Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ccdc18 |
A |
G |
5: 108,359,997 (GRCm39) |
Y1127C |
probably damaging |
Het |
Cdnf |
T |
A |
2: 3,524,863 (GRCm39) |
L134* |
probably null |
Het |
Col11a1 |
A |
G |
3: 113,883,902 (GRCm39) |
D257G |
unknown |
Het |
Cthrc1 |
T |
A |
15: 38,940,529 (GRCm39) |
I44N |
probably benign |
Het |
Dlec1 |
T |
C |
9: 118,952,288 (GRCm39) |
Y545H |
probably benign |
Het |
Drosha |
T |
G |
15: 12,885,069 (GRCm39) |
|
probably null |
Het |
Ebf2 |
A |
G |
14: 67,661,558 (GRCm39) |
N562S |
probably benign |
Het |
Fem1b |
G |
A |
9: 62,704,246 (GRCm39) |
A338V |
probably benign |
Het |
Gga3 |
A |
T |
11: 115,477,820 (GRCm39) |
|
probably null |
Het |
Gm7247 |
A |
T |
14: 51,760,914 (GRCm39) |
H161L |
probably benign |
Het |
Gm7367 |
A |
G |
7: 59,805,517 (GRCm39) |
|
noncoding transcript |
Het |
Inpp5a |
T |
G |
7: 139,105,664 (GRCm39) |
V213G |
probably benign |
Het |
Kcns3 |
T |
C |
12: 11,141,233 (GRCm39) |
T489A |
probably benign |
Het |
Kifc3 |
G |
A |
8: 95,835,241 (GRCm39) |
A211V |
probably damaging |
Het |
Krt71 |
T |
C |
15: 101,642,987 (GRCm39) |
D507G |
possibly damaging |
Het |
Lama5 |
T |
C |
2: 179,849,011 (GRCm39) |
Y224C |
probably damaging |
Het |
Lrrc37a |
A |
G |
11: 103,386,857 (GRCm39) |
L2421P |
unknown |
Het |
Mtch2 |
C |
T |
2: 90,689,894 (GRCm39) |
T205I |
probably benign |
Het |
Or1o11 |
T |
C |
17: 37,757,255 (GRCm39) |
V281A |
probably benign |
Het |
Prkdc |
T |
A |
16: 15,488,490 (GRCm39) |
C537* |
probably null |
Het |
Prl2a1 |
T |
C |
13: 27,985,699 (GRCm39) |
V5A |
probably benign |
Het |
Prob1 |
T |
C |
18: 35,787,192 (GRCm39) |
Y354C |
probably benign |
Het |
Rimklb |
C |
T |
6: 122,433,280 (GRCm39) |
S347N |
possibly damaging |
Het |
Rnase2a |
T |
C |
14: 51,492,945 (GRCm39) |
D140G |
probably damaging |
Het |
Ryr2 |
G |
A |
13: 11,787,302 (GRCm39) |
P1017S |
probably benign |
Het |
Slc3a1 |
A |
G |
17: 85,340,205 (GRCm39) |
D209G |
probably damaging |
Het |
Sntn |
T |
A |
14: 13,682,205 (GRCm38) |
|
probably benign |
Het |
Tal2 |
G |
T |
4: 53,785,994 (GRCm39) |
L58F |
probably damaging |
Het |
Trim39 |
T |
C |
17: 36,571,463 (GRCm39) |
K432E |
probably damaging |
Het |
Trmt5 |
A |
T |
12: 73,329,501 (GRCm39) |
M219K |
probably benign |
Het |
Vmn2r3 |
T |
A |
3: 64,182,767 (GRCm39) |
I311L |
possibly damaging |
Het |
Wfdc17 |
A |
T |
11: 83,595,611 (GRCm39) |
|
probably benign |
Het |
Zbtb6 |
T |
G |
2: 37,319,584 (GRCm39) |
I115L |
probably damaging |
Het |
Zfp750 |
A |
T |
11: 121,402,770 (GRCm39) |
C659* |
probably null |
Het |
|
Other mutations in 2810004N23Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02977:2810004N23Rik
|
APN |
8 |
125,587,930 (GRCm39) |
missense |
probably benign |
0.01 |
FR4342:2810004N23Rik
|
UTSW |
8 |
125,566,572 (GRCm39) |
frame shift |
probably null |
|
R0519:2810004N23Rik
|
UTSW |
8 |
125,566,668 (GRCm39) |
missense |
possibly damaging |
0.90 |
R1302:2810004N23Rik
|
UTSW |
8 |
125,566,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R1349:2810004N23Rik
|
UTSW |
8 |
125,587,992 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1640:2810004N23Rik
|
UTSW |
8 |
125,566,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R6614:2810004N23Rik
|
UTSW |
8 |
125,587,986 (GRCm39) |
splice site |
probably null |
|
R7150:2810004N23Rik
|
UTSW |
8 |
125,589,653 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7806:2810004N23Rik
|
UTSW |
8 |
125,569,143 (GRCm39) |
missense |
probably benign |
|
R9450:2810004N23Rik
|
UTSW |
8 |
125,567,215 (GRCm39) |
missense |
probably damaging |
1.00 |
RF061:2810004N23Rik
|
UTSW |
8 |
125,566,570 (GRCm39) |
frame shift |
probably null |
|
|