Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
A |
T |
1: 71,302,717 (GRCm39) |
D2167E |
possibly damaging |
Het |
Acadsb |
T |
A |
7: 131,045,327 (GRCm39) |
Y420N |
probably benign |
Het |
Adcy1 |
T |
A |
11: 7,014,126 (GRCm39) |
L176Q |
probably damaging |
Het |
Amdhd1 |
T |
A |
10: 93,367,398 (GRCm39) |
K252M |
possibly damaging |
Het |
Aspa |
C |
A |
11: 73,213,094 (GRCm39) |
E83* |
probably null |
Het |
Atat1 |
A |
G |
17: 36,220,899 (GRCm39) |
L10P |
probably damaging |
Het |
Ccdc141 |
T |
A |
2: 76,869,919 (GRCm39) |
N862I |
probably damaging |
Het |
Cdkal1 |
A |
T |
13: 29,809,692 (GRCm39) |
C217* |
probably null |
Het |
Cttnbp2 |
C |
T |
6: 18,435,240 (GRCm39) |
S206N |
probably benign |
Het |
Dner |
A |
T |
1: 84,361,656 (GRCm39) |
I651N |
possibly damaging |
Het |
Efcab3 |
G |
A |
11: 104,890,485 (GRCm39) |
G4189E |
possibly damaging |
Het |
Epha8 |
G |
T |
4: 136,665,897 (GRCm39) |
L420M |
probably damaging |
Het |
Ercc6l2 |
T |
C |
13: 63,982,438 (GRCm39) |
V91A |
probably damaging |
Het |
Gask1a |
A |
G |
9: 121,805,421 (GRCm39) |
D404G |
probably damaging |
Het |
Gm13941 |
A |
G |
2: 110,931,518 (GRCm39) |
L38S |
unknown |
Het |
Golph3l |
G |
A |
3: 95,517,085 (GRCm39) |
E198K |
possibly damaging |
Het |
Hecw2 |
A |
C |
1: 53,963,074 (GRCm39) |
D812E |
probably damaging |
Het |
Ikzf2 |
T |
A |
1: 69,587,835 (GRCm39) |
E212V |
possibly damaging |
Het |
Il6st |
C |
T |
13: 112,627,051 (GRCm39) |
S281F |
probably damaging |
Het |
Kmt2d |
CTGTTG |
CTG |
15: 98,743,057 (GRCm39) |
|
probably benign |
Het |
Krt71 |
T |
G |
15: 101,646,757 (GRCm39) |
K317T |
probably damaging |
Het |
Lgi4 |
T |
C |
7: 30,760,020 (GRCm39) |
F72S |
probably damaging |
Het |
Map3k1 |
C |
T |
13: 111,912,499 (GRCm39) |
R174H |
probably damaging |
Het |
Marveld3 |
T |
A |
8: 110,688,375 (GRCm39) |
H122L |
probably benign |
Het |
Mrgprb2 |
A |
G |
7: 48,202,174 (GRCm39) |
S184P |
probably benign |
Het |
Mylk |
G |
T |
16: 34,699,482 (GRCm39) |
G282* |
probably null |
Het |
Myo16 |
T |
A |
8: 10,450,528 (GRCm39) |
M510K |
unknown |
Het |
Naip5 |
C |
G |
13: 100,367,269 (GRCm39) |
A276P |
probably damaging |
Het |
Or10a3 |
T |
A |
7: 108,480,874 (GRCm39) |
|
probably benign |
Het |
Or10a3n |
T |
G |
7: 108,493,210 (GRCm39) |
I140L |
probably benign |
Het |
Or3a1d |
T |
C |
11: 74,238,041 (GRCm39) |
Y3C |
probably damaging |
Het |
Or4e5 |
T |
G |
14: 52,728,307 (GRCm39) |
Y38S |
probably damaging |
Het |
Or8j3 |
A |
T |
2: 86,028,181 (GRCm39) |
M305K |
probably benign |
Het |
Or9g20 |
T |
G |
2: 85,630,060 (GRCm39) |
N185H |
possibly damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,668,376 (GRCm39) |
Y843H |
probably damaging |
Het |
Prkca |
A |
G |
11: 107,903,867 (GRCm39) |
V242A |
possibly damaging |
Het |
Rbbp8 |
A |
T |
18: 11,865,261 (GRCm39) |
M717L |
probably benign |
Het |
Rtraf |
A |
G |
14: 19,866,314 (GRCm39) |
V134A |
probably damaging |
Het |
Rubcnl |
T |
A |
14: 75,287,108 (GRCm39) |
L592* |
probably null |
Het |
Slc23a1 |
A |
G |
18: 35,755,364 (GRCm39) |
S484P |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,204,118 (GRCm39) |
Y68H |
probably damaging |
Het |
Speer4b |
