Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap12 |
A |
G |
10: 4,304,368 (GRCm39) |
S393G |
probably damaging |
Het |
Ankrd28 |
A |
G |
14: 31,430,083 (GRCm39) |
F862L |
probably damaging |
Het |
Ankrd31 |
T |
C |
13: 97,046,037 (GRCm39) |
*1546Q |
probably null |
Het |
Ankrd33b |
T |
C |
15: 31,297,894 (GRCm39) |
T288A |
probably benign |
Het |
Aox1 |
T |
C |
1: 58,145,227 (GRCm39) |
I1331T |
possibly damaging |
Het |
Atp13a5 |
A |
G |
16: 29,146,601 (GRCm39) |
L231P |
probably damaging |
Het |
C1qtnf12 |
T |
C |
4: 156,050,882 (GRCm39) |
F284L |
probably damaging |
Het |
Caprin1 |
A |
T |
2: 103,608,378 (GRCm39) |
H250Q |
probably damaging |
Het |
Cd2bp2 |
A |
C |
7: 126,793,923 (GRCm39) |
I122S |
probably damaging |
Het |
Cd300lf |
T |
A |
11: 115,024,738 (GRCm39) |
|
probably benign |
Het |
Ceacam14 |
A |
G |
7: 17,547,999 (GRCm39) |
I30V |
probably benign |
Het |
Chchd1 |
T |
A |
14: 20,753,385 (GRCm39) |
*56R |
probably null |
Het |
Ckap5 |
A |
G |
2: 91,409,861 (GRCm39) |
T948A |
probably benign |
Het |
Clec12a |
A |
T |
6: 129,340,949 (GRCm39) |
N243I |
possibly damaging |
Het |
Col11a2 |
A |
G |
17: 34,270,757 (GRCm39) |
M462V |
probably benign |
Het |
Col6a5 |
C |
T |
9: 105,822,833 (GRCm39) |
E175K |
unknown |
Het |
Csnka2ip |
T |
C |
16: 64,300,667 (GRCm39) |
|
probably benign |
Het |
D130040H23Rik |
C |
A |
8: 69,755,033 (GRCm39) |
T146N |
possibly damaging |
Het |
Dennd5b |
T |
C |
6: 148,943,485 (GRCm39) |
|
probably benign |
Het |
Fanci |
A |
G |
7: 79,045,726 (GRCm39) |
T23A |
probably benign |
Het |
Fmnl1 |
T |
C |
11: 103,071,741 (GRCm39) |
Y83H |
probably damaging |
Het |
Galnt13 |
C |
A |
2: 54,770,075 (GRCm39) |
T289N |
probably benign |
Het |
Gcn1 |
A |
G |
5: 115,733,404 (GRCm39) |
D1074G |
probably benign |
Het |
Gm10801 |
ATTTTCAGTTTTCTTGCCATATTCCACGTCCTGCACTGGACATTTCTAAATTTTCCACCTTTTTCAGTTTTC |
ATTTTCAGTTTTC |
2: 98,492,669 (GRCm39) |
|
probably null |
Het |
Gnl1 |
T |
C |
17: 36,294,479 (GRCm39) |
I366T |
probably benign |
Het |
Gtf2ird2 |
A |
T |
5: 134,245,161 (GRCm39) |
Y473F |
probably damaging |
Het |
Ikzf1 |
T |
A |
11: 11,719,485 (GRCm39) |
D397E |
possibly damaging |
Het |
Ints15 |
C |
G |
5: 143,300,795 (GRCm39) |
E19Q |
probably benign |
Het |
Intu |
C |
T |
3: 40,637,789 (GRCm39) |
A425V |
possibly damaging |
Het |
Irag1 |
A |
T |
7: 110,477,347 (GRCm39) |
|
probably null |
Het |
Jakmip1 |
G |
A |
5: 37,343,084 (GRCm39) |
|
probably null |
Het |
Lif |
C |
A |
11: 4,219,225 (GRCm39) |
P168Q |
possibly damaging |
Het |
Myh11 |
A |
C |
16: 14,048,580 (GRCm39) |
S576A |
probably benign |
Het |
Neb |
A |
G |
2: 52,041,425 (GRCm39) |
V6559A |
probably damaging |
Het |
Nphs1 |
A |
G |
7: 30,162,625 (GRCm39) |
N368S |
probably damaging |
Het |
Npsr1 |
G |
A |
9: 24,224,525 (GRCm39) |
V148I |
probably benign |
Het |
Or51f1 |
C |
A |
7: 102,505,725 (GRCm39) |
G255* |
probably null |
Het |
Or52ab4 |
T |
C |
7: 102,987,573 (GRCm39) |
F104S |
probably damaging |
Het |
Or56a5 |
