Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700013D24Rik |
T |
C |
6: 124,324,745 (GRCm39) |
E92G |
possibly damaging |
Het |
Aasdh |
A |
T |
5: 77,034,124 (GRCm39) |
Y476N |
possibly damaging |
Het |
Abca13 |
G |
T |
11: 9,264,623 (GRCm39) |
V3002F |
possibly damaging |
Het |
Adam23 |
C |
T |
1: 63,624,536 (GRCm39) |
T788I |
probably damaging |
Het |
Adgrb2 |
A |
G |
4: 129,898,850 (GRCm39) |
T282A |
possibly damaging |
Het |
Adgrg1 |
T |
C |
8: 95,735,035 (GRCm39) |
Y402H |
probably damaging |
Het |
Agpat2 |
A |
T |
2: 26,483,666 (GRCm39) |
L257Q |
probably benign |
Het |
Agpat3 |
A |
T |
10: 78,118,211 (GRCm39) |
V255E |
possibly damaging |
Het |
Akap6 |
A |
G |
12: 52,933,404 (GRCm39) |
I299V |
probably benign |
Het |
Anapc1 |
A |
T |
2: 128,511,788 (GRCm39) |
F468L |
probably damaging |
Het |
Apob |
T |
A |
12: 8,038,842 (GRCm39) |
N431K |
possibly damaging |
Het |
Asprv1 |
T |
A |
6: 86,605,851 (GRCm39) |
D232E |
probably benign |
Het |
AW209491 |
A |
G |
13: 14,811,921 (GRCm39) |
Y258C |
probably damaging |
Het |
Bach2 |
C |
T |
4: 32,562,316 (GRCm39) |
P261L |
probably benign |
Het |
Cap2 |
T |
A |
13: 46,763,208 (GRCm39) |
I146K |
probably damaging |
Het |
Catsperb |
A |
T |
12: 101,569,028 (GRCm39) |
Q900L |
probably benign |
Het |
Ccdc187 |
A |
T |
2: 26,171,548 (GRCm39) |
V310D |
probably damaging |
Het |
Cenpe |
G |
T |
3: 134,948,388 (GRCm39) |
G1275* |
probably null |
Het |
Chd8 |
C |
T |
14: 52,448,012 (GRCm39) |
G1663D |
probably damaging |
Het |
Col6a5 |
T |
A |
9: 105,823,156 (GRCm39) |
Y67F |
unknown |
Het |
Cuzd1 |
G |
T |
7: 130,919,720 (GRCm39) |
T132K |
possibly damaging |
Het |
Ddr2 |
T |
A |
1: 169,863,585 (GRCm39) |
|
probably benign |
Het |
Ddx42 |
T |
C |
11: 106,138,550 (GRCm39) |
I783T |
probably benign |
Het |
Dennd4a |
T |
A |
9: 64,746,256 (GRCm39) |
D47E |
probably damaging |
Het |
Dvl2 |
T |
G |
11: 69,898,673 (GRCm39) |
W379G |
probably damaging |
Het |
Ehbp1 |
A |
G |
11: 21,963,495 (GRCm39) |
L1160P |
probably damaging |
Het |
Ephb6 |
T |
C |
6: 41,595,580 (GRCm39) |
S780P |
probably damaging |
Het |
Exo5 |
G |
A |
4: 120,779,560 (GRCm39) |
L102F |
probably benign |
Het |
Fam220a |
A |
T |
5: 143,548,594 (GRCm39) |
K2M |
possibly damaging |
Het |
Fanci |
A |
T |
7: 79,083,289 (GRCm39) |
I731L |
probably benign |
Het |
Gbp8 |
A |
G |
5: 105,165,640 (GRCm39) |
S338P |
probably damaging |
Het |
H2-M11 |
T |
C |
17: 36,859,649 (GRCm39) |
I214T |
probably benign |
Het |
Hhatl |
C |
A |
9: 121,618,168 (GRCm39) |
A196S |
probably benign |
Het |
Hspg2 |
C |
A |
4: 137,278,178 (GRCm39) |
C2988* |
probably null |
Het |
Ifi213 |
A |
G |
1: 173,417,426 (GRCm39) |
S329P |
probably benign |
Het |
Lingo3 |
G |
T |
10: 80,670,816 (GRCm39) |
F371L |
probably benign |
Het |
Maml2 |
C |
T |
9: 13,531,413 (GRCm39) |
T209I |
|
Het |
Ndufaf3 |
T |
C |
9: 108,444,182 (GRCm39) |
|
probably benign |
Het |
Nfatc2 |
C |
T |
2: 168,378,216 (GRCm39) |
G483E |
probably damaging |
Het |
Npy6r |
A |
C |
18: 44,409,070 (GRCm39) |
T164P |
probably benign |
Het |
Omg |
T |
C |
11: 79,392,826 (GRCm39) |
E344G |
possibly damaging |
Het |
Or2g25 |
T |
A |
17: 37,970,975 (GRCm39) |
N83I |
probably damaging |
