Other mutations in this stock |
Total: 83 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2510009E07Rik |
T |
C |
16: 21,472,496 (GRCm39) |
Y68C |
probably damaging |
Het |
6820408C15Rik |
A |
T |
2: 152,276,031 (GRCm39) |
H81L |
probably damaging |
Het |
Acbd4 |
A |
G |
11: 102,994,785 (GRCm39) |
T48A |
probably damaging |
Het |
Acp3 |
T |
A |
9: 104,197,200 (GRCm39) |
E146D |
probably benign |
Het |
Acsm1 |
T |
A |
7: 119,251,796 (GRCm39) |
I307N |
probably damaging |
Het |
Adcy4 |
T |
C |
14: 56,019,384 (GRCm39) |
T89A |
possibly damaging |
Het |
Agl |
T |
C |
3: 116,580,895 (GRCm39) |
T356A |
probably benign |
Het |
Ago1 |
A |
G |
4: 126,357,534 (GRCm39) |
I47T |
probably damaging |
Het |
Akr1c6 |
T |
A |
13: 4,496,363 (GRCm39) |
Y75N |
probably benign |
Het |
Anxa2 |
T |
A |
9: 69,386,990 (GRCm39) |
S92T |
probably benign |
Het |
Arid4b |
T |
C |
13: 14,358,979 (GRCm39) |
S585P |
probably damaging |
Het |
Arl4d |
T |
C |
11: 101,557,842 (GRCm39) |
S123P |
possibly damaging |
Het |
Atad2 |
A |
T |
15: 57,963,415 (GRCm39) |
D1067E |
probably damaging |
Het |
Brap |
C |
A |
5: 121,820,922 (GRCm39) |
T403K |
possibly damaging |
Het |
Brwd1 |
A |
T |
16: 95,809,344 (GRCm39) |
N1895K |
possibly damaging |
Het |
Ccdc187 |
T |
C |
2: 26,171,087 (GRCm39) |
T464A |
probably benign |
Het |
Ccn6 |
G |
A |
10: 39,029,239 (GRCm39) |
R230W |
probably damaging |
Het |
Cdh11 |
T |
C |
8: 103,391,233 (GRCm39) |
|
probably benign |
Het |
Chd9 |
A |
T |
8: 91,725,163 (GRCm39) |
Y691F |
probably benign |
Het |
Clhc1 |
A |
T |
11: 29,519,287 (GRCm39) |
I365F |
possibly damaging |
Het |
Col11a1 |
A |
G |
3: 113,951,804 (GRCm39) |
Q1078R |
probably damaging |
Het |
Creb3 |
G |
A |
4: 43,566,375 (GRCm39) |
V294I |
possibly damaging |
Het |
Cspg4 |
T |
C |
9: 56,795,754 (GRCm39) |
I1163T |
probably damaging |
Het |
Cyp3a57 |
A |
C |
5: 145,327,225 (GRCm39) |
|
probably null |
Het |
Dnah3 |
A |
T |
7: 119,618,918 (GRCm39) |
I1661N |
probably damaging |
Het |
Dpysl4 |
A |
C |
7: 138,669,469 (GRCm39) |
D49A |
probably damaging |
Het |
Efhb |
T |
A |
17: 53,733,306 (GRCm39) |
I522F |
probably damaging |
Het |
Epha4 |
T |
C |
1: 77,376,329 (GRCm39) |
T517A |
probably damaging |
Het |
Fasn |
A |
G |
11: 120,703,937 (GRCm39) |
S1466P |
probably damaging |
Het |
Fgd6 |
A |
T |
10: 93,973,298 (GRCm39) |
D1253V |
probably benign |
Het |
Fjx1 |
G |
A |
2: 102,281,509 (GRCm39) |
A142V |
probably benign |
Het |
Foxb1 |
T |
C |
9: 69,666,598 (GRCm39) |
T311A |
probably benign |
Het |
Fpgs |
A |
G |
2: 32,581,200 (GRCm39) |
|
probably null |
Het |
Gm10024 |
A |
G |
10: 77,547,606 (GRCm39) |
|
probably null |
Het |
Gnat3 |
A |
T |
5: 18,208,841 (GRCm39) |
T182S |
possibly damaging |
Het |
Igsf3 |
T |
A |
3: 101,362,543 (GRCm39) |
F875I |
probably benign |
Het |
Kif13b |
A |
G |
14: 64,976,068 (GRCm39) |
E461G |
probably damaging |
Het |
Kif23 |
A |
T |
9: 61,832,982 (GRCm39) |
|
probably null |
Het |
Kntc1 |
G |
A |
5: 123,896,540 (GRCm39) |
R134Q |
possibly damaging |
Het |
Krt33a |
A |
T |
11: 99,905,072 (GRCm39) |
Y145N |
probably damaging |
Het |
Lama5 |
A |
G |
2: 179,848,551 (GRCm39) |
V313A |
probably benign |
