Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam21 |
A |
C |
12: 81,607,064 (GRCm39) |
S233A |
probably damaging |
Het |
Adcy8 |
T |
A |
15: 64,571,067 (GRCm39) |
H1222L |
probably benign |
Het |
Aftph |
T |
C |
11: 20,676,836 (GRCm39) |
T258A |
probably benign |
Het |
Ano3 |
A |
C |
2: 110,715,194 (GRCm39) |
|
probably null |
Het |
Aox4 |
A |
G |
1: 58,303,013 (GRCm39) |
D1148G |
probably damaging |
Het |
Bcl11b |
A |
T |
12: 107,955,750 (GRCm39) |
I133N |
probably damaging |
Het |
Borcs7 |
T |
A |
19: 46,688,057 (GRCm39) |
D67E |
probably damaging |
Het |
Cacna2d4 |
T |
A |
6: 119,285,670 (GRCm39) |
I774N |
probably benign |
Het |
Catsperd |
A |
T |
17: 56,957,801 (GRCm39) |
Y236F |
probably benign |
Het |
Cblc |
T |
C |
7: 19,526,828 (GRCm39) |
S135G |
probably benign |
Het |
Ccdc168 |
C |
A |
1: 44,100,537 (GRCm39) |
R187L |
probably benign |
Het |
Ccdc178 |
A |
G |
18: 22,263,195 (GRCm39) |
V138A |
probably benign |
Het |
Cd300ld |
C |
T |
11: 114,878,186 (GRCm39) |
G109R |
probably damaging |
Het |
Cdh3 |
T |
A |
8: 107,279,109 (GRCm39) |
N690K |
probably damaging |
Het |
Ceacam1 |
T |
A |
7: 25,174,145 (GRCm39) |
Y170F |
possibly damaging |
Het |
Ceacam9 |
A |
C |
7: 16,457,652 (GRCm39) |
H55P |
possibly damaging |
Het |
Celsr1 |
C |
T |
15: 85,914,875 (GRCm39) |
V1033I |
possibly damaging |
Het |
Cep97 |
T |
C |
16: 55,725,683 (GRCm39) |
S807G |
probably benign |
Het |
Ces1b |
A |
G |
8: 93,783,982 (GRCm39) |
|
probably null |
Het |
Chn1 |
T |
C |
2: 73,510,234 (GRCm39) |
T92A |
probably damaging |
Het |
Cimap1b |
C |
A |
15: 89,263,365 (GRCm39) |
W6L |
probably damaging |
Het |
Cngb3 |
A |
C |
4: 19,425,575 (GRCm39) |
Y461S |
possibly damaging |
Het |
Col24a1 |
A |
G |
3: 145,049,459 (GRCm39) |
N629S |
probably benign |
Het |
Cpd |
T |
C |
11: 76,737,437 (GRCm39) |
D119G |
probably benign |
Het |
Cpsf1 |
T |
C |
15: 76,484,775 (GRCm39) |
D594G |
probably damaging |
Het |
Cpsf7 |
C |
T |
19: 10,509,203 (GRCm39) |
A38V |
probably benign |
Het |
Cry1 |
A |
T |
10: 84,983,783 (GRCm39) |
H224Q |
probably benign |
Het |
Ctr9 |
T |
A |
7: 110,633,014 (GRCm39) |
D87E |
probably damaging |
Het |
Cyp2u1 |
T |
A |
3: 131,087,144 (GRCm39) |
N479I |
probably benign |
Het |
Dip2c |
A |
G |
13: 9,642,785 (GRCm39) |
N672D |
probably benign |
Het |
Dnah14 |
T |
C |
1: 181,454,450 (GRCm39) |
V820A |
probably benign |
Het |
Efnb2 |
T |
C |
8: 8,710,524 (GRCm39) |
I31V |
probably benign |
Het |
Fgb |
T |
C |
3: 82,953,359 (GRCm39) |
Y137C |
probably damaging |
Het |
Fkbp15 |
A |
G |
4: 62,239,293 (GRCm39) |
V604A |
possibly damaging |
Het |
Flii |
A |
T |
11: 60,609,090 (GRCm39) |
N682K |
probably benign |
Het |
Fmo3 |
A |
G |
1: 162,781,796 (GRCm39) |
L519P |
possibly damaging |
Het |
Gapvd1 |
T |
A |
2: 34,607,385 (GRCm39) |
M538L |
probably benign |
Het |
Gbp11 |
A |
G |
5: 105,489,971 (GRCm39) |
V69A |
probably benign |
Het |
Ggn |
T |
A |
7: 28,871,605 (GRCm39) |
D364E |
probably benign |
Het |
Gm10377 |
G |
A |
14: 42,614,853 (GRCm39) |
P171S |
probably benign |
Het |
Gramd4 |
C |
T |
15: 86,019,607 (GRCm39) |
A625V |
probably benign |
Het |
Il2ra |
T |
A |
2: 11,647,831 (GRCm39) |
M7K |
probably benign |
Het |
Iqgap2 |
A |
T |