Het |
Or2h15 |
T |
C |
17: 38,441,927 (GRCm39) |
D52G |
possibly damaging |
Het |
Or4c116 |
T |
A |
2: 88,942,737 (GRCm39) |
N40Y |
probably damaging |
Het |
Or52n20 |
A |
G |
7: 104,320,502 (GRCm39) |
N198D |
probably damaging |
Het |
Or5k1 |
A |
G |
16: 58,617,966 (GRCm39) |
M81T |
probably benign |
Het |
Or9i1 |
T |
C |
19: 13,839,849 (GRCm39) |
S231P |
probably benign |
Het |
P2rx7 |
A |
G |
5: 122,808,521 (GRCm39) |
E301G |
probably damaging |
Het |
Phf8-ps |
C |
A |
17: 33,286,038 (GRCm39) |
A255S |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,437,911 (GRCm39) |
S3569P |
probably benign |
Het |
Pkn3 |
G |
A |
2: 29,976,513 (GRCm39) |
|
probably null |
Het |
Proc |
C |
T |
18: 32,256,411 (GRCm39) |
V419M |
probably damaging |
Het |
Prss37 |
C |
T |
6: 40,493,052 (GRCm39) |
W138* |
probably null |
Het |
Prss52 |
T |
A |
14: 64,350,009 (GRCm39) |
L212* |
probably null |
Het |
Rnps1 |
A |
G |
17: 24,637,143 (GRCm39) |
K8E |
unknown |
Het |
Rpf2 |
A |
T |
10: 40,101,429 (GRCm39) |
L202* |
probably null |
Het |
Saraf |
C |
T |
8: 34,632,602 (GRCm39) |
P227L |
probably benign |
Het |
Serpinb5 |
T |
A |
1: 106,809,515 (GRCm39) |
M307K |
possibly damaging |
Het |
Slc46a1 |
T |
C |
11: 78,359,471 (GRCm39) |
S368P |
possibly damaging |
Het |
Slc49a4 |
A |
T |
16: 35,555,967 (GRCm39) |
N164K |
probably benign |
Het |
Slfn8 |
T |
A |
11: 82,895,441 (GRCm39) |
Q455L |
possibly damaging |
Het |
Sv2b |
A |
G |
7: 74,767,347 (GRCm39) |
M683T |
probably damaging |
Het |
Tacc3 |
G |
T |
5: 33,821,874 (GRCm39) |
L211F |
unknown |
Het |
Tbc1d8 |
A |
G |
1: 39,420,490 (GRCm39) |
V681A |
probably damaging |
Het |
Tbkbp1 |
T |
C |
11: 97,029,677 (GRCm39) |
E493G |
unknown |
Het |
Th |
A |
T |
7: 142,447,823 (GRCm39) |
V420E |
possibly damaging |
Het |
Tmem132c |
T |
G |
5: 127,641,421 (GRCm39) |
V115G |
|
Het |
Usp40 |
G |
A |
1: 87,887,558 (GRCm39) |
R915C |
probably benign |
Het |
Wdr81 |
T |
A |
11: 75,342,348 (GRCm39) |
H973L |
possibly damaging |
Het |
Zdhhc6 |
A |
G |
19: 55,302,876 (GRCm39) |
S42P |
probably benign |
Het |
Zfp369 |
T |
A |
13: 65,444,489 (GRCm39) |
I544N |
possibly damaging |
Het |
|
Other mutations in Eml6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01071:Eml6
|
APN |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01407:Eml6
|
APN |
11 |
29,705,021 (GRCm39) |
nonsense |
probably null |
|
IGL01434:Eml6
|
APN |
11 |
29,769,090 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01578:Eml6
|
APN |
11 |
29,800,870 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01780:Eml6
|
APN |
11 |
29,755,175 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01821:Eml6
|
APN |
11 |
29,771,699 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01837:Eml6
|
APN |
11 |
29,727,055 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01904:Eml6
|
APN |
11 |
29,788,613 (GRCm39) |
nonsense |
probably null |
|
IGL01972:Eml6
|
APN |
11 |
29,788,451 (GRCm39) |
missense |
possibly damaging |
0.67 |
IGL02134:Eml6
|
APN |
11 |
29,709,066 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02192:Eml6
|
APN |
11 |
29,755,743 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02377:Eml6
|
APN |
11 |
