Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700001K19Rik |
A |
G |
12: 110,668,754 |
S117P |
possibly damaging |
Het |
Aars2 |
T |
C |
17: 45,507,510 |
|
probably benign |
Het |
Acot11 |
T |
C |
4: 106,749,988 |
D466G |
probably damaging |
Het |
Adgrd1 |
G |
A |
5: 129,139,594 |
A342T |
probably benign |
Het |
Apbb2 |
A |
T |
5: 66,302,611 |
N714K |
probably benign |
Het |
Aqp12 |
C |
A |
1: 93,006,850 |
H150N |
possibly damaging |
Het |
Brinp3 |
T |
A |
1: 146,682,680 |
L114* |
probably null |
Het |
Ccng2 |
T |
C |
5: 93,271,289 |
|
probably benign |
Het |
Cd36 |
T |
A |
5: 17,798,252 |
R265S |
probably benign |
Het |
Ces4a |
T |
C |
8: 105,141,966 |
L104S |
probably benign |
Het |
Clca4b |
T |
C |
3: 144,922,786 |
I387V |
probably damaging |
Het |
Cul7 |
T |
A |
17: 46,654,595 |
H566Q |
probably benign |
Het |
Ddx60 |
A |
T |
8: 62,033,493 |
H1646L |
possibly damaging |
Het |
Dntt |
T |
C |
19: 41,059,127 |
I503T |
probably damaging |
Het |
Dynlt1a |
T |
G |
17: 6,317,395 |
E2D |
probably benign |
Het |
Efemp2 |
G |
T |
19: 5,477,999 |
C78F |
probably damaging |
Het |
Esco1 |
T |
C |
18: 10,594,605 |
E227G |
probably benign |
Het |
Fezf2 |
T |
A |
14: 12,342,607 |
K419N |
probably damaging |
Het |
Gm17541 |
A |
T |
12: 4,689,487 |
|
probably benign |
Het |
Gm2381 |
G |
A |
7: 42,819,948 |
Q251* |
probably null |
Het |
Gm4782 |
T |
G |
6: 50,610,694 |
S686R |
probably damaging |
Het |
Grin3a |
G |
A |
4: 49,665,501 |
R1045* |
probably null |
Het |
Grm8 |
T |
C |
6: 27,285,896 |
Y839C |
probably damaging |
Het |
Gtf3c1 |
G |
A |
7: 125,644,134 |
P1766L |
possibly damaging |
Het |
Herc2 |
T |
A |
7: 56,206,578 |
H3921Q |
probably damaging |
Het |
Hes6 |
A |
T |
1: 91,412,304 |
D143E |
possibly damaging |
Het |
Hmcn2 |
A |
G |
2: 31,394,827 |
E2055G |
probably benign |
Het |
Hmcn2 |
G |
A |
2: 31,445,353 |
|
probably benign |
Het |
Ikzf3 |
A |
G |
11: 98,467,317 |
L398P |
probably benign |
Het |
Il10ra |
A |
T |
9: 45,265,652 |
I125N |
probably benign |
Het |
Kcnb2 |
G |
A |
1: 15,712,913 |
|
probably benign |
Het |
Krt77 |
T |
C |
15: 101,869,378 |
R81G |
possibly damaging |
Het |
Lrrc40 |
T |
A |
3: 158,041,661 |
|
probably null |
Het |
Man1a2 |
C |
T |
3: 100,582,034 |
R543Q |
probably damaging |
Het |
Mansc1 |
T |
C |
6: 134,610,707 |
D169G |
probably benign |
Het |
Mdn1 |
T |
A |
4: 32,741,835 |
S3869T |
probably damaging |
Het |
Mettl14 |
A |
T |
3: 123,382,826 |
S58T |
probably benign |
Het |
Mrpl4 |
T |
C |
9: 21,003,314 |
V62A |
probably benign |
Het |
