Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
T |
C |
16: 20,152,479 (GRCm39) |
T1356A |
possibly damaging |
Het |
Ace3 |
A |
G |
11: 105,886,701 (GRCm39) |
T154A |
probably benign |
Het |
Arhgap31 |
C |
A |
16: 38,422,966 (GRCm39) |
Q1033H |
probably damaging |
Het |
C1qtnf1 |
C |
T |
11: 118,337,340 (GRCm39) |
R57* |
probably null |
Het |
Cacna1g |
T |
C |
11: 94,319,962 (GRCm39) |
T1405A |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,260,011 (GRCm39) |
|
probably benign |
Het |
Cdca4 |
T |
A |
12: 112,785,734 (GRCm39) |
|
probably null |
Het |
Cpa4 |
T |
A |
6: 30,585,158 (GRCm39) |
M314K |
probably damaging |
Het |
Crebbp |
A |
G |
16: 3,902,322 (GRCm39) |
S2306P |
probably damaging |
Het |
Cspg4b |
A |
G |
13: 113,488,163 (GRCm39) |
R9G |
|
Het |
Dcaf5 |
T |
C |
12: 80,385,807 (GRCm39) |
H773R |
probably benign |
Het |
Dcun1d2 |
A |
T |
8: 13,311,406 (GRCm39) |
D194E |
probably benign |
Het |
Dnah1 |
G |
T |
14: 30,989,767 (GRCm39) |
R3250S |
possibly damaging |
Het |
Dnajc25 |
A |
C |
4: 59,020,195 (GRCm39) |
K206T |
possibly damaging |
Het |
Dnajc27 |
T |
C |
12: 4,146,325 (GRCm39) |
L118P |
possibly damaging |
Het |
Etl4 |
C |
T |
2: 20,714,288 (GRCm39) |
T129I |
probably damaging |
Het |
Faap100 |
A |
G |
11: 120,263,003 (GRCm39) |
I785T |
probably damaging |
Het |
Fam227b |
A |
T |
2: 125,830,928 (GRCm39) |
D425E |
probably benign |
Het |
Fat4 |
C |
G |
3: 39,064,842 (GRCm39) |
L4933V |
probably damaging |
Het |
Fbrsl1 |
A |
G |
5: 110,526,086 (GRCm39) |
F39L |
probably damaging |
Het |
Fezf1 |
A |
G |
6: 23,247,769 (GRCm39) |
V102A |
probably benign |
Het |
Gabra2 |
T |
C |
5: 71,170,040 (GRCm39) |
|
probably benign |
Het |
Garnl3 |
C |
A |
2: 32,916,106 (GRCm39) |
R346L |
probably damaging |
Het |
Grin2a |
A |
T |
16: 9,403,089 (GRCm39) |
I799N |
possibly damaging |
Het |
Hspa4 |
A |
G |
11: 53,160,691 (GRCm39) |
F462L |
probably damaging |
Het |
Iars1 |
C |
A |
13: 49,856,675 (GRCm39) |
|
probably benign |
Het |
Igkv6-32 |
C |
T |
6: 70,051,063 (GRCm39) |
V98M |
possibly damaging |
Het |
Il31ra |
A |
G |
13: 112,662,372 (GRCm39) |
F560S |
possibly damaging |
Het |
Itpr3 |
G |
A |
17: 27,337,651 (GRCm39) |
|
probably benign |
Het |
Kif2a |
G |
A |
13: 107,116,049 (GRCm39) |
T299I |
probably damaging |
Het |
Leo1 |
T |
A |
9: 75,373,544 (GRCm39) |
Y656* |
probably null |
Het |
Lpcat2 |
T |
A |
8: 93,635,864 (GRCm39) |
V422D |
probably damaging |
Het |
Lrrcc1 |
T |
A |
3: 14,601,084 (GRCm39) |
S39T |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,405,869 (GRCm39) |
S341T |
probably benign |
Het |
Mc2r |
T |
A |
18: 68,540,879 (GRCm39) |
Y138F |
probably damaging |
Het |
Mepe |
A |
G |
5: 104,485,754 (GRCm39) |
N298S |
possibly damaging |
Het |
Mmp15 |
C |
A |
8: 96,092,982 (GRCm39) |
N120K |
possibly damaging |
Het |
Mrps9 |
A |
G |
1: 42,918,915 (GRCm39) |
R106G |
probably damaging |
Het |
Muc16 |
T |
A |
9: 18,557,744 (GRCm39) |
M2850L |
unknown |
Het |
Mxra8 |
T |
A |
4: 155,927,122 (GRCm39) |
I352N |
probably damaging |
Het |
Myo16 |
G |
A |
8: 10,411,042 (GRCm39) |
V167I |
unknown |
Het |
Neb |
T |
C |
2: 52,215,051 (GRCm39) |
D209G |
probably damaging |
