Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alpk2 |
G |
T |
18: 65,438,532 (GRCm39) |
Q1421K |
possibly damaging |
Het |
Ankub1 |
G |
A |
3: 57,580,258 (GRCm39) |
T133M |
probably benign |
Het |
Bcar3 |
G |
A |
3: 122,248,736 (GRCm39) |
V112M |
possibly damaging |
Het |
Cacna1s |
A |
G |
1: 136,039,804 (GRCm39) |
K1476R |
probably benign |
Het |
Cdc42ep1 |
C |
A |
15: 78,733,977 (GRCm39) |
A359E |
possibly damaging |
Het |
Cemip |
T |
A |
7: 83,624,387 (GRCm39) |
D483V |
probably damaging |
Het |
Cyp4f39 |
G |
A |
17: 32,700,799 (GRCm39) |
R156H |
probably damaging |
Het |
Dpys |
T |
A |
15: 39,720,553 (GRCm39) |
H69L |
probably damaging |
Het |
Fbxl21 |
A |
G |
13: 56,674,885 (GRCm39) |
I79V |
probably benign |
Het |
Fgf9 |
T |
C |
14: 58,347,022 (GRCm39) |
L205P |
probably damaging |
Het |
Fkbp14 |
A |
G |
6: 54,562,835 (GRCm39) |
F144L |
probably damaging |
Het |
Flnb |
A |
C |
14: 7,929,073 (GRCm38) |
D1934A |
probably damaging |
Het |
Garre1 |
G |
A |
7: 33,939,941 (GRCm39) |
Q717* |
probably null |
Het |
Glul |
T |
C |
1: 153,782,243 (GRCm39) |
|
probably benign |
Het |
Helz |
T |
A |
11: 107,517,347 (GRCm39) |
|
probably null |
Het |
Kap |
A |
G |
6: 133,828,956 (GRCm39) |
Y42H |
probably benign |
Het |
Kcnh8 |
T |
C |
17: 53,285,150 (GRCm39) |
V1040A |
probably benign |
Het |
Kptn |
A |
G |
7: 15,854,683 (GRCm39) |
|
probably null |
Het |
Lypd3 |
A |
G |
7: 24,338,494 (GRCm39) |
T182A |
possibly damaging |
Het |
Mcm5 |
A |
C |
8: 75,847,538 (GRCm39) |
D445A |
probably damaging |
Het |
Mios |
T |
A |
6: 8,215,434 (GRCm39) |
I210K |
probably damaging |
Het |
Nat8f2 |
A |
G |
6: 85,844,891 (GRCm39) |
V157A |
probably benign |
Het |
Or1e16 |
T |
A |
11: 73,286,187 (GRCm39) |
|
probably null |
Het |
Pard3b |
C |
A |
1: 62,677,075 (GRCm39) |
A1140E |
probably null |
Het |
Pcnt |
A |
T |
10: 76,256,325 (GRCm39) |
D638E |
probably damaging |
Het |
Pdgfra |
T |
C |
5: 75,346,673 (GRCm39) |
I834T |
probably damaging |
Het |
Phyhd1 |
T |
A |
2: 30,169,994 (GRCm39) |
L162H |
probably damaging |
Het |
Polg |
C |
A |
7: 79,101,739 (GRCm39) |
A1026S |
possibly damaging |
Het |
Rars2 |
T |
A |
4: 34,645,779 (GRCm39) |
M232K |
probably benign |
Het |
Rtl1 |
A |
G |
12: 109,560,114 (GRCm39) |
V575A |
probably damaging |
Het |
Slc18b1 |
A |
T |
10: 23,674,664 (GRCm39) |
T40S |
probably benign |
Het |
Slc22a19 |
T |
C |
19: 7,688,387 (GRCm39) |
T58A |
probably damaging |
Het |
Slc27a6 |
A |
T |
18: 58,731,625 (GRCm39) |
E325V |
probably damaging |
Het |
Slc35e2 |
C |
T |
4: 155,694,483 (GRCm39) |
P10L |
probably benign |
Het |
Srd5a3 |
T |
A |
5: 76,301,413 (GRCm39) |
F214Y |
probably benign |
Het |
Tgfbr2 |
A |
T |
9: 116,004,092 (GRCm39) |
L5Q |
probably damaging |
Het |
Tmem94 |
C |
A |
