Other mutations in this stock |
Total: 24 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca3 |
T |
C |
17: 24,603,538 (GRCm39) |
S577P |
probably damaging |
Het |
Agrn |
T |
C |
4: 156,251,785 (GRCm39) |
T1826A |
possibly damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Btnl6 |
C |
A |
17: 34,734,498 (GRCm39) |
R88I |
possibly damaging |
Het |
Cfap52 |
T |
A |
11: 67,830,617 (GRCm39) |
Y281F |
probably benign |
Het |
CK137956 |
T |
C |
4: 127,845,300 (GRCm39) |
T148A |
probably benign |
Het |
Fpr3 |
C |
T |
17: 18,191,130 (GRCm39) |
Q134* |
probably null |
Het |
Gbp4 |
A |
T |
5: 105,284,886 (GRCm39) |
M1K |
probably null |
Het |
Gpsm1 |
G |
A |
2: 26,209,843 (GRCm39) |
|
probably benign |
Het |
Nedd4 |
A |
G |
9: 72,638,185 (GRCm39) |
D440G |
probably benign |
Het |
Nlgn1 |
C |
T |
3: 25,490,162 (GRCm39) |
D522N |
probably damaging |
Het |
Oprk1 |
T |
C |
1: 5,672,955 (GRCm39) |
V364A |
probably benign |
Het |
Or1e35 |
T |
C |
11: 73,797,541 (GRCm39) |
Y259C |
probably damaging |
Het |
Or5d18 |
A |
G |
2: 87,865,301 (GRCm39) |
Y61H |
probably damaging |
Het |
Polr1e |
T |
C |
4: 45,027,473 (GRCm39) |
|
probably null |
Het |
Psmd11 |
T |
C |
11: 80,351,493 (GRCm39) |
Y239H |
probably damaging |
Het |
Ripor2 |
A |
T |
13: 24,885,610 (GRCm39) |
D576V |
probably damaging |
Het |
Rundc3a |
C |
T |
11: 102,291,489 (GRCm39) |
T327I |
probably damaging |
Het |
Sh3rf1 |
A |
G |
8: 61,825,609 (GRCm39) |
T535A |
probably benign |
Het |
Slc13a2 |
T |
A |
11: 78,295,563 (GRCm39) |
E101V |
probably damaging |
Het |
Tg |
A |
T |
15: 66,553,802 (GRCm39) |
T406S |
probably benign |
Het |
Zfp459 |
G |
A |
13: 67,556,853 (GRCm39) |
P77S |
possibly damaging |
Het |
Zfp612 |
A |
G |
8: 110,816,049 (GRCm39) |
K380E |
probably damaging |
Het |
Zfp629 |
T |
C |
7: 127,210,228 (GRCm39) |
E527G |
probably damaging |
Het |
|
Other mutations in Tjp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01151:Tjp2
|
APN |
19 |
24,116,174 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01412:Tjp2
|
APN |
19 |
24,078,139 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01681:Tjp2
|
APN |
19 |
24,112,213 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02044:Tjp2
|
APN |
19 |
24,098,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02212:Tjp2
|
APN |
19 |
24,116,150 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02629:Tjp2
|
APN |
19 |
24,099,743 (GRCm39) |
splice site |
probably benign |
|
IGL02819:Tjp2
|
APN |
19 |
24,091,469 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02931:Tjp2
|
APN |
19 |
24,073,996 (GRCm39) |
missense |
probably benign |
0.11 |
PIT4402001:Tjp2
|
UTSW |
19 |
24,075,493 (GRCm39) |
nonsense |
probably null |
|
R0032:Tjp2
|
UTSW |
19 |
24,086,059 (GRCm39) |
missense |
probably damaging |
1.00 |
R0667:Tjp2
|
UTSW |
19 |
24,086,113 (GRCm39) |
missense |
probably benign |
0.36 |
R0674:Tjp2
|
UTSW |
19 |
24,108,680 (GRCm39) |
missense |
probably benign |
0.37 |
R0749:Tjp2
|
UTSW |
19 |
24,099,636 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1185:Tjp2
|
UTSW |
19 |
24,108,527 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1563:Tjp2
