Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abat |
A |
G |
16: 8,423,414 (GRCm39) |
I236V |
probably benign |
Het |
Abca8a |
T |
C |
11: 109,961,249 (GRCm39) |
T558A |
probably benign |
Het |
Ace3 |
A |
C |
11: 105,885,764 (GRCm39) |
M57L |
probably benign |
Het |
Adgrg1 |
T |
C |
8: 95,729,129 (GRCm39) |
S18P |
probably benign |
Het |
Ahi1 |
A |
G |
10: 20,934,064 (GRCm39) |
D60G |
probably benign |
Het |
Ap4e1 |
T |
A |
2: 126,870,080 (GRCm39) |
|
probably null |
Het |
Arnt2 |
C |
A |
7: 84,010,773 (GRCm39) |
K34N |
probably damaging |
Het |
Ascc3 |
T |
A |
10: 50,494,021 (GRCm39) |
M152K |
probably benign |
Het |
AW551984 |
A |
T |
9: 39,505,051 (GRCm39) |
F480L |
probably benign |
Het |
Blvrb |
G |
A |
7: 27,158,773 (GRCm39) |
A58T |
possibly damaging |
Het |
Bpifa1 |
C |
T |
2: 153,985,892 (GRCm39) |
T69I |
probably benign |
Het |
Cacna1g |
T |
A |
11: 94,320,997 (GRCm39) |
M1366L |
probably benign |
Het |
Ccdc82 |
A |
G |
9: 13,266,880 (GRCm39) |
I361V |
probably benign |
Het |
Clca4b |
T |
A |
3: 144,631,927 (GRCm39) |
I193F |
possibly damaging |
Het |
Crb1 |
A |
T |
1: 139,176,686 (GRCm39) |
Y371* |
probably null |
Het |
Cul9 |
T |
C |
17: 46,832,854 (GRCm39) |
D1363G |
possibly damaging |
Het |
Cyp2j8 |
C |
T |
4: 96,332,877 (GRCm39) |
A490T |
probably benign |
Het |
D430041D05Rik |
A |
T |
2: 104,086,637 (GRCm39) |
S780T |
probably benign |
Het |
Fzd5 |
G |
T |
1: 64,774,815 (GRCm39) |
C315* |
probably null |
Het |
Gabrr1 |
T |
C |
4: 33,161,695 (GRCm39) |
S340P |
probably damaging |
Het |
Galnt7 |
T |
C |
8: 57,979,200 (GRCm39) |
D641G |
probably damaging |
Het |
Gm7133 |
A |
G |
1: 97,110,948 (GRCm39) |
|
noncoding transcript |
Het |
Heatr5b |
A |
G |
17: 79,120,602 (GRCm39) |
L774P |
possibly damaging |
Het |
Itch |
T |
A |
2: 155,015,985 (GRCm39) |
S157T |
probably benign |
Het |
Itgam |
A |
C |
7: 127,684,824 (GRCm39) |
D398A |
probably damaging |
Het |
Kalrn |
G |
T |
16: 33,805,561 (GRCm39) |
L2659M |
possibly damaging |
Het |
Kcnj14 |
C |
A |
7: 45,468,875 (GRCm39) |
R210L |
possibly damaging |
Het |
Kmt2d |
T |
C |
15: 98,758,573 (GRCm39) |
|
probably benign |
Het |
Krt1c |
G |
C |
15: 101,724,349 (GRCm39) |
T305S |
probably damaging |
Het |
Mcm3ap |
A |
G |
10: 76,342,441 (GRCm39) |
N1645D |
probably damaging |
Het |
Naf1 |
T |
A |
8: 67,336,096 (GRCm39) |
I341K |
probably damaging |
Het |
Nbea |
G |
T |
3: 55,937,317 (GRCm39) |
H765N |
probably damaging |
Het |
Ncapd3 |
A |
G |
9: 26,975,278 (GRCm39) |
I776V |
probably benign |
Het |
Neo1 |
A |
T |
9: 58,824,291 (GRCm39) |
D712E |
probably benign |
Het |
Neu1 |
G |
A |
17: 35,153,730 (GRCm39) |
V385I |
probably benign |
Het |
Or14j3 |
C |
A |
17: 37,900,817 (GRCm39) |
R142S |
probably benign |
Het |
Or51a6 |
C |
A |
7: 102,604,011 (GRCm39) |
G273C |
probably damaging |
Het |
Or51a6 |
A |
G |
7: 102,604,737 (GRCm39) |
Y24H |
probably benign |
Het |
Pgghg |
A |
C |
7: 140,523,308 (GRCm39) |
T196P |
possibly damaging |
Het |
Pira2 |
A |
T |
7: 3,845,445 (GRCm39) |
V313E |
probably damaging |
Het |
Pkd1l2 |
T |
C |
8: 117,809,107 (GRCm39) |
R28G |
probably benign |
Het |
Pkhd1l1 |
T |
C |
15: 44,421,336 (GRCm39) |
S3035P |
probably damaging |
Het |
