Incidental Mutation 'R2143:Pde4dip'
ID |
236465 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Pde4dip
|
Ensembl Gene |
ENSMUSG00000038170 |
Gene Name |
phosphodiesterase 4D interacting protein (myomegalin) |
Synonyms |
Usmg4, D3Bwg1078e, D130016K21Rik, 9430063L05Rik, 4732458A06Rik |
MMRRC Submission |
040146-MU
|
Accession Numbers |
|
Essential gene? |
Essential
(E-score: 1.000)
|
Stock # |
R2143 (G1)
|
Quality Score |
109 |
Status
|
Not validated
|
Chromosome |
3 |
Chromosomal Location |
97597144-97796023 bp(-) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 97795835 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Glutamic Acid to Valine
at position 51
(E51V)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000131170
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000090750]
[ENSMUST00000168438]
|
AlphaFold |
no structure available at present |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000090750
AA Change: E51V
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000088254 Gene: ENSMUSG00000038170 AA Change: E51V
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
40 |
N/A |
INTRINSIC |
low complexity region
|
45 |
57 |
N/A |
INTRINSIC |
Pfam:Cnn_1N
|
124 |
196 |
3.2e-26 |
PFAM |
low complexity region
|
204 |
219 |
N/A |
INTRINSIC |
coiled coil region
|
282 |
325 |
N/A |
INTRINSIC |
internal_repeat_1
|
397 |
438 |
4.03e-5 |
PROSPERO |
low complexity region
|
567 |
578 |
N/A |
INTRINSIC |
internal_repeat_2
|
617 |
667 |
6.59e-5 |
PROSPERO |
internal_repeat_1
|
620 |
661 |
4.03e-5 |
PROSPERO |
coiled coil region
|
866 |
942 |
N/A |
INTRINSIC |
low complexity region
|
1038 |
1056 |
N/A |
INTRINSIC |
low complexity region
|
1067 |
1082 |
N/A |
INTRINSIC |
coiled coil region
|
1118 |
1163 |
N/A |
INTRINSIC |
coiled coil region
|
1336 |
1363 |
N/A |
INTRINSIC |
low complexity region
|
1403 |
1420 |
N/A |
INTRINSIC |
coiled coil region
|
1470 |
1508 |
N/A |
INTRINSIC |
internal_repeat_2
|
1597 |
1644 |
6.59e-5 |
PROSPERO |
DUF1220
|
1680 |
1747 |
1.17e-17 |
SMART |
low complexity region
|
1758 |
1780 |
N/A |
INTRINSIC |
low complexity region
|
1836 |
1851 |
N/A |
INTRINSIC |
low complexity region
|
1860 |
1874 |
N/A |
INTRINSIC |
low complexity region
|
1940 |
1951 |
N/A |
INTRINSIC |
coiled coil region
|
1962 |
2138 |
N/A |
INTRINSIC |
coiled coil region
|
2162 |
2197 |
N/A |
INTRINSIC |
coiled coil region
|
2387 |
2431 |
N/A |
INTRINSIC |
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000127317
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000168438
AA Change: E51V
PolyPhen 2
Score 0.861 (Sensitivity: 0.83; Specificity: 0.93)
|
SMART Domains |
Protein: ENSMUSP00000131170 Gene: ENSMUSG00000038170 AA Change: E51V
Domain | Start | End | E-Value | Type |
low complexity region
|
10 |
40 |
N/A |
INTRINSIC |
low complexity region
|
45 |
57 |
N/A |
INTRINSIC |
Pfam:Microtub_assoc