Het |
Nlgn2 |
A |
G |
11: 69,716,309 (GRCm39) |
V744A |
probably benign |
Het |
Notch2 |
A |
G |
3: 98,029,218 (GRCm39) |
|
probably null |
Het |
Nr1d1 |
G |
C |
11: 98,660,073 (GRCm39) |
R484G |
probably damaging |
Het |
Or14c42-ps1 |
A |
T |
7: 86,211,147 (GRCm39) |
H69L |
unknown |
Het |
Or5ak20 |
T |
C |
2: 85,183,953 (GRCm39) |
T106A |
probably benign |
Het |
Or5k16 |
G |
A |
16: 58,736,843 (GRCm39) |
R54C |
probably benign |
Het |
Or9k2b |
T |
C |
10: 130,016,702 (GRCm39) |
I16V |
probably benign |
Het |
Oxa1l |
A |
G |
14: 54,605,248 (GRCm39) |
|
probably null |
Het |
Piwil4 |
T |
C |
9: 14,616,322 (GRCm39) |
D15G |
|
Het |
Plcz1 |
C |
A |
6: 139,949,612 (GRCm39) |
W461L |
probably damaging |
Het |
Plek |
A |
T |
11: 16,944,676 (GRCm39) |
I118N |
probably damaging |
Het |
Poc1b |
C |
A |
10: 99,000,728 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
T |
2: 111,059,567 (GRCm39) |
M64K |
possibly damaging |
Het |
Ppp1r16b |
G |
A |
2: 158,593,098 (GRCm39) |
D226N |
probably damaging |
Het |
Prss36 |
T |
C |
7: 127,532,635 (GRCm39) |
T739A |
possibly damaging |
Het |
Psme2 |
A |
T |
14: 55,827,074 (GRCm39) |
|
probably null |
Het |
Ptprb |
T |
G |
10: 116,203,495 (GRCm39) |
V1802G |
probably damaging |
Het |
Rabep2 |
C |
A |
7: 126,034,848 (GRCm39) |
Y84* |
probably null |
Het |
Rbbp6 |
T |
G |
7: 122,600,516 (GRCm39) |
S1508A |
unknown |
Het |
Rel |
A |
T |
11: 23,692,430 (GRCm39) |
D534E |
probably benign |
Het |
Rpgrip1 |
G |
A |
14: 52,396,852 (GRCm39) |
S1258N |
probably damaging |
Het |
Rprml |
T |
C |
11: 103,540,953 (GRCm39) |
L116P |
probably damaging |
Het |
Rsph10b |
A |
G |
5: 143,887,112 (GRCm39) |
T323A |
possibly damaging |
Het |
Rtn4rl1 |
A |
G |
11: 75,156,099 (GRCm39) |
H177R |
probably damaging |
Het |
Sag |
A |
G |
1: 87,738,032 (GRCm39) |
T24A |
probably benign |
Het |
Scgb2b26 |
G |
T |
7: 33,643,784 (GRCm39) |
T52N |
probably damaging |
Het |
Scn10a |
T |
C |
9: 119,501,194 (GRCm39) |
I197V |
probably damaging |
Het |
Sec24c |
T |
A |
14: 20,742,927 (GRCm39) |
V1003D |
possibly damaging |
Het |
Sirt2 |
G |
A |
7: 28,471,261 (GRCm39) |
G30E |
probably damaging |
Het |
Slc13a5 |
T |
A |
11: 72,149,919 (GRCm39) |
Q197L |
probably benign |
Het |
Slc44a3 |
A |
T |
3: 121,283,918 (GRCm39) |
S445T |
probably damaging |
Het |
Slc7a7 |
A |
T |
14: 54,610,449 (GRCm39) |
V399E |
probably benign |
Het |
Smarcad1 |
T |
A |
6: 65,088,865 (GRCm39) |
D1000E |
probably benign |
Het |
Sorcs2 |
G |
T |
5: 36,196,657 (GRCm39) |
Q663K |
probably benign |
Het |
Stat4 |
A |
G |
1: 52,118,991 (GRCm39) |
R345G |
probably null |
Het |
Sycp2 |
G |
A |
2: 177,992,768 (GRCm39) |
R1261C |
probably damaging |
Het |
Tcf19 |
T |
C |
17: 35,825,381 (GRCm39) |
I259V |
probably benign |
Het |
Thada |
T |
A |
17: 84,536,637 (GRCm39) |
R1636S |
probably benign |
Het |
Tnrc6c |
T |
C |
11: 117,604,961 (GRCm39) |
L32P |
probably benign |
Het |
Tonsl |
G |
A |
15: 76,517,076 (GRCm39) |
T881I |
probably benign |
Het |
Tonsl |
A |
C |
15: 76,518,263 (GRCm39) |
C570G |
probably damaging |
Het |
Ube2o |
C |
A |
11: 116,432,273 (GRCm39) |
E898* |
probably null |
Het |
Usp5 |
T |
C |
6: 124,794,394 (GRCm39) |
