Incidental Mutation 'R2156:Inpp4b'
ID |
234823 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Inpp4b
|
Ensembl Gene |
ENSMUSG00000037940 |
Gene Name |
inositol polyphosphate-4-phosphatase, type II |
Synonyms |
E130107I17Rik |
MMRRC Submission |
040159-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.230)
|
Stock # |
R2156 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
82069185-82854543 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
T to A
at 82775118 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Isoleucine to Asparagine
at position 772
(I772N)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000150520
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042529]
[ENSMUST00000109851]
[ENSMUST00000109852]
[ENSMUST00000169116]
[ENSMUST00000169387]
[ENSMUST00000170160]
[ENSMUST00000172031]
[ENSMUST00000213285]
[ENSMUST00000217122]
[ENSMUST00000215332]
|
AlphaFold |
Q6P1Y8 |
Predicted Effect |
probably damaging
Transcript: ENSMUST00000042529
AA Change: I755N
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000044466 Gene: ENSMUSG00000037940 AA Change: I755N
Domain | Start | End | E-Value | Type |
C2
|
40 |
147 |
1.72e0 |
SMART |
low complexity region
|
302 |
319 |
N/A |
INTRINSIC |
low complexity region
|
425 |
434 |
N/A |
INTRINSIC |
transmembrane domain
|
898 |
920 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109851
AA Change: I640N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000105477 Gene: ENSMUSG00000037940 AA Change: I640N
Domain | Start | End | E-Value | Type |
low complexity region
|
22 |
35 |
N/A |
INTRINSIC |
low complexity region
|
187 |
204 |
N/A |
INTRINSIC |
low complexity region
|
310 |
319 |
N/A |
INTRINSIC |
transmembrane domain
|
783 |
805 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000109852
AA Change: I772N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000105478 Gene: ENSMUSG00000037940 AA Change: I772N
Domain | Start | End | E-Value | Type |
C2
|
40 |
164 |
5.29e0 |
SMART |
low complexity region
|
319 |
336 |
N/A |
INTRINSIC |
low complexity region
|
442 |
451 |
N/A |
INTRINSIC |
transmembrane domain
|
915 |
937 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000169116
AA Change: I772N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000131947 Gene: ENSMUSG00000037940 AA Change: I772N
Domain | Start | End | E-Value | Type |
C2
|
40 |
164 |
5.29e0 |
SMART |
low complexity region
|
319 |
336 |
N/A |
INTRINSIC |
low complexity region
|
442 |
451 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000169387
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000170160
AA Change: I587N
PolyPhen 2
Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
|
SMART Domains |
Protein: ENSMUSP00000132156 Gene: ENSMUSG00000037940 AA Change: I587N
Domain | Start | End | E-Value | Type |
low complexity region
|
134 |
151 |
N/A |
INTRINSIC |
low complexity region
|
257 |
266 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000172031
AA Change: I772N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
SMART Domains |
