Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
G |
A |
7: 41,276,400 (GRCm39) |
G701D |
probably damaging |
Het |
6030468B19Rik |
T |
A |
11: 117,693,780 (GRCm39) |
N82K |
probably damaging |
Het |
Abca17 |
A |
T |
17: 24,554,564 (GRCm39) |
V130E |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,399,348 (GRCm39) |
K2077* |
probably null |
Het |
Aox1 |
T |
C |
1: 58,322,651 (GRCm39) |
F73S |
probably benign |
Het |
Ap3b1 |
T |
A |
13: 94,668,542 (GRCm39) |
C965* |
probably null |
Het |
Arhgef10 |
T |
A |
8: 14,980,030 (GRCm39) |
V90E |
probably damaging |
Het |
Atr |
T |
A |
9: 95,751,953 (GRCm39) |
H523Q |
probably benign |
Het |
Bicdl1 |
G |
T |
5: 115,789,916 (GRCm39) |
Q511K |
possibly damaging |
Het |
Capn15 |
A |
T |
17: 26,184,228 (GRCm39) |
N150K |
probably damaging |
Het |
Card6 |
A |
T |
15: 5,129,591 (GRCm39) |
W602R |
probably benign |
Het |
Clnk |
A |
T |
5: 38,927,234 (GRCm39) |
S82T |
possibly damaging |
Het |
Cmah |
T |
C |
13: 24,620,612 (GRCm39) |
I282T |
probably damaging |
Het |
Cog8 |
A |
G |
8: 107,779,131 (GRCm39) |
I382T |
probably benign |
Het |
Dhrs7c |
G |
T |
11: 67,700,722 (GRCm39) |
|
probably null |
Het |
Dhrs9 |
T |
A |
2: 69,223,502 (GRCm39) |
D83E |
probably damaging |
Het |
Dmac2l |
A |
T |
12: 69,788,562 (GRCm39) |
N154Y |
probably benign |
Het |
Dmgdh |
G |
A |
13: 93,852,043 (GRCm39) |
G624E |
probably damaging |
Het |
Dnajc30 |
C |
A |
5: 135,093,569 (GRCm39) |
F155L |
probably damaging |
Het |
Drc7 |
A |
C |
8: 95,800,778 (GRCm39) |
K600T |
probably damaging |
Het |
Efhb |
A |
C |
17: 53,707,928 (GRCm39) |
I745S |
probably damaging |
Het |
Elp1 |
ACTTCTTCTTCTTCTTCTTCTTC |
ACTTCTTCTTCTTCTTCTTC |
4: 56,781,176 (GRCm39) |
|
probably benign |
Het |
Fasn |
T |
A |
11: 120,701,291 (GRCm39) |
K1988* |
probably null |
Het |
Gad2 |
T |
C |
2: 22,525,035 (GRCm39) |
L273P |
probably damaging |
Het |
Gm45861 |
A |
T |
8: 28,032,536 (GRCm39) |
K887* |
probably null |
Het |
Gm45861 |
A |
T |
8: 28,032,537 (GRCm39) |
K887I |
unknown |
Het |
Gm9195 |
A |
G |
14: 72,718,221 (GRCm39) |
Y152H |
probably damaging |
Het |
Grip1 |
G |
A |
10: 119,781,061 (GRCm39) |
D237N |
probably damaging |
Het |
Hamp |
A |
C |
7: 30,641,961 (GRCm39) |
C65G |
possibly damaging |
Het |
Hes3 |
A |
G |
4: 152,372,581 (GRCm39) |
|
probably benign |
Het |
Hgh1 |
T |
C |
15: 76,254,650 (GRCm39) |
I342T |
probably damaging |
Het |
Ift80 |
A |
T |
3: 68,898,277 (GRCm39) |
C19* |
probably null |
Het |
Kbtbd12 |
C |
T |
6: 88,595,650 (GRCm39) |
C60Y |
probably damaging |
Het |
Kdm4c |
T |
A |
4: 74,263,804 (GRCm39) |
V696E |
probably benign |
Het |
Lect2 |
A |
G |
13: 56,690,803 (GRCm39) |
I117T |
unknown |
Het |
Lipn |
T |
A |
19: 34,054,390 (GRCm39) |
Y209* |
probably null |
Het |
Lpin3 |
G |
A |
2: 160,740,627 (GRCm39) |
V391I |
probably benign |
Het |
Mocs2 |
A |
T |
13: 114,961,143 (GRCm39) |
I47L |