Myh3 |
A |
G |
11: 67,093,672 |
D1085G |
possibly damaging |
Het |
Myo5c |
C |
A |
9: 75,284,216 |
|
probably benign |
Het |
Naalad2 |
G |
T |
9: 18,350,943 |
|
probably benign |
Het |
Nat3 |
A |
G |
8: 67,547,780 |
T104A |
probably benign |
Het |
Nek4 |
A |
G |
14: 30,957,296 |
E198G |
probably damaging |
Het |
Olfm1 |
A |
G |
2: 28,229,607 |
Y403C |
probably damaging |
Het |
Olfr1131 |
C |
A |
2: 87,629,282 |
T273K |
possibly damaging |
Het |
Olfr873 |
A |
T |
9: 20,301,158 |
R320S |
probably benign |
Het |
Osbpl1a |
T |
A |
18: 12,871,163 |
|
probably null |
Het |
Pax7 |
G |
A |
4: 139,779,736 |
S330L |
possibly damaging |
Het |
Pcdhb15 |
C |
A |
18: 37,475,276 |
D520E |
probably damaging |
Het |
Pgm3 |
T |
C |
9: 86,567,533 |
T145A |
probably benign |
Het |
Phox2b |
G |
A |
5: 67,096,625 |
|
probably null |
Het |
Pik3r6 |
A |
T |
11: 68,526,408 |
R59* |
probably null |
Het |
Pold1 |
A |
G |
7: 44,541,025 |
|
probably benign |
Het |
Ppp1r21 |
T |
C |
17: 88,569,072 |
|
probably benign |
Het |
Prl5a1 |
A |
G |
13: 28,149,987 |
K158E |
possibly damaging |
Het |
Rag2 |
T |
G |
2: 101,630,603 |
C419W |
probably damaging |
Het |
Reln |
A |
G |
5: 21,988,776 |
S1395P |
probably damaging |
Het |
Retnlb |
T |
G |
16: 48,818,659 |
Y74* |
probably null |
Het |
Robo3 |
A |
G |
9: 37,422,640 |
S633P |
probably damaging |
Het |
Ryr1 |
A |
G |
7: 29,040,679 |
S3941P |
probably damaging |
Het |
Scnn1b |
A |
G |
7: 121,912,475 |
N370S |
probably damaging |
Het |
Slc6a5 |
C |
A |
7: 49,938,408 |
|
probably benign |
Het |
Sort1 |
T |
A |
3: 108,344,931 |
N481K |
probably benign |
Het |
Sptlc3 |
T |
A |
2: 139,596,037 |
I417K |
possibly damaging |
Het |
Svil |
T |
A |
18: 5,099,063 |
|
probably benign |
Het |
Taf4b |
T |
C |
18: 14,813,077 |
|
probably benign |
Het |
Tchp |
T |
C |
5: 114,709,333 |
M71T |
possibly damaging |
Het |
Thsd4 |
T |
A |
9: 59,997,134 |
H233L |
probably benign |
Het |
Tmem217 |
G |
T |
17: 29,526,599 |
N52K |
possibly damaging |
Het |
Tmem38b |
T |
C |
4: 53,840,765 |
L60S |
probably damaging |
Het |
Uqcrfs1 |
A |
C |
13: 30,541,163 |
N131K |
probably benign |
Het |
Vars |
T |
A |
17: 35,013,869 |
S896R |
probably benign |
Het |
Vmn1r170 |
A |
T |
7: 23,606,481 |
M103L |
probably benign |
Het |
Vmn2r22 |
T |
C |
6: 123,637,404 |
Y409C |
probably damaging |
Het |
Wdr49 |
A |
T |
3: 75,451,796 |
I8N |
possibly damaging |
Het |
Zfp648 |
T |
A |
1: 154,204,886 |
Y264N |
probably damaging |
Het |
Zmym1 |
A |
C |
4: 127,048,025 |
F857V |
possibly damaging |
Het |
|