Other mutations in this stock |
Total: 23 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ablim1 |
T |
C |
19: 57,140,722 (GRCm39) |
E142G |
possibly damaging |
Het |
Arid4a |
C |
T |
12: 71,122,492 (GRCm39) |
P958S |
probably damaging |
Het |
Cct5 |
T |
C |
15: 31,591,073 (GRCm39) |
|
probably benign |
Het |
Cntnap4 |
C |
T |
8: 113,494,251 (GRCm39) |
|
probably benign |
Het |
Col4a3 |
C |
T |
1: 82,695,590 (GRCm39) |
L1597F |
probably damaging |
Het |
Gla |
C |
A |
X: 133,495,947 (GRCm39) |
V179L |
probably benign |
Het |
Gm20422 |
A |
T |
8: 70,195,642 (GRCm39) |
C212* |
probably null |
Het |
Hace1 |
T |
A |
10: 45,548,453 (GRCm39) |
Y14* |
probably null |
Het |
Hcfc2 |
T |
A |
10: 82,577,112 (GRCm39) |
|
probably null |
Het |
Helz2 |
T |
C |
2: 180,874,038 (GRCm39) |
D2152G |
possibly damaging |
Het |
Lypd10 |
A |
G |
7: 24,413,673 (GRCm39) |
T230A |
probably benign |
Het |
Mcm8 |
T |
G |
2: 132,661,594 (GRCm39) |
L74V |
probably benign |
Het |
Myo18b |
A |
G |
5: 112,978,255 (GRCm39) |
|
probably benign |
Het |
Rad21l |
C |
A |
2: 151,502,635 (GRCm39) |
A192S |
probably benign |
Het |
Scn2a |
A |
G |
2: 65,501,078 (GRCm39) |
D80G |
probably damaging |
Het |
Serpinb3c |
A |
G |
1: 107,203,990 (GRCm39) |
|
probably null |
Het |
Sgip1 |
A |
G |
4: 102,786,118 (GRCm39) |
|
probably benign |
Het |
Slc25a41 |
G |
T |
17: 57,341,957 (GRCm39) |
|
probably null |
Het |
Snx14 |
C |
A |
9: 88,302,382 (GRCm39) |
R140S |
probably damaging |
Het |
Svs6 |
A |
C |
2: 164,159,507 (GRCm39) |
K90T |
possibly damaging |
Het |
Tlcd1 |
T |
A |
11: 78,070,914 (GRCm39) |
Y168N |
probably damaging |
Het |
Vps13d |
A |
G |
4: 144,811,978 (GRCm39) |
I3312T |
probably benign |
Het |
Zfp11 |
A |
G |
5: 129,734,978 (GRCm39) |
V161A |
probably benign |
Het |
|
Other mutations in Ptprg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Ptprg
|
APN |
14 |
12,215,992 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL00484:Ptprg
|
APN |
14 |
12,215,220 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01089:Ptprg
|
APN |
14 |
12,215,286 (GRCm38) |
missense |
probably damaging |
0.97 |
IGL01382:Ptprg
|
APN |
14 |
12,237,797 (GRCm38) |
missense |
probably benign |
0.16 |
IGL01470:Ptprg
|
APN |
14 |
12,213,702 (GRCm38) |
nonsense |
probably null |
|
IGL01762:Ptprg
|
APN |
14 |
12,037,386 (GRCm38) |
missense |
probably benign |
0.00 |
IGL01886:Ptprg
|
APN |
14 |
12,179,280 (GRCm38) |
missense |
probably benign |
0.22 |
IGL01963:Ptprg
|
APN |
14 |
12,220,661 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02015:Ptprg
|
APN |
14 |
12,237,782 (GRCm38) |
missense |
possibly damaging |
0.46 |
IGL02086:Ptprg
|
APN |
14 |
12,110,080 (GRCm38) |
nonsense |
probably null |
|
IGL02197:Ptprg
|
APN |
14 |
12,220,613 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02341:Ptprg
|
APN |
14 |
12,154,360 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02732:Ptprg
|
APN |
14 |
12,225,617 (GRCm38) |
critical splice donor site |
probably null |
|
IGL03011:Ptprg
|
APN |
14 |
12,219,029 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03261:Ptprg
|
APN |
14 |
12,225,552 (GRCm38) |
missense |
probably damaging |
0.99 |
R0038:Ptprg
|
UTSW |
14 |
12,213,710 (GRCm38) |