11: 115,684,016 (GRCm39) |
Q779K |
probably benign |
Het |
Ttn |
G |
A |
2: 76,652,837 (GRCm39) |
P216S |
probably benign |
Het |
Ush2a |
A |
T |
1: 188,132,454 (GRCm39) |
Q892L |
probably benign |
Het |
Vgll4 |
A |
T |
6: 114,867,737 (GRCm39) |
M38K |
possibly damaging |
Het |
Vmn2r109 |
A |
G |
17: 20,773,121 (GRCm39) |
I500T |
probably damaging |
Het |
Vps33a |
T |
C |
5: 123,707,563 (GRCm39) |
I135V |
probably benign |
Het |
Wscd1 |
T |
C |
11: 71,675,261 (GRCm39) |
|
probably null |
Het |
Zfp457 |
C |
A |
13: 67,444,490 (GRCm39) |
M4I |
possibly damaging |
Het |
Zfp532 |
G |
A |
18: 65,756,606 (GRCm39) |
G180R |
possibly damaging |
Het |
Zfp97 |
A |
G |
17: 17,365,871 (GRCm39) |
T457A |
possibly damaging |
Het |
|
Other mutations in Prl7c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01388:Prl7c1
|
APN |
13 |
27,960,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Prl7c1
|
APN |
13 |
27,957,689 (GRCm39) |
missense |
probably damaging |
0.96 |
PIT4458001:Prl7c1
|
UTSW |
13 |
27,957,741 (GRCm39) |
missense |
probably benign |
|
R0566:Prl7c1
|
UTSW |
13 |
27,962,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0856:Prl7c1
|
UTSW |
13 |
27,957,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0908:Prl7c1
|
UTSW |
13 |
27,957,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1585:Prl7c1
|
UTSW |
13 |
27,962,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R4193:Prl7c1
|
UTSW |
13 |
27,960,261 (GRCm39) |
missense |
probably benign |
0.01 |
R4628:Prl7c1
|
UTSW |
13 |
27,962,065 (GRCm39) |
missense |
probably benign |
|
R4728:Prl7c1
|
UTSW |
13 |
27,960,268 (GRCm39) |
missense |
probably benign |
0.00 |
R4873:Prl7c1
|
UTSW |
13 |
27,957,742 (GRCm39) |
missense |
probably benign |
0.01 |
R4875:Prl7c1
|
UTSW |
13 |
27,957,742 (GRCm39) |
missense |
probably benign |
0.01 |
R6353:Prl7c1
|
UTSW |
13 |
27,957,709 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6505:Prl7c1
|
UTSW |
13 |
27,957,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6878:Prl7c1
|
UTSW |
13 |
27,962,827 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7104:Prl7c1
|
UTSW |
13 |
27,962,952 (GRCm39) |
nonsense |
probably null |
|
R7879:Prl7c1
|
UTSW |
13 |
27,962,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Prl7c1
|
UTSW |
13 |
27,962,070 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8828:Prl7c1
|
UTSW |
13 |
27,957,854 (GRCm39) |
missense |
probably benign |
0.14 |
R9142:Prl7c1
|
UTSW |
13 |
27,964,751 (GRCm39) |
start gained |
probably benign |
|
R9215:Prl7c1
|
UTSW |
13 |
27,960,204 (GRCm39) |
missense |
probably benign |
0.32 |
R9296:Prl7c1
|
UTSW |
13 |
27,962,812 (GRCm39) |
missense |
probably benign |
0.06 |
R9453:Prl7c1
|
UTSW |
13 |
27,957,870 (GRCm39) |
missense |
probably benign |
0.44 |
|