Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ambn |
G |
A |
5: 88,607,218 (GRCm39) |
A29T |
probably damaging |
Het |
Ankrd11 |
T |
C |
8: 123,621,467 (GRCm39) |
K795R |
probably damaging |
Het |
Atg3 |
T |
C |
16: 45,004,174 (GRCm39) |
|
probably null |
Het |
Ccdc169 |
T |
C |
3: 55,078,739 (GRCm39) |
V200A |
possibly damaging |
Het |
Cdr2l |
C |
A |
11: 115,283,564 (GRCm39) |
Q141K |
probably damaging |
Het |
Cts3 |
T |
A |
13: 61,715,988 (GRCm39) |
I93F |
probably damaging |
Het |
Eif2ak2 |
A |
G |
17: 79,171,287 (GRCm39) |
L372S |
probably damaging |
Het |
Elovl5 |
T |
C |
9: 77,888,853 (GRCm39) |
I240T |
possibly damaging |
Het |
Farp1 |
C |
T |
14: 121,510,186 (GRCm39) |
A728V |
possibly damaging |
Het |
Fbln1 |
A |
G |
15: 85,128,390 (GRCm39) |
D529G |
possibly damaging |
Het |
Flnb |
G |
T |
14: 7,917,390 (GRCm38) |
|
probably benign |
Het |
Gm14401 |
A |
T |
2: 176,778,625 (GRCm39) |
H237L |
probably damaging |
Het |
Hivep3 |
T |
A |
4: 119,956,443 (GRCm39) |
H1586Q |
probably damaging |
Het |
Igkv12-98 |
T |
A |
6: 68,548,093 (GRCm39) |
L74* |
probably null |
Het |
Iigp1c |
T |
A |
18: 60,378,508 (GRCm39) |
D14E |
possibly damaging |
Het |
Ktn1 |
T |
C |
14: 47,946,335 (GRCm39) |
S917P |
probably benign |
Het |
Lama3 |
T |
C |
18: 12,574,200 (GRCm39) |
|
probably null |
Het |
Lamb1 |
A |
G |
12: 31,351,063 (GRCm39) |
D723G |
possibly damaging |
Het |
Lrrc39 |
A |
T |
3: 116,364,500 (GRCm39) |
R130S |
probably benign |
Het |
Mcm3 |
A |
C |
1: 20,875,039 (GRCm39) |
|
probably null |
Het |
Muc19 |
T |
G |
15: 91,764,901 (GRCm39) |
|
noncoding transcript |
Het |
Necap2 |
A |
G |
4: 140,794,879 (GRCm39) |
F266S |
probably damaging |
Het |
Nfil3 |
C |
T |
13: 53,122,055 (GRCm39) |
G283D |
probably damaging |
Het |
Nlrp4e |
A |
T |
7: 23,021,092 (GRCm39) |
K526N |
possibly damaging |
Het |
Or13a20 |
A |
G |
7: 140,232,389 (GRCm39) |
T166A |
probably benign |
Het |
Or4p7 |
T |
A |
2: 88,222,245 (GRCm39) |
V218E |
possibly damaging |
Het |
Pelp1 |
G |
A |
11: 70,287,720 (GRCm39) |
R401W |
probably damaging |
Het |
Phldb3 |
G |
T |
7: 24,328,295 (GRCm39) |
C613F |
probably damaging |
Het |
Ppp1ca |
T |
C |
19: 4,243,110 (GRCm39) |
Y93H |
probably damaging |
Het |
Ppp1r3b |
A |
G |
8: 35,851,476 (GRCm39) |
E105G |
probably benign |
Het |
Ryr1 |
A |
T |
7: 28,781,968 (GRCm39) |
I2007N |
probably damaging |
Het |
Scgb1b27 |
A |
G |
7: 33,721,228 (GRCm39) |
T39A |
probably damaging |
Het |
Serpinb3b |
T |
C |
1: 107,082,187 (GRCm39) |
D359G |
probably benign |
Het |
Sgo2b |
G |
T |
8: 64,379,557 (GRCm39) |
R1092S |
probably benign |
Het |
Sh3pxd2b |