|
124 |
198 |
1.4e-31 |
PFAM |
low complexity region
|
204 |
219 |
N/A |
INTRINSIC |
coiled coil region
|
282 |
325 |
N/A |
INTRINSIC |
internal_repeat_1
|
397 |
438 |
3.56e-5 |
PROSPERO |
low complexity region
|
567 |
578 |
N/A |
INTRINSIC |
internal_repeat_2
|
617 |
667 |
5.83e-5 |
PROSPERO |
internal_repeat_1
|
620 |
661 |
3.56e-5 |
PROSPERO |
coiled coil region
|
866 |
942 |
N/A |
INTRINSIC |
low complexity region
|
1038 |
1056 |
N/A |
INTRINSIC |
low complexity region
|
1067 |
1082 |
N/A |
INTRINSIC |
coiled coil region
|
1118 |
1163 |
N/A |
INTRINSIC |
coiled coil region
|
1336 |
1363 |
N/A |
INTRINSIC |
low complexity region
|
1403 |
1420 |
N/A |
INTRINSIC |
coiled coil region
|
1470 |
1508 |
N/A |
INTRINSIC |
internal_repeat_2
|
1597 |
1644 |
5.83e-5 |
PROSPERO |
DUF1220
|
1680 |
1747 |
1.17e-17 |
SMART |
low complexity region
|
1758 |
1769 |
N/A |
INTRINSIC |
low complexity region
|
1785 |
1800 |
N/A |
INTRINSIC |
low complexity region
|
1809 |
1823 |
N/A |
INTRINSIC |
low complexity region
|
1889 |
1900 |
N/A |
INTRINSIC |
coiled coil region
|
1911 |
2087 |
N/A |
INTRINSIC |
coiled coil region
|
2111 |
2146 |
N/A |
INTRINSIC |
coiled coil region
|
2336 |
2380 |
N/A |
INTRINSIC |
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.4%
- 20x: 95.3%
|
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 serves to anchor phosphodiesterase 4D to the Golgi/centrosome region of the cell. Defects in this gene may be a cause of myeloproliferative disorder (MBD) associated with eosinophilia. Several transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2010] PHENOTYPE: Mice homozygous for a null allele exhibit partial (in utero or perinatal) lethality, hyperactivity, and increased vertical activity. [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 |
2310034C09Rik |
G |
C |
16: 88,556,053 (GRCm39) |
S89T |
probably benign |
Het |
4930522L14Rik |
C |
G |
5: 109,884,616 (GRCm39) |
C414S |
probably damaging |
Het |
4930553M12Rik |
G |
A |
4: 88,786,411 (GRCm39) |
T69I |
unknown |
Het |
4930553M12Rik |
T |
A |
4: 88,786,412 (GRCm39) |
T69S |
unknown |
Het |
Apobr |
G |
A |
7: 126,186,288 (GRCm39) |
E600K |
probably benign |
Het |
Armc8 |
C |
A |
9: 99,387,361 (GRCm39) |
R419L |
probably damaging |
Het |
Ash1l |
T |
A |
3: 88,892,726 (GRCm39) |
M1535K |
probably benign |
Het |
Atf7ip2 |
A |
G |
16: 10,058,509 (GRCm39) |
E316G |
probably null |
Het |
Atp2a1 |
G |
A |
7: 126,047,897 (GRCm39) |
R638* |
probably null |
Het |
Atp8b4 |
A |
T |
2: 126,216,430 (GRCm39) |
I672N |
probably damaging |
Het |
Atrn |
T |
C |
2: 130,799,916 (GRCm39) |
V431A |
probably benign |
Het |
Babam1 |
T |
C |
8: 71,851,084 (GRCm39) |
S116P |
probably damaging |
Het |
Ccdc142 |
T |
C |
6: 83,079,203 (GRCm39) |
L180P |
probably damaging |
Het |
Cd52 |
T |
C |
4: 133,821,048 (GRCm39) |
|
probably benign |
Het |
Cdk17 |
T |
C |
