Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310002L09Rik |
T |
A |
4: 73,860,986 (GRCm39) |
M205L |
probably benign |
Het |
Aass |
A |
T |
6: 23,075,810 (GRCm39) |
C776S |
probably benign |
Het |
Abi3bp |
T |
C |
16: 56,488,639 (GRCm39) |
S1257P |
possibly damaging |
Het |
Arhgap9 |
T |
A |
10: 127,165,508 (GRCm39) |
M639K |
probably damaging |
Het |
Ctsj |
C |
T |
13: 61,150,357 (GRCm39) |
S214N |
probably damaging |
Het |
Dnali1 |
T |
C |
4: 124,959,340 (GRCm39) |
S18G |
possibly damaging |
Het |
Eif4g3 |
C |
T |
4: 137,893,129 (GRCm39) |
T959M |
probably damaging |
Het |
Eml3 |
G |
A |
19: 8,915,049 (GRCm39) |
M635I |
probably benign |
Het |
Eml6 |
A |
G |
11: 29,727,430 (GRCm39) |
F1231L |
probably benign |
Het |
Fat4 |
A |
C |
3: 39,050,147 (GRCm39) |
K4003T |
probably damaging |
Het |
Fcho1 |
C |
T |
8: 72,165,204 (GRCm39) |
A418T |
probably benign |
Het |
Fgfr2 |
G |
A |
7: 129,863,635 (GRCm39) |
P4S |
probably benign |
Het |
Fgfr2 |
T |
C |
7: 130,373,737 (GRCm39) |
|
probably benign |
Het |
Glp1r |
T |
C |
17: 31,138,406 (GRCm39) |
V160A |
probably benign |
Het |
Gm9726 |
C |
T |
12: 93,895,054 (GRCm39) |
|
noncoding transcript |
Het |
Gm9956 |
C |
A |
10: 56,621,424 (GRCm39) |
L29M |
unknown |
Het |
Gm9956 |
T |
A |
10: 56,621,425 (GRCm39) |
L29Q |
unknown |
Het |
Hddc3 |
T |
A |
7: 79,995,401 (GRCm39) |
S139T |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,555,358 (GRCm39) |
|
probably null |
Het |
Inpp5k |
T |
C |
11: 75,524,285 (GRCm39) |
|
probably benign |
Het |
Kcnq1 |
A |
G |
7: 142,661,189 (GRCm39) |
K32E |
probably benign |
Het |
Krtdap |
A |
T |
7: 30,488,975 (GRCm39) |
|
probably benign |
Het |
Ldb2 |
A |
G |
5: 44,690,016 (GRCm39) |
L201P |
probably damaging |
Het |
Mdn1 |
T |
C |
4: 32,752,032 (GRCm39) |
V4590A |
probably benign |
Het |
Nip7 |
C |
A |
8: 107,784,007 (GRCm39) |
H82Q |
probably benign |
Het |
Odad2 |
G |
T |
18: 7,268,436 (GRCm39) |
P361Q |
probably damaging |
Het |
Or52l1 |
A |
T |
7: 104,830,061 (GRCm39) |
V168E |
probably damaging |
Het |
Otud6b |
T |
A |
4: 14,812,532 (GRCm39) |
T272S |
probably benign |
Het |
Plxna1 |
A |
G |
6: 89,309,186 (GRCm39) |
V1131A |
probably damaging |
Het |
Sipa1 |
C |
A |
19: 5,704,835 (GRCm39) |
A587S |
probably benign |
Het |
Slc17a6 |
A |
T |
7: 51,275,063 (GRCm39) |
I41F |
probably benign |
Het |
Slc43a2 |
T |
A |
11: 75,457,815 (GRCm39) |
Y363* |
probably null |
Het |
Smg1 |
A |
T |
7: 117,742,524 (GRCm39) |
L3230Q |
possibly damaging |
Het |
Snapc1 |
C |
T |
12: 74,021,780 (GRCm39) |
|
probably benign |
Het |
Syne2 |
T |
C |
12: 76,121,209 (GRCm39) |
|
probably benign |
Het |
Tap2 |
C |
A |
17: 34,434,914 (GRCm39) |
D652E |
possibly damaging |
Het |
Trp53rkb |
T |
C |
2: 166,637,430 (GRCm39) |
C129R |
probably benign |
Het |
Ugt2a2 |
T |
C |
5: 87,622,648 (GRCm39) |
T317A |
probably benign |
Het |
Ugt3a1 |
G |
A |
15: 9,306,214 (GRCm39) |
S121N |
probably benign |
Het |
Unc80 |
T |
C |
1: 66,511,247 (GRCm39) |
V85A |
probably damaging |
Het |
Vmn2r71 |
A |
G |
7: 85,267,749 (GRCm39) |
T68A |
possibly damaging |
Het |
Zfp7 |
G |
A |
15: 76,775,704 (GRCm39) |
C582Y |
probably damaging |
Het |
|
Other mutations in Prl7a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00826:Prl7a1
|
APN |
13 |
27,824,778 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02862:Prl7a1
|
APN |
13 |
27,823,872 (GRCm39) |
missense |
probably benign |
0.05 |
R1005:Prl7a1
|
UTSW |
13 |
27,826,429 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1641:Prl7a1
|
UTSW |
13 |
27,817,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R1991:Prl7a1
|
UTSW |
13 |
27,817,655 (GRCm39) |
missense |
probably damaging |
0.96 |
R2233:Prl7a1
|
UTSW |
13 |
27,826,402 (GRCm39) |
critical splice donor site |
probably null |
|
R4061:Prl7a1
|
UTSW |
13 |
27,819,832 (GRCm39) |
missense |
possibly damaging |
0.83 |
R4239:Prl7a1
|
UTSW |
13 |
27,821,549 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4817:Prl7a1
|
UTSW |
13 |
27,819,747 (GRCm39) |
missense |
probably damaging |
0.99 |
R4976:Prl7a1
|
UTSW |
13 |
27,817,564 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4992:Prl7a1
|
UTSW |
13 |
27,819,669 (GRCm39) |
splice site |
probably null |
|
R5119:Prl7a1
|
UTSW |
13 |
27,817,564 (GRCm39) |
missense |
possibly damaging |
0.52 |
R5857:Prl7a1
|
UTSW |
13 |
27,824,684 (GRCm39) |
missense |
probably damaging |
0.99 |
R6060:Prl7a1
|
UTSW |
13 |
27,821,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R6164:Prl7a1
|
UTSW |
13 |
27,821,626 (GRCm39) |
missense |
probably benign |
0.00 |
R6581:Prl7a1
|
UTSW |
13 |
27,817,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R7126:Prl7a1
|
UTSW |
13 |
27,826,402 (GRCm39) |
critical splice donor site |
probably null |
|
R7892:Prl7a1
|
UTSW |
13 |
27,817,661 (GRCm39) |
missense |
not run |
|
R7908:Prl7a1
|
UTSW |
13 |
27,826,433 (GRCm39) |
start codon destroyed |
probably null |
0.91 |
R8376:Prl7a1
|
UTSW |
13 |
27,821,638 (GRCm39) |
missense |
probably benign |
0.00 |
R8771:Prl7a1
|
UTSW |
13 |
27,819,811 (GRCm39) |
missense |
probably damaging |
1.00 |
|