Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
G |
A |
5: 8,744,153 (GRCm39) |
V260M |
probably damaging |
Het |
Accsl |
T |
A |
2: 93,686,092 (GRCm39) |
H575L |
probably benign |
Het |
Armc3 |
A |
T |
2: 19,253,512 (GRCm39) |
I218F |
possibly damaging |
Het |
Bora |
C |
A |
14: 99,310,178 (GRCm39) |
N502K |
probably damaging |
Het |
Brd4 |
T |
A |
17: 32,432,046 (GRCm39) |
D606V |
probably damaging |
Het |
Ccdc190 |
T |
A |
1: 169,757,544 (GRCm39) |
M1K |
probably null |
Het |
Ccl25 |
T |
C |
8: 4,399,898 (GRCm39) |
|
probably benign |
Het |
Cep78 |
G |
T |
19: 15,936,987 (GRCm39) |
T573K |
probably damaging |
Het |
Ces1d |
C |
A |
8: 93,896,346 (GRCm39) |
|
probably null |
Het |
Cntn4 |
C |
T |
6: 106,632,550 (GRCm39) |
H525Y |
probably damaging |
Het |
D630039A03Rik |
T |
C |
4: 57,910,509 (GRCm39) |
E101G |
probably benign |
Het |
Dnah2 |
A |
G |
11: 69,387,403 (GRCm39) |
V941A |
probably benign |
Het |
Exoc6b |
A |
G |
6: 84,821,112 (GRCm39) |
I559T |
probably damaging |
Het |
Fmr1 |
T |
C |
X: 67,731,942 (GRCm39) |
|
probably null |
Het |
Ghr |
A |
T |
15: 3,377,024 (GRCm39) |
C66S |
probably damaging |
Het |
Hook1 |
C |
A |
4: 95,886,929 (GRCm39) |
|
probably benign |
Het |
Igsf1 |
T |
C |
X: 48,876,376 (GRCm39) |
T73A |
probably benign |
Het |
Ipo8 |
T |
C |
6: 148,701,755 (GRCm39) |
K451R |
probably benign |
Het |
Irs1 |
A |
G |
1: 82,266,122 (GRCm39) |
V698A |
probably benign |
Het |
Kat2a |
T |
C |
11: 100,602,301 (GRCm39) |
D151G |
probably benign |
Het |
Lyrm1 |
A |
T |
7: 119,513,469 (GRCm39) |
Q78L |
probably benign |
Het |
Madd |
C |
T |
2: 90,992,507 (GRCm39) |
G1012E |
possibly damaging |
Het |
Mboat1 |
T |
A |
13: 30,320,742 (GRCm39) |
D31E |
probably benign |
Het |
Myh8 |
C |
A |
11: 67,189,172 (GRCm39) |
A1116D |
probably damaging |
Het |
Nop2 |
G |
A |
6: 125,116,695 (GRCm39) |
|
probably null |
Het |
Notch1 |
A |
G |
2: 26,349,971 (GRCm39) |
S2390P |
probably benign |
Het |
Or10ag57 |
T |
G |
2: 87,218,470 (GRCm39) |
N140K |
probably benign |
Het |
Or52z14 |
T |
A |
7: 103,253,615 (GRCm39) |
C251* |
probably null |
Het |
Or6c66b |
A |
G |
10: 129,376,925 (GRCm39) |
D173G |
probably damaging |
Het |
Pigg |
T |
C |
5: 108,467,816 (GRCm39) |
S272P |
probably damaging |
Het |
Plg |
A |
G |
17: 12,637,959 (GRCm39) |
Y795C |
probably damaging |
Het |
Polr3e |
A |
G |
7: 120,536,843 (GRCm39) |
K335R |
probably benign |
Het |
Pramel13 |
T |
A |
4: 144,121,397 (GRCm39) |
Y209F |
probably benign |
Het |
Pramel28 |
T |
C |
4: 143,692,411 (GRCm39) |
I197V |
probably benign |
Het |
Pramel28 |
T |
A |
4: 143,692,608 (GRCm39) |
Q131L |
probably benign |
Het |
Prdm4 |
A |
T |
10: 85,743,685 (GRCm39) |
M190K |
possibly damaging |
Het |
Prex2 |
T |
A |
1: 11,210,489 (GRCm39) |
F597L |
probably benign |
Het |
Ranbp3l |
A |
G |
15: 9,060,940 (GRCm39) |
E403G |
probably damaging |
Het |
Rgmb |
C |
T |
17: 16,027,565 (GRCm39) |
A385T |
possibly damaging |
Het |
Scn4a |
T |
A |
11: 106,211,671 (GRCm39) |
I1449F |
probably damaging |
Het |
Slc17a9 |
T |
C |
2: 180,382,311 (GRCm39) |
|
probably benign |
Het |
Slc26a2 |
T |
C |
18: 61,331,974 (GRCm39) |
I486V |
probably damaging |
