Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd28 |
C |
T |
14: 31,432,904 (GRCm39) |
V548I |
probably benign |
Het |
Aspm |
T |
C |
1: 139,385,300 (GRCm39) |
S315P |
probably benign |
Het |
Caln1 |
G |
T |
5: 130,534,993 (GRCm39) |
E70* |
probably null |
Het |
Cd69 |
A |
T |
6: 129,246,567 (GRCm39) |
W114R |
probably damaging |
Het |
Cnbd2 |
T |
C |
2: 156,177,275 (GRCm39) |
Y90H |
probably damaging |
Het |
Crebrf |
C |
T |
17: 26,961,320 (GRCm39) |
S147F |
probably damaging |
Het |
Cts7 |
A |
T |
13: 61,500,586 (GRCm39) |
C320* |
probably null |
Het |
Dgat1 |
T |
C |
15: 76,386,513 (GRCm39) |
I474V |
possibly damaging |
Het |
Dmxl2 |
T |
A |
9: 54,301,146 (GRCm39) |
I2322F |
probably damaging |
Het |
Dnah11 |
A |
T |
12: 117,892,065 (GRCm39) |
F3703I |
probably damaging |
Het |
Foxb2 |
A |
G |
19: 16,850,433 (GRCm39) |
L191P |
unknown |
Het |
Gli3 |
A |
T |
13: 15,836,977 (GRCm39) |
E453D |
probably benign |
Het |
Gnl3 |
C |
T |
14: 30,738,783 (GRCm39) |
|
probably null |
Het |
Golgb1 |
A |
T |
16: 36,718,921 (GRCm39) |
T276S |
probably damaging |
Het |
Grk4 |
T |
C |
5: 34,826,520 (GRCm39) |
M40T |
probably benign |
Het |
Hoxb1 |
A |
G |
11: 96,257,203 (GRCm39) |
N184S |
possibly damaging |
Het |
Insr |
G |
T |
8: 3,242,593 (GRCm39) |
T42N |
probably damaging |
Het |
Iqgap3 |
A |
G |
3: 88,011,815 (GRCm39) |
K836E |
possibly damaging |
Het |
Kremen1 |
CGGG |
CGGGGGG |
11: 5,151,791 (GRCm39) |
|
probably benign |
Het |
Leng9 |
T |
A |
7: 4,152,409 (GRCm39) |
E89V |
probably damaging |
Het |
Lhcgr |
C |
T |
17: 89,049,727 (GRCm39) |
V600I |
possibly damaging |
Het |
Lima1 |
T |
C |
15: 99,692,396 (GRCm39) |
N183S |
probably benign |
Het |
Lmtk2 |
A |
G |
5: 144,110,729 (GRCm39) |
D483G |
probably benign |
Het |
Lpcat2b |
T |
G |
5: 107,581,307 (GRCm39) |
L212R |
probably damaging |
Het |
Lrrc61 |
A |
T |
6: 48,545,806 (GRCm39) |
I210F |
probably benign |
Het |
Lypd8l |
G |
A |
11: 58,502,934 (GRCm39) |
Q72* |
probably null |
Het |
Lypd8l |
A |
T |
11: 58,503,676 (GRCm39) |
L10H |
probably damaging |
Het |
Med12l |
C |
T |
3: 59,148,113 (GRCm39) |
L977F |
probably damaging |
Het |
Mical1 |
A |
T |
10: 41,358,229 (GRCm39) |
D414V |
probably benign |
Het |
Mmp14 |
C |
T |
14: 54,678,002 (GRCm39) |
A541V |
probably benign |
Het |
Mtmr10 |
A |
G |
7: 63,947,328 (GRCm39) |
D81G |
possibly damaging |
Het |
Myh1 |
G |
A |
11: 67,111,363 (GRCm39) |
V1601M |
probably benign |
Het |
Myo16 |
G |
A |
8: 10,644,905 (GRCm39) |
D1746N |
possibly damaging |
Het |
Neb |
T |
C |
2: 52,177,348 (GRCm39) |
Y1331C |
probably damaging |
Het |
Otop2 |
T |
C |
11: 115,219,927 (GRCm39) |
S256P |
probably damaging |
Het |
Rrp1b |
A |
T |
17: 32,278,302 (GRCm39) |
M658L |
possibly damaging |
Het |
Sema4b |
C |
A |
7: 79,870,627 (GRCm39) |
A525D |
probably damaging |
Het |
Slc13a5 |
T |
A |
11: 72,143,147 (GRCm39) |
I369F |
probably benign |
Het |
Slc22a18 |
T |
C |
7: 143,051,152 (GRCm39) |
S344P |
probably benign |
Het |
Slc25a4 |
