Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcg5 |
T |
C |
17: 84,983,667 (GRCm39) |
D124G |
possibly damaging |
Het |
Ackr3 |
C |
G |
1: 90,141,923 (GRCm39) |
N127K |
probably damaging |
Het |
AL732309.1 |
A |
C |
2: 25,136,151 (GRCm39) |
M21R |
possibly damaging |
Het |
Ankrd52 |
C |
A |
10: 128,222,032 (GRCm39) |
T552K |
possibly damaging |
Het |
Arhgap28 |
T |
C |
17: 68,202,879 (GRCm39) |
|
probably null |
Het |
Arid5b |
A |
T |
10: 67,964,752 (GRCm39) |
N306K |
probably benign |
Het |
C1qtnf3 |
A |
C |
15: 10,952,707 (GRCm39) |
K56N |
probably benign |
Het |
C2 |
C |
T |
17: 35,100,664 (GRCm39) |
G52D |
probably benign |
Het |
Casz1 |
C |
T |
4: 149,031,490 (GRCm39) |
T1247M |
probably damaging |
Het |
Cc2d2b |
A |
G |
19: 40,797,552 (GRCm39) |
D778G |
unknown |
Het |
Cdh5 |
A |
G |
8: 104,869,425 (GRCm39) |
D717G |
probably damaging |
Het |
Clca3a2 |
G |
A |
3: 144,514,372 (GRCm39) |
A445V |
probably damaging |
Het |
Clca3b |
T |
A |
3: 144,547,181 (GRCm39) |
M319L |
possibly damaging |
Het |
Csmd1 |
G |
A |
8: 16,108,721 (GRCm39) |
S1894L |
probably damaging |
Het |
Csnk1g3 |
A |
G |
18: 54,052,090 (GRCm39) |
T220A |
probably damaging |
Het |
Cyp2d10 |
T |
G |
15: 82,287,961 (GRCm39) |
T381P |
probably damaging |
Het |
Ddb2 |
G |
A |
2: 91,067,229 (GRCm39) |
|
probably benign |
Het |
Ddx24 |
C |
A |
12: 103,382,518 (GRCm39) |
L688F |
probably damaging |
Het |
Dennd4c |
T |
C |
4: 86,747,975 (GRCm39) |
L1615P |
unknown |
Het |
Dnah8 |
T |
A |
17: 31,003,099 (GRCm39) |
D3599E |
probably benign |
Het |
Dst |
T |
C |
1: 34,045,305 (GRCm39) |
S13P |
possibly damaging |
Het |
Efcab12 |
T |
C |
6: 115,800,555 (GRCm39) |
D156G |
probably benign |
Het |
Enpp2 |
A |
G |
15: 54,741,170 (GRCm39) |
|
probably null |
Het |
Ephx2 |
A |
G |
14: 66,322,803 (GRCm39) |
V490A |
probably damaging |
Het |
Etnppl |
A |
G |
3: 130,423,224 (GRCm39) |
N308D |
probably damaging |
Het |
F5 |
TCAGAAGACCTCCTCCCCAGACCTGGGCCAGGTGCCCCTTTCTCCAGATGACAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGTCCCTTTCTCCAGATGATAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCTAGATGACAACCAGAAGACGACCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCCAGATGACAACCAGA |
TCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGTCCCTTTCTCCAGATGATAACCAGAAGACCTCCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCTAGATGACAACCAGAAGACGACCTCCCCAGACCTGGGTCAGGTGCCCCTTTCTCCAGATGACAACCAGA |
1: 164,021,150 (GRCm39) |
|
probably benign |
Het |
Fam162b |
A |
T |
10: 51,466,282 (GRCm39) |
|
probably null |
Het |
Fancl |
A |
G |
11: 26,353,362 (GRCm39) |
E86G |
probably damaging |
Het |
Flii |
G |
A |
11: 60,609,866 (GRCm39) |
T615I |
probably benign |
Het |
Fndc7 |
G |
T |
3: 108,779,537 (GRCm39) |
Q336K |
probably benign |
Het |
Gm26661 |
T |
C |
14: 7,791,911 (GRCm38) |
C109R |
unknown |
