Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700006A11Rik |
A |
C |
3: 124,208,042 (GRCm39) |
S212R |
probably benign |
Het |
4930562C15Rik |
T |
C |
16: 4,682,196 (GRCm39) |
S170P |
probably benign |
Het |
9330182O14Rik |
G |
A |
15: 40,008,303 (GRCm39) |
C59Y |
unknown |
Het |
AA986860 |
A |
G |
1: 130,670,624 (GRCm39) |
E282G |
possibly damaging |
Het |
Adam1a |
G |
T |
5: 121,657,397 (GRCm39) |
T632K |
probably benign |
Het |
Aspg |
G |
T |
12: 112,089,417 (GRCm39) |
A402S |
probably damaging |
Het |
Capn7 |
C |
T |
14: 31,058,642 (GRCm39) |
|
probably benign |
Het |
Card9 |
C |
T |
2: 26,246,896 (GRCm39) |
|
probably null |
Het |
Cdh13 |
T |
C |
8: 119,694,912 (GRCm39) |
V254A |
probably damaging |
Het |
Colec10 |
T |
C |
15: 54,325,767 (GRCm39) |
V199A |
probably damaging |
Het |
Copb2 |
T |
C |
9: 98,459,106 (GRCm39) |
S283P |
probably damaging |
Het |
Csmd1 |
G |
T |
8: 15,953,202 (GRCm39) |
S3426R |
probably damaging |
Het |
Cyp4f14 |
A |
G |
17: 33,133,562 (GRCm39) |
V98A |
probably benign |
Het |
Disp1 |
C |
A |
1: 182,869,030 (GRCm39) |
R1130L |
probably damaging |
Het |
Dysf |
A |
G |
6: 84,167,883 (GRCm39) |
|
probably null |
Het |
Efcab3 |
T |
C |
11: 104,629,100 (GRCm39) |
F926S |
probably benign |
Het |
Eif4ebp1 |
T |
C |
8: 27,763,447 (GRCm39) |
V80A |
probably damaging |
Het |
Eloa |
T |
A |
4: 135,736,452 (GRCm39) |
I565F |
probably damaging |
Het |
Espn |
G |
T |
4: 152,215,721 (GRCm39) |
H513N |
probably benign |
Het |
Fam83c |
C |
T |
2: 155,671,491 (GRCm39) |
S648N |
probably benign |
Het |
Fdxr |
C |
T |
11: 115,160,403 (GRCm39) |
V351M |
probably benign |
Het |
Fras1 |
A |
T |
5: 96,862,260 (GRCm39) |
D2213V |
probably damaging |
Het |
Gbp4 |
T |
A |
5: 105,267,825 (GRCm39) |
I474F |
possibly damaging |
Het |
Golgb1 |
T |
C |
16: 36,734,035 (GRCm39) |
V1135A |
probably benign |
Het |
Gpt2 |
G |
A |
8: 86,244,681 (GRCm39) |
E325K |
probably benign |
Het |
Hipk2 |
A |
T |
6: 38,795,413 (GRCm39) |
Y285* |
probably null |
Het |
Ifi27l2b |
T |
C |
12: 103,417,579 (GRCm39) |
I203V |
probably damaging |
Het |
Itga10 |
T |
A |
3: 96,559,081 (GRCm39) |
M390K |
probably damaging |
Het |
Itgb8 |
G |
T |
12: 119,166,159 (GRCm39) |
S124* |
probably null |
Het |
Klhdc10 |
T |
A |
6: 30,441,826 (GRCm39) |
F173I |
probably damaging |
Het |
Kng2 |
T |
G |
16: 22,830,805 (GRCm39) |
N168T |
probably damaging |
Het |
Krtap24-1 |
T |
C |
16: 88,408,434 (GRCm39) |
T231A |
probably damaging |
Het |
Lbx2 |
A |
T |
6: 83,065,045 (GRCm39) |
D194V |
probably damaging |
Het |
Lrrc39 |
C |
A |
3: 116,359,562 (GRCm39) |
Q36K |
probably benign |
Het |
Madd |
T |
C |
2: 90,992,393 (GRCm39) |
E1093G |
possibly damaging |
Het |
Mfap3l |
A |
G |
8: 61,124,303 (GRCm39) |
T182A |
probably damaging |
Het |
Myo9b |
T |
A |
8: 71,786,345 (GRCm39) |
Y670* |
probably null |
Het |
Nbea |
A |
G |
3: 55,899,865 (GRCm39) |
L1428P |
probably damaging |
Het |
Nkx2-3 |
T |
C |
19: 43,603,245 (GRCm39) |
Y284H |
possibly damaging |
Het |
Nphp4 |
A |
G |
4: 152,640,141 (GRCm39) |
D1009G |
probably benign |
Het |
Npy2r |
G |
A |
3: 82,448,490 (GRCm39) |
A95V |
probably damaging |
Het |
Or5ap2 |
T |
C |
2: 85,680,254 (GRCm39) |
S153P |
probably benign |
Het |
