Incidental Mutation 'R1538:Pdzd2'
ID |
169741 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pdzd2
|
Ensembl Gene |
ENSMUSG00000022197 |
Gene Name |
PDZ domain containing 2 |
Synonyms |
Gm21706, A930022H17Rik, Pdzk3, 4930537L06Rik, LOC223364 |
MMRRC Submission |
039577-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.117)
|
Stock # |
R1538 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
15 |
Chromosomal Location |
12359797-12740010 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to C
at 12373047 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Serine to Alanine
at position 2363
(S2363A)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000074788
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000075317]
|
AlphaFold |
no structure available at present |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000075317
AA Change: S2363A
PolyPhen 2
Score 0.996 (Sensitivity: 0.55; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000074788 Gene: ENSMUSG00000022197 AA Change: S2363A
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: 99.0%
- 3x: 98.1%
- 10x: 95.5%
- 20x: 89.6%
|
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: 104 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
G |
T |
3: 137,771,162 (GRCm39) |
R117L |
probably benign |
Het |
4930447C04Rik |
G |
A |
12: 72,928,120 (GRCm39) |
A537V |
possibly damaging |
Het |
4930579F01Rik |
A |
C |
3: 137,889,517 (GRCm39) |
D33E |
probably damaging |
Het |
Acnat1 |
T |
C |
4: 49,447,835 (GRCm39) |
K249E |
possibly damaging |
Het |
Ankrd13a |
T |
C |
5: 114,942,295 (GRCm39) |
I526T |
possibly damaging |
Het |
Aplp1 |
C |
A |
7: 30,135,452 (GRCm39) |
E535D |
probably benign |
Het |
Armc8 |
T |
A |
9: 99,387,343 (GRCm39) |
H425L |
probably damaging |
Het |
Arsi |
G |
A |
18: 61,049,723 (GRCm39) |
G202E |
probably benign |
Het |
Asprv1 |
C |
T |
6: 86,605,618 (GRCm39) |
Q155* |
probably null |
Het |
Atl1 |
A |
G |
12: 69,972,962 (GRCm39) |
Q94R |
probably benign |
Het |
Atp2a2 |
A |
G |
5: 122,595,440 (GRCm39) |
L970P |
probably damaging |
Het |
Atp8a2 |
T |
C |
14: 60,097,719 (GRCm39) |
K770E |
probably benign |
Het |
Bod1l |
A |
G |
5: 41,973,772 (GRCm39) |
M2514T |
probably benign |
Het |
Cacfd1 |
T |
A |
2: 26,908,951 (GRCm39) |
D97E |
probably benign |
Het |
Cacna1e |
A |
G |
1: 154,437,504 (GRCm39) |
L344P |
probably damaging |
Het |
Cacna2d2 |
C |
A |
9: 107,394,615 (GRCm39) |
R596S |
probably damaging |
Het |
Catip |
C |
A |
1: 74,403,811 (GRCm39) |
S176* |
probably null |
Het |
Cdcp1 |
G |
A |
9: 123,002,653 (GRCm39) |
S806L |
probably damaging |
Het |
Cdk6 |
A |
T |
5: 3,570,675 (GRCm39) |
I289L |
probably benign |
Het |
Cers3 |
C |
T |
7: 66,431,571 (GRCm39) |
T182I |
probably damaging |
Het |
Cfap46 |
T |
A |
7: 139,262,924 (GRCm39) |
N43I |
probably null |
Het |
Clec4n |
A |
T |
6: 123,206,992 (GRCm39) |
R5S |
possibly damaging |
Het |
Cnr2 |
G |
T |
4: 135,644,012 (GRCm39) |
S30I |
probably benign |
Het |
Col18a1 |
C |
T |
10: 76,907,170 (GRCm39) |
G870E |
probably damaging |
Het |
Cpne6 |
T |
C |
14: 55,752,677 (GRCm39) |
V289A |
possibly damaging |
Het |
Crym |
G |
A |
7: 119,796,938 (GRCm39) |
L141F |
probably benign |
Het |
Cxxc5 |
T |
C |
18: 35,991,622 (GRCm39) |
