Incidental Mutation 'R1754:Inpp4b'
ID |
193849 |
Institutional Source |
Beutler Lab
|
Gene Symbol |
Inpp4b
|
Ensembl Gene |
ENSMUSG00000037940 |
Gene Name |
inositol polyphosphate-4-phosphatase, type II |
Synonyms |
E130107I17Rik |
MMRRC Submission |
039786-MU
|
Accession Numbers |
|
Essential gene? |
Probably non essential
(E-score: 0.230)
|
Stock # |
R1754 (G1)
|
Quality Score |
225 |
Status
|
Not validated
|
Chromosome |
8 |
Chromosomal Location |
82069185-82854543 bp(+) (GRCm39) |
Type of Mutation |
missense |
DNA Base Change (assembly) |
A to T
at 82497440 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Threonine to Serine
at position 87
(T87S)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000148972
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000042529]
[ENSMUST00000109852]
[ENSMUST00000169116]
[ENSMUST00000169387]
[ENSMUST00000170160]
[ENSMUST00000172031]
[ENSMUST00000213285]
[ENSMUST00000217122]
[ENSMUST00000215332]
|
AlphaFold |
Q6P1Y8 |
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000042529
AA Change: T87S
PolyPhen 2
Score 0.762 (Sensitivity: 0.85; Specificity: 0.92)
|
SMART Domains |
Protein: ENSMUSP00000044466 Gene: ENSMUSG00000037940 AA Change: T87S
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 |
possibly damaging
Transcript: ENSMUST00000109852
AA Change: T87S
PolyPhen 2
Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000105478 Gene: ENSMUSG00000037940 AA Change: T87S
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 |
noncoding transcript
Transcript: ENSMUST00000164870
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000169116
AA Change: T87S
PolyPhen 2
Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
|
SMART Domains |
Protein: ENSMUSP00000131947 Gene: ENSMUSG00000037940 AA Change: T87S
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
AA Change: N47I
PolyPhen 2
Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000170160
|
SMART Domains |
Protein: ENSMUSP00000132156 Gene: ENSMUSG00000037940
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: T87S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
SMART Domains |
Protein: ENSMUSP00000131324 Gene: ENSMUSG00000037940 AA Change: T87S
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 |
possibly damaging
Transcript: ENSMUST00000213285
AA Change: T87S
PolyPhen 2
Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
possibly damaging
Transcript: ENSMUST00000217122
AA Change: T87S
PolyPhen 2
Score 0.574 (Sensitivity: 0.88; Specificity: 0.91)
|
Predicted Effect |
probably damaging
Transcript: ENSMUST00000215332
AA Change: T87S
PolyPhen 2
Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
|
Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000216036
|
Coding Region Coverage |
- 1x: 97.5%
- 3x: 97.0%
- 10x: 95.6%
- 20x: 93.3%
|
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: 87 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
T |
A |
2: 25,324,345 (GRCm39) |
L234M |
probably benign |
Het |
Abca3 |
G |
A |
17: 24,596,753 (GRCm39) |
S402N |
probably benign |
Het |
Acad12 |
A |
T |
5: 121,745,544 (GRCm39) |
V249D |
probably benign |
Het |
Acp4 |
T |
C |
7: 43,904,428 (GRCm39) |
I212V |
probably benign |
Het |
Actl6a |
T |
A |
3: 32,772,723 (GRCm39) |
V233D |
