Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700066M21Rik |
G |
T |
1: 57,416,927 (GRCm39) |
R33L |
probably benign |
Het |
Abhd16b |
A |
T |
2: 181,136,518 (GRCm39) |
R473S |
probably benign |
Het |
Adcyap1r1 |
A |
G |
6: 55,474,140 (GRCm39) |
D492G |
probably damaging |
Het |
Ano5 |
A |
T |
7: 51,229,309 (GRCm39) |
N617I |
probably damaging |
Het |
Clasp2 |
T |
A |
9: 113,738,614 (GRCm39) |
|
probably null |
Het |
Dock8 |
G |
A |
19: 25,133,388 (GRCm39) |
|
probably null |
Het |
Dscaml1 |
T |
C |
9: 45,654,315 (GRCm39) |
V1449A |
probably damaging |
Het |
Ercc6 |
A |
G |
14: 32,282,703 (GRCm39) |
D732G |
probably damaging |
Het |
Fam174c |
T |
A |
10: 80,010,161 (GRCm39) |
|
probably null |
Het |
Fhip2b |
A |
T |
14: 70,825,179 (GRCm39) |
S386T |
possibly damaging |
Het |
Gimap6 |
T |
C |
6: 48,684,951 (GRCm39) |
E45G |
probably benign |
Het |
Glt1d1 |
C |
A |
5: 127,771,364 (GRCm39) |
T285K |
probably damaging |
Het |
Gm14412 |
A |
T |
2: 177,007,636 (GRCm39) |
Y86* |
probably null |
Het |
Grip2 |
A |
G |
6: 91,742,318 (GRCm39) |
S912P |
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,108,290 (GRCm39) |
I741N |
probably damaging |
Het |
Hrh2 |
A |
T |
13: 54,368,299 (GRCm39) |
N92Y |
probably damaging |
Het |
Klrc2 |
T |
A |
6: 129,637,452 (GRCm39) |
Q23L |
possibly damaging |
Het |
Patl2 |
T |
C |
2: 121,955,591 (GRCm39) |
D285G |
probably damaging |
Het |
Prpf40a |
A |
G |
2: 53,035,735 (GRCm39) |
V685A |
probably benign |
Het |
Rspry1 |
A |
G |
8: 95,380,857 (GRCm39) |
H511R |
probably benign |
Het |
Scarb1 |
G |
T |
5: 125,374,296 (GRCm39) |
A279E |
probably damaging |
Het |
Sell |
A |
G |
1: 163,893,114 (GRCm39) |
E110G |
probably damaging |
Het |
Sftpc |
A |
T |
14: 70,760,143 (GRCm39) |
I38N |
probably damaging |
Het |
Shank1 |
G |
A |
7: 43,962,342 (GRCm39) |
S71N |
unknown |
Het |
Slc5a4b |
C |
A |
10: 75,946,674 (GRCm39) |
V33F |
probably damaging |
Het |
Smad7 |
A |
G |
18: 75,527,161 (GRCm39) |
S336G |
probably damaging |
Het |
Tnpo3 |
C |
T |
6: 29,565,768 (GRCm39) |
V529I |
probably benign |
Het |
Trafd1 |
A |
G |
5: 121,517,727 (GRCm39) |
V22A |
probably benign |
Het |
Tssk1 |
A |
G |
16: 17,712,545 (GRCm39) |
E110G |
probably damaging |
Het |
Vmn1r159 |
A |
T |
7: 22,542,675 (GRCm39) |
V119D |
probably damaging |
Het |
Vmn1r191 |
A |
G |
13: 22,363,355 (GRCm39) |
F133S |
probably benign |
Het |
Vwa1 |
G |
A |
4: 155,857,336 (GRCm39) |
P154L |
probably damaging |
Het |
Zfp830 |
C |
T |
11: 82,655,805 (GRCm39) |
T203I |
possibly damaging |
Het |
Zw10 |
G |
T |
9: 48,966,942 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Cdh15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01329:Cdh15
|
APN |
8 |
123,592,062 (GRCm39) |
intron |
probably benign |
|
IGL01958:Cdh15
|
APN |
8 |
123,586,089 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02588:Cdh15
|
APN |
8 |
123,583,291 (GRCm39) |
nonsense |
probably null |
|
IGL02793:Cdh15
|
APN |
8 |
123,587,721 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02947:Cdh15
|
APN |
8 |
123,592,111 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Cdh15
|
UTSW |
8 |
123,592,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R0441:Cdh15
|
UTSW |
8 |
123,587,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R0766:Cdh15
|
UTSW |
8 |
123,588,188 (GRCm39) |
intron |
probably benign |
|
R0898:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1023:Cdh15
|
UTSW |
8 |
123,591,939 (GRCm39) |
missense |
probably damaging |
0.98 |
R1054:Cdh15
|
UTSW |
8 |
123,591,076 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1072:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R1081:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1101:Cdh15
|
UTSW |
8 |
123,587,585 (GRCm39) |
missense |
possibly damaging |
0.93 |
R1208:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1208:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1209:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1210:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1312:Cdh15
|
UTSW |
8 |
123,588,188 (GRCm39) |
intron |
probably benign |
|
R1317:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1318:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1393:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1428:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1429:Cdh15