Het |
Lamb1 |
T |
C |
12: 31,328,651 (GRCm39) |
|
probably null |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mtor |
C |
T |
4: 148,632,133 (GRCm39) |
L2336F |
probably damaging |
Het |
Naglu |
T |
C |
11: 100,967,351 (GRCm39) |
S434P |
probably damaging |
Het |
Ncoa7 |
T |
A |
10: 30,580,655 (GRCm39) |
H101L |
possibly damaging |
Het |
Nlrc4 |
G |
A |
17: 74,752,184 (GRCm39) |
T733I |
possibly damaging |
Het |
Nr3c2 |
A |
G |
8: 77,636,573 (GRCm39) |
E558G |
probably damaging |
Het |
Nsun4 |
A |
T |
4: 115,891,397 (GRCm39) |
N327K |
probably benign |
Het |
Or11g27 |
A |
G |
14: 50,771,100 (GRCm39) |
Y77C |
probably damaging |
Het |
Or1x2 |
T |
C |
11: 50,917,952 (GRCm39) |
V41A |
probably damaging |
Het |
Or2m13 |
T |
A |
16: 19,226,454 (GRCm39) |
Y104F |
probably benign |
Het |
Or4f6 |
T |
A |
2: 111,838,877 (GRCm39) |
Y218F |
probably damaging |
Het |
Or6b13 |
T |
C |
7: 139,781,864 (GRCm39) |
N273S |
probably damaging |
Het |
Pdia2 |
T |
A |
17: 26,415,495 (GRCm39) |
I441F |
probably damaging |
Het |
Phyh |
T |
C |
2: 4,930,494 (GRCm39) |
S74P |
probably benign |
Het |
Pigo |
A |
G |
4: 43,024,661 (GRCm39) |
L146P |
probably damaging |
Het |
Plce1 |
A |
G |
19: 38,713,219 (GRCm39) |
D1191G |
probably damaging |
Het |
Plrg1 |
T |
C |
3: 82,975,301 (GRCm39) |
|
probably benign |
Het |
Plrg1 |
G |
A |
3: 82,977,051 (GRCm39) |
R364Q |
probably damaging |
Het |
Polr3b |
T |
C |
10: 84,515,669 (GRCm39) |
L614S |
probably damaging |
Het |
Pramel16 |
A |
T |
4: 143,676,400 (GRCm39) |
C235S |
possibly damaging |
Het |
Prrg4 |
A |
G |
2: 104,663,027 (GRCm39) |
V193A |
probably damaging |
Het |
Prss16 |
T |
A |
13: 22,187,483 (GRCm39) |
E47V |
probably benign |
Het |
Ptpru |
G |
A |
4: 131,499,861 (GRCm39) |
T1261I |
probably damaging |
Het |
Pycard |
A |
G |
7: 127,591,970 (GRCm39) |
S124P |
possibly damaging |
Het |
Riok1 |
C |
A |
13: 38,221,487 (GRCm39) |
D17E |
probably damaging |
Het |
Scin |
T |
A |
12: 40,177,929 (GRCm39) |
Y102F |
probably benign |
Het |
Scmh1 |
A |
G |
4: 120,386,425 (GRCm39) |
H655R |
probably damaging |
Het |
Scyl2 |
A |
T |
10: 89,476,598 (GRCm39) |
N842K |
probably benign |
Het |
Sec23b |
T |
A |
2: 144,409,049 (GRCm39) |
M211K |
probably benign |
Het |
Serpina3i |
A |
C |
12: 104,234,897 (GRCm39) |
*409C |
probably null |
Het |
Sgk2 |
G |
A |
2: 162,839,779 (GRCm39) |
R129H |
probably benign |
Het |
Slc39a13 |
A |
G |
2: 90,898,871 (GRCm39) |
I80T |
probably damaging |
Het |
Smarcad1 |
A |
G |
6: 65,029,631 (GRCm39) |
D73G |
probably benign |
Het |
Srgap1 |
T |
G |
10: 121,691,278 (GRCm39) |
M319L |
probably benign |
Het |
Stx7 |
T |
A |
10: 24,060,903 (GRCm39) |
V210E |
probably damaging |
Het |
Tjp2 |
T |
A |
19: 24,108,776 (GRCm39) |
H112L |
probably benign |
Het |
Tuba8 |
A |
T |
6: 121,197,385 (GRCm39) |
I16F |
probably damaging |
Het |
Ube3c |
G |
A |
5: 29,851,617 (GRCm39) |
A815T |
probably benign |
Het |
Vmn2r5 |
A |
T |
3: 64,417,116 (GRCm39) |
V14E |
probably benign |
Het |
Vmn2r79 |
A |
T |
7: 86,653,247 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
A |
G |
1: 63,343,018 (GRCm39) |
T466A |
possibly damaging |
Het |
|
