Incidental Mutation 'R7748:Pdzd2'
ID |
597052 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pdzd2
|
Ensembl Gene |
ENSMUSG00000022197 |
Gene Name |
PDZ domain containing 2 |
Synonyms |
Gm21706, A930022H17Rik, Pdzk3, 4930537L06Rik, LOC223364 |
MMRRC Submission |
045804-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.117)
|
Stock # |
R7748 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
15 |
Chromosomal Location |
12359797-12740010 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
C to A
at 12385872 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Leucine
at position 966
(R966L)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000074788
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075317]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000075317
AA Change: R966L
PolyPhen 2
Score 0.600 (Sensitivity: 0.87; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000074788 Gene: ENSMUSG00000022197 AA Change: R966L
Domain | Start | End | E-Value | Type |
PDZ
|
81 |
179 |
1.27e-2 |
SMART |
PDZ
|
342 |
419 |
1.51e-18 |
SMART |
PDZ
|
597 |
675 |
5.25e-18 |
SMART |
low complexity region
|
690 |
718 |
N/A |
INTRINSIC |
PDZ
|
738 |
817 |
1.64e-10 |
SMART |
low complexity region
|
861 |
869 |
N/A |
INTRINSIC |
low complexity region
|
969 |
984 |
N/A |
INTRINSIC |
low complexity region
|
986 |
1000 |
N/A |
INTRINSIC |
low complexity region
|
1436 |
1459 |
N/A |
INTRINSIC |
low complexity region
|
1525 |
1537 |
N/A |
INTRINSIC |
low complexity region
|
1538 |
1553 |
N/A |
INTRINSIC |
low complexity region
|
1567 |
1586 |
N/A |
INTRINSIC |
low complexity region
|
2111 |
2129 |
N/A |
INTRINSIC |
low complexity region
|
2190 |
2198 |
N/A |
INTRINSIC |
low complexity region
|
2335 |
2354 |
N/A |
INTRINSIC |
low complexity region
|
2469 |
2479 |
N/A |
INTRINSIC |
PDZ
|
2589 |
2666 |
1.3e-13 |
SMART |
PDZ
|
2716 |
2794 |
9.42e-20 |
SMART |
|
Coding Region Coverage |
- 1x: 100.0%
- 3x: 100.0%
- 10x: 99.8%
- 20x: 99.2%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene contains six PDZ domains and shares sequence similarity with pro-interleukin-16 (pro-IL-16). Like pro-IL-16, the encoded protein localizes to the endoplasmic reticulum and is thought to be cleaved by a caspase to produce a secreted peptide containing two PDZ domains. In addition, this gene is upregulated in primary prostate tumors and may be involved in the early stages of prostate tumorigenesis. [provided by RefSeq, Dec 2015] PHENOTYPE: Mice homozygous for a gene trapped allele exhibit normal response to acute and chronic pain. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310057M21Rik |
T |
A |
7: 130,963,521 (GRCm39) |
L103F |
probably benign |
Het |
5330417H12Rik |
A |
G |
7: 107,223,765 (GRCm39) |
L103P |
unknown |
Het |
Actb |
T |
C |
5: 142,890,450 (GRCm39) |
I151V |
probably benign |
Het |
Adcy6 |
T |
A |
15: 98,502,437 (GRCm39) |
H59L |
probably benign |
Het |
Adss2 |
G |
C |
1: 177,599,768 (GRCm39) |
S272* |
probably null |
Het |
Aga |
A |
T |
8: 53,964,840 (GRCm39) |
M1L |
possibly damaging |
Het |
Ajm1 |
T |
A |
2: 25,468,971 (GRCm39) |
E313D |
possibly damaging |
Het |
Anxa5 |
G |
A |
3: 36,519,480 (GRCm39) |
T3M |
probably damaging |
Het |
