Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adck5 |
G |
A |
15: 76,478,383 (GRCm39) |
D277N |
probably damaging |
Het |
Adgrv1 |
A |
T |
13: 81,670,288 (GRCm39) |
S2353T |
probably benign |
Het |
Adgrv1 |
A |
T |
13: 81,743,371 (GRCm39) |
N43K |
probably damaging |
Het |
Adnp2 |
A |
G |
18: 80,185,937 (GRCm39) |
I12T |
probably damaging |
Het |
Ahnak2 |
A |
G |
12: 112,741,363 (GRCm39) |
L903P |
probably damaging |
Het |
Ankhd1 |
T |
G |
18: 36,780,878 (GRCm39) |
S1977A |
probably benign |
Het |
Ap1m2 |
T |
C |
9: 21,216,983 (GRCm39) |
M118V |
probably benign |
Het |
Ap3d1 |
T |
C |
10: 80,548,639 (GRCm39) |
K846R |
possibly damaging |
Het |
Aqr |
C |
A |
2: 113,971,396 (GRCm39) |
E480* |
probably null |
Het |
Arl6 |
G |
T |
16: 59,434,199 (GRCm39) |
Q182K |
probably benign |
Het |
Arpc2 |
A |
G |
1: 74,294,034 (GRCm39) |
K106E |
probably benign |
Het |
Atp8a1 |
A |
C |
5: 67,889,524 (GRCm39) |
F599V |
|
Het |
B3galt5 |
A |
T |
16: 96,117,203 (GRCm39) |
I279F |
probably damaging |
Het |
Calcoco2 |
G |
T |
11: 95,991,104 (GRCm39) |
A211D |
unknown |
Het |
Ccdc33 |
T |
C |
9: 57,993,855 (GRCm39) |
E342G |
possibly damaging |
Het |
Ccdc88a |
C |
A |
11: 29,405,484 (GRCm39) |
Q386K |
probably benign |
Het |
Cdh20 |
A |
G |
1: 104,862,065 (GRCm39) |
K82E |
probably benign |
Het |
Clca3a2 |
A |
T |
3: 144,503,575 (GRCm39) |
Y792N |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,658,254 (GRCm39) |
I653V |
probably benign |
Het |
Col7a1 |
C |
T |
9: 108,812,649 (GRCm39) |
R2826W |
unknown |
Het |
D6Ertd527e |
A |
G |
6: 87,088,908 (GRCm39) |
N357S |
unknown |
Het |
Dmgdh |
T |
A |
13: 93,857,123 (GRCm39) |
N742K |
probably benign |
Het |
Dnai3 |
T |
C |
3: 145,748,594 (GRCm39) |
N840S |
probably benign |
Het |
Dnajc6 |
A |
G |
4: 101,475,821 (GRCm39) |
N565D |
probably benign |
Het |
Doc2g |
A |
G |
19: 4,054,390 (GRCm39) |
Y155C |
probably damaging |
Het |
Dot1l |
G |
A |
10: 80,624,361 (GRCm39) |
G943D |
probably damaging |
Het |
Dst |
T |
C |
1: 34,220,736 (GRCm39) |
V2180A |
probably benign |
Het |
Eftud2 |
A |
C |
11: 102,759,422 (GRCm39) |
Y160* |
probably null |
Het |
Ehd1 |
A |
T |
19: 6,331,262 (GRCm39) |
Q140L |
probably benign |
Het |
Etv3 |
T |
C |
3: 87,443,172 (GRCm39) |
V252A |
probably benign |
Het |
F11 |
A |
T |
8: 45,694,566 (GRCm39) |
C598* |
probably null |
Het |
Fancm |
T |
A |
12: 65,137,758 (GRCm39) |
N316K |
probably benign |
Het |
Flnc |
T |
C |
6: 29,457,214 (GRCm39) |
V2372A |
probably damaging |
Het |
Fry |
A |
G |
5: 150,282,488 (GRCm39) |
R338G |
probably damaging |
Het |
Gfra3 |
T |
C |
18: 34,837,591 (GRCm39) |
T136A |
probably benign |
Het |
Golga7b |
T |
C |
19: 42,255,462 (GRCm39) |
V113A |
possibly damaging |
Het |
Gpn3 |
G |
T |
5: 122,520,306 (GRCm39) |
V102L |
|
Het |
Herc2 |
A |
G |
7: 55,820,338 (GRCm39) |
N2859S |
possibly damaging |
Het |
Hpd |
A |
T |
5: 123,318,948 (GRCm39) |
|
probably null |
Het |
Hspg2 |
C |
