Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
C |
6: 23,074,629 (GRCm39) |
K854E |
probably damaging |
Het |
Abcd2 |
G |
T |
15: 91,074,885 (GRCm39) |
Y309* |
probably null |
Het |
Ache |
G |
A |
5: 137,289,751 (GRCm39) |
G360D |
probably damaging |
Het |
Acot12 |
T |
C |
13: 91,929,361 (GRCm39) |
L396P |
probably benign |
Het |
Acox2 |
T |
G |
14: 8,241,303 (GRCm38) |
D603A |
probably benign |
Het |
Adam3 |
C |
A |
8: 25,201,417 (GRCm39) |
K245N |
probably damaging |
Het |
Ankhd1 |
T |
C |
18: 36,758,081 (GRCm39) |
I925T |
probably benign |
Het |
Arhgap27 |
C |
T |
11: 103,251,585 (GRCm39) |
V48M |
probably damaging |
Het |
Atm |
A |
T |
9: 53,423,308 (GRCm39) |
|
probably null |
Het |
B4galt4 |
T |
A |
16: 38,574,302 (GRCm39) |
F92Y |
probably damaging |
Het |
Brwd1 |
C |
T |
16: 95,837,159 (GRCm39) |
R891Q |
probably damaging |
Het |
Calcr |
T |
C |
6: 3,687,612 (GRCm39) |
Q462R |
probably benign |
Het |
Ccdc112 |
T |
C |
18: 46,420,698 (GRCm39) |
R351G |
probably damaging |
Het |
Ccdc80 |
T |
G |
16: 44,917,073 (GRCm39) |
S610A |
probably benign |
Het |
Cdh20 |
C |
A |
1: 104,881,796 (GRCm39) |
N420K |
possibly damaging |
Het |
Cntn3 |
G |
A |
6: 102,255,383 (GRCm39) |
R172* |
probably null |
Het |
Ctnnd1 |
G |
T |
2: 84,452,390 (GRCm39) |
Q78K |
possibly damaging |
Het |
D16Ertd472e |
A |
T |
16: 78,372,814 (GRCm39) |
L41H |
probably damaging |
Het |
Dclk2 |
A |
T |
3: 86,706,909 (GRCm39) |
|
probably null |
Het |
Dmwd |
C |
T |
7: 18,814,234 (GRCm39) |
H295Y |
probably benign |
Het |
Dnai2 |
T |
C |
11: 114,647,988 (GRCm39) |
V588A |
unknown |
Het |
Dnai4 |
T |
G |
4: 102,923,549 (GRCm39) |
I427L |
probably benign |
Het |
Dtx4 |
C |
T |
19: 12,459,437 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
C |
A |
9: 7,141,059 (GRCm39) |
D1323Y |
probably damaging |
Het |
Fcgbp |
T |
A |
7: 27,803,446 (GRCm39) |
H1683Q |
probably benign |
Het |
Fndc3c1 |
G |
C |
X: 105,478,679 (GRCm39) |
L724V |
possibly damaging |
Het |
Gm9195 |
A |
G |
14: 72,689,192 (GRCm39) |
S1876P |
possibly damaging |
Het |
Grhl2 |
A |
C |
15: 37,335,980 (GRCm39) |
K431T |
probably damaging |
Het |
Grm7 |
T |
G |
6: 111,335,530 (GRCm39) |
I647S |
possibly damaging |
Het |
Gtf2ird1 |
T |
C |
5: 134,439,948 (GRCm39) |
N94S |
probably benign |
Het |
Gvin2 |
A |
C |
7: 105,551,386 (GRCm39) |
S555R |
possibly damaging |
Het |
Hmgcs1 |
G |
T |
13: 120,162,620 (GRCm39) |
G195W |
probably damaging |
Het |
Hrc |
A |
T |
7: 44,985,989 (GRCm39) |
Y380F |
possibly damaging |
Het |
Kcnu1 |
C |
T |
8: 26,409,665 (GRCm39) |
Q863* |
probably null |
Het |
Lemd2 |
G |
A |
17: 27,415,165 (GRCm39) |
P300L |
probably damaging |
Het |
Lnpep |
A |
T |
17: 17,773,172 (GRCm39) |
Y665* |
probably null |
Het |
Lrfn1 |
A |
G |
7: 28,166,564 (GRCm39) |
T653A |
probably benign |
Het |
Ly6g6c |
A |
G |
17: 35,286,387 (GRCm39) |
T8A |
unknown |
Het |
Mcm5 |
T |
C |
8: 75,848,344 (GRCm39) |
|
probably null |
Het |
Med28 |
A |
T |
5: 45,680,794 (GRCm39) |
D86V |
probably damaging |
Het |
Mup11 |
A |
G |
4: 60,615,725 (GRCm39) |