|
UTSW |
19 |
24,110,067 (GRCm39) |
missense |
probably damaging |
0.99 |
R1571:Tjp2
|
UTSW |
19 |
24,078,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R1624:Tjp2
|
UTSW |
19 |
24,108,776 (GRCm39) |
missense |
probably benign |
0.01 |
R1658:Tjp2
|
UTSW |
19 |
24,090,311 (GRCm39) |
missense |
probably damaging |
0.99 |
R1851:Tjp2
|
UTSW |
19 |
24,076,899 (GRCm39) |
missense |
possibly damaging |
0.67 |
R1968:Tjp2
|
UTSW |
19 |
24,088,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R2068:Tjp2
|
UTSW |
19 |
24,099,687 (GRCm39) |
missense |
probably benign |
0.22 |
R2273:Tjp2
|
UTSW |
19 |
24,090,171 (GRCm39) |
missense |
probably benign |
|
R3767:Tjp2
|
UTSW |
19 |
24,078,190 (GRCm39) |
missense |
probably benign |
0.01 |
R3770:Tjp2
|
UTSW |
19 |
24,078,190 (GRCm39) |
missense |
probably benign |
0.01 |
R4077:Tjp2
|
UTSW |
19 |
24,086,182 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4079:Tjp2
|
UTSW |
19 |
24,086,182 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4505:Tjp2
|
UTSW |
19 |
24,086,195 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4720:Tjp2
|
UTSW |
19 |
24,078,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R4739:Tjp2
|
UTSW |
19 |
24,097,475 (GRCm39) |
splice site |
probably null |
|
R4745:Tjp2
|
UTSW |
19 |
24,074,030 (GRCm39) |
missense |
possibly damaging |
0.56 |
R4858:Tjp2
|
UTSW |
19 |
24,099,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Tjp2
|
UTSW |
19 |
24,108,568 (GRCm39) |
missense |
probably benign |
|
R5887:Tjp2
|
UTSW |
19 |
24,073,963 (GRCm39) |
missense |
probably benign |
|
R5988:Tjp2
|
UTSW |
19 |
24,091,464 (GRCm39) |
missense |
probably benign |
|
R6144:Tjp2
|
UTSW |
19 |
24,097,437 (GRCm39) |
missense |
probably damaging |
0.99 |
R6163:Tjp2
|
UTSW |
19 |
24,103,068 (GRCm39) |
critical splice donor site |
probably null |
|
R6183:Tjp2
|
UTSW |
19 |
24,078,155 (GRCm39) |
missense |
probably damaging |
0.99 |
R6242:Tjp2
|
UTSW |
19 |
24,076,967 (GRCm39) |
splice site |
probably null |
|
R6683:Tjp2
|
UTSW |
19 |
24,098,207 (GRCm39) |
missense |
probably damaging |
0.99 |
R6866:Tjp2
|
UTSW |
19 |
24,079,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R7025:Tjp2
|
UTSW |
19 |
24,110,052 (GRCm39) |
missense |
probably benign |
0.28 |
R7153:Tjp2
|
UTSW |
19 |
24,079,345 (GRCm39) |
missense |
probably benign |
0.40 |
R7514:Tjp2
|
UTSW |
19 |
24,088,886 (GRCm39) |
missense |
probably benign |
0.03 |
R8004:Tjp2
|
UTSW |
19 |
24,091,484 (GRCm39) |
missense |
probably damaging |
1.00 |
R8505:Tjp2
|
UTSW |
19 |
24,088,438 (GRCm39) |
missense |
probably null |
1.00 |
R8527:Tjp2
|
UTSW |
19 |
24,088,937 (GRCm39) |
missense |
probably damaging |
0.99 |
R8710:Tjp2
|
UTSW |
19 |
24,072,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R9718:Tjp2
|
UTSW |
19 |
24,078,207 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:Tjp2
|
UTSW |
19 |
24,075,391 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Tjp2
|
UTSW |
19 |
24,108,729 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Tjp2
|
UTSW |
19 |
24,072,824 (GRCm39) |
missense |
possibly damaging |
0.74 |
|