Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2200002J24Rik |
T |
G |
7: 30,399,368 (GRCm39) |
I54S |
probably damaging |
Het |
2310002L09Rik |
C |
T |
4: 73,861,172 (GRCm39) |
V143M |
probably benign |
Het |
Abca1 |
T |
C |
4: 53,042,367 (GRCm39) |
I1902V |
not run |
Het |
Apob |
A |
C |
12: 8,058,124 (GRCm39) |
D2202A |
probably damaging |
Het |
Arhgap44 |
T |
A |
11: 64,900,750 (GRCm39) |
S623C |
probably damaging |
Het |
Arhgef7 |
T |
A |
8: 11,874,507 (GRCm39) |
W713R |
possibly damaging |
Het |
Axdnd1 |
A |
C |
1: 156,166,313 (GRCm39) |
|
probably null |
Het |
Bcl9l |
C |
A |
9: 44,420,994 (GRCm39) |
H1467N |
probably damaging |
Het |
Bcl9l |
T |
C |
9: 44,420,263 (GRCm39) |
M1223T |
probably benign |
Het |
Bltp2 |
C |
T |
11: 78,164,031 (GRCm39) |
P1124L |
possibly damaging |
Het |
Brinp3 |
A |
G |
1: 146,622,306 (GRCm39) |
N236S |
probably benign |
Het |
Cckbr |
T |
G |
7: 105,082,798 (GRCm39) |
L54V |
probably benign |
Het |
Cd6 |
G |
A |
19: 10,775,722 (GRCm39) |
Q246* |
probably null |
Het |
Cep89 |
G |
A |
7: 35,129,353 (GRCm39) |
R630H |
probably damaging |
Het |
Ces3a |
T |
A |
8: 105,782,293 (GRCm39) |
|
probably null |
Het |
Cgnl1 |
T |
A |
9: 71,632,917 (GRCm39) |
N145Y |
probably damaging |
Het |
Col6a5 |
T |
C |
9: 105,775,934 (GRCm39) |
D1707G |
probably damaging |
Het |
Cyp2w1 |
A |
G |
5: 139,341,895 (GRCm39) |
T103A |
probably damaging |
Het |
Dip2a |
A |
T |
10: 76,114,417 (GRCm39) |
I1021N |
probably benign |
Het |
Dnah2 |
T |
C |
11: 69,386,040 (GRCm39) |
T981A |
probably benign |
Het |
Dnah8 |
A |
G |
17: 31,074,918 (GRCm39) |
I4546V |
probably benign |
Het |
E2f8 |
A |
C |
7: 48,527,823 (GRCm39) |
F106L |
probably benign |
Het |
Ecpas |
T |
C |
4: 58,853,150 (GRCm39) |
N395S |
probably damaging |
Het |
Eif4g1 |
G |
A |
16: 20,507,364 (GRCm39) |
V1413I |
probably benign |
Het |
Epha10 |
G |
A |
4: 124,808,246 (GRCm39) |
V688I |
probably benign |
Het |
Exoc2 |
A |
T |
13: 31,095,161 (GRCm39) |
V245D |
probably benign |
Het |
Eya4 |
T |
A |
10: 23,102,714 (GRCm39) |
E23D |
probably benign |
Het |
Fbxw10 |
T |
A |
11: 62,738,213 (GRCm39) |
W36R |
possibly damaging |
Het |
Gabbr1 |
G |
A |
17: 37,358,393 (GRCm39) |
G44S |
probably benign |
Het |
Gabrg3 |
T |
A |
7: 56,829,328 (GRCm39) |
Q143L |
probably benign |
Het |
Gm14412 |
A |
C |
2: 177,007,660 (GRCm39) |
I78M |
possibly damaging |
Het |
Gm7298 |
T |
C |
6: 121,737,563 (GRCm39) |
|
probably null |
Het |
Hpse2 |
A |
T |
19: 43,376,509 (GRCm39) |
L81Q |
probably damaging |
Het |
Il18r1 |
A |
G |
1: 40,510,924 (GRCm39) |
H3R |
probably benign |
Het |
Kansl1l |
T |
C |
1: 66,817,173 (GRCm39) |
K396E |
probably damaging |
Het |
Kbtbd3 |
T |
A |
9: 4,331,221 (GRCm39) |
S532T |
probably damaging |
Het |
Lrrtm4 |
T |
C |
6: 79,999,841 (GRCm39) |
Y418H |
probably damaging |
Het |
Mfng |
G |
A |
15: 78,657,265 (GRCm39) |
R70C |
probably damaging |
Het |
Mx2 |
T |
A |
16: 97,348,083 (GRCm39) |
I236K |