T |
A |
7: 104,792,832 (GRCm39) |
I223F |
probably damaging |
Het |
Or5b111 |
A |
T |
19: 13,291,502 (GRCm39) |
L49Q |
probably damaging |
Het |
Or7e166 |
C |
T |
9: 19,624,885 (GRCm39) |
T254I |
probably damaging |
Het |
Patz1 |
T |
C |
11: 3,241,856 (GRCm39) |
C415R |
probably damaging |
Het |
Pcdha9 |
A |
T |
18: 37,131,546 (GRCm39) |
N205I |
possibly damaging |
Het |
Pcdhga12 |
A |
T |
18: 37,899,711 (GRCm39) |
E181V |
probably benign |
Het |
Pcnx1 |
T |
C |
12: 82,018,158 (GRCm39) |
Y1333H |
probably damaging |
Het |
Phf7 |
A |
T |
14: 30,970,106 (GRCm39) |
|
probably benign |
Het |
Pomc |
T |
G |
12: 4,010,298 (GRCm39) |
S180A |
probably benign |
Het |
Ppp1r7 |
T |
A |
1: 93,288,536 (GRCm39) |
|
probably null |
Het |
Prrc2c |
A |
T |
1: 162,536,478 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
GGC |
GGCCACGGCCGC |
7: 97,229,113 (GRCm39) |
|
probably benign |
Het |
Semp2l1 |
C |
T |
1: 32,585,685 (GRCm39) |
R75Q |
probably benign |
Het |
Skint7 |
A |
G |
4: 111,839,198 (GRCm39) |
N164S |
possibly damaging |
Het |
Smg1 |
C |
A |
7: 117,751,900 (GRCm39) |
R2775M |
probably null |
Het |
Snrnp27 |
C |
T |
6: 86,653,226 (GRCm39) |
V131M |
probably damaging |
Het |
Spire1 |
C |
A |
18: 67,629,686 (GRCm39) |
R357L |
probably damaging |
Het |
Sspo |
G |
A |
6: 48,434,071 (GRCm39) |
V959I |
probably damaging |
Het |
St6galnac2 |
T |
C |
11: 116,568,458 (GRCm39) |
H335R |
probably damaging |
Het |
Stard13 |
C |
T |
5: 150,984,267 (GRCm39) |
R623H |
probably damaging |
Het |
Syde1 |
T |
A |
10: 78,424,683 (GRCm39) |
E383V |
probably damaging |
Het |
Taf10 |
A |
G |
7: 105,393,524 (GRCm39) |
M1T |
probably null |
Het |
Traf3ip3 |
A |
G |
1: 192,869,415 (GRCm39) |
C257R |
probably damaging |
Het |
Trpm8 |
G |
A |
1: 88,276,061 (GRCm39) |
|
probably benign |
Het |
Veph1 |
A |
G |
3: 66,171,301 (GRCm39) |
|
probably null |
Het |
Vmn1r169 |
A |
T |
7: 23,276,640 (GRCm39) |
T11S |
possibly damaging |
Het |
Wdhd1 |
A |
T |
14: 47,482,752 (GRCm39) |
S961T |
probably benign |
Het |
Zfp773 |
T |
C |
7: 7,135,469 (GRCm39) |
T376A |
possibly damaging |
Het |
|
Other mutations in Senp1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00684:Senp1
|
APN |
15 |
97,962,719 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01431:Senp1
|
APN |
15 |
97,980,144 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02674:Senp1
|
APN |
15 |
97,954,840 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03289:Senp1
|
APN |
15 |
97,982,926 (GRCm39) |
missense |
probably damaging |
1.00 |
Calmate
|
UTSW |
15 |
97,964,379 (GRCm39) |
missense |
probably benign |
0.00 |
mustard
|
UTSW |
15 |
97,946,152 (GRCm39) |
missense |
probably damaging |
1.00 |
nitrogen
|
UTSW |
15 |
97,964,412 (GRCm39) |
missense |
possibly damaging |
0.61 |
Sinapis
|
UTSW |
15 |
97,962,761 (GRCm39) |
splice site |
probably benign |
|
PIT1430001:Senp1
|
UTSW |
15 |
97,982,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R0026:Senp1
|
UTSW |
15 |