13: 95,836,846 (GRCm39) |
|
probably null |
Het |
Itgb4 |
T |
C |
11: 115,888,906 (GRCm39) |
V1083A |
probably benign |
Het |
Kcnma1 |
G |
A |
14: 23,544,638 (GRCm39) |
A573V |
possibly damaging |
Het |
Kirrel1 |
T |
C |
3: 86,995,729 (GRCm39) |
T402A |
probably benign |
Het |
Krt15 |
A |
T |
11: 100,026,386 (GRCm39) |
V100E |
possibly damaging |
Het |
Krt4 |
T |
A |
15: 101,828,823 (GRCm39) |
Q347L |
probably damaging |
Het |
Map3k21 |
T |
A |
8: 126,661,804 (GRCm39) |
I467N |
probably damaging |
Het |
Mastl |
A |
T |
2: 23,030,585 (GRCm39) |
S195T |
probably damaging |
Het |
Mis18bp1 |
G |
T |
12: 65,205,368 (GRCm39) |
T268K |
probably benign |
Het |
Mmp17 |
G |
A |
5: 129,682,836 (GRCm39) |
G492S |
probably null |
Het |
Myc |
T |
A |
15: 61,860,031 (GRCm39) |
S236T |
probably damaging |
Het |
Nlrp5 |
A |
T |
7: 23,117,848 (GRCm39) |
E524V |
probably damaging |
Het |
Nopchap1 |
T |
C |
10: 83,201,680 (GRCm39) |
V151A |
probably benign |
Het |
Oog4 |
T |
C |
4: 143,165,346 (GRCm39) |
N267S |
possibly damaging |
Het |
Or2a12 |
T |
A |
6: 42,904,469 (GRCm39) |
Y101* |
probably null |
Het |
Or4l15 |
A |
T |
14: 50,198,563 (GRCm39) |
|
probably null |
Het |
Or56a5 |
A |
G |
7: 104,793,086 (GRCm39) |
I138T |
possibly damaging |
Het |
Pde4dip |
T |
C |
3: 97,664,587 (GRCm39) |
E425G |
probably benign |
Het |
Piwil4 |
A |
C |
9: 14,638,729 (GRCm39) |
N312K |
probably benign |
Het |
Pmepa1 |
A |
G |
2: 173,076,212 (GRCm39) |
M47T |
possibly damaging |
Het |
Potefam1 |
A |
T |
2: 111,023,826 (GRCm39) |
S475T |
unknown |
Het |
Prkcg |
G |
A |
7: 3,368,069 (GRCm39) |
G372D |
probably benign |
Het |
Prune2 |
A |
G |
19: 17,096,734 (GRCm39) |
H746R |
probably benign |
Het |
Ptma |
GGAAGAAG |
GGAAGAAGAAG |
1: 86,457,261 (GRCm39) |
|
probably benign |
Het |
Rab3gap2 |
C |
G |
1: 184,983,265 (GRCm39) |
A468G |
probably damaging |
Het |
Ralb |
A |
G |
1: 119,400,129 (GRCm39) |
L123P |
|
Het |
Ralgapa2 |
G |
A |
2: 146,189,046 (GRCm39) |
T1288I |
probably benign |
Het |
Samd4b |
C |
A |
7: 28,122,926 (GRCm39) |
C44F |
probably benign |
Het |
Satb1 |
C |
A |
17: 52,090,008 (GRCm39) |
E280* |
probably null |
Het |
Sec1 |
T |
C |
7: 45,328,034 (GRCm39) |
T338A |
probably damaging |
Het |
Sec16a |
T |
C |
2: 26,331,734 (GRCm39) |
T94A |
probably benign |
Het |
Serpina1f |
G |
A |
12: 103,656,086 (GRCm39) |
R381W |
probably damaging |
Het |
Sfswap |
A |
T |
5: 129,620,305 (GRCm39) |
T525S |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,054,169 (GRCm39) |
|
probably null |
Het |
Spc24 |
A |
G |
9: 21,668,664 (GRCm39) |
L111P |
probably damaging |
Het |
St8sia2 |
T |
C |
7: 73,616,675 (GRCm39) |
D121G |
probably damaging |
Het |
Tanc2 |
A |
G |
11: 105,689,422 (GRCm39) |
T195A |
probably benign |
Het |
Tbc1d9 |
T |
A |
8: 83,997,890 (GRCm39) |
I1149N |
probably damaging |
Het |
Tph2 |
A |
T |
10: 114,987,016 (GRCm39) |
L258Q |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,879,557 (GRCm39) |
M781L |
probably benign |
Het |
Ubap2 |
G |
T |
4: 41,195,779 (GRCm39) |
P1005T |
probably benign |
Het |
Upf2 |
A |
G |
2: 5,965,851 (GRCm39) |
E157G |
unknown |
Het |
Urb2 |
C |
A |
8: 124,755,008 (GRCm39) |
D238E |
probably benign |
Het |
Vipr1 |
T |
C |
9: 121,497,621 (GRCm39) |
