Other mutations in this stock |
Total: 95 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930488N24Rik |
T |
C |
17: 14,326,481 (GRCm39) |
|
noncoding transcript |
Het |
5730455P16Rik |
A |
T |
11: 80,266,346 (GRCm39) |
S132T |
possibly damaging |
Het |
Aadacl3 |
T |
A |
4: 144,184,527 (GRCm39) |
H77L |
probably damaging |
Het |
Actr5 |
T |
A |
2: 158,467,426 (GRCm39) |
V122D |
probably damaging |
Het |
Adamts7 |
A |
G |
9: 90,071,739 (GRCm39) |
D678G |
possibly damaging |
Het |
Alpk1 |
T |
A |
3: 127,464,708 (GRCm39) |
D1190V |
probably benign |
Het |
Apbb1ip |
A |
T |
2: 22,765,265 (GRCm39) |
N649Y |
unknown |
Het |
Atp6v0a1 |
A |
G |
11: 100,933,776 (GRCm39) |
I522V |
probably benign |
Het |
Brd10 |
T |
C |
19: 29,695,809 (GRCm39) |
N1228S |
possibly damaging |
Het |
Cars1 |
T |
C |
7: 143,124,301 (GRCm39) |
D375G |
probably damaging |
Het |
Catspere1 |
A |
T |
1: 177,687,441 (GRCm39) |
|
noncoding transcript |
Het |
Ccdc87 |
A |
G |
19: 4,890,579 (GRCm39) |
D357G |
probably damaging |
Het |
Cfap65 |
C |
T |
1: 74,966,791 (GRCm39) |
A299T |
probably benign |
Het |
Cic |
T |
C |
7: 24,971,157 (GRCm39) |
V296A |
possibly damaging |
Het |
Col7a1 |
T |
A |
9: 108,797,675 (GRCm39) |
S1686T |
possibly damaging |
Het |
Ctbp2 |
A |
C |
7: 132,615,423 (GRCm39) |
L504R |
probably damaging |
Het |
Cttnbp2nl |
T |
C |
3: 104,918,640 (GRCm39) |
K67E |
probably benign |
Het |
Cyp2c50 |
C |
T |
19: 40,102,024 (GRCm39) |
P480S |
probably damaging |
Het |
Dcdc5 |
A |
C |
2: 106,166,420 (GRCm39) |
|
noncoding transcript |
Het |
Defb2 |
G |
T |
8: 22,333,317 (GRCm39) |
E31* |
probably null |
Het |
Dhrs1 |
T |
A |
14: 55,977,083 (GRCm39) |
N244I |
possibly damaging |
Het |
Dop1b |
A |
G |
16: 93,589,978 (GRCm39) |
I134V |
probably benign |
Het |
Eif1ad11 |
A |
T |
12: 87,994,158 (GRCm39) |
I129F |
unknown |
Het |
Etl4 |
A |
G |
2: 20,811,496 (GRCm39) |
D1193G |
possibly damaging |
Het |
Ezh1 |
A |
C |
11: 101,094,594 (GRCm39) |
S399R |
probably damaging |
Het |
Fam161a |
T |
C |
11: 22,970,076 (GRCm39) |
S26P |
probably damaging |
Het |
Fcgbp |
C |
A |
7: 27,813,383 (GRCm39) |
S2306Y |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,876,512 (GRCm39) |
I2415T |
probably benign |
Het |
Gas2l3 |
A |
G |
10: 89,252,907 (GRCm39) |
L246P |
probably damaging |
Het |
Gdf15 |
C |
T |
8: 71,082,246 (GRCm39) |
V287M |
probably damaging |
Het |
Gm7742 |
T |
C |
17: 21,420,235 (GRCm39) |
|
noncoding transcript |
Het |
Grin2d |
T |
C |
7: 45,507,363 (GRCm39) |
D446G |
probably damaging |
Het |
Hemk1 |
A |
G |
9: 107,205,385 (GRCm39) |
F107L |
probably benign |
Het |
Hmgcr |
C |
T |
13: 96,796,700 (GRCm39) |
G197S |
probably damaging |
Het |
Ift52 |
G |
A |
2: 162,873,108 (GRCm39) |
G207D |
probably benign |
Het |
Il17re |
A |
G |
6: 113,442,816 (GRCm39) |
T275A |
probably benign |
Het |
Iqcf3 |
T |
C |
9: 106,430,788 (GRCm39) |
|
probably benign |
Het |
Kcna1 |
A |
G |
6: 126,619,099 (GRCm39) |
I407T |
probably damaging |
Het |
Kcnrg |
T |
A |
14: 61,845,386 (GRCm39) |
M142K |
probably benign |
Het |
Lhx9 |
C |
A |
1: 138,766,105 (GRCm39) |
V237L |
probably benign |
Het |
Lipo3 |
A |
C |
19: 33,560,497 (GRCm39) |
I56S |
