Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts14 |
C |
T |
10: 61,038,780 (GRCm39) |
S907N |
probably damaging |
Het |
Adgrf1 |
A |
T |
17: 43,614,651 (GRCm39) |
Y245F |
possibly damaging |
Het |
Adgrl3 |
C |
T |
5: 81,613,065 (GRCm39) |
A98V |
probably damaging |
Het |
Afmid |
A |
T |
11: 117,726,349 (GRCm39) |
I186F |
probably damaging |
Het |
Ago4 |
A |
G |
4: 126,400,596 (GRCm39) |
Y706H |
probably damaging |
Het |
Appl1 |
A |
T |
14: 26,685,652 (GRCm39) |
S55R |
possibly damaging |
Het |
Ash1l |
A |
G |
3: 88,892,576 (GRCm39) |
H1485R |
probably damaging |
Het |
Atp6v0a2 |
C |
T |
5: 124,796,138 (GRCm39) |
T734M |
possibly damaging |
Het |
B3gat1 |
T |
C |
9: 26,663,069 (GRCm39) |
|
probably benign |
Het |
Bcl7c |
T |
C |
7: 127,306,504 (GRCm39) |
N96D |
probably benign |
Het |
Brca2 |
T |
C |
5: 150,465,360 (GRCm39) |
L1708P |
probably benign |
Het |
Ccl8 |
C |
T |
11: 82,006,873 (GRCm39) |
P29S |
possibly damaging |
Het |
Clpx |
T |
A |
9: 65,234,115 (GRCm39) |
C587S |
probably null |
Het |
Coro2b |
T |
C |
9: 62,332,978 (GRCm39) |
D168G |
|
Het |
Dst |
T |
C |
1: 34,153,105 (GRCm39) |
|
probably null |
Het |
Eps8l1 |
C |
T |
7: 4,477,042 (GRCm39) |
Q443* |
probably null |
Het |
Fam131b |
G |
T |
6: 42,298,946 (GRCm39) |
N11K |
possibly damaging |
Het |
Firrm |
A |
T |
1: 163,818,300 (GRCm39) |
I47N |
possibly damaging |
Het |
Fry |
T |
C |
5: 150,360,768 (GRCm39) |
V125A |
probably benign |
Het |
Ftcd |
T |
C |
10: 76,417,413 (GRCm39) |
F284S |
probably damaging |
Het |
Glg1 |
A |
G |
8: 111,904,380 (GRCm39) |
I617T |
probably damaging |
Het |
Gm4847 |
C |
T |
1: 166,469,332 (GRCm39) |
V111M |
probably damaging |
Het |
Hcrtr2 |
C |
T |
9: 76,161,854 (GRCm39) |
V179I |
probably damaging |
Het |
Herc6 |
A |
G |
6: 57,595,612 (GRCm39) |
N430S |
probably benign |
Het |
Knl1 |
T |
C |
2: 118,900,761 (GRCm39) |
S821P |
probably benign |
Het |
Letm2 |
C |
T |
8: 26,077,236 (GRCm39) |
V285I |
|
Het |
Map3k14 |
T |
C |
11: 103,129,835 (GRCm39) |
T361A |
possibly damaging |
Het |
Mmp10 |
A |
T |
9: 7,504,913 (GRCm39) |
M236L |
probably damaging |
Het |
Mmp16 |
A |
G |
4: 17,996,202 (GRCm39) |
K97R |
probably benign |
Het |
Muc6 |
T |
A |
7: 141,237,432 (GRCm39) |
K194* |
probably null |
Het |
Myo18a |
A |
G |
11: 77,718,477 (GRCm39) |
Y949C |
probably damaging |
Het |
Nat8f1 |
A |
G |
6: 85,887,369 (GRCm39) |
L197P |
probably damaging |
Het |
Nlrp9a |
T |
G |
7: 26,273,291 (GRCm39) |
N976K |
possibly damaging |
Het |
Or2aa1 |
A |
T |
11: 59,480,367 (GRCm39) |
C183S |
probably damaging |
Het |
Or56b1 |
C |
T |
7: 104,285,291 (GRCm39) |
R137C |
probably benign |
Het |
Or8g24 |
T |
C |
9: 38,989,307 (GRCm39) |
I245V |
probably benign |
Het |
Parp3 |
T |
C |
9: 106,348,490 (GRCm39) |
Y515C |
probably damaging |
Het |
Pde11a |
C |
G |
2: 75,966,803 (GRCm39) |
A549P |
probably damaging |
Het |
Pdlim4 |
T |
C |
11: 53,959,662 (GRCm39) |
|
probably benign |
Het |
Pla2g4e |
T |
C |
2: 120,001,718 (GRCm39) |
T644A |
probably benign |
Het |
Pmm1 |
C |
T |
15: 81,839,896 (GRCm39) |
R143H |
probably damaging |
Het |
Poglut2 |
T |
C |
1: 44,153,925 (GRCm39) |
I175V |
possibly damaging |
Het |
Prb1b |
GAGGGGGTCTCTGCTGGGGGCCTCTCTGTGGGGGTGGGCCTTGTTGGTTTCCAGGCT |
G |
6: 132,289,174 (GRCm39) |
|
probably null |
Het |
Prr7 |
A |
G |
13: 55,620,234 (GRCm39) |
S133G |
possibly damaging |
Het |
Pten |
C |
A |
19: 32,795,412 (GRCm39) |
D326E |
possibly damaging |
Het |
Ranbp2 |
T |
A |
10: 58,315,343 (GRCm39) |
L2021* |
probably null |
Het |
Rassf5 |
T |
C |
1: 131,140,077 (GRCm39) |
I161V |
probably benign |
Het |
Ric1 |
C |
A |
19: 29,548,143 (GRCm39) |
|
probably benign |
Het |
Samd9l |
A |
G |
6: 3,373,791 (GRCm39) |
S1157P |