missense |
probably damaging |
1.00 |
R0383:Ptprg
|
UTSW |
14 |
12,219,024 (GRCm38) |
missense |
possibly damaging |
0.93 |
R0433:Ptprg
|
UTSW |
14 |
12,220,620 (GRCm38) |
missense |
probably damaging |
1.00 |
R0488:Ptprg
|
UTSW |
14 |
12,220,653 (GRCm38) |
missense |
probably damaging |
1.00 |
R0503:Ptprg
|
UTSW |
14 |
12,237,138 (GRCm38) |
missense |
possibly damaging |
0.89 |
R0520:Ptprg
|
UTSW |
14 |
12,199,783 (GRCm38) |
missense |
possibly damaging |
0.92 |
R0570:Ptprg
|
UTSW |
14 |
12,215,896 (GRCm38) |
missense |
probably damaging |
1.00 |
R0606:Ptprg
|
UTSW |
14 |
12,154,131 (GRCm38) |
missense |
probably benign |
|
R1086:Ptprg
|
UTSW |
14 |
11,952,706 (GRCm38) |
splice site |
probably benign |
|
R1468:Ptprg
|
UTSW |
14 |
12,190,767 (GRCm38) |
missense |
probably benign |
0.02 |
R1468:Ptprg
|
UTSW |
14 |
12,190,767 (GRCm38) |
missense |
probably benign |
0.02 |
R1519:Ptprg
|
UTSW |
14 |
12,220,596 (GRCm38) |
missense |
probably damaging |
1.00 |
R1662:Ptprg
|
UTSW |
14 |
12,207,357 (GRCm38) |
missense |
probably damaging |
1.00 |
R1714:Ptprg
|
UTSW |
14 |
12,213,697 (GRCm38) |
missense |
probably damaging |
1.00 |
R1716:Ptprg
|
UTSW |
14 |
12,154,360 (GRCm38) |
missense |
probably benign |
0.00 |
R1797:Ptprg
|
UTSW |
14 |
12,199,743 (GRCm38) |
missense |
probably damaging |
1.00 |
R1803:Ptprg
|
UTSW |
14 |
12,091,410 (GRCm38) |
splice site |
probably null |
|
R2104:Ptprg
|
UTSW |
14 |
11,952,897 (GRCm38) |
critical splice donor site |
probably null |
|
R2125:Ptprg
|
UTSW |
14 |
12,179,283 (GRCm38) |
missense |
possibly damaging |
0.74 |
R2126:Ptprg
|
UTSW |
14 |
12,154,355 (GRCm38) |
missense |
probably benign |
|
R2133:Ptprg
|
UTSW |
14 |
12,211,637 (GRCm38) |
missense |
probably damaging |
1.00 |
R2471:Ptprg
|
UTSW |
14 |
12,210,327 (GRCm38) |
missense |
probably damaging |
1.00 |
R2571:Ptprg
|
UTSW |
14 |
12,122,135 (GRCm38) |
missense |
probably benign |
|
R3821:Ptprg
|
UTSW |
14 |
12,226,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4196:Ptprg
|
UTSW |
14 |
12,122,002 (GRCm38) |
missense |
possibly damaging |
0.51 |
R4392:Ptprg
|
UTSW |
14 |
12,142,467 (GRCm38) |
missense |
possibly damaging |
0.80 |
R4665:Ptprg
|
UTSW |
14 |
12,215,288 (GRCm38) |
missense |
possibly damaging |
0.90 |
R4730:Ptprg
|
UTSW |
14 |
12,213,713 (GRCm38) |
missense |
probably damaging |
1.00 |
R4737:Ptprg
|
UTSW |
14 |
12,226,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R4764:Ptprg
|
UTSW |
14 |
12,122,068 (GRCm38) |
missense |
probably benign |
0.01 |
R4801:Ptprg
|
UTSW |
14 |
11,554,233 (GRCm38) |
utr 5 prime |
probably benign |
|
R4825:Ptprg
|
UTSW |
14 |
12,220,654 (GRCm38) |
missense |
probably damaging |
1.00 |
R4960:Ptprg
|
UTSW |
14 |
12,237,837 (GRCm38) |
missense |
probably benign |
0.07 |
R4972:Ptprg
|
UTSW |
14 |
12,226,427 (GRCm38) |
missense |
possibly damaging |
0.94 |
R4980:Ptprg
|
UTSW |
14 |
12,154,421 (GRCm38) |
missense |
probably benign |
0.16 |
R5004:Ptprg
|
UTSW |
14 |
12,220,667 (GRCm38) |
missense |
probably damaging |
1.00 |
R5058:Ptprg
|
UTSW |
14 |
12,037,387 (GRCm38) |
missense |
possibly damaging |
0.82 |
R5182:Ptprg
|
UTSW |
14 |
12,154,174 (GRCm38) |
missense |
probably benign |
|
R5258:Ptprg
|
UTSW |
