Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcf3 |
C |
T |
16: 20,371,316 (GRCm39) |
R437C |
probably damaging |
Het |
Abhd3 |
A |
G |
18: 10,647,840 (GRCm39) |
Y315H |
possibly damaging |
Het |
Adam19 |
C |
T |
11: 46,033,861 (GRCm39) |
P891L |
probably damaging |
Het |
Ampd1 |
T |
A |
3: 102,999,046 (GRCm39) |
Y400* |
probably null |
Het |
Ap1g1 |
T |
C |
8: 110,582,267 (GRCm39) |
S724P |
probably benign |
Het |
Bst2 |
T |
A |
8: 71,989,861 (GRCm39) |
T71S |
possibly damaging |
Het |
C3 |
A |
G |
17: 57,531,851 (GRCm39) |
|
probably null |
Het |
Cacna2d1 |
C |
A |
5: 16,566,815 (GRCm39) |
|
probably benign |
Het |
Cacna2d4 |
C |
T |
6: 119,213,709 (GRCm39) |
H43Y |
possibly damaging |
Het |
Ccdc71 |
T |
G |
9: 108,341,336 (GRCm39) |
V383G |
probably benign |
Het |
Cd109 |
A |
T |
9: 78,596,214 (GRCm39) |
Q849L |
possibly damaging |
Het |
Cdkn2a |
A |
T |
4: 89,195,004 (GRCm39) |
H115Q |
possibly damaging |
Het |
Ces1e |
T |
C |
8: 93,946,057 (GRCm39) |
E161G |
probably benign |
Het |
Cggbp1 |
C |
T |
16: 64,676,201 (GRCm39) |
S89L |
possibly damaging |
Het |
Crocc |
A |
T |
4: 140,769,553 (GRCm39) |
|
probably benign |
Het |
Cspg4b |
T |
A |
13: 113,505,687 (GRCm39) |
L2272* |
probably null |
Het |
Eef1akmt3 |
G |
A |
10: 126,869,142 (GRCm39) |
Q111* |
probably null |
Het |
Exoc7 |
T |
C |
11: 116,186,118 (GRCm39) |
N361S |
probably benign |
Het |
Fat2 |
G |
T |
11: 55,187,011 (GRCm39) |
S1278R |
probably benign |
Het |
Fbxo42 |
A |
G |
4: 140,927,640 (GRCm39) |
N640S |
probably benign |
Het |
Fbxw25 |
A |
G |
9: 109,483,720 (GRCm39) |
V164A |
possibly damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,854,917 (GRCm39) |
I1848V |
probably damaging |
Het |
Foxs1 |
T |
C |
2: 152,774,330 (GRCm39) |
E241G |
probably damaging |
Het |
Fras1 |
A |
T |
5: 96,924,493 (GRCm39) |
I3645F |
possibly damaging |
Het |
Gm14496 |
T |
A |
2: 181,639,206 (GRCm39) |
V432E |
probably benign |
Het |
H3c2 |
T |
A |
13: 23,936,693 (GRCm39) |
C111S |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,403,203 (GRCm39) |
L4374* |
probably null |
Het |
Ift122 |
T |
C |
6: 115,901,445 (GRCm39) |
|
probably benign |
Het |
Itgav |
C |
A |
2: 83,622,381 (GRCm39) |
N654K |
probably benign |
Het |
Itih5 |
T |
C |
2: 10,239,803 (GRCm39) |
|
probably benign |
Het |
Jak2 |
C |
A |
19: 29,289,157 (GRCm39) |
T1103K |
probably benign |
Het |
Kcnc4 |
C |
A |
3: 107,365,920 (GRCm39) |
C96F |
probably benign |
Het |
Med13l |
C |
A |
5: 118,880,514 (GRCm39) |
S1202Y |
unknown |
Het |
Mefv |
T |
C |
16: 3,533,320 (GRCm39) |
E317G |
possibly damaging |
Het |
Ncoa2 |
T |
C |
1: 13,222,608 (GRCm39) |
T1226A |
probably benign |
Het |
Nktr |
C |
T |
9: 121,579,757 (GRCm39) |
|
probably benign |
Het |
Nudt5 |
G |
A |
2: 5,867,114 (GRCm39) |
V61M |
probably damaging |
Het |
Or51a39 |
C |
T |
7: 102,363,162 (GRCm39) |
A153T |
probably benign |
Het |
Pakap |
A |
G |
4: 57,709,649 (GRCm39) |
D198G |
possibly damaging |
Het |
Pcdhb2 |
A |
C |
18: 37,430,283 (GRCm39) |
Y752S |
probably damaging |
Het |
Pcnx4 |
A |
G |
12: 72,603,076 (GRCm39) |
D446G |