10: 93,053,881 (GRCm39) |
L125P |
probably damaging |
Het |
Ckap5 |
A |
G |
2: 91,396,090 (GRCm39) |
D531G |
probably benign |
Het |
Cntn5 |
G |
T |
9: 9,748,420 (GRCm39) |
P487Q |
probably damaging |
Het |
Crispld1 |
C |
T |
1: 17,819,860 (GRCm39) |
T286I |
probably benign |
Het |
Crtap |
T |
C |
9: 114,209,036 (GRCm39) |
Y336C |
probably damaging |
Het |
Ctu2 |
T |
A |
8: 123,205,891 (GRCm39) |
I213K |
probably benign |
Het |
Dmac2l |
A |
G |
12: 69,787,828 (GRCm39) |
Q88R |
probably damaging |
Het |
Dsc3 |
A |
G |
18: 20,113,743 (GRCm39) |
F393S |
possibly damaging |
Het |
Dsg2 |
T |
A |
18: 20,712,218 (GRCm39) |
I118N |
probably damaging |
Het |
Dstyk |
T |
A |
1: 132,391,113 (GRCm39) |
M838K |
probably damaging |
Het |
Elmo3 |
T |
C |
8: 106,035,305 (GRCm39) |
V450A |
probably damaging |
Het |
Eml5 |
A |
C |
12: 98,776,864 (GRCm39) |
F1417C |
probably damaging |
Het |
Enam |
T |
A |
5: 88,640,779 (GRCm39) |
M147K |
probably benign |
Het |
Entpd1 |
T |
C |
19: 40,725,227 (GRCm39) |
Y409H |
probably damaging |
Het |
Extl1 |
C |
A |
4: 134,098,355 (GRCm39) |
E225D |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,186,065 (GRCm39) |
V1761A |
possibly damaging |
Het |
Fsip2 |
A |
T |
2: 82,820,615 (GRCm39) |
L5449F |
possibly damaging |
Het |
Gabra5 |
G |
A |
7: 57,138,763 (GRCm39) |
T95I |
probably damaging |
Het |
Gal3st2c |
C |
T |
1: 93,937,173 (GRCm39) |
Q373* |
probably null |
Het |
Gbp5 |
A |
C |
3: 142,209,593 (GRCm39) |
T180P |
probably damaging |
Het |
Glb1 |
T |
C |
9: 114,266,892 (GRCm39) |
L212P |
probably damaging |
Het |
Gm11596 |
A |
T |
11: 99,683,789 (GRCm39) |
C110* |
probably null |
Het |
Gpat2 |
T |
C |
2: 127,275,682 (GRCm39) |
F487L |
probably damaging |
Het |
Hsph1 |
A |
T |
5: 149,554,951 (GRCm39) |
H110Q |
probably damaging |
Het |
Ikbke |
C |
A |
1: 131,201,211 (GRCm39) |
V176L |
probably damaging |
Het |
Ildr2 |
T |
C |
1: 166,096,895 (GRCm39) |
V38A |
probably damaging |
Het |
Inpp4a |
G |
T |
1: 37,426,827 (GRCm39) |
C326F |
probably damaging |
Het |
Irak2 |
T |
A |
6: 113,649,788 (GRCm39) |
V141D |
probably benign |
Het |
Jade1 |
G |
A |
3: 41,559,143 (GRCm39) |
R408Q |
probably benign |
Het |
Jmjd7 |
C |
A |
2: 119,860,601 (GRCm39) |
|
probably null |
Het |
Kdm7a |
C |
T |
6: 39,145,884 (GRCm39) |
V348I |
possibly damaging |
Het |
Kif20a |
A |
G |
18: 34,758,657 (GRCm39) |
D42G |
possibly damaging |
Het |
Klhl7 |
A |
T |
5: 24,305,861 (GRCm39) |
M37L |
probably benign |
Het |
Krt5 |
A |
G |
15: 101,620,794 (GRCm39) |
I151T |
probably damaging |
Het |
Krtap1-5 |
T |
C |
11: 99,471,644 (GRCm39) |
I50V |
probably benign |
Het |
Letm1 |
A |
AG |
5: 33,926,859 (GRCm39) |
|
probably null |
Het |
Lrrc71 |
C |
T |
3: 87,652,828 (GRCm39) |
W148* |
probably null |
Het |
Lsmem1 |
GTACATACATACATACATACATACATACA |
GTACATACATACATACATACATACATACATACA |
12: 40,235,260 (GRCm39) |
|
probably null |
Het |
Map1a |