14 |
12,142,431 (GRCm38) |
missense |
probably benign |
0.11 |
R5338:Ptprg
|
UTSW |
14 |
12,154,111 (GRCm38) |
missense |
probably benign |
|
R5353:Ptprg
|
UTSW |
14 |
11,554,235 (GRCm38) |
utr 5 prime |
probably benign |
|
R5373:Ptprg
|
UTSW |
14 |
12,213,665 (GRCm38) |
missense |
probably benign |
0.00 |
R5387:Ptprg
|
UTSW |
14 |
12,153,873 (GRCm38) |
missense |
probably damaging |
1.00 |
R5616:Ptprg
|
UTSW |
14 |
12,122,120 (GRCm38) |
missense |
probably benign |
|
R5623:Ptprg
|
UTSW |
14 |
12,153,857 (GRCm38) |
missense |
probably damaging |
1.00 |
R5976:Ptprg
|
UTSW |
14 |
12,211,625 (GRCm38) |
missense |
probably damaging |
0.96 |
R6027:Ptprg
|
UTSW |
14 |
12,220,613 (GRCm38) |
missense |
possibly damaging |
0.87 |
R6091:Ptprg
|
UTSW |
14 |
12,215,979 (GRCm38) |
missense |
probably damaging |
1.00 |
R6184:Ptprg
|
UTSW |
14 |
12,153,943 (GRCm38) |
missense |
probably benign |
0.00 |
R6234:Ptprg
|
UTSW |
14 |
12,213,747 (GRCm38) |
missense |
probably damaging |
1.00 |
R6318:Ptprg
|
UTSW |
14 |
12,237,118 (GRCm38) |
missense |
probably damaging |
1.00 |
R6324:Ptprg
|
UTSW |
14 |
12,226,314 (GRCm38) |
missense |
probably damaging |
1.00 |
R6334:Ptprg
|
UTSW |
14 |
12,166,832 (GRCm38) |
missense |
probably damaging |
1.00 |
R6646:Ptprg
|
UTSW |
14 |
11,962,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R6647:Ptprg
|
UTSW |
14 |
11,962,714 (GRCm38) |
missense |
probably damaging |
1.00 |
R6992:Ptprg
|
UTSW |
14 |
11,962,602 (GRCm38) |
missense |
probably damaging |
1.00 |
R7088:Ptprg
|
UTSW |
14 |
12,207,365 (GRCm38) |
missense |
probably damaging |
1.00 |
R7250:Ptprg
|
UTSW |
14 |
12,166,767 (GRCm38) |
missense |
probably benign |
0.18 |
R7342:Ptprg
|
UTSW |
14 |
12,237,151 (GRCm38) |
missense |
possibly damaging |
0.90 |
R7358:Ptprg
|
UTSW |
14 |
12,154,198 (GRCm38) |
missense |
possibly damaging |
0.59 |
R7410:Ptprg
|
UTSW |
14 |
11,962,657 (GRCm38) |
missense |
probably damaging |
1.00 |
R7448:Ptprg
|
UTSW |
14 |
12,142,461 (GRCm38) |
missense |
probably benign |
0.12 |
R7514:Ptprg
|
UTSW |
14 |
12,179,342 (GRCm38) |
missense |
possibly damaging |
0.86 |
R7523:Ptprg
|
UTSW |
14 |
12,237,130 (GRCm38) |
missense |
probably damaging |
0.97 |
R7672:Ptprg
|
UTSW |
14 |
12,211,668 (GRCm38) |
missense |
probably benign |
0.04 |
R7709:Ptprg
|
UTSW |
14 |
12,226,452 (GRCm38) |
missense |
probably damaging |
1.00 |
R7720:Ptprg
|
UTSW |
14 |
12,211,703 (GRCm38) |
missense |
probably benign |
0.31 |
R8860:Ptprg
|
UTSW |
14 |
12,213,685 (GRCm38) |
missense |
probably damaging |
1.00 |
R8992:Ptprg
|
UTSW |
14 |
12,154,170 (GRCm38) |
missense |
probably benign |
0.00 |
R9054:Ptprg
|
UTSW |
14 |
12,213,638 (GRCm38) |
missense |
possibly damaging |
0.58 |
R9587:Ptprg
|
UTSW |
14 |
12,215,992 (GRCm38) |
missense |
probably damaging |
1.00 |
R9621:Ptprg
|
UTSW |
14 |
12,237,809 (GRCm38) |
missense |
probably benign |
|
R9625:Ptprg
|
UTSW |
14 |
12,152,027 (GRCm38) |
missense |
probably damaging |
1.00 |
R9773:Ptprg
|
UTSW |
14 |
12,199,806 (GRCm38) |
missense |
probably damaging |
0.97 |
X0020:Ptprg
|
UTSW |
14 |
12,110,070 (GRCm38) |
frame shift |
probably null |
|
X0027:Ptprg
|
UTSW |
14 |
12,110,070 (GRCm38) |
frame shift |
probably null |
|
|