Other mutations in this stock |
Total: 99 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy3 |
G |
A |
12: 4,248,434 (GRCm39) |
V499M |
possibly damaging |
Het |
Aff4 |
T |
C |
11: 53,295,184 (GRCm39) |
S795P |
probably damaging |
Het |
Ank |
G |
A |
15: 27,562,819 (GRCm39) |
V176I |
probably damaging |
Het |
Ankfn1 |
A |
G |
11: 89,332,268 (GRCm39) |
I446T |
possibly damaging |
Het |
Arhgap33 |
C |
A |
7: 30,232,441 (GRCm39) |
S32I |
possibly damaging |
Het |
Ascc3 |
T |
A |
10: 50,699,744 (GRCm39) |
Y1856N |
probably damaging |
Het |
Atf3 |
T |
C |
1: 190,909,472 (GRCm39) |
T66A |
probably benign |
Het |
Atf7ip |
T |
C |
6: 136,538,386 (GRCm39) |
C548R |
probably damaging |
Het |
Bag6 |
A |
G |
17: 35,364,152 (GRCm39) |
T841A |
probably damaging |
Het |
Bbof1 |
A |
T |
12: 84,473,630 (GRCm39) |
Q320L |
possibly damaging |
Het |
Bmp2k |
A |
T |
5: 97,201,001 (GRCm39) |
Q307L |
probably damaging |
Het |
Btaf1 |
T |
A |
19: 36,964,052 (GRCm39) |
N874K |
possibly damaging |
Het |
Calr4 |
G |
A |
4: 109,096,179 (GRCm39) |
|
probably null |
Het |
Camk1d |
T |
C |
2: 5,317,912 (GRCm39) |
I248V |
possibly damaging |
Het |
Ccdc177 |
G |
A |
12: 80,804,160 (GRCm39) |
R705C |
unknown |
Het |
Cdk18 |
C |
T |
1: 132,046,587 (GRCm39) |
|
probably null |
Het |
Cers4 |
A |
G |
8: 4,565,565 (GRCm39) |
S4G |
probably benign |
Het |
Cfap54 |
A |
G |
10: 92,800,396 (GRCm39) |
V1604A |
probably benign |
Het |
Chd8 |
C |
T |
14: 52,441,372 (GRCm39) |
G907S |
probably benign |
Het |
Cilk1 |
T |
C |
9: 78,038,801 (GRCm39) |
S17P |
probably damaging |
Het |
Cnksr3 |
G |
A |
10: 7,076,746 (GRCm39) |
Q149* |
probably null |
Het |
Cntd1 |
T |
C |
11: 101,176,557 (GRCm39) |
V218A |
possibly damaging |
Het |
Cog7 |
A |
T |
7: 121,549,109 (GRCm39) |
V384E |
probably damaging |
Het |
Col5a2 |
A |
G |
1: 45,542,058 (GRCm39) |
V6A |
unknown |
Het |
Col7a1 |
T |
C |
9: 108,794,146 (GRCm39) |
|
probably null |
Het |
Cpsf6 |
T |
A |
10: 117,203,866 (GRCm39) |
I29L |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,897,178 (GRCm39) |
T379A |
probably benign |
Het |
Ddx46 |
T |
C |
13: 55,800,732 (GRCm39) |
S296P |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,651,742 (GRCm39) |
D328G |
probably damaging |
Het |
Dnah8 |
T |
G |
17: 31,006,159 (GRCm39) |
L3692W |
probably damaging |
Het |
Dnmt3l |
A |
C |
10: 77,895,565 (GRCm39) |
S368R |
probably null |
Het |
Egfr |
A |
G |
11: 16,854,434 (GRCm39) |
K869E |
probably damaging |
Het |
Ehd1 |
G |
A |
19: 6,347,724 (GRCm39) |
M359I |
probably benign |
Het |
F5 |
A |
T |
1: 164,023,139 (GRCm39) |
T1566S |
probably benign |
Het |
Flrt2 |
T |
C |
12: 95,745,725 (GRCm39) |
I21T |
probably benign |
Het |
Galnt1 |
T |
A |
18: 24,404,812 (GRCm39) |
I383K |
probably benign |
Het |
Ghdc |
G |
T |
11: 100,657,660 (GRCm39) |
A523D |
probably damaging |
Het |
Gm24022 |
A |
G |
12: 113,393,399 (GRCm39) |
|
probably benign |
Het |
Golga3 |
T |
C |
5: 110,353,643 (GRCm39) |
S934P |
probably damaging |
Het |
Gpr135 |
T |
A |
12: 72,117,282 (GRCm39) |
T162S |
probably benign |
Het |
Gucd1 |
G |
A |
10: 75,353,036 (GRCm39) |
|
probably null |
Het |
Hcrtr2 |
T |
A |
9: 76,137,886 (GRCm39) |
