Other mutations in this stock |
Total: 98 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
A |
G |
1: 183,765,828 (GRCm39) |
V77A |
probably benign |
Het |
Actl7a |
G |
A |
4: 56,744,135 (GRCm39) |
V221M |
probably damaging |
Het |
Alkbh2 |
C |
T |
5: 114,262,287 (GRCm39) |
E148K |
probably damaging |
Het |
Arhgef10 |
C |
T |
8: 15,006,987 (GRCm39) |
|
probably benign |
Het |
Asgr2 |
T |
C |
11: 69,989,123 (GRCm39) |
L86P |
possibly damaging |
Het |
Atp12a |
A |
G |
14: 56,624,308 (GRCm39) |
R919G |
probably benign |
Het |
Atrn |
A |
G |
2: 130,836,971 (GRCm39) |
Y1145C |
probably damaging |
Het |
B3gnt5 |
T |
G |
16: 19,588,294 (GRCm39) |
L171R |
probably benign |
Het |
Bbof1 |
T |
A |
12: 84,457,859 (GRCm39) |
N41K |
possibly damaging |
Het |
Bdp1 |
A |
T |
13: 100,235,097 (GRCm39) |
W166R |
probably benign |
Het |
Bean1 |
A |
T |
8: 104,937,742 (GRCm39) |
H107L |
possibly damaging |
Het |
Brd4 |
T |
C |
17: 32,417,060 (GRCm39) |
|
probably benign |
Het |
Cadps |
T |
C |
14: 12,465,859 (GRCm38) |
K1017R |
possibly damaging |
Het |
Cep78 |
G |
A |
19: 15,951,715 (GRCm39) |
|
probably benign |
Het |
Cfap70 |
C |
T |
14: 20,445,020 (GRCm39) |
A1087T |
probably damaging |
Het |
Cideb |
A |
G |
14: 55,992,700 (GRCm39) |
V72A |
probably benign |
Het |
Cpz |
T |
C |
5: 35,675,012 (GRCm39) |
E79G |
probably damaging |
Het |
Crybg1 |
A |
G |
10: 43,873,544 (GRCm39) |
L1188P |
probably damaging |
Het |
Cuzd1 |
G |
A |
7: 130,911,425 (GRCm39) |
P518L |
probably benign |
Het |
Cyp2j5 |
A |
T |
4: 96,551,491 (GRCm39) |
N77K |
probably damaging |
Het |
Cyp4f39 |
T |
G |
17: 32,702,265 (GRCm39) |
F254C |
probably benign |
Het |
Dkk1 |
C |
A |
19: 30,524,731 (GRCm39) |
V225L |
probably damaging |
Het |
Dlg5 |
T |
C |
14: 24,226,639 (GRCm39) |
Y421C |
probably damaging |
Het |
Dnhd1 |
T |
C |
7: 105,362,614 (GRCm39) |
C3766R |
probably benign |
Het |
Dock9 |
G |
T |
14: 121,820,792 (GRCm39) |
S1534Y |
probably damaging |
Het |
Dst |
T |
C |
1: 34,200,110 (GRCm39) |
V96A |
probably damaging |
Het |
F2r |
A |
G |
13: 95,740,698 (GRCm39) |
F279S |
probably damaging |
Het |
Farp1 |
C |
A |
14: 121,492,908 (GRCm39) |
N503K |
probably benign |
Het |
Fbxw2 |
G |
A |
2: 34,712,776 (GRCm39) |
T95I |
probably damaging |
Het |
Fis1 |
A |
G |
5: 136,994,461 (GRCm39) |
T50A |
probably benign |
Het |
Frzb |
T |
G |
2: 80,276,772 (GRCm39) |
E138A |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,817,164 (GRCm39) |
D4299V |
probably benign |
Het |
Fyco1 |
C |
T |
9: 123,659,478 (GRCm39) |
D233N |
probably damaging |
Het |
Gmpr |
A |
G |
13: 45,667,997 (GRCm39) |
|
probably benign |
Het |
Hc |
C |
T |
2: 34,919,407 (GRCm39) |
|
probably benign |
Het |
Hnrnpa1 |
T |
C |
15: 103,150,699 (GRCm39) |
M186T |
possibly damaging |
Het |
Kl |
A |
G |
5: 150,906,132 (GRCm39) |
K501E |
probably benign |
Het |
Klhl42 |
A |
G |
6: 147,009,427 (GRCm39) |
N422S |
probably damaging |
Het |
Kmt2d |
C |
G |
15: 98,753,471 (GRCm39) |
K127N |
probably damaging |
Het |
Kmt2d |
T |
A |
15: 98,753,472 (GRCm39) |
K127M |
probably damaging |
Het |
Krt39 |
T |
A |
11: 99,405,461 (GRCm39) |
T480S |
probably benign |
Het |
Lims2 |
T |
A |
18: 32,088,395 (GRCm39) |
C198* |
probably null |
Het |
Mctp1 |
A |
G |
