Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
G |
T |
11: 9,248,304 (GRCm39) |
V2684L |
probably benign |
Het |
Adamts9 |
T |
A |
6: 92,866,886 (GRCm39) |
I718F |
probably damaging |
Het |
Adcyap1r1 |
A |
G |
6: 55,455,067 (GRCm39) |
D110G |
probably benign |
Het |
Adgrd1 |
G |
A |
5: 129,208,641 (GRCm39) |
G281D |
probably damaging |
Het |
Afg1l |
A |
T |
10: 42,330,366 (GRCm39) |
C100* |
probably null |
Het |
Atp2a2 |
G |
A |
5: 122,595,372 (GRCm39) |
Q993* |
probably null |
Het |
Baz1a |
A |
G |
12: 54,977,095 (GRCm39) |
M389T |
probably benign |
Het |
Btnl4 |
T |
A |
17: 34,693,242 (GRCm39) |
M58L |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Cpeb1 |
A |
T |
7: 80,998,180 (GRCm39) |
F533Y |
probably damaging |
Het |
Ctnna1 |
T |
A |
18: 35,308,179 (GRCm39) |
N166K |
possibly damaging |
Het |
Ecsit |
T |
C |
9: 21,987,580 (GRCm39) |
H153R |
probably damaging |
Het |
Gbp8 |
T |
C |
5: 105,162,955 (GRCm39) |
K480E |
probably benign |
Het |
Glyat |
A |
T |
19: 12,625,373 (GRCm39) |
T66S |
probably benign |
Het |
Gm1110 |
T |
C |
9: 26,792,124 (GRCm39) |
Q632R |
probably benign |
Het |
Gm12185 |
C |
T |
11: 48,798,738 (GRCm39) |
R585Q |
probably damaging |
Het |
Gm17669 |
TAA |
TAAA |
18: 67,695,819 (GRCm39) |
|
probably null |
Het |
Gm7489 |
A |
C |
15: 53,749,195 (GRCm39) |
E89A |
unknown |
Het |
Grb7 |
C |
T |
11: 98,344,655 (GRCm39) |
Q353* |
probably null |
Het |
Ifi207 |
G |
A |
1: 173,562,738 (GRCm39) |
T136I |
unknown |
Het |
Ighv3-1 |
T |
C |
12: 113,928,224 (GRCm39) |
Y45C |
probably benign |
Het |
Ing5 |
A |
G |
1: 93,739,668 (GRCm39) |
M92V |
possibly damaging |
Het |
Ivl |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
TTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
3: 92,479,608 (GRCm39) |
|
probably benign |
Het |
Kdm6b |
A |
T |
11: 69,290,778 (GRCm39) |
D1630E |
unknown |
Het |
Lmo7 |
C |
T |
14: 102,124,923 (GRCm39) |
Q583* |
probably null |
Het |
Lrrc37a |
T |
C |
11: 103,395,338 (GRCm39) |
D29G |
probably benign |
Het |
Mpdz |
G |
T |
4: 81,337,263 (GRCm39) |
A10D |
probably damaging |
Het |
Myh4 |
A |
G |
11: 67,131,821 (GRCm39) |
M94V |
possibly damaging |
Het |
Nectin2 |
A |
C |
7: 19,472,252 (GRCm39) |
L46V |
probably benign |
Het |
Nynrin |
A |
T |
14: 56,101,425 (GRCm39) |
T365S |
probably benign |
Het |
Or4c120 |
A |
T |
2: 89,000,977 (GRCm39) |
I193K |
probably benign |
Het |
Pde4b |
A |
C |
4: 102,459,875 (GRCm39) |
E570A |
probably damaging |
Het |
Phf3 |
T |
C |
1: 30,855,622 (GRCm39) |
H988R |
probably damaging |
Het |
Ppfia2 |
A |
G |
10: 106,763,708 (GRCm39) |
K1234E |
probably benign |
Het |
Prp2 |
C |
T |
6: 132,577,510 (GRCm39) |
P266S |
unknown |
Het |
Ralgds |
T |
C |
2: 28,432,486 (GRCm39) |
L160P |
probably damaging |
Het |
Rasa1 |
A |
T |
13: 85,375,237 (GRCm39) |
M664K |
possibly damaging |
Het |
Ryr2 |
T |
C |