T |
A |
2: 121,132,426 (GRCm39) |
S843T |
probably damaging |
Het |
Map1s |
T |
A |
8: 71,363,608 (GRCm39) |
D48E |
probably damaging |
Het |
Mast4 |
A |
G |
13: 102,871,983 (GRCm39) |
F2462L |
possibly damaging |
Het |
Mettl21e |
T |
A |
1: 44,249,398 (GRCm39) |
Y86F |
probably benign |
Het |
Myh6 |
A |
T |
14: 55,190,411 (GRCm39) |
D1035E |
probably damaging |
Het |
Naip6 |
C |
T |
13: 100,436,367 (GRCm39) |
D719N |
probably damaging |
Het |
Nat8f2 |
T |
G |
6: 85,845,239 (GRCm39) |
H41P |
probably benign |
Het |
Ncam1 |
T |
A |
9: 49,454,319 (GRCm39) |
Q597L |
possibly damaging |
Het |
Nek1 |
T |
A |
8: 61,481,730 (GRCm39) |
I215K |
probably damaging |
Het |
Nol11 |
A |
T |
11: 107,071,881 (GRCm39) |
S237R |
probably benign |
Het |
Npr2 |
T |
C |
4: 43,648,166 (GRCm39) |
F870S |
probably damaging |
Het |
Nsd1 |
T |
C |
13: 55,408,210 (GRCm39) |
Y1285H |
probably damaging |
Het |
Nup93 |
C |
T |
8: 95,023,108 (GRCm39) |
Q229* |
probably null |
Het |
Or4a15 |
C |
T |
2: 89,193,447 (GRCm39) |
E109K |
probably damaging |
Het |
Or7g12 |
G |
A |
9: 18,900,099 (GRCm39) |
A272T |
probably benign |
Het |
Pappa |
T |
A |
4: 65,099,186 (GRCm39) |
Y568* |
probably null |
Het |
Parva |
A |
G |
7: 112,159,274 (GRCm39) |
D180G |
possibly damaging |
Het |
Pask |
C |
T |
1: 93,249,019 (GRCm39) |
A794T |
probably benign |
Het |
Pax1 |
T |
A |
2: 147,207,802 (GRCm39) |
C225S |
probably damaging |
Het |
Pde6c |
A |
T |
19: 38,150,777 (GRCm39) |
H562L |
probably damaging |
Het |
Pet100 |
T |
G |
8: 3,672,355 (GRCm39) |
L14R |
probably damaging |
Het |
Pfkfb2 |
T |
C |
1: 130,626,460 (GRCm39) |
T438A |
probably benign |
Het |
Pira2 |
A |
T |
7: 3,847,344 (GRCm39) |
L115Q |
probably damaging |
Het |
Polr2d |
T |
A |
18: 31,929,132 (GRCm39) |
L127Q |
probably damaging |
Het |
Prkd1 |
A |
G |
12: 50,536,694 (GRCm39) |
V130A |
possibly damaging |
Het |
Psd3 |
T |
C |
8: 68,417,003 (GRCm39) |
D45G |
probably damaging |
Het |
Ptpn13 |
A |
G |
5: 103,703,999 (GRCm39) |
T1344A |
probably benign |
Het |
Ptpn6 |
T |
A |
6: 124,701,947 (GRCm39) |
H406L |
probably benign |
Het |
Ric1 |
A |
T |
19: 29,510,652 (GRCm39) |
S78C |
probably damaging |
Het |
Ric1 |
G |
A |
19: 29,510,653 (GRCm39) |
S78N |
probably damaging |
Het |
Scgb1b2 |
G |
T |
7: 30,991,188 (GRCm39) |
|
probably benign |
Het |
Senp7 |
A |
G |
16: 55,990,169 (GRCm39) |
H639R |
probably benign |
Het |
Sgtb |
A |
T |
13: 104,260,767 (GRCm39) |
D72V |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,964,086 (GRCm39) |
M484T |
probably benign |
Het |
Slc5a1 |
A |
G |
5: 33,318,140 (GRCm39) |
K598E |
probably benign |
Het |
Slit3 |
T |
A |
11: 35,503,088 (GRCm39) |
|
probably null |
Het |
Smc1b |
T |
C |
15: 85,008,003 (GRCm39) |
H258R |
probably benign |
Het |
Smu1 |
T |
C |
4: 40,744,073 (GRCm39) |
D318G |
probably damaging |
Het |
Sned1 |
T |
A |
1: 93,199,406 (GRCm39) |
F495L |