S171P |
possibly damaging |
Het |
Nckap1 |
A |
G |
2: 80,370,542 (GRCm39) |
F383L |
probably benign |
Het |
Nid1 |
G |
C |
13: 13,642,970 (GRCm39) |
G303R |
probably benign |
Het |
Nkain3 |
A |
G |
4: 20,282,892 (GRCm39) |
V147A |
probably benign |
Het |
Or12k8 |
A |
G |
2: 36,975,670 (GRCm39) |
V30A |
probably benign |
Het |
Pde9a |
G |
A |
17: 31,639,258 (GRCm39) |
V63I |
possibly damaging |
Het |
Pdlim2 |
T |
A |
14: 70,411,826 (GRCm39) |
I69F |
probably damaging |
Het |
Peg10 |
CCACATCAGGATCCACATCAGGATGCACATCAGCATCAGGATCCCCATCAGGATGCACATCAGGATCCACATCAGGATGCACATCAG |
CCACATCAGGATCCACATCAGGATGCACATCAG |
6: 4,756,398 (GRCm39) |
|
probably benign |
Het |
Phf20l1 |
T |
C |
15: 66,476,638 (GRCm39) |
I245T |
probably benign |
Het |
Prmt8 |
C |
T |
6: 127,666,792 (GRCm39) |
R394H |
possibly damaging |
Het |
Prorp |
A |
G |
12: 55,355,430 (GRCm39) |
|
probably null |
Het |
Prpf4b |
T |
A |
13: 35,067,994 (GRCm39) |
D274E |
unknown |
Het |
Psmd6 |
A |
T |
14: 14,112,225 (GRCm38) |
|
probably null |
Het |
Rgs16 |
T |
C |
1: 153,617,416 (GRCm39) |
L69P |
probably damaging |
Het |
Robo3 |
A |
T |
9: 37,336,020 (GRCm39) |
I482N |
probably damaging |
Het |
Serpina1b |
T |
A |
12: 103,694,553 (GRCm39) |
H397L |
probably benign |
Het |
Skint11 |
T |
A |
4: 114,088,944 (GRCm39) |
L246Q |
probably damaging |
Het |
Skint5 |
T |
A |
4: 113,396,536 (GRCm39) |
R1212S |
unknown |
Het |
Slc11a2 |
T |
C |
15: 100,300,213 (GRCm39) |
D348G |
probably benign |
Het |
Slc15a2 |
T |
C |
16: 36,576,643 (GRCm39) |
K495E |
probably benign |
Het |
Son |
T |
G |
16: 91,458,990 (GRCm39) |
D2072E |
unknown |
Het |
Stau1 |
A |
G |
2: 166,805,494 (GRCm39) |
V34A |
probably damaging |
Het |
Stk3 |
G |
T |
15: 35,073,262 (GRCm39) |
L153I |
possibly damaging |
Het |
Swi5 |
A |
T |
2: 32,177,922 (GRCm39) |
V13E |
probably benign |
Het |
Syne2 |
A |
T |
12: 76,078,172 (GRCm39) |
|
probably null |
Het |
Synm |
T |
C |
7: 67,384,663 (GRCm39) |
M558V |
probably benign |
Het |
Tep1 |
T |
A |
14: 51,062,013 (GRCm39) |
|
probably null |
Het |
Tmc6 |
A |
G |
11: 117,667,151 (GRCm39) |
V149A |
probably benign |
Het |
Tmem214 |
T |
A |
5: 31,028,065 (GRCm39) |
V95E |
possibly damaging |
Het |
Tnnt2 |
T |
A |
1: 135,778,114 (GRCm39) |
|
probably null |
Het |
Txlna |
A |
G |
4: 129,525,071 (GRCm39) |
|
probably null |
Het |
Vmn2r26 |
T |
C |
6: 124,038,948 (GRCm39) |
I841T |
probably damaging |
Het |
Wasf2 |
G |
A |
4: 132,923,045 (GRCm39) |
V452I |
probably damaging |
Het |
Wdr62 |
C |
T |
7: 29,951,761 (GRCm39) |
D673N |
probably damaging |
Het |
Wdr95 |
C |
T |
5: 149,518,836 (GRCm39) |
T559I |
probably benign |
Het |
Zbtb40 |
A |
T |
4: 136,726,937 (GRCm39) |
|
probably null |
Het |
Zfat |
T |
C |
15: 68,051,856 (GRCm39) |
E646G |
probably benign |
Het |
|
Other mutations in Scara3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00229:Scara3
|
APN |
14 |
66,170,570 (GRCm39) |
missense |
probably benign |
0.01 |
IGL00646:Scara3
|
APN |
14 |
66,158,605 (GRCm39) |
nonsense |
probably null |
|
IGL00718:Scara3
|
APN |