I410F |
probably benign |
Het |
Igkv6-15 |
T |
C |
6: 70,383,633 (GRCm39) |
Y56C |
probably damaging |
Het |
Il22ra1 |
A |
T |
4: 135,460,415 (GRCm39) |
Y57F |
probably damaging |
Het |
Irak4 |
A |
G |
15: 94,456,154 (GRCm39) |
E247G |
possibly damaging |
Het |
Kank3 |
T |
C |
17: 34,040,746 (GRCm39) |
V13A |
possibly damaging |
Het |
Klhl1 |
A |
T |
14: 96,374,046 (GRCm39) |
S667T |
probably damaging |
Het |
Klhl6 |
T |
G |
16: 19,765,741 (GRCm39) |
*620C |
probably null |
Het |
Lct |
A |
G |
1: 128,235,978 (GRCm39) |
L343P |
probably damaging |
Het |
Lgr6 |
G |
T |
1: 134,918,370 (GRCm39) |
P264T |
probably benign |
Het |
Lilrb4a |
T |
A |
10: 51,367,516 (GRCm39) |
|
probably null |
Het |
Lin7a |
G |
T |
10: 107,218,530 (GRCm39) |
G25* |
probably null |
Het |
Manba |
T |
C |
3: 135,273,391 (GRCm39) |
F775S |
probably benign |
Het |
Marchf6 |
A |
G |
15: 31,465,468 (GRCm39) |
V812A |
probably damaging |
Het |
Megf6 |
T |
A |
4: 154,352,517 (GRCm39) |
L1292H |
probably damaging |
Het |
Myo18b |
T |
G |
5: 112,909,206 (GRCm39) |
Q1979P |
probably damaging |
Het |
Myoz1 |
T |
C |
14: 20,703,769 (GRCm39) |
M59V |
probably damaging |
Het |
Naa35 |
T |
C |
13: 59,773,345 (GRCm39) |
I100T |
possibly damaging |
Het |
Nox4 |
A |
T |
7: 87,010,011 (GRCm39) |
Y404F |
probably damaging |
Het |
Ntn1 |
T |
C |
11: 68,151,358 (GRCm39) |
Y441C |
probably damaging |
Het |
Onecut3 |
A |
G |
10: 80,331,154 (GRCm39) |
T105A |
unknown |
Het |
Or10ak8 |
C |
A |
4: 118,774,440 (GRCm39) |
V75F |
probably damaging |
Het |
Or1n1 |
T |
C |
2: 36,750,082 (GRCm39) |
T93A |
probably benign |
Het |
Or4d5 |
G |
A |
9: 40,012,523 (GRCm39) |
H88Y |
probably benign |
Het |
Pabpc1l |
A |
G |
2: 163,884,438 (GRCm39) |
S392G |
probably benign |
Het |
Pan3 |
T |
A |
5: 147,463,492 (GRCm39) |
|
probably null |
Het |
Pcdha4 |
G |
A |
18: 37,088,001 (GRCm39) |
S728N |
probably benign |
Het |
Pds5a |
T |
C |
5: 65,854,128 (GRCm39) |
D38G |
probably damaging |
Het |
Pgm2l1 |
A |
G |
7: 99,921,583 (GRCm39) |
I605V |
probably benign |
Het |
Phip |
T |
C |
9: 82,778,072 (GRCm39) |
|
probably null |
Het |
Pilra |
T |
C |
5: 137,833,777 (GRCm39) |
I96M |
probably damaging |
Het |
Ppig |
T |
A |
2: 69,571,830 (GRCm39) |
V183D |
unknown |
Het |
Ppp2r2a |
A |
T |
14: 67,259,757 (GRCm39) |
L313* |
probably null |
Het |
Ppp4c |
A |
G |
7: 126,386,709 (GRCm39) |
F126S |
probably damaging |
Het |
Ptger2 |
C |
A |
14: 45,226,824 (GRCm39) |
R135S |
probably damaging |
Het |
Rab11fip5 |
T |
A |
6: 85,324,788 (GRCm39) |
E506D |
probably damaging |
Het |
Rdh12 |
G |
A |
12: 79,259,516 (GRCm39) |
G133R |
probably damaging |
Het |
Rims2 |
A |
T |
15: 39,315,824 (GRCm39) |
D610V |
probably benign |
Het |
Saa1 |
T |
A |
7: 46,390,132 (GRCm39) |
Y122F |
probably damaging |
Het |
Septin10 |
A |
T |
10: 59,012,811 (GRCm39) |
V269E |
probably damaging |
Het |
Serpina3n |
T |
A |
12: 104,374,998 (GRCm39) |
D23E |
probably benign |
Het |
Serpinb11 |
A |
G |
1: 107,304,598 (GRCm39) |
K188E |
possibly damaging |
Het |
Slc18a3 |
C |
T |
14: 32,185,736 (GRCm39) |
V216M |
possibly damaging |
Het |
Slc19a3 |
G |
T |
1: 83,000,341 (GRCm39) |
N225K |
probably benign |
Het |
Slc4a1 |
