Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,815,526 (GRCm39) |
F258S |
probably damaging |
Het |
Abca3 |
A |
G |
17: 24,602,959 (GRCm39) |
Y518C |
probably damaging |
Het |
Ank2 |
A |
T |
3: 126,840,431 (GRCm39) |
N274K |
probably damaging |
Het |
Ankrd31 |
C |
T |
13: 96,969,329 (GRCm39) |
L989F |
probably damaging |
Het |
Ano6 |
A |
G |
15: 95,825,463 (GRCm39) |
R354G |
probably benign |
Het |
Arfgef1 |
T |
C |
1: 10,211,838 (GRCm39) |
Y1735C |
probably damaging |
Het |
B3gnt8 |
G |
A |
7: 25,328,659 (GRCm39) |
G363D |
probably benign |
Het |
Calcrl |
T |
C |
2: 84,203,729 (GRCm39) |
|
probably null |
Het |
Cc2d2b |
A |
T |
19: 40,797,726 (GRCm39) |
D782V |
unknown |
Het |
Ccdc162 |
A |
G |
10: 41,531,440 (GRCm39) |
|
probably null |
Het |
Cdkal1 |
A |
T |
13: 29,809,918 (GRCm39) |
*219R |
probably null |
Het |
Clcnkb |
A |
T |
4: 141,135,160 (GRCm39) |
V526D |
possibly damaging |
Het |
Cnbp |
A |
T |
6: 87,821,074 (GRCm39) |
C162S |
probably damaging |
Het |
Coq2 |
A |
G |
5: 100,811,656 (GRCm39) |
|
probably benign |
Het |
D6Wsu163e |
T |
A |
6: 126,931,778 (GRCm39) |
L270Q |
probably damaging |
Het |
Dennd10 |
C |
T |
19: 60,823,423 (GRCm39) |
Q353* |
probably null |
Het |
Dnhd1 |
C |
T |
7: 105,362,855 (GRCm39) |
Q3806* |
probably null |
Het |
Eepd1 |
T |
C |
9: 25,394,518 (GRCm39) |
F261L |
probably benign |
Het |
Fes |
C |
T |
7: 80,036,559 (GRCm39) |
|
probably benign |
Het |
Fsip2 |
T |
A |
2: 82,807,681 (GRCm39) |
D1333E |
possibly damaging |
Het |
Gm10800 |
CAAGAAAACTGAAAATCAAAGAAAACTGAAAATCA |
CAAGAAAACTGAAAATCA |
2: 98,497,361 (GRCm39) |
|
probably null |
Het |
Gm5113 |
T |
C |
7: 29,878,292 (GRCm39) |
F127L |
probably benign |
Het |
Grk3 |
A |
G |
5: 113,066,697 (GRCm39) |
S596P |
possibly damaging |
Het |
Gsk3a |
A |
G |
7: 24,936,814 (GRCm39) |
V91A |
possibly damaging |
Het |
Gss |
T |
C |
2: 155,420,279 (GRCm39) |
K141E |
probably damaging |
Het |
Il1rl2 |
A |
T |
1: 40,366,530 (GRCm39) |
|
probably null |
Het |
Kcnmb1 |
A |
G |
11: 33,914,825 (GRCm39) |
Y42C |
probably damaging |
Het |
Krtap16-1 |
A |
T |
11: 99,877,170 (GRCm39) |
I78N |
probably damaging |
Het |
Lrp2 |
C |
T |
2: 69,379,382 (GRCm39) |
S110N |
possibly damaging |
Het |
Lrrfip1 |
T |
A |
1: 91,012,781 (GRCm39) |
|
probably benign |
Het |
Magel2 |
G |
T |
7: 62,029,441 (GRCm39) |
A782S |
unknown |
Het |
Map1b |
C |
A |
13: 99,569,017 (GRCm39) |
E1235* |
probably null |
Het |
Mcpt1 |
A |
C |
14: 56,257,520 (GRCm39) |
H222P |
probably benign |
Het |
Met |
T |
A |
6: 17,549,137 (GRCm39) |
N996K |
probably benign |
Het |
Mia |
C |
A |
7: 26,880,230 (GRCm39) |
Q52H |
probably damaging |
Het |
Mia |
T |
A |
7: 26,880,231 (GRCm39) |
Q52L |
possibly damaging |
Het |
Myh7 |
T |
A |
14: 55,230,228 (GRCm39) |
K35* |
probably null |
Het |
Myt1l |
T |
A |
12: 29,861,468 (GRCm39) |
D83E |
unknown |
Het |
Nbl1 |
A |
G |
4: 138,810,861 (GRCm39) |
V111A |
probably damaging |
Het |
Nid1 |
T |
A |
13: 13,638,515 (GRCm39) |
V145D |
probably benign |
Het |
Nif3l1 |
C |
T |
1: 58,486,653 (GRCm39) |
|
probably benign |
Het |
Npnt |
T |
C |
3: 132,591,764 (GRCm39) |
Y500C |
probably damaging |
Het |
Nubpl |
T |
A |
12: 52,144,676 (GRCm39) |
|
probably null |
Het |
Nxpe4 |
T |
A |
9: 48,310,250 (GRCm39) |
D504E |
probably damaging |
Het |
Obsl1 |
A |
G |
1: 75,463,917 (GRCm39) |
V1696A |
possibly damaging |
Het |
Or56a3 |
A |
T |
7: 104,735,329 (GRCm39) |