13: 76,532,729 (GRCm39) |
N26D |
possibly damaging |
Het |
Mdm4 |
A |
G |
1: 132,931,538 (GRCm39) |
S168P |
probably benign |
Het |
Myo3a |
A |
G |
2: 22,455,008 (GRCm39) |
Y71C |
probably benign |
Het |
Nlrp9c |
T |
A |
7: 26,084,319 (GRCm39) |
D420V |
probably damaging |
Het |
Ntf3 |
A |
T |
6: 126,079,485 (GRCm39) |
I7N |
possibly damaging |
Het |
Or10ag52 |
G |
A |
2: 87,043,721 (GRCm39) |
G162S |
probably benign |
Het |
Or13c25 |
G |
T |
4: 52,910,849 (GRCm39) |
T315K |
probably benign |
Het |
Or4c119 |
A |
G |
2: 88,986,925 (GRCm39) |
V198A |
probably benign |
Het |
Or8b38 |
T |
C |
9: 37,972,981 (GRCm39) |
Y122H |
probably damaging |
Het |
Papln |
C |
A |
12: 83,836,028 (GRCm39) |
Y1222* |
probably null |
Het |
Pgm3 |
T |
G |
9: 86,440,531 (GRCm39) |
I387L |
possibly damaging |
Het |
Pira12 |
G |
C |
7: 3,900,871 (GRCm39) |
P20R |
probably damaging |
Het |
Pkd1 |
C |
A |
17: 24,814,131 (GRCm39) |
P4167Q |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,854,947 (GRCm39) |
V1174E |
probably damaging |
Het |
Polr1b |
A |
G |
2: 128,943,031 (GRCm39) |
N9D |
probably benign |
Het |
Prkaa2 |
G |
A |
4: 104,893,950 (GRCm39) |
Q456* |
probably null |
Het |
Ptch2 |
G |
T |
4: 116,965,858 (GRCm39) |
V425L |
probably benign |
Het |
Ptprh |
A |
T |
7: 4,552,394 (GRCm39) |
S957T |
probably benign |
Het |
Riok1 |
A |
G |
13: 38,241,177 (GRCm39) |
D444G |
probably benign |
Het |
Rrbp1 |
A |
T |
2: 143,830,211 (GRCm39) |
V652E |
probably benign |
Het |
Rrp36 |
C |
T |
17: 46,983,671 (GRCm39) |
R47Q |
possibly damaging |
Het |
Sec24c |
T |
C |
14: 20,736,955 (GRCm39) |
S304P |
probably damaging |
Het |
Serpinb6b |
A |
T |
13: 33,158,991 (GRCm39) |
D64V |
possibly damaging |
Het |
Serpinb9b |
A |
T |
13: 33,223,531 (GRCm39) |
|
probably null |
Het |
Six6 |
T |
A |
12: 72,988,538 (GRCm39) |
I237N |
probably damaging |
Het |
Slc25a36 |
A |
T |
9: 96,975,135 (GRCm39) |
M127K |
probably benign |
Het |
Slc2a10 |
A |
G |
2: 165,356,550 (GRCm39) |
D70G |
probably damaging |
Het |
Slc2a3 |
T |
A |
6: 122,713,700 (GRCm39) |
I171F |
probably damaging |
Het |
Smc4 |
A |
G |
3: 68,940,401 (GRCm39) |
T1087A |
probably damaging |
Het |
Spg21 |
A |
G |
9: 65,391,779 (GRCm39) |
Y242C |
probably damaging |
Het |
St14 |
A |
G |
9: 31,001,166 (GRCm39) |
V855A |
possibly damaging |
Het |
Stx2 |
G |
A |
5: 129,065,903 (GRCm39) |
T251M |
probably damaging |
Het |
Svs3b |
A |
T |
2: 164,097,848 (GRCm39) |
S158T |
probably benign |
Het |
Synpo |
C |
T |
18: 60,736,661 (GRCm39) |
M428I |
probably benign |
Het |
Tasor2 |
A |
T |
13: 3,626,612 (GRCm39) |
Y1113N |
possibly damaging |
Het |
Tbc1d31 |
G |
A |
15: 57,775,760 (GRCm39) |
R17H |
probably damaging |
Het |
Tbl3 |
G |
A |
17: 24,923,477 (GRCm39) |
T284I |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,971,927 (GRCm39) |
T127A |
possibly damaging |
Het |
Tgoln1 |
T |
C |
6: 72,593,084 (GRCm39) |
E132G |
probably benign |
Het |
Timeless |
T |
C |
10: 128,077,583 (GRCm39) |
I221T |
probably damaging |
Het |
Tmem176b |
C |
T |
6: 48,815,138 (GRCm39) |
A52T |
possibly damaging |
Het |
Tmem192 |
C |
T |
8: 65,418,235 (GRCm39) |
L207F |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,176,996 (GRCm39) |
|
probably null |
Het |
Ttc7b |
