Incidental Mutation 'IGL01401:Inpp5b'
| ID |
79636 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Inpp5b
|
| Ensembl Gene |
ENSMUSG00000028894 |
| Gene Name |
inositol polyphosphate-5-phosphatase B |
| Synonyms |
75kDa |
| Accession Numbers |
|
| Essential gene? |
Probably non essential
(E-score: 0.217)
|
| Stock # |
IGL01401
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
4 |
| Chromosomal Location |
124635643-124695304 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to C
at 124639880 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Alanine
at position 99
(V99A)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000139221
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000094782]
[ENSMUST00000153837]
[ENSMUST00000154229]
[ENSMUST00000184454]
|
| AlphaFold |
Q8K337 |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000094782
AA Change: V99A
PolyPhen 2
Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000092375
Gene: ENSMUSG00000028894
AA Change: V99A
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:INPP5B_PH
|
1 |
150 |
4.3e-61 |
PFAM |
|
low complexity region
|
206 |
220 |
N/A |
INTRINSIC |
|
IPPc
|
343 |
644 |
6.29e-126 |
SMART |
|
Blast:RhoGAP
|
706 |
732 |
1e-7 |
BLAST |
|
Blast:RhoGAP
|
755 |
809 |
2e-24 |
BLAST |
|
RhoGAP
|
827 |
993 |
6.77e-37 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000102164
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000131381
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000153837
AA Change: V99A
PolyPhen 2
Score 0.904 (Sensitivity: 0.82; Specificity: 0.94)
|
| SMART Domains |
Protein: ENSMUSP00000122568
Gene: ENSMUSG00000028894
AA Change: V99A
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:2KIG|A
|
1 |
156 |
1e-113 |
PDB |
|
| Predicted Effect |
possibly damaging
Transcript: ENSMUST00000154229
AA Change: V145A
PolyPhen 2
Score 0.857 (Sensitivity: 0.83; Specificity: 0.93)
|
| SMART Domains |
Protein: ENSMUSP00000115176
Gene: ENSMUSG00000028894
AA Change: V145A
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:2KIG|A
|
1 |
202 |
1e-104 |
PDB |
|
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000184454
AA Change: V99A
PolyPhen 2
Score 0.968 (Sensitivity: 0.77; Specificity: 0.95)
|
| SMART Domains |
Protein: ENSMUSP00000139221
Gene: ENSMUSG00000028894
AA Change: V99A
| Domain | Start | End | E-Value | Type |
|---|
|
PDB:2KIG|A
|
1 |
156 |
1e-105 |
PDB |
|
low complexity region
|
206 |
220 |
N/A |
INTRINSIC |
|
IPPc
|
343 |
644 |
6.29e-126 |
SMART |
|
PDB:3QBT|H
|
645 |
782 |
6e-49 |
PDB |
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: This gene encodes a member of the inositol polyphosphate-5-phosphatase (INPP5) family. This protein hydrolyzes the 5' phosphate from phosphatidylinositol 4,5-bisphosphate and phosphatidylinositol-1,4,5-trisphosphate, which results in changes to multiple signaling pathways. This protein may be involved in protein trafficking and secretion. Homozygous knockout mice exhibit impaired spermatogenesis and male sterility. Alternative splicing of this gene results in multiple transcript variants. [provided by RefSeq, Nov 2014]
PHENOTYPE: Homozygous null male mice are infertile with a disruption in spermatogenesis and a defect in adherens junctions processing. [provided by MGI curators]
|
| Allele List at MGI |
All alleles(24) : Targeted(6) Gene trapped(18)
|
| Other mutations in this stock |