29,727,282 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02584:Eml6
|
APN |
11 |
29,699,387 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02587:Eml6
|
APN |
11 |
29,734,236 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL02810:Eml6
|
APN |
11 |
29,799,016 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02873:Eml6
|
APN |
11 |
29,830,700 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02880:Eml6
|
APN |
11 |
29,699,959 (GRCm39) |
missense |
probably benign |
0.03 |
IGL03289:Eml6
|
APN |
11 |
29,745,328 (GRCm39) |
missense |
possibly damaging |
0.49 |
IGL03301:Eml6
|
APN |
11 |
29,714,083 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03386:Eml6
|
APN |
11 |
29,699,934 (GRCm39) |
missense |
probably benign |
|
IGL03407:Eml6
|
APN |
11 |
29,856,330 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4453001:Eml6
|
UTSW |
11 |
29,752,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R0125:Eml6
|
UTSW |
11 |
29,832,088 (GRCm39) |
missense |
probably benign |
0.19 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0240:Eml6
|
UTSW |
11 |
29,742,367 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0271:Eml6
|
UTSW |
11 |
29,798,949 (GRCm39) |
missense |
possibly damaging |
0.48 |
R0304:Eml6
|
UTSW |
11 |
29,727,441 (GRCm39) |
missense |
probably benign |
0.00 |
R0415:Eml6
|
UTSW |
11 |
29,699,392 (GRCm39) |
missense |
possibly damaging |
0.84 |
R0449:Eml6
|
UTSW |
11 |
29,843,213 (GRCm39) |
missense |
probably benign |
0.01 |
R0538:Eml6
|
UTSW |
11 |
29,710,010 (GRCm39) |
splice site |
probably benign |
|
R0671:Eml6
|
UTSW |
11 |
29,755,065 (GRCm39) |
missense |
probably benign |
0.00 |
R0766:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R0800:Eml6
|
UTSW |
11 |
29,699,877 (GRCm39) |
missense |
probably benign |
0.08 |
R0841:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R0879:Eml6
|
UTSW |
11 |
29,800,816 (GRCm39) |
critical splice donor site |
probably null |
|
R1061:Eml6
|
UTSW |
11 |
29,727,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1145:Eml6
|
UTSW |
11 |
29,727,430 (GRCm39) |
missense |
probably benign |
0.41 |
R1172:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1173:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1174:Eml6
|
UTSW |
11 |
29,699,824 (GRCm39) |
missense |
possibly damaging |
0.54 |
R1199:Eml6
|
UTSW |
11 |
29,705,044 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1311:Eml6
|
UTSW |
11 |
29,781,088 (GRCm39) |
splice site |
probably benign |
|
R1312:Eml6
|
UTSW |
11 |
29,781,219 (GRCm39) |
splice site |
probably benign |
|
R1355:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1370:Eml6
|
UTSW |
11 |
29,783,085 (GRCm39) |
missense |
probably benign |
0.03 |
R1457:Eml6
|
UTSW |
11 |
29,974,459 (GRCm39) |
missense |
probably damaging |
1.00 |
R1486:Eml6
|
UTSW |
11 |
29,755,114 (GRCm39) |
missense |
possibly damaging |
0.83 |
R1511:Eml6
|
UTSW |
11 |
29,768,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Eml6
|
UTSW |
11 |
29,742,256 (GRCm39) |
splice site |
probably null |
|
R1642:Eml6
|
UTSW |
11 |
29,727,001 (GRCm39) |
critical splice donor site |
probably null |
|
R1682:Eml6
|
UTSW |
11 |
29,709,065 (GRCm39) |
missense |