probably damaging |
Het |
Svs3a |
C |
A |
2: 164,131,804 (GRCm39) |
S124Y |
probably damaging |
Het |
Syngr4 |
A |
G |
7: 45,536,464 (GRCm39) |
V186A |
probably benign |
Het |
Tars3 |
G |
A |
7: 65,305,539 (GRCm39) |
M254I |
possibly damaging |
Het |
Tdpoz1 |
T |
A |
3: 93,578,143 (GRCm39) |
R214* |
probably null |
Het |
Tm2d3 |
A |
G |
7: 65,344,987 (GRCm39) |
D54G |
probably damaging |
Het |
Trim66 |
A |
T |
7: 109,074,320 (GRCm39) |
I647N |
probably damaging |
Het |
Triml2 |
T |
A |
8: 43,646,548 (GRCm39) |
W346R |
probably damaging |
Het |
Trp53bp1 |
A |
T |
2: 121,046,545 (GRCm39) |
V1085D |
probably benign |
Het |
Trpv2 |
T |
C |
11: 62,483,612 (GRCm39) |
V483A |
probably benign |
Het |
Ugp2 |
G |
T |
11: 21,278,949 (GRCm39) |
N412K |
probably benign |
Het |
Upf1 |
T |
C |
8: 70,792,004 (GRCm39) |
D418G |
probably null |
Het |
Vmn2r77 |
C |
A |
7: 86,461,152 (GRCm39) |
P826Q |
probably damaging |
Het |
Vrtn |
T |
C |
12: 84,696,936 (GRCm39) |
M562T |
probably benign |
Het |
Wdr55 |
A |
G |
18: 36,895,419 (GRCm39) |
N132S |
possibly damaging |
Het |
Wipf2 |
A |
T |
11: 98,787,040 (GRCm39) |
R356S |
possibly damaging |
Het |
Zdhhc6 |
T |
C |
19: 55,287,228 (GRCm39) |
K411E |
probably benign |
Het |
Zfp260 |
A |
G |
7: 29,804,765 (GRCm39) |
K222E |
probably damaging |
Het |
Zfp280d |
A |
G |
9: 72,220,011 (GRCm39) |
N237S |
probably damaging |
Het |
Zfp445 |
T |
G |
9: 122,682,547 (GRCm39) |
S465R |
possibly damaging |
Het |
Zfp821 |
A |
G |
8: 110,450,979 (GRCm39) |
D324G |
probably damaging |
Het |
|
Other mutations in Pde4dip |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00332:Pde4dip
|
APN |
3 |
97,674,593 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00543:Pde4dip
|
APN |
3 |
97,664,940 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00979:Pde4dip
|
APN |
3 |
97,655,074 (GRCm39) |
splice site |
probably benign |
|
IGL01483:Pde4dip
|
APN |
3 |
97,661,465 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02122:Pde4dip
|
APN |
3 |
97,674,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02398:Pde4dip
|
APN |
3 |
97,674,097 (GRCm39) |
missense |
probably benign |
|
IGL02814:Pde4dip
|
APN |
3 |
97,674,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02826:Pde4dip
|
APN |
3 |
97,674,403 (GRCm39) |
missense |
probably damaging |
1.00 |
D3080:Pde4dip
|
UTSW |
3 |
97,674,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R0077:Pde4dip
|
UTSW |
3 |
97,660,442 (GRCm39) |
nonsense |
probably null |
|
R0096:Pde4dip
|
UTSW |
3 |
97,674,783 (GRCm39) |
missense |
probably damaging |
0.99 |
R0277:Pde4dip
|
UTSW |
3 |
97,751,028 (GRCm39) |
missense |
probably benign |
0.01 |
R0304:Pde4dip
|
UTSW |
3 |
97,751,028 (GRCm39) |
missense |
probably benign |
0.01 |
R0616:Pde4dip
|
UTSW |
3 |
97,654,849 (GRCm39) |
missense |
probably benign |
0.09 |
R0676:Pde4dip
|
UTSW |
3 |
97,624,413 (GRCm39) |
splice site |
