Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
T |
A |
12: 55,107,957 (GRCm39) |
T81S |
possibly damaging |
Het |
Ablim2 |
C |
T |
5: 36,030,518 (GRCm39) |
A581V |
possibly damaging |
Het |
Acbd5 |
T |
A |
2: 22,979,710 (GRCm39) |
S210T |
probably benign |
Het |
Adam10 |
T |
A |
9: 70,655,505 (GRCm39) |
F324L |
probably damaging |
Het |
Ak6 |
A |
G |
13: 100,791,857 (GRCm39) |
N100S |
possibly damaging |
Het |
Angptl3 |
G |
T |
4: 98,925,759 (GRCm39) |
V362L |
probably benign |
Het |
Ano9 |
C |
A |
7: 140,684,220 (GRCm39) |
W514L |
probably benign |
Het |
Asb8 |
T |
C |
15: 98,034,108 (GRCm39) |
Y149C |
probably damaging |
Het |
Bcl6b |
C |
A |
11: 70,117,447 (GRCm39) |
A392S |
probably damaging |
Het |
Cad |
T |
A |
5: 31,232,500 (GRCm39) |
I1855N |
possibly damaging |
Het |
Calm5 |
G |
A |
13: 3,904,277 (GRCm39) |
G4R |
probably damaging |
Het |
Carm1 |
T |
C |
9: 21,480,808 (GRCm39) |
V94A |
probably damaging |
Het |
Ccnl1 |
A |
T |
3: 65,855,165 (GRCm39) |
S399R |
possibly damaging |
Het |
Cdh17 |
T |
A |
4: 11,783,163 (GRCm39) |
I168N |
probably benign |
Het |
Ces2g |
C |
T |
8: 105,693,605 (GRCm39) |
R429C |
probably benign |
Het |
Chd3 |
T |
C |
11: 69,246,648 (GRCm39) |
|
probably benign |
Het |
Cmtr2 |
T |
A |
8: 110,948,977 (GRCm39) |
M429K |
probably benign |
Het |
Cnga1 |
T |
G |
5: 72,761,835 (GRCm39) |
I560L |
probably benign |
Het |
Col6a5 |
A |
G |
9: 105,759,796 (GRCm39) |
Y1975H |
probably damaging |
Het |
Copb1 |
T |
C |
7: 113,849,463 (GRCm39) |
I47V |
probably benign |
Het |
Crbn |
G |
A |
6: 106,777,010 (GRCm39) |
|
probably benign |
Het |
Ddx41 |
A |
G |
13: 55,680,939 (GRCm39) |
L324P |
probably damaging |
Het |
Dhx57 |
A |
G |
17: 80,577,794 (GRCm39) |
|
probably benign |
Het |
Dlgap2 |
A |
T |
8: 14,793,430 (GRCm39) |
I475F |
probably benign |
Het |
Dock2 |
T |
A |
11: 34,618,287 (GRCm39) |
K110* |
probably null |
Het |
Dpp7 |
T |
C |
2: 25,245,645 (GRCm39) |
D147G |
probably damaging |
Het |
Dync2h1 |
G |
T |
9: 7,075,824 (GRCm39) |
D3014E |
probably damaging |
Het |
Efcab5 |
A |
T |
11: 76,994,115 (GRCm39) |
F1291I |
probably damaging |
Het |
Endov |
T |
A |
11: 119,382,736 (GRCm39) |
V61D |
probably benign |
Het |
Etv3 |
C |
A |
3: 87,443,786 (GRCm39) |
P457T |
possibly damaging |
Het |
Fam185a |
T |
A |
5: 21,638,766 (GRCm39) |
H199Q |
probably benign |
Het |
Fat3 |
T |
A |
9: 15,878,397 (GRCm39) |
E3361D |
probably benign |
Het |
Fbn1 |
T |
C |
2: 125,186,015 (GRCm39) |
|
probably benign |
Het |
Gm17079 |
A |
T |
14: 51,932,787 (GRCm39) |
W37R |
|
Het |
Gpr68 |
T |
C |
12: 100,845,292 (GRCm39) |
H84R |
probably benign |
Het |
Gramd1b |
A |
T |
9: 40,215,674 (GRCm39) |
S725R |
probably damaging |
Het |
Greb1 |
T |
A |
12: 16,746,548 (GRCm39) |
T1241S |
probably benign |
Het |
Hcn4 |
T |
C |
9: 58,751,193 (GRCm39) |
M273T |
probably benign |
Het |
Hdlbp |
A |
G |
1: 93,341,640 (GRCm39) |
V973A |
probably damaging |
Het |
Ighv8-11 |
A |
T |
12: 115,531,164 (GRCm39) |
|
probably benign |
Het |
Itpkb |
A |
T |
1: 180,249,346 (GRCm39) |
Q907L |
probably benign |
Het |
Lmo7 |
T |
A |
14: 102,168,644 (GRCm39) |
N1634K |
unknown |
Het |
Lrrk1 |
C |
A |
7: 65,952,477 (GRCm39) |
L486F |
