Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abl2 |
T |
G |
1: 156,450,104 (GRCm39) |
N90K |
possibly damaging |
Het |
Acox1 |
T |
C |
11: 116,069,001 (GRCm39) |
T415A |
possibly damaging |
Het |
Acy1 |
T |
C |
9: 106,314,921 (GRCm39) |
M1V |
probably null |
Het |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Alpk3 |
C |
A |
7: 80,750,746 (GRCm39) |
Y1505* |
probably null |
Het |
Ankrd17 |
T |
C |
5: 90,390,902 (GRCm39) |
N2256S |
probably benign |
Het |
Ankrd22 |
C |
A |
19: 34,126,692 (GRCm39) |
C46F |
possibly damaging |
Het |
Arhgef5 |
A |
T |
6: 43,257,605 (GRCm39) |
K1291* |
probably null |
Het |
Arl9 |
T |
A |
5: 77,158,276 (GRCm39) |
Y119* |
probably null |
Het |
Asb14 |
T |
C |
14: 26,622,805 (GRCm39) |
V89A |
probably benign |
Het |
Banp |
T |
G |
8: 122,676,588 (GRCm39) |
|
probably null |
Het |
Btn2a2 |
T |
C |
13: 23,666,933 (GRCm39) |
N224S |
probably benign |
Het |
C1ra |
C |
T |
6: 124,499,403 (GRCm39) |
Q530* |
probably null |
Het |
C2cd6 |
A |
C |
1: 59,107,844 (GRCm39) |
S273A |
probably benign |
Het |
Cd1d2 |
A |
T |
3: 86,895,583 (GRCm39) |
|
probably null |
Het |
Cdc42bpb |
T |
C |
12: 111,306,307 (GRCm39) |
D132G |
probably damaging |
Het |
Cfap45 |
C |
A |
1: 172,362,877 (GRCm39) |
Y289* |
probably null |
Het |
Chrdl2 |
T |
C |
7: 99,659,332 (GRCm39) |
|
probably null |
Het |
Cilk1 |
A |
G |
9: 78,065,221 (GRCm39) |
K377R |
probably benign |
Het |
Cst5 |
C |
T |
2: 149,247,496 (GRCm39) |
L71F |
probably benign |
Het |
Dcaf11 |
T |
C |
14: 55,802,966 (GRCm39) |
F292L |
possibly damaging |
Het |
Dgcr8 |
A |
G |
16: 18,077,487 (GRCm39) |
F641S |
probably damaging |
Het |
Dnm3 |
G |
A |
1: 162,149,198 (GRCm39) |
|
probably null |
Het |
Efcab3 |
G |
T |
11: 104,640,526 (GRCm39) |
S1088I |
probably benign |
Het |
Eral1 |
T |
C |
11: 77,966,219 (GRCm39) |
K320E |
probably damaging |
Het |
Eva1a |
A |
G |
6: 82,069,002 (GRCm39) |
T110A |
possibly damaging |
Het |
Fbxo42 |
A |
G |
4: 140,926,917 (GRCm39) |
D399G |
possibly damaging |
Het |
Frs2 |
T |
C |
10: 116,910,007 (GRCm39) |
T452A |
possibly damaging |
Het |
Git2 |
T |
A |
5: 114,871,958 (GRCm39) |
D542V |
probably damaging |
Het |
Grk2 |
T |
A |
19: 4,356,063 (GRCm39) |
|
probably benign |
Het |
Gsg1l2 |
A |
G |
11: 67,676,110 (GRCm39) |
N158S |
possibly damaging |
Het |
Hc |
T |
C |
2: 34,918,063 (GRCm39) |
N740S |
probably benign |
Het |
Hectd1 |
T |
C |
12: 51,791,588 (GRCm39) |
|
probably null |
Het |
Hemk1 |
A |
G |
9: 107,208,288 (GRCm39) |
|
probably null |
Het |
Hormad2 |
G |
T |
11: 4,362,245 (GRCm39) |
Y126* |
probably null |
Het |
Hr |
A |
G |
14: 70,795,652 (GRCm39) |
E399G |
possibly damaging |
Het |
Ilf3 |
C |
A |
9: 21,314,707 (GRCm39) |
H780N |
unknown |
Het |
Inpp5e |
A |
T |
2: 26,298,161 (GRCm39) |
S147T |
probably benign |
Het |
Irag2 |
C |
A |
6: 145,119,427 (GRCm39) |
|
probably null |
Het |
Jmjd6 |
T |
C |
11: 116,733,275 (GRCm39) |
D134G |
probably damaging |
Het |
Kif23 |
G |
T |
9: 61,844,457 (GRCm39) |
Y120* |
probably null |
Het |
Klk12 |
T |
A |
7: 43,422,780 (GRCm39) |
Y236N |
probably damaging |
Het |
Kmt5b |
C |
A |
19: 3,852,799 (GRCm39) |
Y186* |
