Other mutations in this stock |
Total: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca15 |
A |
T |
7: 119,965,044 (GRCm39) |
I769F |
possibly damaging |
Het |
Ackr1 |
A |
C |
1: 173,159,779 (GRCm39) |
W247G |
probably damaging |
Het |
Adgrl4 |
G |
A |
3: 151,197,946 (GRCm39) |
G69S |
probably damaging |
Het |
Agrn |
C |
T |
4: 156,260,886 (GRCm39) |
S710N |
probably damaging |
Het |
Aox3 |
A |
G |
1: 58,218,494 (GRCm39) |
M1103V |
probably benign |
Het |
Asb18 |
G |
A |
1: 89,896,206 (GRCm39) |
A278V |
probably benign |
Het |
B3gat2 |
A |
G |
1: 23,801,945 (GRCm39) |
E77G |
probably benign |
Het |
Camta1 |
T |
C |
4: 151,232,863 (GRCm39) |
|
probably null |
Het |
Cbll1 |
A |
T |
12: 31,537,579 (GRCm39) |
I392N |
probably damaging |
Het |
Ccdc113 |
A |
G |
8: 96,264,829 (GRCm39) |
D113G |
possibly damaging |
Het |
Cd79a |
T |
C |
7: 24,599,092 (GRCm39) |
F148L |
probably benign |
Het |
Chad |
T |
A |
11: 94,455,999 (GRCm39) |
C26S |
probably damaging |
Het |
Cog4 |
T |
C |
8: 111,607,600 (GRCm39) |
F696L |
probably damaging |
Het |
Csf2rb |
T |
G |
15: 78,225,839 (GRCm39) |
S303R |
probably damaging |
Het |
Cstpp1 |
A |
T |
2: 91,214,118 (GRCm39) |
L79H |
probably damaging |
Het |
Cubn |
C |
T |
2: 13,365,176 (GRCm39) |
G1621R |
probably damaging |
Het |
Dennd4c |
T |
A |
4: 86,747,179 (GRCm39) |
N1454K |
probably benign |
Het |
Dennd5b |
T |
C |
6: 148,918,604 (GRCm39) |
I853V |
probably benign |
Het |
Dnaaf11 |
T |
C |
15: 66,321,412 (GRCm39) |
E243G |
probably benign |
Het |
Dop1a |
A |
T |
9: 86,389,783 (GRCm39) |
D561V |
probably benign |
Het |
Dpysl4 |
A |
G |
7: 138,669,456 (GRCm39) |
I45V |
probably benign |
Het |
Ect2l |
A |
C |
10: 18,045,153 (GRCm39) |
S301A |
possibly damaging |
Het |
Elf2 |
A |
G |
3: 51,165,035 (GRCm39) |
V323A |
probably damaging |
Het |
Epcam |
C |
T |
17: 87,947,904 (GRCm39) |
R125* |
probably null |
Het |
Ephb4 |
T |
C |
5: 137,363,937 (GRCm39) |
V612A |
probably damaging |
Het |
Erich3 |
C |
T |
3: 154,469,426 (GRCm39) |
R1293C |
unknown |
Het |
F830045P16Rik |
C |
A |
2: 129,302,367 (GRCm39) |
L408F |
probably damaging |
Het |
Gask1a |
G |
A |
9: 121,793,887 (GRCm39) |
V14I |
probably benign |
Het |
Gm13102 |
T |
C |
4: 143,835,787 (GRCm39) |
I485T |
probably benign |
Het |
Gm16494 |
A |
T |
17: 47,327,800 (GRCm39) |
L28* |
probably null |
Het |
Grin2c |
A |
G |
11: 115,144,696 (GRCm39) |
V610A |
probably damaging |
Het |
Hacd2 |
T |
A |
16: 34,922,434 (GRCm39) |
Y208N |
probably damaging |
Het |
Hlf |
A |
T |
11: 90,278,821 (GRCm39) |
F81Y |
probably damaging |
Het |
Igfbp7 |
G |
A |
5: 77,499,134 (GRCm39) |
A257V |
probably damaging |
Het |
Il12a |
A |
T |
3: 68,605,235 (GRCm39) |
N167I |
probably damaging |
Het |
Il1r2 |
G |
A |
1: 40,162,371 (GRCm39) |
C338Y |
probably damaging |
Het |
Irf2bpl |
G |
T |
12: 86,930,489 (GRCm39) |
H61Q |
probably damaging |
Het |
Kansl1 |
A |
G |
11: 104,314,890 (GRCm39) |
F383L |
probably benign |
Het |
Kcnh8 |
A |
G |
17: 53,268,871 (GRCm39) |
T863A |
probably damaging |
Het |
Klhl36 |
C |
A |
8: 120,596,397 (GRCm39) |
Q33K |
probably benign |
Het |
Lrig2 |
A |
T |
3: 104,401,985 (GRCm39) |
Y113* |
probably null |
Het |
Lrrc36 |
T |
A |
8: 106,178,667 (GRCm39) |
S287R |
possibly damaging |
Het |
Mr1 |
A |
T |
1: 155,005,054 (GRCm39) |
Y329N |
probably damaging |
Het |
Muc5ac |
G |
C |
7: 141,363,040 (GRCm39) |
G2117A |
unknown |
Het |
Nectin4 |
G |
A |
1: 171,211,326 (GRCm39) |
|
probably null |
Het |
Nsrp1 |
A |
G |
11: 76,940,097 (GRCm39) |
|
probably null |
Het |
Or1e21 |
A |
T |
