Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810055G02Rik |
A |
T |
19: 3,765,784 (GRCm39) |
M20L |
probably benign |
Het |
Aadacl4fm1 |
C |
T |
4: 144,255,354 (GRCm39) |
A258V |
probably benign |
Het |
Abca8b |
T |
A |
11: 109,833,163 (GRCm39) |
D1241V |
probably benign |
Het |
Adam20 |
G |
A |
8: 41,248,490 (GRCm39) |
R200H |
probably benign |
Het |
Adcy10 |
T |
C |
1: 165,340,681 (GRCm39) |
F229L |
probably damaging |
Het |
Adsl |
A |
T |
15: 80,839,840 (GRCm39) |
N126I |
probably benign |
Het |
Ahnak |
GATCTCTAT |
GAT |
19: 8,984,393 (GRCm39) |
|
probably benign |
Het |
Ahnak |
AGATCTC |
A |
19: 8,984,392 (GRCm39) |
|
probably benign |
Het |
Aktip |
G |
A |
8: 91,856,355 (GRCm39) |
P41S |
probably damaging |
Het |
Alkbh3 |
C |
A |
2: 93,811,318 (GRCm39) |
R258L |
probably damaging |
Het |
Arfgap3 |
A |
G |
15: 83,197,734 (GRCm39) |
Y341H |
probably benign |
Het |
Arhgef26 |
C |
T |
3: 62,331,034 (GRCm39) |
L583F |
probably damaging |
Het |
Arhgef40 |
T |
C |
14: 52,226,415 (GRCm39) |
I153T |
probably damaging |
Het |
Atp1a1 |
T |
C |
3: 101,498,757 (GRCm39) |
S179G |
probably benign |
Het |
Bok |
T |
C |
1: 93,614,229 (GRCm39) |
S21P |
probably damaging |
Het |
Ccdc136 |
A |
G |
6: 29,417,441 (GRCm39) |
E754G |
probably benign |
Het |
Cers3 |
A |
G |
7: 66,423,378 (GRCm39) |
K108E |
probably benign |
Het |
Cmya5 |
T |
C |
13: 93,201,881 (GRCm39) |
|
probably null |
Het |
Col19a1 |
T |
C |
1: 24,367,148 (GRCm39) |
E478G |
possibly damaging |
Het |
Colec10 |
T |
A |
15: 54,323,180 (GRCm39) |
S134R |
possibly damaging |
Het |
Ctnnb1 |
A |
T |
9: 120,784,895 (GRCm39) |
I514F |
probably damaging |
Het |
Cux1 |
C |
T |
5: 136,338,673 (GRCm39) |
E664K |
probably benign |
Het |
Dars1 |
T |
C |
1: 128,333,199 (GRCm39) |
Q75R |
probably benign |
Het |
Disp1 |
T |
A |
1: 182,917,379 (GRCm39) |
S16C |
probably damaging |
Het |
Dnah7a |
A |
T |
1: 53,598,299 (GRCm39) |
V1412E |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,044,182 (GRCm39) |
V226I |
probably benign |
Het |
Ep400 |
T |
A |
5: 110,904,509 (GRCm39) |
H30L |
unknown |
Het |
Ephx4 |
A |
G |
5: 107,567,647 (GRCm39) |
I202V |
probably benign |
Het |
Exoc3 |
A |
T |
13: 74,341,027 (GRCm39) |
F259Y |
probably damaging |
Het |
Ezr |
T |
C |
17: 7,020,394 (GRCm39) |
E229G |
probably damaging |
Het |
Fat1 |
A |
T |
8: 45,470,417 (GRCm39) |
I1472L |
probably benign |
Het |
Fsd1l |
T |
G |
4: 53,679,972 (GRCm39) |
D223E |
probably benign |
Het |
Gata6 |
A |
T |
18: 11,059,064 (GRCm39) |
D377V |
possibly damaging |
Het |
Gm12185 |
A |
T |
11: 48,798,216 (GRCm39) |
M759K |
probably benign |
Het |
Gm9922 |
C |
T |
14: 101,966,893 (GRCm39) |
A120T |
unknown |
Het |
Hectd4 |
A |
T |
5: 121,448,744 (GRCm39) |
Y364F |
probably benign |
Het |
Hnrnph1 |
A |
G |
11: 50,276,696 (GRCm39) |
S465G |
unknown |
Het |
Ifi204 |
T |
C |
1: 173,576,924 (GRCm39) |
Y559C |
probably damaging |
Het |
Ift88 |
T |
C |
14: 57,718,853 (GRCm39) |
S613P |
probably damaging |
Het |
Kif21a |
G |
C |
15: 90,869,528 (GRCm39) |
A441G |
probably damaging |
Het |
Kif21a |
G |
T |
15: 90,879,715 (GRCm39) |
T191K |
probably benign |
Het |
Lrit1 |
T |
A |
14: 36,782,084 (GRCm39) |
C252* |
probably null |
Het |
Ncbp1 |
T |
A |
4: 46,144,837 (GRCm39) |
D29E |
probably benign |
Het |
Nphp4 |
T |
G |
4: 152,631,521 (GRCm39) |
V807G |
probably benign |
Het |
Nsd1 |
T |
C |