probably benign |
Het |
Pnp2 |
G |
A |
14: 51,201,761 (GRCm39) |
R249H |
probably damaging |
Het |
Rgs3 |
A |
T |
4: 62,542,121 (GRCm39) |
I32F |
probably damaging |
Het |
Rnf139 |
A |
G |
15: 58,770,727 (GRCm39) |
T251A |
probably benign |
Het |
Rnf41 |
A |
G |
10: 128,274,104 (GRCm39) |
E252G |
probably damaging |
Het |
Rxfp2 |
T |
A |
5: 149,975,093 (GRCm39) |
F220Y |
probably benign |
Het |
Sdcbp |
A |
G |
4: 6,379,042 (GRCm39) |
D43G |
possibly damaging |
Het |
Serpina3f |
A |
G |
12: 104,183,267 (GRCm39) |
D43G |
probably damaging |
Het |
Sftpc |
T |
C |
14: 70,758,887 (GRCm39) |
K154R |
probably null |
Het |
Simc1 |
A |
G |
13: 54,672,530 (GRCm39) |
T293A |
probably benign |
Het |
Slc6a15 |
T |
C |
10: 103,225,208 (GRCm39) |
|
probably benign |
Het |
Spata31e2 |
T |
G |
1: 26,723,032 (GRCm39) |
H716P |
probably damaging |
Het |
Ston2 |
A |
T |
12: 91,707,376 (GRCm39) |
I78N |
probably damaging |
Het |
Taok3 |
T |
C |
5: 117,355,307 (GRCm39) |
|
probably null |
Het |
Tent4b |
G |
A |
8: 88,977,371 (GRCm39) |
G391D |
probably damaging |
Het |
Tiam1 |
C |
T |
16: 89,589,889 (GRCm39) |
|
probably benign |
Het |
Tnfsf15 |
T |
C |
4: 63,648,229 (GRCm39) |
H137R |
possibly damaging |
Het |
Tpte |
G |
A |
8: 22,817,755 (GRCm39) |
R247H |
possibly damaging |
Het |
Trim2 |
T |
C |
3: 84,117,476 (GRCm39) |
|
probably benign |
Het |
Ulk1 |
A |
T |
5: 110,936,810 (GRCm39) |
|
probably benign |
Het |
Utp4 |
T |
G |
8: 107,640,018 (GRCm39) |
H442Q |
probably null |
Het |
Vmn1r193 |
T |
A |
13: 22,403,798 (GRCm39) |
I65F |
probably damaging |
Het |
Vps54 |
A |
T |
11: 21,256,962 (GRCm39) |
Q690L |
probably damaging |
Het |
Ybx2 |
T |
C |
11: 69,831,145 (GRCm39) |
|
probably benign |
Het |
Zbtb38 |
C |
T |
9: 96,568,993 (GRCm39) |
G697D |
possibly damaging |
Het |
Zfp202 |
C |
T |
9: 40,120,212 (GRCm39) |
Q218* |
probably null |
Het |
Zfp820 |
G |
A |
17: 22,038,800 (GRCm39) |
T176I |
probably benign |
Het |
|
Other mutations in Skint6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01123:Skint6
|
APN |
4 |
112,661,879 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL01296:Skint6
|
APN |
4 |
113,093,637 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01343:Skint6
|
APN |
4 |
113,140,823 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01543:Skint6
|
APN |
4 |
112,757,160 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01633:Skint6
|
APN |
4 |
113,095,246 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01818:Skint6
|
APN |
4 |
112,805,766 (GRCm39) |
missense |
probably benign |
0.18 |
IGL02124:Skint6
|
APN |
4 |
112,944,993 (GRCm39) |
missense |
probably benign |
|
IGL02517:Skint6
|
APN |
4 |
112,805,737 (GRCm39) |
splice site |
probably benign |
|
IGL02647:Skint6
|
APN |
4 |
112,985,088 (GRCm39) |
splice site |
probably benign |
|
IGL02887:Skint6
|
APN |
4 |
113,095,381 (GRCm39) |
nonsense |
probably null |
|
IGL03026:Skint6
|
APN |
4 |
112,848,441 (GRCm39) |
splice site |
probably null |
|
IGL03030:Skint6
|
APN |
4 |
112,870,153 (GRCm39) |
missense |
probably benign |
0.03 |
meissner
|