Protein: ENSMUSP00000131324 Gene: ENSMUSG00000037940 AA Change: I772N
Domain | Start | End | E-Value | Type |
C2
|
40 |
164 |
5.29e0 |
SMART |
low complexity region
|
319 |
336 |
N/A |
INTRINSIC |
low complexity region
|
442 |
451 |
N/A |
INTRINSIC |
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000213285
AA Change: I772N
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000217122
AA Change: I772N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000215332
AA Change: I772N
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
Coding Region Coverage |
- 1x: 99.2%
- 3x: 98.7%
- 10x: 97.5%
- 20x: 95.6%
|
Validation Efficiency |
|
MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] INPP4B encodes the inositol polyphosphate 4-phosphatase type II, one of the enzymes involved in phosphatidylinositol signaling pathways. This enzyme removes the phosphate group at position 4 of the inositol ring from inositol 3,4-bisphosphate. There is limited data to suggest that the human type II enzyme is subject to alternative splicing, as has been established for the type I enzyme. [provided by RefSeq, Jul 2008] PHENOTYPE: Mice homozygous for a knock-out allele exhibit osteoporosis, reduced long bone length, increased osteoclast numbers and size, increased osteoblast numbers, and increased bone resorption and resorption. [provided by MGI curators]
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1810065E05Rik |
T |
A |
11: 58,313,134 (GRCm39) |
|
probably null |
Het |
Acaa2 |
T |
C |
18: 74,926,476 (GRCm39) |
|
probably null |
Het |
Adam7 |
T |
C |
14: 68,748,792 (GRCm39) |
Q485R |
probably benign |
Het |
Adcy4 |
T |
G |
14: 56,006,627 (GRCm39) |
T1069P |
probably benign |
Het |
Arsj |
T |
C |
3: 126,232,337 (GRCm39) |
L361P |
probably damaging |
Het |
Birc2 |
A |
C |
9: 7,826,939 (GRCm39) |
L349R |
probably damaging |
Het |
C1qa |
T |
C |
4: 136,623,727 (GRCm39) |
Y159C |
probably damaging |
Het |
Cdh13 |
A |
G |
8: 119,963,703 (GRCm39) |
K428E |
probably damaging |
Het |
Cenpe |
T |
C |
3: 134,953,235 (GRCm39) |
M1563T |
probably benign |
Het |
Col10a1 |
T |
C |
10: 34,271,696 (GRCm39) |
V556A |
probably benign |
Het |
Creg2 |
G |
A |
1: 39,662,338 (GRCm39) |
L265F |
probably damaging |
Het |
Cyp1a2 |
T |
A |
9: 57,589,433 (GRCm39) |
D127V |
probably damaging |
Het |
Cyp3a44 |
A |
T |
5: 145,740,480 (GRCm39) |
Y53* |
probably null |
Het |
Cyth1 |
C |
T |
11: 118,073,634 (GRCm39) |
R233Q |
probably damaging |
Het |
Dnmbp |
G |
A |
19: 43,890,346 (GRCm39) |
H474Y |
possibly damaging |
Het |
Dvl1 |
G |
A |
4: 155,932,273 (GRCm39) |
V28I |
possibly damaging |
Het |
Ercc2 |
G |
A |
7: 19,120,717 (GRCm39) |
R206H |
possibly damaging |
Het |
Evx2 |
T |
A |
2: 74,486,360 (GRCm39) |
H343L |
probably damaging |
Het |
Fcrl2 |
T |
A |
3: 87,164,648 (GRCm39) |
I293F |
probably benign |
Het |
Gcnt4 |
A |
G |
13: 97,082,974 (GRCm39) |
E90G |
probably damaging |
Het |
Gid8 |
T |
G |
2: 180,358,751 (GRCm39) |
C139G |
probably benign |
Het |
Gm11938 |
C |
A |
11: 99,493,933 (GRCm39) |
C54F |
probably damaging |
Het |
Gm3336 |
G |
A |
8: 71,174,509 (GRCm39) |
V158I |
probably benign |