13: 55,393,856 (GRCm39) |
S589P |
possibly damaging |
Het |
Oas1b |
T |
A |
5: 120,952,550 (GRCm39) |
N80K |
probably damaging |
Het |
Oprk1 |
T |
A |
1: 5,669,096 (GRCm39) |
C181S |
probably damaging |
Het |
Oprl1 |
T |
A |
2: 181,360,212 (GRCm39) |
N89K |
probably damaging |
Het |
Or5w12 |
A |
T |
2: 87,502,105 (GRCm39) |
I202N |
probably benign |
Het |
Or8k53 |
G |
A |
2: 86,177,583 (GRCm39) |
H176Y |
probably benign |
Het |
Pdcd11 |
A |
G |
19: 47,117,741 (GRCm39) |
K1697E |
probably damaging |
Het |
Pdp1 |
G |
A |
4: 11,961,607 (GRCm39) |
H254Y |
probably benign |
Het |
Pds5b |
A |
T |
5: 150,729,128 (GRCm39) |
D1419V |
possibly damaging |
Het |
Per1 |
G |
T |
11: 68,991,475 (GRCm39) |
G3V |
probably benign |
Het |
Pex16 |
C |
A |
2: 92,206,988 (GRCm39) |
N55K |
probably damaging |
Het |
Phldb2 |
C |
A |
16: 45,595,340 (GRCm39) |
L862F |
probably benign |
Het |
Pld5 |
T |
A |
1: 175,791,572 (GRCm39) |
D478V |
probably benign |
Het |
Pms2 |
T |
C |
5: 143,851,614 (GRCm39) |
I177T |
probably damaging |
Het |
Pou1f1 |
A |
T |
16: 65,326,758 (GRCm39) |
E119D |
probably benign |
Het |
Ppp2r1a |
A |
C |
17: 21,179,058 (GRCm39) |
E295A |
probably damaging |
Het |
Qrfprl |
A |
G |
6: 65,433,124 (GRCm39) |
I315V |
probably benign |
Het |
Rad51ap2 |
A |
T |
12: 11,507,593 (GRCm39) |
N505I |
possibly damaging |
Het |
Rasal3 |
A |
C |
17: 32,615,536 (GRCm39) |
V434G |
probably damaging |
Het |
Rasgrf2 |
C |
T |
13: 92,136,092 (GRCm39) |
V6M |
|
Het |
Rwdd1 |
A |
T |
10: 33,877,152 (GRCm39) |
D197E |
|
Het |
Scn11a |
A |
T |
9: 119,619,076 (GRCm39) |
C755* |
probably null |
Het |
Skil |
T |
C |
3: 31,171,009 (GRCm39) |
S443P |
probably benign |
Het |
Slc12a6 |
T |
C |
2: 112,186,817 (GRCm39) |
C939R |
probably damaging |
Het |
Slc25a36 |
A |
G |
9: 96,961,230 (GRCm39) |
S269P |
probably benign |
Het |
Srrm4 |
T |
A |
5: 116,620,452 (GRCm39) |
H92L |
unknown |
Het |
Styk1 |
CTCTTCATGATTTTCTT |
CTCTT |
6: 131,278,612 (GRCm39) |
|
probably benign |
Het |
Tbc1d4 |
A |
T |
14: 101,744,846 (GRCm39) |
V260E |
probably benign |
Het |
Tbc1d8 |
T |
C |
1: 39,424,313 (GRCm39) |
N593D |
probably damaging |
Het |
Trex1 |
C |
A |
9: 108,887,805 (GRCm39) |
R62L |
probably damaging |
Het |
Trpm3 |
A |
T |
19: 22,692,716 (GRCm39) |
D269V |
possibly damaging |
Het |
Trpv4 |
G |
T |
5: 114,771,211 (GRCm39) |
Y439* |
probably null |
Het |
Ttn |
G |
A |
2: 76,564,592 (GRCm39) |
T28515I |
probably damaging |
Het |
Ucn2 |
G |
A |
9: 108,815,571 (GRCm39) |
G111D |
probably damaging |
Het |
Uhrf2 |
A |
G |
19: 30,033,881 (GRCm39) |
I212V |
possibly damaging |
Het |
Usp24 |
T |
A |
4: 106,204,564 (GRCm39) |
M261K |
probably benign |
Het |
Vmn1r235 |
A |
T |
17: 21,481,960 (GRCm39) |
D95V |
probably benign |
Het |
Vwf |
G |
A |
6: 125,601,536 (GRCm39) |
R826Q |
|
Het |
Zfp1002 |
C |
T |
2: 150,096,496 (GRCm39) |
R311Q |
probably benign |
Het |
Zfp28 |
T |
C |
7: 6,396,878 (GRCm39) |
C438R |
probably damaging |
Het |
|
Other mutations in Nlrp10 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01374:Nlrp10
|
APN |
7 |
108,523,788 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL01482:Nlrp10
|
APN |
7 |
108,526,159 (GRCm39) |
missense |
probably benign |
|
IGL02043:Nlrp10
|
APN |
7 |
108,524,709 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03129:Nlrp10
|
APN |
7 |
108,524,118 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02835:Nlrp10