R135S |
possibly damaging |
Het |
Or8s2 |
A |
T |
15: 98,276,475 (GRCm39) |
I172N |
probably damaging |
Het |
P2rx1 |
A |
T |
11: 72,900,821 (GRCm39) |
H224L |
probably benign |
Het |
Pald1 |
A |
T |
10: 61,182,815 (GRCm39) |
|
probably null |
Het |
Pard6g |
C |
T |
18: 80,160,411 (GRCm39) |
R175* |
probably null |
Het |
Pisd |
A |
G |
5: 32,895,755 (GRCm39) |
I271T |
probably benign |
Het |
Prrt3 |
T |
C |
6: 113,472,796 (GRCm39) |
S459G |
probably damaging |
Het |
Psd3 |
A |
T |
8: 68,165,945 (GRCm39) |
C328S |
unknown |
Het |
Psme1 |
A |
G |
14: 55,817,853 (GRCm39) |
E120G |
|
Het |
Pum3 |
A |
T |
19: 27,397,457 (GRCm39) |
M306K |
possibly damaging |
Het |
Pxdn |
T |
C |
12: 30,040,992 (GRCm39) |
F423L |
probably benign |
Het |
Rac3 |
A |
G |
11: 120,614,071 (GRCm39) |
D118G |
probably damaging |
Het |
Rnf14 |
A |
G |
18: 38,446,267 (GRCm39) |
K357E |
probably benign |
Het |
Rpl23a |
T |
C |
11: 78,073,720 (GRCm39) |
I40V |
probably benign |
Het |
Slc5a5 |
A |
T |
8: 71,345,227 (GRCm39) |
S27T |
probably damaging |
Het |
Slc7a14 |
A |
T |
3: 31,277,595 (GRCm39) |
L670Q |
probably damaging |
Het |
Snorc |
C |
T |
1: 87,402,826 (GRCm39) |
T52I |
probably damaging |
Het |
Sst |
T |
A |
16: 23,708,499 (GRCm39) |
K111* |
probably null |
Het |
Stxbp4 |
A |
G |
11: 90,426,267 (GRCm39) |
S514P |
unknown |
Het |
Susd1 |
T |
A |
4: 59,390,576 (GRCm39) |
T300S |
probably benign |
Het |
Tecpr1 |
C |
T |
5: 144,150,845 (GRCm39) |
|
probably benign |
Het |
Tmem185b |
C |
T |
1: 119,454,198 (GRCm39) |
|
probably benign |
Het |
Tor2a |
T |
A |
2: 32,651,699 (GRCm39) |
F305I |
probably damaging |
Het |
Ttk |
T |
A |
9: 83,750,113 (GRCm39) |
D689E |
probably damaging |
Het |
Tut4 |
A |
T |
4: 108,336,408 (GRCm39) |
D44V |
probably damaging |
Het |
Usp25 |
A |
G |
16: 76,878,421 (GRCm39) |
D615G |
probably damaging |
Het |
Vmn1r209 |
A |
G |
13: 22,990,684 (GRCm39) |
V2A |
probably benign |
Het |
Vmn2r80 |
A |
C |
10: 79,017,928 (GRCm39) |
E551A |
probably damaging |
Het |
Wac |
G |
T |
18: 7,926,104 (GRCm39) |
E636* |
probably null |
Het |
Wdr53 |
T |
A |
16: 32,071,130 (GRCm39) |
D158E |
probably damaging |
Het |
Zbtb7c |
T |
C |
18: 76,270,152 (GRCm39) |
V80A |
probably damaging |
Het |
|
Other mutations in Ano8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00338:Ano8
|
APN |
8 |
71,936,902 (GRCm39) |
splice site |
probably benign |
|
IGL00501:Ano8
|
APN |
8 |
71,931,793 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01380:Ano8
|
APN |
8 |
71,933,453 (GRCm39) |
unclassified |
probably benign |
|
IGL02138:Ano8
|
APN |
8 |
71,937,486 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02516:Ano8
|
APN |
8 |
71,937,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02675:Ano8
|
APN |
8 |
71,936,184 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02995:Ano8
|
APN |
8 |
71,935,761 (GRCm39) |
missense |
possibly damaging |
0.72 |
H8786:Ano8
|
UTSW |
8 |
71,931,388 (GRCm39) |
unclassified |
probably benign |
|
R0265:Ano8
|
UTSW |
8 |
71,933,168 (GRCm39) |
unclassified |
probably benign |
|
R0282:Ano8
|
UTSW |
8 |
71,933,258 (GRCm39) |
unclassified |
probably benign |
|
R0518:Ano8
|
UTSW |
8 |
71,931,902 (GRCm39) |
missense |
probably benign |
0.39 |
R0521:Ano8
|
UTSW |
8 |
71,931,902 (GRCm39) |
missense |
probably benign |
0.39 |
R1028:Ano8
|
UTSW |
8 |
71,933,615 (GRCm39) |
small deletion |
probably benign |
|
R1147:Ano8
|
UTSW |