Arhgap45 |
A |
T |
10: 79,852,766 (GRCm39) |
|
probably benign |
Het |
Atp6v0a2 |
A |
T |
5: 124,793,560 (GRCm39) |
H639L |
probably benign |
Het |
BC005537 |
C |
T |
13: 24,987,382 (GRCm39) |
R7W |
possibly damaging |
Het |
Bcl2l2 |
C |
T |
14: 55,121,836 (GRCm39) |
|
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,013,484 (GRCm39) |
|
probably null |
Het |
Bod1l |
A |
C |
5: 41,989,683 (GRCm39) |
S347A |
probably damaging |
Het |
Calcoco1 |
T |
C |
15: 102,627,996 (GRCm39) |
D46G |
probably damaging |
Het |
Camk1 |
T |
C |
6: 113,317,289 (GRCm39) |
E60G |
probably damaging |
Het |
Capza1 |
A |
T |
3: 104,732,721 (GRCm39) |
|
probably null |
Het |
Ccdc18 |
T |
A |
5: 108,296,907 (GRCm39) |
|
probably null |
Het |
Cdh20 |
G |
A |
1: 104,869,024 (GRCm39) |
A172T |
probably damaging |
Het |
Cdk4 |
C |
T |
10: 126,900,298 (GRCm39) |
A65V |
possibly damaging |
Het |
Cftr |
T |
C |
6: 18,277,888 (GRCm39) |
|
probably null |
Het |
Chd3 |
T |
C |
11: 69,246,459 (GRCm39) |
M1092V |
probably benign |
Het |
Chd6 |
A |
T |
2: 160,808,539 (GRCm39) |
H1558Q |
probably benign |
Het |
Chi3l1 |
A |
G |
1: 134,116,966 (GRCm39) |
H318R |
probably benign |
Het |
Cps1 |
A |
G |
1: 67,178,965 (GRCm39) |
Y59C |
probably damaging |
Het |
Cyb5r4 |
T |
C |
9: 86,914,434 (GRCm39) |
V111A |
probably damaging |
Het |
Ddx39b |
G |
A |
17: 35,471,726 (GRCm39) |
V291M |
probably damaging |
Het |
Dhx57 |
A |
G |
17: 80,572,546 (GRCm39) |
F709S |
probably damaging |
Het |
Eef1b2 |
A |
T |
1: 63,217,024 (GRCm39) |
K64N |
probably damaging |
Het |
Eef1ece2 |
A |
T |
16: 20,451,834 (GRCm39) |
D407V |
probably damaging |
Het |
Fam135a |
A |
G |
1: 24,068,050 (GRCm39) |
S940P |
probably benign |
Het |
Fam234b |
T |
A |
6: 135,186,349 (GRCm39) |
V119E |
probably damaging |
Het |
Fbxo46 |
G |
C |
7: 18,870,458 (GRCm39) |
C359S |
probably damaging |
Het |
Fkbp14 |
C |
A |
6: 54,572,505 (GRCm39) |
|
probably benign |
Het |
Fmn2 |
T |
A |
1: 174,494,215 (GRCm39) |
V1243E |
probably damaging |
Het |
Fsbp |
C |
A |
4: 11,579,924 (GRCm39) |
T64K |
probably damaging |
Het |
Fscb |
A |
T |
12: 64,521,181 (GRCm39) |
M95K |
probably benign |
Het |
Fyb1 |
T |
G |
15: 6,668,307 (GRCm39) |
V500G |
probably damaging |
Het |
G2e3 |
A |
G |
12: 51,418,450 (GRCm39) |
N615S |
probably benign |
Het |
Gart |
T |
C |
16: 91,427,540 (GRCm39) |
D486G |
possibly damaging |
Het |
Gas2l2 |
T |
A |
11: 83,313,224 (GRCm39) |
D696V |
probably benign |
Het |
Glmn |
C |
T |
5: 107,710,110 (GRCm39) |
|
probably null |
Het |
Gm47985 |
A |
T |
1: 151,058,725 (GRCm39) |
D122V |
probably damaging |
Het |
Gm7168 |
A |
G |
17: 14,168,914 (GRCm39) |
K94E |
probably benign |
Het |
Gnai2 |
T |
C |
9: 107,492,934 (GRCm39) |
H323R |
|
Het |
Helz2 |
C |
T |
2: 180,876,324 (GRCm39) |
R1390H |
probably damaging |
Het |
Igf2bp1 |
T |
C |
11: 95,858,413 (GRCm39) |
M453V |
probably benign |
Het |
Ighv3-1 |
C |
T |
12: 113,928,270 (GRCm39) |
V30M |
probably damaging |
Het |
Inpp5a |
A |
T |
7: 139,154,911 (GRCm39) |
R343S |
probably damaging |
Het |
Itga8 |
T |
A |
2: 12,235,050 (GRCm39) |
I403F |
possibly damaging |
Het |
Katnip |
A |
T |
7: 125,428,973 (GRCm39) |
M558L |
probably benign |
Het |
Krt33a |
C |
T |