Total: 38 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adgrl3 |
T |
C |
5: 81,836,516 (GRCm39) |
V758A |
possibly damaging |
Het |
| Arf4 |
T |
C |
14: 26,359,609 (GRCm39) |
L12P |
probably damaging |
Het |
| Bltp1 |
A |
G |
3: 36,996,441 (GRCm39) |
N1051S |
probably benign |
Het |
| C4bp |
A |
T |
1: 130,575,801 (GRCm39) |
V230E |
possibly damaging |
Het |
| Carm1 |
T |
A |
9: 21,480,878 (GRCm39) |
|
probably null |
Het |
| Cd4 |
G |
A |
6: 124,856,341 (GRCm39) |
T50I |
probably benign |
Het |
| Ceacam16 |
T |
C |
7: 19,595,054 (GRCm39) |
Y8C |
probably benign |
Het |
| Ckap2l |
A |
T |
2: 129,111,136 (GRCm39) |
V687E |
probably damaging |
Het |
| Dcaf4 |
A |
G |
12: 83,588,148 (GRCm39) |
D449G |
probably damaging |
Het |
| Dhx38 |
T |
C |
8: 110,278,746 (GRCm39) |
Y1113C |
probably benign |
Het |
| Fry |
A |
G |
5: 150,362,253 (GRCm39) |
I161V |
probably benign |
Het |
| Gm17093 |
A |
C |
14: 44,758,984 (GRCm39) |
M169L |
unknown |
Het |
| Gm20721 |
A |
G |
2: 174,187,295 (GRCm39) |
D999G |
probably damaging |
Het |
| Grin2b |
T |
C |
6: 135,713,361 (GRCm39) |
H840R |
probably damaging |
Het |
| Hoxc12 |
C |
A |
15: 102,845,755 (GRCm39) |
H156Q |
probably benign |
Het |
| Htr3b |
T |
C |
9: 48,858,934 (GRCm39) |
D68G |
probably damaging |
Het |
| Klhl42 |
C |
T |
6: 147,009,241 (GRCm39) |
T360M |
probably benign |
Het |
| Lmo7 |
C |
T |
14: 102,031,713 (GRCm39) |
R36* |
probably null |
Het |
| Lmod3 |
T |
G |
6: 97,229,513 (GRCm39) |
N7T |
probably damaging |
Het |
| Malrd1 |
G |
A |
2: 16,106,768 (GRCm39) |
|
probably null |
Het |
| Mthfd2l |
T |
A |
5: 91,148,425 (GRCm39) |
I284K |
possibly damaging |
Het |
| Myo1e |
T |
A |
9: 70,234,448 (GRCm39) |
I267N |
probably damaging |
Het |
| Or13c7d |
T |
C |
4: 43,770,112 (GRCm39) |
R300G |
probably damaging |
Het |
| Or2y1g |
T |
A |
11: 49,171,314 (GRCm39) |
V113E |
possibly damaging |
Het |
| Prkce |
T |
C |
17: 86,476,268 (GRCm39) |
V83A |
probably damaging |
Het |
| Pxdn |
G |
T |
12: 30,051,983 (GRCm39) |
C540F |
probably damaging |
Het |
| Resf1 |
A |
G |
6: 149,228,394 (GRCm39) |
E480G |
probably damaging |
Het |
| Ryr2 |
T |
A |
13: 11,606,238 (GRCm39) |
E4448V |
possibly damaging |
Het |
| Scn1a |
A |
T |
2: 66,119,455 (GRCm39) |
N1349K |
probably damaging |
Het |
| Smarcc1 |
T |
C |
9: 109,979,033 (GRCm39) |
I172T |
possibly damaging |
Het |
| Syt16 |
T |
C |
12: 74,269,437 (GRCm39) |
V92A |
possibly damaging |
Het |
| Tenm4 |
A |
G |
7: 96,523,474 (GRCm39) |
Y1672C |
probably damaging |
Het |
| Tmem131 |
A |
G |
1: 36,838,468 (GRCm39) |
Y1486H |
probably damaging |
Het |
| Tmem132a |
A |
G |
19: 10,838,888 (GRCm39) |
|
probably benign |
Het |
| Usp40 |
A |
T |
1: 87,921,920 (GRCm39) |
D314E |
probably damaging |
Het |
| Vmn2r79 |
G |
A |
7: 86,686,481 (GRCm39) |
V621I |
probably benign |
Het |
| Wnk4 |
A |
G |
11: 101,167,509 (GRCm39) |
|
probably benign |
Het |
| Wwc1 |
C |
A |
11: 35,789,445 (GRCm39) |
|
probably null |
Het |
|
| Other mutations in Inpp5b |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL00338:Inpp5b
|
APN |
4 |
124,678,168 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
IGL00696:Inpp5b
|
APN |
4 |
124,636,328 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
IGL00969:Inpp5b
|
APN |
4 |
124,677,787 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL01481:Inpp5b
|
APN |
4 |
124,694,492 (GRCm39) |
splice site |
probably null |
|
|
IGL01517:Inpp5b
|
APN |
4 |
124,676,229 (GRCm39) |
