Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agl |
A |
T |
3: 116,566,145 (GRCm39) |
F992I |
probably damaging |
Het |
Ampd1 |
T |
C |
3: 102,992,713 (GRCm39) |
F152L |
probably damaging |
Het |
Ank2 |
T |
C |
3: 126,806,335 (GRCm39) |
H602R |
possibly damaging |
Het |
Ankib1 |
T |
C |
5: 3,797,071 (GRCm39) |
D247G |
probably damaging |
Het |
Bccip |
T |
A |
7: 133,322,594 (GRCm39) |
H313Q |
probably benign |
Het |
Ccdc198 |
A |
T |
14: 49,470,403 (GRCm39) |
L172H |
probably damaging |
Het |
Cep250 |
A |
G |
2: 155,821,197 (GRCm39) |
E929G |
probably damaging |
Het |
Chl1 |
C |
A |
6: 103,686,152 (GRCm39) |
L954I |
probably benign |
Het |
Cog5 |
A |
T |
12: 31,710,716 (GRCm39) |
D32V |
probably benign |
Het |
Cyp4f16 |
C |
A |
17: 32,763,116 (GRCm39) |
A187E |
probably benign |
Het |
Dffb |
A |
T |
4: 154,050,050 (GRCm39) |
V271E |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 31,070,604 (GRCm39) |
Y4430C |
possibly damaging |
Het |
Dpp3 |
T |
C |
19: 4,968,385 (GRCm39) |
E229G |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,909,613 (GRCm39) |
N2130Y |
probably benign |
Het |
Kcnk3 |
T |
C |
5: 30,745,722 (GRCm39) |
V21A |
possibly damaging |
Het |
Kif9 |
G |
A |
9: 110,319,094 (GRCm39) |
S186N |
probably benign |
Het |
Lhfpl3 |
C |
A |
5: 22,951,424 (GRCm39) |
N78K |
probably benign |
Het |
Ly6c1 |
A |
G |
15: 74,917,457 (GRCm39) |
S64P |
probably damaging |
Het |
Mapk10 |
T |
C |
5: 103,186,446 (GRCm39) |
T59A |
probably benign |
Het |
Mars1 |
A |
T |
10: 127,140,171 (GRCm39) |
C394* |
probably null |
Het |
Mettl16 |
T |
A |
11: 74,683,063 (GRCm39) |
D168E |
possibly damaging |
Het |
Mgat2 |
A |
T |
12: 69,232,158 (GRCm39) |
Q244L |
probably benign |
Het |
Mrps30 |
A |
G |
13: 118,521,101 (GRCm39) |
|
probably null |
Het |
Myrip |
C |
A |
9: 120,290,487 (GRCm39) |
A702E |
probably damaging |
Het |
Nepn |
T |
C |
10: 52,280,168 (GRCm39) |
L420P |
probably damaging |
Het |
Nrn1 |
A |
T |
13: 36,918,238 (GRCm39) |
Y9* |
probably null |
Het |
Nup107 |
T |
C |
10: 117,595,081 (GRCm39) |
Y752C |
probably damaging |
Het |
Nutm2 |
A |
T |
13: 50,628,496 (GRCm39) |
D520V |
probably damaging |
Het |
Olfm2 |
C |
T |
9: 20,586,946 (GRCm39) |
C48Y |
probably damaging |
Het |
Or52j3 |
T |
C |
7: 102,836,735 (GRCm39) |
F309S |
possibly damaging |
Het |
Or8g19 |
A |
G |
9: 39,056,278 (GRCm39) |
N294S |
probably null |
Het |
Osbpl1a |
T |
A |
18: 13,038,138 (GRCm39) |
D271V |
probably damaging |
Het |
Osmr |
G |
T |
15: 6,873,934 (GRCm39) |
D154E |
probably benign |
Het |
Pcdh9 |
A |
G |
14: 94,124,484 (GRCm39) |
V562A |
probably damaging |
Het |
Peak1 |
A |
C |
9: 56,166,726 (GRCm39) |
S401A |
probably benign |
Het |
Pigk |
A |
T |
3: 152,446,486 (GRCm39) |
H195L |
probably benign |
Het |
Plekha6 |
G |
C |
1: 133,200,045 (GRCm39) |
R208P |
possibly damaging |
Het |
Ppp2r1a |
C |
T |
17: 21,171,608 (GRCm39) |
R28C |
probably damaging |
Het |
Pramel30 |
G |
T |
4: 144,059,323 (GRCm39) |
V345F |
probably damaging |
Het |
Ptbp3 |
T |
C |
4: 59,493,311 (GRCm39) |
D123G |
probably benign |
Het |
Ptgr2 |
G |
A |
12: 84,355,120 (GRCm39) |
E285K |
possibly damaging |
Het |
Rassf1 |