11: 99,902,428 (GRCm39) |
R404H |
probably benign |
Het |
Krt34 |
T |
A |
11: 99,929,764 (GRCm39) |
E244V |
probably damaging |
Het |
Krt42 |
T |
C |
11: 100,157,792 (GRCm39) |
E224G |
probably damaging |
Het |
Krtap5-2 |
TCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACCACAGCCCCCACAGGAACTACA |
TCCACAGGAACTACA |
7: 141,728,845 (GRCm39) |
|
probably benign |
Het |
Lama1 |
T |
C |
17: 68,057,585 (GRCm39) |
L553P |
|
Het |
Lcn9 |
T |
A |
2: 25,714,926 (GRCm39) |
*179K |
probably null |
Het |
Ldaf1 |
A |
T |
7: 119,714,702 (GRCm39) |
I64F |
possibly damaging |
Het |
Lrrc2 |
T |
G |
9: 110,809,999 (GRCm39) |
M345R |
possibly damaging |
Het |
Marchf11 |
T |
C |
15: 26,387,916 (GRCm39) |
V257A |
probably damaging |
Het |
Masp2 |
T |
C |
4: 148,690,163 (GRCm39) |
I224T |
probably benign |
Het |
Mpz |
A |
T |
1: 170,987,509 (GRCm39) |
|
probably null |
Het |
Mtr |
C |
T |
13: 12,242,725 (GRCm39) |
A442T |
probably benign |
Het |
Muc5b |
A |
G |
7: 141,401,542 (GRCm39) |
K596R |
unknown |
Het |
Myo15a |
T |
G |
11: 60,395,727 (GRCm39) |
F1397C |
|
Het |
Ncor2 |
T |
C |
5: 125,187,031 (GRCm39) |
I173V |
unknown |
Het |
Ngly1 |
T |
A |
14: 16,290,820 (GRCm38) |
I434K |
possibly damaging |
Het |
Notch2 |
A |
G |
3: 98,045,800 (GRCm39) |
H1655R |
possibly damaging |
Het |
Notum |
C |
T |
11: 120,545,627 (GRCm39) |
A390T |
probably damaging |
Het |
Or10a3n |
T |
C |
7: 108,493,285 (GRCm39) |
T115A |
probably benign |
Het |
Or1e22 |
T |
G |
11: 73,376,994 (GRCm39) |
I219L |
probably benign |
Het |
Pds5a |
T |
A |
5: 65,777,009 (GRCm39) |
I51F |
possibly damaging |
Het |
Plk3 |
T |
C |
4: 116,988,925 (GRCm39) |
Y278C |
probably damaging |
Het |
Plxna1 |
C |
G |
6: 89,314,334 (GRCm39) |
|
probably null |
Het |
Plxna1 |
T |
A |
6: 89,314,335 (GRCm39) |
|
probably null |
Het |
Ppp4r4 |
G |
A |
12: 103,571,320 (GRCm39) |
|
probably null |
Het |
Pramel6 |
T |
A |
2: 87,339,043 (GRCm39) |
V81E |
probably damaging |
Het |
Prdm2 |
T |
C |
4: 142,862,459 (GRCm39) |
E277G |
possibly damaging |
Het |
Prkg1 |
T |
A |
19: 30,970,491 (GRCm39) |
I222F |
possibly damaging |
Het |
Proser3 |
A |
T |
7: 30,239,497 (GRCm39) |
S536T |
possibly damaging |
Het |
Prrt4 |
C |
A |
6: 29,177,190 (GRCm39) |
G193V |
probably damaging |
Het |
Ptpn21 |
A |
T |
12: 98,655,031 (GRCm39) |
H645Q |
probably benign |
Het |
Ptprd |
T |
C |
4: 76,017,741 (GRCm39) |
I744V |
probably null |
Het |
Rad54l2 |
A |
G |
9: 106,596,233 (GRCm39) |
V235A |
possibly damaging |
Het |
Repin1 |
G |
T |
6: 48,574,279 (GRCm39) |
E403* |
probably null |
Het |
Rgs22 |
C |
T |
15: 36,122,415 (GRCm39) |
|
probably null |
Het |
Rtcb |
A |
T |
10: 85,777,832 (GRCm39) |
D447E |
probably benign |
Het |
Rtn1 |
C |
T |
12: 72,263,700 (GRCm39) |
V744I |
possibly damaging |
Het |
Scfd1 |
T |
G |
12: 51,436,140 (GRCm39) |
I96M |
probably benign |
Het |
Serpina3b |
T |
C |
12: 104,096,722 (GRCm39) |
M1T |
probably null |
Het |
Slc1a4 |
T |
C |
11: 20,282,252 (GRCm39) |
Y74C |
probably damaging |
Het |
Slc9b2 |
A |
T |
3: 135,031,940 (GRCm39) |
I267F |
possibly damaging |
Het |
Sorcs2 |
A |
T |
5: 36,386,519 (GRCm39) |
M173K |
possibly damaging |
Het |
Sparc |
T |
C |
11: 55,289,426 (GRCm39) |
I226V |
probably benign |
Het |
