Incidental Mutation 'R6035:Pde8b'
ID |
479173 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pde8b
|
Ensembl Gene |
ENSMUSG00000021684 |
Gene Name |
phosphodiesterase 8B |
Synonyms |
B230331L10Rik, C030047E14Rik |
MMRRC Submission |
044207-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.110)
|
Stock # |
R6035 (G1)
|
Quality Score |
225.009 |
Status
|
Not validated
|
Chromosome |
13 |
Chromosomal Location |
95160962-95386844 bp(-) (GRCm39) |
Type of Mutation |
intron |
DNA Base Change (assembly) |
A to G
at 95164105 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
|
Ref Sequence |
ENSEMBL: ENSMUSP00000128987
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000022192]
[ENSMUST00000056512]
[ENSMUST00000067082]
[ENSMUST00000160801]
[ENSMUST00000162153]
[ENSMUST00000162292]
[ENSMUST00000162412]
[ENSMUST00000172104]
|
AlphaFold |
E9Q4S1 |
Predicted Effect |
probably benign
Transcript: ENSMUST00000022192
|
SMART Domains |
Protein: ENSMUSP00000022192 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:PDE8
|
1 |
52 |
2.2e-39 |
PFAM |
low complexity region
|
75 |
98 |
N/A |
INTRINSIC |
Pfam:Response_reg
|
134 |
252 |
2.9e-15 |
PFAM |
Blast:HDc
|
420 |
481 |
1e-20 |
BLAST |
HDc
|
565 |
748 |
3.01e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000056512
|
SMART Domains |
Protein: ENSMUSP00000055145 Gene: ENSMUSG00000042015
Domain | Start | End | E-Value | Type |
WD40
|
32 |
70 |
4.48e-2 |
SMART |
WD40
|
73 |
119 |
1.24e-4 |
SMART |
WD40
|
122 |
159 |
1.28e1 |
SMART |
WD40
|
211 |
249 |
2.86e0 |
SMART |
WD40
|
308 |
350 |
7.92e-3 |
SMART |
WD40
|
394 |
432 |
1.67e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000067082
|
SMART Domains |
Protein: ENSMUSP00000070465 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:PDE8
|
1 |
47 |
1.4e-32 |
PFAM |
low complexity region
|
75 |
98 |
N/A |
INTRINSIC |
Blast:REC
|
112 |
235 |
6e-45 |
BLAST |
PAS
|
249 |
316 |
3.59e-3 |
SMART |
Blast:HDc
|
447 |
508 |
1e-20 |
BLAST |
HDc
|
592 |
775 |
3.01e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000160801
|
SMART Domains |
Protein: ENSMUSP00000124033 Gene: ENSMUSG00000042015
Domain | Start | End | E-Value | Type |
WD40
|
32 |
70 |
4.48e-2 |
SMART |
WD40
|
73 |
119 |
1.24e-4 |
SMART |
WD40
|
122 |
159 |
1.28e1 |
SMART |
WD40
|
211 |
249 |
2.86e0 |
SMART |
WD40
|
308 |
350 |
7.92e-3 |
SMART |
WD40
|
394 |
432 |
1.67e-1 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162153
|
SMART Domains |
Protein: ENSMUSP00000124704 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:Response_reg
|
29 |
147 |
2.6e-15 |
PFAM |
PAS
|
164 |
231 |
3.59e-3 |
SMART |
Blast:HDc
|
362 |
423 |
1e-20 |
BLAST |
HDc
|
507 |
690 |
3.01e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162292
|
SMART Domains |
Protein: ENSMUSP00000124068 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:PDE8
|
1 |
52 |
2.1e-39 |
PFAM |
low complexity region
|
75 |
98 |
N/A |
INTRINSIC |
Pfam:Response_reg
|
134 |
252 |
2.6e-15 |
PFAM |
Blast:HDc
|
370 |
431 |
1e-20 |
BLAST |
HDc
|
515 |
698 |
3.01e-3 |
SMART |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000162412
|
SMART Domains |
Protein: ENSMUSP00000124409 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:Response_reg
|
29 |
147 |
2.3e-15 |
PFAM |
PAS
|
164 |
231 |