missense |
probably benign |
0.00 |
|
IGL03085:Inpp5b
|
APN |
4 |
124,686,115 (GRCm39) |
missense |
probably benign |
0.01 |
|
IGL03178:Inpp5b
|
APN |
4 |
124,679,047 (GRCm39) |
missense |
probably benign |
0.02 |
|
reduced
|
UTSW |
4 |
124,686,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
P0042:Inpp5b
|
UTSW |
4 |
124,691,703 (GRCm39) |
critical splice donor site |
probably null |
|
|
R0504:Inpp5b
|
UTSW |
4 |
124,676,201 (GRCm39) |
nonsense |
probably null |
|
|
R0531:Inpp5b
|
UTSW |
4 |
124,689,249 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R1396:Inpp5b
|
UTSW |
4 |
124,682,873 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1626:Inpp5b
|
UTSW |
4 |
124,677,696 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1768:Inpp5b
|
UTSW |
4 |
124,687,069 (GRCm39) |
nonsense |
probably null |
|
|
R2037:Inpp5b
|
UTSW |
4 |
124,692,092 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R2119:Inpp5b
|
UTSW |
4 |
124,691,662 (GRCm39) |
missense |
probably benign |
0.00 |
|
R2132:Inpp5b
|
UTSW |
4 |
124,678,961 (GRCm39) |
splice site |
probably benign |
|
|
R2190:Inpp5b
|
UTSW |
4 |
124,678,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R3237:Inpp5b
|
UTSW |
4 |
124,674,279 (GRCm39) |
missense |
probably benign |
0.04 |
|
R3800:Inpp5b
|
UTSW |
4 |
124,679,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4735:Inpp5b
|
UTSW |
4 |
124,677,760 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4827:Inpp5b
|
UTSW |
4 |
124,637,643 (GRCm39) |
intron |
probably benign |
|
|
R4865:Inpp5b
|
UTSW |
4 |
124,645,288 (GRCm39) |
missense |
probably benign |
|
|
R4868:Inpp5b
|
UTSW |
4 |
124,645,203 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4913:Inpp5b
|
UTSW |
4 |
124,674,214 (GRCm39) |
missense |
probably benign |
0.09 |
|
R5055:Inpp5b
|
UTSW |
4 |
124,636,824 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5068:Inpp5b
|
UTSW |
4 |
124,636,442 (GRCm39) |
splice site |
probably null |
|
|
R5208:Inpp5b
|
UTSW |
4 |
124,645,110 (GRCm39) |
missense |
possibly damaging |
0.62 |
|
R5642:Inpp5b
|
UTSW |
4 |
124,676,229 (GRCm39) |
missense |
probably benign |
0.00 |
|
R5875:Inpp5b
|
UTSW |
4 |
124,674,199 (GRCm39) |
missense |
possibly damaging |
0.66 |
|
R6015:Inpp5b
|
UTSW |
4 |
124,692,143 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R6288:Inpp5b
|
UTSW |
4 |
124,679,020 (GRCm39) |
missense |
probably benign |
0.00 |
|
R6450:Inpp5b
|
UTSW |
4 |
124,686,045 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7138:Inpp5b
|
UTSW |
4 |
124,679,065 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7235:Inpp5b
|
UTSW |
4 |
124,645,185 (GRCm39) |
missense |
probably benign |
0.04 |
|
R7382:Inpp5b
|
UTSW |
4 |
124,645,370 (GRCm39) |
missense |
probably benign |
0.00 |
|
R7659:Inpp5b
|
UTSW |
4 |
124,689,219 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7806:Inpp5b
|
UTSW |
4 |
124,678,881 (GRCm39) |
splice site |
probably null |
|
|
R8348:Inpp5b
|
UTSW |
4 |
124,678,967 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8509:Inpp5b
|
UTSW |
4 |
124,637,698 (GRCm39) |
critical splice donor site |
probably null |
|
|
R9430:Inpp5b
|
UTSW |
4 |
124,636,340 (GRCm39) |
missense |
possibly damaging |
0.84 |
|
R9794:Inpp5b
|
UTSW |
4 |
124,687,174 (GRCm39) |
missense |
probably damaging |
0.98 |
|
Z1176:Inpp5b
|
UTSW |
4 |
124,691,633 (GRCm39) |
frame shift |
probably null |
|
|
| Posted On |
2013-11-05 |
Incidental Mutation