probably damaging |
Het |
Mysm1 |
T |
C |
4: 94,853,369 (GRCm39) |
Q410R |
probably damaging |
Het |
Nlrp12 |
T |
C |
7: 3,294,030 (GRCm39) |
N100S |
probably benign |
Het |
Nlrp4b |
T |
A |
7: 10,459,001 (GRCm39) |
H773Q |
probably benign |
Het |
Nlrp5 |
T |
A |
7: 23,123,343 (GRCm39) |
S735T |
possibly damaging |
Het |
Nt5c2 |
G |
A |
19: 46,880,020 (GRCm39) |
R363W |
probably benign |
Het |
Or12k8 |
A |
G |
2: 36,974,933 (GRCm39) |
F276L |
possibly damaging |
Het |
Or3a10 |
T |
A |
11: 73,935,614 (GRCm39) |
H162L |
possibly damaging |
Het |
Otud7b |
A |
T |
3: 96,062,528 (GRCm39) |
Y589F |
probably benign |
Het |
P2rx1 |
T |
A |
11: 72,900,079 (GRCm39) |
C165* |
probably null |
Het |
Pax8 |
T |
C |
2: 24,319,609 (GRCm39) |
D354G |
possibly damaging |
Het |
Pdcd11 |
G |
A |
19: 47,094,871 (GRCm39) |
V552I |
probably benign |
Het |
Pde6c |
G |
T |
19: 38,148,201 (GRCm39) |
C485F |
possibly damaging |
Het |
Pex5 |
T |
C |
6: 124,376,300 (GRCm39) |
Y434C |
probably benign |
Het |
Ppargc1a |
T |
C |
5: 51,619,851 (GRCm39) |
|
probably null |
Het |
Prss2 |
A |
T |
6: 41,501,886 (GRCm39) |
D224V |
possibly damaging |
Het |
Psd2 |
A |
G |
18: 36,136,032 (GRCm39) |
N440S |
probably benign |
Het |
Psmb3 |
T |
A |
11: 97,603,265 (GRCm39) |
D159E |
probably benign |
Het |
Ptgr2 |
T |
G |
12: 84,354,575 (GRCm39) |
L252R |
probably damaging |
Het |
Ptpro |
A |
T |
6: 137,393,818 (GRCm39) |
N829Y |
probably damaging |
Het |
Rhobtb2 |
C |
A |
14: 70,034,280 (GRCm39) |
R315L |
probably benign |
Het |
Rimbp2 |
A |
T |
5: 128,866,759 (GRCm39) |
V520D |
possibly damaging |
Het |
Schip1 |
A |
T |
3: 68,401,911 (GRCm39) |
Y24F |
probably benign |
Het |
Sdha |
A |
T |
13: 74,479,555 (GRCm39) |
V432E |
probably damaging |
Het |
Sez6 |
T |
C |
11: 77,868,426 (GRCm39) |
L929P |
probably damaging |
Het |
Shcbp1l |
A |
G |
1: 153,323,571 (GRCm39) |
I466V |
probably benign |
Het |
Skor1 |
T |
C |
9: 63,052,167 (GRCm39) |
S601G |
probably damaging |
Het |
Slc6a7 |
A |
C |
18: 61,138,851 (GRCm39) |
L219R |
probably damaging |
Het |
Smok2a |
T |
C |
17: 13,444,513 (GRCm39) |
M30T |
possibly damaging |
Het |
Sp8 |
A |
G |
12: 118,813,144 (GRCm39) |
D333G |
probably damaging |
Het |
Spp1 |
G |
A |
5: 104,588,200 (GRCm39) |
D201N |
probably damaging |
Het |
Sstr3 |
A |
T |
15: 78,424,588 (GRCm39) |
L53Q |
probably damaging |
Het |
Tacc2 |
T |
A |
7: 130,224,843 (GRCm39) |
N509K |
probably benign |
Het |
Tdrd1 |
T |
C |
19: 56,852,809 (GRCm39) |
V1030A |
probably damaging |
Het |
Tfrc |
A |
G |
16: 32,437,985 (GRCm39) |
K346R |
probably benign |
Het |
Tgm3 |
G |
A |
2: 129,854,330 (GRCm39) |
|
probably null |
Het |
Tomm5 |
C |
A |
4: 45,106,651 (GRCm39) |
L88F |
unknown |
Het |
Trak1 |
T |
A |
9: 121,245,264 (GRCm39) |
C46* |
probably null |
Het |
Trim8 |
A |
T |
19: 46,504,053 (GRCm39) |
D535V |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,665,995 (GRCm39) |
Y870* |
probably null |
Het |
Tspoap1 |
T |
C |