probably benign |
0.13 |
R1687:Eml6
|
UTSW |
11 |
29,783,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Eml6
|
UTSW |
11 |
29,696,282 (GRCm39) |
nonsense |
probably null |
|
R1796:Eml6
|
UTSW |
11 |
29,831,975 (GRCm39) |
missense |
probably benign |
0.19 |
R1797:Eml6
|
UTSW |
11 |
29,832,041 (GRCm39) |
missense |
probably benign |
0.09 |
R1837:Eml6
|
UTSW |
11 |
29,699,802 (GRCm39) |
splice site |
probably null |
|
R1874:Eml6
|
UTSW |
11 |
29,781,136 (GRCm39) |
missense |
probably damaging |
0.99 |
R1967:Eml6
|
UTSW |
11 |
29,974,545 (GRCm39) |
missense |
probably damaging |
1.00 |
R1969:Eml6
|
UTSW |
11 |
29,783,075 (GRCm39) |
missense |
probably benign |
|
R2007:Eml6
|
UTSW |
11 |
29,798,814 (GRCm39) |
critical splice donor site |
probably null |
|
R2012:Eml6
|
UTSW |
11 |
29,781,128 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2198:Eml6
|
UTSW |
11 |
29,800,935 (GRCm39) |
missense |
probably benign |
0.01 |
R2217:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2218:Eml6
|
UTSW |
11 |
29,768,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R2403:Eml6
|
UTSW |
11 |
29,752,434 (GRCm39) |
missense |
probably benign |
0.05 |
R2520:Eml6
|
UTSW |
11 |
29,741,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R2937:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R2938:Eml6
|
UTSW |
11 |
29,783,049 (GRCm39) |
splice site |
probably benign |
|
R3085:Eml6
|
UTSW |
11 |
29,759,332 (GRCm39) |
missense |
probably damaging |
0.96 |
R3236:Eml6
|
UTSW |
11 |
29,781,097 (GRCm39) |
critical splice donor site |
probably null |
|
R3738:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3739:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R3752:Eml6
|
UTSW |
11 |
29,759,360 (GRCm39) |
missense |
probably benign |
0.06 |
R3854:Eml6
|
UTSW |
11 |
29,699,905 (GRCm39) |
missense |
possibly damaging |
0.76 |
R3941:Eml6
|
UTSW |
11 |
29,753,167 (GRCm39) |
missense |
probably damaging |
0.98 |
R4034:Eml6
|
UTSW |
11 |
29,753,137 (GRCm39) |
missense |
probably benign |
0.20 |
R4049:Eml6
|
UTSW |
11 |
29,788,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R4108:Eml6
|
UTSW |
11 |
29,755,136 (GRCm39) |
missense |
probably damaging |
0.98 |
R4657:Eml6
|
UTSW |
11 |
29,755,108 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4662:Eml6
|
UTSW |
11 |
29,727,390 (GRCm39) |
missense |
probably damaging |
1.00 |
R4665:Eml6
|
UTSW |
11 |
29,769,007 (GRCm39) |
nonsense |
probably null |
|
R4721:Eml6
|
UTSW |
11 |
29,788,525 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4729:Eml6
|
UTSW |
11 |
29,783,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R4766:Eml6
|
UTSW |
11 |
29,755,757 (GRCm39) |
missense |
probably benign |
0.22 |
R4810:Eml6
|
UTSW |
11 |
29,705,011 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4831:Eml6
|
UTSW |
11 |
29,727,052 (GRCm39) |
nonsense |
probably null |
|
R5035:Eml6
|
UTSW |
11 |
29,804,187 (GRCm39) |
missense |
probably benign |
0.00 |
R5064:Eml6
|
UTSW |
11 |
29,699,300 (GRCm39) |
missense |
probably benign |
0.12 |
R5103:Eml6
|
UTSW |
11 |
29,800,905 (GRCm39) |
missense |
possibly damaging |
0.65 |
R5121:Eml6
|
UTSW |
11 |
29,694,606 (GRCm39) |
missense |
