Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
T |
C |
9: 53,408,065 (GRCm38) |
S2P |
probably benign |
Het |
Abca16 |
A |
C |
7: 120,435,893 (GRCm38) |
T301P |
probably damaging |
Het |
Acer2 |
A |
G |
4: 86,887,162 (GRCm38) |
D121G |
possibly damaging |
Het |
Adgrd1 |
T |
C |
5: 129,171,931 (GRCm38) |
|
probably null |
Het |
Arhgap11a |
T |
C |
2: 113,841,711 (GRCm38) |
I249V |
probably benign |
Het |
Arhgap22 |
A |
G |
14: 33,366,714 (GRCm38) |
E219G |
probably benign |
Het |
C2cd4b |
T |
A |
9: 67,759,751 (GRCm38) |
S10T |
probably benign |
Het |
Cnot6 |
A |
T |
11: 49,683,171 (GRCm38) |
I224N |
probably damaging |
Het |
Ctrc |
T |
C |
4: 141,841,518 (GRCm38) |
T125A |
probably damaging |
Het |
Cxxc5 |
T |
G |
18: 35,858,589 (GRCm38) |
S14R |
unknown |
Het |
Cyp4f37 |
T |
G |
17: 32,634,678 (GRCm38) |
F445L |
probably damaging |
Het |
Dcbld1 |
T |
G |
10: 52,312,850 (GRCm38) |
I186S |
probably benign |
Het |
Dmxl2 |
T |
C |
9: 54,382,702 (GRCm38) |
T2510A |
probably benign |
Het |
Dnah3 |
A |
G |
7: 120,071,887 (GRCm38) |
I591T |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 67,841,163 (GRCm38) |
I204N |
probably benign |
Het |
Dysf |
G |
A |
6: 84,111,987 (GRCm38) |
|
probably null |
Het |
Erich5 |
A |
G |
15: 34,471,369 (GRCm38) |
E248G |
probably damaging |
Het |
Fhip1a |
A |
G |
3: 85,730,500 (GRCm38) |
V164A |
possibly damaging |
Het |
Foxm1 |
A |
G |
6: 128,373,871 (GRCm38) |
S712G |
probably damaging |
Het |
Frmpd1 |
A |
G |
4: 45,284,055 (GRCm38) |
T959A |
probably benign |
Het |
Gfra4 |
C |
T |
2: 131,040,256 (GRCm38) |
V277I |
probably null |
Het |
Hacd4 |
T |
C |
4: 88,435,010 (GRCm38) |
I82V |
probably benign |
Het |
Itih2 |
C |
T |
2: 10,123,414 (GRCm38) |
V159I |
possibly damaging |
Het |
Itpr2 |
T |
A |
6: 146,166,651 (GRCm38) |
M2410L |
probably benign |
Het |
Marchf11 |
A |
G |
15: 26,311,043 (GRCm38) |
I202V |
probably damaging |
Het |
Marchf3 |
A |
G |
18: 56,811,830 (GRCm38) |
|
probably null |
Het |
Med12l |
G |
A |
3: 59,247,437 (GRCm38) |
E1135K |
probably damaging |
Het |
Mib2 |
C |
T |
4: 155,659,460 (GRCm38) |
G42S |
probably damaging |
Het |
Mlx |
T |
C |
11: 101,087,782 (GRCm38) |
L78P |
possibly damaging |
Het |
Muc5b |
T |
C |
7: 141,846,427 (GRCm38) |
C473R |
unknown |
Het |
N4bp2l1 |
T |
A |
5: 150,576,745 (GRCm38) |
R66* |
probably null |
Het |
Nes |
A |
G |
3: 87,977,172 (GRCm38) |
T913A |
possibly damaging |
Het |
Oas1a |
T |
C |
5: 120,899,259 (GRCm38) |
E235G |
probably damaging |
Het |
Or5p56 |
T |
C |
7: 107,991,189 (GRCm38) |
S275P |
probably damaging |
Het |
Or8b1c |
T |
C |
9: 38,473,208 (GRCm38) |
S154P |
possibly damaging |
Het |
Or8i2 |
T |
A |
2: 87,021,620 (GRCm38) |
H308L |
probably benign |
Het |
Parn |
C |
T |
16: 13,640,294 (GRCm38) |
V286I |
probably benign |
Het |
Paxip1 |
G |
A |
5: 27,765,942 (GRCm38) |
Q470* |
probably null |
Het |
Phc2 |
C |
G |
4: 128,723,710 (GRCm38) |
H510D |
possibly damaging |
Het |
Pla2g4f |
T |
A |
2: 120,305,041 (GRCm38) |
D384V |
probably damaging |
Het |
Plpbp |
A |
T |
8: 27,045,131 (GRCm38) |
N68I |
probably damaging |
Het |
Podxl2 |
G |
A |
6: 88,849,955 (GRCm38) |
A123V |
possibly damaging |
Het |
Pole |
A |
T |
5: 110,325,550 (GRCm38) |
T1737S |
possibly damaging |
Het |
Ppp3cc |
T |
C |
14: 70,225,027 (GRCm38) |
E396G |
probably damaging |
Het |
Pramel7 |
T |
A |
2: 87,491,008 (GRCm38) |
I228F |
probably benign |
Het |
Qtrt1 |
G |
T |
9: 21,418,288 (GRCm38) |
M217I |
probably benign |
Het |
Sec24a |
T |