probably benign |
|
R1166:Pde4dip
|
UTSW |
3 |
97,620,512 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1376:Pde4dip
|
UTSW |
3 |
97,650,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R1376:Pde4dip
|
UTSW |
3 |
97,650,533 (GRCm39) |
missense |
probably damaging |
0.99 |
R1452:Pde4dip
|
UTSW |
3 |
97,631,418 (GRCm39) |
missense |
probably damaging |
1.00 |
R1550:Pde4dip
|
UTSW |
3 |
97,627,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R1700:Pde4dip
|
UTSW |
3 |
97,610,639 (GRCm39) |
missense |
probably benign |
0.00 |
R1704:Pde4dip
|
UTSW |
3 |
97,661,576 (GRCm39) |
missense |
probably benign |
0.28 |
R1769:Pde4dip
|
UTSW |
3 |
97,603,246 (GRCm39) |
missense |
probably benign |
0.00 |
R1934:Pde4dip
|
UTSW |
3 |
97,600,007 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1980:Pde4dip
|
UTSW |
3 |
97,664,312 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2088:Pde4dip
|
UTSW |
3 |
97,661,749 (GRCm39) |
missense |
probably null |
1.00 |
R2149:Pde4dip
|
UTSW |
3 |
97,700,152 (GRCm39) |
missense |
possibly damaging |
0.64 |
R2156:Pde4dip
|
UTSW |
3 |
97,631,534 (GRCm39) |
missense |
probably damaging |
0.98 |
R2158:Pde4dip
|
UTSW |
3 |
97,664,937 (GRCm39) |
missense |
probably benign |
0.15 |
R2240:Pde4dip
|
UTSW |
3 |
97,631,480 (GRCm39) |
missense |
probably benign |
0.00 |
R2249:Pde4dip
|
UTSW |
3 |
97,700,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R2256:Pde4dip
|
UTSW |
3 |
97,625,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R2680:Pde4dip
|
UTSW |
3 |
97,608,933 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2921:Pde4dip
|
UTSW |
3 |
97,626,885 (GRCm39) |
missense |
probably benign |
|
R3407:Pde4dip
|
UTSW |
3 |
97,661,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R3736:Pde4dip
|
UTSW |
3 |
97,631,427 (GRCm39) |
missense |
probably damaging |
1.00 |
R3787:Pde4dip
|
UTSW |
3 |
97,622,868 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3883:Pde4dip
|
UTSW |
3 |
97,620,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R4437:Pde4dip
|
UTSW |
3 |
97,673,885 (GRCm39) |
missense |
possibly damaging |
0.52 |
R4528:Pde4dip
|
UTSW |
3 |
97,624,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4576:Pde4dip
|
UTSW |
3 |
97,661,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Pde4dip
|
UTSW |
3 |
97,603,260 (GRCm39) |
missense |
probably damaging |
0.98 |
R4653:Pde4dip
|
UTSW |
3 |
97,674,654 (GRCm39) |
missense |
probably damaging |
0.99 |
R4678:Pde4dip
|
UTSW |
3 |
97,602,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R4679:Pde4dip
|
UTSW |
3 |
97,602,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R4688:Pde4dip
|
UTSW |
3 |
97,750,993 (GRCm39) |
nonsense |
probably null |
|
R4770:Pde4dip
|
UTSW |
3 |
97,674,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Pde4dip
|
UTSW |
3 |
97,700,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R4842:Pde4dip