G |
T |
9: 107,429,021 (GRCm39) |
V76L |
possibly damaging |
Het |
Sec22a |
A |
G |
16: 35,134,461 (GRCm39) |
V307A |
probably damaging |
Het |
Slc1a5 |
T |
C |
7: 16,516,151 (GRCm39) |
V109A |
probably benign |
Het |
St8sia5 |
T |
A |
18: 77,342,478 (GRCm39) |
M396K |
possibly damaging |
Het |
Tiam1 |
T |
C |
16: 89,586,074 (GRCm39) |
E602G |
probably benign |
Het |
Tll1 |
T |
C |
8: 64,527,297 (GRCm39) |
E408G |
probably damaging |
Het |
Tpsb2 |
G |
A |
17: 25,586,108 (GRCm39) |
V109M |
probably benign |
Het |
Trib1 |
T |
A |
15: 59,526,451 (GRCm39) |
|
probably null |
Het |
Trio |
G |
T |
15: 27,852,019 (GRCm39) |
A765E |
possibly damaging |
Het |
Uggt2 |
A |
T |
14: 119,286,838 (GRCm39) |
V193E |
probably damaging |
Het |
Vmn1r115 |
G |
A |
7: 20,578,447 (GRCm39) |
P155L |
probably benign |
Het |
Wdr31 |
A |
G |
4: 62,374,113 (GRCm39) |
L292S |
probably benign |
Het |
Xrra1 |
T |
C |
7: 99,525,462 (GRCm39) |
I127T |
probably benign |
Het |
Yju2 |
G |
A |
17: 56,269,030 (GRCm39) |
C46Y |
probably damaging |
Het |
Zfp442 |
G |
A |
2: 150,249,944 (GRCm39) |
Q596* |
probably null |
Het |
|
Other mutations in Skint5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Skint5
|
APN |
4 |
113,400,070 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01288:Skint5
|
APN |
4 |
113,381,332 (GRCm39) |
intron |
probably benign |
|
IGL01313:Skint5
|
APN |
4 |
113,662,361 (GRCm39) |
missense |
unknown |
|
IGL01446:Skint5
|
APN |
4 |
113,800,019 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01861:Skint5
|
APN |
4 |
113,417,021 (GRCm39) |
splice site |
probably benign |
|
IGL01955:Skint5
|
APN |
4 |
113,480,933 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02150:Skint5
|
APN |
4 |
113,742,988 (GRCm39) |
missense |
unknown |
|
IGL02190:Skint5
|
APN |
4 |
113,797,962 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02271:Skint5
|
APN |
4 |
113,794,778 (GRCm39) |
splice site |
probably null |
|
IGL02426:Skint5
|
APN |
4 |
113,797,981 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02484:Skint5
|
APN |
4 |
113,799,750 (GRCm39) |
nonsense |
probably null |
|
IGL02548:Skint5
|
APN |
4 |
113,588,273 (GRCm39) |
missense |
unknown |
|
IGL02556:Skint5
|
APN |
4 |
113,797,932 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02674:Skint5
|
APN |
4 |
113,487,582 (GRCm39) |
splice site |
probably benign |
|
IGL02697:Skint5
|
APN |
4 |
113,336,910 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02710:Skint5
|
APN |
4 |
113,335,156 (GRCm39) |
missense |
unknown |
|
IGL02721:Skint5
|
APN |
4 |
113,799,746 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02750:Skint5
|
APN |
4 |
113,396,559 (GRCm39) |
missense |
unknown |
|
IGL03121:Skint5
|
APN |
4 |
113,574,284 (GRCm39) |
missense |
unknown |
|
IGL03167:Skint5
|
APN |
4 |
113,751,047 (GRCm39) |
missense |
unknown |
|
IGL03247:Skint5
|
APN |
4 |
113,798,005 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03264:Skint5
|
APN |
4 |
113,343,854 (GRCm39) |
missense |
unknown |
|
IGL03281:Skint5
|
APN |
4 |
113,524,415 (GRCm39) |
missense |
unknown |
|
IGL03353:Skint5
|
APN |
4 |
113,599,379 (GRCm39) |
missense |
