Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433N12Rik |
A |
T |
9: 3,134,008 (GRCm39) |
|
noncoding transcript |
Het |
Akap12 |
A |
G |
10: 4,304,060 (GRCm39) |
E290G |
probably damaging |
Het |
Akap6 |
T |
A |
12: 52,933,601 (GRCm39) |
C364* |
probably null |
Het |
Akr1c18 |
A |
T |
13: 4,187,143 (GRCm39) |
Y198N |
probably damaging |
Het |
Aurka |
T |
C |
2: 172,210,899 (GRCm39) |
|
probably benign |
Het |
Bloc1s6 |
T |
A |
2: 122,586,135 (GRCm39) |
|
probably null |
Het |
Clca3a1 |
C |
T |
3: 144,713,539 (GRCm39) |
M697I |
probably benign |
Het |
Csn2 |
T |
C |
5: 87,843,879 (GRCm39) |
|
probably benign |
Het |
Dsc1 |
T |
C |
18: 20,232,195 (GRCm39) |
E271G |
probably damaging |
Het |
Eif1ad4 |
A |
T |
12: 87,862,158 (GRCm39) |
K7* |
probably null |
Het |
Evi5 |
G |
A |
5: 107,963,513 (GRCm39) |
A354V |
probably damaging |
Het |
Fcer2a |
T |
A |
8: 3,738,151 (GRCm39) |
R137S |
probably benign |
Het |
Fto |
A |
G |
8: 92,168,344 (GRCm39) |
T266A |
probably benign |
Het |
Fzd4 |
G |
A |
7: 89,053,943 (GRCm39) |
V17I |
unknown |
Het |
Gadd45b |
T |
C |
10: 80,767,075 (GRCm39) |
L105P |
probably damaging |
Het |
Galntl6 |
T |
C |
8: 58,880,743 (GRCm39) |
S137G |
probably damaging |
Het |
Gpr135 |
T |
C |
12: 72,116,442 (GRCm39) |
M442V |
probably benign |
Het |
Kcnq1 |
T |
A |
7: 142,748,015 (GRCm39) |
Y330* |
probably null |
Het |
Kdm5b |
A |
G |
1: 134,549,724 (GRCm39) |
R1106G |
possibly damaging |
Het |
Lrrc8e |
C |
T |
8: 4,286,141 (GRCm39) |
R789W |
probably damaging |
Het |
Myo16 |
T |
C |
8: 10,485,853 (GRCm39) |
L644P |
probably damaging |
Het |
Nbeal1 |
G |
T |
1: 60,281,784 (GRCm39) |
|
probably null |
Het |
Nlrp4c |
T |
C |
7: 6,103,783 (GRCm39) |
C906R |
possibly damaging |
Het |
Or10ag56 |
C |
T |
2: 87,139,826 (GRCm39) |
T251I |
probably damaging |
Het |
Or1e29 |
A |
T |
11: 73,667,532 (GRCm39) |
I207N |
probably benign |
Het |
Or1j15 |
T |
A |
2: 36,458,754 (GRCm39) |
L48H |
probably damaging |
Het |
Ovgp1 |
A |
G |
3: 105,882,307 (GRCm39) |
N70D |
probably benign |
Het |
Panx3 |
A |
T |
9: 37,572,443 (GRCm39) |
M369K |
probably damaging |
Het |
Plet1 |
A |
G |
9: 50,406,017 (GRCm39) |
N52S |
probably benign |
Het |
Psg18 |
A |
T |
7: 18,088,741 (GRCm39) |
M1K |
probably null |
Het |
Ptprz1 |
A |
T |
6: 22,972,843 (GRCm39) |
D251V |
probably damaging |
Het |
Serpinb6a |
A |
G |
13: 34,114,064 (GRCm39) |
Y88H |
possibly damaging |
Het |
Siglecf |
G |
A |
7: 43,004,562 (GRCm39) |
R297Q |
possibly damaging |
Het |
Tbx15 |
T |
C |
3: 99,223,544 (GRCm39) |
V244A |
probably damaging |
Het |
Top2a |
A |
T |
11: 98,901,856 (GRCm39) |
L458Q |
probably damaging |
Het |
Trim39 |
A |
G |
17: 36,574,855 (GRCm39) |
|
probably benign |
Het |
Vps37c |
T |
C |
19: 10,687,781 (GRCm39) |
C81R |
probably damaging |
Het |
Wdr62 |
A |
T |
7: 29,941,187 (GRCm39) |
S744T |
probably benign |
Het |
Zyg11a |
G |
A |
4: 108,062,099 (GRCm39) |
T234I |
probably damaging |
Het |
|
Other mutations in Prss1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Prss1l
|
APN |
6 |
41,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00586:Prss1l
|
APN |
6 |
41,373,049 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01103:Prss1l
|
APN |
6 |
41,374,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01368:Prss1l
|
APN |
6 |
41,373,620 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL03114:Prss1l
|
APN |
6 |
41,374,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Prss1l
|
UTSW |
6 |
41,373,195 (GRCm39) |
splice site |
probably benign |
|
R1548:Prss1l
|
UTSW |
6 |
41,372,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Prss1l
|
UTSW |
6 |
41,373,701 (GRCm39) |
missense |
probably benign |
0.35 |
R5622:Prss1l
|
UTSW |
6 |
41,373,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R5664:Prss1l
|
UTSW |
6 |
41,371,605 (GRCm39) |
missense |
probably benign |
0.04 |
R6222:Prss1l
|
UTSW |
6 |
41,374,100 (GRCm39) |
missense |
probably damaging |
0.98 |
R6325:Prss1l
|
UTSW |
6 |
41,373,590 (GRCm39) |
missense |
probably benign |
0.00 |
R7816:Prss1l
|
UTSW |
6 |
41,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Prss1l
|
UTSW |
6 |
41,373,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8016:Prss1l
|
UTSW |
6 |
41,374,100 (GRCm39) |
missense |
probably damaging |
0.98 |
|