|
UTSW |
3 |
97,700,844 (GRCm39) |
missense |
probably damaging |
1.00 |
R4899:Pde4dip
|
UTSW |
3 |
97,616,874 (GRCm39) |
missense |
probably damaging |
1.00 |
R4914:Pde4dip
|
UTSW |
3 |
97,622,644 (GRCm39) |
missense |
probably benign |
0.10 |
R4943:Pde4dip
|
UTSW |
3 |
97,662,827 (GRCm39) |
missense |
probably damaging |
0.99 |
R5131:Pde4dip
|
UTSW |
3 |
97,616,830 (GRCm39) |
missense |
probably damaging |
0.98 |
R5408:Pde4dip
|
UTSW |
3 |
97,704,052 (GRCm39) |
missense |
probably benign |
0.35 |
R5583:Pde4dip
|
UTSW |
3 |
97,654,892 (GRCm39) |
missense |
possibly damaging |
0.67 |
R5677:Pde4dip
|
UTSW |
3 |
97,748,964 (GRCm39) |
nonsense |
probably null |
|
R5689:Pde4dip
|
UTSW |
3 |
97,599,683 (GRCm39) |
nonsense |
probably null |
|
R5696:Pde4dip
|
UTSW |
3 |
97,616,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R5860:Pde4dip
|
UTSW |
3 |
97,631,504 (GRCm39) |
missense |
possibly damaging |
0.68 |
R6279:Pde4dip
|
UTSW |
3 |
97,606,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Pde4dip
|
UTSW |
3 |
97,602,227 (GRCm39) |
missense |
probably benign |
|
R6440:Pde4dip
|
UTSW |
3 |
97,674,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R6464:Pde4dip
|
UTSW |
3 |
97,617,660 (GRCm39) |
missense |
probably damaging |
1.00 |
R6489:Pde4dip
|
UTSW |
3 |
97,662,907 (GRCm39) |
nonsense |
probably null |
|
R6706:Pde4dip
|
UTSW |
3 |
97,648,709 (GRCm39) |
missense |
probably damaging |
1.00 |
R6722:Pde4dip
|
UTSW |
3 |
97,625,555 (GRCm39) |
nonsense |
probably null |
|
R6798:Pde4dip
|
UTSW |
3 |
97,795,850 (GRCm39) |
missense |
probably benign |
|
R6804:Pde4dip
|
UTSW |
3 |
97,700,564 (GRCm39) |
nonsense |
probably null |
|
R6862:Pde4dip
|
UTSW |
3 |
97,674,340 (GRCm39) |
missense |
possibly damaging |
0.52 |
R6957:Pde4dip
|
UTSW |
3 |
97,731,649 (GRCm39) |
splice site |
probably null |
|
R6983:Pde4dip
|
UTSW |
3 |
97,625,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Pde4dip
|
UTSW |
3 |
97,622,738 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7025:Pde4dip
|
UTSW |
3 |
97,631,499 (GRCm39) |
nonsense |
probably null |
|
R7136:Pde4dip
|
UTSW |
3 |
97,601,379 (GRCm39) |
missense |
probably benign |
0.03 |
R7178:Pde4dip
|
UTSW |
3 |
97,622,946 (GRCm39) |
missense |
probably benign |
0.26 |
R7269:Pde4dip
|
UTSW |
3 |
97,674,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R7283:Pde4dip
|
UTSW |
3 |
97,666,198 (GRCm39) |
missense |
probably benign |
0.03 |
R7354:Pde4dip
|
UTSW |
3 |
97,626,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R7357:Pde4dip
|
UTSW |
3 |
97,622,857 (GRCm39) |
missense |
probably benign |
0.01 |
R7360:Pde4dip
|
UTSW |
3 |
97,625,632 (GRCm39) |
missense |
probably benign |
0.01 |
R7371:Pde4dip
|
UTSW |
3 |
97,664,587 (GRCm39) |
missense |
probably benign |
0.08 |
R7432:Pde4dip
|
UTSW |
3 |
97,602,408 (GRCm39) |
missense |
probably benign |
|
R7536:Pde4dip
|
UTSW |
