Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc5 |
T |
A |
16: 20,218,759 (GRCm39) |
T208S |
probably benign |
Het |
Acaa2 |
A |
G |
18: 74,926,380 (GRCm39) |
E112G |
probably benign |
Het |
Adgrb1 |
A |
G |
15: 74,421,873 (GRCm39) |
N881S |
probably damaging |
Het |
Adgre1 |
A |
G |
17: 57,717,844 (GRCm39) |
E314G |
probably benign |
Het |
Adgre1 |
A |
G |
17: 57,727,399 (GRCm39) |
E443G |
probably benign |
Het |
Akp3 |
A |
G |
1: 87,053,353 (GRCm39) |
Y102C |
probably damaging |
Het |
Birc6 |
A |
G |
17: 74,886,526 (GRCm39) |
N618S |
probably benign |
Het |
Bpifc |
A |
G |
10: 85,815,078 (GRCm39) |
V296A |
probably benign |
Het |
Cacna2d3 |
G |
A |
14: 28,691,275 (GRCm39) |
|
probably benign |
Het |
Cacnb4 |
T |
C |
2: 52,364,966 (GRCm39) |
N99S |
probably damaging |
Het |
Cd38 |
A |
G |
5: 44,065,348 (GRCm39) |
Y283C |
probably damaging |
Het |
Celf4 |
T |
A |
18: 25,629,293 (GRCm39) |
Q411L |
probably damaging |
Het |
Cemip |
A |
T |
7: 83,647,755 (GRCm39) |
H108Q |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,024,045 (GRCm39) |
E1902G |
probably damaging |
Het |
Dst |
A |
G |
1: 34,229,571 (GRCm39) |
D2063G |
probably damaging |
Het |
Fsip2 |
A |
T |
2: 82,823,184 (GRCm39) |
I6306L |
probably benign |
Het |
Furin |
A |
G |
7: 80,040,838 (GRCm39) |
S667P |
possibly damaging |
Het |
Glmp |
T |
A |
3: 88,233,139 (GRCm39) |
S92R |
probably benign |
Het |
Gm11563 |
C |
G |
11: 99,549,298 (GRCm39) |
C152S |
unknown |
Het |
Gm3486 |
A |
G |
14: 41,206,518 (GRCm39) |
V185A |
probably benign |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
Hyal1 |
C |
A |
9: 107,456,369 (GRCm39) |
A102E |
probably damaging |
Het |
Invs |
T |
C |
4: 48,421,785 (GRCm39) |
C806R |
probably benign |
Het |
L1td1 |
T |
C |
4: 98,621,933 (GRCm39) |
V165A |
probably benign |
Het |
Lama1 |
A |
G |
17: 68,120,861 (GRCm39) |
T2666A |
|
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrrc8a |
A |
G |
2: 30,146,239 (GRCm39) |
Y351C |
probably damaging |
Het |
Myh7b |
T |
C |
2: 155,464,152 (GRCm39) |
F551S |
possibly damaging |
Het |
Myo19 |
A |
G |
11: 84,788,386 (GRCm39) |
T333A |
probably benign |
Het |
Nrp2 |
A |
T |
1: 62,799,947 (GRCm39) |
N387I |
probably damaging |
Het |
Oas2 |
T |
C |
5: 120,874,204 (GRCm39) |
D543G |
probably benign |
Het |
Or2g25 |
A |
G |
17: 37,970,405 (GRCm39) |
I273T |
possibly damaging |
Het |
Or5al6 |
A |
G |
2: 85,976,428 (GRCm39) |
S217P |
probably damaging |
Het |
Pak5 |
A |
G |
2: 135,942,859 (GRCm39) |
V427A |
probably benign |
Het |
Pfas |
G |
A |
11: 68,891,356 (GRCm39) |
A247V |
probably benign |
Het |
Pramel52-ps |
C |
T |
5: 94,531,490 (GRCm39) |
H125Y |
possibly damaging |
Het |
Psat1 |
T |
A |
19: 15,894,545 (GRCm39) |
T115S |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,787,437 (GRCm39) |
D1077E |
probably benign |
Het |
Rabgap1l |
A |
G |
1: 160,509,752 (GRCm39) |
S442P |
probably benign |
Het |
Ralgapa1 |
A |
G |
12: 55,822,976 (GRCm39) |
M280T |