3.59e-3 |
SMART |
Blast:HDc
|
312 |
373 |
1e-20 |
BLAST |
HDc
|
457 |
640 |
3.01e-3 |
SMART |
|
Predicted Effect |
unknown
Transcript: ENSMUST00000162670
AA Change: S175P
|
SMART Domains |
Protein: ENSMUSP00000125237 Gene: ENSMUSG00000021684 AA Change: S175P
Domain | Start | End | E-Value | Type |
Pfam:PDEase_I
|
1 |
182 |
6.6e-56 |
PFAM |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000162882
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000223486
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000220923
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000172104
|
SMART Domains |
Protein: ENSMUSP00000128987 Gene: ENSMUSG00000021684
Domain | Start | End | E-Value | Type |
Pfam:PDE8
|
1 |
52 |
2.2e-39 |
PFAM |
low complexity region
|
75 |
98 |
N/A |
INTRINSIC |
Pfam:Response_reg
|
134 |
252 |
2.8e-15 |
PFAM |
PAS
|
269 |
336 |
3.59e-3 |
SMART |
HDc
|
557 |
740 |
3.01e-3 |
SMART |
|
Coding Region Coverage |
- 1x: 99.8%
- 3x: 98.9%
- 10x: 91.8%
- 20x: 70.9%
|
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 is a cyclic nucleotide phosphodiesterase (PDE) that catalyzes the hydrolysis of the second messenger cAMP. The encoded protein, which does not hydrolyze cGMP, is resistant to several PDE inhibitors. Defects in this gene are a cause of autosomal dominant striatal degeneration (ADSD). Several transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, Jul 2010] PHENOTYPE: Mice homozygous for a knock-out allele exhibit increased uring corticosterone, decreased serum adrenocorticotropin and decreased sensitivity to a PDE8-selective inhibitor. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
G |
T |
6: 121,615,353 (GRCm39) |
G76W |
probably damaging |
Het |
Abca17 |
A |
T |
17: 24,500,219 (GRCm39) |
F1324Y |
possibly damaging |
Het |
Abca8b |
A |
T |
11: 109,862,686 (GRCm39) |
|
probably null |
Het |
Abcc12 |
A |
G |
8: 87,244,033 (GRCm39) |
M1040T |
probably damaging |
Het |
Abtb1 |
A |
G |
6: 88,818,788 (GRCm39) |
F7L |
probably damaging |
Het |
Adcy9 |
T |
C |
16: 4,122,377 (GRCm39) |
T558A |
probably benign |
Het |
Adgrb1 |
A |
T |
15: 74,412,292 (GRCm39) |
T424S |
possibly damaging |
Het |
Afg3l2 |
G |
T |
18: 67,554,329 (GRCm39) |
L458M |
probably damaging |
Het |
Ankrd31 |
C |
A |
13: 96,968,721 (GRCm39) |
P786Q |
probably benign |
Het |
Arhgap39 |
G |
T |
15: 76,621,424 (GRCm39) |
Y392* |
probably null |
Het |
Ash1l |
T |
C |
3: 88,892,326 (GRCm39) |
Y1402H |
probably damaging |
Het |
Carmil2 |
G |
T |
8: 106,419,195 (GRCm39) |
W749L |
probably benign |
Het |
Ccar1 |
A |
G |
10: 62,587,564 (GRCm39) |
Y867H |
unknown |
Het |
Cdh13 |
A |
G |
8: 119,232,437 (GRCm39) |
D47G |
probably benign |
Het |
Chst9 |
T |
A |
18: 15,585,910 (GRCm39) |
T218S |
probably benign |
Het |
Clec2i |
G |
A |
6: 128,870,587 (GRCm39) |
V67I |
probably benign |
Het |
Cox7a2 |
T |
A |
9: 79,667,028 (GRCm39) |
|
probably benign |
Het |
Cplx3 |
A |
G |
9: 57,519,030 (GRCm39) |
|
probably null |
Het |
Cpz |
A |
G |
5: 35,674,929 (GRCm39) |
C107R |
probably damaging |
Het |
Dapk1 |
T |
A |
13: 60,909,013 (GRCm39) |
C1209S |
possibly damaging |
Het |
Ddx41 |
T |
C |
13: 55,681,781 (GRCm39) |
M307V |
probably benign |
Het |
Defa24 |
A |
G |
8: 22,224,565 (GRCm39) |
I5V |
probably benign |
Het |
Dgcr8 |
A |
T |
