Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AI837181 |
CGG |
CGGTGG |
19: 5,475,262 (GRCm39) |
|
probably benign |
Het |
AI837181 |
GGC |
GGCTGC |
19: 5,475,263 (GRCm39) |
|
probably benign |
Het |
Angptl1 |
A |
T |
1: 156,684,794 (GRCm39) |
Q321L |
possibly damaging |
Het |
AY358078 |
T |
TAGGATAATGC |
14: 52,043,050 (GRCm39) |
|
probably null |
Het |
Blm |
CCTCCTCCTCCTCCTCCTCCTCCT |
CCTCCTCCTCCTGCTCCTCCTCCTCCTCCTCCTCCT |
7: 80,162,653 (GRCm39) |
|
probably benign |
Het |
Blm |
CTC |
CTCATCCTCCTCATC |
7: 80,162,675 (GRCm39) |
|
probably benign |
Het |
Car13 |
T |
C |
3: 14,719,974 (GRCm39) |
Y129H |
probably damaging |
Het |
Cd109 |
TTATTTATTTAT |
TTATTTATTTATGTATTTATTTAT |
9: 78,619,805 (GRCm39) |
|
probably benign |
Het |
Cd109 |
TATTTAT |
TATTTATTTATTCATTTAT |
9: 78,619,810 (GRCm39) |
|
probably benign |
Het |
Cdh26 |
T |
C |
2: 178,108,424 (GRCm39) |
C341R |
probably damaging |
Het |
Chga |
GCA |
GCACCA |
12: 102,527,680 (GRCm39) |
|
probably benign |
Het |
Col11a1 |
A |
T |
3: 114,010,650 (GRCm39) |
I1689L |
unknown |
Het |
Dnah6 |
T |
G |
6: 73,078,872 (GRCm39) |
S2364R |
probably benign |
Het |
E4f1 |
CCG |
CCGACG |
17: 24,674,160 (GRCm39) |
|
probably benign |
Het |
Fah |
A |
C |
7: 84,238,836 (GRCm39) |
N336K |
probably damaging |
Het |
Fbxo11 |
A |
T |
17: 88,303,481 (GRCm39) |
I664K |
|
Het |
Fcgbp |
A |
G |
7: 27,789,180 (GRCm39) |
D582G |
probably benign |
Het |
Gabre |
C |
CCGGCTA |
X: 71,313,663 (GRCm39) |
|
probably null |
Het |
Garin5a |
CCTGGGTCTGAGGGAGGA |
CCTGGGTCTGAGGGAGGAAGGCTGGATCCTGGATAACTGGGTCTGAGGGAGGA |
7: 44,149,944 (GRCm39) |
|
probably null |
Het |
Gm1110 |
A |
G |
9: 26,831,936 (GRCm39) |
Y72H |
probably damaging |
Het |
Inpp5e |
C |
T |
2: 26,298,389 (GRCm39) |
A71T |
possibly damaging |
Het |
Iqcm |
C |
T |
8: 76,304,527 (GRCm39) |
T96I |
probably benign |
Het |
Lce1m |
TGCCACCGCTGC |
TGCCACCGCTGCCGCCACCGCTGC |
3: 92,925,590 (GRCm39) |
|
probably benign |
Het |
Lce1m |
AC |
ACCGCCGCTGCCCC |
3: 92,925,606 (GRCm39) |
|
probably benign |
Het |
Lrch1 |
TTGGTGGTGCTGGTGG |
TTGGTGG |
14: 75,185,014 (GRCm39) |
|
probably benign |
Het |
Lyst |
A |
G |
13: 13,808,948 (GRCm39) |
D206G |
probably benign |
Het |
Map4k5 |
A |
T |
12: 69,903,630 (GRCm39) |
D58E |
probably damaging |
Het |
Mapkapk2 |
A |
G |
1: 130,984,250 (GRCm39) |
S251P |
probably damaging |
Het |
Mcph1 |
CCTG |
CCTGCTG |
8: 18,702,545 (GRCm39) |
|
probably benign |
Het |
Men1 |
T |
C |
19: 6,390,146 (GRCm39) |
S600P |
probably damaging |
Het |
Mllt1 |
C |
T |
17: 57,203,300 (GRCm39) |
V394M |
probably benign |
Het |
Mllt1 |
C |
A |
17: 57,203,301 (GRCm39) |
M393I |
possibly damaging |
Het |
Nacc1 |
T |
C |
8: 85,402,848 (GRCm39) |
E315G |
possibly damaging |
Het |
Nefh |
GGGGACTTGGCCTC |
GGGGACTTGGCCTCACCTAGGGACTTGGCCTC |
11: 4,891,047 (GRCm39) |
|
probably benign |
Het |
Nefh |
GACTTGGCCTC |
GACTTGGCCTCACCTGGGGACTTGGCCTC |
11: 4,891,050 (GRCm39) |
|
probably benign |
Het |
Nid2 |
TAACACCGCCA |
TA |
14: 19,801,434 (GRCm39) |
|
probably benign |
Het |
Or5b122 |
T |
A |
19: 13,563,415 (GRCm39) |
I206N |
probably damaging |
Het |
Parp2 |
A |
G |
14: 51,054,843 (GRCm39) |