probably benign |
Het |
Mogs |
T |
A |
6: 83,095,488 (GRCm39) |
H768Q |
probably benign |
Het |
Nbeal1 |
T |
A |
1: 60,276,317 (GRCm39) |
I686N |
probably damaging |
Het |
Nbeal1 |
T |
A |
1: 60,299,793 (GRCm39) |
C1376* |
probably null |
Het |
Ninl |
A |
G |
2: 150,791,263 (GRCm39) |
Y1087H |
possibly damaging |
Het |
Or10a3 |
A |
G |
7: 108,480,475 (GRCm39) |
F113L |
probably benign |
Het |
Or10ak14 |
A |
G |
4: 118,611,615 (GRCm39) |
V42A |
possibly damaging |
Het |
Or4k5 |
A |
G |
14: 50,385,689 (GRCm39) |
L214S |
probably damaging |
Het |
Or51b6b |
A |
C |
7: 103,309,788 (GRCm39) |
L223R |
probably damaging |
Het |
Or6s1 |
A |
G |
14: 51,308,616 (GRCm39) |
V78A |
possibly damaging |
Het |
Or8k30 |
T |
A |
2: 86,339,369 (GRCm39) |
C189S |
probably damaging |
Het |
Pkn1 |
A |
G |
8: 84,398,363 (GRCm39) |
F768S |
probably damaging |
Het |
Plekha2 |
A |
G |
8: 25,553,957 (GRCm39) |
F82L |
probably damaging |
Het |
Ppie |
T |
C |
4: 123,028,900 (GRCm39) |
E111G |
probably benign |
Het |
Rps6ka5 |
T |
C |
12: 100,547,679 (GRCm39) |
Y277C |
probably damaging |
Het |
Scgb2b12 |
A |
G |
7: 32,026,102 (GRCm39) |
V30A |
probably benign |
Het |
Serac1 |
A |
T |
17: 6,124,476 (GRCm39) |
S16T |
probably benign |
Het |
Sf3a3 |
T |
C |
4: 124,616,693 (GRCm39) |
Y192H |
probably damaging |
Het |
Slc14a1 |
A |
G |
18: 78,145,626 (GRCm39) |
V436A |
probably benign |
Het |
Smc3 |
T |
A |
19: 53,630,329 (GRCm39) |
M1112K |
probably damaging |
Het |
Tnk2 |
G |
A |
16: 32,499,986 (GRCm39) |
G1017E |
probably damaging |
Het |
Tnn |
T |
A |
1: 159,953,947 (GRCm39) |
K603* |
probably null |
Het |
Trpm6 |
T |
C |
19: 18,815,462 (GRCm39) |
S1183P |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,614,724 (GRCm39) |
V16964E |
possibly damaging |
Het |
Usp17le |
G |
A |
7: 104,417,696 (GRCm39) |
T482I |
probably benign |
Het |
Vmn1r219 |
T |
A |
13: 23,347,525 (GRCm39) |
M238K |
probably damaging |
Het |
Wfs1 |
C |
T |
5: 37,124,516 (GRCm39) |
G792S |
probably benign |
Het |
Xpa |
A |
T |
4: 46,185,612 (GRCm39) |
L122Q |
probably damaging |
Het |
|
Other mutations in Hlcs |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01078:Hlcs
|
APN |
16 |
93,934,019 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02026:Hlcs
|
APN |
16 |
93,935,564 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02341:Hlcs
|
APN |
16 |
94,031,969 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03075:Hlcs
|
APN |
16 |
93,939,706 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4515001:Hlcs
|
UTSW |
16 |
94,068,275 (GRCm39) |
missense |
probably benign |
0.45 |
R0372:Hlcs
|
UTSW |
16 |
93,939,766 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0664:Hlcs
|
UTSW |
16 |
94,032,170 (GRCm39) |
missense |
probably damaging |
1.00 |
R0731:Hlcs
|
UTSW |
16 |
93,932,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Hlcs
|
UTSW |
16 |
