Other mutations in this stock |
Total: 97 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,771,419 (GRCm39) |
R203* |
probably null |
Het |
Acp6 |
T |
C |
3: 97,083,054 (GRCm39) |
L355P |
probably damaging |
Het |
Aebp2 |
T |
C |
6: 140,579,464 (GRCm39) |
S234P |
probably damaging |
Het |
Anapc7 |
A |
G |
5: 122,577,567 (GRCm39) |
D374G |
probably benign |
Het |
Apob |
A |
T |
12: 8,051,039 (GRCm39) |
I1088F |
probably damaging |
Het |
Armc3 |
T |
C |
2: 19,297,953 (GRCm39) |
Y575H |
probably damaging |
Het |
Asxl2 |
G |
T |
12: 3,534,558 (GRCm39) |
G252* |
probably null |
Het |
Atl1 |
A |
T |
12: 70,010,102 (GRCm39) |
K556M |
probably damaging |
Het |
AU018091 |
A |
G |
7: 3,212,104 (GRCm39) |
V206A |
probably benign |
Het |
Bcas1 |
A |
T |
2: 170,212,397 (GRCm39) |
D383E |
possibly damaging |
Het |
Bmx |
A |
G |
X: 163,015,192 (GRCm39) |
W257R |
probably benign |
Het |
Bpifb6 |
T |
C |
2: 153,747,270 (GRCm39) |
|
probably null |
Het |
Cacna1b |
G |
A |
2: 24,622,318 (GRCm39) |
P222L |
probably damaging |
Het |
Cand1 |
A |
G |
10: 119,045,972 (GRCm39) |
S978P |
probably damaging |
Het |
Cap2 |
T |
A |
13: 46,791,357 (GRCm39) |
Y175N |
possibly damaging |
Het |
Caps2 |
G |
A |
10: 112,036,591 (GRCm39) |
A384T |
probably benign |
Het |
Catsperg2 |
A |
T |
7: 29,420,470 (GRCm39) |
Y223* |
probably null |
Het |
Cd81 |
G |
T |
7: 142,620,938 (GRCm39) |
G206* |
probably null |
Het |
Cd84 |
A |
G |
1: 171,700,317 (GRCm39) |
T145A |
possibly damaging |
Het |
Cdkn2aip |
G |
T |
8: 48,165,211 (GRCm39) |
N167K |
probably benign |
Het |
Ceacam14 |
T |
A |
7: 17,549,290 (GRCm39) |
L227* |
probably null |
Het |
Ceacam5 |
A |
T |
7: 17,491,805 (GRCm39) |
D725V |
probably damaging |
Het |
Cldn34a |
A |
T |
X: 151,346,841 (GRCm39) |
H171L |
probably benign |
Het |
Col18a1 |
T |
C |
10: 76,916,988 (GRCm39) |
I114V |
unknown |
Het |
Cp |
A |
G |
3: 20,033,177 (GRCm39) |
D667G |
probably damaging |
Het |
Cr2 |
G |
A |
1: 194,836,458 (GRCm39) |
P1278S |
possibly damaging |
Het |
Crat |
A |
G |
2: 30,295,060 (GRCm39) |
Y452H |
possibly damaging |
Het |
Cyp4f13 |
T |
A |
17: 33,144,542 (GRCm39) |
H318L |
probably damaging |
Het |
Dab1 |
C |
T |
4: 104,588,948 (GRCm39) |
A524V |
probably benign |
Het |
Dmbt1 |
A |
G |
7: 130,660,018 (GRCm39) |
N527S |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,853,785 (GRCm39) |
D1583V |
probably damaging |
Het |
Fgb |
G |
T |
3: 82,951,560 (GRCm39) |
Y256* |
probably null |
Het |
Frmd3 |
T |
A |
4: 74,105,676 (GRCm39) |
S441T |
probably damaging |
Het |
Glp1r |
T |
A |
17: 31,149,722 (GRCm39) |
C329S |
possibly damaging |
Het |
Gm14190 |
G |
T |
11: 99,581,431 (GRCm39) |
Q46K |
unknown |
Het |
Golt1b |
T |
A |
6: 142,338,080 (GRCm39) |
F17Y |
probably damaging |
Het |
Gsdmc |
A |
G |
15: 63,673,748 (GRCm39) |
I179T |
probably benign |
Het |
Gsdmc2 |
T |
A |
15: 63,700,086 (GRCm39) |
M229L |
probably benign |
Het |
Gulp1 |
A |
C |
1: 44,805,274 (GRCm39) |
N121T |
