Other mutations in this stock |
Total: 76 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2900026A02Rik |
T |
C |
5: 113,332,567 (GRCm39) |
D549G |
probably benign |
Het |
Aamdc |
A |
G |
7: 97,199,902 (GRCm39) |
V120A |
probably benign |
Het |
Acp2 |
A |
T |
2: 91,037,174 (GRCm39) |
Q251L |
probably benign |
Het |
AI597479 |
C |
T |
1: 43,150,505 (GRCm39) |
A205V |
possibly damaging |
Het |
Apob |
A |
G |
12: 8,029,261 (GRCm39) |
T44A |
possibly damaging |
Het |
Arhgap18 |
G |
A |
10: 26,648,610 (GRCm39) |
V11M |
probably damaging |
Het |
Arhgef10l |
T |
G |
4: 140,319,265 (GRCm39) |
H156P |
probably benign |
Het |
Aste1 |
G |
A |
9: 105,273,880 (GRCm39) |
C40Y |
probably benign |
Het |
Ccn2 |
A |
T |
10: 24,473,501 (GRCm39) |
M347L |
possibly damaging |
Het |
Chd9 |
G |
A |
8: 91,725,335 (GRCm39) |
|
probably null |
Het |
Clec4n |
T |
A |
6: 123,207,662 (GRCm39) |
F42L |
probably benign |
Het |
Cngb1 |
T |
C |
8: 96,026,350 (GRCm39) |
K144E |
unknown |
Het |
Cyp4f17 |
A |
G |
17: 32,747,746 (GRCm39) |
T485A |
probably damaging |
Het |
Defa30 |
C |
T |
8: 21,624,686 (GRCm39) |
T3I |
probably damaging |
Het |
Dmxl1 |
T |
A |
18: 50,091,477 (GRCm39) |
W2854R |
probably damaging |
Het |
Dnah11 |
G |
A |
12: 117,884,703 (GRCm39) |
T3783I |
possibly damaging |
Het |
Dync1i1 |
T |
A |
6: 5,913,443 (GRCm39) |
F225L |
possibly damaging |
Het |
Elp6 |
T |
A |
9: 110,144,852 (GRCm39) |
Y119* |
probably null |
Het |
Enpep |
A |
T |
3: 129,125,529 (GRCm39) |
M201K |
probably benign |
Het |
Fam161a |
A |
T |
11: 22,970,661 (GRCm39) |
R280W |
probably damaging |
Het |
Fam98a |
T |
C |
17: 75,848,330 (GRCm39) |
N128S |
possibly damaging |
Het |
Fpgt |
A |
T |
3: 154,792,934 (GRCm39) |
D364E |
probably benign |
Het |
G3bp1 |
T |
A |
11: 55,390,439 (GRCm39) |
M448K |
probably damaging |
Het |
Gadd45b |
T |
C |
10: 80,766,284 (GRCm39) |
M16T |
probably benign |
Het |
Gdi2 |
A |
T |
13: 3,614,869 (GRCm39) |
I383F |
probably benign |
Het |
H2-T13 |
T |
C |
17: 36,391,993 (GRCm39) |
T27A |
possibly damaging |
Het |
Igtp |
T |
G |
11: 58,097,026 (GRCm39) |
L66V |
probably damaging |
Het |
Kcne4 |
G |
A |
1: 78,795,623 (GRCm39) |
M90I |
probably benign |
Het |
Lmo7 |
T |
A |
14: 102,136,123 (GRCm39) |
M732K |
probably damaging |
Het |
Ltbp2 |
G |
A |
12: 84,837,864 (GRCm39) |
P1192L |
probably benign |
Het |
Mast4 |
T |
G |
13: 102,917,753 (GRCm39) |
S552R |
probably damaging |
Het |
Meak7 |
G |
A |
8: 120,498,096 (GRCm39) |
A136V |
probably benign |
Het |
Mff |
A |
T |
1: 82,707,007 (GRCm39) |
M11L |
probably benign |
Het |
Mterf2 |
T |
C |
10: 84,956,327 (GRCm39) |
E99G |
probably damaging |
Het |
Myef2l |
T |
C |
3: 10,153,791 (GRCm39) |
S187P |
probably benign |
Het |
Myom2 |
T |
A |
8: 15,149,210 (GRCm39) |
N560K |
probably damaging |
Het |
Nab2 |
A |
G |
10: 127,500,580 (GRCm39) |
S171P |
probably damaging |
Het |
Nhlrc3 |
T |
C |
3: 53,369,190 (GRCm39) |
N83S |
possibly damaging |
Het |
Nod2 |
A |
T |
8: 89,391,033 (GRCm39) |
I447F |
probably damaging |
Het |
Npat |
T |
A |
9: 53,474,456 (GRCm39) |
D749E |
possibly damaging |
Het |
Nxph4 |
