Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd17 |
T |
C |
5: 90,391,395 (GRCm39) |
S1841G |
possibly damaging |
Het |
Anxa10 |
T |
C |
8: 62,516,093 (GRCm39) |
E193G |
possibly damaging |
Het |
Ap3d1 |
T |
C |
10: 80,545,284 (GRCm39) |
S1056G |
probably benign |
Het |
Apbb1 |
T |
C |
7: 105,214,242 (GRCm39) |
N62D |
probably damaging |
Het |
Apobec2 |
A |
T |
17: 48,730,022 (GRCm39) |
Y215N |
probably damaging |
Het |
Apobec2 |
T |
A |
17: 48,730,024 (GRCm39) |
Y214F |
probably damaging |
Het |
Appl2 |
A |
T |
10: 83,436,871 (GRCm39) |
V630E |
probably benign |
Het |
Bud23 |
T |
C |
5: 135,089,877 (GRCm39) |
|
probably benign |
Het |
Cacna1b |
A |
T |
2: 24,580,797 (GRCm39) |
M683K |
possibly damaging |
Het |
Cbfa2t2 |
T |
A |
2: 154,373,293 (GRCm39) |
D187E |
probably damaging |
Het |
Cfap54 |
G |
T |
10: 92,773,753 (GRCm39) |
F96L |
probably benign |
Het |
Cimap1a |
A |
T |
7: 140,429,461 (GRCm39) |
S197C |
probably benign |
Het |
Crebbp |
A |
G |
16: 3,906,295 (GRCm39) |
|
probably benign |
Het |
Crocc |
C |
T |
4: 140,755,722 (GRCm39) |
R1102Q |
probably damaging |
Het |
Dcaf12 |
T |
C |
4: 41,298,329 (GRCm39) |
D273G |
possibly damaging |
Het |
Dchs1 |
T |
C |
7: 105,414,221 (GRCm39) |
T865A |
probably benign |
Het |
Dhfr |
A |
T |
13: 92,491,788 (GRCm39) |
I8F |
probably damaging |
Het |
Dnaja2 |
A |
T |
8: 86,279,887 (GRCm39) |
F97L |
possibly damaging |
Het |
Dnase1l1 |
C |
T |
X: 73,320,644 (GRCm39) |
|
probably null |
Het |
Doc2b |
T |
C |
11: 75,667,967 (GRCm39) |
D261G |
probably benign |
Het |
Ear1 |
A |
G |
14: 44,056,485 (GRCm39) |
Y128H |
probably benign |
Het |
Elac2 |
T |
A |
11: 64,883,142 (GRCm39) |
I171N |
probably damaging |
Het |
Entpd3 |
C |
A |
9: 120,395,380 (GRCm39) |
N454K |
possibly damaging |
Het |
Flrt3 |
A |
G |
2: 140,502,663 (GRCm39) |
S322P |
possibly damaging |
Het |
Fn1 |
C |
T |
1: 71,688,394 (GRCm39) |
C170Y |
probably damaging |
Het |
Gabbr1 |
T |
A |
17: 37,382,920 (GRCm39) |
|
probably benign |
Het |
Gm7247 |
T |
G |
14: 51,602,774 (GRCm39) |
S37A |
probably damaging |
Het |
Gm8775 |
T |
A |
3: 4,277,008 (GRCm39) |
|
noncoding transcript |
Het |
Gprc5c |
G |
T |
11: 114,755,093 (GRCm39) |
V257L |
possibly damaging |
Het |
Gria4 |
A |
C |
9: 4,472,168 (GRCm39) |
N440K |
probably damaging |
Het |
H2-T22 |
T |
A |
17: 36,350,113 (GRCm39) |
R334* |
probably null |
Het |
Ift172 |
T |
C |
5: 31,423,330 (GRCm39) |
D817G |
probably benign |
Het |
Igkv9-124 |
T |
A |
6: 67,919,348 (GRCm39) |
R21S |
possibly damaging |
Het |
Itgam |
G |
A |
7: 127,712,390 (GRCm39) |
V846I |
probably benign |
Het |
Kif11 |
T |
A |
19: 37,373,063 (GRCm39) |
M94K |
possibly damaging |
Het |
Krtcap2 |
T |
C |
3: 89,154,085 (GRCm39) |
V2A |
probably benign |
Het |
Lrrc47 |
A |
G |
4: 154,101,933 (GRCm39) |
D400G |
probably damaging |
Het |
Man2a1 |
T |
A |
17: 65,059,443 (GRCm39) |
V1110E |
probably benign |
Het |
Mfsd9 |
T |
A |
1: 40,813,365 (GRCm39) |
I317F |
probably damaging |
Het |
Mindy4 |
A |
T |
6: 55,193,730 (GRCm39) |
|
probably null |
Het |
Mrpl53 |
A |
G |
6: 83,086,541 (GRCm39) |
T82A |
probably damaging |
Het |
Myo3b |
A |
G |
2: 69,925,637 (GRCm39) |
K35E |
possibly damaging |
Het |
Nalcn |
A |
G |
14: 123,515,650 (GRCm39) |
V1717A |
possibly damaging |
Het |
Ncoa2 |
A |
G |
1: 13,257,070 (GRCm39) |
V143A |
probably damaging |
Het |
Or10ag60 |
G |
A |
2: 87,438,319 (GRCm39) |
G196R |
possibly damaging |
Het |
Or10ag60 |
G |
A |
2: 87,437,755 (GRCm39) |
A8T |
possibly damaging |
Het |
Or12e9 |
A |
G |
2: 87,201,878 (GRCm39) |
M1V |
probably null |
Het |
Or5k17 |
A |
G |
16: 58,746,422 (GRCm39) |
S171P |