probably damaging |
Het |
Loxhd1 |
C |
G |
18: 77,472,663 (GRCm39) |
P1060R |
probably damaging |
Het |
Map2k4 |
A |
C |
11: 65,587,201 (GRCm39) |
|
probably benign |
Het |
Methig1 |
A |
G |
15: 100,251,416 (GRCm39) |
K109R |
possibly damaging |
Het |
Mmrn1 |
G |
A |
6: 60,950,027 (GRCm39) |
V326I |
probably benign |
Het |
Myo15a |
G |
A |
11: 60,367,741 (GRCm39) |
R167H |
probably damaging |
Het |
Ncoa7 |
G |
A |
10: 30,524,472 (GRCm39) |
T142M |
probably damaging |
Het |
Nfkb2 |
C |
A |
19: 46,296,493 (GRCm39) |
Q254K |
probably damaging |
Het |
Nherf1 |
A |
G |
11: 115,070,918 (GRCm39) |
E290G |
probably benign |
Het |
Nol6 |
G |
T |
4: 41,121,508 (GRCm39) |
P278Q |
probably damaging |
Het |
Nptxr |
T |
A |
15: 79,677,027 (GRCm39) |
D285V |
probably damaging |
Het |
Oosp3 |
T |
C |
19: 11,688,997 (GRCm39) |
W82R |
probably damaging |
Het |
Or6b3 |
A |
T |
1: 92,438,812 (GRCm39) |
*313K |
probably null |
Het |
Or6n1 |
A |
G |
1: 173,916,742 (GRCm39) |
I45M |
possibly damaging |
Het |
Pa2g4 |
G |
T |
10: 128,395,199 (GRCm39) |
T322K |
probably damaging |
Het |
Parp16 |
C |
A |
9: 65,145,175 (GRCm39) |
F291L |
probably damaging |
Het |
Pdzd9 |
A |
T |
7: 120,267,619 (GRCm39) |
D65E |
probably damaging |
Het |
Pgap3 |
A |
G |
11: 98,281,300 (GRCm39) |
W238R |
probably damaging |
Het |
Pgf |
G |
A |
12: 85,218,538 (GRCm39) |
H67Y |
probably benign |
Het |
Pik3cb |
T |
C |
9: 98,955,679 (GRCm39) |
T413A |
probably benign |
Het |
Plcxd2 |
A |
T |
16: 45,800,700 (GRCm39) |
C175S |
probably benign |
Het |
Pou2f1 |
A |
T |
1: 165,719,517 (GRCm39) |
|
probably benign |
Het |
Ppfia1 |
T |
G |
7: 144,052,106 (GRCm39) |
N846T |
probably benign |
Het |
Ppid |
T |
A |
3: 79,502,504 (GRCm39) |
|
probably null |
Het |
Prkcq |
G |
A |
2: 11,231,797 (GRCm39) |
|
probably null |
Het |
Ptgds |
T |
C |
2: 25,359,058 (GRCm39) |
K66E |
probably benign |
Het |
Ptpmt1 |
A |
G |
2: 90,748,283 (GRCm39) |
|
noncoding transcript |
Het |
Rab3il1 |
G |
A |
19: 10,004,034 (GRCm39) |
G51D |
probably benign |
Het |
Rdx |
T |
C |
9: 51,974,891 (GRCm39) |
V9A |
probably damaging |
Het |
Rpl7l1 |
T |
C |
17: 47,089,014 (GRCm39) |
N239S |
probably benign |
Het |
Rrbp1 |
C |
A |
2: 143,806,685 (GRCm39) |
A978S |
possibly damaging |
Het |
Rsf1 |
GCGGCGGCG |
GCGGCGGCGCCGGCGGCG |
7: 97,229,126 (GRCm39) |
|
probably benign |
Het |
Scn3a |
A |
T |
2: 65,291,622 (GRCm39) |
I1708N |
probably damaging |
Het |
Serinc1 |
A |
G |
10: 57,401,466 (GRCm39) |
I109T |
possibly damaging |
Het |
Shroom1 |
G |
A |
11: 53,355,966 (GRCm39) |
V339I |
probably benign |
Het |
Slc30a8 |
T |
A |
15: 52,169,880 (GRCm39) |
C36S |
probably benign |
Het |
Slco1b2 |
A |
G |
6: 141,631,158 (GRCm39) |
I597M |
probably benign |
Het |
Snx27 |
A |
G |
3: 94,427,518 (GRCm39) |
F228S |
probably damaging |
Het |
Spata31f1a |
T |
A |
4: 42,851,815 (GRCm39) |
I114F |
probably damaging |
Het |
Speer4e2 |
G |
T |
5: 15,026,225 (GRCm39) |
T144K |
probably benign |
Het |
Stim1 |
T |
A |
7: 102,064,571 (GRCm39) |
F214I |
probably damaging |
Het |
Svep1 |
T |
C |
4: 58,082,664 (GRCm39) |
T1987A |
probably benign |
Het |
Tamm41 |
A |
G |
6: 115,002,378 (GRCm39) |
I18T |
possibly damaging |
Het |