probably null |
Het |
Krtap9-5 |
A |
G |
11: 99,840,132 (GRCm39) |
T278A |
unknown |
Het |
Lca5 |
T |
A |
9: 83,305,509 (GRCm39) |
D99V |
probably damaging |
Het |
Leng9 |
A |
G |
7: 4,151,800 (GRCm39) |
V292A |
probably benign |
Het |
Lime1 |
A |
G |
2: 181,025,135 (GRCm39) |
R231G |
probably benign |
Het |
Mrpl28 |
T |
A |
17: 26,343,589 (GRCm39) |
S116R |
probably damaging |
Het |
Muc15 |
A |
T |
2: 110,561,862 (GRCm39) |
R99S |
probably benign |
Het |
Myh2 |
G |
A |
11: 67,083,368 (GRCm39) |
A1444T |
probably benign |
Het |
Mynn |
T |
A |
3: 30,657,825 (GRCm39) |
Y48N |
probably damaging |
Het |
Myo1b |
A |
T |
1: 51,836,639 (GRCm39) |
V274E |
possibly damaging |
Het |
Nemp1 |
T |
A |
10: 127,528,923 (GRCm39) |
M209K |
possibly damaging |
Het |
Nlrc4 |
G |
T |
17: 74,752,507 (GRCm39) |
D625E |
probably benign |
Het |
Or10al6 |
C |
T |
17: 38,082,910 (GRCm39) |
A122V |
probably damaging |
Het |
Or11a4 |
T |
C |
17: 37,536,276 (GRCm39) |
F87L |
probably benign |
Het |
Or4p4 |
T |
C |
2: 88,482,622 (GRCm39) |
L42P |
probably damaging |
Het |
Otog |
T |
C |
7: 45,913,543 (GRCm39) |
V792A |
probably benign |
Het |
Paqr8 |
T |
C |
1: 21,005,442 (GRCm39) |
Y199H |
probably damaging |
Het |
Popdc3 |
A |
G |
10: 45,191,117 (GRCm39) |
D76G |
probably damaging |
Het |
Ppme1 |
T |
C |
7: 99,991,069 (GRCm39) |
N210D |
probably benign |
Het |
Prdm15 |
A |
C |
16: 97,636,842 (GRCm39) |
Y158* |
probably null |
Het |
Prrg2 |
A |
T |
7: 44,709,687 (GRCm39) |
L70Q |
probably benign |
Het |
Psmg4 |
C |
T |
13: 34,361,966 (GRCm39) |
R85W |
probably damaging |
Het |
Rab11fip4 |
A |
T |
11: 79,580,478 (GRCm39) |
T437S |
probably benign |
Het |
Rap2a |
T |
A |
14: 120,716,338 (GRCm39) |
M67K |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,946,208 (GRCm39) |
H322Q |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,990,801 (GRCm39) |
T521S |
possibly damaging |
Het |
Scrn2 |
T |
G |
11: 96,923,992 (GRCm39) |
V292G |
possibly damaging |
Het |
Serpina3n |
C |
A |
12: 104,377,656 (GRCm39) |
P303H |
probably benign |
Het |
Spop |
C |
T |
11: 95,376,727 (GRCm39) |
T260M |
probably damaging |
Het |
Surf2 |
G |
A |
2: 26,809,354 (GRCm39) |
G224D |
probably benign |
Het |
Synm |
T |
G |
7: 67,382,971 (GRCm39) |
N669T |
unknown |
Het |
Tmprss13 |
T |
C |
9: 45,239,721 (GRCm39) |
S10P |
unknown |
Het |
Trav9d-1 |
T |
A |
14: 53,029,970 (GRCm39) |
S25T |
probably benign |
Het |
Trpc3 |
A |
T |
3: 36,678,565 (GRCm39) |
I840K |
probably damaging |
Het |
Tsbp1 |
T |
A |
17: 34,636,539 (GRCm39) |
|
probably null |
Het |
Tssc4 |
C |
A |
7: 142,622,999 (GRCm39) |
|
probably benign |
Het |
Ttc39d |
G |
T |
17: 80,523,579 (GRCm39) |
R79S |
possibly damaging |
Het |
Txlnb |
T |
A |
10: 17,675,082 (GRCm39) |
S78R |
probably damaging |
Het |
Vmn1r142 |
T |
A |
7: 21,862,784 (GRCm39) |
Q226L |
possibly damaging |
Het |
Vmn1r230 |
T |
C |
17: 21,067,146 (GRCm39) |
S112P |
probably damaging |
Het |
Wrnip1 |
T |
C |
13: 33,000,360 (GRCm39) |
F456L |
possibly damaging |
Het |
Zc3h8 |
G |
T |
2: 128,775,215 (GRCm39) |
H148Q |
probably benign |
Het |
Zcchc3 |
A |
G |
2: 152,256,615 (GRCm39) |
V28A |