11: 87,655,136 (GRCm39) |
L286P |
probably benign |
Het |
Ttll3 |
AAGTA |
AAGTAGAGTA |
6: 113,376,120 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,562,389 (GRCm39) |
I28819F |
probably damaging |
Het |
Twf2 |
T |
C |
9: 106,089,079 (GRCm39) |
S89P |
probably damaging |
Het |
Ulk4 |
C |
T |
9: 121,092,734 (GRCm39) |
E168K |
possibly damaging |
Het |
Unc13b |
T |
A |
4: 43,172,737 (GRCm39) |
N1188K |
unknown |
Het |
Utp6 |
C |
T |
11: 79,828,556 (GRCm39) |
V528I |
probably benign |
Het |
Vmn1r78 |
T |
C |
7: 11,887,241 (GRCm39) |
F284S |
probably benign |
Het |
Vmn2r54 |
T |
A |
7: 12,366,196 (GRCm39) |
Q246L |
probably damaging |
Het |
Vmn2r87 |
A |
G |
10: 130,313,413 (GRCm39) |
M451T |
probably benign |
Het |
Vwf |
C |
T |
6: 125,663,483 (GRCm39) |
P2808L |
|
Het |
Wdr97 |
T |
C |
15: 76,243,307 (GRCm39) |
L989P |
|
Het |
Wwc1 |
T |
C |
11: 35,759,936 (GRCm39) |
Q693R |
probably benign |
Het |
Zfp582 |
C |
T |
7: 6,356,886 (GRCm39) |
S233L |
probably damaging |
Het |
Zfp658 |
T |
A |
7: 43,224,108 (GRCm39) |
H794Q |
possibly damaging |
Het |
|
Other mutations in Zfp882 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00676:Zfp882
|
APN |
8 |
72,667,671 (GRCm39) |
missense |
probably benign |
|
R0244:Zfp882
|
UTSW |
8 |
72,667,367 (GRCm39) |
missense |
possibly damaging |
0.79 |
R0270:Zfp882
|
UTSW |
8 |
72,668,459 (GRCm39) |
missense |
probably benign |
0.05 |
R0636:Zfp882
|
UTSW |
8 |
72,668,181 (GRCm39) |
missense |
probably benign |
0.01 |
R0840:Zfp882
|
UTSW |
8 |
72,668,530 (GRCm39) |
nonsense |
probably null |
|
R1299:Zfp882
|
UTSW |
8 |
72,667,317 (GRCm39) |
missense |
probably damaging |
1.00 |
R4439:Zfp882
|
UTSW |
8 |
72,667,453 (GRCm39) |
missense |
probably damaging |
0.97 |
R4829:Zfp882
|
UTSW |
8 |
72,668,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R5028:Zfp882
|
UTSW |
8 |
72,668,498 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5296:Zfp882
|
UTSW |
8 |
72,668,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R5882:Zfp882
|
UTSW |
8 |
72,667,303 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5974:Zfp882
|
UTSW |
8 |
72,666,999 (GRCm39) |
missense |
probably damaging |
1.00 |
R6052:Zfp882
|
UTSW |
8 |
72,668,349 (GRCm39) |
missense |
probably benign |
0.01 |
R6383:Zfp882
|
UTSW |
8 |
72,668,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R6888:Zfp882
|
UTSW |
8 |
72,668,130 (GRCm39) |
missense |
probably benign |
0.01 |
R6987:Zfp882
|
UTSW |
8 |
72,668,517 (GRCm39) |
missense |
probably benign |
0.01 |
R7045:Zfp882
|
UTSW |
8 |
72,667,093 (GRCm39) |
critical splice donor site |
probably null |
|
R7780:Zfp882
|
UTSW |
8 |
72,668,073 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8386:Zfp882
|
UTSW |
8 |
72,667,962 (GRCm39) |
missense |
probably benign |
0.00 |
R9452:Zfp882
|
UTSW |
8 |
72,668,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Zfp882
|
UTSW |
8 |
72,667,915 (GRCm39) |
missense |
probably benign |
0.01 |
|