8 |
71,934,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ano8
|
UTSW |
8 |
71,934,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1748:Ano8
|
UTSW |
8 |
71,931,602 (GRCm39) |
unclassified |
probably benign |
|
R1852:Ano8
|
UTSW |
8 |
71,936,131 (GRCm39) |
missense |
probably damaging |
0.99 |
R4161:Ano8
|
UTSW |
8 |
71,935,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R4192:Ano8
|
UTSW |
8 |
71,935,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R4274:Ano8
|
UTSW |
8 |
71,931,385 (GRCm39) |
unclassified |
probably benign |
|
R4834:Ano8
|
UTSW |
8 |
71,936,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R4961:Ano8
|
UTSW |
8 |
71,935,640 (GRCm39) |
missense |
probably damaging |
1.00 |
R5252:Ano8
|
UTSW |
8 |
71,935,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Ano8
|
UTSW |
8 |
71,937,641 (GRCm39) |
splice site |
probably null |
|
R5598:Ano8
|
UTSW |
8 |
71,935,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R5695:Ano8
|
UTSW |
8 |
71,935,887 (GRCm39) |
missense |
probably damaging |
0.98 |
R5994:Ano8
|
UTSW |
8 |
71,937,478 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Ano8
|
UTSW |
8 |
71,935,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6153:Ano8
|
UTSW |
8 |
71,933,441 (GRCm39) |
unclassified |
probably benign |
|
R6405:Ano8
|
UTSW |
8 |
71,935,674 (GRCm39) |
missense |
probably damaging |
1.00 |
R6516:Ano8
|
UTSW |
8 |
71,934,424 (GRCm39) |
splice site |
probably null |
|
R6539:Ano8
|
UTSW |
8 |
71,937,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7194:Ano8
|
UTSW |
8 |
71,935,007 (GRCm39) |
missense |
possibly damaging |
0.66 |
R7204:Ano8
|
UTSW |
8 |
71,931,669 (GRCm39) |
missense |
probably benign |
0.39 |
R7340:Ano8
|
UTSW |
8 |
71,935,655 (GRCm39) |
missense |
probably damaging |
0.99 |
R7365:Ano8
|
UTSW |
8 |
71,937,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R7417:Ano8
|
UTSW |
8 |
71,933,477 (GRCm39) |
missense |
unknown |
|
R7486:Ano8
|
UTSW |
8 |
71,937,642 (GRCm39) |
critical splice donor site |
probably null |
|
R7644:Ano8
|
UTSW |
8 |
71,937,474 (GRCm39) |
missense |
probably damaging |
0.98 |
R7709:Ano8
|
UTSW |
8 |
71,934,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R7719:Ano8
|
UTSW |
8 |
71,935,784 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8040:Ano8
|
UTSW |
8 |
71,934,812 (GRCm39) |
missense |
probably benign |
0.26 |
R8219:Ano8
|
UTSW |
8 |
71,933,357 (GRCm39) |
missense |
unknown |
|
R8355:Ano8
|
UTSW |
8 |
71,933,210 (GRCm39) |
unclassified |
probably benign |
|
R8401:Ano8
|
UTSW |
8 |
71,936,011 (GRCm39) |
missense |
probably damaging |
1.00 |
R8713:Ano8
|
UTSW |
8 |
71,937,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8755:Ano8
|
UTSW |
8 |
71,935,724 (GRCm39) |
missense |
probably benign |
0.11 |
R8871:Ano8
|
UTSW |
8 |
71,931,944 (GRCm39) |
missense |
probably benign |
0.39 |
R8990:Ano8
|
UTSW |
8 |
71,929,201 (GRCm39) |
missense |
unknown |
|
R9037:Ano8
|
UTSW |
8 |
71,937,088 (GRCm39) |
missense |
probably damaging |
1.00 |
R9379:Ano8
|
UTSW |
8 |
71,936,178 (GRCm39) |
missense |
probably benign |
0.28 |
R9432:Ano8
|
UTSW |
8 |
71,933,561 (GRCm39) |
missense |
unknown |
|
R9492:Ano8
|
UTSW |
8 |
71,934,784 (GRCm39) |
missense |
possibly damaging |
0.66 |
R9609:Ano8
|
UTSW |
8 |
71,933,726 (GRCm39) |
missense |
unknown |
|
X0026:Ano8
|
UTSW |
8 |
71,931,801 (GRCm39) |
unclassified |
probably benign |
|
|