Mutagenetix > Incidental Mutation

Incidental Mutation 'R4202:Pip4p1'

318805

Institutional Source

Beutler Lab

Gene Symbol

Pip4p1

Ensembl Gene

ENSMUSG00000035953

Gene Name

phosphatidylinositol-4,5-bisphosphate 4-phosphatase 1

Synonyms

Tmem55b

MMRRC Submission

041032-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.314) question?

Stock #

R4202 (G1)

Quality Score

146

Status

Validated

Chromosome

Chromosomal Location

51164672-51168306 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 51168112 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Proline at position 41 (S41P)

Ref Sequence

ENSEMBL: ENSMUSP00000125414 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000049312] [ENSMUST00000049411] [ENSMUST00000128395] [ENSMUST00000136753] [ENSMUST00000154288] [ENSMUST00000162957] [ENSMUST00000160538] [ENSMUST00000161166] [ENSMUST00000160835] [ENSMUST00000226871]

AlphaFold

Q3TWL2

Predicted Effect

probably damaging
Transcript: ENSMUST00000049312
AA Change: S41P

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000038276
Gene: ENSMUSG00000035953
AA Change: S41P

Domain	Start	End	E-Value	Type
Pfam:Tmemb_55A	1	270	9.8e-132	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000049411

SMART Domains

Protein: ENSMUSP00000042602
Gene: ENSMUSG00000035960

Domain	Start	End	E-Value	Type
low complexity region	14	40	N/A	INTRINSIC
Pfam:Exo_endo_phos	64	308	1.5e-31	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000128395

SMART Domains

Protein: ENSMUSP00000116319
Gene: ENSMUSG00000035960

Domain	Start	End	E-Value	Type
low complexity region	9	35	N/A	INTRINSIC
Pfam:Exo_endo_phos	59	280	2.3e-24	PFAM
Pfam:Exo_endo_phos_2	138	284	4e-12	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000136753

SMART Domains

Protein: ENSMUSP00000123148
Gene: ENSMUSG00000035960

Domain	Start	End	E-Value	Type
low complexity region	14	40	N/A	INTRINSIC
Pfam:Exo_endo_phos	64	177	3.8e-13	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000154288

SMART Domains

Protein: ENSMUSP00000122343
Gene: ENSMUSG00000035960

Domain	Start	End	E-Value	Type
low complexity region	14	40	N/A	INTRINSIC
Pfam:Exo_endo_phos	64	214	1.1e-18	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159047

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000159745

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000163043

Predicted Effect

possibly damaging
Transcript: ENSMUST00000162957
AA Change: S41P

PolyPhen 2 Score 0.932 (Sensitivity: 0.80; Specificity: 0.94)

SMART Domains

Protein: ENSMUSP00000123697
Gene: ENSMUSG00000035953
AA Change: S41P

Domain	Start	End	E-Value	Type
Pfam:Tmemb_55A	1	174	2.9e-64	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000163088

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000162935

Predicted Effect

probably damaging
Transcript: ENSMUST00000160538
AA Change: S41P

PolyPhen 2 Score 0.962 (Sensitivity: 0.78; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000124259
Gene: ENSMUSG00000035953
AA Change: S41P

Domain	Start	End	E-Value	Type
Pfam:Tmemb_55A	1	197	1.9e-82	PFAM
low complexity region	221	235	N/A	INTRINSIC

Predicted Effect

probably damaging
Transcript: ENSMUST00000161166
AA Change: S41P

PolyPhen 2 Score 0.969 (Sensitivity: 0.77; Specificity: 0.95)

SMART Domains

Protein: ENSMUSP00000125414
Gene: ENSMUSG00000035953
AA Change: S41P

Domain	Start	End	E-Value	Type
Pfam:Tmemb_55A	1	168	3.6e-65	PFAM

Predicted Effect

possibly damaging
Transcript: ENSMUST00000160835
AA Change: S41P

PolyPhen 2 Score 0.502 (Sensitivity: 0.88; Specificity: 0.90)

SMART Domains

Protein: ENSMUSP00000124782
Gene: ENSMUSG00000035953
AA Change: S41P

Domain	Start	End	E-Value	Type
Pfam:Tmemb_55A	4	277	2.8e-129	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000226871

Predicted Effect

probably benign
Transcript: ENSMUST00000161669

Meta Mutation Damage Score

0.1109

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.3%
20x: 95.5%

Validation Efficiency

92% (33/36)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] TMEM55B catalyzes the degradation of phosphatidylinositol 4,5-bisphosphate (PtdIns-4,5-P2) by removing the 4-phosphate (Ungewickell et al., 2005 [PubMed 16365287]).[supplied by OMIM, Mar 2008]