13: 11,570,334 (GRCm39) |
T4930A |
probably benign |
Het |
Senp8 |
T |
C |
9: 59,644,763 (GRCm39) |
Y131C |
probably damaging |
Het |
Sp100 |
A |
G |
1: 85,635,837 (GRCm39) |
I547M |
probably benign |
Het |
Spata20 |
A |
G |
11: 94,375,434 (GRCm39) |
M120T |
probably damaging |
Het |
Spata31 |
A |
G |
13: 65,069,664 (GRCm39) |
H604R |
probably benign |
Het |
Sycp1 |
A |
T |
3: 102,842,149 (GRCm39) |
S53T |
probably benign |
Het |
Tgm1 |
T |
C |
14: 55,950,022 (GRCm39) |
D62G |
unknown |
Het |
Trpm1 |
G |
C |
7: 63,918,309 (GRCm39) |
E1434Q |
possibly damaging |
Het |
Tshb |
A |
T |
3: 102,685,480 (GRCm39) |
Y50N |
probably damaging |
Het |
Wdr17 |
A |
T |
8: 55,126,614 (GRCm39) |
Y413* |
probably null |
Het |
Zdhhc16 |
G |
A |
19: 41,926,209 (GRCm39) |
G55R |
possibly damaging |
Het |
|
Other mutations in Prl7c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01388:Prl7c1
|
APN |
13 |
27,960,198 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03096:Prl7c1
|
APN |
13 |
27,957,689 (GRCm39) |
missense |
probably damaging |
0.96 |
R0566:Prl7c1
|
UTSW |
13 |
27,962,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R0856:Prl7c1
|
UTSW |
13 |
27,957,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0908:Prl7c1
|
UTSW |
13 |
27,957,717 (GRCm39) |
missense |
possibly damaging |
0.84 |
R1585:Prl7c1
|
UTSW |
13 |
27,962,838 (GRCm39) |
missense |
probably damaging |
0.99 |
R4193:Prl7c1
|
UTSW |
13 |
27,960,261 (GRCm39) |
missense |
probably benign |
0.01 |
R4628:Prl7c1
|
UTSW |
13 |
27,962,065 (GRCm39) |
missense |
probably benign |
|
R4728:Prl7c1
|
UTSW |
13 |
27,960,268 (GRCm39) |
missense |
probably benign |
0.00 |
R4873:Prl7c1
|
UTSW |
13 |
27,957,742 (GRCm39) |
missense |
probably benign |
0.01 |
R4875:Prl7c1
|
UTSW |
13 |
27,957,742 (GRCm39) |
missense |
probably benign |
0.01 |
R5714:Prl7c1
|
UTSW |
13 |
27,962,949 (GRCm39) |
nonsense |
probably null |
|
R6353:Prl7c1
|
UTSW |
13 |
27,957,709 (GRCm39) |
missense |
possibly damaging |
0.64 |
R6505:Prl7c1
|
UTSW |
13 |
27,957,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6878:Prl7c1
|
UTSW |
13 |
27,962,827 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7104:Prl7c1
|
UTSW |
13 |
27,962,952 (GRCm39) |
nonsense |
probably null |
|
R7879:Prl7c1
|
UTSW |
13 |
27,962,817 (GRCm39) |
missense |
probably damaging |
1.00 |
R7896:Prl7c1
|
UTSW |
13 |
27,962,070 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8828:Prl7c1
|
UTSW |
13 |
27,957,854 (GRCm39) |
missense |
probably benign |
0.14 |
R9142:Prl7c1
|
UTSW |
13 |
27,964,751 (GRCm39) |
start gained |
probably benign |
|
R9215:Prl7c1
|
UTSW |
13 |
27,960,204 (GRCm39) |
missense |
probably benign |
0.32 |
R9296:Prl7c1
|
UTSW |
13 |
27,962,812 (GRCm39) |
missense |
probably benign |
0.06 |
R9453:Prl7c1
|
UTSW |
13 |
27,957,870 (GRCm39) |
missense |
probably benign |
0.44 |
|