25 |
G |
T |
11: 88,906,598 (GRCm39) |
V437L |
probably benign |
Het |
Ttn |
T |
C |
2: 76,574,027 (GRCm39) |
D25622G |
probably damaging |
Het |
Ube3b |
T |
A |
5: 114,536,912 (GRCm39) |
S303R |
probably benign |
Het |
Ush2a |
T |
A |
1: 188,310,688 (GRCm39) |
V2088D |
probably damaging |
Het |
Vmn2r103 |
A |
G |
17: 20,032,241 (GRCm39) |
T672A |
probably damaging |
Het |
Wdr11 |
G |
T |
7: 129,200,785 (GRCm39) |
G79C |
probably damaging |
Het |
Wdr89 |
T |
A |
12: 75,679,367 (GRCm39) |
T296S |
probably benign |
Het |
Zdhhc24 |
T |
A |
19: 4,930,402 (GRCm39) |
L179M |
possibly damaging |
Het |
Zfp981 |
T |
C |
4: 146,622,217 (GRCm39) |
C381R |
probably damaging |
Het |
Zim1 |
A |
G |
7: 6,679,947 (GRCm39) |
I572T |
probably benign |
Het |
|
Other mutations in Adam19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01433:Adam19
|
APN |
11 |
46,003,610 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01727:Adam19
|
APN |
11 |
46,012,380 (GRCm39) |
missense |
probably benign |
|
IGL01758:Adam19
|
APN |
11 |
46,003,751 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02160:Adam19
|
APN |
11 |
46,030,522 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02421:Adam19
|
APN |
11 |
46,028,380 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02572:Adam19
|
APN |
11 |
46,022,548 (GRCm39) |
nonsense |
probably null |
|
IGL02995:Adam19
|
APN |
11 |
46,027,176 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03171:Adam19
|
APN |
11 |
46,029,681 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03237:Adam19
|
APN |
11 |
46,028,383 (GRCm39) |
missense |
probably benign |
|
R0026:Adam19
|
UTSW |
11 |
46,027,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R0158:Adam19
|
UTSW |
11 |
46,033,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R0304:Adam19
|
UTSW |
11 |
46,018,219 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0488:Adam19
|
UTSW |
11 |
46,029,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R0501:Adam19
|
UTSW |
11 |
46,013,957 (GRCm39) |
missense |
probably damaging |
1.00 |
R0591:Adam19
|
UTSW |
11 |
46,012,238 (GRCm39) |
splice site |
probably benign |
|
R0734:Adam19
|
UTSW |
11 |
46,018,230 (GRCm39) |
missense |
probably damaging |
0.99 |
R0747:Adam19
|
UTSW |
11 |
46,009,322 (GRCm39) |
splice site |
probably null |
|
R0771:Adam19
|
UTSW |
11 |
46,012,280 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1052:Adam19
|
UTSW |
11 |
46,018,092 (GRCm39) |
missense |
probably damaging |
0.99 |
R1573:Adam19
|
UTSW |
11 |
46,004,445 (GRCm39) |
splice site |
probably benign |
|
R1735:Adam19
|
UTSW |
11 |
46,029,744 (GRCm39) |
missense |
probably benign |
0.26 |
R1830:Adam19
|
UTSW |
11 |
46,018,105 (GRCm39) |
missense |
probably damaging |
0.98 |
R1911:Adam19
|
UTSW |
11 |
46,012,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:Adam19
|
UTSW |
11 |
45,951,731 (GRCm39) |
splice site |
probably null |
|
R3749:Adam19
|
UTSW |
11 |
46,028,437 (GRCm39) |
missense |
probably benign |
0.00 |
R3893:Adam19
|
UTSW |
11 |
46,019,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R3916:Adam19
|
UTSW |
11 |
45,951,762 (GRCm39) |
missense |
probably benign |
0.25 |
R3917:Adam19
|
UTSW |
11 |
45,951,762 (GRCm39) |
missense |
probably benign |
0.25 |
R4506:Adam19
|
UTSW |
11 |
46,009,271 (GRCm39) |
missense |
possibly damaging |
0.67 |
R4767:Adam19
|
UTSW |
11 |
46,029,804 (GRCm39) |
critical splice donor site |
probably null |
|
R5055:Adam19
|
UTSW |
11 |
46,013,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R5313:Adam19
|
UTSW |
11 |
46,022,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R5329:Adam19
|
UTSW |
11 |
46,015,853 (GRCm39) |
missense |
probably damaging |
0.99 |
R5567:Adam19
|
UTSW |
11 |
46,027,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R5602:Adam19
|
UTSW |
11 |
46,027,142 (GRCm39) |
missense |
probably benign |
|
R6198:Adam19
|
UTSW |
11 |
46,012,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R6875:Adam19
|
UTSW |
11 |
46,003,702 (GRCm39) |
missense |
probably benign |
|
R7011:Adam19
|
UTSW |
11 |
46,033,845 (GRCm39) |
missense |
probably benign |
0.00 |
R7163:Adam19
|
UTSW |
11 |
46,022,544 (GRCm39) |
missense |
probably benign |
|
R7213:Adam19
|
UTSW |
11 |
46,012,298 (GRCm39) |
missense |
probably benign |
0.20 |
R7267:Adam19
|
UTSW |
11 |
46,012,403 (GRCm39) |
nonsense |
probably null |
|
R7896:Adam19
|
UTSW |
11 |
46,028,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R8012:Adam19
|
UTSW |
11 |
45,955,873 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8059:Adam19
|
UTSW |
11 |
46,027,293 (GRCm39) |
splice site |
probably benign |
|
R8243:Adam19
|
UTSW |
11 |
46,015,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R8357:Adam19
|
UTSW |
11 |
46,030,939 (GRCm39) |
missense |
probably damaging |
0.96 |
R8419:Adam19
|
UTSW |
11 |
46,015,850 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8457:Adam19
|
UTSW |
11 |
46,030,939 (GRCm39) |
missense |
probably damaging |
0.96 |
R9163:Adam19
|
UTSW |
11 |
46,018,176 (GRCm39) |
missense |
probably benign |
0.02 |
R9349:Adam19
|
UTSW |
11 |
46,022,570 (GRCm39) |
nonsense |
probably null |
|
R9489:Adam19
|
UTSW |
11 |
46,028,449 (GRCm39) |
missense |
probably benign |
0.10 |
R9579:Adam19
|
UTSW |
11 |
46,009,262 (GRCm39) |
missense |
probably benign |
0.00 |
R9641:Adam19
|
UTSW |
11 |
46,027,149 (GRCm39) |
missense |
probably damaging |
1.00 |
X0067:Adam19
|
UTSW |
11 |
45,946,942 (GRCm39) |
start codon destroyed |
probably null |
0.06 |
|