Allele List at MGI

Other mutations in this stock

Total: 30 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adsl	C	T	15: 80,836,417 (GRCm39)	T58I	probably damaging	Het
Ano7	A	G	1: 93,308,200 (GRCm39)	D77G	probably benign	Het
Ap2b1	T	A	11: 83,226,430 (GRCm39)		probably null	Het
Bclaf3	T	A	X: 158,336,829 (GRCm39)	S419T	probably damaging	Het
Bysl	A	G	17: 47,915,251 (GRCm39)	S166P	probably benign	Het
Cd101	A	C	3: 100,926,001 (GRCm39)	D239E	probably damaging	Het
Cdc42bpb	G	A	12: 111,260,573 (GRCm39)	P1702S	probably benign	Het
Cfap65	G	T	1: 74,959,701 (GRCm39)	F816L	probably damaging	Het
Cnot6	T	C	11: 49,593,463 (GRCm39)	Y6C	probably damaging	Het
Csrp1	T	G	1: 135,673,065 (GRCm39)	C61G	probably damaging	Het
Gmeb2	A	G	2: 180,895,766 (GRCm39)	V468A	possibly damaging	Het
Gucy2g	A	G	19: 55,218,201 (GRCm39)	S416P	possibly damaging	Het
Hormad1	G	A	3: 95,492,509 (GRCm39)	R362H	probably benign	Het
Lancl2	T	A	6: 57,689,977 (GRCm39)	V61D	probably benign	Het
Lta4h	A	G	10: 93,306,669 (GRCm39)	D287G	probably damaging	Het
Maml1	A	T	11: 50,148,740 (GRCm39)	L1000Q	probably damaging	Het
Or6c206	T	C	10: 129,097,646 (GRCm39)	V272A	probably benign	Het
Or7a42	T	C	10: 78,791,129 (GRCm39)	V30A	probably benign	Het
Osbpl9	G	T	4: 109,029,437 (GRCm39)		probably benign	Het
Oser1	T	C	2: 163,253,375 (GRCm39)	T45A	probably benign	Het
Ppfibp1	C	A	6: 146,931,079 (GRCm39)	S878R	probably damaging	Het
Prss43	T	A	9: 110,656,529 (GRCm39)	V72D	probably benign	Het
Sdhb	T	A	4: 140,706,379 (GRCm39)	M272K	possibly damaging	Het
Shroom3	G	T	5: 93,090,945 (GRCm39)	V1151F	probably damaging	Het
Stx17	T	A	4: 48,158,870 (GRCm39)	D83E	probably damaging	Het
Tas2r138	T	C	6: 40,589,410 (GRCm39)	M279V	possibly damaging	Het
Tsku	C	T	7: 98,002,205 (GRCm39)	R42H	probably damaging	Het
Tyr	A	G	7: 87,078,276 (GRCm39)	L528P	possibly damaging	Het
Vmn2r87	T	C	10: 130,308,448 (GRCm39)	I597V	probably benign	Het
Wnt5b	T	C	6: 119,417,272 (GRCm39)	N198D	probably damaging	Het

Other mutations in Pip4p1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02310:Pip4p1	APN	14	51,166,667 (GRCm39)	missense	possibly damaging	0.83
R0016:Pip4p1	UTSW	14	51,166,351 (GRCm39)	missense	probably damaging	1.00
R0885:Pip4p1	UTSW	14	51,167,763 (GRCm39)	missense	probably damaging	1.00
R2483:Pip4p1	UTSW	14	51,167,749 (GRCm39)	missense	probably damaging	1.00
R2509:Pip4p1	UTSW	14	51,167,115 (GRCm39)	nonsense	probably null
R4992:Pip4p1	UTSW	14	51,166,690 (GRCm39)	missense	probably damaging	0.98
R5381:Pip4p1	UTSW	14	51,166,495 (GRCm39)	missense	probably benign	0.00
R5629:Pip4p1	UTSW	14	51,165,373 (GRCm39)	missense	probably benign	0.05
R5844:Pip4p1	UTSW	14	51,166,499 (GRCm39)	missense	probably benign	0.03
R5865:Pip4p1	UTSW	14	51,166,332 (GRCm39)	unclassified	probably benign
R7177:Pip4p1	UTSW	14	51,167,634 (GRCm39)	missense	possibly damaging	0.65
R7732:Pip4p1	UTSW	14	51,168,090 (GRCm39)	missense	possibly damaging	0.69
R8773:Pip4p1	UTSW	14	51,166,503 (GRCm39)	missense	possibly damaging	0.48
R9751:Pip4p1	UTSW	14	51,165,436 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- CCAGGCTTAGGCAGTGATTG -3'
(R):5'- TGTTTCAGGTCCACGAATGACAG -3'

Sequencing Primer
(F):5'- TGATTGCGGACCGAGGATGC -3'
(R):5'- GTCCACGAATGACAGCGCAG -3'

Posted On

2015-06-10