probably damaging |
Het |
Serpinb1a |
A |
G |
13: 33,029,763 (GRCm39) |
V153A |
probably damaging |
Het |
Shank1 |
T |
C |
7: 43,968,531 (GRCm39) |
Y275H |
unknown |
Het |
Slc6a18 |
C |
T |
13: 73,823,889 (GRCm39) |
G84R |
probably damaging |
Het |
Smarcc2 |
A |
G |
10: 128,301,093 (GRCm39) |
E187G |
probably damaging |
Het |
Stxbp4 |
A |
G |
11: 90,426,249 (GRCm39) |
S520P |
unknown |
Het |
Taar8b |
C |
T |
10: 23,967,205 (GRCm39) |
E330K |
probably benign |
Het |
Tdpoz6 |
A |
G |
3: 93,599,742 (GRCm39) |
F209S |
probably damaging |
Het |
Tex14 |
T |
A |
11: 87,365,239 (GRCm39) |
V61D |
|
Het |
Tg |
T |
C |
15: 66,555,522 (GRCm39) |
F738S |
probably damaging |
Het |
Trpc4 |
T |
C |
3: 54,102,254 (GRCm39) |
S51P |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,626,231 (GRCm39) |
S14975G |
probably benign |
Het |
Usp15 |
C |
T |
10: 122,961,498 (GRCm39) |
G685R |
possibly damaging |
Het |
Usp17lc |
C |
T |
7: 103,067,539 (GRCm39) |
P278L |
possibly damaging |
Het |
Wasf1 |
T |
C |
10: 40,810,571 (GRCm39) |
V271A |
possibly damaging |
Het |
Zbtb46 |
C |
T |
2: 181,065,935 (GRCm39) |
V72I |
possibly damaging |
Het |
Zfp462 |
A |
G |
4: 55,007,563 (GRCm39) |
M1V |
probably null |
Het |
Zfp648 |
T |
C |
1: 154,080,914 (GRCm39) |
F358L |
probably damaging |
Het |
|
Other mutations in A2m |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00494:A2m
|
APN |
6 |
121,621,108 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL00798:A2m
|
APN |
6 |
121,647,969 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01154:A2m
|
APN |
6 |
121,650,501 (GRCm39) |
nonsense |
probably null |
|
IGL01313:A2m
|
APN |
6 |
121,621,969 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01337:A2m
|
APN |
6 |
121,645,529 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01505:A2m
|
APN |
6 |
121,653,906 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL01508:A2m
|
APN |
6 |
121,636,326 (GRCm39) |
nonsense |
probably null |
|
IGL01672:A2m
|
APN |
6 |
121,618,316 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01951:A2m
|
APN |
6 |
121,644,149 (GRCm39) |
missense |
possibly damaging |
0.78 |
IGL02012:A2m
|
APN |
6 |
121,651,820 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02066:A2m
|
APN |
6 |
121,626,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:A2m
|
APN |
6 |
121,645,179 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02397:A2m
|
APN |
6 |
121,623,834 (GRCm39) |
missense |
probably benign |
|
IGL02407:A2m
|
APN |
6 |
121,645,575 (GRCm39) |
nonsense |
probably null |
|
IGL02408:A2m
|
APN |
6 |
121,621,130 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02469:A2m
|
APN |
6 |
121,645,074 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02527:A2m
|
APN |
6 |
121,638,392 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02612:A2m
|
APN |
6 |
121,654,971 (GRCm39) |
missense |
probably benign |
|
IGL02746:A2m
|
APN |
6 |
121,646,462 (GRCm39) |
splice site |
probably benign |
|
IGL02952:A2m
|
APN |
6 |
121,654,984 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03056:A2m
|
APN |
6 |
121,647,862 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03121:A2m
|
APN |
6 |
121,618,265 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03303:A2m
|
APN |
6 |
121,644,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03369:A2m
|
APN |
6 |
121,653,862 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03046:A2m
|
UTSW |
6 |
121,636,282 (GRCm39) |
missense |
probably benign |
0.04 |
R0040:A2m
|
UTSW |
6 |
121,622,165 (GRCm39) |
missense |
possibly damaging |
0.93 |
R0049:A2m
|
UTSW |
6 |
121,615,267 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0049:A2m
|
UTSW |
6 |