probably benign |
0.03 |
R5161:Eml6
|
UTSW |
11 |
29,974,467 (GRCm39) |
missense |
probably damaging |
0.99 |
R5211:Eml6
|
UTSW |
11 |
29,804,145 (GRCm39) |
missense |
probably benign |
0.02 |
R5268:Eml6
|
UTSW |
11 |
29,753,108 (GRCm39) |
missense |
probably benign |
0.15 |
R5390:Eml6
|
UTSW |
11 |
29,710,096 (GRCm39) |
missense |
probably damaging |
1.00 |
R5529:Eml6
|
UTSW |
11 |
29,714,126 (GRCm39) |
missense |
probably benign |
0.04 |
R6239:Eml6
|
UTSW |
11 |
29,699,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R6326:Eml6
|
UTSW |
11 |
29,769,066 (GRCm39) |
missense |
probably damaging |
1.00 |
R6395:Eml6
|
UTSW |
11 |
29,759,321 (GRCm39) |
missense |
probably benign |
0.00 |
R6476:Eml6
|
UTSW |
11 |
29,741,971 (GRCm39) |
critical splice donor site |
probably null |
|
R6483:Eml6
|
UTSW |
11 |
29,699,875 (GRCm39) |
missense |
probably benign |
0.00 |
R6701:Eml6
|
UTSW |
11 |
29,735,748 (GRCm39) |
missense |
probably damaging |
0.98 |
R6753:Eml6
|
UTSW |
11 |
29,704,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R6809:Eml6
|
UTSW |
11 |
29,753,161 (GRCm39) |
missense |
probably benign |
0.23 |
R6847:Eml6
|
UTSW |
11 |
29,768,447 (GRCm39) |
missense |
probably benign |
0.00 |
R6855:Eml6
|
UTSW |
11 |
29,701,381 (GRCm39) |
splice site |
probably null |
|
R7168:Eml6
|
UTSW |
11 |
29,788,529 (GRCm39) |
missense |
probably benign |
0.01 |
R7175:Eml6
|
UTSW |
11 |
29,734,231 (GRCm39) |
missense |
probably benign |
0.00 |
R7305:Eml6
|
UTSW |
11 |
29,727,258 (GRCm39) |
missense |
probably benign |
0.01 |
R7615:Eml6
|
UTSW |
11 |
29,752,501 (GRCm39) |
missense |
possibly damaging |
0.49 |
R7692:Eml6
|
UTSW |
11 |
29,703,085 (GRCm39) |
missense |
probably damaging |
0.98 |
R7980:Eml6
|
UTSW |
11 |
29,783,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Eml6
|
UTSW |
11 |
29,699,973 (GRCm39) |
missense |
possibly damaging |
0.63 |
R8046:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably damaging |
0.99 |
R8049:Eml6
|
UTSW |
11 |
29,843,201 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8114:Eml6
|
UTSW |
11 |
29,704,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R8799:Eml6
|
UTSW |
11 |
29,708,981 (GRCm39) |
missense |
probably benign |
0.11 |
R8945:Eml6
|
UTSW |
11 |
29,703,110 (GRCm39) |
missense |
probably damaging |
0.98 |
R8977:Eml6
|
UTSW |
11 |
29,734,182 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8986:Eml6
|
UTSW |
11 |
29,755,181 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9088:Eml6
|
UTSW |
11 |
29,768,424 (GRCm39) |
missense |
probably damaging |
0.96 |
R9150:Eml6
|
UTSW |
11 |
29,755,791 (GRCm39) |
missense |
probably benign |
0.15 |
R9209:Eml6
|
UTSW |
11 |
29,781,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9467:Eml6
|
UTSW |
11 |
29,769,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R9481:Eml6
|
UTSW |
11 |
29,788,641 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9534:Eml6
|
UTSW |
11 |
29,734,155 (GRCm39) |
missense |
possibly damaging |
0.45 |
RF037:Eml6
|
UTSW |
11 |
29,702,549 (GRCm39) |
critical splice acceptor site |
probably benign |
|
RF039:Eml6
|
UTSW |
11 |
29,702,551 (GRCm39) |
critical splice acceptor site |
probably benign |
|
|