11: 73,344,372 (GRCm39) |
I222N |
possibly damaging |
Het |
Or9g3 |
A |
G |
2: 85,583,836 (GRCm39) |
T44A |
probably benign |
Het |
Pcdh8 |
A |
T |
14: 80,008,143 (GRCm39) |
I140N |
probably damaging |
Het |
Pdzd8 |
A |
G |
19: 59,333,208 (GRCm39) |
V271A |
probably damaging |
Het |
Pex3 |
T |
A |
10: 13,403,550 (GRCm39) |
I324L |
possibly damaging |
Het |
Pira12 |
T |
A |
7: 3,898,603 (GRCm39) |
I282F |
probably damaging |
Het |
Pitpnm1 |
T |
A |
19: 4,153,470 (GRCm39) |
F209I |
probably benign |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 110,350,827 (GRCm39) |
|
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,271,149 (GRCm39) |
T3135S |
probably damaging |
Het |
Prdm16 |
T |
C |
4: 154,412,756 (GRCm39) |
N1082S |
probably damaging |
Het |
Psmd12 |
A |
T |
11: 107,370,439 (GRCm39) |
I13F |
possibly damaging |
Het |
Ptgs2 |
A |
T |
1: 149,980,258 (GRCm39) |
I399F |
probably benign |
Het |
Rasa3 |
A |
T |
8: 13,618,708 (GRCm39) |
S830T |
probably benign |
Het |
Rasgef1c |
A |
T |
11: 49,861,120 (GRCm39) |
R362W |
probably damaging |
Het |
Resf1 |
A |
G |
6: 149,226,936 (GRCm39) |
|
probably benign |
Het |
Rictor |
C |
T |
15: 6,801,635 (GRCm39) |
S441L |
probably benign |
Het |
Rnf217 |
C |
A |
10: 31,393,415 (GRCm39) |
G389W |
probably damaging |
Het |
Sec16b |
A |
T |
1: 157,385,630 (GRCm39) |
D675V |
probably damaging |
Het |
Serpinb12 |
A |
G |
1: 106,877,401 (GRCm39) |
Y137C |
probably damaging |
Het |
Slc2a5 |
T |
A |
4: 150,227,591 (GRCm39) |
I470N |
probably damaging |
Het |
Slc5a1 |
T |
C |
5: 33,290,761 (GRCm39) |
I115T |
possibly damaging |
Het |
Slco1a4 |
A |
T |
6: 141,780,413 (GRCm39) |
S126T |
possibly damaging |
Het |
St6galnac2 |
T |
C |
11: 116,568,410 (GRCm39) |
D351G |
probably damaging |
Het |
Stat4 |
G |
A |
1: 52,121,711 (GRCm39) |
V357M |
possibly damaging |
Het |
Taf4 |
G |
A |
2: 179,573,822 (GRCm39) |
T682M |
probably damaging |
Het |
Tdrd9 |
T |
A |
12: 111,958,982 (GRCm39) |
C139S |
probably benign |
Het |
Tmed9 |
G |
A |
13: 55,741,054 (GRCm39) |
R23Q |
not run |
Het |
Tmem150a |
A |
C |
6: 72,336,028 (GRCm39) |
H205P |
probably damaging |
Het |
Tns2 |
C |
A |
15: 102,018,163 (GRCm39) |
L350I |
probably benign |
Het |
Tpr |
A |
G |
1: 150,295,646 (GRCm39) |
T964A |
probably benign |
Het |
Traf3ip1 |
G |
T |
1: 91,422,479 (GRCm39) |
|
probably benign |
Het |
Trem2 |
G |
T |
17: 48,653,567 (GRCm39) |
|
probably benign |
Het |
Ttc14 |
G |
A |
3: 33,863,590 (GRCm39) |
G666D |
unknown |
Het |
Ulk1 |
T |
C |
5: 110,957,078 (GRCm39) |
D40G |
probably damaging |
Het |
Vmn1r30 |
A |
G |
6: 58,412,397 (GRCm39) |
V145A |
probably benign |
Het |
Vmn1r79 |
C |
T |
7: 11,910,762 (GRCm39) |
Q215* |
probably null |
Het |
Wnk2 |
G |
A |
13: 49,231,493 (GRCm39) |
T16I |
unknown |
Het |
Yme1l1 |
T |
C |
2: 23,077,856 (GRCm39) |
|
probably null |
Het |
Zbtb16 |
T |
A |
9: 48,654,769 (GRCm39) |
H454L |
probably damaging |
Het |
Zkscan5 |
A |
C |
5: 145,157,676 (GRCm39) |
H726P |
probably damaging |
Het |
Zrsr2-ps1 |
A |
G |
11: 22,923,595 (GRCm39) |
Q123R |
possibly damaging |
Het |
|
Other mutations in Pramel32 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00088:Pramel32
|
APN |
4 |
88,547,307 (GRCm39) |
missense |
probably benign |
0.43 |
IGL00229:Pramel32
|
APN |
4 |
88,547,290 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01938:Pramel32
|
APN |
4 |
88,547,600 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02321:Pramel32
|
APN |
4 |
88,548,340 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02351:Pramel32
|
APN |
4 |