121,615,267 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0109:A2m
|
UTSW |
6 |
121,636,262 (GRCm39) |
missense |
probably benign |
0.00 |
R0147:A2m
|
UTSW |
6 |
121,639,405 (GRCm39) |
critical splice donor site |
probably null |
|
R0148:A2m
|
UTSW |
6 |
121,639,405 (GRCm39) |
critical splice donor site |
probably null |
|
R0345:A2m
|
UTSW |
6 |
121,615,231 (GRCm39) |
splice site |
probably benign |
|
R0445:A2m
|
UTSW |
6 |
121,634,914 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:A2m
|
UTSW |
6 |
121,653,849 (GRCm39) |
splice site |
probably benign |
|
R1186:A2m
|
UTSW |
6 |
121,638,493 (GRCm39) |
missense |
probably benign |
0.00 |
R1436:A2m
|
UTSW |
6 |
121,621,172 (GRCm39) |
missense |
probably benign |
0.09 |
R1452:A2m
|
UTSW |
6 |
121,655,015 (GRCm39) |
missense |
probably benign |
0.01 |
R1636:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1637:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1638:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1698:A2m
|
UTSW |
6 |
121,622,117 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1776:A2m
|
UTSW |
6 |
121,618,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R1791:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1918:A2m
|
UTSW |
6 |
121,621,895 (GRCm39) |
missense |
probably benign |
0.16 |
R1921:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R1927:A2m
|
UTSW |
6 |
121,613,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R1934:A2m
|
UTSW |
6 |
121,626,792 (GRCm39) |
missense |
probably damaging |
0.98 |
R1943:A2m
|
UTSW |
6 |
121,645,506 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1996:A2m
|
UTSW |
6 |
121,646,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R2039:A2m
|
UTSW |
6 |
121,636,908 (GRCm39) |
missense |
probably benign |
0.32 |
R2085:A2m
|
UTSW |
6 |
121,653,918 (GRCm39) |
missense |
probably damaging |
1.00 |
R2092:A2m
|
UTSW |
6 |
121,651,896 (GRCm39) |
nonsense |
probably null |
|
R2105:A2m
|
UTSW |
6 |
121,650,459 (GRCm39) |
missense |
probably benign |
0.04 |
R2107:A2m
|
UTSW |
6 |
121,631,571 (GRCm39) |
missense |
probably benign |
0.04 |
R2235:A2m
|
UTSW |
6 |
121,619,023 (GRCm39) |
missense |
probably benign |
0.21 |
R2292:A2m
|
UTSW |
6 |
121,650,518 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2350:A2m
|
UTSW |
6 |
121,655,047 (GRCm39) |
splice site |
probably benign |
|
R3001:A2m
|
UTSW |
6 |
121,638,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3002:A2m
|
UTSW |
6 |
121,638,406 (GRCm39) |
missense |
possibly damaging |
0.88 |
R3023:A2m
|
UTSW |
6 |
121,646,531 (GRCm39) |
missense |
probably benign |
0.08 |
R3429:A2m
|
UTSW |
6 |
121,613,249 (GRCm39) |
start codon destroyed |
probably null |
|
R3437:A2m
|
UTSW |
6 |
121,616,253 (GRCm39) |
missense |
probably null |
0.03 |
R3909:A2m
|
UTSW |
6 |
121,625,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R4300:A2m
|
UTSW |
6 |
121,650,434 (GRCm39) |
missense |
probably benign |
0.00 |
R4332:A2m
|
UTSW |
6 |
121,634,406 (GRCm39) |
missense |
probably benign |
0.01 |
R4584:A2m
|
UTSW |
6 |
121,634,365 (GRCm39) |
missense |
probably benign |
0.07 |
R4697:A2m
|
UTSW |
6 |
121,615,243 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
R4710:A2m
|
UTSW |
6 |
121,618,262 (GRCm39) |
missense |
probably benign |
0.03 |
R4841:A2m
|
UTSW |
6 |
121,623,803 (GRCm39) |
missense |
probably benign |
0.06 |
R5206:A2m
|
UTSW |
6 |
121,651,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:A2m
|
UTSW |
6 |
121,653,909 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5230:A2m
|
UTSW |
6 |
121,651,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:A2m
|
UTSW |
6 |
121,615,375 (GRCm39) |
missense |
probably benign |
0.11 |
R5331:A2m
|
UTSW |