unknown |
|
IGL03377:Skint5
|
APN |
4 |
113,620,735 (GRCm39) |
missense |
unknown |
|
PIT4377001:Skint5
|
UTSW |
4 |
113,454,900 (GRCm39) |
missense |
unknown |
|
R0006:Skint5
|
UTSW |
4 |
113,751,059 (GRCm39) |
splice site |
probably benign |
|
R0026:Skint5
|
UTSW |
4 |
113,403,665 (GRCm39) |
splice site |
probably benign |
|
R0096:Skint5
|
UTSW |
4 |
113,454,965 (GRCm39) |
splice site |
probably benign |
|
R0096:Skint5
|
UTSW |
4 |
113,454,965 (GRCm39) |
splice site |
probably benign |
|
R0277:Skint5
|
UTSW |
4 |
113,794,818 (GRCm39) |
missense |
probably benign |
0.04 |
R0323:Skint5
|
UTSW |
4 |
113,794,818 (GRCm39) |
missense |
probably benign |
0.04 |
R0369:Skint5
|
UTSW |
4 |
113,369,220 (GRCm39) |
critical splice donor site |
probably null |
|
R0375:Skint5
|
UTSW |
4 |
113,562,793 (GRCm39) |
missense |
unknown |
|
R0464:Skint5
|
UTSW |
4 |
113,392,928 (GRCm39) |
missense |
unknown |
|
R0479:Skint5
|
UTSW |
4 |
113,512,869 (GRCm39) |
missense |
unknown |
|
R0507:Skint5
|
UTSW |
4 |
113,425,127 (GRCm39) |
splice site |
probably null |
|
R0533:Skint5
|
UTSW |
4 |
113,685,064 (GRCm39) |
missense |
unknown |
|
R0628:Skint5
|
UTSW |
4 |
113,588,266 (GRCm39) |
nonsense |
probably null |
|
R0645:Skint5
|
UTSW |
4 |
113,620,679 (GRCm39) |
missense |
unknown |
|
R1201:Skint5
|
UTSW |
4 |
113,413,342 (GRCm39) |
missense |
unknown |
|
R1240:Skint5
|
UTSW |
4 |
113,574,304 (GRCm39) |
missense |
unknown |
|
R1270:Skint5
|
UTSW |
4 |
113,799,856 (GRCm39) |
nonsense |
probably null |
|
R1390:Skint5
|
UTSW |
4 |
113,512,881 (GRCm39) |
missense |
unknown |
|
R1398:Skint5
|
UTSW |
4 |
113,636,268 (GRCm39) |
missense |
unknown |
|
R1438:Skint5
|
UTSW |
4 |
113,413,308 (GRCm39) |
splice site |
probably benign |
|
R1591:Skint5
|
UTSW |
4 |
113,856,651 (GRCm39) |
critical splice donor site |
probably null |
|
R1631:Skint5
|
UTSW |
4 |
113,341,123 (GRCm39) |
missense |
probably benign |
0.23 |
R1653:Skint5
|
UTSW |
4 |
113,347,875 (GRCm39) |
missense |
unknown |
|
R1722:Skint5
|
UTSW |
4 |
113,703,508 (GRCm39) |
splice site |
probably null |
|
R1735:Skint5
|
UTSW |
4 |
113,420,656 (GRCm39) |
missense |
unknown |
|
R1765:Skint5
|
UTSW |
4 |
113,434,858 (GRCm39) |
missense |
unknown |
|
R2054:Skint5
|
UTSW |
4 |
113,676,360 (GRCm39) |
critical splice donor site |
probably null |
|
R2058:Skint5
|
UTSW |
4 |
113,727,897 (GRCm39) |
missense |
possibly damaging |
0.53 |
R2197:Skint5
|
UTSW |
4 |
113,798,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R2239:Skint5
|
UTSW |
4 |
113,403,733 (GRCm39) |
missense |
unknown |
|
R2380:Skint5
|
UTSW |
4 |
113,403,733 (GRCm39) |
missense |
unknown |
|
R2406:Skint5
|
UTSW |
4 |
113,799,864 (GRCm39) |
missense |
probably damaging |
0.97 |
R2512:Skint5
|
UTSW |
4 |
113,487,616 (GRCm39) |
missense |
unknown |
|
R2913:Skint5
|
UTSW |
4 |
113,381,289 (GRCm39) |
intron |
probably benign |
|
R3522:Skint5
|
UTSW |
4 |
113,614,102 (GRCm39) |
critical splice donor site |
probably null |
|
R3779:Skint5
|
UTSW |
4 |
113,636,237 (GRCm39) |
splice site |
probably benign |
|
R3815:Skint5
|
UTSW |
4 |