Het |
Gucy1b1 |
T |
C |
3: 81,968,327 (GRCm39) |
N60D |
probably benign |
Het |
Hdac7 |
T |
C |
15: 97,691,944 (GRCm39) |
K810E |
probably benign |
Het |
Hsp90ab1 |
A |
G |
17: 45,880,629 (GRCm39) |
F361L |
possibly damaging |
Het |
Igf2bp3 |
A |
T |
6: 49,085,858 (GRCm39) |
|
probably null |
Het |
Iqca1 |
A |
G |
1: 90,017,238 (GRCm39) |
L390P |
possibly damaging |
Het |
Itgb2 |
C |
T |
10: 77,396,082 (GRCm39) |
R586W |
probably benign |
Het |
Itih1 |
A |
G |
14: 30,655,432 (GRCm39) |
S588P |
possibly damaging |
Het |
Iyd |
T |
A |
10: 3,497,166 (GRCm39) |
|
probably null |
Het |
Kl |
A |
G |
5: 150,912,425 (GRCm39) |
K725E |
probably benign |
Het |
Layn |
T |
A |
9: 50,968,697 (GRCm39) |
M349L |
probably benign |
Het |
Map3k5 |
T |
C |
10: 19,900,683 (GRCm39) |
Y286H |
probably damaging |
Het |
Med4 |
C |
T |
14: 73,755,472 (GRCm39) |
|
probably benign |
Het |
Mfn1 |
T |
A |
3: 32,588,400 (GRCm39) |
N42K |
possibly damaging |
Het |
Mindy2 |
T |
C |
9: 70,563,874 (GRCm39) |
D152G |
probably benign |
Het |
Mrc2 |
A |
G |
11: 105,238,682 (GRCm39) |
|
probably null |
Het |
Mrpl11 |
C |
A |
19: 5,012,497 (GRCm39) |
A26E |
probably damaging |
Het |
Msh6 |
G |
A |
17: 88,293,568 (GRCm39) |
W774* |
probably null |
Het |
Mtch1 |
A |
T |
17: 29,561,841 (GRCm39) |
V121E |
probably damaging |
Het |
Mtg2 |
G |
T |
2: 179,725,923 (GRCm39) |
E178* |
probably null |
Het |
Nbas |
A |
T |
12: 13,491,510 (GRCm39) |
N1461Y |
probably damaging |
Het |
Ndfip2 |
A |
G |
14: 105,525,204 (GRCm39) |
T65A |
probably benign |
Het |
Ninl |
G |
T |
2: 150,786,503 (GRCm39) |
Q1146K |
probably damaging |
Het |
Notch1 |
T |
C |
2: 26,350,873 (GRCm39) |
D2089G |
possibly damaging |
Het |
Notch3 |
C |
T |
17: 32,366,818 (GRCm39) |
V906M |
probably damaging |
Het |
Or51l14 |
A |
G |
7: 103,101,371 (GRCm39) |
I276V |
probably benign |
Het |
Or6b6 |
A |
G |
7: 106,570,775 (GRCm39) |
Y259H |
probably damaging |
Het |
Osmr |
A |
T |
15: 6,873,891 (GRCm39) |
Y169N |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,885,033 (GRCm39) |
V124A |
possibly damaging |
Het |
P2rx1 |
T |
C |
11: 72,904,939 (GRCm39) |
M369T |
probably benign |
Het |
Pde4dip |
T |
C |
3: 97,631,534 (GRCm39) |
Q1125R |
probably damaging |
Het |
Podn |
A |
T |
4: 107,878,892 (GRCm39) |
V180E |
probably damaging |
Het |
Pold1 |
A |
T |
7: 44,188,542 (GRCm39) |
V475E |
probably damaging |
Het |
Polg |
A |
G |
7: 79,111,468 (GRCm39) |
I261T |
possibly damaging |
Het |
Satb1 |
G |
T |
17: 52,047,438 (GRCm39) |
Q595K |
probably benign |
Het |
Scaf8 |
T |
A |
17: 3,214,407 (GRCm39) |
|
probably null |
Het |
Semp2l1 |
T |
A |
1: 32,585,128 (GRCm39) |
M261L |
probably benign |
Het |
Serpinb3a |
C |
T |
1: 106,975,202 (GRCm39) |
|
probably null |
Het |
Slc22a26 |
T |
C |
19: 7,779,480 (GRCm39) |
D112G |
probably damaging |
Het |
Slc25a23 |
A |
G |
17: 57,352,562 (GRCm39) |
F441L |
probably benign |
Het |
Slc25a53 |
T |
C |
X: 135,884,216 (GRCm39) |
T42A |
probably damaging |
Het |
Slc6a15 |
T |
C |
10: 103,229,269 (GRCm39) |
Y103H |
probably damaging |
Het |
Slx4 |
A |
G |
16: 3,804,223 (GRCm39) |