probably damaging |
Het |
Aire |
T |
A |
10: 77,866,124 (GRCm39) |
Q533L |
probably damaging |
Het |
Aldh3b3 |
T |
C |
19: 4,018,517 (GRCm39) |
S411P |
probably benign |
Het |
Amer2 |
A |
G |
14: 60,617,206 (GRCm39) |
K467R |
probably damaging |
Het |
Apol9b |
A |
T |
15: 77,619,962 (GRCm39) |
I253F |
probably benign |
Het |
Arid1b |
A |
G |
17: 5,329,476 (GRCm39) |
|
probably null |
Het |
Atp6v0a4 |
T |
C |
6: 38,044,764 (GRCm39) |
T494A |
probably benign |
Het |
Atp6v1b2 |
A |
G |
8: 69,554,613 (GRCm39) |
D106G |
probably benign |
Het |
Avpr1b |
T |
C |
1: 131,527,839 (GRCm39) |
S121P |
probably damaging |
Het |
Bcl11a |
A |
C |
11: 24,114,724 (GRCm39) |
E689A |
probably damaging |
Het |
Brpf3 |
T |
G |
17: 29,040,297 (GRCm39) |
L906R |
probably benign |
Het |
Btn1a1 |
T |
C |
13: 23,644,638 (GRCm39) |
K287E |
probably benign |
Het |
Cacna1i |
A |
G |
15: 80,255,730 (GRCm39) |
H871R |
probably damaging |
Het |
Cd14 |
A |
T |
18: 36,858,567 (GRCm39) |
L296Q |
probably damaging |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Colgalt1 |
G |
T |
8: 72,075,823 (GRCm39) |
W490L |
probably damaging |
Het |
Ctnna2 |
A |
G |
6: 77,613,732 (GRCm39) |
I273T |
possibly damaging |
Het |
Dnah7a |
A |
T |
1: 53,543,344 (GRCm39) |
D2275E |
probably benign |
Het |
Dnah7a |
A |
C |
1: 53,601,059 (GRCm39) |
|
probably null |
Het |
Egfem1 |
T |
C |
3: 29,722,482 (GRCm39) |
Y404H |
possibly damaging |
Het |
Esm1 |
A |
T |
13: 113,353,230 (GRCm39) |
N171Y |
probably damaging |
Het |
Exoc1 |
T |
G |
5: 76,708,169 (GRCm39) |
|
probably null |
Het |
Fam243 |
A |
G |
16: 92,117,919 (GRCm39) |
V123A |
probably damaging |
Het |
Fcho1 |
A |
G |
8: 72,163,890 (GRCm39) |
I580T |
probably benign |
Het |
Fgfr1 |
A |
G |
8: 26,060,226 (GRCm39) |
H552R |
probably damaging |
Het |
Fsbp |
A |
G |
4: 11,583,906 (GRCm39) |
R202G |
probably damaging |
Het |
Gabra6 |
A |
G |
11: 42,207,388 (GRCm39) |
V231A |
probably damaging |
Het |
Gmeb1 |
A |
G |
4: 131,959,338 (GRCm39) |
S239P |
probably benign |
Het |
Gnpat |
T |
A |
8: 125,603,745 (GRCm39) |
Y208N |
probably damaging |
Het |
Il21 |
T |
C |
3: 37,279,674 (GRCm39) |
K114R |
possibly damaging |
Het |
Inhbc |
T |
C |
10: 127,206,162 (GRCm39) |
D35G |
possibly damaging |
Het |
Kcns2 |
T |
C |
15: 34,839,663 (GRCm39) |
I342T |
possibly damaging |
Het |
Ky |
A |
T |
9: 102,419,126 (GRCm39) |
T378S |
possibly damaging |
Het |
Lcat |
CAT |
C |
8: 106,668,446 (GRCm39) |
|
probably null |
Het |
Lrrc8d |
T |
C |
5: 105,960,523 (GRCm39) |
V311A |
probably benign |
Het |
Mief1 |
A |
G |
15: 80,133,803 (GRCm39) |
I287V |
probably damaging |
Het |
Mrpl47 |
A |
G |
3: 32,784,233 (GRCm39) |
V179A |
probably benign |
Het |
Mtcl1 |
T |
C |
17: 66,687,178 (GRCm39) |
K576R |
probably damaging |
Het |
Myh10 |
C |
A |
11: 68,703,884 (GRCm39) |
A1902E |
probably damaging |
Het |
Nlrp3 |
A |
G |
11: 59,449,228 (GRCm39) |
T837A |
possibly damaging |
Het |
Nr1i3 |
T |
C |
1: 171,044,963 (GRCm39) |
Y132H |
probably damaging |
Het |
Oit3 |
T |
C |
10: 59,263,762 (GRCm39) |
|
probably null |
Het |
Or12j4 |
A |
T |
7: 140,046,773 (GRCm39) |
I220F |
probably damaging |
Het |
Or2z2 |
A |
T |
11: 58,346,088 (GRCm39) |
M229K |
probably damaging |
Het |
Or4c100 |
A |
T |
2: 88,356,159 (GRCm39) |
R77S |