probably benign |
Het |
Or5p55 |
T |
C |
7: 107,567,104 (GRCm39) |
S167P |
probably benign |
Het |
Or6c202 |
T |
C |
10: 128,996,106 (GRCm39) |
Y249C |
probably damaging |
Het |
Or7g28 |
A |
T |
9: 19,272,438 (GRCm39) |
I71N |
probably damaging |
Het |
Or9g8 |
G |
A |
2: 85,607,668 (GRCm39) |
V247M |
probably damaging |
Het |
Pde4b |
G |
T |
4: 102,458,741 (GRCm39) |
A466S |
probably damaging |
Het |
Pfkfb3 |
A |
T |
2: 11,491,162 (GRCm39) |
|
probably benign |
Het |
Ppp1r21 |
A |
G |
17: 88,866,268 (GRCm39) |
K355E |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,741,095 (GRCm39) |
Y90* |
probably null |
Het |
Rbms1 |
G |
A |
2: 60,612,284 (GRCm39) |
L161F |
probably damaging |
Het |
Rdh16f2 |
A |
G |
10: 127,702,672 (GRCm39) |
D83G |
probably damaging |
Het |
Sec16b |
C |
T |
1: 157,392,361 (GRCm39) |
R910* |
probably null |
Het |
Sema4c |
CTGGGCTT |
C |
1: 36,591,381 (GRCm39) |
|
probably null |
Het |
Spata31e5 |
T |
C |
1: 28,816,636 (GRCm39) |
I465M |
possibly damaging |
Het |
Stambp |
A |
G |
6: 83,540,803 (GRCm39) |
|
probably null |
Het |
Tcf21 |
T |
C |
10: 22,695,558 (GRCm39) |
N82S |
probably damaging |
Het |
Tlr2 |
A |
T |
3: 83,745,030 (GRCm39) |
V351D |
probably damaging |
Het |
Tmem39a |
G |
A |
16: 38,411,326 (GRCm39) |
G359D |
probably damaging |
Het |
Ttc23l |
G |
T |
15: 10,551,636 (GRCm39) |
T30K |
possibly damaging |
Het |
Vmn2r17 |
C |
A |
5: 109,577,342 (GRCm39) |
F464L |
probably benign |
Het |
Vmn2r49 |
T |
A |
7: 9,710,204 (GRCm39) |
T843S |
probably benign |
Het |
Vmn2r7 |
T |
C |
3: 64,598,088 (GRCm39) |
D823G |
probably null |
Het |
Wrnip1 |
T |
A |
13: 33,000,319 (GRCm39) |
L442Q |
probably damaging |
Het |
Zbtb38 |
G |
T |
9: 96,569,062 (GRCm39) |
S674Y |
probably damaging |
Het |
Zfp639 |
T |
G |
3: 32,574,585 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ndufa9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01739:Ndufa9
|
APN |
6 |
126,821,777 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02167:Ndufa9
|
APN |
6 |
126,821,748 (GRCm39) |
splice site |
probably benign |
|
IGL02206:Ndufa9
|
APN |
6 |
126,821,366 (GRCm39) |
nonsense |
probably null |
|
IGL03186:Ndufa9
|
APN |
6 |
126,821,855 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL03356:Ndufa9
|
APN |
6 |
126,821,813 (GRCm39) |
missense |
possibly damaging |
0.89 |
R0310:Ndufa9
|
UTSW |
6 |
126,804,495 (GRCm39) |
splice site |
probably benign |
|
R1118:Ndufa9
|
UTSW |
6 |
126,799,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1119:Ndufa9
|
UTSW |
6 |
126,799,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R1714:Ndufa9
|
UTSW |
6 |
126,799,154 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2207:Ndufa9
|
UTSW |
6 |
126,821,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R2483:Ndufa9
|
UTSW |
6 |
126,821,362 (GRCm39) |
missense |
possibly damaging |
0.48 |
R3617:Ndufa9
|
UTSW |
6 |
126,826,071 (GRCm39) |
unclassified |
probably benign |
|
R3623:Ndufa9
|
UTSW |
6 |
126,821,362 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4619:Ndufa9
|
UTSW |
6 |
126,804,498 (GRCm39) |
splice site |
probably null |
|
R4855:Ndufa9
|
UTSW |
6 |
126,804,505 (GRCm39) |
nonsense |
probably null |
|
R4931:Ndufa9
|
UTSW |
6 |
126,813,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R4965:Ndufa9
|
UTSW |
6 |
126,799,026 (GRCm39) |
missense |
probably benign |
0.01 |
R7373:Ndufa9
|
UTSW |
6 |
126,811,421 (GRCm39) |
missense |
probably damaging |
1.00 |
R9178:Ndufa9
|
UTSW |
6 |
126,826,050 (GRCm39) |
missense |
probably benign |
|
Z1176:Ndufa9
|
UTSW |
6 |
126,821,778 (GRCm39) |
missense |
probably damaging |
1.00 |
|