S864P |
probably benign |
Het |
Snap91 |
T |
C |
9: 86,707,130 (GRCm39) |
E220G |
probably damaging |
Het |
Spam1 |
T |
C |
6: 24,796,267 (GRCm39) |
F73L |
probably damaging |
Het |
Sphkap |
C |
T |
1: 83,255,710 (GRCm39) |
V393M |
probably benign |
Het |
Spred2 |
T |
C |
11: 19,971,241 (GRCm39) |
Y370H |
probably damaging |
Het |
Sqle |
T |
C |
15: 59,195,578 (GRCm39) |
|
probably null |
Het |
Srrm2 |
A |
G |
17: 24,037,237 (GRCm39) |
T1390A |
probably benign |
Het |
Tas1r2 |
A |
G |
4: 139,396,352 (GRCm39) |
R564G |
possibly damaging |
Het |
Tbl2 |
G |
T |
5: 135,185,374 (GRCm39) |
|
probably null |
Het |
Tcof1 |
T |
C |
18: 60,964,901 (GRCm39) |
D606G |
possibly damaging |
Het |
Tdpoz3 |
T |
A |
3: 93,734,087 (GRCm39) |
L254H |
probably damaging |
Het |
Trpm1 |
A |
T |
7: 63,884,736 (GRCm39) |
I806F |
probably damaging |
Het |
Ttc22 |
A |
G |
4: 106,496,237 (GRCm39) |
D429G |
probably benign |
Het |
Ube2o |
C |
A |
11: 116,471,972 (GRCm39) |
G90C |
probably damaging |
Het |
Usp34 |
T |
A |
11: 23,332,602 (GRCm39) |
F1110I |
probably damaging |
Het |
Vmn2r82 |
T |
C |
10: 79,214,722 (GRCm39) |
L235P |
probably damaging |
Het |
Vps35 |
A |
G |
8: 86,013,129 (GRCm39) |
V116A |
probably benign |
Het |
Wdfy3 |
A |
G |
5: 102,046,291 (GRCm39) |
|
probably null |
Het |
Zeb2 |
T |
C |
2: 44,878,821 (GRCm39) |
K1138E |
probably benign |
Het |
Zfp513 |
G |
A |
5: 31,357,866 (GRCm39) |
T169I |
probably benign |
Het |
Zfp629 |
T |
C |
7: 127,211,551 (GRCm39) |
D86G |
probably benign |
Het |
|
Other mutations in Inpp4b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00850:Inpp4b
|
APN |
8 |
82,583,379 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01481:Inpp4b
|
APN |
8 |
82,724,009 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01509:Inpp4b
|
APN |
8 |
82,617,332 (GRCm39) |
splice site |
probably benign |
|
IGL01515:Inpp4b
|
APN |
8 |
82,679,340 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01607:Inpp4b
|
APN |
8 |
82,737,292 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01643:Inpp4b
|
APN |
8 |
82,798,400 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01736:Inpp4b
|
APN |
8 |
82,723,968 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02154:Inpp4b
|
APN |
8 |
82,696,130 (GRCm39) |
splice site |
probably benign |
|
IGL02327:Inpp4b
|
APN |
8 |
82,768,591 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02413:Inpp4b
|
APN |
8 |
82,759,800 (GRCm39) |
missense |
probably benign |
|
IGL02652:Inpp4b
|
APN |
8 |
82,497,429 (GRCm39) |
splice site |
probably benign |
|
IGL02678:Inpp4b
|
APN |
8 |
82,583,373 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03146:Inpp4b
|
APN |
8 |
82,470,410 (GRCm39) |
missense |
possibly damaging |
0.61 |
LCD18:Inpp4b
|
UTSW |
8 |
82,419,639 (GRCm39) |
intron |
probably benign |
|
PIT4280001:Inpp4b
|
UTSW |
8 |
82,761,046 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4480001:Inpp4b
|
UTSW |
8 |
82,772,896 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4504001:Inpp4b
|
UTSW |
8 |
82,768,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R0083:Inpp4b
|
