Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adtrp |
A |
T |
13: 41,828,146 |
N82K |
probably damaging |
Het |
Ankrd36 |
T |
A |
11: 5,628,906 |
S57T |
possibly damaging |
Het |
Aoc3 |
A |
G |
11: 101,331,817 |
N293S |
probably benign |
Het |
Aup1 |
A |
T |
6: 83,056,621 |
H302L |
probably damaging |
Het |
Bptf |
G |
A |
11: 107,040,380 |
R277W |
probably damaging |
Het |
Cald1 |
A |
G |
6: 34,758,011 |
I346V |
unknown |
Het |
Cd44 |
T |
C |
2: 102,834,300 |
T519A |
possibly damaging |
Het |
Cela1 |
A |
G |
15: 100,682,885 |
|
probably null |
Het |
Ces2g |
T |
C |
8: 104,962,563 |
V57A |
possibly damaging |
Het |
Cpt1b |
G |
C |
15: 89,424,425 |
T100S |
probably benign |
Het |
D6Wsu163e |
A |
T |
6: 126,955,896 |
I361F |
possibly damaging |
Het |
Dock5 |
A |
T |
14: 67,846,000 |
D153E |
possibly damaging |
Het |
Dync2h1 |
G |
T |
9: 7,168,326 |
R430S |
probably damaging |
Het |
Eml5 |
C |
T |
12: 98,815,959 |
G1405R |
probably damaging |
Het |
Ergic2 |
G |
A |
6: 148,201,477 |
A91V |
probably damaging |
Het |
Fancl |
A |
T |
11: 26,469,754 |
I336L |
probably benign |
Het |
Fpr3 |
A |
G |
17: 17,970,961 |
T165A |
possibly damaging |
Het |
Gm11639 |
T |
A |
11: 104,804,274 |
F1730L |
probably benign |
Het |
Gon4l |
A |
G |
3: 88,899,984 |
I1662V |
possibly damaging |
Het |
Gpr153 |
C |
T |
4: 152,279,101 |
|
probably benign |
Het |
Hdac4 |
C |
A |
1: 91,947,517 |
A911S |
probably damaging |
Het |
Ighd |
T |
C |
12: 113,414,563 |
N139D |
|
Het |
Klhl22 |
T |
A |
16: 17,771,826 |
L117Q |
probably damaging |
Het |
Kntc1 |
A |
G |
5: 123,790,117 |
S1226G |
probably benign |
Het |
Lama5 |
A |
T |
2: 180,186,688 |
C2126S |
probably damaging |
Het |
Ldlr |
A |
G |
9: 21,739,689 |
I468V |
probably benign |
Het |
Lmtk3 |
G |
A |
7: 45,798,288 |
A1253T |
unknown |
Het |
Lta |
T |
A |
17: 35,204,069 |
N93Y |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,509,770 |
|
probably null |
Het |
Mink1 |
A |
G |
11: 70,610,076 |
|
probably null |
Het |
Myl10 |
G |
C |
5: 136,697,971 |
V70L |
probably benign |
Het |
Ntpcr |
A |
G |
8: 125,745,335 |
M132V |
probably benign |
Het |
Olfr298 |
A |
G |
7: 86,488,853 |
S233P |
probably damaging |
Het |
Olfr664 |
A |
G |
7: 104,733,908 |
M152T |
probably benign |
Het |
Olfr851 |
T |
C |
9: 19,496,802 |
I18T |
probably benign |
Het |
Padi2 |
A |
G |
4: 140,933,279 |
I357V |
probably benign |
Het |
Pax7 |
G |
T |
4: 139,779,609 |
H372Q |
probably benign |
Het |
Paxip1 |
A |
G |
5: 27,744,543 |
Y966H |
probably damaging |
Het |
Pde4b |
A |
C |
4: 102,555,625 |
D199A |
probably null |
Het |
Pkd1l2 |
T |
C |
8: 117,065,572 |
N494D |
probably benign |
Het |
Prdm2 |
G |
T |
4: 143,136,010 |
Q237K |
probably benign |
Het |
Prune2 |
T |
C |
19: 17,120,405 |
L1091P |
probably damaging |
Het |
Rab9 |
C |
T |
X: 166,457,758 |
D186N |
probably benign |
Het |
Rassf5 |
A |
G |
1: 131,178,527 |
*414Q |
probably null |
Het |
Repin1 |
G |
T |
6: 48,597,345 |
E403* |
probably null |
Het |
Rrp9 |
C |
A |
9: 106,483,189 |
T238K |
probably benign |
Het |
Slc44a2 |
A |
G |
9: 21,348,586 |
D630G |
probably benign |
Het |
Slc7a9 |
A |
G |
7: 35,457,018 |
D295G |
probably benign |
Het |
Slco3a1 |
A |
T |
7: 74,284,306 |
M706K |
possibly damaging |
Het |
Spag9 |
T |
C |
11: 94,071,688 |
|
probably null |
Het |
Stam2 |
A |
T |
2: 52,700,168 |
Y394N |
probably damaging |
Het |
Steap3 |
A |
T |
1: 120,243,894 |
H160Q |
probably damaging |
Het |
Stxbp5l |
A |
T |
16: 37,241,447 |
C334S |
probably benign |
Het |
Tcof1 |
G |
C |
18: 60,829,051 |
A702G |
possibly damaging |
Het |
Thap1 |
CAGCATCTGCTCGGAGCA |
CAGCA |
8: 26,160,856 |
|
probably null |
Het |
Tmem74 |
A |
T |
15: 43,868,060 |
|
probably benign |
Het |
Ttn |
T |
C |
2: 76,707,136 |
K34816R |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,797,391 |
N14736I |
probably damaging |
Het |
Vmn1r183 |
A |
G |
7: 24,055,465 |
Q231R |
possibly damaging |
Het |
Vmn1r235 |
A |
G |
17: 21,262,177 |
T255A |
probably damaging |
Het |
Wasl |
A |
T |
6: 24,619,210 |
I437K |
unknown |
Het |
Wdr34 |
T |
A |
2: 30,032,208 |
T414S |
possibly damaging |
Het |
Ywhae |
A |
G |
11: 75,751,943 |
N43D |
probably damaging |
Het |
Zfp583 |
A |
T |
7: 6,317,211 |
Y267* |
probably null |
Het |
Zfp608 |
C |
T |
18: 54,988,000 |
G172R |
probably benign |
Het |
|