A |
11: 51,729,454 (GRCm38) |
D456V |
probably damaging |
Het |
Shox2 |
T |
G |
3: 66,981,544 (GRCm38) |
|
probably null |
Het |
Skint2 |
T |
A |
4: 112,624,086 (GRCm38) |
S49T |
probably damaging |
Het |
Smarca5 |
A |
G |
8: 80,720,686 (GRCm38) |
|
probably null |
Het |
Sorcs2 |
T |
A |
5: 36,024,572 (GRCm38) |
D1068V |
possibly damaging |
Het |
Tmem114 |
T |
C |
16: 8,412,102 (GRCm38) |
|
probably null |
Het |
Ttc7b |
T |
A |
12: 100,355,046 (GRCm38) |
M24L |
probably benign |
Het |
Ttll3 |
A |
G |
6: 113,408,903 (GRCm38) |
|
probably null |
Het |
Usp7 |
C |
T |
16: 8,704,982 (GRCm38) |
D102N |
probably benign |
Het |
|
Other mutations in Prl7d1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01390:Prl7d1
|
APN |
13 |
27,710,166 (GRCm38) |
missense |
possibly damaging |
0.91 |
IGL01735:Prl7d1
|
APN |
13 |
27,714,389 (GRCm38) |
missense |
possibly damaging |
0.83 |
IGL02139:Prl7d1
|
APN |
13 |
27,712,083 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4305001:Prl7d1
|
UTSW |
13 |
27,714,337 (GRCm38) |
missense |
possibly damaging |
0.90 |
PIT4531001:Prl7d1
|
UTSW |
13 |
27,710,178 (GRCm38) |
missense |
probably damaging |
1.00 |
R0555:Prl7d1
|
UTSW |
13 |
27,712,055 (GRCm38) |
missense |
probably benign |
0.13 |
R0631:Prl7d1
|
UTSW |
13 |
27,710,182 (GRCm38) |
missense |
probably benign |
0.32 |
R0837:Prl7d1
|
UTSW |
13 |
27,714,338 (GRCm38) |
missense |
probably benign |
0.06 |
R1403:Prl7d1
|
UTSW |
13 |
27,709,197 (GRCm38) |
missense |
possibly damaging |
0.89 |
R1403:Prl7d1
|
UTSW |
13 |
27,709,197 (GRCm38) |
missense |
possibly damaging |
0.89 |
R1459:Prl7d1
|
UTSW |
13 |
27,709,257 (GRCm38) |
missense |
possibly damaging |
0.81 |
R1643:Prl7d1
|
UTSW |
13 |
27,712,131 (GRCm38) |
missense |
possibly damaging |
0.53 |
R1691:Prl7d1
|
UTSW |
13 |
27,709,382 (GRCm38) |
missense |
probably damaging |
0.97 |
R2016:Prl7d1
|
UTSW |
13 |
27,710,173 (GRCm38) |
missense |
probably damaging |
1.00 |
R3873:Prl7d1
|
UTSW |
13 |
27,716,668 (GRCm38) |
start codon destroyed |
probably null |
0.92 |
R3874:Prl7d1
|
UTSW |
13 |
27,716,668 (GRCm38) |
start codon destroyed |
probably null |
0.92 |
R5251:Prl7d1
|
UTSW |
13 |
27,709,244 (GRCm38) |
missense |
probably benign |
0.33 |
R5275:Prl7d1
|
UTSW |
13 |
27,709,247 (GRCm38) |
missense |
probably damaging |
0.99 |
R5295:Prl7d1
|
UTSW |
13 |
27,709,247 (GRCm38) |
missense |
probably damaging |
0.99 |
R5398:Prl7d1
|
UTSW |
13 |
27,710,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R6798:Prl7d1
|
UTSW |
13 |
27,709,397 (GRCm38) |
critical splice acceptor site |
probably null |
|
R6818:Prl7d1
|
UTSW |
13 |
27,714,471 (GRCm38) |
missense |
probably benign |
0.07 |
R6825:Prl7d1
|
UTSW |
13 |
27,710,142 (GRCm38) |
missense |
probably benign |
0.01 |
R7478:Prl7d1
|
UTSW |
13 |
27,710,185 (GRCm38) |
nonsense |
probably null |
|
R7795:Prl7d1
|
UTSW |
13 |
27,709,280 (GRCm38) |
missense |
probably damaging |
1.00 |
R7995:Prl7d1
|
UTSW |
13 |
27,710,071 (GRCm38) |
missense |
probably benign |
|
R8193:Prl7d1
|
UTSW |
13 |
27,709,247 (GRCm38) |
missense |
|
|
R9313:Prl7d1
|
UTSW |
13 |
27,709,199 (GRCm38) |
missense |
probably benign |
|
R9424:Prl7d1
|
UTSW |
13 |
27,710,202 (GRCm38) |
missense |
probably benign |
0.00 |
R9430:Prl7d1
|
UTSW |
13 |
27,714,377 (GRCm38) |
missense |
possibly damaging |
0.80 |
R9733:Prl7d1
|
UTSW |
13 |
27,714,356 (GRCm38) |
missense |
probably benign |
0.00 |
R9758:Prl7d1
|
UTSW |
13 |
27,709,277 (GRCm38) |
missense |
possibly damaging |
0.91 |
|