probably damaging |
Het |
Or5b113 |
T |
C |
19: 13,342,717 (GRCm39) |
S242P |
probably damaging |
Het |
Or5h25 |
T |
A |
16: 58,930,944 (GRCm39) |
I10F |
probably benign |
Het |
Or6k14 |
A |
G |
1: 173,927,599 (GRCm39) |
T192A |
probably benign |
Het |
Or7a42 |
T |
A |
10: 78,791,531 (GRCm39) |
V164E |
probably damaging |
Het |
Or9k2 |
G |
A |
10: 129,999,033 (GRCm39) |
T54I |
probably benign |
Het |
Pdlim4 |
T |
C |
11: 53,946,699 (GRCm39) |
E196G |
possibly damaging |
Het |
Pigs |
A |
G |
11: 78,228,673 (GRCm39) |
Y293C |
probably damaging |
Het |
Pkd1l2 |
A |
T |
8: 117,757,458 (GRCm39) |
S1527T |
possibly damaging |
Het |
Pkd2l1 |
A |
T |
19: 44,144,040 (GRCm39) |
Y344* |
probably null |
Het |
Pmp2 |
T |
C |
3: 10,247,284 (GRCm39) |
|
probably null |
Het |
Polr3e |
T |
C |
7: 120,538,521 (GRCm39) |
|
probably null |
Het |
Ppp3ca |
C |
G |
3: 136,587,209 (GRCm39) |
I230M |
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,739,235 (GRCm39) |
H463R |
probably benign |
Het |
Ptger1 |
A |
G |
8: 84,395,926 (GRCm39) |
N328D |
probably benign |
Het |
Rhno1 |
A |
T |
6: 128,334,822 (GRCm39) |
I167N |
probably benign |
Het |
Rictor |
C |
A |
15: 6,764,849 (GRCm39) |
P34H |
probably damaging |
Het |
Rnf10 |
A |
C |
5: 115,383,924 (GRCm39) |
S630R |
probably damaging |
Het |
Rnf168 |
A |
G |
16: 32,117,942 (GRCm39) |
Q501R |
probably benign |
Het |
Rngtt |
T |
G |
4: 33,329,634 (GRCm39) |
|
probably null |
Het |
Samd9l |
G |
T |
6: 3,373,126 (GRCm39) |
F1378L |
probably damaging |
Het |
Slc9c1 |
T |
A |
16: 45,409,872 (GRCm39) |
M864K |
probably benign |
Het |
Slitrk5 |
T |
C |
14: 111,917,951 (GRCm39) |
F525S |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,076,290 (GRCm39) |
M784V |
probably benign |
Het |
Spata31e4 |
A |
T |
13: 50,855,123 (GRCm39) |
T254S |
probably damaging |
Het |
Spint2 |
C |
T |
7: 28,959,791 (GRCm39) |
|
probably null |
Het |
Ssh1 |
A |
T |
5: 114,093,906 (GRCm39) |
I276N |
probably damaging |
Het |
Trank1 |
T |
A |
9: 111,221,939 (GRCm39) |
V2892D |
probably benign |
Het |
Ttn |
C |
A |
2: 76,581,384 (GRCm39) |
E21424* |
probably null |
Het |
Usp17lc |
T |
C |
7: 103,068,055 (GRCm39) |
I450T |
probably benign |
Het |
Vcan |
A |
G |
13: 89,852,854 (GRCm39) |
V702A |
probably benign |
Het |
Vmn1r36 |
TA |
TAA |
6: 66,693,517 (GRCm39) |
|
probably null |
Het |
Vmn2r51 |
G |
T |
7: 9,833,873 (GRCm39) |
D388E |
probably benign |
Het |
Zfp106 |
A |
C |
2: 120,364,245 (GRCm39) |
S721A |
probably damaging |
Het |
Zfp106 |
G |
A |
2: 120,364,244 (GRCm39) |
S721L |
probably damaging |
Het |
Zfp189 |
T |
A |
4: 49,529,342 (GRCm39) |
H148Q |
possibly damaging |
Het |
Zfp352 |
A |
T |
4: 90,112,046 (GRCm39) |
Y62F |
probably benign |
Het |
Zfp839 |
T |
C |
12: 110,821,891 (GRCm39) |
V235A |
probably damaging |
Het |
Zfp871 |
T |
C |
17: 32,994,308 (GRCm39) |
Y289C |
probably damaging |
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 |
|
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 |
R2156:Inpp4b
|
UTSW |
8 |
82,775,118 (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'- AGCAATCACACGCATAGAGGATAGC -3'
(R):5'- CCACAGCTTGGCAAAGTATGACGAC -3'
Sequencing Primer
(F):5'- GGGttttgtttgtttgtttgtttttg -3'
(R):5'- TTGGCAAAGTATGACGACCTCTC -3'
|
Posted On |
2014-05-23 |