97,974,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R0026:Senp1
|
UTSW |
15 |
97,974,549 (GRCm39) |
missense |
probably damaging |
0.99 |
R0125:Senp1
|
UTSW |
15 |
97,946,112 (GRCm39) |
missense |
probably damaging |
0.99 |
R0531:Senp1
|
UTSW |
15 |
97,962,761 (GRCm39) |
splice site |
probably benign |
|
R1389:Senp1
|
UTSW |
15 |
97,973,734 (GRCm39) |
missense |
probably benign |
0.03 |
R1396:Senp1
|
UTSW |
15 |
97,974,435 (GRCm39) |
missense |
probably benign |
0.01 |
R1786:Senp1
|
UTSW |
15 |
97,973,848 (GRCm39) |
missense |
probably benign |
0.00 |
R1999:Senp1
|
UTSW |
15 |
97,956,196 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2045:Senp1
|
UTSW |
15 |
97,957,825 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2130:Senp1
|
UTSW |
15 |
97,973,848 (GRCm39) |
missense |
probably benign |
0.00 |
R2132:Senp1
|
UTSW |
15 |
97,973,848 (GRCm39) |
missense |
probably benign |
0.00 |
R2133:Senp1
|
UTSW |
15 |
97,973,848 (GRCm39) |
missense |
probably benign |
0.00 |
R2150:Senp1
|
UTSW |
15 |
97,956,196 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2327:Senp1
|
UTSW |
15 |
97,980,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R3815:Senp1
|
UTSW |
15 |
97,954,713 (GRCm39) |
missense |
probably damaging |
1.00 |
R4719:Senp1
|
UTSW |
15 |
97,954,731 (GRCm39) |
missense |
probably benign |
0.42 |
R4766:Senp1
|
UTSW |
15 |
97,943,777 (GRCm39) |
missense |
probably damaging |
0.98 |
R4866:Senp1
|
UTSW |
15 |
97,964,729 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5141:Senp1
|
UTSW |
15 |
97,974,488 (GRCm39) |
missense |
probably benign |
0.08 |
R5485:Senp1
|
UTSW |
15 |
97,964,377 (GRCm39) |
missense |
probably benign |
0.00 |
R5651:Senp1
|
UTSW |
15 |
97,974,498 (GRCm39) |
missense |
probably benign |
|
R5668:Senp1
|
UTSW |
15 |
97,946,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5729:Senp1
|
UTSW |
15 |
97,964,412 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6041:Senp1
|
UTSW |
15 |
97,956,097 (GRCm39) |
missense |
probably damaging |
0.97 |
R6395:Senp1
|
UTSW |
15 |
97,946,074 (GRCm39) |
missense |
probably damaging |
1.00 |
R6521:Senp1
|
UTSW |
15 |
97,946,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R7070:Senp1
|
UTSW |
15 |
97,980,187 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7075:Senp1
|
UTSW |
15 |
97,956,207 (GRCm39) |
missense |
probably benign |
0.00 |
R7262:Senp1
|
UTSW |
15 |
97,964,379 (GRCm39) |
missense |
probably benign |
0.00 |
R7625:Senp1
|
UTSW |
15 |
97,964,679 (GRCm39) |
missense |
probably benign |
0.10 |
R8318:Senp1
|
UTSW |
15 |
97,962,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R8368:Senp1
|
UTSW |
15 |
97,943,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R9373:Senp1
|
UTSW |
15 |
97,964,435 (GRCm39) |
missense |
probably benign |
0.00 |
R9650:Senp1
|
UTSW |
15 |
97,946,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R9756:Senp1
|
UTSW |
15 |
97,957,806 (GRCm39) |
missense |
possibly damaging |
0.92 |
|