Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acin1 |
C |
T |
14: 54,901,172 (GRCm39) |
G685R |
probably benign |
Het |
Ahdc1 |
T |
C |
4: 132,791,129 (GRCm39) |
F790S |
possibly damaging |
Het |
Alg10b |
T |
C |
15: 90,109,893 (GRCm39) |
Y69H |
probably damaging |
Het |
Amer3 |
A |
T |
1: 34,626,465 (GRCm39) |
S235C |
probably damaging |
Het |
Ankfy1 |
G |
T |
11: 72,644,469 (GRCm39) |
S722I |
probably benign |
Het |
Baz1a |
T |
C |
12: 55,032,624 (GRCm39) |
|
probably benign |
Het |
Ccdc177 |
A |
G |
12: 80,804,208 (GRCm39) |
S689P |
unknown |
Het |
Cdh24 |
C |
A |
14: 54,869,874 (GRCm39) |
R681L |
probably damaging |
Het |
Cdk14 |
T |
G |
5: 5,060,862 (GRCm39) |
I338L |
probably benign |
Het |
Clec2m |
T |
C |
6: 129,308,494 (GRCm39) |
T12A |
probably benign |
Het |
Col18a1 |
G |
T |
10: 76,949,044 (GRCm39) |
S156* |
probably null |
Het |
Col6a6 |
T |
C |
9: 105,663,348 (GRCm39) |
Y63C |
probably damaging |
Het |
Dnah5 |
T |
C |
15: 28,459,502 (GRCm39) |
|
probably benign |
Het |
Dock3 |
T |
C |
9: 106,855,927 (GRCm39) |
Y744C |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,406,404 (GRCm39) |
|
probably null |
Het |
Dse |
A |
T |
10: 34,029,934 (GRCm39) |
D385E |
probably damaging |
Het |
Efhc1 |
A |
C |
1: 21,037,573 (GRCm39) |
D250A |
|
Het |
Epha3 |
T |
A |
16: 63,431,348 (GRCm39) |
T519S |
probably benign |
Het |
Gas2l3 |
A |
G |
10: 89,250,282 (GRCm39) |
Y279H |
probably damaging |
Het |
Gatd3a |
A |
G |
10: 78,005,461 (GRCm39) |
S35P |
probably damaging |
Het |
Gemin6 |
G |
A |
17: 80,535,432 (GRCm39) |
V131I |
probably damaging |
Het |
Gm40460 |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
CACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 141,794,554 (GRCm39) |
|
probably benign |
Het |
Gnai2 |
C |
A |
9: 107,512,326 (GRCm39) |
A31S |
|
Het |
Greb1l |
A |
G |
18: 10,555,042 (GRCm39) |
D1696G |
possibly damaging |
Het |
Itfg2 |
T |
C |
6: 128,394,668 (GRCm39) |
E35G |
probably damaging |
Het |
Kctd10 |
A |
G |
5: 114,503,921 (GRCm39) |
F244L |
probably damaging |
Het |
Kif19b |
C |
A |
5: 140,472,534 (GRCm39) |
P686Q |
probably damaging |
Het |
Krtap5-1 |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
ACAGGGCTTGCAGCAGCTGGACTGACAGCAGCAGGGCTTGCAGCAGCTGGACTGACAGCAG |
7: 141,850,333 (GRCm39) |
|
probably benign |
Het |
Lgals9 |
G |
T |
11: 78,860,716 (GRCm39) |
|
probably benign |
Het |
Lrriq4 |
A |
T |
3: 30,705,088 (GRCm39) |
N372I |
probably damaging |
Het |
Mical2 |
A |
G |
7: 111,910,574 (GRCm39) |
N248S |
probably damaging |
Het |
Mipep |
T |
A |
14: 61,080,689 (GRCm39) |
C560* |
probably null |
Het |
Myo1a |
G |
A |
10: 127,548,653 (GRCm39) |
V396M |
probably benign |
Het |
Myod1 |
A |
G |
7: 46,026,487 (GRCm39) |
T131A |
probably damaging |
Het |
Nalcn |
T |
A |
14: 123,647,199 (GRCm39) |
D558V |
possibly damaging |
Het |
Odf2l |
T |
A |
3: 144,833,758 (GRCm39) |
|
probably benign |
Het |
Or6d13 |
G |
A |
6: 116,518,186 (GRCm39) |
M257I |
probably benign |
Het |
Plbd2 |
A |
T |
5: 120,624,728 (GRCm39) |
M480K |
probably damaging |
Het |
Ppargc1a |
A |
G |
5: 51,631,235 (GRCm39) |
F465L |
possibly damaging |
Het |
Ppp1r15b |
A |
T |
1: 133,064,506 (GRCm39) |
I659F |
probably damaging |
Het |
Prune2 |
C |
T |
19: 17,097,510 (GRCm39) |
L1005F |
probably benign |
Het |
Pter |
T |
C |
2: 12,985,341 (GRCm39) |
S224P |
probably damaging |
Het |
Ralgapa2 |
A |
G |
2: 146,266,731 (GRCm39) |