H762R |
possibly damaging |
Het |
Vmn2r15 |
A |
G |
5: 109,434,779 (GRCm39) |
S642P |
probably benign |
Het |
Vmn2r23 |
T |
C |
6: 123,690,431 (GRCm39) |
W436R |
probably damaging |
Het |
Vps13d |
A |
C |
4: 144,811,977 (GRCm39) |
I3343M |
|
Het |
Wbp11 |
T |
C |
6: 136,799,932 (GRCm39) |
K83E |
probably damaging |
Het |
Zfp26 |
T |
A |
9: 20,356,201 (GRCm39) |
N36Y |
possibly damaging |
Het |
Zfp57 |
T |
A |
17: 37,320,938 (GRCm39) |
I264N |
probably damaging |
Het |
|
Other mutations in Cpn2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00895:Cpn2
|
APN |
16 |
30,079,338 (GRCm39) |
missense |
probably benign |
0.42 |
IGL01954:Cpn2
|
APN |
16 |
30,079,138 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02458:Cpn2
|
APN |
16 |
30,079,653 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03036:Cpn2
|
APN |
16 |
30,079,647 (GRCm39) |
missense |
probably benign |
0.00 |
BB002:Cpn2
|
UTSW |
16 |
30,079,619 (GRCm39) |
missense |
probably damaging |
1.00 |
BB012:Cpn2
|
UTSW |
16 |
30,079,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0118:Cpn2
|
UTSW |
16 |
30,079,186 (GRCm39) |
missense |
probably benign |
0.04 |
R0541:Cpn2
|
UTSW |
16 |
30,078,169 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1300:Cpn2
|
UTSW |
16 |
30,078,481 (GRCm39) |
missense |
probably benign |
0.01 |
R1470:Cpn2
|
UTSW |
16 |
30,079,003 (GRCm39) |
missense |
probably benign |
0.00 |
R1470:Cpn2
|
UTSW |
16 |
30,079,003 (GRCm39) |
missense |
probably benign |
0.00 |
R1751:Cpn2
|
UTSW |
16 |
30,078,485 (GRCm39) |
nonsense |
probably null |
|
R1753:Cpn2
|
UTSW |
16 |
30,078,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R1761:Cpn2
|
UTSW |
16 |
30,079,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Cpn2
|
UTSW |
16 |
30,078,485 (GRCm39) |
nonsense |
probably null |
|
R1793:Cpn2
|
UTSW |
16 |
30,078,142 (GRCm39) |
missense |
probably damaging |
1.00 |
R2360:Cpn2
|
UTSW |
16 |
30,078,321 (GRCm39) |
missense |
probably benign |
0.01 |
R2414:Cpn2
|
UTSW |
16 |
30,079,392 (GRCm39) |
missense |
probably benign |
0.41 |
R3842:Cpn2
|
UTSW |
16 |
30,079,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R4934:Cpn2
|
UTSW |
16 |
30,079,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Cpn2
|
UTSW |
16 |
30,079,233 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5593:Cpn2
|
UTSW |
16 |
30,078,898 (GRCm39) |
missense |
probably benign |
0.02 |
R5864:Cpn2
|
UTSW |
16 |
30,078,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R6755:Cpn2
|
UTSW |
16 |
30,079,149 (GRCm39) |
missense |
probably damaging |
1.00 |
R7833:Cpn2
|
UTSW |
16 |
30,079,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R7925:Cpn2
|
UTSW |
16 |
30,079,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R8441:Cpn2
|
UTSW |
16 |
30,078,849 (GRCm39) |
missense |
probably damaging |
1.00 |
R8844:Cpn2
|
UTSW |
16 |
30,078,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R9406:Cpn2
|
UTSW |
16 |
30,078,360 (GRCm39) |
missense |
probably benign |
0.02 |
R9523:Cpn2
|
UTSW |
16 |
30,078,759 (GRCm39) |
missense |
possibly damaging |
0.89 |
RF021:Cpn2
|
UTSW |
16 |
30,078,156 (GRCm39) |
missense |
probably benign |
|
|