16: 18,076,178 (GRCm39) |
N2K |
probably damaging |
Het |
Ebf2 |
A |
G |
14: 67,476,423 (GRCm39) |
D131G |
probably damaging |
Het |
Fam149b |
C |
T |
14: 20,427,985 (GRCm39) |
R424C |
probably damaging |
Het |
Fbln2 |
G |
A |
6: 91,240,335 (GRCm39) |
V714M |
probably damaging |
Het |
Fgf5 |
T |
C |
5: 98,423,385 (GRCm39) |
Y257H |
probably damaging |
Het |
Fmo3 |
A |
C |
1: 162,791,605 (GRCm39) |
V224G |
probably damaging |
Het |
Gigyf2 |
T |
C |
1: 87,338,450 (GRCm39) |
I394T |
possibly damaging |
Het |
Glmn |
T |
A |
5: 107,741,746 (GRCm39) |
|
probably null |
Het |
Greb1l |
T |
C |
18: 10,501,025 (GRCm39) |
I385T |
possibly damaging |
Het |
Grhl1 |
C |
A |
12: 24,658,449 (GRCm39) |
Q365K |
probably benign |
Het |
Gsdme |
G |
A |
6: 50,206,306 (GRCm39) |
T179M |
probably damaging |
Het |
Gtf2a1l |
A |
G |
17: 89,018,962 (GRCm39) |
T349A |
probably benign |
Het |
Hax1 |
GTCATCATCATCATCATC |
GTCATCATCATCATCATCATC |
3: 89,905,247 (GRCm39) |
|
probably benign |
Het |
Il5ra |
G |
A |
6: 106,718,226 (GRCm39) |
T76I |
probably damaging |
Het |
Itga8 |
T |
C |
2: 12,196,525 (GRCm39) |
T631A |
probably benign |
Het |
Kcnh6 |
G |
A |
11: 105,909,978 (GRCm39) |
|
probably null |
Het |
Krt26 |
C |
T |
11: 99,224,415 (GRCm39) |
E368K |
probably benign |
Het |
Lhx9 |
T |
C |
1: 138,766,281 (GRCm39) |
D169G |
possibly damaging |
Het |
Lmod3 |
A |
G |
6: 97,224,234 (GRCm39) |
L529P |
probably damaging |
Het |
Mroh2a |
G |
A |
1: 88,158,390 (GRCm39) |
V146M |
probably damaging |
Het |
Nup155 |
A |
G |
15: 8,173,577 (GRCm39) |
T891A |
probably benign |
Het |
Or11g24 |
A |
G |
14: 50,661,984 (GRCm39) |
T3A |
probably benign |
Het |
Or1e1 |
T |
C |
11: 73,244,582 (GRCm39) |
M1T |
probably null |
Het |
Or1j13 |
T |
A |
2: 36,369,996 (GRCm39) |
I49F |
probably damaging |
Het |
Or1p4-ps1 |
T |
C |
11: 74,208,285 (GRCm39) |
*145R |
probably null |
Het |
Or8b36 |
ATTGCTGTTT |
ATTGCTGTTTGCTGTTT |
9: 37,937,836 (GRCm39) |
|
probably null |
Het |
Papln |
G |
C |
12: 83,821,454 (GRCm39) |
G262A |
probably damaging |
Het |
Pdcd1lg2 |
G |
A |
19: 29,423,435 (GRCm39) |
V160I |
probably benign |
Het |
Ppme1 |
G |
A |
7: 100,004,002 (GRCm39) |
R68* |
probably null |
Het |
Ptprn2 |
A |
T |
12: 117,219,215 (GRCm39) |
N949Y |
probably damaging |
Het |
Qser1 |
C |
A |
2: 104,617,468 (GRCm39) |
D1115Y |
probably damaging |
Het |
Rad54l |
G |
T |
4: 115,954,666 (GRCm39) |
D674E |
probably damaging |
Het |
Ripk4 |
T |
A |
16: 97,545,387 (GRCm39) |
D420V |
probably damaging |
Het |
Ros1 |
G |
T |
10: 51,954,067 (GRCm39) |
S1857R |
probably benign |
Het |
Rsf1 |
ATGGCG |
ATGGCGACGGTGGCG |
7: 97,229,111 (GRCm39) |
|
probably benign |
Het |
Rsf1 |
A |
G |
7: 97,311,316 (GRCm39) |
E682G |
probably benign |
Het |
Samd4 |
G |
A |
14: 47,325,329 (GRCm39) |
R515H |
probably damaging |
Het |
Selp |
T |
A |
1: 163,969,079 (GRCm39) |
W560R |
probably benign |
Het |
Shc3 |
A |
T |
13: 51,615,468 (GRCm39) |
L163Q |
probably damaging |
Het |
Shh |
G |
A |
5: 28,666,397 (GRCm39) |
A163V |
probably damaging |
Het |
Slc17a8 |
T |
C |
10: 89,427,937 (GRCm39) |
R113G |
possibly damaging |
Het |
Slc5a6 |
C |
A |
5: 31,206,168 (GRCm39) |
|
probably benign |
Het |
Smarcd2 |
A |
G |
11: 106,157,715 (GRCm39) |
|
probably null |
Het |
Sytl3 |
A |
G |
17: 6,995,664 (GRCm39) |
D148G |
