Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AAdacl4fm3 |
A |
G |
4: 144,430,263 (GRCm39) |
V242A |
possibly damaging |
Het |
Antxr2 |
T |
C |
5: 98,152,155 (GRCm39) |
D152G |
probably benign |
Het |
Blmh |
A |
T |
11: 76,856,758 (GRCm39) |
K118* |
probably null |
Het |
Bnip3 |
G |
A |
7: 138,499,801 (GRCm39) |
P62L |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,554,357 (GRCm39) |
T684S |
probably damaging |
Het |
Chd3 |
C |
A |
11: 69,248,209 (GRCm39) |
K894N |
possibly damaging |
Het |
Chkb |
T |
A |
15: 89,311,794 (GRCm39) |
R133S |
probably benign |
Het |
Dennd5a |
T |
C |
7: 109,507,579 (GRCm39) |
N803S |
probably benign |
Het |
Dync2li1 |
A |
T |
17: 84,956,668 (GRCm39) |
D276V |
possibly damaging |
Het |
Erap1 |
T |
C |
13: 74,822,908 (GRCm39) |
|
probably benign |
Het |
Hgsnat |
C |
T |
8: 26,462,965 (GRCm39) |
V70M |
probably benign |
Het |
Leprot |
T |
C |
4: 101,509,673 (GRCm39) |
|
probably null |
Het |
Lhcgr |
G |
A |
17: 89,057,546 (GRCm39) |
A315V |
probably benign |
Het |
Lrrn4 |
C |
T |
2: 132,712,588 (GRCm39) |
V412I |
probably benign |
Het |
Macrod2 |
G |
A |
2: 140,261,824 (GRCm39) |
|
probably null |
Het |
Mmaa |
G |
A |
8: 80,008,199 (GRCm39) |
R13C |
probably damaging |
Het |
Plpp4 |
T |
A |
7: 128,918,023 (GRCm39) |
I66N |
probably damaging |
Het |
Prss1 |
G |
T |
6: 41,439,553 (GRCm39) |
K95N |
possibly damaging |
Het |
Rasa2 |
C |
T |
9: 96,459,606 (GRCm39) |
|
probably benign |
Het |
Relb |
A |
G |
7: 19,350,336 (GRCm39) |
V208A |
possibly damaging |
Het |
Sema3d |
T |
C |
5: 12,555,806 (GRCm39) |
S178P |
probably damaging |
Het |
Slc18a1 |
A |
T |
8: 69,526,383 (GRCm39) |
W102R |
probably benign |
Het |
Slc39a8 |
A |
C |
3: 135,563,873 (GRCm39) |
K239N |
probably benign |
Het |
Stap1 |
A |
G |
5: 86,229,132 (GRCm39) |
H100R |
probably benign |
Het |
Suz12 |
T |
A |
11: 79,889,918 (GRCm39) |
V143E |
probably damaging |
Het |
Tmf1 |
A |
G |
6: 97,153,455 (GRCm39) |
V206A |
probably benign |
Het |
Trim16 |
T |
A |
11: 62,728,058 (GRCm39) |
|
probably benign |
Het |
Ube2b |
C |
T |
11: 51,891,119 (GRCm39) |
|
probably null |
Het |
Vmn1r223 |
T |
C |
13: 23,434,254 (GRCm39) |
S283P |
probably damaging |
Het |
Wrn |
T |
A |
8: 33,809,173 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Prl4a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Prl4a1
|
APN |
13 |
28,205,443 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02192:Prl4a1
|
APN |
13 |
28,202,554 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03006:Prl4a1
|
APN |
13 |
28,207,359 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03071:Prl4a1
|
APN |
13 |
28,204,246 (GRCm39) |
missense |
probably benign |
0.32 |
R4974:Prl4a1
|
UTSW |
13 |
28,207,308 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5208:Prl4a1
|
UTSW |
13 |
28,202,467 (GRCm39) |
missense |
probably benign |
0.33 |
R5946:Prl4a1
|
UTSW |
13 |
28,202,499 (GRCm39) |
missense |
probably damaging |
0.98 |
R6387:Prl4a1
|
UTSW |
13 |
28,202,482 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7236:Prl4a1
|
UTSW |
13 |
28,202,556 (GRCm39) |
missense |
probably benign |
|
R8213:Prl4a1
|
UTSW |
13 |
28,207,369 (GRCm39) |
nonsense |
probably null |
|
R8445:Prl4a1
|
UTSW |
13 |
28,205,445 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8828:Prl4a1
|
UTSW |
13 |
28,207,307 (GRCm39) |
missense |
probably damaging |
0.99 |
|