Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
T |
A |
5: 77,039,626 (GRCm39) |
T228S |
probably benign |
Het |
Adamts2 |
C |
T |
11: 50,683,612 (GRCm39) |
P965S |
probably damaging |
Het |
Ankrd11 |
A |
G |
8: 123,618,485 (GRCm39) |
I1768T |
probably benign |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Baz2b |
A |
T |
2: 59,743,234 (GRCm39) |
L1579Q |
probably damaging |
Het |
Btbd7 |
A |
G |
12: 102,757,034 (GRCm39) |
V684A |
probably damaging |
Het |
Camk1g |
T |
A |
1: 193,038,665 (GRCm39) |
I86F |
probably benign |
Het |
Capn13 |
A |
T |
17: 73,689,889 (GRCm39) |
S41T |
possibly damaging |
Het |
Cep192 |
C |
A |
18: 67,980,504 (GRCm39) |
L1422I |
probably damaging |
Het |
Chaf1a |
T |
C |
17: 56,354,380 (GRCm39) |
F217L |
unknown |
Het |
Clca3b |
A |
T |
3: 144,529,274 (GRCm39) |
M800K |
possibly damaging |
Het |
Cplane1 |
A |
G |
15: 8,258,443 (GRCm39) |
T2230A |
probably benign |
Het |
Crocc |
A |
G |
4: 140,744,388 (GRCm39) |
V1836A |
probably benign |
Het |
Csmd2 |
G |
A |
4: 128,377,188 (GRCm39) |
V2023M |
possibly damaging |
Het |
Cul9 |
A |
G |
17: 46,854,486 (GRCm39) |
V72A |
possibly damaging |
Het |
Ddx52 |
T |
C |
11: 83,834,269 (GRCm39) |
|
probably null |
Het |
Dennd5b |
A |
C |
6: 148,969,703 (GRCm39) |
V250G |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Gtpbp4 |
A |
T |
13: 9,023,285 (GRCm39) |
M593K |
probably benign |
Het |
Il21 |
A |
G |
3: 37,286,681 (GRCm39) |
F12L |
probably benign |
Het |
Lrit2 |
T |
A |
14: 36,791,105 (GRCm39) |
N261K |
probably benign |
Het |
Lrrc39 |
G |
T |
3: 116,364,562 (GRCm39) |
C151F |
probably damaging |
Het |
Lsm14a |
C |
A |
7: 34,050,799 (GRCm39) |
R426L |
probably damaging |
Het |
Maml1 |
G |
A |
11: 50,157,774 (GRCm39) |
P134S |
probably benign |
Het |
Map3k13 |
T |
C |
16: 21,722,542 (GRCm39) |
C235R |
probably damaging |
Het |
Naip2 |
C |
T |
13: 100,298,489 (GRCm39) |
A516T |
possibly damaging |
Het |
Nsmaf |
T |
C |
4: 6,409,884 (GRCm39) |
E663G |
probably benign |
Het |
Ntrk3 |
T |
C |
7: 78,005,822 (GRCm39) |
N513S |
probably damaging |
Het |
Nufip1 |
T |
G |
14: 76,363,692 (GRCm39) |
N305K |
possibly damaging |
Het |
Or10al5 |
C |
T |
17: 38,062,916 (GRCm39) |
T57I |
possibly damaging |
Het |
Or2ag1b |
T |
A |
7: 106,288,918 (GRCm39) |
T7S |
probably benign |
Het |
Or4c10b |
A |
T |
2: 89,711,745 (GRCm39) |
T192S |
probably benign |
Het |
Or51a6 |
T |
A |
7: 102,604,175 (GRCm39) |
D218V |
probably benign |
Het |
Or9r3 |
A |
T |
10: 129,947,872 (GRCm39) |
Y262* |
probably null |
Het |
Pi4ka |
A |
G |
16: 17,194,894 (GRCm39) |
V168A |
probably benign |
Het |
Prex2 |
T |
C |
1: 11,301,996 (GRCm39) |
V1433A |
probably damaging |
Het |
Prr3 |
G |
A |
17: 36,285,484 (GRCm39) |
R86* |
probably null |
Het |
Ptprz1 |
T |
C |
6: 23,049,605 (GRCm39) |
F1350L |
probably damaging |
Het |
R3hcc1l |
T |
C |
19: 42,552,046 (GRCm39) |
S348P |
possibly damaging |
Het |
Rag2 |
A |
T |
2: 101,459,960 (GRCm39) |
Q90L |
probably benign |
Het |
Scel |
T |
C |
14: 103,770,752 (GRCm39) |
L62P |
probably damaging |
Het |
Serpini1 |
A |
T |
3: 75,521,977 (GRCm39) |
E156V |
possibly damaging |
Het |
Skint4 |
T |
A |
4: 111,993,240 (GRCm39) |
I321K |
possibly damaging |
Het |
Slc28a2 |
A |
G |
2: 122,286,098 (GRCm39) |
D478G |
probably damaging |
Het |
Sppl2b |
G |
T |
10: 80,700,965 (GRCm39) |
V164F |
probably damaging |
Het |
Traf5 |
T |
A |
1: 191,729,470 (GRCm39) |
N527I |
probably benign |
Het |
Ttc3 |
T |
A |
16: 94,244,176 (GRCm39) |
D17E |
probably benign |
Het |
Txlnb |
G |
A |
10: 17,682,521 (GRCm39) |
A148T |
possibly damaging |
Het |
Ubtf |
A |
G |
11: 102,201,757 (GRCm39) |
Y256H |
probably damaging |
Het |
Usp25 |
T |
C |
16: 76,868,559 (GRCm39) |
F320S |
possibly damaging |
Het |
Utp14b |
T |
C |
1: 78,643,656 (GRCm39) |
V518A |
probably benign |
Het |
Utp20 |
A |
G |
10: 88,593,834 (GRCm39) |
V2192A |
possibly damaging |
Het |
Vmn1r173 |
T |
A |
7: 23,402,533 (GRCm39) |
M256K |
probably benign |
Het |
Vmn2r114 |
T |
A |
17: 23,515,962 (GRCm39) |
M510L |
probably benign |
Het |
Xdh |
T |
A |
17: 74,233,547 (GRCm39) |
Q189L |
probably benign |
Het |
Zfat |
C |
T |
15: 68,051,959 (GRCm39) |
A605T |
probably benign |
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 |
R0841:Prl7a1
|
UTSW |
13 |
27,826,393 (GRCm39) |
splice site |
probably benign |
|
R1005:Prl7a1
|
UTSW |
13 |
27,826,429 (GRCm39) |
missense |
possibly damaging |
0.75 |
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 |
|