UTSW |
8 |
82,468,091 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0212:Inpp4b
|
UTSW |
8 |
82,497,546 (GRCm39) |
missense |
probably benign |
0.00 |
R0285:Inpp4b
|
UTSW |
8 |
82,761,145 (GRCm39) |
splice site |
probably benign |
|
R0363:Inpp4b
|
UTSW |
8 |
82,610,886 (GRCm39) |
splice site |
probably benign |
|
R0364:Inpp4b
|
UTSW |
8 |
82,723,943 (GRCm39) |
missense |
probably benign |
0.09 |
R0471:Inpp4b
|
UTSW |
8 |
82,768,528 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0550:Inpp4b
|
UTSW |
8 |
82,723,966 (GRCm39) |
missense |
probably benign |
0.00 |
R0562:Inpp4b
|
UTSW |
8 |
82,494,780 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0661:Inpp4b
|
UTSW |
8 |
82,468,091 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0693:Inpp4b
|
UTSW |
8 |
82,723,943 (GRCm39) |
missense |
probably benign |
0.09 |
R1081:Inpp4b
|
UTSW |
8 |
82,795,653 (GRCm39) |
missense |
probably damaging |
0.97 |
R1251:Inpp4b
|
UTSW |
8 |
82,617,382 (GRCm39) |
missense |
probably benign |
0.01 |
R1374:Inpp4b
|
UTSW |
8 |
82,470,445 (GRCm39) |
critical splice donor site |
probably null |
|
R1445:Inpp4b
|
UTSW |
8 |
82,679,463 (GRCm39) |
splice site |
probably null |
|
R1465:Inpp4b
|
UTSW |
8 |
82,494,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Inpp4b
|
UTSW |
8 |
82,494,786 (GRCm39) |
missense |
probably damaging |
1.00 |
R1647:Inpp4b
|
UTSW |
8 |
82,583,403 (GRCm39) |
splice site |
probably benign |
|
R1754:Inpp4b
|
UTSW |
8 |
82,497,440 (GRCm39) |
missense |
probably damaging |
1.00 |
R1759:Inpp4b
|
UTSW |
8 |
82,494,732 (GRCm39) |
missense |
probably benign |
0.06 |
R2085:Inpp4b
|
UTSW |
8 |
82,678,903 (GRCm39) |
missense |
probably damaging |
1.00 |
R2160:Inpp4b
|
UTSW |
8 |
82,848,004 (GRCm39) |
nonsense |
probably null |
|
R2175:Inpp4b
|
UTSW |
8 |
82,583,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R2191:Inpp4b
|
UTSW |
8 |
82,723,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R2401:Inpp4b
|
UTSW |
8 |
82,723,968 (GRCm39) |
missense |
probably benign |
0.00 |
R2475:Inpp4b
|
UTSW |
8 |
82,768,607 (GRCm39) |
missense |
probably benign |
0.09 |
R2512:Inpp4b
|
UTSW |
8 |
82,737,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R2919:Inpp4b
|
UTSW |
8 |
82,711,958 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3021:Inpp4b
|
UTSW |
8 |
82,629,467 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3423:Inpp4b
|
UTSW |
8 |
82,678,890 (GRCm39) |
missense |
possibly damaging |
0.63 |
R3777:Inpp4b
|
UTSW |
8 |
82,768,621 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3778:Inpp4b
|
UTSW |
8 |
82,768,621 (GRCm39) |
missense |
possibly damaging |
0.89 |
R3794:Inpp4b
|
UTSW |
8 |
82,759,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Inpp4b
|
UTSW |
8 |
82,759,845 (GRCm39) |
missense |
probably damaging |
1.00 |
R4590:Inpp4b
|
UTSW |
8 |
82,468,040 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R4602:Inpp4b
|
UTSW |
8 |
82,696,164 (GRCm39) |
missense |
probably damaging |
0.99 |
R4691:Inpp4b
|
UTSW |
8 |
82,849,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R4924:Inpp4b
|
UTSW |
8 |