Spata22 |
T |
G |
11: 73,227,080 (GRCm39) |
I98S |
probably null |
Het |
Spef2 |
C |
T |
15: 9,653,031 (GRCm39) |
V917M |
probably damaging |
Het |
Sspo |
C |
A |
6: 48,426,399 (GRCm39) |
C139* |
probably null |
Het |
Tenm4 |
A |
G |
7: 96,543,909 (GRCm39) |
D2012G |
probably damaging |
Het |
Tgm5 |
G |
A |
2: 120,883,289 (GRCm39) |
R351C |
probably damaging |
Het |
Tmem145 |
G |
A |
7: 25,006,753 (GRCm39) |
W82* |
probably null |
Het |
Topors |
T |
A |
4: 40,262,654 (GRCm39) |
D210V |
probably damaging |
Het |
Tssk4 |
A |
T |
14: 55,888,569 (GRCm39) |
H146L |
probably damaging |
Het |
Unc93b1 |
T |
A |
19: 3,985,250 (GRCm39) |
D19E |
unknown |
Het |
Usp17lc |
A |
G |
7: 103,067,688 (GRCm39) |
T328A |
probably damaging |
Het |
Utrn |
A |
G |
10: 12,490,252 (GRCm39) |
Y43H |
probably benign |
Het |
Vmn1r25 |
T |
A |
6: 57,955,549 (GRCm39) |
I247F |
probably damaging |
Het |
Vmn2r78 |
A |
T |
7: 86,570,343 (GRCm39) |
Q287L |
probably benign |
Het |
Vps13c |
T |
A |
9: 67,870,371 (GRCm39) |
I3170N |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,236,720 (GRCm39) |
M398K |
probably benign |
Het |
Zfp354c |
TCACACTCGGCACA |
TCACA |
11: 50,706,067 (GRCm39) |
|
probably benign |
Het |
Zfp773 |
T |
C |
7: 7,135,907 (GRCm39) |
R230G |
probably benign |
Het |
|
Other mutations in Pdzd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Pdzd2
|
APN |
15 |
12,458,069 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL00586:Pdzd2
|
APN |
15 |
12,365,853 (GRCm39) |
splice site |
probably null |
|
IGL00697:Pdzd2
|
APN |
15 |
12,373,733 (GRCm39) |
missense |
possibly damaging |
0.81 |
IGL00721:Pdzd2
|
APN |
15 |
12,374,498 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00971:Pdzd2
|
APN |
15 |
12,374,804 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01066:Pdzd2
|
APN |
15 |
12,402,718 (GRCm39) |
unclassified |
probably benign |
|
IGL01389:Pdzd2
|
APN |
15 |
12,374,712 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL01505:Pdzd2
|
APN |
15 |
12,458,293 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01527:Pdzd2
|
APN |
15 |
12,445,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01584:Pdzd2
|
APN |
15 |
12,592,569 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01763:Pdzd2
|
APN |
15 |
12,372,632 (GRCm39) |
missense |
probably benign |
|
IGL01915:Pdzd2
|
APN |
15 |
12,371,725 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01947:Pdzd2
|
APN |
15 |
12,592,440 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02058:Pdzd2
|
APN |
15 |
12,376,382 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02274:Pdzd2
|
APN |
15 |
12,445,735 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Pdzd2
|
APN |
15 |
12,375,851 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02600:Pdzd2
|
APN |
15 |
12,411,105 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02637:Pdzd2
|
APN |
15 |
12,385,720 (GRCm39) |
missense |
probably benign |
0.13 |
IGL02639:Pdzd2
|
APN |
15 |
12,592,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02712:Pdzd2
|
APN |
15 |
12,376,113 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02967:Pdzd2
|
APN |
15 |
12,374,427 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02992:Pdzd2
|
APN |