Other mutations in Spata18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00228:Spata18
|
APN |
5 |
73,815,097 (GRCm39) |
missense |
possibly damaging |
0.80 |
IGL01331:Spata18
|
APN |
5 |
73,827,024 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01394:Spata18
|
APN |
5 |
73,836,688 (GRCm39) |
splice site |
probably null |
|
IGL01994:Spata18
|
APN |
5 |
73,814,944 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02192:Spata18
|
APN |
5 |
73,829,861 (GRCm39) |
splice site |
probably null |
|
IGL02253:Spata18
|
APN |
5 |
73,825,939 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL03195:Spata18
|
APN |
5 |
73,828,591 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03204:Spata18
|
APN |
5 |
73,828,449 (GRCm39) |
splice site |
probably benign |
|
ANU74:Spata18
|
UTSW |
5 |
73,828,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R0312:Spata18
|
UTSW |
5 |
73,824,224 (GRCm39) |
missense |
probably benign |
0.00 |
R0557:Spata18
|
UTSW |
5 |
73,809,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Spata18
|
UTSW |
5 |
73,828,482 (GRCm39) |
missense |
probably damaging |
1.00 |
R1937:Spata18
|
UTSW |
5 |
73,834,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R2228:Spata18
|
UTSW |
5 |
73,824,244 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2229:Spata18
|
UTSW |
5 |
73,824,244 (GRCm39) |
missense |
possibly damaging |
0.57 |
R2896:Spata18
|
UTSW |
5 |
73,815,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R3082:Spata18
|
UTSW |
5 |
73,836,423 (GRCm39) |
intron |
probably benign |
|
R3716:Spata18
|
UTSW |
5 |
73,824,193 (GRCm39) |
critical splice acceptor site |
probably null |
|
R3717:Spata18
|
UTSW |
5 |
73,824,193 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4061:Spata18
|
UTSW |
5 |
73,828,509 (GRCm39) |
missense |
probably damaging |
1.00 |
R4299:Spata18
|
UTSW |
5 |
73,824,245 (GRCm39) |
missense |
probably benign |
0.36 |
R4963:Spata18
|
UTSW |
5 |
73,836,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R5603:Spata18
|
UTSW |
5 |
73,828,575 (GRCm39) |
missense |
probably benign |
0.12 |
R6381:Spata18
|
UTSW |
5 |
73,832,559 (GRCm39) |
missense |
probably damaging |
1.00 |
R6581:Spata18
|
UTSW |
5 |
73,826,859 (GRCm39) |
missense |
probably benign |
0.14 |
R7062:Spata18
|
UTSW |
5 |
73,816,636 (GRCm39) |
missense |
probably benign |
0.08 |
R7591:Spata18
|
UTSW |
5 |
73,829,759 (GRCm39) |
missense |
|
|
R7682:Spata18
|
UTSW |
5 |
73,826,008 (GRCm39) |
missense |
|
|
R7688:Spata18
|
UTSW |
5 |
73,809,005 (GRCm39) |
missense |
probably benign |
0.14 |
R7783:Spata18
|
UTSW |
5 |
73,825,953 (GRCm39) |
missense |
|
|
R8051:Spata18
|
UTSW |
5 |
73,827,063 (GRCm39) |
missense |
|
|
R8765:Spata18
|
UTSW |
5 |
73,825,992 (GRCm39) |
missense |
|
|
R8951:Spata18
|
UTSW |
5 |
73,828,572 (GRCm39) |
missense |
probably damaging |
0.99 |
R9505:Spata18
|
UTSW |
5 |
73,809,017 (GRCm39) |
critical splice donor site |
probably null |
|
R9514:Spata18
|
UTSW |
5 |
73,829,840 (GRCm39) |
missense |
|
|
R9515:Spata18
|
UTSW |
5 |
73,829,840 (GRCm39) |
missense |
|
|
X0061:Spata18
|
UTSW |
5 |
73,824,202 (GRCm39) |
missense |
possibly damaging |
0.68 |
|