113,703,496 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3815:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3816:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3817:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3818:Skint5
|
UTSW |
4 |
113,486,319 (GRCm39) |
splice site |
probably benign |
|
R3837:Skint5
|
UTSW |
4 |
113,797,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R3943:Skint5
|
UTSW |
4 |
113,799,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3944:Skint5
|
UTSW |
4 |
113,799,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4038:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4039:Skint5
|
UTSW |
4 |
113,743,011 (GRCm39) |
missense |
unknown |
|
R4280:Skint5
|
UTSW |
4 |
113,799,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4308:Skint5
|
UTSW |
4 |
113,341,164 (GRCm39) |
missense |
unknown |
|
R4386:Skint5
|
UTSW |
4 |
113,341,090 (GRCm39) |
missense |
probably benign |
0.23 |
R4513:Skint5
|
UTSW |
4 |
113,599,382 (GRCm39) |
missense |
unknown |
|
R4575:Skint5
|
UTSW |
4 |
113,524,390 (GRCm39) |
missense |
unknown |
|
R4631:Skint5
|
UTSW |
4 |
113,486,314 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4722:Skint5
|
UTSW |
4 |
113,751,052 (GRCm39) |
missense |
unknown |
|
R4854:Skint5
|
UTSW |
4 |
113,437,725 (GRCm39) |
missense |
unknown |
|
R5010:Skint5
|
UTSW |
4 |
113,403,734 (GRCm39) |
missense |
unknown |
|
R5070:Skint5
|
UTSW |
4 |
113,652,735 (GRCm39) |
missense |
unknown |
|
R5158:Skint5
|
UTSW |
4 |
113,599,409 (GRCm39) |
missense |
unknown |
|
R5163:Skint5
|
UTSW |
4 |
113,652,762 (GRCm39) |
missense |
unknown |
|
R5190:Skint5
|
UTSW |
4 |
113,620,711 (GRCm39) |
missense |
unknown |
|
R5232:Skint5
|
UTSW |
4 |
113,434,841 (GRCm39) |
missense |
unknown |
|
R5257:Skint5
|
UTSW |
4 |
113,434,859 (GRCm39) |
missense |
unknown |
|
R5499:Skint5
|
UTSW |
4 |
113,799,700 (GRCm39) |
critical splice donor site |
probably null |
|
R5569:Skint5
|
UTSW |
4 |
113,545,903 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5776:Skint5
|
UTSW |
4 |
113,620,700 (GRCm39) |
missense |
unknown |
|
R5987:Skint5
|
UTSW |
4 |
113,743,005 (GRCm39) |
missense |
unknown |
|
R5995:Skint5
|
UTSW |
4 |
113,751,029 (GRCm39) |
missense |
unknown |
|
R6063:Skint5
|
UTSW |
4 |
113,347,842 (GRCm39) |
missense |
probably benign |
0.23 |
R6074:Skint5
|
UTSW |
4 |
113,662,397 (GRCm39) |
missense |
unknown |
|
R6111:Skint5
|
UTSW |
4 |
113,562,845 (GRCm39) |
missense |
unknown |
|
R6173:Skint5
|
UTSW |
4 |
113,392,907 (GRCm39) |
missense |
unknown |
|
R6238:Skint5
|
UTSW |
4 |
113,800,064 (GRCm39) |
splice site |
probably null |
|
R6248:Skint5
|
UTSW |
4 |
113,636,286 (GRCm39) |
missense |
unknown |
|
R6318:Skint5
|
UTSW |
4 |
113,374,330 (GRCm39) |
missense |
unknown |
|
R6370:Skint5
|
UTSW |
4 |
113,471,307 (GRCm39) |
missense |
unknown |
|
R6404:Skint5
|
UTSW |
4 |
113,799,806 (GRCm39) |
missense |
probably damaging |
0.97 |
R6499:Skint5
|
UTSW |
4 |
113,396,552 (GRCm39) |
missense |
unknown |
|
R6646:Skint5
|
UTSW |
4 |
113,797,974 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6737:Skint5
|
UTSW |
4 |
113,392,936 (GRCm39) |
missense |
unknown |
|
R6795:Skint5
|
UTSW |
4 |
113,524,420 (GRCm39) |