94,069,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R1465:Hlcs
|
UTSW |
16 |
94,069,151 (GRCm39) |
missense |
probably damaging |
0.99 |
R1761:Hlcs
|
UTSW |
16 |
94,068,866 (GRCm39) |
missense |
probably benign |
0.05 |
R2013:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
R2014:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
R2015:Hlcs
|
UTSW |
16 |
94,063,599 (GRCm39) |
missense |
probably benign |
0.17 |
R2204:Hlcs
|
UTSW |
16 |
94,032,011 (GRCm39) |
missense |
probably benign |
0.30 |
R2371:Hlcs
|
UTSW |
16 |
94,068,926 (GRCm39) |
missense |
probably damaging |
0.98 |
R3816:Hlcs
|
UTSW |
16 |
93,933,947 (GRCm39) |
missense |
probably benign |
0.11 |
R3822:Hlcs
|
UTSW |
16 |
94,068,840 (GRCm39) |
missense |
probably benign |
0.04 |
R4422:Hlcs
|
UTSW |
16 |
93,939,819 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4657:Hlcs
|
UTSW |
16 |
94,063,557 (GRCm39) |
missense |
probably benign |
0.00 |
R4783:Hlcs
|
UTSW |
16 |
94,069,398 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5347:Hlcs
|
UTSW |
16 |
94,068,383 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5808:Hlcs
|
UTSW |
16 |
94,063,491 (GRCm39) |
missense |
probably benign |
0.00 |
R5940:Hlcs
|
UTSW |
16 |
93,935,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R6341:Hlcs
|
UTSW |
16 |
94,032,022 (GRCm39) |
missense |
probably damaging |
1.00 |
R6943:Hlcs
|
UTSW |
16 |
93,942,261 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7053:Hlcs
|
UTSW |
16 |
94,068,874 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7166:Hlcs
|
UTSW |
16 |
94,063,585 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7313:Hlcs
|
UTSW |
16 |
94,068,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R7427:Hlcs
|
UTSW |
16 |
94,068,758 (GRCm39) |
missense |
probably benign |
0.00 |
R7428:Hlcs
|
UTSW |
16 |
94,068,758 (GRCm39) |
missense |
probably benign |
0.00 |
R7547:Hlcs
|
UTSW |
16 |
94,032,031 (GRCm39) |
nonsense |
probably null |
|
R7548:Hlcs
|
UTSW |
16 |
93,933,876 (GRCm39) |
nonsense |
probably null |
|
R8172:Hlcs
|
UTSW |
16 |
94,068,485 (GRCm39) |
missense |
probably damaging |
1.00 |
R8241:Hlcs
|
UTSW |
16 |
94,068,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Hlcs
|
UTSW |
16 |
94,063,617 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8940:Hlcs
|
UTSW |
16 |
94,032,085 (GRCm39) |
missense |
probably benign |
|
R9274:Hlcs
|
UTSW |
16 |
94,088,785 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9360:Hlcs
|
UTSW |
16 |
93,932,672 (GRCm39) |
missense |
probably damaging |
1.00 |
R9361:Hlcs
|
UTSW |
16 |
93,939,799 (GRCm39) |
missense |
probably benign |
0.10 |
R9564:Hlcs
|
UTSW |
16 |
93,935,580 (GRCm39) |
missense |
probably benign |
0.01 |
X0065:Hlcs
|
UTSW |
16 |
93,934,032 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Hlcs
|
UTSW |
16 |
94,063,518 (GRCm39) |
missense |
probably damaging |
1.00 |
|