82,849,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R4992:Inpp4b
|
UTSW |
8 |
82,759,837 (GRCm39) |
missense |
probably damaging |
1.00 |
R5219:Inpp4b
|
UTSW |
8 |
82,610,785 (GRCm39) |
missense |
probably benign |
0.01 |
R5228:Inpp4b
|
UTSW |
8 |
82,494,744 (GRCm39) |
missense |
probably damaging |
0.99 |
R5557:Inpp4b
|
UTSW |
8 |
82,678,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R5627:Inpp4b
|
UTSW |
8 |
82,470,445 (GRCm39) |
critical splice donor site |
probably benign |
|
R5691:Inpp4b
|
UTSW |
8 |
82,617,323 (GRCm39) |
intron |
probably benign |
|
R6186:Inpp4b
|
UTSW |
8 |
82,772,863 (GRCm39) |
missense |
probably damaging |
0.99 |
R6213:Inpp4b
|
UTSW |
8 |
82,724,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R6232:Inpp4b
|
UTSW |
8 |
82,678,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R6283:Inpp4b
|
UTSW |
8 |
82,497,462 (GRCm39) |
missense |
probably damaging |
1.00 |
R6302:Inpp4b
|
UTSW |
8 |
82,494,806 (GRCm39) |
missense |
probably benign |
0.00 |
R6309:Inpp4b
|
UTSW |
8 |
82,768,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R6360:Inpp4b
|
UTSW |
8 |
82,629,481 (GRCm39) |
missense |
probably benign |
0.20 |
R6477:Inpp4b
|
UTSW |
8 |
82,571,343 (GRCm39) |
splice site |
probably null |
|
R6773:Inpp4b
|
UTSW |
8 |
82,583,249 (GRCm39) |
intron |
probably benign |
|
R6968:Inpp4b
|
UTSW |
8 |
82,571,086 (GRCm39) |
missense |
probably benign |
0.18 |
R7147:Inpp4b
|
UTSW |
8 |
82,629,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R7318:Inpp4b
|
UTSW |
8 |
82,798,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R7409:Inpp4b
|
UTSW |
8 |
82,679,314 (GRCm39) |
splice site |
probably null |
|
R7455:Inpp4b
|
UTSW |
8 |
82,798,332 (GRCm39) |
missense |
probably damaging |
0.99 |
R7632:Inpp4b
|
UTSW |
8 |
82,772,968 (GRCm39) |
missense |
probably damaging |
1.00 |
R7844:Inpp4b
|
UTSW |
8 |
82,467,949 (GRCm39) |
start gained |
probably benign |
|
R7958:Inpp4b
|
UTSW |
8 |
82,696,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R8440:Inpp4b
|
UTSW |
8 |
82,768,524 (GRCm39) |
missense |
probably damaging |
1.00 |
R9160:Inpp4b
|
UTSW |
8 |
82,610,782 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9303:Inpp4b
|
UTSW |
8 |
82,759,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R9390:Inpp4b
|
UTSW |
8 |
82,497,522 (GRCm39) |
missense |
probably damaging |
1.00 |
R9583:Inpp4b
|
UTSW |
8 |
82,497,555 (GRCm39) |
critical splice donor site |
probably null |
|
R9705:Inpp4b
|
UTSW |
8 |
82,772,890 (GRCm39) |
missense |
probably benign |
0.14 |
R9778:Inpp4b
|
UTSW |
8 |
82,775,160 (GRCm39) |
missense |
probably benign |
|
RF003:Inpp4b
|
UTSW |
8 |
82,696,150 (GRCm39) |
nonsense |
probably null |
|
Z1088:Inpp4b
|
UTSW |
8 |
82,795,560 (GRCm39) |
critical splice acceptor site |
probably null |
|
Z1176:Inpp4b
|
UTSW |
8 |
82,795,630 (GRCm39) |
missense |
possibly damaging |
0.60 |
|
Predicted Primers |
PCR Primer
(F):5'- CCTTACAAGCGAGCTGTAAAC -3'
(R):5'- ATGCTACTTTACTCACAGGCC -3'
Sequencing Primer
(F):5'- tcttcttcctcctcctcttc -3'
(R):5'- ACAGGCCTCTTTTGCTTAAGAG -3'
|
Posted On |
2014-10-01 |