15 |
12,382,708 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03005:Pdzd2
|
APN |
15 |
12,385,351 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03067:Pdzd2
|
APN |
15 |
12,388,628 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03335:Pdzd2
|
APN |
15 |
12,373,850 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4280001:Pdzd2
|
UTSW |
15 |
12,399,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Pdzd2
|
UTSW |
15 |
12,371,691 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0241:Pdzd2
|
UTSW |
15 |
12,368,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0241:Pdzd2
|
UTSW |
15 |
12,368,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R0446:Pdzd2
|
UTSW |
15 |
12,375,110 (GRCm39) |
missense |
probably benign |
0.43 |
R0462:Pdzd2
|
UTSW |
15 |
12,592,246 (GRCm39) |
missense |
probably damaging |
1.00 |
R0562:Pdzd2
|
UTSW |
15 |
12,592,364 (GRCm39) |
missense |
probably damaging |
1.00 |
R0589:Pdzd2
|
UTSW |
15 |
12,376,385 (GRCm39) |
missense |
probably benign |
0.03 |
R0639:Pdzd2
|
UTSW |
15 |
12,458,144 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0925:Pdzd2
|
UTSW |
15 |
12,399,356 (GRCm39) |
missense |
probably damaging |
1.00 |
R1015:Pdzd2
|
UTSW |
15 |
12,374,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R1054:Pdzd2
|
UTSW |
15 |
12,371,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R1070:Pdzd2
|
UTSW |
15 |
12,390,052 (GRCm39) |
critical splice donor site |
probably null |
|
R1099:Pdzd2
|
UTSW |
15 |
12,373,173 (GRCm39) |
missense |
probably damaging |
1.00 |
R1122:Pdzd2
|
UTSW |
15 |
12,457,981 (GRCm39) |
missense |
probably benign |
0.25 |
R1126:Pdzd2
|
UTSW |
15 |
12,458,306 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1381:Pdzd2
|
UTSW |
15 |
12,385,525 (GRCm39) |
missense |
probably benign |
0.02 |
R1385:Pdzd2
|
UTSW |
15 |
12,411,108 (GRCm39) |
missense |
probably benign |
0.38 |
R1513:Pdzd2
|
UTSW |
15 |
12,373,915 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1538:Pdzd2
|
UTSW |
15 |
12,373,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R1750:Pdzd2
|
UTSW |
15 |
12,385,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R1775:Pdzd2
|
UTSW |
15 |
12,592,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R1801:Pdzd2
|
UTSW |
15 |
12,387,740 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1832:Pdzd2
|
UTSW |
15 |
12,390,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R1856:Pdzd2
|
UTSW |
15 |
12,373,941 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1870:Pdzd2
|
UTSW |
15 |
12,457,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R1879:Pdzd2
|
UTSW |
15 |
12,373,986 (GRCm39) |
missense |
possibly damaging |
0.61 |
R2072:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2073:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2075:Pdzd2
|
UTSW |
15 |
12,385,905 (GRCm39) |
missense |
probably damaging |
1.00 |
R2125:Pdzd2
|
UTSW |
15 |
12,373,676 (GRCm39) |
missense |
probably benign |
0.37 |
R2142:Pdzd2
|
UTSW |
15 |
12,406,645 (GRCm39) |
missense |
probably damaging |
1.00 |
R2155:Pdzd2
|
UTSW |
15 |
12,375,879 (GRCm39) |
missense |
probably benign |
0.43 |
R2282:Pdzd2
|
UTSW |
15 |
12,373,934 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2407:Pdzd2