C |
A |
11: 32,353,993 (GRCm39) |
S187* |
probably null |
Het |
Slc11a1 |
T |
A |
1: 74,418,955 (GRCm39) |
L92H |
probably damaging |
Het |
Smc3 |
T |
C |
19: 53,617,758 (GRCm39) |
V585A |
probably damaging |
Het |
Sp6 |
A |
G |
11: 96,913,429 (GRCm39) |
|
probably benign |
Het |
Spata16 |
A |
T |
3: 26,894,871 (GRCm39) |
I307F |
possibly damaging |
Het |
Tfpi2 |
T |
A |
6: 3,965,359 (GRCm39) |
H33L |
probably benign |
Het |
Tnxb |
T |
A |
17: 34,912,782 (GRCm39) |
D1642E |
probably damaging |
Het |
Ttc1 |
T |
C |
11: 43,621,320 (GRCm39) |
N287S |
probably damaging |
Het |
Ttc9 |
G |
A |
12: 81,678,536 (GRCm39) |
V120I |
possibly damaging |
Het |
Umps |
A |
G |
16: 33,787,272 (GRCm39) |
V27A |
probably damaging |
Het |
Usp50 |
C |
A |
2: 126,551,334 (GRCm39) |
M48I |
probably damaging |
Het |
Vmn1r76 |
A |
T |
7: 11,664,309 (GRCm39) |
C267S |
possibly damaging |
Het |
Wee1 |
A |
T |
7: 109,725,055 (GRCm39) |
D275V |
possibly damaging |
Het |
Zmym6 |
C |
T |
4: 126,982,152 (GRCm39) |
P63L |
probably benign |
Het |
|
Other mutations in Prb1a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00670:Prb1a
|
APN |
6 |
132,184,109 (GRCm39) |
utr 3 prime |
probably benign |
|
R0369:Prb1a
|
UTSW |
6 |
132,184,620 (GRCm39) |
nonsense |
probably null |
|
R1500:Prb1a
|
UTSW |
6 |
132,184,439 (GRCm39) |
missense |
unknown |
|
R1544:Prb1a
|
UTSW |
6 |
132,186,424 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1544:Prb1a
|
UTSW |
6 |
132,186,423 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1559:Prb1a
|
UTSW |
6 |
132,185,507 (GRCm39) |
missense |
unknown |
|
R2142:Prb1a
|
UTSW |
6 |
132,184,166 (GRCm39) |
missense |
unknown |
|
R2655:Prb1a
|
UTSW |
6 |
132,187,425 (GRCm39) |
missense |
unknown |
|
R4065:Prb1a
|
UTSW |
6 |
132,184,658 (GRCm39) |
missense |
unknown |
|
R4505:Prb1a
|
UTSW |
6 |
132,184,533 (GRCm39) |
nonsense |
probably null |
|
R5925:Prb1a
|
UTSW |
6 |
132,187,475 (GRCm39) |
missense |
unknown |
|
R6391:Prb1a
|
UTSW |
6 |
132,184,139 (GRCm39) |
missense |
unknown |
|
R6525:Prb1a
|
UTSW |
6 |
132,184,467 (GRCm39) |
missense |
unknown |
|
R6745:Prb1a
|
UTSW |
6 |
132,186,383 (GRCm39) |
splice site |
probably null |
|
R7192:Prb1a
|
UTSW |
6 |
132,184,335 (GRCm39) |
missense |
unknown |
|
R7536:Prb1a
|
UTSW |
6 |
132,184,184 (GRCm39) |
missense |
unknown |
|
R8483:Prb1a
|
UTSW |
6 |
132,185,398 (GRCm39) |
missense |
unknown |
|
R9139:Prb1a
|
UTSW |
6 |
132,185,306 (GRCm39) |
missense |
unknown |
|
R9365:Prb1a
|
UTSW |
6 |
132,184,201 (GRCm39) |
missense |
unknown |
|
R9559:Prb1a
|
UTSW |
6 |
132,184,388 (GRCm39) |
missense |
unknown |
|
|