T |
A |
11: 102,242,329 (GRCm39) |
I797F |
probably benign |
Het |
Slx9 |
A |
G |
10: 77,325,850 (GRCm39) |
V154A |
probably benign |
Het |
Spic |
A |
G |
10: 88,511,761 (GRCm39) |
M165T |
possibly damaging |
Het |
Timm44 |
A |
T |
8: 4,325,886 (GRCm39) |
M1K |
probably null |
Het |
Tmc6 |
A |
G |
11: 117,661,610 (GRCm39) |
L572P |
probably benign |
Het |
Tnc |
G |
A |
4: 63,918,299 (GRCm39) |
T1204M |
probably benign |
Het |
Tnc |
G |
A |
4: 63,902,726 (GRCm39) |
T1517I |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,851,169 (GRCm39) |
L680* |
probably null |
Het |
Trps1 |
T |
A |
15: 50,524,703 (GRCm39) |
M887L |
possibly damaging |
Het |
Tulp3 |
A |
C |
6: 128,302,031 (GRCm39) |
V330G |
probably damaging |
Het |
Upf1 |
A |
G |
8: 70,787,350 (GRCm39) |
S835P |
probably damaging |
Het |
Wdr64 |
A |
G |
1: 175,620,525 (GRCm39) |
|
probably null |
Het |
Yju2b |
G |
A |
8: 84,985,304 (GRCm39) |
P322S |
probably benign |
Het |
Zbtb40 |
A |
G |
4: 136,723,461 (GRCm39) |
L643P |
probably damaging |
Het |
Zc3h18 |
A |
T |
8: 123,110,259 (GRCm39) |
D36V |
probably damaging |
Het |
|
Other mutations in Lmnb2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00087:Lmnb2
|
APN |
10 |
80,739,871 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL00908:Lmnb2
|
APN |
10 |
80,745,821 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01365:Lmnb2
|
APN |
10 |
80,740,818 (GRCm39) |
missense |
probably benign |
0.07 |
IGL01598:Lmnb2
|
APN |
10 |
80,742,999 (GRCm39) |
missense |
probably benign |
0.00 |
R0761:Lmnb2
|
UTSW |
10 |
80,742,088 (GRCm39) |
start codon destroyed |
probably null |
0.03 |
R1143:Lmnb2
|
UTSW |
10 |
80,740,149 (GRCm39) |
unclassified |
probably benign |
|
R1324:Lmnb2
|
UTSW |
10 |
80,740,005 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1763:Lmnb2
|
UTSW |
10 |
80,743,025 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Lmnb2
|
UTSW |
10 |
80,740,226 (GRCm39) |
unclassified |
probably benign |
|
R5053:Lmnb2
|
UTSW |
10 |
80,740,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R5334:Lmnb2
|
UTSW |
10 |
80,739,791 (GRCm39) |
missense |
probably benign |
0.08 |
R5713:Lmnb2
|
UTSW |
10 |
80,741,921 (GRCm39) |
missense |
probably damaging |
0.97 |
R5975:Lmnb2
|
UTSW |
10 |
80,740,962 (GRCm39) |
nonsense |
probably null |
|
R6314:Lmnb2
|
UTSW |
10 |
80,745,804 (GRCm39) |
missense |
probably damaging |
1.00 |
R6835:Lmnb2
|
UTSW |
10 |
80,745,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Lmnb2
|
UTSW |
10 |
80,740,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R7776:Lmnb2
|
UTSW |
10 |
80,753,991 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8230:Lmnb2
|
UTSW |
10 |
80,740,982 (GRCm39) |
missense |
probably damaging |
0.97 |
R8728:Lmnb2
|
UTSW |
10 |
80,740,913 (GRCm39) |
critical splice donor site |
probably null |
|
R9032:Lmnb2
|
UTSW |
10 |
80,740,091 (GRCm39) |
missense |
probably benign |
0.03 |
R9063:Lmnb2
|
UTSW |
10 |
80,742,005 (GRCm39) |
missense |
probably benign |
0.00 |
R9085:Lmnb2
|
UTSW |
10 |
80,740,091 (GRCm39) |
missense |
probably benign |
0.03 |
Z1176:Lmnb2
|
UTSW |
10 |
80,739,072 (GRCm39) |
missense |
probably damaging |
0.99 |
|