|
UTSW |
15 |
12,373,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R3545:Pdzd2
|
UTSW |
15 |
12,375,557 (GRCm39) |
missense |
probably benign |
0.00 |
R3878:Pdzd2
|
UTSW |
15 |
12,376,262 (GRCm39) |
missense |
probably benign |
0.00 |
R3879:Pdzd2
|
UTSW |
15 |
12,375,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R4396:Pdzd2
|
UTSW |
15 |
12,387,732 (GRCm39) |
missense |
probably benign |
0.36 |
R4398:Pdzd2
|
UTSW |
15 |
12,376,061 (GRCm39) |
missense |
probably benign |
0.30 |
R4491:Pdzd2
|
UTSW |
15 |
12,385,723 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4492:Pdzd2
|
UTSW |
15 |
12,419,567 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4492:Pdzd2
|
UTSW |
15 |
12,385,723 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4656:Pdzd2
|
UTSW |
15 |
12,385,797 (GRCm39) |
missense |
probably benign |
0.00 |
R4715:Pdzd2
|
UTSW |
15 |
12,419,602 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4803:Pdzd2
|
UTSW |
15 |
12,374,681 (GRCm39) |
missense |
probably benign |
0.04 |
R4893:Pdzd2
|
UTSW |
15 |
12,385,429 (GRCm39) |
missense |
probably benign |
0.00 |
R4959:Pdzd2
|
UTSW |
15 |
12,375,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Pdzd2
|
UTSW |
15 |
12,375,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5030:Pdzd2
|
UTSW |
15 |
12,592,494 (GRCm39) |
nonsense |
probably null |
|
R5174:Pdzd2
|
UTSW |
15 |
12,372,600 (GRCm39) |
missense |
probably benign |
0.01 |
R5230:Pdzd2
|
UTSW |
15 |
12,390,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Pdzd2
|
UTSW |
15 |
12,373,028 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5268:Pdzd2
|
UTSW |
15 |
12,592,263 (GRCm39) |
missense |
probably damaging |
1.00 |
R5488:Pdzd2
|
UTSW |
15 |
12,382,762 (GRCm39) |
missense |
probably benign |
0.00 |
R5489:Pdzd2
|
UTSW |
15 |
12,382,762 (GRCm39) |
missense |
probably benign |
0.00 |
R5588:Pdzd2
|
UTSW |
15 |
12,374,367 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5605:Pdzd2
|
UTSW |
15 |
12,592,436 (GRCm39) |
nonsense |
probably null |
|
R5704:Pdzd2
|
UTSW |
15 |
12,385,761 (GRCm39) |
missense |
probably benign |
0.02 |
R5858:Pdzd2
|
UTSW |
15 |
12,442,675 (GRCm39) |
missense |
probably damaging |
0.97 |
R6048:Pdzd2
|
UTSW |
15 |
12,592,656 (GRCm39) |
splice site |
probably null |
|
R6222:Pdzd2
|
UTSW |
15 |
12,374,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R6311:Pdzd2
|
UTSW |
15 |
12,458,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Pdzd2
|
UTSW |
15 |
12,592,551 (GRCm39) |
missense |
probably damaging |
1.00 |
R6897:Pdzd2
|
UTSW |
15 |
12,385,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R6900:Pdzd2
|
UTSW |
15 |
12,374,123 (GRCm39) |
missense |
probably benign |
|
R6955:Pdzd2
|
UTSW |
15 |
12,401,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R6959:Pdzd2
|
UTSW |
15 |
12,375,993 (GRCm39) |
missense |
probably benign |
0.17 |
R6992:Pdzd2
|
UTSW |
15 |
12,457,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Pdzd2
|
UTSW |
15 |
12,373,061 (GRCm39) |
missense |
probably benign |
0.14 |
R7014:Pdzd2
|
UTSW |
15 |
12,372,647 (GRCm39) |
missense |
probably benign |
0.13 |
R7110:Pdzd2
|
UTSW |
15 |
12,368,099 (GRCm39) |
missense |