Tmem150b |
T |
A |
7: 4,726,871 (GRCm39) |
D79V |
probably damaging |
Het |
Tmem167 |
T |
A |
13: 90,252,548 (GRCm39) |
I68N |
probably benign |
Het |
Traf3 |
A |
G |
12: 111,227,204 (GRCm39) |
E339G |
possibly damaging |
Het |
Tspan12 |
G |
A |
6: 21,795,660 (GRCm39) |
P177S |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,783,562 (GRCm39) |
I810T |
probably benign |
Het |
Ulk1 |
T |
C |
5: 110,939,996 (GRCm39) |
T407A |
probably benign |
Het |
Uroc1 |
G |
A |
6: 90,334,600 (GRCm39) |
|
probably null |
Het |
Vmn2r-ps69 |
T |
C |
7: 84,959,584 (GRCm39) |
|
noncoding transcript |
Het |
Wdr59 |
T |
C |
8: 112,207,446 (GRCm39) |
N476S |
probably benign |
Het |
Zfp472 |
A |
G |
17: 33,196,416 (GRCm39) |
M164V |
probably benign |
Het |
Zfp608 |
T |
C |
18: 55,120,756 (GRCm39) |
N277S |
probably benign |
Het |
Zfp831 |
T |
C |
2: 174,547,097 (GRCm39) |
C1427R |
possibly damaging |
Het |
|
Other mutations in Cd101 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00958:Cd101
|
APN |
3 |
100,911,018 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01443:Cd101
|
APN |
3 |
100,910,887 (GRCm39) |
missense |
probably benign |
|
IGL02000:Cd101
|
APN |
3 |
100,919,398 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02178:Cd101
|
APN |
3 |
100,901,082 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02224:Cd101
|
APN |
3 |
100,924,318 (GRCm39) |
missense |
probably benign |
|
IGL02450:Cd101
|
APN |
3 |
100,901,054 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02502:Cd101
|
APN |
3 |
100,919,141 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02536:Cd101
|
APN |
3 |
100,910,913 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02749:Cd101
|
APN |
3 |
100,927,715 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02818:Cd101
|
APN |
3 |
100,919,245 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02829:Cd101
|
APN |
3 |
100,925,881 (GRCm39) |
splice site |
probably benign |
|
IGL02902:Cd101
|
APN |
3 |
100,926,310 (GRCm39) |
splice site |
probably benign |
|
tax_day
|
UTSW |
3 |
100,911,021 (GRCm39) |
missense |
possibly damaging |
0.86 |
R0069:Cd101
|
UTSW |
3 |
100,915,533 (GRCm39) |
missense |
probably benign |
0.08 |
R0069:Cd101
|
UTSW |
3 |
100,915,533 (GRCm39) |
missense |
probably benign |
0.08 |
R0411:Cd101
|
UTSW |
3 |
100,925,843 (GRCm39) |
splice site |
probably null |
|
R0486:Cd101
|
UTSW |
3 |
100,915,408 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0556:Cd101
|
UTSW |
3 |
100,927,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R0726:Cd101
|
UTSW |
3 |
100,927,938 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0966:Cd101
|
UTSW |
3 |
100,915,538 (GRCm39) |
missense |
probably benign |
0.13 |
R1344:Cd101
|
UTSW |
3 |
100,926,091 (GRCm39) |
nonsense |
probably null |
|
R1418:Cd101
|
UTSW |
3 |
100,926,091 (GRCm39) |
nonsense |
probably null |
|
R1547:Cd101
|
UTSW |
3 |
100,926,267 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1551:Cd101
|
UTSW |
3 |
100,919,329 (GRCm39) |
missense |
probably damaging |
0.99 |
R1845:Cd101
|
UTSW |
3 |
100,936,764 (GRCm39) |
splice site |
probably null |
|
R1919:Cd101
|
UTSW |
3 |