|
UTSW |
7 |
108,523,869 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0106:Nlrp10
|
UTSW |
7 |
108,524,529 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0106:Nlrp10
|
UTSW |
7 |
108,524,529 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0540:Nlrp10
|
UTSW |
7 |
108,523,492 (GRCm39) |
missense |
probably benign |
0.26 |
R0607:Nlrp10
|
UTSW |
7 |
108,523,492 (GRCm39) |
missense |
probably benign |
0.26 |
R1166:Nlrp10
|
UTSW |
7 |
108,524,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R1248:Nlrp10
|
UTSW |
7 |
108,525,088 (GRCm39) |
missense |
probably benign |
0.08 |
R1450:Nlrp10
|
UTSW |
7 |
108,524,595 (GRCm39) |
missense |
probably damaging |
0.98 |
R1459:Nlrp10
|
UTSW |
7 |
108,523,555 (GRCm39) |
missense |
probably benign |
|
R1567:Nlrp10
|
UTSW |
7 |
108,526,257 (GRCm39) |
missense |
probably benign |
0.02 |
R1635:Nlrp10
|
UTSW |
7 |
108,523,737 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1845:Nlrp10
|
UTSW |
7 |
108,526,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R1912:Nlrp10
|
UTSW |
7 |
108,524,602 (GRCm39) |
nonsense |
probably null |
|
R1952:Nlrp10
|
UTSW |
7 |
108,523,770 (GRCm39) |
missense |
probably benign |
0.20 |
R1953:Nlrp10
|
UTSW |
7 |
108,524,325 (GRCm39) |
missense |
probably benign |
0.00 |
R2079:Nlrp10
|
UTSW |
7 |
108,524,835 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3615:Nlrp10
|
UTSW |
7 |
108,523,683 (GRCm39) |
missense |
probably benign |
|
R3616:Nlrp10
|
UTSW |
7 |
108,523,683 (GRCm39) |
missense |
probably benign |
|
R4207:Nlrp10
|
UTSW |
7 |
108,523,548 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4786:Nlrp10
|
UTSW |
7 |
108,524,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R5048:Nlrp10
|
UTSW |
7 |
108,523,772 (GRCm39) |
missense |
probably benign |
0.01 |
R5568:Nlrp10
|
UTSW |
7 |
108,523,468 (GRCm39) |
missense |
probably benign |
0.00 |
R5993:Nlrp10
|
UTSW |
7 |
108,526,220 (GRCm39) |
missense |
probably benign |
0.00 |
R6033:Nlrp10
|
UTSW |
7 |
108,523,784 (GRCm39) |
missense |
probably benign |
0.17 |
R6033:Nlrp10
|
UTSW |
7 |
108,523,784 (GRCm39) |
missense |
probably benign |
0.17 |
R6170:Nlrp10
|
UTSW |
7 |
108,523,671 (GRCm39) |
missense |
probably benign |
0.00 |
R6320:Nlrp10
|
UTSW |
7 |
108,524,953 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6935:Nlrp10
|
UTSW |
7 |
108,526,107 (GRCm39) |
missense |
probably damaging |
0.99 |
R7024:Nlrp10
|
UTSW |
7 |
108,524,405 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7081:Nlrp10
|
UTSW |
7 |
108,523,855 (GRCm39) |
missense |
probably benign |
0.02 |
R7397:Nlrp10
|
UTSW |
7 |
108,523,899 (GRCm39) |
missense |
probably damaging |
1.00 |
R7720:Nlrp10
|
UTSW |
7 |
108,523,695 (GRCm39) |
missense |
probably benign |
0.36 |
R7763:Nlrp10
|
UTSW |
7 |
108,525,033 (GRCm39) |
missense |
probably damaging |
0.99 |
R7776:Nlrp10
|
UTSW |
7 |
108,524,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Nlrp10
|
UTSW |
7 |
108,523,468 (GRCm39) |
missense |
probably benign |
0.00 |
R7852:Nlrp10
|
UTSW |
7 |
108,524,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R8272:Nlrp10
|
UTSW |
7 |
108,525,103 (GRCm39) |
missense |
probably benign |
0.00 |
R9181:Nlrp10
|
UTSW |
7 |
108,524,108 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Nlrp10
|
UTSW |
7 |
108,525,058 (GRCm39) |
nonsense |
probably null |
|
|