S380P |
probably damaging |
Het |
Zc3h18 |
T |
A |
8: 123,139,760 (GRCm39) |
S734T |
unknown |
Het |
Zmym6 |
T |
A |
4: 126,998,106 (GRCm39) |
Y381N |
probably damaging |
Het |
Zscan4e |
T |
C |
7: 11,041,251 (GRCm39) |
K207R |
probably benign |
Het |
|
Other mutations in Npr3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00326:Npr3
|
APN |
15 |
11,895,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01420:Npr3
|
APN |
15 |
11,858,718 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01599:Npr3
|
APN |
15 |
11,895,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01977:Npr3
|
APN |
15 |
11,858,804 (GRCm39) |
missense |
probably damaging |
1.00 |
eel
|
UTSW |
15 |
11,858,733 (GRCm39) |
missense |
probably damaging |
0.99 |
Electric
|
UTSW |
15 |
11,848,689 (GRCm39) |
missense |
possibly damaging |
0.73 |
Morray
|
UTSW |
15 |
11,851,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R0581:Npr3
|
UTSW |
15 |
11,851,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R0607:Npr3
|
UTSW |
15 |
11,845,368 (GRCm39) |
missense |
probably benign |
0.32 |
R1554:Npr3
|
UTSW |
15 |
11,848,649 (GRCm39) |
missense |
probably benign |
|
R1779:Npr3
|
UTSW |
15 |
11,851,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R1793:Npr3
|
UTSW |
15 |
11,848,665 (GRCm39) |
missense |
probably benign |
0.05 |
R1968:Npr3
|
UTSW |
15 |
11,905,055 (GRCm39) |
missense |
probably benign |
0.31 |
R2379:Npr3
|
UTSW |
15 |
11,883,449 (GRCm39) |
missense |
probably damaging |
0.99 |
R2883:Npr3
|
UTSW |
15 |
11,883,410 (GRCm39) |
missense |
possibly damaging |
0.50 |
R3080:Npr3
|
UTSW |
15 |
11,905,235 (GRCm39) |
missense |
probably benign |
0.01 |
R3745:Npr3
|
UTSW |
15 |
11,905,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R3803:Npr3
|
UTSW |
15 |
11,895,876 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Npr3
|
UTSW |
15 |
11,848,599 (GRCm39) |
missense |
probably benign |
0.32 |
R4411:Npr3
|
UTSW |
15 |
11,905,235 (GRCm39) |
missense |
probably benign |
0.01 |
R4412:Npr3
|
UTSW |
15 |
11,905,235 (GRCm39) |
missense |
probably benign |
0.01 |
R4667:Npr3
|
UTSW |
15 |
11,905,553 (GRCm39) |
missense |
possibly damaging |
0.58 |
R5209:Npr3
|
UTSW |
15 |
11,848,689 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5742:Npr3
|
UTSW |
15 |
11,883,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R6339:Npr3
|
UTSW |
15 |
11,845,361 (GRCm39) |
missense |
probably damaging |
0.99 |
R6605:Npr3
|
UTSW |
15 |
11,905,518 (GRCm39) |
missense |
probably damaging |
1.00 |
R6890:Npr3
|
UTSW |
15 |
11,883,478 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7009:Npr3
|
UTSW |
15 |
11,905,334 (GRCm39) |
missense |
probably damaging |
1.00 |
R7582:Npr3
|
UTSW |
15 |
11,895,768 (GRCm39) |
missense |
probably null |
1.00 |
R7743:Npr3
|
UTSW |
15 |
11,905,724 (GRCm39) |
start codon destroyed |
probably null |
0.90 |
R7896:Npr3
|
UTSW |
15 |
11,883,448 (GRCm39) |
missense |
probably damaging |
1.00 |
R8672:Npr3
|
UTSW |
15 |
11,851,579 (GRCm39) |
missense |
probably damaging |
1.00 |
R8840:Npr3
|
UTSW |
15 |
11,905,329 (GRCm39) |
missense |
probably damaging |
0.98 |
S24628:Npr3
|
UTSW |
15 |
11,848,649 (GRCm39) |
missense |
probably benign |
|
|