T |
4: 137,266,887 (GRCm39) |
T1964I |
probably benign |
Het |
Hydin |
A |
T |
8: 111,220,965 (GRCm39) |
T1454S |
probably benign |
Het |
Irgm2 |
A |
T |
11: 58,110,872 (GRCm39) |
T188S |
possibly damaging |
Het |
Jak3 |
A |
G |
8: 72,131,366 (GRCm39) |
D77G |
probably damaging |
Het |
Kcnj4 |
G |
T |
15: 79,369,220 (GRCm39) |
F253L |
possibly damaging |
Het |
Kidins220 |
T |
A |
12: 25,106,895 (GRCm39) |
D1358E |
probably benign |
Het |
Klf1 |
C |
A |
8: 85,630,061 (GRCm39) |
C295* |
probably null |
Het |
Kmt2a |
C |
T |
9: 44,760,102 (GRCm39) |
W582* |
probably null |
Het |
Lrig2 |
A |
G |
3: 104,371,556 (GRCm39) |
C716R |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,765,004 (GRCm39) |
D2941N |
|
Het |
Lrpprc |
A |
T |
17: 85,020,262 (GRCm39) |
V1141E |
probably damaging |
Het |
Mrgprx1 |
C |
T |
7: 47,671,273 (GRCm39) |
G158D |
probably benign |
Het |
Muc5b |
C |
A |
7: 141,409,279 (GRCm39) |
A1121D |
unknown |
Het |
Nf1 |
G |
T |
11: 79,334,733 (GRCm39) |
V852L |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,118,286 (GRCm39) |
E670G |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,784,601 (GRCm39) |
T101A |
probably benign |
Het |
Or10a49 |
T |
C |
7: 108,467,563 (GRCm39) |
Y266C |
probably damaging |
Het |
Or2t35 |
T |
A |
14: 14,407,963 (GRCm38) |
I245K |
probably benign |
Het |
Or5b123 |
G |
A |
19: 13,597,365 (GRCm39) |
V237I |
probably benign |
Het |
P2rx2 |
T |
C |
5: 110,488,172 (GRCm39) |
T461A |
probably benign |
Het |
Pank1 |
G |
A |
19: 34,799,194 (GRCm39) |
T419I |
probably damaging |
Het |
Patz1 |
T |
C |
11: 3,244,562 (GRCm39) |
V481A |
unknown |
Het |
Pdlim5 |
A |
G |
3: 142,018,058 (GRCm39) |
L179P |
probably benign |
Het |
Pik3ap1 |
A |
T |
19: 41,296,967 (GRCm39) |
V461D |
probably damaging |
Het |
Polq |
T |
C |
16: 36,848,176 (GRCm39) |
V261A |
probably damaging |
Het |
Ppm1a |
G |
A |
12: 72,837,451 (GRCm39) |
V333M |
possibly damaging |
Het |
R3hcc1l |
T |
C |
19: 42,552,671 (GRCm39) |
L556P |
probably benign |
Het |
Rabggta |
G |
A |
14: 55,956,375 (GRCm39) |
Q365* |
probably null |
Het |
Ranbp9 |
T |
C |
13: 43,578,519 (GRCm39) |
T185A |
probably benign |
Het |
Rd3l |
T |
G |
12: 111,945,913 (GRCm39) |
N189H |
probably damaging |
Het |
Rnf213 |
G |
A |
11: 119,332,794 (GRCm39) |
A2669T |
|
Het |
Ros1 |
T |
A |
10: 51,996,931 (GRCm39) |
H1268L |
probably benign |
Het |
Rps6ka4 |
G |
T |
19: 6,809,354 (GRCm39) |
S433R |
possibly damaging |
Het |
Ryr1 |
A |
G |
7: 28,759,092 (GRCm39) |
L3362P |
probably damaging |
Het |
Setd1b |
A |
T |
5: 123,298,046 (GRCm39) |
T1361S |
unknown |
Het |
Setd2 |
T |
C |
9: 110,377,570 (GRCm39) |
S462P |
probably damaging |
Het |
Sgsm3 |
A |
T |
15: 80,890,935 (GRCm39) |
Q132L |
probably benign |
Het |
Slx1b |
C |
A |
7: 126,291,698 (GRCm39) |
R122L |
probably damaging |
Het |
Sorbs2 |
A |
T |
8: 46,276,788 (GRCm39) |
T1167S |
probably benign |
Het |
Spdya |
A |
C |
17: 71,869,513 (GRCm39) |