Het |
H2-DMb1 |
T |
C |
17: 34,378,436 (GRCm39) |
|
probably null |
Het |
H2-T10 |
C |
T |
17: 36,430,189 (GRCm39) |
G251R |
probably damaging |
Het |
Harbi1 |
T |
C |
2: 91,551,044 (GRCm39) |
I339T |
probably benign |
Het |
Hsp90aa1 |
A |
G |
12: 110,661,659 (GRCm39) |
M119T |
unknown |
Het |
Ighe |
T |
A |
12: 113,235,954 (GRCm39) |
Y124F |
|
Het |
Ighv7-1 |
T |
C |
12: 113,860,149 (GRCm39) |
Y81C |
probably damaging |
Het |
Ilkap |
A |
T |
1: 91,313,115 (GRCm39) |
|
probably null |
Het |
Inpp5a |
A |
G |
7: 139,105,586 (GRCm39) |
D179G |
probably damaging |
Het |
Itgad |
A |
T |
7: 127,788,979 (GRCm39) |
D510V |
probably damaging |
Het |
Kcnn2 |
A |
T |
18: 45,693,138 (GRCm39) |
H238L |
probably benign |
Het |
Kctd17 |
T |
A |
15: 78,319,842 (GRCm39) |
C189S |
probably damaging |
Het |
Larp4b |
C |
A |
13: 9,208,616 (GRCm39) |
A423E |
probably benign |
Het |
Llgl2 |
A |
G |
11: 115,741,556 (GRCm39) |
E562G |
possibly damaging |
Het |
Macf1 |
T |
C |
4: 123,268,218 (GRCm39) |
T6734A |
probably benign |
Het |
Maz |
G |
A |
7: 126,623,765 (GRCm39) |
T377M |
probably damaging |
Het |
Mmrn1 |
G |
T |
6: 60,921,917 (GRCm39) |
G125* |
probably null |
Het |
Mvp |
A |
G |
7: 126,592,781 (GRCm39) |
S377P |
probably benign |
Het |
Nin |
C |
T |
12: 70,090,508 (GRCm39) |
R969Q |
|
Het |
Nod2 |
T |
A |
8: 89,379,694 (GRCm39) |
V65D |
probably damaging |
Het |
Opa1 |
A |
T |
16: 29,405,799 (GRCm39) |
E121D |
probably benign |
Het |
Or10w3 |
C |
T |
19: 13,704,270 (GRCm39) |
A215V |
probably benign |
Het |
Or1r1 |
A |
G |
11: 73,874,669 (GRCm39) |
V255A |
probably benign |
Het |
Or2n1c |
T |
C |
17: 38,519,607 (GRCm39) |
V157A |
probably benign |
Het |
Or4a76 |
A |
T |
2: 89,460,447 (GRCm39) |
I265N |
possibly damaging |
Het |
Or5ac21 |
T |
C |
16: 59,123,611 (GRCm39) |
F32L |
probably benign |
Het |
Or5b123 |
A |
G |
19: 13,596,942 (GRCm39) |
I96V |
probably benign |
Het |
Or6c88 |
T |
A |
10: 129,406,718 (GRCm39) |
S65T |
probably damaging |
Het |
Or7e174 |
A |
T |
9: 20,012,726 (GRCm39) |
I224F |
possibly damaging |
Het |
Osbpl2 |
A |
G |
2: 179,791,994 (GRCm39) |
T233A |
probably benign |
Het |
Pcp4l1 |
G |
A |
1: 171,002,034 (GRCm39) |
A42V |
possibly damaging |
Het |
Plekhh3 |
T |
A |
11: 101,061,600 (GRCm39) |
D38V |
possibly damaging |
Het |
Prtg |
C |
T |
9: 72,798,122 (GRCm39) |
A696V |
probably damaging |
Het |
Ptpn14 |
T |
G |
1: 189,595,621 (GRCm39) |
V748G |
possibly damaging |
Het |
Reg2 |
A |
T |
6: 78,383,137 (GRCm39) |
D28V |
probably benign |
Het |
Rhpn1 |
A |
T |
15: 75,576,246 (GRCm39) |
I2F |
possibly damaging |
Het |
Rundc3a |
A |
G |
11: 102,290,799 (GRCm39) |
E294G |
possibly damaging |
Het |
Scara3 |
T |
A |
14: 66,168,865 (GRCm39) |
I251L |
probably benign |
Het |
Slc23a2 |
G |
A |
2: 131,931,043 (GRCm39) |
T152I |
probably damaging |
Het |