6 |
121,615,375 (GRCm39) |
missense |
probably benign |
0.11 |
R5377:A2m
|
UTSW |
6 |
121,622,212 (GRCm39) |
missense |
probably benign |
|
R5590:A2m
|
UTSW |
6 |
121,653,891 (GRCm39) |
missense |
probably damaging |
1.00 |
R5835:A2m
|
UTSW |
6 |
121,616,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5910:A2m
|
UTSW |
6 |
121,645,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R5915:A2m
|
UTSW |
6 |
121,644,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R5949:A2m
|
UTSW |
6 |
121,655,032 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:A2m
|
UTSW |
6 |
121,647,862 (GRCm39) |
missense |
probably benign |
0.38 |
R5996:A2m
|
UTSW |
6 |
121,636,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R6035:A2m
|
UTSW |
6 |
121,615,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R6035:A2m
|
UTSW |
6 |
121,615,353 (GRCm39) |
missense |
probably damaging |
0.99 |
R6090:A2m
|
UTSW |
6 |
121,624,972 (GRCm39) |
missense |
probably benign |
0.45 |
R6241:A2m
|
UTSW |
6 |
121,623,788 (GRCm39) |
missense |
probably benign |
0.09 |
R6294:A2m
|
UTSW |
6 |
121,631,440 (GRCm39) |
missense |
probably benign |
|
R6492:A2m
|
UTSW |
6 |
121,631,464 (GRCm39) |
missense |
probably benign |
0.35 |
R6554:A2m
|
UTSW |
6 |
121,618,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R6597:A2m
|
UTSW |
6 |
121,625,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R6742:A2m
|
UTSW |
6 |
121,654,995 (GRCm39) |
missense |
probably benign |
0.01 |
R6795:A2m
|
UTSW |
6 |
121,625,281 (GRCm39) |
splice site |
probably null |
|
R6843:A2m
|
UTSW |
6 |
121,615,360 (GRCm39) |
missense |
probably benign |
0.01 |
R7013:A2m
|
UTSW |
6 |
121,618,345 (GRCm39) |
missense |
probably null |
0.00 |
R7137:A2m
|
UTSW |
6 |
121,654,944 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7167:A2m
|
UTSW |
6 |
121,624,930 (GRCm39) |
missense |
probably benign |
|
R7294:A2m
|
UTSW |
6 |
121,650,541 (GRCm39) |
nonsense |
probably null |
|
R7452:A2m
|
UTSW |
6 |
121,618,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7507:A2m
|
UTSW |
6 |
121,652,177 (GRCm39) |
missense |
probably benign |
0.01 |
R7602:A2m
|
UTSW |
6 |
121,647,895 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7602:A2m
|
UTSW |
6 |
121,618,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:A2m
|
UTSW |
6 |
121,637,063 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7766:A2m
|
UTSW |
6 |
121,615,300 (GRCm39) |
missense |
probably benign |
0.08 |
R7921:A2m
|
UTSW |
6 |
121,654,954 (GRCm39) |
missense |
probably benign |
0.00 |
R8007:A2m
|
UTSW |
6 |
121,647,845 (GRCm39) |
intron |
probably benign |
|
R8291:A2m
|
UTSW |
6 |
121,655,017 (GRCm39) |
missense |
probably damaging |
1.00 |
R8542:A2m
|
UTSW |
6 |
121,634,369 (GRCm39) |
missense |
probably benign |
0.03 |
R8856:A2m
|
UTSW |
6 |
121,618,349 (GRCm39) |
missense |
probably benign |
0.00 |
R9154:A2m
|
UTSW |
6 |
121,645,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R9156:A2m
|
UTSW |
6 |
121,647,957 (GRCm39) |
missense |
probably damaging |
0.98 |
R9255:A2m
|
UTSW |
6 |
121,626,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R9269:A2m
|
UTSW |
6 |
121,637,865 (GRCm39) |
missense |
probably benign |
0.38 |
R9325:A2m
|
UTSW |
6 |
121,646,578 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9393:A2m
|
UTSW |
6 |
121,616,270 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9563:A2m
|
UTSW |
6 |
121,645,009 (GRCm39) |
missense |
probably damaging |
0.99 |
X0057:A2m
|
UTSW |
6 |
121,645,135 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:A2m
|
UTSW |
6 |
121,653,039 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:A2m
|
UTSW |
6 |
121,623,835 (GRCm39) |
missense |
probably benign |
|
|