probably damaging |
Het |
Tnks |
G |
T |
8: 35,385,615 (GRCm39) |
H297Q |
possibly damaging |
Het |
Trbv21 |
A |
T |
6: 41,179,568 (GRCm39) |
|
probably benign |
Het |
Ube3c |
T |
C |
5: 29,806,161 (GRCm39) |
F268L |
probably benign |
Het |
Ugt2b5 |
T |
C |
5: 87,287,541 (GRCm39) |
I209V |
probably benign |
Het |
Usp1 |
A |
G |
4: 98,818,082 (GRCm39) |
N140S |
probably damaging |
Het |
Vcam1 |
T |
C |
3: 115,919,606 (GRCm39) |
Y226C |
probably damaging |
Het |
Vmn1r129 |
T |
A |
7: 21,094,534 (GRCm39) |
Q228L |
probably damaging |
Het |
Vmn1r209 |
T |
A |
13: 22,990,202 (GRCm39) |
N163Y |
probably benign |
Het |
Vmn1r85 |
A |
G |
7: 12,818,854 (GRCm39) |
S97P |
probably damaging |
Het |
Vmn2r30 |
C |
T |
7: 7,337,350 (GRCm39) |
M95I |
probably benign |
Het |
Vmn2r74 |
G |
A |
7: 85,601,098 (GRCm39) |
R847C |
probably damaging |
Het |
Wdr70 |
G |
A |
15: 7,916,830 (GRCm39) |
T529I |
possibly damaging |
Het |
Zfp532 |
T |
G |
18: 65,757,005 (GRCm39) |
S313A |
possibly damaging |
Het |
Zhx3 |
A |
T |
2: 160,621,463 (GRCm39) |
N901K |
probably benign |
Het |
|
Other mutations in Pde8b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Pde8b
|
APN |
13 |
95,170,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01517:Pde8b
|
APN |
13 |
95,237,395 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01736:Pde8b
|
APN |
13 |
95,166,910 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01756:Pde8b
|
APN |
13 |
95,182,895 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01867:Pde8b
|
APN |
13 |
95,237,446 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01939:Pde8b
|
APN |
13 |
95,232,232 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02026:Pde8b
|
APN |
13 |
95,170,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02685:Pde8b
|
APN |
13 |
95,162,628 (GRCm39) |
makesense |
probably null |
|
IGL02830:Pde8b
|
APN |
13 |
95,189,409 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02966:Pde8b
|
APN |
13 |
95,232,156 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03003:Pde8b
|
APN |
13 |
95,178,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03064:Pde8b
|
APN |
13 |
95,182,906 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03349:Pde8b
|
APN |
13 |
95,179,551 (GRCm39) |
splice site |
probably benign |
|
R0356:Pde8b
|
UTSW |
13 |
95,182,962 (GRCm39) |
missense |
probably damaging |
0.96 |
R0464:Pde8b
|
UTSW |
13 |
95,241,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R0711:Pde8b
|
UTSW |
13 |
95,244,325 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1436:Pde8b
|
UTSW |
13 |
95,162,678 (GRCm39) |
missense |
probably benign |
0.00 |
R1467:Pde8b
|
UTSW |
13 |
95,170,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R1467:Pde8b
|
UTSW |
13 |
95,170,680 (GRCm39) |
missense |
probably damaging |
0.99 |
R1494:Pde8b
|
UTSW |
13 |
95,184,304 (GRCm39) |
missense |
probably damaging |
1.00 |
R1546:Pde8b
|
UTSW |
13 |
95,182,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1699:Pde8b
|
UTSW |
13 |
95,169,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R1795:Pde8b
|
UTSW |
13 |
95,178,527 (GRCm39) |
missense |
probably benign |
0.10 |
R1879:Pde8b
|
UTSW |
13 |
95,221,723 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2184:Pde8b
|
UTSW |
13 |