Or5m11 |
T |
A |
2: 85,781,817 (GRCm39) |
S137T |
possibly damaging |
Het |
Palld |
A |
T |
8: 61,969,679 (GRCm39) |
V1215D |
unknown |
Het |
Pard6g |
T |
C |
18: 80,160,340 (GRCm39) |
I151T |
possibly damaging |
Het |
Parp12 |
T |
C |
6: 39,088,670 (GRCm39) |
I189V |
probably benign |
Het |
Parp4 |
A |
G |
14: 56,840,256 (GRCm39) |
I554V |
probably benign |
Het |
Pcnx2 |
G |
A |
8: 126,480,356 (GRCm39) |
P1984S |
probably damaging |
Het |
Piwil4 |
T |
C |
9: 14,648,196 (GRCm39) |
M128V |
probably benign |
Het |
Polr2a |
C |
A |
11: 69,628,288 (GRCm39) |
E1302* |
probably null |
Het |
Psg17 |
C |
A |
7: 18,548,421 (GRCm39) |
G450V |
probably damaging |
Het |
Psg17 |
C |
G |
7: 18,548,422 (GRCm39) |
G450R |
probably damaging |
Het |
Rag1 |
T |
C |
2: 101,474,128 (GRCm39) |
E338G |
probably damaging |
Het |
Rev3l |
A |
T |
10: 39,698,163 (GRCm39) |
K887* |
probably null |
Het |
Rragd |
T |
C |
4: 32,996,027 (GRCm39) |
F124S |
possibly damaging |
Het |
Scube1 |
A |
T |
15: 83,513,712 (GRCm39) |
|
probably null |
Het |
Sfpq |
A |
T |
4: 126,919,725 (GRCm39) |
D490V |
possibly damaging |
Het |
Smc1b |
G |
T |
15: 84,955,798 (GRCm39) |
Q1034K |
probably damaging |
Het |
Smg7 |
T |
C |
1: 152,753,831 (GRCm39) |
N5S |
probably benign |
Het |
Spata31d1a |
A |
C |
13: 59,850,301 (GRCm39) |
L609R |
probably damaging |
Het |
Ssh2 |
A |
G |
11: 77,345,164 (GRCm39) |
K1050E |
probably benign |
Het |
Stab1 |
G |
A |
14: 30,882,824 (GRCm39) |
T393I |
possibly damaging |
Het |
Sult2a4 |
C |
T |
7: 13,722,320 (GRCm39) |
W49* |
probably null |
Het |
Thrap3 |
A |
T |
4: 126,074,231 (GRCm39) |
S172T |
unknown |
Het |
Tmem130 |
A |
G |
5: 144,687,721 (GRCm39) |
V205A |
probably damaging |
Het |
Ube2d2b |
A |
G |
5: 107,978,717 (GRCm39) |
I123V |
probably benign |
Het |
Unc79 |
G |
T |
12: 103,027,652 (GRCm39) |
L414F |
probably damaging |
Het |
Vmn2r30 |
C |
T |
7: 7,337,183 (GRCm39) |
S151N |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,356,078 (GRCm39) |
T443S |
probably benign |
Het |
Zfp229 |
T |
A |
17: 21,961,597 (GRCm39) |
S51T |
probably damaging |
Het |
Zfp617 |
T |
C |
8: 72,686,384 (GRCm39) |
L238P |
probably damaging |
Het |
Zfp707 |
T |
A |
15: 75,845,398 (GRCm39) |
C87* |
probably null |
Het |
Zfp853 |
T |
C |
5: 143,275,362 (GRCm39) |
K101R |
unknown |
Het |
|
Other mutations in Nuggc |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01359:Nuggc
|
APN |
14 |
65,860,656 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01403:Nuggc
|
APN |
14 |
65,860,635 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01413:Nuggc
|
APN |
14 |
65,876,030 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02588:Nuggc
|
APN |
14 |
65,855,226 (GRCm39) |
splice site |
probably benign |
|
R0102:Nuggc
|
UTSW |
14 |
65,851,000 (GRCm39) |
missense |
probably null |
1.00 |
R0102:Nuggc
|
UTSW |
14 |
65,851,000 (GRCm39) |
missense |
probably null |
1.00 |
R0395:Nuggc
|
UTSW |
14 |
65,850,921 (GRCm39) |
nonsense |
probably null |
|
R0827:Nuggc
|
UTSW |
14 |
65,846,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R1496:Nuggc
|
UTSW |
14 |
65,861,582 (GRCm39) |
missense |
probably damaging |
0.96 |
R1861:Nuggc
|
UTSW |
14 |
65,879,450 (GRCm39) |
splice site |