possibly damaging |
Het |
Ift122 |
T |
A |
6: 115,901,328 (GRCm39) |
F1037I |
probably damaging |
Het |
Ildr1 |
A |
T |
16: 36,536,568 (GRCm39) |
Y199F |
probably damaging |
Het |
Ints2 |
T |
A |
11: 86,139,760 (GRCm39) |
H278L |
possibly damaging |
Het |
Invs |
T |
C |
4: 48,392,599 (GRCm39) |
V271A |
possibly damaging |
Het |
Kcnj2 |
T |
C |
11: 110,963,709 (GRCm39) |
I367T |
probably benign |
Het |
Kif21b |
T |
C |
1: 136,089,508 (GRCm39) |
S1115P |
probably damaging |
Het |
Lce1k |
A |
T |
3: 92,714,125 (GRCm39) |
C20S |
unknown |
Het |
Lcmt2 |
C |
A |
2: 120,970,762 (GRCm39) |
R107L |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lrrc9 |
A |
C |
12: 72,544,635 (GRCm39) |
R71S |
probably damaging |
Het |
Mcc |
C |
A |
18: 44,624,382 (GRCm39) |
E213* |
probably null |
Het |
Mis18bp1 |
T |
C |
12: 65,205,468 (GRCm39) |
T235A |
probably benign |
Het |
Mta2 |
C |
T |
19: 8,919,696 (GRCm39) |
|
probably benign |
Het |
Nebl |
T |
A |
2: 17,457,321 (GRCm39) |
I80F |
probably damaging |
Het |
Nek10 |
A |
G |
14: 14,860,764 (GRCm38) |
T467A |
probably benign |
Het |
Nexn |
A |
T |
3: 151,958,576 (GRCm39) |
F106I |
probably damaging |
Het |
Nrdc |
T |
A |
4: 108,896,972 (GRCm39) |
Y282* |
probably null |
Het |
Nxf3 |
G |
A |
X: 134,976,583 (GRCm39) |
P380S |
possibly damaging |
Het |
Oma1 |
C |
T |
4: 103,178,971 (GRCm39) |
T208I |
probably damaging |
Het |
Or1a1 |
T |
C |
11: 74,086,989 (GRCm39) |
V220A |
probably damaging |
Het |
Or4c31 |
A |
G |
2: 88,291,686 (GRCm39) |
M1V |
probably null |
Het |
Or4d10c |
C |
A |
19: 12,065,620 (GRCm39) |
V179F |
probably damaging |
Het |
Or4p21 |
A |
G |
2: 88,277,033 (GRCm39) |
L83P |
probably damaging |
Het |
Or51a42 |
A |
T |
7: 103,708,335 (GRCm39) |
I158N |
possibly damaging |
Het |
Or52l1 |
A |
T |
7: 104,830,221 (GRCm39) |
C115S |
probably damaging |
Het |
Or5p66 |
C |
A |
7: 107,885,566 (GRCm39) |
G256* |
probably null |
Het |
Or5p70 |
A |
G |
7: 107,995,041 (GRCm39) |
Y238C |
probably benign |
Het |
Panx2 |
A |
T |
15: 88,953,941 (GRCm39) |
Y632F |
possibly damaging |
Het |
Pdia4 |
T |
C |
6: 47,773,589 (GRCm39) |
T587A |
probably benign |
Het |
Piezo2 |
A |
T |
18: 63,207,733 (GRCm39) |
L1426Q |
probably null |
Het |
Pigk |
T |
A |
3: 152,450,131 (GRCm39) |
Y212N |
probably damaging |
Het |
Pramel22 |
T |
A |
4: 143,380,838 (GRCm39) |
Y395F |
probably damaging |
Het |
Prl3b1 |
C |
T |
13: 27,429,775 (GRCm39) |
T71I |
possibly damaging |
Het |
Rab3gap1 |
A |
G |
1: 127,870,166 (GRCm39) |
E929G |
possibly damaging |
Het |
Rabl3 |
T |
C |
16: 37,384,079 (GRCm39) |
I162T |
probably benign |
Het |
Rasgrf2 |
T |
A |
13: 92,172,473 (GRCm39) |
T188S |
probably damaging |
Het |
Slc12a2 |
A |
G |
18: 58,043,358 (GRCm39) |
I601V |
possibly damaging |
Het |
Slc25a42 |
A |
T |
8: 70,644,519 (GRCm39) |
I60N |
probably benign |
Het |
Slc2a3 |
C |
T |
6: 122,713,694 (GRCm39) |
G173S |
probably damaging |
Het |
Slc46a3 |
G |
A |
5: 147,823,404 (GRCm39) |
T146M |