|
UTSW |
8 |
123,584,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R1695:Cdh15
|
UTSW |
8 |
123,588,755 (GRCm39) |
missense |
probably benign |
0.05 |
R2157:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2170:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2178:Cdh15
|
UTSW |
8 |
123,591,715 (GRCm39) |
splice site |
probably null |
|
R2252:Cdh15
|
UTSW |
8 |
123,584,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R2290:Cdh15
|
UTSW |
8 |
123,586,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R2317:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2330:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2345:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2349:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2353:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2354:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2566:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2567:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2568:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2893:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2894:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R2937:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2938:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2990:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2992:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R2993:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3029:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3030:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3195:Cdh15
|
UTSW |
8 |
123,583,374 (GRCm39) |
missense |
probably benign |
0.10 |
R3441:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3442:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3608:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R3686:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4119:Cdh15
|
UTSW |
8 |
123,590,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Cdh15
|
UTSW |
8 |
123,590,162 (GRCm39) |
missense |
probably damaging |
1.00 |
R4477:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4478:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4480:Cdh15
|
UTSW |
8 |
123,591,415 (GRCm39) |
missense |
probably benign |
0.00 |
R4580:Cdh15
|
UTSW |
8 |
123,591,897 (GRCm39) |
missense |
probably damaging |
0.99 |
R4583:Cdh15
|
UTSW |
8 |
123,591,767 (GRCm39) |
missense |
probably damaging |
0.98 |
R4619:Cdh15
|
UTSW |
8 |
123,587,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R4694:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4731:Cdh15
|
UTSW |
8 |
123,588,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5076:Cdh15
|
UTSW |
8 |
123,591,087 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5347:Cdh15
|
UTSW |
8 |
123,588,802 (GRCm39) |
missense |
probably null |
1.00 |
R5375:Cdh15
|
UTSW |
8 |
123,591,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R5498:Cdh15
|
UTSW |
8 |
123,591,917 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5778:Cdh15
|
UTSW |
8 |
123,583,326 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6320:Cdh15
|
UTSW |
8 |
123,591,086 (GRCm39) |
missense |
probably benign |
0.01 |
R6570:Cdh15
|
UTSW |
8 |
123,584,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Cdh15
|
UTSW |
8 |
123,590,294 (GRCm39) |
missense |
probably benign |
0.32 |
R7505:Cdh15
|
UTSW |
8 |
123,575,231 (GRCm39) |
missense |
probably benign |
0.01 |
R7527:Cdh15
|
UTSW |
8 |
123,588,865 (GRCm39) |
missense |
probably damaging |
1.00 |
R7724:Cdh15
|
UTSW |
8 |
123,593,700 (GRCm39) |
missense |
probably damaging |
1.00 |
R8093:Cdh15
|
UTSW |
8 |
123,593,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8485:Cdh15
|
UTSW |
8 |
123,584,105 (GRCm39) |
missense |
probably damaging |
1.00 |
R8759:Cdh15
|
UTSW |
8 |
123,587,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R8910:Cdh15
|
UTSW |
8 |
123,575,240 (GRCm39) |
missense |
probably benign |
0.04 |
R9017:Cdh15
|
UTSW |
8 |
123,584,256 (GRCm39) |
critical splice donor site |
probably null |
|
R9453:Cdh15
|
UTSW |
8 |
123,586,029 (GRCm39) |
missense |
probably damaging |
0.99 |
R9705:Cdh15
|
UTSW |
8 |
123,591,024 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Cdh15
|
UTSW |
8 |
123,590,998 (GRCm39) |
missense |
probably damaging |
1.00 |
|