A |
G |
10: 127,362,631 (GRCm39) |
S87P |
probably benign |
Het |
Or2y1f |
T |
A |
11: 49,184,902 (GRCm39) |
Y251* |
probably null |
Het |
Or51i2 |
G |
T |
7: 103,689,273 (GRCm39) |
R90L |
possibly damaging |
Het |
Or5d47 |
G |
A |
2: 87,804,526 (GRCm39) |
T161M |
possibly damaging |
Het |
Or6c6 |
T |
A |
10: 129,186,989 (GRCm39) |
S186T |
probably damaging |
Het |
Or9q2 |
T |
A |
19: 13,772,214 (GRCm39) |
T254S |
probably damaging |
Het |
Pcdha3 |
G |
A |
18: 37,079,353 (GRCm39) |
V32I |
probably benign |
Het |
Pcdhgc3 |
A |
T |
18: 37,939,691 (GRCm39) |
T31S |
probably benign |
Het |
Phldb3 |
A |
G |
7: 24,323,297 (GRCm39) |
R391G |
probably damaging |
Het |
Piezo1 |
A |
G |
8: 123,228,604 (GRCm39) |
V257A |
|
Het |
Pip5k1b |
T |
A |
19: 24,416,442 (GRCm39) |
Q15L |
probably benign |
Het |
Plxnc1 |
T |
C |
10: 94,649,093 (GRCm39) |
N1229D |
probably benign |
Het |
Ptpn12 |
A |
G |
5: 21,224,212 (GRCm39) |
V127A |
probably benign |
Het |
Ptprr |
T |
A |
10: 116,109,724 (GRCm39) |
V655D |
probably benign |
Het |
Rbbp8 |
A |
G |
18: 11,838,888 (GRCm39) |
T190A |
probably benign |
Het |
Rnf17 |
T |
A |
14: 56,719,579 (GRCm39) |
V943E |
probably damaging |
Het |
Rnpc3 |
C |
T |
3: 113,404,913 (GRCm39) |
G414D |
probably damaging |
Het |
Robo4 |
T |
A |
9: 37,316,158 (GRCm39) |
N387K |
probably damaging |
Het |
Sall4 |
G |
A |
2: 168,597,781 (GRCm39) |
T353M |
probably damaging |
Het |
Serpinb13 |
T |
C |
1: 106,909,997 (GRCm39) |
I38T |
probably damaging |
Het |
Sgsm1 |
A |
T |
5: 113,422,139 (GRCm39) |
I218N |
unknown |
Het |
Sntg2 |
T |
A |
12: 30,293,343 (GRCm39) |
|
probably null |
Het |
Taf1c |
G |
A |
8: 120,325,393 (GRCm39) |
S823F |
probably damaging |
Het |
Timd6 |
T |
A |
11: 46,468,246 (GRCm39) |
C107S |
probably damaging |
Het |
Trhde |
T |
G |
10: 114,244,598 (GRCm39) |
I963L |
probably damaging |
Het |
Trim43b |
T |
C |
9: 88,967,619 (GRCm39) |
Y339C |
probably damaging |
Het |
Trp53 |
T |
A |
11: 69,480,537 (GRCm39) |
|
probably null |
Het |
Tubg2 |
T |
C |
11: 101,051,621 (GRCm39) |
V282A |
probably benign |
Het |
Ube2g1 |
C |
T |
11: 72,553,943 (GRCm39) |
|
probably benign |
Het |
Usp34 |
C |
A |
11: 23,437,203 (GRCm39) |
A3341E |
|
Het |
Vmn2r12 |
T |
A |
5: 109,233,986 (GRCm39) |
H742L |
probably damaging |
Het |
Vmn2r24 |
T |
C |
6: 123,792,542 (GRCm39) |
V623A |
probably damaging |
Het |
Vmn2r5 |
A |
T |
3: 64,411,316 (GRCm39) |
D417E |
probably damaging |
Het |
Vmn2r-ps158 |
C |
T |
7: 42,673,499 (GRCm39) |
P193S |
possibly damaging |
Het |
Xirp2 |
A |
T |
2: 67,342,118 (GRCm39) |
D1453V |
probably damaging |
Het |
Zfp2 |
T |
C |
11: 50,791,042 (GRCm39) |
S334G |
probably damaging |
Het |
|
Other mutations in Dcaf6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00828:Dcaf6
|
APN |
1 |
165,165,916 (GRCm39) |
splice site |
probably benign |
|
IGL01377:Dcaf6
|
APN |
1 |
165,216,293 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02027:Dcaf6
|
APN |
1 |
165,251,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02390:Dcaf6
|
APN |
1 |
165,250,490 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL02754:Dcaf6