Ppp1r9a |
T |
A |
6: 4,905,509 (GRCm39) |
N21K |
probably damaging |
Het |
Prune1 |
T |
C |
3: 95,169,554 (GRCm39) |
D216G |
probably benign |
Het |
Ptpn23 |
G |
T |
9: 110,216,893 (GRCm39) |
|
probably benign |
Het |
Ranbp2 |
T |
A |
10: 58,301,351 (GRCm39) |
M668K |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rpsa |
G |
T |
9: 119,960,102 (GRCm39) |
V222L |
probably benign |
Het |
Septin2 |
A |
G |
1: 93,425,098 (GRCm39) |
T45A |
probably damaging |
Het |
Slc12a8 |
A |
T |
16: 33,445,384 (GRCm39) |
D260V |
probably damaging |
Het |
Srrm2 |
G |
T |
17: 24,039,330 (GRCm39) |
M2087I |
possibly damaging |
Het |
Tg |
T |
C |
15: 66,700,306 (GRCm39) |
L88P |
probably damaging |
Het |
Tns1 |
A |
G |
1: 73,991,578 (GRCm39) |
|
probably null |
Het |
Topbp1 |
A |
T |
9: 103,224,160 (GRCm39) |
D1429V |
probably benign |
Het |
Tprg1 |
A |
G |
16: 25,241,151 (GRCm39) |
|
probably null |
Het |
Trit1 |
T |
C |
4: 122,933,261 (GRCm39) |
I66T |
possibly damaging |
Het |
Usf3 |
A |
T |
16: 44,037,670 (GRCm39) |
I717L |
probably damaging |
Het |
|
Other mutations in 1700034J05Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01654:1700034J05Rik
|
APN |
6 |
146,854,838 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01725:1700034J05Rik
|
APN |
6 |
146,853,767 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01860:1700034J05Rik
|
APN |
6 |
146,853,914 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL01991:1700034J05Rik
|
APN |
6 |
146,854,608 (GRCm39) |
missense |
probably benign |
0.32 |
IGL02375:1700034J05Rik
|
APN |
6 |
146,854,813 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0254:1700034J05Rik
|
UTSW |
6 |
146,853,902 (GRCm39) |
missense |
probably benign |
0.00 |
R0361:1700034J05Rik
|
UTSW |
6 |
146,853,869 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0835:1700034J05Rik
|
UTSW |
6 |
146,855,036 (GRCm39) |
intron |
probably benign |
|
R1101:1700034J05Rik
|
UTSW |
6 |
146,853,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1428:1700034J05Rik
|
UTSW |
6 |
146,853,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1487:1700034J05Rik
|
UTSW |
6 |
146,854,877 (GRCm39) |
missense |
probably benign |
0.16 |
R1887:1700034J05Rik
|
UTSW |
6 |
146,853,909 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1988:1700034J05Rik
|
UTSW |
6 |
146,854,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R1989:1700034J05Rik
|
UTSW |
6 |
146,854,394 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4063:1700034J05Rik
|
UTSW |
6 |
146,854,606 (GRCm39) |
missense |
probably benign |
0.32 |
R6578:1700034J05Rik
|
UTSW |
6 |
146,854,812 (GRCm39) |
nonsense |
probably null |
|
R7029:1700034J05Rik
|
UTSW |
6 |
146,853,841 (GRCm39) |
missense |
probably benign |
0.00 |
R7585:1700034J05Rik
|
UTSW |
6 |
146,854,851 (GRCm39) |
missense |
probably benign |
0.00 |
R7842:1700034J05Rik
|
UTSW |
6 |
146,855,034 (GRCm39) |
missense |
unknown |
|
R9272:1700034J05Rik
|
UTSW |
6 |
146,854,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R9444:1700034J05Rik
|
UTSW |
6 |
146,854,724 (GRCm39) |
missense |
probably damaging |
1.00 |
X0066:1700034J05Rik
|
UTSW |
6 |
146,855,038 (GRCm39) |
start codon destroyed |
probably null |
|
|