95,162,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Pde8b
|
UTSW |
13 |
95,179,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R2892:Pde8b
|
UTSW |
13 |
95,170,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R3034:Pde8b
|
UTSW |
13 |
95,359,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R4204:Pde8b
|
UTSW |
13 |
95,359,053 (GRCm39) |
missense |
probably benign |
0.22 |
R4206:Pde8b
|
UTSW |
13 |
95,359,053 (GRCm39) |
missense |
probably benign |
0.22 |
R4623:Pde8b
|
UTSW |
13 |
95,178,447 (GRCm39) |
missense |
possibly damaging |
0.69 |
R4711:Pde8b
|
UTSW |
13 |
95,166,958 (GRCm39) |
missense |
probably benign |
0.00 |
R5133:Pde8b
|
UTSW |
13 |
95,223,250 (GRCm39) |
missense |
probably benign |
0.05 |
R5134:Pde8b
|
UTSW |
13 |
95,223,250 (GRCm39) |
missense |
probably benign |
0.05 |
R5314:Pde8b
|
UTSW |
13 |
95,223,361 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5342:Pde8b
|
UTSW |
13 |
95,178,498 (GRCm39) |
missense |
probably damaging |
0.99 |
R5376:Pde8b
|
UTSW |
13 |
95,162,654 (GRCm39) |
missense |
probably benign |
0.00 |
R5806:Pde8b
|
UTSW |
13 |
95,178,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R5830:Pde8b
|
UTSW |
13 |
95,178,398 (GRCm39) |
missense |
probably benign |
0.01 |
R6021:Pde8b
|
UTSW |
13 |
95,162,670 (GRCm39) |
missense |
possibly damaging |
0.47 |
R6035:Pde8b
|
UTSW |
13 |
95,164,105 (GRCm39) |
intron |
probably benign |
|
R6129:Pde8b
|
UTSW |
13 |
95,178,467 (GRCm39) |
missense |
probably damaging |
0.98 |
R6181:Pde8b
|
UTSW |
13 |
95,223,316 (GRCm39) |
missense |
probably benign |
0.36 |
R6313:Pde8b
|
UTSW |
13 |
95,178,508 (GRCm39) |
nonsense |
probably null |
|
R6849:Pde8b
|
UTSW |
13 |
95,184,307 (GRCm39) |
missense |
possibly damaging |
0.89 |
R6914:Pde8b
|
UTSW |
13 |
95,223,352 (GRCm39) |
missense |
probably benign |
0.06 |
R6999:Pde8b
|
UTSW |
13 |
95,223,342 (GRCm39) |
missense |
possibly damaging |
0.91 |
R7149:Pde8b
|
UTSW |
13 |
95,223,349 (GRCm39) |
missense |
probably benign |
0.03 |
R7275:Pde8b
|
UTSW |
13 |
95,179,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R7483:Pde8b
|
UTSW |
13 |
95,164,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R7553:Pde8b
|
UTSW |
13 |
95,223,258 (GRCm39) |
missense |
probably benign |
0.21 |
R7790:Pde8b
|
UTSW |
13 |
95,170,679 (GRCm39) |
missense |
probably benign |
0.00 |
R7802:Pde8b
|
UTSW |
13 |
95,237,446 (GRCm39) |
missense |
probably damaging |
0.99 |
R7852:Pde8b
|
UTSW |
13 |
95,244,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R7872:Pde8b
|
UTSW |
13 |
95,223,347 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7897:Pde8b
|
UTSW |
13 |
95,244,202 (GRCm39) |
missense |
probably benign |
0.01 |
R8144:Pde8b
|
UTSW |
13 |
95,359,278 (GRCm39) |
missense |
probably damaging |
0.99 |
R8792:Pde8b
|
UTSW |
13 |
95,179,534 (GRCm39) |
missense |
probably benign |
|
R8850:Pde8b
|
UTSW |
13 |
95,226,793 (GRCm39) |
missense |
probably benign |
0.01 |
R8905:Pde8b
|
UTSW |
13 |
95,182,993 (GRCm39) |
missense |
probably damaging |
1.00 |
R9252:Pde8b
|
UTSW |
13 |
95,169,424 (GRCm39) |
missense |
probably damaging |
1.00 |
R9256:Pde8b
|
UTSW |
13 |
95,164,204 (GRCm39) |
missense |
probably damaging |
1.00 |
R9582:Pde8b
|
UTSW |
13 |
95,169,369 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
|
Posted On |
2017-06-26 |