C |
A |
5: 27,705,206 (GRCm39) |
V56L |
probably damaging |
Het |
Sycp2l |
T |
A |
13: 41,306,232 (GRCm39) |
S84T |
|
Het |
Syne1 |
T |
C |
10: 5,007,858 (GRCm39) |
D122G |
probably benign |
Het |
Timd2 |
G |
T |
11: 46,573,540 (GRCm39) |
P155T |
probably benign |
Het |
Topbp1 |
G |
A |
9: 103,223,923 (GRCm39) |
R1401Q |
probably benign |
Het |
Trim36 |
C |
A |
18: 46,309,125 (GRCm39) |
D312Y |
probably benign |
Het |
Vps13c |
A |
G |
9: 67,818,860 (GRCm39) |
T1094A |
probably benign |
Het |
Vwa8 |
T |
A |
14: 79,186,988 (GRCm39) |
Y465N |
probably damaging |
Het |
Zfpm1 |
T |
C |
8: 123,062,531 (GRCm39) |
L530P |
probably damaging |
Het |
Zmynd10 |
A |
T |
9: 107,425,965 (GRCm39) |
T100S |
probably benign |
Het |
|
Other mutations in Rnf150 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02183:Rnf150
|
APN |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R0512:Rnf150
|
UTSW |
8 |
83,590,807 (GRCm39) |
missense |
probably benign |
0.01 |
R1848:Rnf150
|
UTSW |
8 |
83,590,639 (GRCm39) |
start codon destroyed |
possibly damaging |
0.67 |
R2078:Rnf150
|
UTSW |
8 |
83,730,234 (GRCm39) |
missense |
probably damaging |
0.96 |
R2192:Rnf150
|
UTSW |
8 |
83,591,020 (GRCm39) |
missense |
probably damaging |
0.98 |
R3918:Rnf150
|
UTSW |
8 |
83,591,090 (GRCm39) |
missense |
probably benign |
0.25 |
R4365:Rnf150
|
UTSW |
8 |
83,590,744 (GRCm39) |
missense |
probably benign |
0.05 |
R4781:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R4810:Rnf150
|
UTSW |
8 |
83,716,991 (GRCm39) |
missense |
possibly damaging |
0.66 |
R4859:Rnf150
|
UTSW |
8 |
83,590,712 (GRCm39) |
missense |
probably damaging |
1.00 |
R5677:Rnf150
|
UTSW |
8 |
83,730,228 (GRCm39) |
nonsense |
probably null |
|
R6022:Rnf150
|
UTSW |
8 |
83,769,358 (GRCm39) |
missense |
probably benign |
0.00 |
R6241:Rnf150
|
UTSW |
8 |
83,591,093 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6283:Rnf150
|
UTSW |
8 |
83,717,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Rnf150
|
UTSW |
8 |
83,810,131 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7014:Rnf150
|
UTSW |
8 |
83,769,292 (GRCm39) |
missense |
probably benign |
|
R7023:Rnf150
|
UTSW |
8 |
83,590,706 (GRCm39) |
missense |
probably damaging |
0.97 |
R7394:Rnf150
|
UTSW |
8 |
83,717,100 (GRCm39) |
nonsense |
probably null |
|
R7710:Rnf150
|
UTSW |
8 |
83,590,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7771:Rnf150
|
UTSW |
8 |
83,590,832 (GRCm39) |
missense |
probably benign |
0.00 |
R8073:Rnf150
|
UTSW |
8 |
83,590,546 (GRCm39) |
start gained |
probably benign |
|
R8856:Rnf150
|
UTSW |
8 |
83,762,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R8980:Rnf150
|
UTSW |
8 |
83,717,087 (GRCm39) |
missense |
probably benign |
0.19 |
R9139:Rnf150
|
UTSW |
8 |
83,590,588 (GRCm39) |
start gained |
probably benign |
|
R9289:Rnf150
|
UTSW |
8 |
83,716,982 (GRCm39) |
missense |
probably benign |
|
R9410:Rnf150
|
UTSW |
8 |
83,762,722 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9594:Rnf150
|
UTSW |
8 |
83,717,144 (GRCm39) |
missense |
probably damaging |
1.00 |
R9603:Rnf150
|
UTSW |
8 |
83,717,208 (GRCm39) |
missense |
possibly damaging |
0.64 |
|