UTSW |
4 |
112,661,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
Tegmentum
|
UTSW |
4 |
112,700,019 (GRCm39) |
splice site |
probably null |
|
PIT4576001:Skint6
|
UTSW |
4 |
112,910,564 (GRCm39) |
missense |
possibly damaging |
0.91 |
R0058:Skint6
|
UTSW |
4 |
112,904,012 (GRCm39) |
splice site |
probably benign |
|
R0058:Skint6
|
UTSW |
4 |
112,904,012 (GRCm39) |
splice site |
probably benign |
|
R0099:Skint6
|
UTSW |
4 |
112,668,698 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0164:Skint6
|
UTSW |
4 |
112,848,433 (GRCm39) |
splice site |
probably benign |
|
R0312:Skint6
|
UTSW |
4 |
112,666,297 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0591:Skint6
|
UTSW |
4 |
112,715,366 (GRCm39) |
splice site |
probably benign |
|
R0762:Skint6
|
UTSW |
4 |
112,722,848 (GRCm39) |
splice site |
probably benign |
|
R0941:Skint6
|
UTSW |
4 |
113,095,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Skint6
|
UTSW |
4 |
113,095,300 (GRCm39) |
missense |
probably benign |
0.20 |
R1132:Skint6
|
UTSW |
4 |
112,755,296 (GRCm39) |
critical splice donor site |
probably null |
|
R1228:Skint6
|
UTSW |
4 |
112,711,649 (GRCm39) |
missense |
probably benign |
|
R1338:Skint6
|
UTSW |
4 |
112,870,158 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1432:Skint6
|
UTSW |
4 |
112,726,721 (GRCm39) |
splice site |
probably benign |
|
R1512:Skint6
|
UTSW |
4 |
113,095,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R1577:Skint6
|
UTSW |
4 |
113,005,720 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1733:Skint6
|
UTSW |
4 |
113,034,234 (GRCm39) |
splice site |
probably benign |
|
R1762:Skint6
|
UTSW |
4 |
113,093,678 (GRCm39) |
missense |
probably damaging |
0.98 |
R1891:Skint6
|
UTSW |
4 |
112,703,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1908:Skint6
|
UTSW |
4 |
112,749,187 (GRCm39) |
missense |
probably benign |
|
R2069:Skint6
|
UTSW |
4 |
113,095,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R2089:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2091:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2091:Skint6
|
UTSW |
4 |
112,703,881 (GRCm39) |
missense |
probably benign |
|
R2144:Skint6
|
UTSW |
4 |
113,093,457 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2166:Skint6
|
UTSW |
4 |
112,711,649 (GRCm39) |
missense |
probably benign |
0.01 |
R2192:Skint6
|
UTSW |
4 |
112,722,909 (GRCm39) |
nonsense |
probably null |
|
R2267:Skint6
|
UTSW |
4 |
112,700,019 (GRCm39) |
splice site |
probably null |
|
R2312:Skint6
|
UTSW |
4 |
113,095,339 (GRCm39) |
missense |
probably damaging |
1.00 |
R2324:Skint6
|
UTSW |
4 |
112,729,654 (GRCm39) |
splice site |
probably null |
|
R2342:Skint6
|
UTSW |
4 |
113,034,180 (GRCm39) |
missense |
probably benign |
0.00 |
R3028:Skint6
|
UTSW |
4 |
113,093,690 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3704:Skint6
|
UTSW |
4 |
112,993,669 (GRCm39) |
missense |
possibly damaging |
0.86 |
R3752:Skint6
|
UTSW |
4 |
112,700,096 (GRCm39) |
splice site |
probably benign |
|
R3760:Skint6
|
UTSW |
4 |
112,794,655 (GRCm39) |
missense |
possibly damaging |