probably damaging |
Het |
Specc1 |
C |
A |
11: 61,920,120 (GRCm39) |
P7T |
possibly damaging |
Het |
Sptbn4 |
T |
C |
7: 27,123,235 (GRCm39) |
D229G |
probably benign |
Het |
Sspo |
T |
C |
6: 48,427,984 (GRCm39) |
I154T |
probably benign |
Het |
Stx5a |
T |
C |
19: 8,726,254 (GRCm39) |
|
probably null |
Het |
Stxbp6 |
A |
T |
12: 44,902,640 (GRCm39) |
C210* |
probably null |
Het |
Tagap1 |
C |
T |
17: 7,224,285 (GRCm39) |
R137Q |
probably benign |
Het |
Tbc1d9 |
A |
G |
8: 83,997,932 (GRCm39) |
Y1163C |
probably damaging |
Het |
Tex14 |
T |
G |
11: 87,440,296 (GRCm39) |
L1367R |
probably damaging |
Het |
Tnnt3 |
C |
T |
7: 142,065,262 (GRCm39) |
R131C |
possibly damaging |
Het |
Tpx2 |
T |
A |
2: 152,732,544 (GRCm39) |
M606K |
probably benign |
Het |
Trim46 |
A |
T |
3: 89,145,008 (GRCm39) |
Y489N |
probably damaging |
Het |
Ttc28 |
C |
T |
5: 111,424,188 (GRCm39) |
S1485L |
probably benign |
Het |
Txnl1 |
T |
C |
18: 63,812,585 (GRCm39) |
T70A |
probably benign |
Het |
Unc80 |
T |
C |
1: 66,731,708 (GRCm39) |
L3053P |
probably damaging |
Het |
Wars1 |
G |
T |
12: 108,854,359 (GRCm39) |
N18K |
possibly damaging |
Het |
Wnt8a |
A |
G |
18: 34,677,937 (GRCm39) |
D115G |
probably damaging |
Het |
Xndc1 |
T |
A |
7: 101,722,398 (GRCm39) |
V21E |
probably damaging |
Het |
Zfp493 |
T |
A |
13: 67,934,388 (GRCm39) |
C114S |
probably damaging |
Het |
|
Other mutations in Arid4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00482:Arid4b
|
APN |
13 |
14,365,719 (GRCm39) |
unclassified |
probably benign |
|
IGL00581:Arid4b
|
APN |
13 |
14,334,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00808:Arid4b
|
APN |
13 |
14,310,846 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01150:Arid4b
|
APN |
13 |
14,369,959 (GRCm39) |
nonsense |
probably null |
|
IGL01570:Arid4b
|
APN |
13 |
14,361,394 (GRCm39) |
unclassified |
probably benign |
|
IGL01942:Arid4b
|
APN |
13 |
14,310,749 (GRCm39) |
intron |
probably benign |
|
IGL02031:Arid4b
|
APN |
13 |
14,327,997 (GRCm39) |
splice site |
probably benign |
|
IGL02183:Arid4b
|
APN |
13 |
14,344,575 (GRCm39) |
missense |
possibly damaging |
0.68 |
R0096:Arid4b
|
UTSW |
13 |
14,303,779 (GRCm39) |
missense |
probably benign |
0.08 |
R0096:Arid4b
|
UTSW |
13 |
14,303,779 (GRCm39) |
missense |
probably benign |
0.08 |
R0514:Arid4b
|
UTSW |
13 |
14,358,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0694:Arid4b
|
UTSW |
13 |
14,362,419 (GRCm39) |
missense |
probably damaging |
0.96 |
R0746:Arid4b
|
UTSW |
13 |
14,317,623 (GRCm39) |
missense |
probably benign |
0.01 |
R1624:Arid4b
|
UTSW |
13 |
14,358,979 (GRCm39) |
missense |
probably damaging |
0.99 |
R1625:Arid4b
|
UTSW |
13 |
14,361,699 (GRCm39) |
missense |
probably damaging |
0.99 |
R1812:Arid4b
|
UTSW |
13 |
14,370,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R1891:Arid4b
|
UTSW |
13 |
14,310,821 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2051:Arid4b
|
UTSW |
13 |