probably benign |
|
R1986:Nuggc
|
UTSW |
14 |
65,879,370 (GRCm39) |
missense |
probably damaging |
0.98 |
R1995:Nuggc
|
UTSW |
14 |
65,848,623 (GRCm39) |
missense |
probably benign |
0.02 |
R2283:Nuggc
|
UTSW |
14 |
65,876,061 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2317:Nuggc
|
UTSW |
14 |
65,861,591 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3799:Nuggc
|
UTSW |
14 |
65,857,087 (GRCm39) |
missense |
probably benign |
0.00 |
R3980:Nuggc
|
UTSW |
14 |
65,856,542 (GRCm39) |
critical splice donor site |
probably null |
|
R4303:Nuggc
|
UTSW |
14 |
65,848,621 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4431:Nuggc
|
UTSW |
14 |
65,848,659 (GRCm39) |
missense |
probably benign |
0.19 |
R4734:Nuggc
|
UTSW |
14 |
65,860,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R5095:Nuggc
|
UTSW |
14 |
65,872,539 (GRCm39) |
nonsense |
probably null |
|
R5108:Nuggc
|
UTSW |
14 |
65,876,129 (GRCm39) |
missense |
probably damaging |
0.99 |
R5360:Nuggc
|
UTSW |
14 |
65,876,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R5547:Nuggc
|
UTSW |
14 |
65,879,330 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5636:Nuggc
|
UTSW |
14 |
65,885,637 (GRCm39) |
nonsense |
probably null |
|
R6494:Nuggc
|
UTSW |
14 |
65,885,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R6922:Nuggc
|
UTSW |
14 |
65,855,092 (GRCm39) |
missense |
probably damaging |
1.00 |
R6971:Nuggc
|
UTSW |
14 |
65,846,305 (GRCm39) |
missense |
probably benign |
0.04 |
R7273:Nuggc
|
UTSW |
14 |
65,857,057 (GRCm39) |
missense |
probably damaging |
0.99 |
R7282:Nuggc
|
UTSW |
14 |
65,855,072 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:Nuggc
|
UTSW |
14 |
65,885,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R7670:Nuggc
|
UTSW |
14 |
65,850,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R7780:Nuggc
|
UTSW |
14 |
65,882,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R7871:Nuggc
|
UTSW |
14 |
65,860,700 (GRCm39) |
missense |
probably benign |
0.01 |
R8250:Nuggc
|
UTSW |
14 |
65,879,318 (GRCm39) |
missense |
probably benign |
0.10 |
R8329:Nuggc
|
UTSW |
14 |
65,878,731 (GRCm39) |
missense |
probably benign |
0.01 |
R8334:Nuggc
|
UTSW |
14 |
65,882,478 (GRCm39) |
missense |
probably benign |
0.04 |
R8463:Nuggc
|
UTSW |
14 |
65,851,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8503:Nuggc
|
UTSW |
14 |
65,878,797 (GRCm39) |
critical splice donor site |
probably null |
|
R8737:Nuggc
|
UTSW |
14 |
65,882,535 (GRCm39) |
missense |
probably benign |
0.00 |
R8861:Nuggc
|
UTSW |
14 |
65,847,484 (GRCm39) |
critical splice donor site |
probably null |
|
R8914:Nuggc
|
UTSW |
14 |
65,879,354 (GRCm39) |
missense |
probably benign |
|
R9573:Nuggc
|
UTSW |
14 |
65,848,603 (GRCm39) |
missense |
probably benign |
0.37 |
R9666:Nuggc
|
UTSW |
14 |
65,857,045 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9792:Nuggc
|
UTSW |
14 |
65,847,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R9793:Nuggc
|
UTSW |
14 |
65,847,345 (GRCm39) |
missense |
probably damaging |
1.00 |
R9795:Nuggc
|
UTSW |
14 |
65,847,345 (GRCm39) |
missense |
probably damaging |
1.00 |
RF019:Nuggc
|
UTSW |
14 |
65,885,713 (GRCm39) |
missense |
probably damaging |
1.00 |
|