0.53 |
R3827:Skint6
|
UTSW |
4 |
112,794,634 (GRCm39) |
missense |
probably benign |
|
R4377:Skint6
|
UTSW |
4 |
113,093,715 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4406:Skint6
|
UTSW |
4 |
113,013,683 (GRCm39) |
missense |
probably benign |
0.01 |
R4611:Skint6
|
UTSW |
4 |
112,931,273 (GRCm39) |
missense |
probably benign |
|
R4780:Skint6
|
UTSW |
4 |
113,093,594 (GRCm39) |
missense |
probably damaging |
0.98 |
R4788:Skint6
|
UTSW |
4 |
113,095,533 (GRCm39) |
missense |
possibly damaging |
0.54 |
R4818:Skint6
|
UTSW |
4 |
112,812,589 (GRCm39) |
intron |
probably benign |
|
R4900:Skint6
|
UTSW |
4 |
112,924,667 (GRCm39) |
missense |
probably benign |
0.03 |
R4972:Skint6
|
UTSW |
4 |
112,692,265 (GRCm39) |
missense |
probably benign |
|
R5008:Skint6
|
UTSW |
4 |
112,848,452 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5016:Skint6
|
UTSW |
4 |
113,028,730 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5085:Skint6
|
UTSW |
4 |
113,093,465 (GRCm39) |
missense |
probably damaging |
0.99 |
R5165:Skint6
|
UTSW |
4 |
112,722,865 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5221:Skint6
|
UTSW |
4 |
112,752,121 (GRCm39) |
splice site |
probably null |
|
R5310:Skint6
|
UTSW |
4 |
113,041,965 (GRCm39) |
nonsense |
probably null |
|
R5423:Skint6
|
UTSW |
4 |
112,707,937 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5436:Skint6
|
UTSW |
4 |
112,953,788 (GRCm39) |
missense |
probably benign |
0.08 |
R5447:Skint6
|
UTSW |
4 |
112,963,106 (GRCm39) |
missense |
probably benign |
0.34 |
R5564:Skint6
|
UTSW |
4 |
112,846,162 (GRCm39) |
missense |
possibly damaging |
0.72 |
R5629:Skint6
|
UTSW |
4 |
112,870,176 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5936:Skint6
|
UTSW |
4 |
112,953,790 (GRCm39) |
missense |
probably benign |
0.33 |
R5993:Skint6
|
UTSW |
4 |
112,666,276 (GRCm39) |
missense |
probably benign |
0.02 |
R6027:Skint6
|
UTSW |
4 |
112,953,761 (GRCm39) |
splice site |
probably null |
|
R6174:Skint6
|
UTSW |
4 |
112,696,510 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6497:Skint6
|
UTSW |
4 |
113,093,595 (GRCm39) |
missense |
probably damaging |
0.98 |
R6552:Skint6
|
UTSW |
4 |
112,924,687 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6645:Skint6
|
UTSW |
4 |
112,749,235 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6810:Skint6
|
UTSW |
4 |
112,805,577 (GRCm39) |
splice site |
probably null |
|
R7003:Skint6
|
UTSW |
4 |
112,963,109 (GRCm39) |
missense |
probably benign |
0.01 |
R7211:Skint6
|
UTSW |
4 |
113,095,566 (GRCm39) |
missense |
probably benign |
0.09 |
R7269:Skint6
|
UTSW |
4 |
112,711,686 (GRCm39) |
splice site |
probably null |
|
R7398:Skint6
|
UTSW |
4 |
112,755,335 (GRCm39) |
missense |
probably benign |
0.00 |
R7438:Skint6
|
UTSW |
4 |
113,095,425 (GRCm39) |
missense |
probably damaging |
1.00 |
R7461:Skint6
|
UTSW |
4 |
113,034,243 (GRCm39) |
splice site |
probably null |
|
R7536:Skint6
|
UTSW |
4 |
112,668,744 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7613:Skint6
|
UTSW |
4 |
113,034,243 (GRCm39) |
splice site |