14,362,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R2060:Arid4b
|
UTSW |
13 |
14,370,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R2344:Arid4b
|
UTSW |
13 |
14,328,075 (GRCm39) |
missense |
probably benign |
0.26 |
R3605:Arid4b
|
UTSW |
13 |
14,294,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R3606:Arid4b
|
UTSW |
13 |
14,294,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R3844:Arid4b
|
UTSW |
13 |
14,361,645 (GRCm39) |
missense |
probably damaging |
0.99 |
R3909:Arid4b
|
UTSW |
13 |
14,307,069 (GRCm39) |
missense |
probably damaging |
1.00 |
R3938:Arid4b
|
UTSW |
13 |
14,361,513 (GRCm39) |
missense |
probably benign |
0.34 |
R4394:Arid4b
|
UTSW |
13 |
14,329,557 (GRCm39) |
splice site |
probably null |
|
R4466:Arid4b
|
UTSW |
13 |
14,307,095 (GRCm39) |
missense |
probably damaging |
1.00 |
R4530:Arid4b
|
UTSW |
13 |
14,301,040 (GRCm39) |
missense |
probably damaging |
0.98 |
R4537:Arid4b
|
UTSW |
13 |
14,294,746 (GRCm39) |
nonsense |
probably null |
|
R4829:Arid4b
|
UTSW |
13 |
14,359,023 (GRCm39) |
missense |
probably benign |
0.23 |
R4930:Arid4b
|
UTSW |
13 |
14,362,062 (GRCm39) |
missense |
probably damaging |
0.99 |
R4972:Arid4b
|
UTSW |
13 |
14,334,857 (GRCm39) |
missense |
probably benign |
0.07 |
R5119:Arid4b
|
UTSW |
13 |
14,338,866 (GRCm39) |
missense |
probably benign |
0.15 |
R5236:Arid4b
|
UTSW |
13 |
14,301,034 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5304:Arid4b
|
UTSW |
13 |
14,361,514 (GRCm39) |
missense |
probably benign |
0.34 |
R5439:Arid4b
|
UTSW |
13 |
14,362,281 (GRCm39) |
missense |
probably damaging |
0.99 |
R5734:Arid4b
|
UTSW |
13 |
14,334,856 (GRCm39) |
missense |
probably benign |
0.09 |
R5950:Arid4b
|
UTSW |
13 |
14,365,849 (GRCm39) |
splice site |
probably benign |
|
R5951:Arid4b
|
UTSW |
13 |
14,317,648 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6645:Arid4b
|
UTSW |
13 |
14,294,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R6765:Arid4b
|
UTSW |
13 |
14,361,900 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6804:Arid4b
|
UTSW |
13 |
14,303,792 (GRCm39) |
missense |
probably benign |
0.44 |
R7342:Arid4b
|
UTSW |
13 |
14,310,804 (GRCm39) |
missense |
probably benign |
0.03 |
R7354:Arid4b
|
UTSW |
13 |
14,339,455 (GRCm39) |
missense |
probably benign |
0.19 |
R7426:Arid4b
|
UTSW |
13 |
14,355,891 (GRCm39) |
critical splice donor site |
probably null |
|
R7863:Arid4b
|
UTSW |
13 |
14,338,734 (GRCm39) |
missense |
probably benign |
0.01 |
R8070:Arid4b
|
UTSW |
13 |
14,310,844 (GRCm39) |
missense |
probably benign |
0.32 |
R8076:Arid4b
|
UTSW |
13 |
14,361,535 (GRCm39) |
missense |
probably benign |
0.01 |
R8239:Arid4b
|
UTSW |
13 |
14,344,594 (GRCm39) |
missense |
probably benign |
|
R8303:Arid4b
|
UTSW |
13 |
14,294,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R9047:Arid4b
|
UTSW |
13 |
14,355,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R9799:Arid4b
|
UTSW |
13 |
14,358,967 (GRCm39) |
missense |
probably benign |
|
|