Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
C |
14: 118,853,858 (GRCm39) |
S425G |
probably benign |
Het |
Adam29 |
A |
G |
8: 56,324,609 (GRCm39) |
I615T |
probably damaging |
Het |
Arap2 |
A |
T |
5: 62,906,818 (GRCm39) |
I67N |
probably damaging |
Het |
Asxl2 |
C |
T |
12: 3,477,108 (GRCm39) |
|
probably benign |
Het |
Atp13a4 |
C |
T |
16: 29,260,014 (GRCm39) |
G607D |
|
Het |
Atp2c2 |
G |
A |
8: 120,474,936 (GRCm39) |
V514M |
probably damaging |
Het |
Baiap3 |
A |
G |
17: 25,468,082 (GRCm39) |
C311R |
possibly damaging |
Het |
Becn1 |
A |
C |
11: 101,185,052 (GRCm39) |
S137R |
probably benign |
Het |
C1qtnf6 |
G |
T |
15: 78,409,574 (GRCm39) |
T91K |
probably benign |
Het |
C8a |
T |
C |
4: 104,718,626 (GRCm39) |
K110E |
probably damaging |
Het |
Camta2 |
A |
G |
11: 70,574,714 (GRCm39) |
|
probably null |
Het |
Capn8 |
T |
A |
1: 182,426,240 (GRCm39) |
Y192N |
probably damaging |
Het |
Ccdc170 |
C |
T |
10: 4,508,512 (GRCm39) |
Q579* |
probably null |
Het |
Cenpa |
G |
T |
5: 30,824,292 (GRCm39) |
|
probably benign |
Het |
Cltc |
A |
G |
11: 86,616,054 (GRCm39) |
V404A |
probably benign |
Het |
Cyp3a11 |
A |
T |
5: 145,802,710 (GRCm39) |
L261Q |
probably benign |
Het |
Daw1 |
T |
A |
1: 83,170,436 (GRCm39) |
S249R |
probably benign |
Het |
Dchs1 |
T |
A |
7: 105,404,155 (GRCm39) |
I2796F |
probably benign |
Het |
Dis3l2 |
T |
C |
1: 86,673,222 (GRCm39) |
|
probably null |
Het |
Dnah5 |
A |
T |
15: 28,347,098 (GRCm39) |
D2527V |
probably damaging |
Het |
Dsg4 |
G |
A |
18: 20,599,685 (GRCm39) |
R767Q |
probably damaging |
Het |
Edaradd |
A |
G |
13: 12,493,338 (GRCm39) |
I118T |
probably damaging |
Het |
Fam83h |
A |
G |
15: 75,876,275 (GRCm39) |
F354S |
possibly damaging |
Het |
Fat3 |
A |
G |
9: 15,899,778 (GRCm39) |
V3085A |
probably benign |
Het |
Fer |
A |
G |
17: 64,440,516 (GRCm39) |
D711G |
possibly damaging |
Het |
G6pc1 |
G |
T |
11: 101,267,503 (GRCm39) |
V318F |
probably benign |
Het |
Gal3st1 |
C |
A |
11: 3,948,227 (GRCm39) |
H145N |
probably benign |
Het |
Helz |
C |
T |
11: 107,552,856 (GRCm39) |
P1211S |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,302,038 (GRCm39) |
I667V |
probably benign |
Het |
Herc2 |
T |
A |
7: 55,753,466 (GRCm39) |
|
probably null |
Het |
Hivep1 |
C |
T |
13: 42,308,387 (GRCm39) |
T209I |
probably damaging |
Het |
Hsph1 |
A |
G |
5: 149,542,485 (GRCm39) |
Y678H |
probably damaging |
Het |
Ift122 |
C |
T |
6: 115,903,263 (GRCm39) |
R1176C |
probably benign |
Het |
Ighv1-23 |
T |
C |
12: 114,728,095 (GRCm39) |
D109G |
probably damaging |
Het |
Itgb3 |
T |
C |
11: 104,534,403 (GRCm39) |
V420A |
possibly damaging |
Het |
Kcnk13 |
C |
A |
12: 100,027,985 (GRCm39) |
N353K |
probably damaging |
Het |
Kif21a |
A |
G |
15: 90,877,999 (GRCm39) |
F270L |
probably benign |
Het |
Kit |
T |
A |