probably benign |
Het |
Mdfic |
G |
A |
6: 15,799,653 (GRCm39) |
C260Y |
probably damaging |
Het |
Mdh2 |
T |
C |
5: 135,814,882 (GRCm39) |
I140T |
probably benign |
Het |
Or1j14 |
T |
C |
2: 36,418,207 (GRCm39) |
V261A |
probably benign |
Het |
Or51d1 |
C |
A |
7: 102,348,028 (GRCm39) |
D194E |
probably damaging |
Het |
Or52n3 |
T |
C |
7: 104,530,762 (GRCm39) |
Y283H |
probably damaging |
Het |
P2rx2 |
C |
T |
5: 110,490,380 (GRCm39) |
V112I |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,787,319 (GRCm39) |
V1038E |
probably benign |
Het |
Rab25 |
T |
A |
3: 88,452,388 (GRCm39) |
R73S |
probably damaging |
Het |
Rab8a |
TA |
TAA |
8: 72,925,130 (GRCm39) |
|
probably null |
Het |
Rnf213 |
T |
C |
11: 119,308,955 (GRCm39) |
Y729H |
|
Het |
Rnf213 |
A |
G |
11: 119,332,038 (GRCm39) |
T2417A |
|
Het |
Rnft2 |
C |
A |
5: 118,366,935 (GRCm39) |
A268S |
probably benign |
Het |
Samhd1 |
T |
C |
2: 156,971,794 (GRCm39) |
D116G |
probably benign |
Het |
Sema6d |
T |
A |
2: 124,506,937 (GRCm39) |
V915E |
probably benign |
Het |
Sp140l2 |
G |
A |
1: 85,235,170 (GRCm39) |
H130Y |
probably benign |
Het |
Srcin1 |
C |
A |
11: 97,414,368 (GRCm39) |
R1045L |
probably damaging |
Het |
St18 |
T |
A |
1: 6,872,788 (GRCm39) |
N174K |
probably benign |
Het |
Stac3 |
G |
A |
10: 127,339,494 (GRCm39) |
C130Y |
probably damaging |
Het |
Stum |
G |
C |
1: 180,310,740 (GRCm39) |
P52R |
probably damaging |
Het |
Tbc1d2 |
C |
T |
4: 46,615,106 (GRCm39) |
E526K |
possibly damaging |
Het |
Tiam1 |
A |
G |
16: 89,694,900 (GRCm39) |
S186P |
probably damaging |
Het |
Tiparp |
G |
C |
3: 65,460,963 (GRCm39) |
V651L |
probably benign |
Het |
Tmem19 |
C |
T |
10: 115,179,765 (GRCm39) |
G244S |
probably damaging |
Het |
Trip11 |
A |
T |
12: 101,839,656 (GRCm39) |
V1658D |
possibly damaging |
Het |
Ttyh3 |
A |
C |
5: 140,612,944 (GRCm39) |
Y453D |
probably damaging |
Het |
Ttyh3 |
G |
T |
5: 140,612,945 (GRCm39) |
S452R |
probably benign |
Het |
Ube2h |
C |
T |
6: 30,262,338 (GRCm39) |
|
probably benign |
Het |
Zbtb4 |
T |
C |
11: 69,667,618 (GRCm39) |
S308P |
probably damaging |
Het |
Zfyve1 |
T |
C |
12: 83,597,681 (GRCm39) |
E672G |
probably damaging |
Het |
Zswim5 |
G |
A |
4: 116,842,002 (GRCm39) |
D861N |
probably damaging |
Het |
|
Other mutations in Myo9a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00427:Myo9a
|
APN |
9 |
59,750,342 (GRCm39) |
splice site |
probably benign |
|
IGL00510:Myo9a
|
APN |
9 |
59,739,464 (GRCm39) |
splice site |
probably benign |
|
IGL00710:Myo9a
|
APN |
9 |
59,782,594 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00963:Myo9a
|
APN |
9 |
59,807,655 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01087:Myo9a
|
APN |
9 |
59,697,361 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL01145:Myo9a
|
APN |
9 |
59,762,658 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01403:Myo9a
|
APN |
9 |
59,778,846 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01528:Myo9a
|
APN |
9 |
59,686,957 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01608:Myo9a
|
APN |
9 |
59,778,119 (GRCm39) |
nonsense |
probably null |
|
IGL01701:Myo9a
|
APN |
9 |
59,791,877 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01918:Myo9a