C |
T |
12: 100,381,389 (GRCm39) |
|
probably null |
Het |
Tubb5 |
T |
C |
17: 36,146,190 (GRCm39) |
Y340C |
probably benign |
Het |
Ubr1 |
G |
A |
2: 120,761,449 (GRCm39) |
T576I |
probably benign |
Het |
Vcan |
T |
C |
13: 89,841,134 (GRCm39) |
E1470G |
probably damaging |
Het |
Vmn1r200 |
T |
A |
13: 22,579,663 (GRCm39) |
N146K |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,831,839 (GRCm39) |
I317F |
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,949,710 (GRCm39) |
I710T |
possibly damaging |
Het |
Wipf1 |
T |
A |
2: 73,270,499 (GRCm39) |
K61N |
probably benign |
Het |
Zfp112 |
T |
C |
7: 23,824,662 (GRCm39) |
V210A |
probably benign |
Het |
Zfp612 |
G |
A |
8: 110,815,095 (GRCm39) |
V101M |
probably benign |
Het |
Zfp637 |
A |
G |
6: 117,822,681 (GRCm39) |
R270G |
probably damaging |
Het |
Zfp652 |
A |
G |
11: 95,654,851 (GRCm39) |
E418G |
possibly damaging |
Het |
Zfp97 |
A |
G |
17: 17,365,265 (GRCm39) |
I255V |
probably benign |
Het |
|
Other mutations in Dll3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0024:Dll3
|
UTSW |
7 |
27,999,586 (GRCm39) |
splice site |
probably benign |
|
R0138:Dll3
|
UTSW |
7 |
28,000,746 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0322:Dll3
|
UTSW |
7 |
27,995,793 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0479:Dll3
|
UTSW |
7 |
28,000,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R1711:Dll3
|
UTSW |
7 |
27,993,922 (GRCm39) |
missense |
probably damaging |
0.98 |
R1742:Dll3
|
UTSW |
7 |
27,993,848 (GRCm39) |
missense |
probably benign |
0.37 |
R1854:Dll3
|
UTSW |
7 |
27,995,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R3037:Dll3
|
UTSW |
7 |
27,998,542 (GRCm39) |
missense |
probably damaging |
0.99 |
R3158:Dll3
|
UTSW |
7 |
27,993,520 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4306:Dll3
|
UTSW |
7 |
28,001,082 (GRCm39) |
splice site |
probably null |
|
R4424:Dll3
|
UTSW |
7 |
27,995,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Dll3
|
UTSW |
7 |
27,995,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Dll3
|
UTSW |
7 |
27,995,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R5604:Dll3
|
UTSW |
7 |
27,994,057 (GRCm39) |
missense |
probably benign |
|
R5770:Dll3
|
UTSW |
7 |
27,998,434 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5988:Dll3
|
UTSW |
7 |
27,993,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R7204:Dll3
|
UTSW |
7 |
27,998,330 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7347:Dll3
|
UTSW |
7 |
27,998,536 (GRCm39) |
missense |
probably damaging |
0.99 |
R7373:Dll3
|
UTSW |
7 |
27,994,057 (GRCm39) |
missense |
probably benign |
|
R7694:Dll3
|
UTSW |
7 |
28,001,170 (GRCm39) |
start codon destroyed |
probably null |
0.83 |
R7829:Dll3
|
UTSW |
7 |
27,994,075 (GRCm39) |
missense |
probably damaging |
0.99 |
R7905:Dll3
|
UTSW |
7 |
28,000,960 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8681:Dll3
|
UTSW |
7 |
27,994,270 (GRCm39) |
missense |
probably damaging |
0.99 |
R8988:Dll3
|
UTSW |
7 |
27,995,793 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9519:Dll3
|
UTSW |
7 |
27,995,764 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Dll3
|
UTSW |
7 |
28,000,808 (GRCm39) |
missense |
probably damaging |
0.99 |
|