S8P |
unknown |
Het |
Dido1 |
A |
C |
2: 180,326,763 (GRCm39) |
S453R |
possibly damaging |
Het |
Dnah2 |
A |
C |
11: 69,368,028 (GRCm39) |
S1770R |
probably benign |
Het |
Dnah7a |
A |
G |
1: 53,535,148 (GRCm39) |
V2704A |
possibly damaging |
Het |
Eml5 |
T |
C |
12: 98,760,535 (GRCm39) |
N1738S |
probably damaging |
Het |
Eri3 |
A |
G |
4: 117,439,836 (GRCm39) |
T138A |
possibly damaging |
Het |
Ext2 |
C |
T |
2: 93,537,632 (GRCm39) |
E585K |
probably damaging |
Het |
Fbxw19 |
T |
A |
9: 109,324,056 (GRCm39) |
S38C |
probably damaging |
Het |
Fcgbpl1 |
A |
T |
7: 27,854,917 (GRCm39) |
I1848F |
probably damaging |
Het |
Fmo6 |
G |
A |
1: 162,753,675 (GRCm39) |
P156S |
probably damaging |
Het |
Frem3 |
A |
T |
8: 81,339,764 (GRCm39) |
I686F |
probably benign |
Het |
Frem3 |
T |
C |
8: 81,339,339 (GRCm39) |
L544P |
probably damaging |
Het |
Gabra1 |
T |
C |
11: 42,031,177 (GRCm39) |
Y251C |
probably benign |
Het |
Gemin4 |
G |
T |
11: 76,101,987 (GRCm39) |
Q925K |
probably benign |
Het |
Gm18856 |
T |
A |
13: 14,139,274 (GRCm39) |
|
probably benign |
Het |
Gnb1 |
A |
T |
4: 155,636,171 (GRCm39) |
T164S |
probably benign |
Het |
Gpx6 |
A |
G |
13: 21,497,822 (GRCm39) |
D31G |
possibly damaging |
Het |
Gzmd |
A |
C |
14: 56,367,802 (GRCm39) |
I157S |
probably benign |
Het |
Il31ra |
T |
A |
13: 112,684,000 (GRCm39) |
N43I |
possibly damaging |
Het |
Irak3 |
T |
C |
10: 120,001,035 (GRCm39) |
T297A |
probably benign |
Het |
Kank2 |
T |
C |
9: 21,685,927 (GRCm39) |
D649G |
probably damaging |
Het |
Kif3b |
AGAGGAGGAGGAGGAGG |
AGAGGAGGAGGAGG |
2: 153,159,382 (GRCm39) |
|
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Klhl18 |
A |
G |
9: 110,275,815 (GRCm39) |
F111S |
probably damaging |
Het |
Lratd2 |
A |
G |
15: 60,695,498 (GRCm39) |
C83R |
probably damaging |
Het |
Lrp5 |
A |
G |
19: 3,697,585 (GRCm39) |
S319P |
possibly damaging |
Het |
Mettl15 |
T |
C |
2: 108,962,010 (GRCm39) |
|
probably null |
Het |
Mtarc1 |
T |
C |
1: 184,534,199 (GRCm39) |
E223G |
probably damaging |
Het |
Ncoa1 |
T |
C |
12: 4,320,748 (GRCm39) |
Q1107R |
possibly damaging |
Het |
Ncoa7 |
T |
G |
10: 30,570,207 (GRCm39) |
M251L |
probably damaging |
Het |
Nos2 |
A |
T |
11: 78,847,396 (GRCm39) |
M1023L |
probably benign |
Het |
Nup107 |
T |
C |
10: 117,626,399 (GRCm39) |
K25E |
probably damaging |
Het |
Or10q1b |
A |
T |
19: 13,682,860 (GRCm39) |
Y223F |
probably damaging |
Het |
Or52s1b |
A |
G |
7: 102,822,193 (GRCm39) |
I217T |
probably damaging |
Het |
Or5k14 |
T |
A |
16: 58,693,261 (GRCm39) |
N84I |
probably damaging |
Het |
Or5p58 |
T |
A |
7: 107,694,493 (GRCm39) |
I95F |
probably damaging |
Het |
Or6b6 |
A |
T |
7: 106,571,190 (GRCm39) |
Y120* |
probably null |
Het |
Or6c206 |
T |
C |
10: 129,097,082 (GRCm39) |
I84T |
probably damaging |
Het |
Parm1 |
G |
A |
5: 91,742,306 (GRCm39) |
E225K |
possibly damaging |
Het |
Piezo1 |
A |
G |
8: 123,218,142 (GRCm39) |
L1199P |
probably damaging |
Het |
Prpsap1 |
A |
T |
11: 116,370,534 (GRCm39) |
M141K |
probably benign |
Het |
Prss29 |
A |
T |
17: 25,539,257 (GRCm39) |
M1L |
possibly damaging |
Het |
Pter |
T |
A |
2: 12,983,417 (GRCm39) |
S141T |
probably benign |
Het |
Ptpru |
A |
T |
4: 131,501,662 (GRCm39) |
D1181E |
