Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahdc1 |
T |
A |
4: 132,792,707 (GRCm39) |
M1316K |
probably benign |
Het |
Alkal1 |
A |
G |
1: 6,459,712 (GRCm39) |
Y96C |
probably damaging |
Het |
Anxa2r1 |
A |
T |
13: 120,496,667 (GRCm39) |
N67K |
probably benign |
Het |
Arhgap17 |
T |
C |
7: 122,913,913 (GRCm39) |
Y199C |
probably damaging |
Het |
Bmp2 |
T |
C |
2: 133,403,388 (GRCm39) |
V313A |
probably damaging |
Het |
Cacna1b |
C |
T |
2: 24,577,757 (GRCm39) |
|
probably null |
Het |
Cars1 |
T |
C |
7: 143,140,876 (GRCm39) |
T141A |
probably damaging |
Het |
Ccdc57 |
A |
G |
11: 120,764,637 (GRCm39) |
|
probably benign |
Het |
Cenpe |
T |
C |
3: 134,970,183 (GRCm39) |
|
probably null |
Het |
Chadl |
T |
C |
15: 81,577,258 (GRCm39) |
S198G |
probably benign |
Het |
Chd6 |
G |
C |
2: 160,872,722 (GRCm39) |
P286R |
probably damaging |
Het |
Clec4a4 |
G |
T |
6: 122,989,671 (GRCm39) |
W104L |
probably benign |
Het |
Coq4 |
G |
A |
2: 29,678,346 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
G |
T |
15: 8,245,971 (GRCm39) |
V1448L |
probably benign |
Het |
Crtc2 |
T |
A |
3: 90,169,940 (GRCm39) |
Y445* |
probably null |
Het |
Dapk1 |
A |
T |
13: 60,844,112 (GRCm39) |
I44F |
probably damaging |
Het |
Dcbld2 |
T |
A |
16: 58,270,204 (GRCm39) |
|
probably null |
Het |
Dcun1d4 |
T |
C |
5: 73,668,455 (GRCm39) |
|
probably benign |
Het |
Depdc7 |
A |
T |
2: 104,560,523 (GRCm39) |
|
probably benign |
Het |
Dna2 |
A |
G |
10: 62,794,977 (GRCm39) |
D416G |
probably benign |
Het |
Dnah2 |
A |
T |
11: 69,390,016 (GRCm39) |
I743N |
probably damaging |
Het |
Dnah9 |
A |
G |
11: 65,975,438 (GRCm39) |
|
probably null |
Het |
Dock3 |
A |
G |
9: 106,846,999 (GRCm39) |
S877P |
probably damaging |
Het |
Eif3l |
T |
A |
15: 78,959,966 (GRCm39) |
|
probably null |
Het |
Epha5 |
A |
T |
5: 84,219,134 (GRCm39) |
|
probably null |
Het |
Ffar3 |
T |
A |
7: 30,554,529 (GRCm39) |
N264Y |
probably damaging |
Het |
Fyb1 |
A |
T |
15: 6,668,381 (GRCm39) |
I525F |
probably damaging |
Het |
Fyco1 |
A |
G |
9: 123,648,218 (GRCm39) |
F1239L |
probably damaging |
Het |
Gcdh |
T |
C |
8: 85,620,071 (GRCm39) |
|
probably benign |
Het |
Gk5 |
T |
C |
9: 96,032,473 (GRCm39) |
|
probably benign |
Het |
Grm1 |
A |
G |
10: 10,595,778 (GRCm39) |
Y617H |
probably benign |
Het |
Gvin-ps3 |
A |
G |
7: 105,683,159 (GRCm39) |
V32A |
probably benign |
Het |
Hhipl2 |
A |
T |
1: 183,206,042 (GRCm39) |
I131L |
probably damaging |
Het |
Larp4b |
T |
C |
13: 9,216,345 (GRCm39) |
|
probably benign |
Het |
Lrig2 |
T |
A |
3: 104,398,227 (GRCm39) |
I301F |
possibly damaging |
Het |
Man2a2 |
A |
T |
7: 80,012,713 (GRCm39) |
I600N |
possibly damaging |
Het |
Mylk2 |
G |
C |
2: 152,755,661 (GRCm39) |
|
probably null |
Het |
Myo6 |
C |
T |
9: 80,193,664 (GRCm39) |
Q870* |
probably null |
Het |
Napg |
T |
G |
18: 63,127,409 (GRCm39) |
H204Q |
probably benign |
Het |
Neb |
G |
A |
2: 52,153,959 (GRCm39) |
T2384M |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,931,325 (GRCm38) |
|
probably benign |
Het |
Or11h23 |
A |
C |
14: 50,948,071 (GRCm39) |
T95P |
probably benign |
Het |
Or4c111 |
A |
G |
2: 88,844,057 (GRCm39) |
M117T |
probably damaging |
Het |
Or5an6 |
T |
C |
19: 12,372,221 (GRCm39) |
V198A |
probably benign |
Het |
Or5b108 |
T |
G |
19: 13,168,739 (GRCm39) |
L236R |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,572,276 (GRCm39) |
T554A |
unknown |
Het |
Perm1 |
C |
A |
4: 156,301,771 (GRCm39) |
T105K |
probably damaging |
Het |
Pik3r1 |
T |
C |
13: 101,822,866 (GRCm39) |
|
probably null |
Het |
Pld5 |
A |
G |
1: 175,872,462 (GRCm39) |
I225T |
probably damaging |
Het |
Plxnc1 |
T |
C |
10: 94,667,195 (GRCm39) |
|
probably benign |
Het |
Ptpn12 |
A |
C |
5: 21,203,354 (GRCm39) |
S475A |
possibly damaging |
Het |
Ptprt |
A |
G |
2: 161,769,692 (GRCm39) |
V391A |
possibly damaging |
Het |
Rac2 |
T |
G |
15: 78,450,145 (GRCm39) |