3 |
97,664,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R7542:Pde4dip
|
UTSW |
3 |
97,673,971 (GRCm39) |
missense |
possibly damaging |
0.59 |
R7609:Pde4dip
|
UTSW |
3 |
97,622,881 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7650:Pde4dip
|
UTSW |
3 |
97,606,423 (GRCm39) |
critical splice donor site |
probably null |
|
R7800:Pde4dip
|
UTSW |
3 |
97,622,599 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Pde4dip
|
UTSW |
3 |
97,622,490 (GRCm39) |
missense |
probably damaging |
1.00 |
R7918:Pde4dip
|
UTSW |
3 |
97,622,539 (GRCm39) |
nonsense |
probably null |
|
R8120:Pde4dip
|
UTSW |
3 |
97,614,254 (GRCm39) |
missense |
probably null |
0.94 |
R8139:Pde4dip
|
UTSW |
3 |
97,604,309 (GRCm39) |
missense |
probably benign |
0.02 |
R8144:Pde4dip
|
UTSW |
3 |
97,622,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Pde4dip
|
UTSW |
3 |
97,674,848 (GRCm39) |
missense |
probably damaging |
0.98 |
R8294:Pde4dip
|
UTSW |
3 |
97,674,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R8406:Pde4dip
|
UTSW |
3 |
97,606,428 (GRCm39) |
missense |
probably benign |
0.04 |
R8911:Pde4dip
|
UTSW |
3 |
97,650,917 (GRCm39) |
missense |
probably benign |
0.22 |
R8912:Pde4dip
|
UTSW |
3 |
97,617,633 (GRCm39) |
missense |
probably damaging |
1.00 |
R8960:Pde4dip
|
UTSW |
3 |
97,700,464 (GRCm39) |
missense |
probably damaging |
1.00 |
R8993:Pde4dip
|
UTSW |
3 |
97,673,810 (GRCm39) |
missense |
probably damaging |
1.00 |
R9031:Pde4dip
|
UTSW |
3 |
97,599,675 (GRCm39) |
missense |
probably damaging |
1.00 |
R9032:Pde4dip
|
UTSW |
3 |
97,601,385 (GRCm39) |
missense |
probably benign |
0.00 |
R9085:Pde4dip
|
UTSW |
3 |
97,601,385 (GRCm39) |
missense |
probably benign |
0.00 |
R9103:Pde4dip
|
UTSW |
3 |
97,749,044 (GRCm39) |
missense |
probably damaging |
1.00 |
R9163:Pde4dip
|
UTSW |
3 |
97,659,123 (GRCm39) |
critical splice donor site |
probably null |
|
R9182:Pde4dip
|
UTSW |
3 |
97,602,314 (GRCm39) |
missense |
probably benign |
0.13 |
R9185:Pde4dip
|
UTSW |
3 |
97,666,132 (GRCm39) |
missense |
probably benign |
0.01 |
R9286:Pde4dip
|
UTSW |
3 |
97,607,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R9357:Pde4dip
|
UTSW |
3 |
97,625,645 (GRCm39) |
missense |
probably benign |
0.00 |
R9415:Pde4dip
|
UTSW |
3 |
97,660,468 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9500:Pde4dip
|
UTSW |
3 |
97,795,896 (GRCm39) |
missense |
unknown |
|
R9595:Pde4dip
|
UTSW |
3 |
97,602,207 (GRCm39) |
critical splice donor site |
probably null |
|
R9689:Pde4dip
|
UTSW |
3 |
97,649,841 (GRCm39) |
missense |
probably damaging |
1.00 |
R9720:Pde4dip
|
UTSW |
3 |
97,603,287 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Predicted Primers |
PCR Primer
(F):5'- CCCGTGACAGCATAGATCTC -3'
(R):5'- TTGGATGCTCTTCCACGCTG -3'
Sequencing Primer
(F):5'- GTGACAGCATAGATCTCCTGCC -3'
(R):5'- TCATAGCAAGGGCACAGTGC -3'
|
Posted On |
2014-10-01 |