Het |
Sntn |
A |
T |
14: 13,678,991 (GRCm38) |
D55V |
probably damaging |
Het |
Snx25 |
T |
A |
8: 46,498,247 (GRCm39) |
R595S |
probably benign |
Het |
Spag11b |
C |
T |
8: 19,191,426 (GRCm39) |
T33I |
probably damaging |
Het |
Sval2 |
A |
G |
6: 41,841,181 (GRCm39) |
I81M |
probably damaging |
Het |
Tab2 |
A |
G |
10: 7,795,039 (GRCm39) |
V481A |
probably damaging |
Het |
Zfp867 |
G |
A |
11: 59,355,003 (GRCm39) |
Q109* |
probably null |
Het |
Zfp935 |
T |
C |
13: 62,602,247 (GRCm39) |
T318A |
probably benign |
Het |
|
Other mutations in Pramel24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00976:Pramel24
|
APN |
4 |
143,453,585 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01122:Pramel24
|
APN |
4 |
143,454,971 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02314:Pramel24
|
APN |
4 |
143,455,012 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03089:Pramel24
|
APN |
4 |
143,452,703 (GRCm39) |
missense |
probably benign |
0.43 |
R0233:Pramel24
|
UTSW |
4 |
143,452,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0233:Pramel24
|
UTSW |
4 |
143,452,633 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0349:Pramel24
|
UTSW |
4 |
143,453,629 (GRCm39) |
missense |
probably benign |
0.00 |
R0681:Pramel24
|
UTSW |
4 |
143,454,622 (GRCm39) |
missense |
probably benign |
|
R0963:Pramel24
|
UTSW |
4 |
143,453,678 (GRCm39) |
missense |
possibly damaging |
0.50 |
R1114:Pramel24
|
UTSW |
4 |
143,453,425 (GRCm39) |
missense |
probably benign |
0.01 |
R2070:Pramel24
|
UTSW |
4 |
143,453,472 (GRCm39) |
nonsense |
probably null |
|
R2475:Pramel24
|
UTSW |
4 |
143,453,395 (GRCm39) |
missense |
probably benign |
0.14 |
R3824:Pramel24
|
UTSW |
4 |
143,453,255 (GRCm39) |
missense |
probably benign |
0.00 |
R4050:Pramel24
|
UTSW |
4 |
143,453,692 (GRCm39) |
missense |
probably benign |
0.01 |
R4125:Pramel24
|
UTSW |
4 |
143,452,850 (GRCm39) |
nonsense |
probably null |
|
R4273:Pramel24
|
UTSW |
4 |
143,453,416 (GRCm39) |
nonsense |
probably null |
|
R4280:Pramel24
|
UTSW |
4 |
143,452,592 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4921:Pramel24
|
UTSW |
4 |
143,454,896 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5223:Pramel24
|
UTSW |
4 |
143,454,591 (GRCm39) |
missense |
probably benign |
0.00 |
R7256:Pramel24
|
UTSW |
4 |
143,452,849 (GRCm39) |
missense |
probably benign |
0.23 |
R7640:Pramel24
|
UTSW |
4 |
143,453,276 (GRCm39) |
missense |
probably benign |
0.00 |
R7666:Pramel24
|
UTSW |
4 |
143,455,085 (GRCm39) |
missense |
probably benign |
0.00 |
R7683:Pramel24
|
UTSW |
4 |
143,453,284 (GRCm39) |
nonsense |
probably null |
|
R7981:Pramel24
|
UTSW |
4 |
143,453,452 (GRCm39) |
missense |
probably benign |
0.01 |
R8856:Pramel24
|
UTSW |
4 |
143,453,303 (GRCm39) |
missense |
probably benign |
0.33 |
R9050:Pramel24
|
UTSW |
4 |
143,453,329 (GRCm39) |
missense |
probably benign |
0.03 |
R9739:Pramel24
|
UTSW |
4 |
143,454,997 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9757:Pramel24
|
UTSW |
4 |
143,454,992 (GRCm39) |
missense |
probably benign |
0.00 |
Z1088:Pramel24
|
UTSW |
4 |
143,453,603 (GRCm39) |
missense |
probably damaging |
1.00 |
|