|
APN |
1 |
165,165,915 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL02900:Dcaf6
|
APN |
1 |
165,227,344 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03119:Dcaf6
|
APN |
1 |
165,167,545 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03211:Dcaf6
|
APN |
1 |
165,250,502 (GRCm39) |
missense |
possibly damaging |
0.55 |
R0588:Dcaf6
|
UTSW |
1 |
165,247,792 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1494:Dcaf6
|
UTSW |
1 |
165,160,942 (GRCm39) |
missense |
probably damaging |
0.99 |
R1512:Dcaf6
|
UTSW |
1 |
165,179,589 (GRCm39) |
missense |
probably benign |
0.22 |
R1840:Dcaf6
|
UTSW |
1 |
165,227,317 (GRCm39) |
missense |
probably damaging |
0.96 |
R2191:Dcaf6
|
UTSW |
1 |
165,250,433 (GRCm39) |
missense |
probably benign |
0.07 |
R2297:Dcaf6
|
UTSW |
1 |
165,227,431 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Dcaf6
|
UTSW |
1 |
165,250,421 (GRCm39) |
splice site |
probably benign |
|
R3861:Dcaf6
|
UTSW |
1 |
165,256,838 (GRCm39) |
missense |
probably damaging |
1.00 |
R3907:Dcaf6
|
UTSW |
1 |
165,251,949 (GRCm39) |
nonsense |
probably null |
|
R4521:Dcaf6
|
UTSW |
1 |
165,218,059 (GRCm39) |
missense |
probably damaging |
0.98 |
R4531:Dcaf6
|
UTSW |
1 |
165,239,036 (GRCm39) |
missense |
probably damaging |
1.00 |
R4906:Dcaf6
|
UTSW |
1 |
165,239,032 (GRCm39) |
critical splice donor site |
probably null |
|
R4916:Dcaf6
|
UTSW |
1 |
165,247,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R4956:Dcaf6
|
UTSW |
1 |
165,216,354 (GRCm39) |
missense |
probably benign |
0.00 |
R5080:Dcaf6
|
UTSW |
1 |
165,247,690 (GRCm39) |
missense |
probably damaging |
1.00 |
R5091:Dcaf6
|
UTSW |
1 |
165,157,572 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5277:Dcaf6
|
UTSW |
1 |
165,251,915 (GRCm39) |
missense |
probably benign |
0.09 |
R5512:Dcaf6
|
UTSW |
1 |
165,227,404 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5914:Dcaf6
|
UTSW |
1 |
165,178,724 (GRCm39) |
missense |
probably benign |
|
R6004:Dcaf6
|
UTSW |
1 |
165,216,254 (GRCm39) |
missense |
probably benign |
0.00 |
R6239:Dcaf6
|
UTSW |
1 |
165,178,839 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6736:Dcaf6
|
UTSW |
1 |
165,227,354 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7051:Dcaf6
|
UTSW |
1 |
165,251,886 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7110:Dcaf6
|
UTSW |
1 |
165,179,537 (GRCm39) |
missense |
probably benign |
0.22 |
R7583:Dcaf6
|
UTSW |
1 |
165,160,879 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Dcaf6
|
UTSW |
1 |
165,179,623 (GRCm39) |
nonsense |
probably null |
|
R7790:Dcaf6
|
UTSW |
1 |
165,227,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R8369:Dcaf6
|
UTSW |
1 |
165,185,043 (GRCm39) |
missense |
probably damaging |
1.00 |
R8411:Dcaf6
|
UTSW |
1 |
165,216,244 (GRCm39) |
missense |
probably benign |
0.03 |
R9061:Dcaf6
|
UTSW |
1 |
165,164,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R9307:Dcaf6
|
UTSW |
1 |
165,227,236 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9626:Dcaf6
|
UTSW |
1 |
165,227,264 (GRCm39) |
nonsense |
probably null |
|
|