88,546,127 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02358:Pramel32
|
APN |
4 |
88,546,127 (GRCm39) |
missense |
probably damaging |
1.00 |
P0005:Pramel32
|
UTSW |
4 |
88,546,187 (GRCm39) |
missense |
probably damaging |
1.00 |
R0521:Pramel32
|
UTSW |
4 |
88,547,559 (GRCm39) |
missense |
probably damaging |
0.96 |
R0578:Pramel32
|
UTSW |
4 |
88,552,376 (GRCm39) |
missense |
probably benign |
0.01 |
R0600:Pramel32
|
UTSW |
4 |
88,547,536 (GRCm39) |
missense |
probably damaging |
1.00 |
R0750:Pramel32
|
UTSW |
4 |
88,545,905 (GRCm39) |
missense |
probably benign |
0.01 |
R1483:Pramel32
|
UTSW |
4 |
88,547,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R1502:Pramel32
|
UTSW |
4 |
88,546,269 (GRCm39) |
missense |
probably benign |
0.00 |
R1911:Pramel32
|
UTSW |
4 |
88,548,309 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2204:Pramel32
|
UTSW |
4 |
88,546,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R2507:Pramel32
|
UTSW |
4 |
88,547,448 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2512:Pramel32
|
UTSW |
4 |
88,547,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R4299:Pramel32
|
UTSW |
4 |
88,546,419 (GRCm39) |
missense |
probably damaging |
0.97 |
R4498:Pramel32
|
UTSW |
4 |
88,547,129 (GRCm39) |
splice site |
probably null |
|
R4656:Pramel32
|
UTSW |
4 |
88,548,202 (GRCm39) |
missense |
probably benign |
0.41 |
R4787:Pramel32
|
UTSW |
4 |
88,547,450 (GRCm39) |
nonsense |
probably null |
|
R4823:Pramel32
|
UTSW |
4 |
88,547,452 (GRCm39) |
missense |
probably damaging |
1.00 |
R4885:Pramel32
|
UTSW |
4 |
88,546,219 (GRCm39) |
missense |
possibly damaging |
0.50 |
R4948:Pramel32
|
UTSW |
4 |
88,547,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R4967:Pramel32
|
UTSW |
4 |
88,547,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R5229:Pramel32
|
UTSW |
4 |
88,548,372 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5426:Pramel32
|
UTSW |
4 |
88,547,647 (GRCm39) |
intron |
probably benign |
|
R5520:Pramel32
|
UTSW |
4 |
88,548,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Pramel32
|
UTSW |
4 |
88,546,280 (GRCm39) |
missense |
probably benign |
0.10 |
R5596:Pramel32
|
UTSW |
4 |
88,548,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6282:Pramel32
|
UTSW |
4 |
88,548,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R6366:Pramel32
|
UTSW |
4 |
88,547,102 (GRCm39) |
missense |
probably damaging |
0.99 |
R6808:Pramel32
|
UTSW |
4 |
88,548,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R6866:Pramel32
|
UTSW |
4 |
88,545,977 (GRCm39) |
missense |
probably damaging |
1.00 |
R7105:Pramel32
|
UTSW |
4 |
88,548,339 (GRCm39) |
missense |
probably damaging |
0.98 |
R7117:Pramel32
|
UTSW |
4 |
88,547,195 (GRCm39) |
missense |
probably damaging |
0.99 |
R7319:Pramel32
|
UTSW |
4 |
88,548,184 (GRCm39) |
missense |
probably benign |
0.25 |
R7345:Pramel32
|
UTSW |
4 |
88,546,416 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7399:Pramel32
|
UTSW |
4 |
88,546,202 (GRCm39) |
missense |
probably benign |
0.01 |
R7626:Pramel32
|
UTSW |
4 |
88,548,279 (GRCm39) |
missense |
probably damaging |
1.00 |
R8044:Pramel32
|
UTSW |
4 |
88,548,212 (GRCm39) |
missense |
possibly damaging |
0.47 |
R8849:Pramel32
|
UTSW |
4 |
88,546,014 (GRCm39) |
missense |
probably benign |
0.03 |
R9334:Pramel32
|
UTSW |
4 |
88,548,186 (GRCm39) |
missense |
probably damaging |
0.99 |
R9515:Pramel32
|
UTSW |
4 |
88,546,219 (GRCm39) |
missense |
possibly damaging |
0.50 |
RF012:Pramel32
|
UTSW |
4 |
88,546,006 (GRCm39) |
missense |
probably damaging |
0.97 |
|