A |
C |
8: 46,662,212 (GRCm39) |
S149A |
probably benign |
Het |
Smc2 |
A |
T |
4: 52,460,266 (GRCm39) |
E547D |
probably benign |
Het |
Stx8 |
A |
G |
11: 67,864,077 (GRCm39) |
T46A |
probably benign |
Het |
Tacr3 |
T |
C |
3: 134,560,631 (GRCm39) |
V190A |
probably benign |
Het |
Tdrkh |
A |
T |
3: 94,336,467 (GRCm39) |
K468M |
possibly damaging |
Het |
Tmem145 |
T |
C |
7: 25,005,598 (GRCm39) |
S4P |
probably benign |
Het |
Tmem74 |
A |
G |
15: 43,730,506 (GRCm39) |
I179T |
probably damaging |
Het |
Vmn1r222 |
A |
C |
13: 23,416,683 (GRCm39) |
W177G |
probably benign |
Het |
Zfp426 |
T |
C |
9: 20,381,401 (GRCm39) |
I529V |
probably benign |
Het |
Zfp462 |
A |
G |
4: 55,008,313 (GRCm39) |
Y93C |
probably null |
Het |
Zfyve26 |
G |
A |
12: 79,330,890 (GRCm39) |
T443I |
probably damaging |
Het |
Zkscan16 |
A |
C |
4: 58,951,869 (GRCm39) |
R181S |
possibly damaging |
Het |
|
Other mutations in Prl8a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02259:Prl8a1
|
APN |
13 |
27,766,089 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02369:Prl8a1
|
APN |
13 |
27,760,924 (GRCm39) |
missense |
possibly damaging |
0.58 |
IGL03257:Prl8a1
|
APN |
13 |
27,759,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02837:Prl8a1
|
UTSW |
13 |
27,759,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R0838:Prl8a1
|
UTSW |
13 |
27,758,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R1480:Prl8a1
|
UTSW |
13 |
27,758,055 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1973:Prl8a1
|
UTSW |
13 |
27,760,917 (GRCm39) |
missense |
probably benign |
0.07 |
R2396:Prl8a1
|
UTSW |
13 |
27,758,007 (GRCm39) |
missense |
probably benign |
0.00 |
R3732:Prl8a1
|
UTSW |
13 |
27,763,716 (GRCm39) |
missense |
probably damaging |
0.98 |
R3874:Prl8a1
|
UTSW |
13 |
27,759,441 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4895:Prl8a1
|
UTSW |
13 |
27,759,513 (GRCm39) |
missense |
probably benign |
0.20 |
R5135:Prl8a1
|
UTSW |
13 |
27,763,802 (GRCm39) |
splice site |
probably null |
|
R5139:Prl8a1
|
UTSW |
13 |
27,758,049 (GRCm39) |
missense |
probably damaging |
0.98 |
R5908:Prl8a1
|
UTSW |
13 |
27,758,040 (GRCm39) |
missense |
probably benign |
0.00 |
R6232:Prl8a1
|
UTSW |
13 |
27,759,557 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6262:Prl8a1
|
UTSW |
13 |
27,758,126 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7203:Prl8a1
|
UTSW |
13 |
27,758,172 (GRCm39) |
missense |
probably damaging |
0.99 |
R7243:Prl8a1
|
UTSW |
13 |
27,766,086 (GRCm39) |
missense |
probably damaging |
1.00 |
R7372:Prl8a1
|
UTSW |
13 |
27,758,089 (GRCm39) |
missense |
probably damaging |
0.97 |
R7485:Prl8a1
|
UTSW |
13 |
27,758,068 (GRCm39) |
missense |
probably damaging |
1.00 |
R8115:Prl8a1
|
UTSW |
13 |
27,758,028 (GRCm39) |
missense |
probably benign |
0.01 |
R8782:Prl8a1
|
UTSW |
13 |
27,758,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Prl8a1
|
UTSW |
13 |
27,766,069 (GRCm39) |
missense |
possibly damaging |
0.73 |
|