|
APN |
9 |
59,686,985 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02026:Myo9a
|
APN |
9 |
59,813,245 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02139:Myo9a
|
APN |
9 |
59,687,275 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02176:Myo9a
|
APN |
9 |
59,777,836 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02272:Myo9a
|
APN |
9 |
59,791,883 (GRCm39) |
splice site |
probably benign |
|
IGL02283:Myo9a
|
APN |
9 |
59,778,956 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02499:Myo9a
|
APN |
9 |
59,722,669 (GRCm39) |
splice site |
probably benign |
|
IGL02652:Myo9a
|
APN |
9 |
59,771,211 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02666:Myo9a
|
APN |
9 |
59,832,187 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02878:Myo9a
|
APN |
9 |
59,815,583 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02982:Myo9a
|
APN |
9 |
59,815,491 (GRCm39) |
nonsense |
probably null |
|
IGL03072:Myo9a
|
APN |
9 |
59,716,725 (GRCm39) |
missense |
possibly damaging |
0.83 |
IGL03090:Myo9a
|
APN |
9 |
59,801,418 (GRCm39) |
splice site |
probably benign |
|
IGL03111:Myo9a
|
APN |
9 |
59,734,526 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03389:Myo9a
|
APN |
9 |
59,776,890 (GRCm39) |
missense |
probably damaging |
1.00 |
essentials
|
UTSW |
9 |
59,802,149 (GRCm39) |
missense |
probably benign |
0.09 |
necessities
|
UTSW |
9 |
59,722,617 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4402001:Myo9a
|
UTSW |
9 |
59,777,719 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0013:Myo9a
|
UTSW |
9 |
59,767,489 (GRCm39) |
splice site |
probably benign |
|
R0013:Myo9a
|
UTSW |
9 |
59,767,489 (GRCm39) |
splice site |
probably benign |
|
R0018:Myo9a
|
UTSW |
9 |
59,779,007 (GRCm39) |
missense |
probably benign |
0.00 |
R0018:Myo9a
|
UTSW |
9 |
59,779,007 (GRCm39) |
missense |
probably benign |
0.00 |
R0329:Myo9a
|
UTSW |
9 |
59,830,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R0423:Myo9a
|
UTSW |
9 |
59,802,619 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Myo9a
|
UTSW |
9 |
59,801,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R0607:Myo9a
|
UTSW |
9 |
59,829,076 (GRCm39) |
missense |
probably benign |
0.02 |
R0652:Myo9a
|
UTSW |
9 |
59,779,209 (GRCm39) |
missense |
probably benign |
|
R0653:Myo9a
|
UTSW |
9 |
59,832,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R0723:Myo9a
|
UTSW |
9 |
59,778,383 (GRCm39) |
missense |
probably benign |
0.01 |
R0784:Myo9a
|
UTSW |
9 |
59,803,828 (GRCm39) |
splice site |
probably benign |
|
R0842:Myo9a
|
UTSW |
9 |
59,778,350 (GRCm39) |
missense |
probably benign |
0.02 |
R1055:Myo9a
|
UTSW |
9 |
59,762,653 (GRCm39) |
missense |
probably benign |
0.01 |
R1056:Myo9a
|
UTSW |
9 |
59,739,484 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1195:Myo9a
|
UTSW |
9 |
59,802,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R1615:Myo9a
|
UTSW |
9 |
59,695,739 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1698:Myo9a
|
UTSW |
9 |
59,775,464 (GRCm39) |
missense |
probably benign |
0.05 |
R1715:Myo9a
|
UTSW |
9 |
59,739,583 (GRCm39) |
missense |
probably damaging |
0.99 |
R1981:Myo9a
|
UTSW |
9 |