missense |
unknown |
|
R6815:Skint5
|
UTSW |
4 |
113,574,324 (GRCm39) |
critical splice acceptor site |
probably null |
|
R6935:Skint5
|
UTSW |
4 |
113,799,793 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7028:Skint5
|
UTSW |
4 |
113,798,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Skint5
|
UTSW |
4 |
113,574,304 (GRCm39) |
missense |
unknown |
|
R7071:Skint5
|
UTSW |
4 |
113,636,277 (GRCm39) |
missense |
unknown |
|
R7142:Skint5
|
UTSW |
4 |
113,428,791 (GRCm39) |
missense |
unknown |
|
R7197:Skint5
|
UTSW |
4 |
113,437,679 (GRCm39) |
critical splice donor site |
probably null |
|
R7208:Skint5
|
UTSW |
4 |
113,396,536 (GRCm39) |
missense |
unknown |
|
R7297:Skint5
|
UTSW |
4 |
113,400,131 (GRCm39) |
missense |
unknown |
|
R7470:Skint5
|
UTSW |
4 |
113,743,000 (GRCm39) |
missense |
unknown |
|
R7470:Skint5
|
UTSW |
4 |
113,614,128 (GRCm39) |
missense |
unknown |
|
R7500:Skint5
|
UTSW |
4 |
113,417,035 (GRCm39) |
missense |
unknown |
|
R7547:Skint5
|
UTSW |
4 |
113,483,785 (GRCm39) |
missense |
unknown |
|
R7556:Skint5
|
UTSW |
4 |
113,425,162 (GRCm39) |
missense |
unknown |
|
R7619:Skint5
|
UTSW |
4 |
113,381,305 (GRCm39) |
missense |
unknown |
|
R7629:Skint5
|
UTSW |
4 |
113,799,857 (GRCm39) |
missense |
probably damaging |
1.00 |
R7646:Skint5
|
UTSW |
4 |
113,620,739 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7725:Skint5
|
UTSW |
4 |
113,685,099 (GRCm39) |
missense |
unknown |
|
R7788:Skint5
|
UTSW |
4 |
113,403,715 (GRCm39) |
missense |
unknown |
|
R7818:Skint5
|
UTSW |
4 |
113,799,923 (GRCm39) |
missense |
possibly damaging |
0.56 |
R7819:Skint5
|
UTSW |
4 |
113,417,032 (GRCm39) |
missense |
unknown |
|
R7958:Skint5
|
UTSW |
4 |
113,480,980 (GRCm39) |
missense |
unknown |
|
R8150:Skint5
|
UTSW |
4 |
113,798,087 (GRCm39) |
missense |
probably benign |
0.21 |
R8214:Skint5
|
UTSW |
4 |
113,662,139 (GRCm39) |
splice site |
probably null |
|
R8413:Skint5
|
UTSW |
4 |
113,572,900 (GRCm39) |
missense |
unknown |
|
R8420:Skint5
|
UTSW |
4 |
113,437,679 (GRCm39) |
critical splice donor site |
probably null |
|
R8459:Skint5
|
UTSW |
4 |
113,703,481 (GRCm39) |
nonsense |
probably null |
|
R8703:Skint5
|
UTSW |
4 |
113,733,207 (GRCm39) |
missense |
unknown |
|
R8710:Skint5
|
UTSW |
4 |
113,483,787 (GRCm39) |
missense |
unknown |
|
R8927:Skint5
|
UTSW |
4 |
113,341,099 (GRCm39) |
missense |
probably benign |
0.23 |
R8928:Skint5
|
UTSW |
4 |
113,341,099 (GRCm39) |
missense |
probably benign |
0.23 |
R8950:Skint5
|
UTSW |
4 |
113,374,349 (GRCm39) |
missense |
unknown |
|
R9047:Skint5
|
UTSW |
4 |
113,512,919 (GRCm39) |
missense |
unknown |
|
R9053:Skint5
|
UTSW |
4 |
113,403,684 (GRCm39) |
missense |
unknown |
|
R9216:Skint5
|
UTSW |
4 |
113,392,955 (GRCm39) |
missense |
unknown |
|
R9441:Skint5
|
UTSW |
4 |
113,347,848 (GRCm39) |
missense |
unknown |
|
R9551:Skint5
|
UTSW |
4 |
113,798,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9552:Skint5
|
UTSW |
4 |
113,798,052 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9750:Skint5
|
UTSW |
4 |
113,727,866 (GRCm39) |
missense |
unknown |
|
X0028:Skint5
|
UTSW |
4 |
113,548,306 (GRCm39) |
missense |
unknown |
|
|