T103P |
probably damaging |
Het |
Stfa2 |
A |
G |
16: 36,228,638 (GRCm39) |
S20P |
probably benign |
Het |
Sulf1 |
A |
G |
1: 12,891,026 (GRCm39) |
T400A |
probably benign |
Het |
Tardbp |
A |
T |
4: 148,709,751 (GRCm39) |
D23E |
probably damaging |
Het |
Tekt2 |
C |
T |
4: 126,217,444 (GRCm39) |
R207H |
probably damaging |
Het |
Tgm1 |
C |
T |
14: 55,948,441 (GRCm39) |
D237N |
probably benign |
Het |
Tgs1 |
T |
A |
4: 3,585,964 (GRCm39) |
N280K |
probably benign |
Het |
Tmem198 |
A |
T |
1: 75,459,272 (GRCm39) |
I76F |
possibly damaging |
Het |
Trpv2 |
A |
T |
11: 62,475,385 (GRCm39) |
Y266F |
probably damaging |
Het |
Ttn |
C |
T |
2: 76,569,845 (GRCm39) |
G27016E |
probably damaging |
Het |
Ttn |
T |
C |
2: 76,781,824 (GRCm39) |
E1074G |
unknown |
Het |
Unc5b |
A |
T |
10: 60,613,322 (GRCm39) |
W305R |
probably damaging |
Het |
Usp38 |
A |
G |
8: 81,741,164 (GRCm39) |
|
probably benign |
Het |
Vmn1r79 |
A |
G |
7: 11,910,582 (GRCm39) |
T155A |
probably benign |
Het |
Vwce |
G |
A |
19: 10,615,481 (GRCm39) |
V121I |
probably benign |
Het |
Wdr91 |
A |
T |
6: 34,865,961 (GRCm39) |
D530E |
probably benign |
Het |
Wnt4 |
A |
G |
4: 137,023,929 (GRCm39) |
T299A |
probably benign |
Het |
Yeats2 |
T |
A |
16: 20,047,491 (GRCm39) |
Y1284* |
probably null |
Het |
Zfp113 |
A |
T |
5: 138,148,888 (GRCm39) |
Y85* |
probably null |
Het |
Zfp184 |
A |
G |
13: 22,144,096 (GRCm39) |
T601A |
probably benign |
Het |
Zfp655 |
A |
G |
5: 145,180,442 (GRCm39) |
E100G |
probably damaging |
Het |
|
Other mutations in Rnf17 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00586:Rnf17
|
APN |
14 |
56,658,539 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00717:Rnf17
|
APN |
14 |
56,703,207 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00978:Rnf17
|
APN |
14 |
56,749,728 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01295:Rnf17
|
APN |
14 |
56,700,521 (GRCm39) |
nonsense |
probably null |
|
IGL01779:Rnf17
|
APN |
14 |
56,699,520 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02132:Rnf17
|
APN |
14 |
56,658,623 (GRCm39) |
missense |
probably benign |
0.27 |
IGL02183:Rnf17
|
APN |
14 |
56,745,325 (GRCm39) |
missense |
probably null |
0.99 |
IGL02387:Rnf17
|
APN |
14 |
56,738,044 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02422:Rnf17
|
APN |
14 |
56,719,592 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03081:Rnf17
|
APN |
14 |
56,671,828 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03269:Rnf17
|
APN |
14 |
56,665,403 (GRCm39) |
missense |
possibly damaging |
0.74 |
divest
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
Shed
|
UTSW |
14 |
56,749,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Rnf17
|
UTSW |
14 |
56,708,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0046:Rnf17
|
UTSW |
14 |
56,708,830 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Rnf17
|
UTSW |
14 |
56,751,563 (GRCm39) |
missense |