I615T |
probably benign |
Het |
Ror1 |
T |
C |
4: 100,191,715 (GRCm39) |
|
probably null |
Het |
Rps2 |
A |
G |
17: 24,940,662 (GRCm39) |
T259A |
probably benign |
Het |
Rsf1 |
GCG |
GCGACGGCGCCG |
7: 97,229,114 (GRCm39) |
|
probably benign |
Het |
S1pr4 |
G |
A |
10: 81,334,533 (GRCm39) |
R314C |
probably damaging |
Het |
Sema4f |
A |
T |
6: 82,891,081 (GRCm39) |
H575Q |
probably benign |
Het |
Son |
A |
G |
16: 91,453,734 (GRCm39) |
D827G |
probably damaging |
Het |
Sox8 |
A |
T |
17: 25,787,045 (GRCm39) |
H219Q |
possibly damaging |
Het |
Spink2 |
C |
T |
5: 77,357,615 (GRCm39) |
D24N |
probably benign |
Het |
Stard9 |
A |
G |
2: 120,534,099 (GRCm39) |
D3452G |
probably benign |
Het |
Syngr2 |
G |
T |
11: 117,703,507 (GRCm39) |
D108Y |
probably damaging |
Het |
Tardbp |
G |
A |
4: 148,702,755 (GRCm39) |
S403L |
possibly damaging |
Het |
Tomm70a |
T |
C |
16: 56,942,546 (GRCm39) |
S108P |
probably benign |
Het |
Ttc12 |
T |
C |
9: 49,351,515 (GRCm39) |
T661A |
probably benign |
Het |
Tubgcp6 |
A |
G |
15: 89,006,824 (GRCm39) |
V66A |
probably benign |
Het |
Unc13b |
T |
A |
4: 43,235,207 (GRCm39) |
L477Q |
probably damaging |
Het |
Vmn1r77 |
T |
A |
7: 11,776,060 (GRCm39) |
C279S |
probably benign |
Het |
Vmn2r79 |
T |
C |
7: 86,645,712 (GRCm39) |
S14P |
probably benign |
Het |
Zan |
T |
C |
5: 137,472,674 (GRCm39) |
T72A |
probably benign |
Het |
Zcchc2 |
A |
G |
1: 105,958,998 (GRCm39) |
*1156W |
probably null |
Het |
Zfp354c |
A |
T |
11: 50,708,718 (GRCm39) |
D26E |
probably benign |
Het |
|
Other mutations in Cytip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01635:Cytip
|
APN |
2 |
58,038,243 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01670:Cytip
|
APN |
2 |
58,023,785 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02184:Cytip
|
APN |
2 |
58,023,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02271:Cytip
|
APN |
2 |
58,023,872 (GRCm39) |
nonsense |
probably null |
|
IGL02468:Cytip
|
APN |
2 |
58,024,025 (GRCm39) |
missense |
probably benign |
0.08 |
R0079:Cytip
|
UTSW |
2 |
58,050,006 (GRCm39) |
missense |
probably benign |
0.37 |
R0304:Cytip
|
UTSW |
2 |
58,038,258 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0612:Cytip
|
UTSW |
2 |
58,024,202 (GRCm39) |
missense |
possibly damaging |
0.46 |
R1448:Cytip
|
UTSW |
2 |
58,035,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R1822:Cytip
|
UTSW |
2 |
58,024,158 (GRCm39) |
missense |
probably benign |
0.00 |
R1954:Cytip
|
UTSW |
2 |
58,038,265 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4401:Cytip
|
UTSW |
2 |
58,023,947 (GRCm39) |
missense |
probably benign |
0.01 |
R4578:Cytip
|
UTSW |
2 |
58,050,024 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5101:Cytip
|
UTSW |
2 |
58,037,911 (GRCm39) |
missense |
probably damaging |
1.00 |
R7104:Cytip
|
UTSW |
2 |
58,049,986 (GRCm39) |
missense |
probably benign |
0.00 |
R7703:Cytip
|
UTSW |
2 |
58,037,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R7966:Cytip
|
UTSW |
2 |
58,037,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R8492:Cytip
|
UTSW |
2 |
58,027,869 (GRCm39) |
critical splice donor site |
probably null |
|
R8711:Cytip
|
UTSW |
2 |
58,041,135 (GRCm39) |
missense |
probably damaging |
0.99 |
R9548:Cytip
|
UTSW |
2 |
58,041,141 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1176:Cytip
|
UTSW |
2 |
58,024,049 (GRCm39) |
missense |
probably damaging |
1.00 |
|