probably damaging |
Het |
Rab3ip |
T |
A |
10: 116,775,159 (GRCm39) |
Q66H |
probably damaging |
Het |
Rgs12 |
A |
T |
5: 35,178,511 (GRCm39) |
T779S |
probably damaging |
Het |
Rgs22 |
A |
G |
15: 36,048,922 (GRCm39) |
F786S |
probably damaging |
Het |
Rnasel |
A |
T |
1: 153,636,540 (GRCm39) |
D640V |
possibly damaging |
Het |
Rp1 |
T |
C |
1: 4,415,899 (GRCm39) |
T1738A |
probably damaging |
Het |
Sacs |
T |
C |
14: 61,447,508 (GRCm39) |
S3185P |
probably damaging |
Het |
Scnn1a |
T |
A |
6: 125,315,856 (GRCm39) |
D321E |
possibly damaging |
Het |
Sec31b |
G |
C |
19: 44,507,025 (GRCm39) |
L1014V |
probably benign |
Het |
Serpinb10 |
A |
G |
1: 107,468,690 (GRCm39) |
Y111C |
probably damaging |
Het |
Shld2 |
C |
G |
14: 33,990,833 (GRCm39) |
Q24H |
probably damaging |
Het |
Siglecg |
A |
G |
7: 43,067,313 (GRCm39) |
K627E |
possibly damaging |
Het |
Sigmar1 |
T |
C |
4: 41,740,845 (GRCm39) |
I95V |
probably benign |
Het |
Sirpb1b |
T |
A |
3: 15,613,819 (GRCm39) |
T88S |
possibly damaging |
Het |
Spire2 |
T |
G |
8: 124,084,895 (GRCm39) |
L245R |
probably damaging |
Het |
Stard9 |
C |
A |
2: 120,527,192 (GRCm39) |
P1150T |
probably benign |
Het |
Stat6 |
C |
A |
10: 127,489,125 (GRCm39) |
T380N |
probably damaging |
Het |
Sult3a1 |
G |
A |
10: 33,746,166 (GRCm39) |
G162E |
probably benign |
Het |
Surf4 |
T |
C |
2: 26,823,710 (GRCm39) |
|
probably null |
Het |
Tacc2 |
T |
C |
7: 130,227,149 (GRCm39) |
M1278T |
probably benign |
Het |
Tacr2 |
T |
A |
10: 62,097,106 (GRCm39) |
|
probably null |
Het |
Tcaf1 |
A |
T |
6: 42,655,923 (GRCm39) |
V351E |
probably damaging |
Het |
Tmcc2 |
A |
G |
1: 132,308,718 (GRCm39) |
S59P |
probably damaging |
Het |
Tmem17 |
G |
A |
11: 22,467,266 (GRCm39) |
S60N |
possibly damaging |
Het |
Tmem63b |
C |
G |
17: 45,989,904 (GRCm39) |
R88P |
possibly damaging |
Het |
Tmprss7 |
A |
T |
16: 45,499,753 (GRCm39) |
I307N |
probably benign |
Het |
Treml2 |
A |
T |
17: 48,609,786 (GRCm39) |
T73S |
possibly damaging |
Het |
Trrap |
A |
G |
5: 144,774,012 (GRCm39) |
H2876R |
possibly damaging |
Het |
Tyw3 |
A |
G |
3: 154,302,506 (GRCm39) |
I53T |
probably damaging |
Het |
Ugp2 |
A |
G |
11: 21,283,791 (GRCm39) |
I92T |
possibly damaging |
Het |
Vmn2r66 |
A |
T |
7: 84,644,166 (GRCm39) |
M748K |
possibly damaging |
Het |
Vmn2r82 |
T |
C |
10: 79,192,578 (GRCm39) |
S52P |
possibly damaging |
Het |
Wdr37 |
A |
T |
13: 8,886,828 (GRCm39) |
S320T |
probably benign |
Het |
Zbtb16 |
A |
T |
9: 48,743,583 (GRCm39) |
M243K |
probably benign |
Het |
Zfr |
C |
T |
15: 12,150,329 (GRCm39) |
T432I |
possibly damaging |
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 |
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 |
12,385,723 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4492:Pdzd2
|
UTSW |
15 |
12,419,567 (GRCm39) |
missense |
possibly damaging |
0.48 |
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 |
R7748:Pdzd2
|
UTSW |
15 |
12,385,872 (GRCm39) |
missense |
possibly damaging |
0.60 |
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'- AGAGTAGTCCTCGCCACTACACAG -3'
(R):5'- TTAGGAACCCACCACCAGTGGATG -3'
Sequencing Primer
(F):5'- ATGCTCAAGGCTCTCAGC -3'
(R):5'- CACTACTACTGTGAGCAGAGCTG -3'
|
Posted On |
2014-04-13 |