E262G |
probably damaging |
Het |
Pdik1l |
TTT |
TTTGTTTTTGTGTT |
4: 134,006,686 (GRCm39) |
|
probably null |
Het |
Pop1 |
G |
A |
15: 34,502,583 (GRCm39) |
G90D |
probably damaging |
Het |
Ppp3cc |
T |
C |
14: 70,504,788 (GRCm39) |
T73A |
possibly damaging |
Het |
Prpf4b |
T |
A |
13: 35,068,219 (GRCm39) |
S349R |
unknown |
Het |
Rassf6 |
TCCTGTAGAGCAATGGGGATTC |
TCCTGTAGAGCAATGGGGATTCTGCCTCACTCATGGGCCTGTAGAGCAATGGGGATTC |
5: 90,756,780 (GRCm39) |
|
probably benign |
Het |
Rassf6 |
GTAGAGCAATGGGGATTC |
GTAGAGCAATGGGGATTCTGCCTCACTCATGGTCCTTTAGAGCAATGGGGATTC |
5: 90,756,784 (GRCm39) |
|
probably null |
Het |
Sdk2 |
T |
C |
11: 113,776,078 (GRCm39) |
E208G |
probably benign |
Het |
Smurf2 |
G |
T |
11: 106,743,413 (GRCm39) |
P211Q |
probably benign |
Het |
Snx25 |
C |
A |
8: 46,569,218 (GRCm39) |
|
probably null |
Het |
Spata6 |
T |
A |
4: 111,685,502 (GRCm39) |
M469K |
probably benign |
Het |
Spta1 |
G |
T |
1: 174,058,926 (GRCm39) |
A1954S |
possibly damaging |
Het |
Sry |
CTGGTCGTGGAACTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGGTGGTGGTCATGGAACTGCTG |
CTGGTCATGGAACTGCTG |
Y: 2,662,564 (GRCm39) |
|
probably benign |
Het |
Stard8 |
GAG |
GAGTAG |
X: 98,110,121 (GRCm39) |
|
probably null |
Het |
Tfeb |
AGC |
AGCGGC |
17: 48,097,027 (GRCm39) |
|
probably benign |
Het |
Tlcd1 |
T |
A |
11: 78,071,020 (GRCm39) |
L203Q |
probably benign |
Het |
Tlr11 |
T |
C |
14: 50,598,682 (GRCm39) |
F223L |
possibly damaging |
Het |
Usp48 |
T |
A |
4: 137,333,106 (GRCm39) |
V100D |
probably damaging |
Het |
Vinac1 |
A |
G |
2: 128,880,714 (GRCm39) |
F404S |
|
Het |
Vmn2r56 |
G |
A |
7: 12,428,757 (GRCm39) |
T503I |
probably benign |
Het |
Vps18 |
T |
C |
2: 119,127,871 (GRCm39) |
L898P |
probably damaging |
Het |
Zfp384 |
GCCCAGGCCCAGGCCCAGGCCCAG |
GCCCAGGCCCAGTCCCAGGCCCAGGCCCAGGCCCAG |
6: 125,013,434 (GRCm39) |
|
probably benign |
Het |
Zfp706 |
T |
A |
15: 37,003,949 (GRCm39) |
Y39F |
probably benign |
Het |
Zhx3 |
T |
A |
2: 160,623,726 (GRCm39) |
N147I |
probably damaging |
Het |
|
Other mutations in Prdm15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00973:Prdm15
|
APN |
16 |
97,607,367 (GRCm39) |
splice site |
probably benign |
|
IGL01325:Prdm15
|
APN |
16 |
97,607,717 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02195:Prdm15
|
APN |
16 |
97,637,029 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02473:Prdm15
|
APN |
16 |
97,638,805 (GRCm39) |
splice site |
probably null |
|
IGL02502:Prdm15
|
APN |
16 |
97,640,539 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Prdm15
|
APN |
16 |
97,623,142 (GRCm39) |
missense |
probably benign |
|
R0408:Prdm15
|
UTSW |
16 |
97,636,986 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0437:Prdm15
|
UTSW |
16 |
97,613,759 (GRCm39) |
missense |
probably benign |
0.00 |
R0497:Prdm15
|
UTSW |
16 |
97,595,534 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0590:Prdm15
|
UTSW |
16 |
97,598,961 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0630:Prdm15
|
UTSW |
16 |
97,638,907 (GRCm39) |
missense |
probably null |
1.00 |
R0661:Prdm15
|
UTSW |
16 |
97,630,882 (GRCm39) |
missense |
probably benign |
0.34 |