59,801,429 (GRCm39) |
missense |
probably benign |
|
R2228:Myo9a
|
UTSW |
9 |
59,801,463 (GRCm39) |
missense |
probably benign |
0.06 |
R2272:Myo9a
|
UTSW |
9 |
59,722,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R2327:Myo9a
|
UTSW |
9 |
59,687,048 (GRCm39) |
missense |
probably benign |
0.11 |
R2990:Myo9a
|
UTSW |
9 |
59,832,172 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3161:Myo9a
|
UTSW |
9 |
59,739,598 (GRCm39) |
splice site |
probably benign |
|
R3721:Myo9a
|
UTSW |
9 |
59,775,463 (GRCm39) |
missense |
probably benign |
|
R3928:Myo9a
|
UTSW |
9 |
59,802,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R4197:Myo9a
|
UTSW |
9 |
59,802,149 (GRCm39) |
missense |
probably benign |
0.09 |
R4212:Myo9a
|
UTSW |
9 |
59,813,349 (GRCm39) |
nonsense |
probably null |
|
R4610:Myo9a
|
UTSW |
9 |
59,779,165 (GRCm39) |
missense |
probably benign |
|
R4616:Myo9a
|
UTSW |
9 |
59,728,932 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Myo9a
|
UTSW |
9 |
59,778,355 (GRCm39) |
missense |
probably benign |
0.00 |
R4623:Myo9a
|
UTSW |
9 |
59,778,355 (GRCm39) |
missense |
probably benign |
0.00 |
R4632:Myo9a
|
UTSW |
9 |
59,776,947 (GRCm39) |
missense |
probably benign |
0.00 |
R4657:Myo9a
|
UTSW |
9 |
59,782,699 (GRCm39) |
critical splice donor site |
probably null |
|
R4892:Myo9a
|
UTSW |
9 |
59,731,525 (GRCm39) |
missense |
probably damaging |
0.98 |
R4897:Myo9a
|
UTSW |
9 |
59,803,800 (GRCm39) |
missense |
probably benign |
0.07 |
R4966:Myo9a
|
UTSW |
9 |
59,779,017 (GRCm39) |
missense |
probably benign |
0.00 |
R4993:Myo9a
|
UTSW |
9 |
59,768,755 (GRCm39) |
nonsense |
probably null |
|
R5160:Myo9a
|
UTSW |
9 |
59,779,085 (GRCm39) |
missense |
probably benign |
0.24 |
R5233:Myo9a
|
UTSW |
9 |
59,817,900 (GRCm39) |
missense |
probably damaging |
1.00 |
R5271:Myo9a
|
UTSW |
9 |
59,814,665 (GRCm39) |
missense |
probably damaging |
1.00 |
R5308:Myo9a
|
UTSW |
9 |
59,771,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R5367:Myo9a
|
UTSW |
9 |
59,807,732 (GRCm39) |
missense |
probably damaging |
0.96 |
R5432:Myo9a
|
UTSW |
9 |
59,772,953 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5459:Myo9a
|
UTSW |
9 |
59,791,803 (GRCm39) |
missense |
probably damaging |
0.98 |
R5511:Myo9a
|
UTSW |
9 |
59,687,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R5568:Myo9a
|
UTSW |
9 |
59,781,911 (GRCm39) |
missense |
probably benign |
|
R5573:Myo9a
|
UTSW |
9 |
59,778,284 (GRCm39) |
missense |
probably benign |
|
R5589:Myo9a
|
UTSW |
9 |
59,802,527 (GRCm39) |
nonsense |
probably null |
|
R5607:Myo9a
|
UTSW |
9 |
59,771,227 (GRCm39) |
missense |
probably damaging |
1.00 |
R5633:Myo9a
|
UTSW |
9 |
59,775,467 (GRCm39) |
missense |
possibly damaging |
0.60 |
R5885:Myo9a
|
UTSW |
9 |
59,778,503 (GRCm39) |
missense |
probably benign |
|
R6024:Myo9a
|
UTSW |
9 |
59,762,671 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6086:Myo9a
|
UTSW |
9 |
59,697,340 (GRCm39) |
nonsense |
probably null |
|
R6146:Myo9a
|
UTSW |
9 |
59,778,512 (GRCm39) |
missense |
probably benign |
0.01 |
R6194:Myo9a
|
UTSW |
9 |
59,777,033 (GRCm39) |
missense |
probably benign |
0.00 |
R6213:Myo9a
|
UTSW |
9 |
59,734,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R6368:Myo9a