probably benign |
Het |
Zdbf2 |
T |
A |
1: 63,346,669 (GRCm39) |
C1683S |
probably benign |
Het |
Zfp874a |
T |
C |
13: 67,573,723 (GRCm39) |
|
probably null |
Het |
Zmym4 |
A |
G |
4: 126,776,029 (GRCm39) |
S1260P |
probably benign |
Het |
|
Other mutations in Mctp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01108:Mctp2
|
APN |
7 |
71,835,563 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01296:Mctp2
|
APN |
7 |
71,878,274 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01509:Mctp2
|
APN |
7 |
71,909,017 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02074:Mctp2
|
APN |
7 |
71,811,006 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02185:Mctp2
|
APN |
7 |
71,730,571 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02238:Mctp2
|
APN |
7 |
71,739,953 (GRCm39) |
nonsense |
probably null |
|
IGL02707:Mctp2
|
APN |
7 |
71,909,089 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02820:Mctp2
|
APN |
7 |
71,895,290 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02869:Mctp2
|
APN |
7 |
71,878,219 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03354:Mctp2
|
APN |
7 |
71,810,992 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03397:Mctp2
|
APN |
7 |
71,909,025 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03407:Mctp2
|
APN |
7 |
71,861,400 (GRCm39) |
missense |
probably benign |
0.05 |
trifecta
|
UTSW |
7 |
71,909,079 (GRCm39) |
missense |
possibly damaging |
0.63 |
triumvirate
|
UTSW |
7 |
71,861,438 (GRCm39) |
missense |
probably damaging |
1.00 |
troika
|
UTSW |
7 |
71,835,568 (GRCm39) |
missense |
probably damaging |
1.00 |
F5770:Mctp2
|
UTSW |
7 |
71,771,499 (GRCm39) |
splice site |
probably benign |
|
PIT4131001:Mctp2
|
UTSW |
7 |
71,740,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0013:Mctp2
|
UTSW |
7 |
71,879,156 (GRCm39) |
missense |
probably benign |
0.00 |
R0079:Mctp2
|
UTSW |
7 |
71,863,864 (GRCm39) |
splice site |
probably benign |
|
R0083:Mctp2
|
UTSW |
7 |
71,878,264 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0173:Mctp2
|
UTSW |
7 |
71,896,855 (GRCm39) |
critical splice donor site |
probably null |
|
R0302:Mctp2
|
UTSW |
7 |
71,740,012 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0533:Mctp2
|
UTSW |
7 |
71,730,570 (GRCm39) |
missense |
probably benign |
0.00 |
R0675:Mctp2
|
UTSW |
7 |
71,732,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1076:Mctp2
|
UTSW |
7 |
71,835,615 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1222:Mctp2
|
UTSW |
7 |
71,908,887 (GRCm39) |
missense |
probably benign |
|
R1356:Mctp2
|
UTSW |
7 |
71,814,471 (GRCm39) |
unclassified |
probably benign |
|
R1628:Mctp2
|
UTSW |
7 |
71,861,337 (GRCm39) |
splice site |
probably null |
|
R1649:Mctp2
|
UTSW |
7 |
71,811,006 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Mctp2
|
UTSW |
7 |
71,814,446 (GRCm39) |
missense |
probably benign |
0.01 |
R2256:Mctp2
|
UTSW |
7 |
71,835,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R2257:Mctp2
|
UTSW |
7 |
71,835,568 (GRCm39) |
missense |
probably damaging |
1.00 |
R2327:Mctp2
|
UTSW |
7 |
71,861,358 (GRCm39) |
missense |
probably damaging |