possibly damaging |
Het |
Rb1cc1 |
A |
T |
1: 6,331,256 (GRCm39) |
E394D |
probably damaging |
Het |
Seh1l |
T |
C |
18: 67,922,460 (GRCm39) |
V271A |
probably benign |
Het |
Sf3b1 |
A |
T |
1: 55,036,315 (GRCm39) |
N919K |
probably benign |
Het |
Sftpd |
A |
G |
14: 40,896,449 (GRCm39) |
S245P |
possibly damaging |
Het |
Slc22a15 |
T |
C |
3: 101,831,430 (GRCm39) |
E2G |
probably damaging |
Het |
Spta1 |
A |
G |
1: 174,036,891 (GRCm39) |
D1134G |
possibly damaging |
Het |
Syna |
A |
G |
5: 134,587,815 (GRCm39) |
V378A |
probably damaging |
Het |
Tchp |
A |
G |
5: 114,847,411 (GRCm39) |
K77E |
possibly damaging |
Het |
Tescl |
T |
C |
7: 24,032,956 (GRCm39) |
N123S |
probably benign |
Het |
Trio |
C |
T |
15: 27,824,176 (GRCm39) |
R1443Q |
probably damaging |
Het |
Trrap |
A |
T |
5: 144,727,665 (GRCm39) |
Y462F |
possibly damaging |
Het |
Vmn1r78 |
A |
G |
7: 11,886,832 (GRCm39) |
T148A |
probably benign |
Het |
Vmn2r111 |
T |
C |
17: 22,778,032 (GRCm39) |
N549S |
possibly damaging |
Het |
Zfp1007 |
A |
C |
5: 109,824,711 (GRCm39) |
N246K |
probably benign |
Het |
|
Other mutations in Col23a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02797:Col23a1
|
APN |
11 |
51,452,743 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02997:Col23a1
|
APN |
11 |
51,467,979 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03237:Col23a1
|
APN |
11 |
51,458,746 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03493:Col23a1
|
APN |
11 |
51,455,632 (GRCm39) |
critical splice donor site |
probably null |
|
R0755:Col23a1
|
UTSW |
11 |
51,467,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1523:Col23a1
|
UTSW |
11 |
51,452,743 (GRCm39) |
critical splice donor site |
probably null |
|
R1721:Col23a1
|
UTSW |
11 |
51,418,716 (GRCm39) |
missense |
unknown |
|
R1939:Col23a1
|
UTSW |
11 |
51,442,816 (GRCm39) |
missense |
unknown |
|
R2032:Col23a1
|
UTSW |
11 |
51,450,835 (GRCm39) |
missense |
unknown |
|
R2139:Col23a1
|
UTSW |
11 |
51,464,861 (GRCm39) |
missense |
probably benign |
0.03 |
R4829:Col23a1
|
UTSW |
11 |
51,448,413 (GRCm39) |
missense |
unknown |
|
R5536:Col23a1
|
UTSW |
11 |
51,458,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R6253:Col23a1
|
UTSW |
11 |
51,464,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R6520:Col23a1
|
UTSW |
11 |
51,440,552 (GRCm39) |
splice site |
probably null |
|
R7145:Col23a1
|
UTSW |
11 |
51,456,050 (GRCm39) |
critical splice donor site |
probably null |
|
R7863:Col23a1
|
UTSW |
11 |
51,463,597 (GRCm39) |
missense |
probably damaging |
1.00 |
R8103:Col23a1
|
UTSW |
11 |
51,461,014 (GRCm39) |
splice site |
probably null |
|
R8347:Col23a1
|
UTSW |
11 |
51,462,083 (GRCm39) |
missense |
probably damaging |
1.00 |
R8681:Col23a1
|
UTSW |
11 |
51,458,756 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9480:Col23a1
|
UTSW |
11 |
51,207,774 (GRCm39) |
missense |
unknown |
|
Z1176:Col23a1
|
UTSW |
11 |
51,440,535 (GRCm39) |
missense |
unknown |
|
|