Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3100002H09Rik |
G |
T |
4: 124,610,642 (GRCm38) |
A39E |
probably damaging |
Het |
Agtr1b |
T |
A |
3: 20,315,749 (GRCm38) |
N231I |
possibly damaging |
Het |
Alpk2 |
T |
C |
18: 65,307,740 (GRCm38) |
E661G |
probably damaging |
Het |
Ankrd26 |
C |
T |
6: 118,507,788 (GRCm38) |
S1496N |
probably benign |
Het |
Asah2 |
T |
C |
19: 31,995,358 (GRCm38) |
N659S |
probably benign |
Het |
Atp12a |
T |
C |
14: 56,384,188 (GRCm38) |
V760A |
possibly damaging |
Het |
Casp2 |
T |
C |
6: 42,279,836 (GRCm38) |
C343R |
probably damaging |
Het |
Cblb |
T |
A |
16: 52,152,644 (GRCm38) |
M446K |
possibly damaging |
Het |
Cipc |
T |
C |
12: 86,962,090 (GRCm38) |
V241A |
probably benign |
Het |
Ddit4l |
A |
G |
3: 137,626,121 (GRCm38) |
K83E |
probably benign |
Het |
E430018J23Rik |
A |
G |
7: 127,393,423 (GRCm38) |
M5T |
probably benign |
Het |
Epc2 |
A |
G |
2: 49,522,669 (GRCm38) |
T220A |
probably damaging |
Het |
Epha5 |
T |
C |
5: 84,071,191 (GRCm38) |
D741G |
probably damaging |
Het |
Flg2 |
A |
T |
3: 93,201,761 (GRCm38) |
R365S |
possibly damaging |
Het |
Ggn |
A |
T |
7: 29,172,668 (GRCm38) |
H491L |
possibly damaging |
Het |
Gm21119 |
T |
C |
8: 20,621,939 (GRCm38) |
S267P |
probably benign |
Het |
Gm8332 |
A |
T |
12: 88,249,705 (GRCm38) |
D132E |
unknown |
Het |
Gpat2 |
G |
C |
2: 127,431,918 (GRCm38) |
G294R |
possibly damaging |
Het |
Ighv6-4 |
A |
G |
12: 114,406,532 (GRCm38) |
V100A |
probably benign |
Het |
Invs |
A |
T |
4: 48,402,870 (GRCm38) |
Y501F |
possibly damaging |
Het |
Iqcm |
G |
T |
8: 75,753,352 (GRCm38) |
G313W |
probably damaging |
Het |
Jph2 |
A |
G |
2: 163,376,286 (GRCm38) |
S157P |
probably damaging |
Het |
Mast4 |
T |
C |
13: 102,737,496 (GRCm38) |
E1596G |
probably damaging |
Het |
Mllt6 |
T |
A |
11: 97,676,934 (GRCm38) |
L759Q |
probably damaging |
Het |
Nalcn |
A |
G |
14: 123,321,323 (GRCm38) |
L837P |
probably damaging |
Het |
Neb |
G |
A |
2: 52,147,189 (GRCm38) |
T6836I |
probably damaging |
Het |
Nol12 |
T |
A |
15: 78,940,080 (GRCm38) |
D133E |
probably benign |
Het |
Olfr1136 |
A |
G |
2: 87,693,570 (GRCm38) |
V104A |
probably benign |
Het |
Oxtr |
C |
A |
6: 112,477,099 (GRCm38) |
|
probably benign |
Het |
Pcmt1 |
A |
G |
10: 7,663,149 (GRCm38) |
L38P |
probably damaging |
Het |
Pik3r2 |
T |
C |
8: 70,769,173 (GRCm38) |
Y617C |
probably damaging |
Het |
Pvr |
G |
T |
7: 19,905,802 (GRCm38) |
Q380K |
probably benign |
Het |
Rtn2 |
A |
G |
7: 19,287,259 (GRCm38) |
E188G |
probably benign |
Het |
Setd4 |
C |
A |
16: 93,590,030 (GRCm38) |
R260L |
probably benign |
Het |
Six5 |
A |
G |
7: 19,096,569 (GRCm38) |
N374D |
probably benign |
Het |
Slc9b1 |
T |
C |
3: 135,371,965 (GRCm38) |
I140T |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,172,063 (GRCm38) |
F797L |
probably damaging |
Het |
Tbata |
T |
C |
10: 61,185,363 (GRCm38) |
L262P |
probably damaging |
Het |
Tti1 |
A |
T |
2: 158,008,427 (GRCm38) |
C297* |
probably null |