Slc39a2 |
T |
G |
14: 52,131,650 (GRCm39) |
S74A |
possibly damaging |
Het |
Tmprss15 |
T |
C |
16: 78,758,907 (GRCm39) |
Y937C |
probably damaging |
Het |
Tpp2 |
T |
C |
1: 44,017,938 (GRCm39) |
L779S |
probably damaging |
Het |
Tssk2 |
T |
C |
16: 17,717,227 (GRCm39) |
V210A |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,725,937 (GRCm39) |
T6100S |
unknown |
Het |
Tufm |
G |
A |
7: 126,088,759 (GRCm39) |
E317K |
possibly damaging |
Het |
Vinac1 |
T |
C |
2: 128,879,772 (GRCm39) |
D718G |
unknown |
Het |
Wdfy4 |
A |
G |
14: 32,769,271 (GRCm39) |
S2219P |
|
Het |
Wtap |
T |
C |
17: 13,199,833 (GRCm39) |
N50S |
possibly damaging |
Het |
|
Other mutations in Nktr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01333:Nktr
|
APN |
9 |
121,560,630 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01402:Nktr
|
APN |
9 |
121,570,218 (GRCm39) |
splice site |
probably null |
|
IGL01404:Nktr
|
APN |
9 |
121,570,218 (GRCm39) |
splice site |
probably null |
|
IGL02945:Nktr
|
APN |
9 |
121,557,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03334:Nktr
|
APN |
9 |
121,577,242 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03134:Nktr
|
UTSW |
9 |
121,575,532 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4131001:Nktr
|
UTSW |
9 |
121,570,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Nktr
|
UTSW |
9 |
121,570,232 (GRCm39) |
splice site |
probably benign |
|
R0158:Nktr
|
UTSW |
9 |
121,579,757 (GRCm39) |
unclassified |
probably benign |
|
R0399:Nktr
|
UTSW |
9 |
121,560,550 (GRCm39) |
missense |
probably damaging |
0.98 |
R0503:Nktr
|
UTSW |
9 |
121,579,806 (GRCm39) |
unclassified |
probably benign |
|
R0585:Nktr
|
UTSW |
9 |
121,583,346 (GRCm39) |
utr 3 prime |
probably benign |
|
R0606:Nktr
|
UTSW |
9 |
121,578,356 (GRCm39) |
unclassified |
probably benign |
|
R1248:Nktr
|
UTSW |
9 |
121,556,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R1899:Nktr
|
UTSW |
9 |
121,577,932 (GRCm39) |
unclassified |
probably benign |
|
R1912:Nktr
|
UTSW |
9 |
121,579,306 (GRCm39) |
unclassified |
probably benign |
|
R2049:Nktr
|
UTSW |
9 |
121,570,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R2279:Nktr
|
UTSW |
9 |
121,560,603 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2912:Nktr
|
UTSW |
9 |
121,578,670 (GRCm39) |
unclassified |
probably benign |
|
R2913:Nktr
|
UTSW |
9 |
121,578,670 (GRCm39) |
unclassified |
probably benign |
|
R2914:Nktr
|
UTSW |
9 |
121,578,670 (GRCm39) |
unclassified |
probably benign |
|
R3939:Nktr
|
UTSW |
9 |
121,578,135 (GRCm39) |
unclassified |
probably benign |
|
R4080:Nktr
|
UTSW |
9 |
121,570,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R4471:Nktr
|
UTSW |
9 |
121,577,962 (GRCm39) |
unclassified |
probably benign |
|
R4472:Nktr
|
UTSW |
9 |
121,577,962 (GRCm39) |
unclassified |
probably benign |