probably damaging |
1.00 |
R0189:Rnf17
|
UTSW |
14 |
56,719,650 (GRCm39) |
missense |
probably null |
1.00 |
R0243:Rnf17
|
UTSW |
14 |
56,719,541 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0245:Rnf17
|
UTSW |
14 |
56,676,066 (GRCm39) |
missense |
probably damaging |
0.97 |
R0486:Rnf17
|
UTSW |
14 |
56,751,632 (GRCm39) |
missense |
probably benign |
0.43 |
R0554:Rnf17
|
UTSW |
14 |
56,760,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R0840:Rnf17
|
UTSW |
14 |
56,712,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Rnf17
|
UTSW |
14 |
56,751,622 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1170:Rnf17
|
UTSW |
14 |
56,663,088 (GRCm39) |
missense |
probably benign |
0.10 |
R1200:Rnf17
|
UTSW |
14 |
56,705,163 (GRCm39) |
missense |
probably benign |
0.44 |
R1464:Rnf17
|
UTSW |
14 |
56,699,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Rnf17
|
UTSW |
14 |
56,699,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R1472:Rnf17
|
UTSW |
14 |
56,665,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R1512:Rnf17
|
UTSW |
14 |
56,705,243 (GRCm39) |
missense |
probably benign |
0.01 |
R1605:Rnf17
|
UTSW |
14 |
56,730,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Rnf17
|
UTSW |
14 |
56,759,856 (GRCm39) |
missense |
probably damaging |
0.99 |
R1791:Rnf17
|
UTSW |
14 |
56,741,464 (GRCm39) |
nonsense |
probably null |
|
R2015:Rnf17
|
UTSW |
14 |
56,724,426 (GRCm39) |
missense |
probably benign |
0.00 |
R2023:Rnf17
|
UTSW |
14 |
56,669,036 (GRCm39) |
missense |
possibly damaging |
0.59 |
R2086:Rnf17
|
UTSW |
14 |
56,720,837 (GRCm39) |
missense |
probably damaging |
0.98 |
R2130:Rnf17
|
UTSW |
14 |
56,730,811 (GRCm39) |
missense |
probably damaging |
1.00 |
R2309:Rnf17
|
UTSW |
14 |
56,743,439 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3003:Rnf17
|
UTSW |
14 |
56,738,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R3611:Rnf17
|
UTSW |
14 |
56,705,197 (GRCm39) |
missense |
probably benign |
0.43 |
R3847:Rnf17
|
UTSW |
14 |
56,749,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R3848:Rnf17
|
UTSW |
14 |
56,749,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R3849:Rnf17
|
UTSW |
14 |
56,749,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R3850:Rnf17
|
UTSW |
14 |
56,749,753 (GRCm39) |
missense |
probably damaging |
1.00 |
R3872:Rnf17
|
UTSW |
14 |
56,712,870 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3874:Rnf17
|
UTSW |
14 |
56,712,870 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4021:Rnf17
|
UTSW |
14 |
56,697,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R4022:Rnf17
|
UTSW |
14 |
56,697,458 (GRCm39) |
missense |
probably damaging |
0.98 |
R4790:Rnf17
|
UTSW |
14 |
56,671,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R4951:Rnf17
|
UTSW |
14 |
56,759,848 (GRCm39) |
missense |
probably benign |
0.02 |
R5068:Rnf17
|
UTSW |
14 |
56,743,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5069:Rnf17