Het |
Ush1c |
C |
A |
7: 46,225,624 (GRCm38) |
G139C |
probably damaging |
Het |
Vmn1r1 |
C |
T |
1: 182,157,777 (GRCm38) |
V108I |
probably benign |
Het |
Vmn2r116 |
C |
T |
17: 23,401,092 (GRCm38) |
T600I |
probably damaging |
Het |
Zfp873 |
A |
G |
10: 82,060,589 (GRCm38) |
T422A |
probably benign |
Het |
Zfp943 |
G |
A |
17: 21,992,908 (GRCm38) |
C325Y |
probably damaging |
Het |
|
Other mutations in Prl7a2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01484:Prl7a2
|
APN |
13 |
27,659,208 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02424:Prl7a2
|
APN |
13 |
27,667,970 (GRCm38) |
missense |
probably null |
0.08 |
IGL02734:Prl7a2
|
APN |
13 |
27,659,207 (GRCm38) |
missense |
probably benign |
0.38 |
IGL02823:Prl7a2
|
APN |
13 |
27,662,751 (GRCm38) |
missense |
possibly damaging |
0.95 |
PIT4260001:Prl7a2
|
UTSW |
13 |
27,659,276 (GRCm38) |
nonsense |
probably null |
|
R0733:Prl7a2
|
UTSW |
13 |
27,662,688 (GRCm38) |
missense |
probably damaging |
1.00 |
R1371:Prl7a2
|
UTSW |
13 |
27,662,767 (GRCm38) |
missense |
probably benign |
0.01 |
R1778:Prl7a2
|
UTSW |
13 |
27,659,271 (GRCm38) |
missense |
probably damaging |
0.98 |
R1857:Prl7a2
|
UTSW |
13 |
27,659,180 (GRCm38) |
nonsense |
probably null |
|
R2063:Prl7a2
|
UTSW |
13 |
27,660,887 (GRCm38) |
missense |
probably damaging |
0.98 |
R2064:Prl7a2
|
UTSW |
13 |
27,660,887 (GRCm38) |
missense |
probably damaging |
0.98 |
R2065:Prl7a2
|
UTSW |
13 |
27,660,887 (GRCm38) |
missense |
probably damaging |
0.98 |
R2067:Prl7a2
|
UTSW |
13 |
27,660,887 (GRCm38) |
missense |
probably damaging |
0.98 |
R2068:Prl7a2
|
UTSW |
13 |
27,660,887 (GRCm38) |
missense |
probably damaging |
0.98 |
R2176:Prl7a2
|
UTSW |
13 |
27,659,106 (GRCm38) |
missense |
probably benign |
0.10 |
R2213:Prl7a2
|
UTSW |
13 |
27,665,068 (GRCm38) |
missense |
probably benign |
0.06 |
R4111:Prl7a2
|
UTSW |
13 |
27,665,067 (GRCm38) |
missense |
possibly damaging |
0.96 |
R4459:Prl7a2
|
UTSW |
13 |
27,665,996 (GRCm38) |
missense |
probably benign |
0.21 |
R4483:Prl7a2
|
UTSW |
13 |
27,660,947 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4722:Prl7a2
|
UTSW |
13 |
27,660,875 (GRCm38) |
missense |
probably damaging |
1.00 |
R5360:Prl7a2
|
UTSW |
13 |
27,659,160 (GRCm38) |
missense |
probably benign |
0.22 |
R5778:Prl7a2
|
UTSW |
13 |
27,661,000 (GRCm38) |
nonsense |
probably null |
|
R7107:Prl7a2
|
UTSW |
13 |
27,659,093 (GRCm38) |
missense |
possibly damaging |
0.89 |
R7600:Prl7a2
|
UTSW |
13 |
27,659,281 (GRCm38) |
missense |
possibly damaging |
0.63 |
R8298:Prl7a2
|
UTSW |
13 |
27,661,011 (GRCm38) |
missense |
probably benign |
0.00 |
R8447:Prl7a2
|
UTSW |
13 |
27,665,958 (GRCm38) |
missense |
possibly damaging |
0.72 |
R9009:Prl7a2
|
UTSW |
13 |
27,666,011 (GRCm38) |
missense |
probably damaging |
1.00 |
R9331:Prl7a2
|
UTSW |
13 |
27,665,079 (GRCm38) |
missense |
probably damaging |
1.00 |
R9624:Prl7a2
|
UTSW |
13 |
27,665,886 (GRCm38) |
nonsense |
probably null |
|
|