|
R4506:Nktr
|
UTSW |
9 |
121,577,949 (GRCm39) |
unclassified |
probably benign |
|
R4556:Nktr
|
UTSW |
9 |
121,570,189 (GRCm39) |
missense |
probably damaging |
0.98 |
R4736:Nktr
|
UTSW |
9 |
121,578,805 (GRCm39) |
unclassified |
probably benign |
|
R4749:Nktr
|
UTSW |
9 |
121,570,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4943:Nktr
|
UTSW |
9 |
121,549,020 (GRCm39) |
intron |
probably benign |
|
R5084:Nktr
|
UTSW |
9 |
121,577,176 (GRCm39) |
missense |
possibly damaging |
0.86 |
R5250:Nktr
|
UTSW |
9 |
121,578,858 (GRCm39) |
unclassified |
probably benign |
|
R5288:Nktr
|
UTSW |
9 |
121,577,659 (GRCm39) |
missense |
probably benign |
0.23 |
R5324:Nktr
|
UTSW |
9 |
121,556,412 (GRCm39) |
missense |
probably damaging |
1.00 |
R5330:Nktr
|
UTSW |
9 |
121,581,834 (GRCm39) |
intron |
probably benign |
|
R5331:Nktr
|
UTSW |
9 |
121,581,834 (GRCm39) |
intron |
probably benign |
|
R5502:Nktr
|
UTSW |
9 |
121,577,672 (GRCm39) |
unclassified |
probably benign |
|
R5587:Nktr
|
UTSW |
9 |
121,577,555 (GRCm39) |
unclassified |
probably benign |
|
R5664:Nktr
|
UTSW |
9 |
121,578,483 (GRCm39) |
nonsense |
probably null |
|
R6005:Nktr
|
UTSW |
9 |
121,577,460 (GRCm39) |
unclassified |
probably benign |
|
R6057:Nktr
|
UTSW |
9 |
121,577,455 (GRCm39) |
unclassified |
probably benign |
|
R6083:Nktr
|
UTSW |
9 |
121,579,202 (GRCm39) |
unclassified |
probably benign |
|
R6274:Nktr
|
UTSW |
9 |
121,560,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6445:Nktr
|
UTSW |
9 |
121,577,480 (GRCm39) |
unclassified |
probably benign |
|
R6467:Nktr
|
UTSW |
9 |
121,560,585 (GRCm39) |
missense |
probably damaging |
1.00 |
R6911:Nktr
|
UTSW |
9 |
121,583,392 (GRCm39) |
nonsense |
probably null |
|
R6960:Nktr
|
UTSW |
9 |
121,571,758 (GRCm39) |
missense |
probably damaging |
0.99 |
R7226:Nktr
|
UTSW |
9 |
121,575,599 (GRCm39) |
missense |
probably damaging |
0.99 |
R7324:Nktr
|
UTSW |
9 |
121,556,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R7451:Nktr
|
UTSW |
9 |
121,558,722 (GRCm39) |
missense |
probably damaging |
0.99 |
R7464:Nktr
|
UTSW |
9 |
121,579,393 (GRCm39) |
missense |
unknown |
|
R7537:Nktr
|
UTSW |
9 |
121,578,345 (GRCm39) |
missense |
unknown |
|
R8126:Nktr
|
UTSW |
9 |
121,575,514 (GRCm39) |
missense |
probably damaging |
1.00 |
R8163:Nktr
|
UTSW |
9 |
121,579,929 (GRCm39) |
unclassified |
probably benign |
|
R8812:Nktr
|
UTSW |
9 |
121,579,317 (GRCm39) |
missense |
unknown |
|
R8829:Nktr
|
UTSW |
9 |
121,583,330 (GRCm39) |
missense |
unknown |
|
R8945:Nktr
|
UTSW |
9 |
121,575,558 (GRCm39) |
missense |
possibly damaging |
0.70 |
R9158:Nktr
|
UTSW |
9 |
121,582,154 (GRCm39) |
missense |
unknown |
|
R9252:Nktr
|
UTSW |
9 |
121,579,415 (GRCm39) |
missense |
unknown |
|
R9378:Nktr
|
UTSW |
9 |
121,577,264 (GRCm39) |
missense |
probably damaging |
1.00 |
|