R0718:Prdm15
|
UTSW |
16 |
97,613,833 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1144:Prdm15
|
UTSW |
16 |
97,609,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R1240:Prdm15
|
UTSW |
16 |
97,638,800 (GRCm39) |
missense |
probably damaging |
0.98 |
R1605:Prdm15
|
UTSW |
16 |
97,640,506 (GRCm39) |
missense |
probably damaging |
1.00 |
R1908:Prdm15
|
UTSW |
16 |
97,638,885 (GRCm39) |
missense |
probably benign |
0.27 |
R2081:Prdm15
|
UTSW |
16 |
97,604,980 (GRCm39) |
nonsense |
probably null |
|
R2208:Prdm15
|
UTSW |
16 |
97,600,464 (GRCm39) |
splice site |
probably null |
|
R3787:Prdm15
|
UTSW |
16 |
97,598,945 (GRCm39) |
missense |
probably benign |
0.00 |
R3890:Prdm15
|
UTSW |
16 |
97,600,771 (GRCm39) |
missense |
probably damaging |
1.00 |
R4326:Prdm15
|
UTSW |
16 |
97,607,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4728:Prdm15
|
UTSW |
16 |
97,622,986 (GRCm39) |
missense |
probably benign |
0.04 |
R4952:Prdm15
|
UTSW |
16 |
97,607,277 (GRCm39) |
missense |
probably damaging |
0.99 |
R4998:Prdm15
|
UTSW |
16 |
97,595,689 (GRCm39) |
missense |
probably damaging |
0.97 |
R5225:Prdm15
|
UTSW |
16 |
97,609,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R5505:Prdm15
|
UTSW |
16 |
97,618,183 (GRCm39) |
missense |
possibly damaging |
0.76 |
R5628:Prdm15
|
UTSW |
16 |
97,600,823 (GRCm39) |
missense |
probably damaging |
0.98 |
R5721:Prdm15
|
UTSW |
16 |
97,608,296 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5873:Prdm15
|
UTSW |
16 |
97,609,889 (GRCm39) |
missense |
probably damaging |
1.00 |
R5980:Prdm15
|
UTSW |
16 |
97,613,770 (GRCm39) |
nonsense |
probably null |
|
R6311:Prdm15
|
UTSW |
16 |
97,600,255 (GRCm39) |
missense |
probably null |
0.08 |
R6540:Prdm15
|
UTSW |
16 |
97,637,005 (GRCm39) |
missense |
probably benign |
0.13 |
R7053:Prdm15
|
UTSW |
16 |
97,595,742 (GRCm39) |
nonsense |
probably null |
|
R7241:Prdm15
|
UTSW |
16 |
97,596,941 (GRCm39) |
missense |
possibly damaging |
0.50 |
R7468:Prdm15
|
UTSW |
16 |
97,636,842 (GRCm39) |
nonsense |
probably null |
|
R7473:Prdm15
|
UTSW |
16 |
97,623,046 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7762:Prdm15
|
UTSW |
16 |
97,619,473 (GRCm39) |
missense |
probably benign |
0.00 |
R7911:Prdm15
|
UTSW |
16 |
97,613,792 (GRCm39) |
missense |
probably benign |
0.35 |
R8053:Prdm15
|
UTSW |
16 |
97,636,807 (GRCm39) |
missense |
probably benign |
0.17 |
R8127:Prdm15
|
UTSW |
16 |
97,638,910 (GRCm39) |
missense |
probably benign |
0.24 |
R8213:Prdm15
|
UTSW |
16 |
97,608,260 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Prdm15
|
UTSW |
16 |
97,618,066 (GRCm39) |
missense |
unknown |
|
R8768:Prdm15
|
UTSW |
16 |
97,638,888 (GRCm39) |
missense |
probably benign |
|
R9000:Prdm15
|
UTSW |
16 |
97,595,470 (GRCm39) |
missense |
probably benign |
0.03 |
R9513:Prdm15
|
UTSW |
16 |
97,607,704 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Prdm15
|
UTSW |
16 |
97,623,142 (GRCm39) |
missense |
probably benign |
|
RF021:Prdm15
|
UTSW |
16 |
97,609,956 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Prdm15
|
UTSW |
16 |
97,618,159 (GRCm39) |
missense |
possibly damaging |
0.54 |
|