5: 75,799,660 (GRCm39) |
V464D |
probably benign |
Het |
Klhl36 |
G |
A |
8: 120,596,914 (GRCm39) |
W205* |
probably null |
Het |
Krt17 |
A |
G |
11: 100,149,291 (GRCm39) |
Y260H |
probably damaging |
Het |
Lats1 |
C |
T |
10: 7,588,706 (GRCm39) |
Q1108* |
probably null |
Het |
Lrch1 |
G |
A |
14: 74,994,477 (GRCm39) |
T709I |
possibly damaging |
Het |
Lrrc58 |
C |
A |
16: 37,689,053 (GRCm39) |
Q66K |
probably benign |
Het |
Mei1 |
G |
A |
15: 81,999,682 (GRCm39) |
A664T |
|
Het |
Mtmr6 |
C |
T |
14: 60,537,753 (GRCm39) |
T546M |
probably benign |
Het |
Ncoa3 |
T |
A |
2: 165,910,449 (GRCm39) |
F1288L |
probably damaging |
Het |
Nwd1 |
G |
T |
8: 73,434,458 (GRCm39) |
V1352L |
probably benign |
Het |
Or4k77 |
T |
A |
2: 111,199,707 (GRCm39) |
H243Q |
probably damaging |
Het |
Or5ac17 |
A |
T |
16: 59,036,761 (GRCm39) |
C72S |
probably benign |
Het |
Ovol3 |
C |
T |
7: 29,934,646 (GRCm39) |
|
probably null |
Het |
Palb2 |
C |
A |
7: 121,716,554 (GRCm39) |
V843L |
probably damaging |
Het |
Pds5a |
T |
A |
5: 65,809,878 (GRCm39) |
|
probably null |
Het |
Per1 |
A |
G |
11: 68,995,561 (GRCm39) |
S714G |
possibly damaging |
Het |
Plch2 |
G |
A |
4: 155,084,917 (GRCm39) |
R442C |
probably damaging |
Het |
Pon2 |
A |
T |
6: 5,289,080 (GRCm39) |
S26R |
probably benign |
Het |
Ppp1r9a |
A |
T |
6: 5,115,378 (GRCm39) |
N834Y |
probably damaging |
Het |
Pramel22 |
T |
C |
4: 143,382,130 (GRCm39) |
I189V |
probably damaging |
Het |
Rbm46 |
C |
T |
3: 82,749,795 (GRCm39) |
W483* |
probably null |
Het |
Rnd1 |
A |
T |
15: 98,571,782 (GRCm39) |
V88E |
probably damaging |
Het |
Sbno2 |
T |
A |
10: 79,905,409 (GRCm39) |
T142S |
unknown |
Het |
Scn9a |
C |
T |
2: 66,377,531 (GRCm39) |
V384M |
possibly damaging |
Het |
Sertad4 |
T |
A |
1: 192,529,018 (GRCm39) |
H266L |
possibly damaging |
Het |
Setd5 |
T |
A |
6: 113,092,043 (GRCm39) |
M288K |
possibly damaging |
Het |
Sinhcaf |
A |
G |
6: 148,834,600 (GRCm39) |
Y10H |
probably benign |
Het |
Skint6 |
T |
A |
4: 113,095,425 (GRCm39) |
N78I |
probably damaging |
Het |
Sltm |
G |
T |
9: 70,480,748 (GRCm39) |
G200V |
unknown |
Het |
Smg1 |
A |
G |
7: 117,795,116 (GRCm39) |
I477T |
unknown |
Het |
Supv3l1 |
C |
T |
10: 62,266,249 (GRCm39) |
|
probably null |
Het |
Syne2 |
A |
G |
12: 76,062,337 (GRCm39) |
R4220G |
probably benign |
Het |
Tbr1 |
A |
T |
2: 61,635,161 (GRCm39) |
H37L |
possibly damaging |
Het |
Tet3 |
TGGCCCAGGCCCAGGC |
TGGCCCAGGCCCAGGCCCAGGC |
6: 83,345,211 (GRCm39) |
|
probably benign |
Het |
Tmem231 |
G |
T |
8: 112,645,040 (GRCm39) |
S155R |
probably damaging |
Het |
Trem3 |
A |
G |
17: 48,565,498 (GRCm39) |
*184W |
probably null |
Het |
Trim33 |
T |
A |
3: 103,253,956 (GRCm39) |
|
probably benign |
Het |
Tsen2 |
G |
A |
6: 115,536,943 (GRCm39) |
W233* |
probably null |
Het |
Ttc21a |
T |
A |
9: 119,774,605 (GRCm39) |