14 |
66,168,876 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL01948:Scara3
|
APN |
14 |
66,168,261 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01979:Scara3
|
APN |
14 |
66,168,412 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02399:Scara3
|
APN |
14 |
66,170,559 (GRCm39) |
nonsense |
probably null |
|
IGL02939:Scara3
|
APN |
14 |
66,169,105 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02945:Scara3
|
APN |
14 |
66,168,660 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03075:Scara3
|
APN |
14 |
66,168,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03100:Scara3
|
APN |
14 |
66,168,722 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03156:Scara3
|
APN |
14 |
66,168,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03179:Scara3
|
APN |
14 |
66,168,603 (GRCm39) |
missense |
probably damaging |
1.00 |
condor
|
UTSW |
14 |
66,168,651 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4362001:Scara3
|
UTSW |
14 |
66,173,851 (GRCm39) |
missense |
probably benign |
|
R0062:Scara3
|
UTSW |
14 |
66,168,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0062:Scara3
|
UTSW |
14 |
66,168,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R0124:Scara3
|
UTSW |
14 |
66,168,670 (GRCm39) |
missense |
probably benign |
0.01 |
R0349:Scara3
|
UTSW |
14 |
66,169,230 (GRCm39) |
missense |
probably damaging |
0.98 |
R1584:Scara3
|
UTSW |
14 |
66,158,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Scara3
|
UTSW |
14 |
66,190,950 (GRCm39) |
start codon destroyed |
probably null |
0.06 |
R5336:Scara3
|
UTSW |
14 |
66,168,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R6307:Scara3
|
UTSW |
14 |
66,175,710 (GRCm39) |
missense |
probably benign |
0.24 |
R6420:Scara3
|
UTSW |
14 |
66,175,701 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6610:Scara3
|
UTSW |
14 |
66,168,670 (GRCm39) |
missense |
probably damaging |
0.97 |
R7159:Scara3
|
UTSW |
14 |
66,158,229 (GRCm39) |
missense |
probably damaging |
0.98 |
R7246:Scara3
|
UTSW |
14 |
66,169,093 (GRCm39) |
missense |
probably damaging |
0.97 |
R7315:Scara3
|
UTSW |
14 |
66,168,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R7324:Scara3
|
UTSW |
14 |
66,168,865 (GRCm39) |
missense |
probably benign |
0.03 |
R7497:Scara3
|
UTSW |
14 |
66,168,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R7504:Scara3
|
UTSW |
14 |
66,168,780 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7554:Scara3
|
UTSW |
14 |
66,158,299 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8143:Scara3
|
UTSW |
14 |
66,169,269 (GRCm39) |
missense |
probably damaging |
0.96 |
R9043:Scara3
|
UTSW |
14 |
66,169,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R9226:Scara3
|
UTSW |
14 |
66,169,233 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9363:Scara3
|
UTSW |
14 |
66,168,720 (GRCm39) |
missense |
probably benign |
0.01 |
R9730:Scara3
|
UTSW |
14 |
66,168,261 (GRCm39) |
missense |
probably damaging |
0.99 |
YA93:Scara3
|
UTSW |
14 |
66,168,398 (GRCm39) |
missense |
probably damaging |
0.98 |
|