100,926,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Cd101
|
UTSW |
3 |
100,915,377 (GRCm39) |
missense |
probably damaging |
0.96 |
R2260:Cd101
|
UTSW |
3 |
100,924,261 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2679:Cd101
|
UTSW |
3 |
100,901,079 (GRCm39) |
missense |
probably benign |
0.00 |
R2873:Cd101
|
UTSW |
3 |
100,911,164 (GRCm39) |
missense |
probably benign |
0.00 |
R3606:Cd101
|
UTSW |
3 |
100,927,913 (GRCm39) |
missense |
probably damaging |
1.00 |
R4201:Cd101
|
UTSW |
3 |
100,926,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R4202:Cd101
|
UTSW |
3 |
100,926,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R4205:Cd101
|
UTSW |
3 |
100,926,001 (GRCm39) |
missense |
probably damaging |
1.00 |
R4349:Cd101
|
UTSW |
3 |
100,920,630 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4574:Cd101
|
UTSW |
3 |
100,920,469 (GRCm39) |
missense |
probably benign |
0.02 |
R4601:Cd101
|
UTSW |
3 |
100,901,204 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4910:Cd101
|
UTSW |
3 |
100,901,205 (GRCm39) |
missense |
probably benign |
0.13 |
R5014:Cd101
|
UTSW |
3 |
100,911,139 (GRCm39) |
missense |
probably damaging |
0.99 |
R5081:Cd101
|
UTSW |
3 |
100,911,021 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5396:Cd101
|
UTSW |
3 |
100,926,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R5425:Cd101
|
UTSW |
3 |
100,926,002 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Cd101
|
UTSW |
3 |
100,927,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R6210:Cd101
|
UTSW |
3 |
100,925,959 (GRCm39) |
missense |
probably damaging |
1.00 |
R6732:Cd101
|
UTSW |
3 |
100,915,515 (GRCm39) |
missense |
probably benign |
0.01 |
R6830:Cd101
|
UTSW |
3 |
100,901,012 (GRCm39) |
missense |
probably benign |
0.12 |
R6897:Cd101
|
UTSW |
3 |
100,920,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R6940:Cd101
|
UTSW |
3 |
100,911,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R7335:Cd101
|
UTSW |
3 |
100,926,045 (GRCm39) |
missense |
probably benign |
0.01 |
R7565:Cd101
|
UTSW |
3 |
100,926,108 (GRCm39) |
missense |
probably benign |
0.00 |
R7880:Cd101
|
UTSW |
3 |
100,915,182 (GRCm39) |
missense |
probably benign |
0.00 |
R8121:Cd101
|
UTSW |
3 |
100,927,898 (GRCm39) |
missense |
probably damaging |
1.00 |
R8233:Cd101
|
UTSW |
3 |
100,900,989 (GRCm39) |
missense |
unknown |
|
R8900:Cd101
|
UTSW |
3 |
100,926,062 (GRCm39) |
missense |
probably benign |
0.19 |
R8960:Cd101
|
UTSW |
3 |
100,910,817 (GRCm39) |
missense |
probably benign |
0.01 |
R9260:Cd101
|
UTSW |
3 |
100,920,599 (GRCm39) |
missense |
probably benign |
0.16 |
R9335:Cd101
|
UTSW |
3 |
100,915,431 (GRCm39) |
missense |
probably benign |
0.18 |
R9663:Cd101
|
UTSW |
3 |
100,911,222 (GRCm39) |
missense |
probably benign |
0.21 |
X0018:Cd101
|
UTSW |
3 |
100,925,948 (GRCm39) |
missense |
possibly damaging |
0.95 |
X0023:Cd101
|
UTSW |
3 |
100,926,171 (GRCm39) |
missense |
probably benign |
|
X0058:Cd101
|
UTSW |
3 |
100,927,737 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Cd101
|
UTSW |
3 |
100,924,456 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Cd101
|
UTSW |
3 |
100,919,232 (GRCm39) |
missense |
probably benign |
0.03 |
|