N286K |
probably damaging |
Het |
Tulp4 |
A |
T |
17: 6,248,983 (GRCm39) |
M194L |
probably benign |
Het |
Ube3b |
C |
A |
5: 114,553,345 (GRCm39) |
R906S |
possibly damaging |
Het |
Ube3b |
A |
C |
5: 114,556,687 (GRCm39) |
D1006A |
probably damaging |
Het |
Vipas39 |
A |
T |
12: 87,288,705 (GRCm39) |
|
probably null |
Het |
Wdr35 |
T |
A |
12: 9,072,785 (GRCm39) |
Y920N |
probably damaging |
Het |
Zan |
T |
G |
5: 137,423,824 (GRCm39) |
I2692L |
unknown |
Het |
Zfp142 |
C |
A |
1: 74,624,679 (GRCm39) |
E48D |
probably benign |
Het |
Zfp598 |
T |
C |
17: 24,896,504 (GRCm39) |
Y194H |
probably damaging |
Het |
Zfp85 |
T |
C |
13: 67,897,064 (GRCm39) |
N336S |
probably benign |
Het |
Zfyve27 |
A |
T |
19: 42,177,959 (GRCm39) |
|
probably null |
Het |
Zp3 |
T |
C |
5: 136,011,559 (GRCm39) |
S126P |
probably damaging |
Het |
|
Other mutations in Sfxn4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01141:Sfxn4
|
APN |
19 |
60,839,452 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL01567:Sfxn4
|
APN |
19 |
60,842,336 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01829:Sfxn4
|
APN |
19 |
60,847,172 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01903:Sfxn4
|
APN |
19 |
60,847,118 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01965:Sfxn4
|
APN |
19 |
60,847,182 (GRCm39) |
splice site |
probably benign |
|
IGL03290:Sfxn4
|
APN |
19 |
60,848,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Sfxn4
|
UTSW |
19 |
60,847,111 (GRCm39) |
missense |
probably benign |
0.01 |
R0550:Sfxn4
|
UTSW |
19 |
60,839,383 (GRCm39) |
splice site |
probably benign |
|
R2228:Sfxn4
|
UTSW |
19 |
60,839,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R2229:Sfxn4
|
UTSW |
19 |
60,839,458 (GRCm39) |
missense |
probably damaging |
1.00 |
R3949:Sfxn4
|
UTSW |
19 |
60,840,501 (GRCm39) |
missense |
probably damaging |
1.00 |
R5074:Sfxn4
|
UTSW |
19 |
60,839,450 (GRCm39) |
missense |
probably damaging |
1.00 |
R6534:Sfxn4
|
UTSW |
19 |
60,827,461 (GRCm39) |
missense |
probably damaging |
1.00 |
R7120:Sfxn4
|
UTSW |
19 |
60,840,477 (GRCm39) |
nonsense |
probably null |
|
R7375:Sfxn4
|
UTSW |
19 |
60,847,112 (GRCm39) |
missense |
probably benign |
0.38 |
R7440:Sfxn4
|
UTSW |
19 |
60,830,642 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7479:Sfxn4
|
UTSW |
19 |
60,847,112 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7577:Sfxn4
|
UTSW |
19 |
60,842,324 (GRCm39) |
missense |
probably benign |
0.21 |
R7883:Sfxn4
|
UTSW |
19 |
60,847,187 (GRCm39) |
splice site |
probably null |
|
R8058:Sfxn4
|
UTSW |
19 |
60,832,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R9335:Sfxn4
|
UTSW |
19 |
60,839,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9523:Sfxn4
|
UTSW |
19 |
60,845,807 (GRCm39) |
missense |
probably damaging |
0.97 |
|