|
UTSW |
14 |
56,743,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Rnf17
|
UTSW |
14 |
56,743,385 (GRCm39) |
missense |
probably damaging |
0.99 |
R5518:Rnf17
|
UTSW |
14 |
56,719,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5628:Rnf17
|
UTSW |
14 |
56,724,409 (GRCm39) |
splice site |
probably null |
|
R5712:Rnf17
|
UTSW |
14 |
56,708,856 (GRCm39) |
missense |
probably benign |
0.19 |
R5747:Rnf17
|
UTSW |
14 |
56,703,276 (GRCm39) |
critical splice donor site |
probably null |
|
R5869:Rnf17
|
UTSW |
14 |
56,743,445 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6336:Rnf17
|
UTSW |
14 |
56,658,626 (GRCm39) |
splice site |
probably null |
|
R6626:Rnf17
|
UTSW |
14 |
56,665,381 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6639:Rnf17
|
UTSW |
14 |
56,676,200 (GRCm39) |
missense |
probably benign |
0.01 |
R6675:Rnf17
|
UTSW |
14 |
56,697,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R6731:Rnf17
|
UTSW |
14 |
56,761,807 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7062:Rnf17
|
UTSW |
14 |
56,703,111 (GRCm39) |
missense |
probably benign |
0.00 |
R7103:Rnf17
|
UTSW |
14 |
56,708,763 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7144:Rnf17
|
UTSW |
14 |
56,749,789 (GRCm39) |
splice site |
probably null |
|
R7527:Rnf17
|
UTSW |
14 |
56,753,895 (GRCm39) |
missense |
probably damaging |
1.00 |
R7664:Rnf17
|
UTSW |
14 |
56,676,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7754:Rnf17
|
UTSW |
14 |
56,699,529 (GRCm39) |
critical splice donor site |
probably null |
|
R7772:Rnf17
|
UTSW |
14 |
56,715,144 (GRCm39) |
missense |
probably benign |
0.27 |
R8092:Rnf17
|
UTSW |
14 |
56,724,479 (GRCm39) |
missense |
probably benign |
0.00 |
R8150:Rnf17
|
UTSW |
14 |
56,658,593 (GRCm39) |
missense |
probably benign |
0.19 |
R8203:Rnf17
|
UTSW |
14 |
56,705,179 (GRCm39) |
missense |
probably benign |
0.17 |
R8320:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8321:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8379:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8380:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8381:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8382:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8383:Rnf17
|
UTSW |
14 |
56,661,999 (GRCm39) |
frame shift |
probably null |
|
R8799:Rnf17
|
UTSW |
14 |
56,737,886 (GRCm39) |
missense |
probably damaging |
1.00 |
R8850:Rnf17
|
UTSW |
14 |
56,722,658 (GRCm39) |
missense |
probably damaging |
1.00 |
R9212:Rnf17
|
UTSW |
14 |
56,761,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R9276:Rnf17
|
UTSW |
14 |
56,719,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R9300:Rnf17
|
UTSW |
14 |
56,697,495 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9375:Rnf17
|
UTSW |
14 |
56,719,579 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Rnf17
|
UTSW |
14 |
56,705,163 (GRCm39) |
missense |
possibly damaging |
0.66 |
|