|
UTSW |
9 |
59,832,231 (GRCm39) |
missense |
probably benign |
0.01 |
R6550:Myo9a
|
UTSW |
9 |
59,775,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R6612:Myo9a
|
UTSW |
9 |
59,734,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R6665:Myo9a
|
UTSW |
9 |
59,779,155 (GRCm39) |
missense |
probably benign |
0.09 |
R6951:Myo9a
|
UTSW |
9 |
59,802,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Myo9a
|
UTSW |
9 |
59,722,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7107:Myo9a
|
UTSW |
9 |
59,778,098 (GRCm39) |
missense |
probably benign |
0.44 |
R7310:Myo9a
|
UTSW |
9 |
59,778,436 (GRCm39) |
missense |
probably benign |
0.08 |
R7473:Myo9a
|
UTSW |
9 |
59,802,527 (GRCm39) |
missense |
probably benign |
0.31 |
R7723:Myo9a
|
UTSW |
9 |
59,687,141 (GRCm39) |
missense |
probably damaging |
1.00 |
R7823:Myo9a
|
UTSW |
9 |
59,719,233 (GRCm39) |
missense |
probably damaging |
1.00 |
R7824:Myo9a
|
UTSW |
9 |
59,767,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7965:Myo9a
|
UTSW |
9 |
59,695,721 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Myo9a
|
UTSW |
9 |
59,687,374 (GRCm39) |
missense |
probably benign |
0.33 |
R8055:Myo9a
|
UTSW |
9 |
59,814,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8071:Myo9a
|
UTSW |
9 |
59,781,931 (GRCm39) |
missense |
probably benign |
|
R8250:Myo9a
|
UTSW |
9 |
59,767,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Myo9a
|
UTSW |
9 |
59,817,961 (GRCm39) |
missense |
probably benign |
0.08 |
R8355:Myo9a
|
UTSW |
9 |
59,817,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R8432:Myo9a
|
UTSW |
9 |
59,687,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R8470:Myo9a
|
UTSW |
9 |
59,739,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8528:Myo9a
|
UTSW |
9 |
59,767,423 (GRCm39) |
missense |
probably damaging |
1.00 |
R8681:Myo9a
|
UTSW |
9 |
59,775,394 (GRCm39) |
missense |
probably benign |
0.16 |
R8793:Myo9a
|
UTSW |
9 |
59,791,850 (GRCm39) |
missense |
probably benign |
0.03 |
R8812:Myo9a
|
UTSW |
9 |
59,687,030 (GRCm39) |
missense |
probably benign |
0.14 |
R9016:Myo9a
|
UTSW |
9 |
59,775,427 (GRCm39) |
nonsense |
probably null |
|
R9026:Myo9a
|
UTSW |
9 |
59,716,757 (GRCm39) |
missense |
probably damaging |
0.96 |
R9036:Myo9a
|
UTSW |
9 |
59,687,584 (GRCm39) |
nonsense |
probably null |
|
R9130:Myo9a
|
UTSW |
9 |
59,739,514 (GRCm39) |
missense |
probably damaging |
0.98 |
R9131:Myo9a
|
UTSW |
9 |
59,768,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Myo9a
|
UTSW |
9 |
59,772,922 (GRCm39) |
missense |
probably benign |
0.04 |
R9498:Myo9a
|
UTSW |
9 |
59,734,466 (GRCm39) |
missense |
probably damaging |
1.00 |
R9575:Myo9a
|
UTSW |
9 |
59,813,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R9651:Myo9a
|
UTSW |
9 |
59,778,764 (GRCm39) |
missense |
probably damaging |
0.96 |
R9672:Myo9a
|
UTSW |
9 |
59,687,332 (GRCm39) |
missense |
probably benign |
0.16 |
RF018:Myo9a
|
UTSW |
9 |
59,776,869 (GRCm39) |
missense |
probably benign |
0.00 |
RF019:Myo9a
|
UTSW |
9 |
59,829,055 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Myo9a
|
UTSW |
9 |
59,802,542 (GRCm39) |
missense |
probably damaging |
1.00 |
|