probably damaging |
1.00 |
R7180:Pdzd2
|
UTSW |
15 |
12,376,209 (GRCm39) |
missense |
probably damaging |
0.99 |
R7228:Pdzd2
|
UTSW |
15 |
12,458,231 (GRCm39) |
nonsense |
probably null |
|
R7228:Pdzd2
|
UTSW |
15 |
12,373,059 (GRCm39) |
missense |
probably benign |
0.01 |
R7317:Pdzd2
|
UTSW |
15 |
12,592,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Pdzd2
|
UTSW |
15 |
12,437,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R7349:Pdzd2
|
UTSW |
15 |
12,399,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7600:Pdzd2
|
UTSW |
15 |
12,372,820 (GRCm39) |
missense |
probably damaging |
1.00 |
R7663:Pdzd2
|
UTSW |
15 |
12,373,289 (GRCm39) |
missense |
probably damaging |
1.00 |
R7712:Pdzd2
|
UTSW |
15 |
12,407,422 (GRCm39) |
missense |
probably damaging |
1.00 |
R7716:Pdzd2
|
UTSW |
15 |
12,373,460 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7740:Pdzd2
|
UTSW |
15 |
12,374,102 (GRCm39) |
missense |
probably benign |
0.00 |
R8017:Pdzd2
|
UTSW |
15 |
12,373,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8019:Pdzd2
|
UTSW |
15 |
12,373,122 (GRCm39) |
missense |
probably damaging |
1.00 |
R8108:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8109:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8110:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8111:Pdzd2
|
UTSW |
15 |
12,373,592 (GRCm39) |
missense |
probably benign |
0.01 |
R8145:Pdzd2
|
UTSW |
15 |
12,407,458 (GRCm39) |
missense |
probably benign |
0.37 |
R8220:Pdzd2
|
UTSW |
15 |
12,592,249 (GRCm39) |
missense |
probably damaging |
0.99 |
R8278:Pdzd2
|
UTSW |
15 |
12,375,995 (GRCm39) |
missense |
probably benign |
|
R8768:Pdzd2
|
UTSW |
15 |
12,437,252 (GRCm39) |
missense |
probably damaging |
1.00 |
R8879:Pdzd2
|
UTSW |
15 |
12,402,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R9019:Pdzd2
|
UTSW |
15 |
12,375,612 (GRCm39) |
missense |
probably damaging |
1.00 |
R9030:Pdzd2
|
UTSW |
15 |
12,374,385 (GRCm39) |
missense |
probably benign |
0.02 |
R9061:Pdzd2
|
UTSW |
15 |
12,374,753 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9302:Pdzd2
|
UTSW |
15 |
12,374,342 (GRCm39) |
missense |
possibly damaging |
0.61 |
R9321:Pdzd2
|
UTSW |
15 |
12,386,023 (GRCm39) |
missense |
probably benign |
0.00 |
R9421:Pdzd2
|
UTSW |
15 |
12,375,114 (GRCm39) |
missense |
|
|
R9515:Pdzd2
|
UTSW |
15 |
12,374,621 (GRCm39) |
missense |
probably damaging |
1.00 |
R9592:Pdzd2
|
UTSW |
15 |
12,458,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9614:Pdzd2
|
UTSW |
15 |
12,375,486 (GRCm39) |
missense |
probably damaging |
1.00 |
R9630:Pdzd2
|
UTSW |
15 |
12,374,443 (GRCm39) |
missense |
probably benign |
0.37 |
R9776:Pdzd2
|
UTSW |
15 |
12,457,909 (GRCm39) |
missense |
probably benign |
0.03 |
X0057:Pdzd2
|
UTSW |
15 |
12,411,113 (GRCm39) |
missense |
probably damaging |
1.00 |
X0063:Pdzd2
|
UTSW |
15 |
12,368,805 (GRCm39) |
missense |
possibly damaging |
0.77 |
X0066:Pdzd2
|
UTSW |
15 |
12,372,942 (GRCm39) |
missense |
probably benign |
0.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CTGGAGTCGTTCATCCTGCTTG -3'
(R):5'- AGCCAGGCCAGATTGGAAAC -3'
Sequencing Primer
(F):5'- GTTCACATCAATACTTTTGGAAGAGG -3'
(R):5'- CAGGCCAGATTGGAAACTTGTGTTC -3'
|
Posted On |
2019-11-26 |