probably null |
|
R7956:Skint6
|
UTSW |
4 |
112,703,894 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8118:Skint6
|
UTSW |
4 |
113,013,691 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8118:Skint6
|
UTSW |
4 |
112,722,872 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8197:Skint6
|
UTSW |
4 |
112,752,040 (GRCm39) |
splice site |
probably null |
|
R8218:Skint6
|
UTSW |
4 |
112,696,471 (GRCm39) |
splice site |
probably null |
|
R8344:Skint6
|
UTSW |
4 |
113,093,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R8518:Skint6
|
UTSW |
4 |
113,095,465 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8776:Skint6
|
UTSW |
4 |
112,661,885 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8776-TAIL:Skint6
|
UTSW |
4 |
112,661,885 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8794:Skint6
|
UTSW |
4 |
113,049,869 (GRCm39) |
missense |
possibly damaging |
0.73 |
R8796:Skint6
|
UTSW |
4 |
112,661,891 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8812:Skint6
|
UTSW |
4 |
112,846,149 (GRCm39) |
missense |
probably benign |
0.00 |
R8866:Skint6
|
UTSW |
4 |
112,711,650 (GRCm39) |
missense |
probably benign |
|
R8881:Skint6
|
UTSW |
4 |
112,672,716 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8949:Skint6
|
UTSW |
4 |
112,931,296 (GRCm39) |
missense |
probably benign |
0.04 |
R8967:Skint6
|
UTSW |
4 |
112,729,701 (GRCm39) |
nonsense |
probably null |
|
R9005:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9007:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9053:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9055:Skint6
|
UTSW |
4 |
113,095,347 (GRCm39) |
missense |
probably damaging |
1.00 |
R9144:Skint6
|
UTSW |
4 |
112,985,102 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9149:Skint6
|
UTSW |
4 |
113,034,173 (GRCm39) |
missense |
probably damaging |
0.98 |
R9297:Skint6
|
UTSW |
4 |
112,668,717 (GRCm39) |
missense |
probably benign |
0.00 |
R9388:Skint6
|
UTSW |
4 |
113,049,838 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9407:Skint6
|
UTSW |
4 |
113,034,224 (GRCm39) |
missense |
possibly damaging |
0.53 |
R9475:Skint6
|
UTSW |
4 |
112,664,037 (GRCm39) |
critical splice donor site |
probably null |
|
R9515:Skint6
|
UTSW |
4 |
112,715,375 (GRCm39) |
missense |
probably benign |
|
R9572:Skint6
|
UTSW |
4 |
112,985,128 (GRCm39) |
missense |
probably benign |
|
R9689:Skint6
|
UTSW |
4 |
113,093,546 (GRCm39) |
missense |
probably damaging |
0.99 |
R9744:Skint6
|
UTSW |
4 |
112,666,360 (GRCm39) |
missense |
probably damaging |
1.00 |
R9785:Skint6
|
UTSW |
4 |
112,740,884 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1176:Skint6
|
UTSW |
4 |
113,095,491 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1176:Skint6
|
UTSW |
4 |
112,749,211 (GRCm39) |
missense |
possibly damaging |
0.53 |
Z1176:Skint6
|
UTSW |
4 |
113,095,492 (GRCm39) |
missense |
possibly damaging |
0.83 |
Z1177:Skint6
|
UTSW |
4 |
112,963,158 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1177:Skint6
|
UTSW |
4 |
112,664,125 (GRCm39) |
missense |
possibly damaging |
0.96 |
|