D65A |
possibly damaging |
Het |
Rgl3 |
A |
G |
9: 21,888,676 (GRCm39) |
|
probably null |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Sebox |
A |
T |
11: 78,394,675 (GRCm39) |
T47S |
probably damaging |
Het |
Sema4b |
A |
G |
7: 79,874,388 (GRCm39) |
T593A |
probably benign |
Het |
Serpina3a |
C |
T |
12: 104,082,787 (GRCm39) |
Q187* |
probably null |
Het |
Serpinb1a |
T |
C |
13: 33,027,199 (GRCm39) |
K248E |
probably benign |
Het |
Serpinb9e |
A |
C |
13: 33,443,757 (GRCm39) |
E259A |
probably benign |
Het |
Slc30a3 |
T |
A |
5: 31,247,510 (GRCm39) |
H44L |
probably damaging |
Het |
Smarca2 |
T |
C |
19: 26,748,333 (GRCm39) |
|
probably benign |
Het |
Snrnp200 |
T |
A |
2: 127,078,737 (GRCm39) |
C1801S |
probably damaging |
Het |
Soat1 |
G |
A |
1: 156,269,944 (GRCm39) |
|
probably null |
Het |
Spink6 |
T |
C |
18: 44,204,605 (GRCm39) |
|
probably benign |
Het |
Spta1 |
G |
A |
1: 174,012,256 (GRCm39) |
R354H |
probably damaging |
Het |
Tbck |
T |
A |
3: 132,543,733 (GRCm39) |
H861Q |
probably benign |
Het |
Tgfbrap1 |
G |
A |
1: 43,088,856 (GRCm39) |
T849M |
possibly damaging |
Het |
Tnrc6a |
A |
G |
7: 122,769,563 (GRCm39) |
N451S |
possibly damaging |
Het |
Trim36 |
T |
C |
18: 46,329,318 (GRCm39) |
T41A |
probably damaging |
Het |
Trmt112 |
C |
A |
19: 6,887,721 (GRCm39) |
|
probably benign |
Het |
Trpc4ap |
A |
G |
2: 155,486,990 (GRCm39) |
|
probably benign |
Het |
Ttll7 |
C |
T |
3: 146,645,746 (GRCm39) |
P535S |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,691,776 (GRCm39) |
|
probably benign |
Het |
Txndc11 |
C |
T |
16: 10,946,364 (GRCm39) |
R149Q |
probably benign |
Het |
Ubr4 |
C |
T |
4: 139,164,509 (GRCm39) |
|
probably benign |
Het |
Usp30 |
G |
A |
5: 114,241,888 (GRCm39) |
|
probably null |
Het |
Vmn1r195 |
A |
G |
13: 22,463,181 (GRCm39) |
Y217C |
probably damaging |
Het |
Vps33b |
T |
A |
7: 79,932,234 (GRCm39) |
D135E |
probably benign |
Het |
Vrk2 |
A |
G |
11: 26,433,331 (GRCm39) |
|
probably benign |
Het |
Wdr81 |
G |
T |
11: 75,343,809 (GRCm39) |
P486Q |
probably damaging |
Het |
Zfp788 |
T |
C |
7: 41,297,750 (GRCm39) |
Y129H |
probably damaging |
Het |
|
Other mutations in 1700003E16Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01087:1700003E16Rik
|
APN |
6 |
83,139,770 (GRCm39) |
splice site |
probably null |
|
IGL02616:1700003E16Rik
|
APN |
6 |
83,138,644 (GRCm39) |
missense |
probably benign |
|
IGL03171:1700003E16Rik
|
APN |
6 |
83,139,377 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL03196:1700003E16Rik
|
APN |
6 |
83,138,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R0124:1700003E16Rik
|
UTSW |
6 |
83,138,656 (GRCm39) |
missense |
probably benign |
|
R1081:1700003E16Rik
|
UTSW |
6 |
83,139,002 (GRCm39) |
missense |
probably benign |
|
R1522:1700003E16Rik
|
UTSW |
6 |
83,139,568 (GRCm39) |
missense |
probably damaging |
0.96 |
R4361:1700003E16Rik
|
UTSW |
6 |
83,139,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R4688:1700003E16Rik
|
UTSW |
6 |
83,139,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R5326:1700003E16Rik
|
UTSW |
6 |
83,138,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R6007:1700003E16Rik
|
UTSW |
6 |
83,137,900 (GRCm39) |
missense |
possibly damaging |
0.80 |
R7212:1700003E16Rik
|
UTSW |
6 |
83,138,654 (GRCm39) |
missense |
probably benign |
0.00 |
R7343:1700003E16Rik
|
UTSW |
6 |
83,139,353 (GRCm39) |
missense |
probably benign |
0.12 |
R8081:1700003E16Rik
|
UTSW |
6 |
83,138,313 (GRCm39) |
missense |
probably damaging |
1.00 |
R8121:1700003E16Rik
|
UTSW |
6 |
83,138,893 (GRCm39) |
missense |
probably benign |
|
R9188:1700003E16Rik
|
UTSW |
6 |
83,139,230 (GRCm39) |
missense |
probably benign |
0.12 |
R9329:1700003E16Rik
|
UTSW |
6 |
83,133,556 (GRCm39) |
start codon destroyed |
probably null |
0.55 |
Z1176:1700003E16Rik
|
UTSW |
6 |
83,138,097 (GRCm39) |
missense |
probably damaging |
1.00 |
|