0.99 |
R2407:Mctp2
|
UTSW |
7 |
71,850,155 (GRCm39) |
missense |
probably benign |
0.40 |
R2471:Mctp2
|
UTSW |
7 |
71,810,909 (GRCm39) |
nonsense |
probably null |
|
R3706:Mctp2
|
UTSW |
7 |
71,863,859 (GRCm39) |
splice site |
probably benign |
|
R4023:Mctp2
|
UTSW |
7 |
71,739,987 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4025:Mctp2
|
UTSW |
7 |
71,739,987 (GRCm39) |
missense |
possibly damaging |
0.88 |
R4176:Mctp2
|
UTSW |
7 |
71,909,085 (GRCm39) |
missense |
probably benign |
|
R4272:Mctp2
|
UTSW |
7 |
71,909,079 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4498:Mctp2
|
UTSW |
7 |
71,833,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R4654:Mctp2
|
UTSW |
7 |
71,739,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R4815:Mctp2
|
UTSW |
7 |
71,909,097 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4946:Mctp2
|
UTSW |
7 |
71,909,017 (GRCm39) |
missense |
probably benign |
0.00 |
R5389:Mctp2
|
UTSW |
7 |
71,863,835 (GRCm39) |
missense |
possibly damaging |
0.50 |
R5682:Mctp2
|
UTSW |
7 |
71,895,207 (GRCm39) |
critical splice donor site |
probably null |
|
R5878:Mctp2
|
UTSW |
7 |
71,863,856 (GRCm39) |
missense |
probably benign |
0.01 |
R5918:Mctp2
|
UTSW |
7 |
71,878,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R5956:Mctp2
|
UTSW |
7 |
71,908,923 (GRCm39) |
missense |
probably benign |
|
R5964:Mctp2
|
UTSW |
7 |
71,752,925 (GRCm39) |
missense |
probably damaging |
0.97 |
R5978:Mctp2
|
UTSW |
7 |
71,739,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R6054:Mctp2
|
UTSW |
7 |
71,908,851 (GRCm39) |
missense |
probably benign |
|
R6475:Mctp2
|
UTSW |
7 |
71,850,092 (GRCm39) |
critical splice donor site |
probably null |
|
R6849:Mctp2
|
UTSW |
7 |
71,861,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R6963:Mctp2
|
UTSW |
7 |
71,877,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R7366:Mctp2
|
UTSW |
7 |
71,908,962 (GRCm39) |
missense |
probably benign |
0.00 |
R7746:Mctp2
|
UTSW |
7 |
71,835,544 (GRCm39) |
missense |
probably benign |
|
R7765:Mctp2
|
UTSW |
7 |
71,740,079 (GRCm39) |
splice site |
probably null |
|
R7822:Mctp2
|
UTSW |
7 |
71,776,935 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7984:Mctp2
|
UTSW |
7 |
71,752,937 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8416:Mctp2
|
UTSW |
7 |
71,852,210 (GRCm39) |
missense |
probably benign |
0.12 |
R8678:Mctp2
|
UTSW |
7 |
71,752,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R8819:Mctp2
|
UTSW |
7 |
71,879,081 (GRCm39) |
missense |
probably benign |
0.20 |
R8820:Mctp2
|
UTSW |
7 |
71,879,081 (GRCm39) |
missense |
probably benign |
0.20 |
R8835:Mctp2
|
UTSW |
7 |
71,852,161 (GRCm39) |
missense |
probably benign |
0.19 |
R8897:Mctp2
|
UTSW |
7 |
71,909,311 (GRCm39) |
start codon destroyed |
probably benign |
0.27 |
R8898:Mctp2
|
UTSW |
7 |
71,752,904 (GRCm39) |
missense |
probably damaging |
0.99 |
R9124:Mctp2
|
UTSW |
7 |
71,909,178 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Mctp2
|
UTSW |
7 |
71,909,028 (GRCm39) |
nonsense |
probably null |
|
Z1191:Mctp2
|
UTSW |
7 |
71,835,568 (GRCm39) |
missense |
probably damaging |
1.00 |
|