Mutagenetix > Incidental Mutation

Incidental Mutation 'R4012:Inpp5j'

311761

Institutional Source

Beutler Lab

Gene Symbol

Inpp5j

Ensembl Gene

ENSMUSG00000034570

Gene Name

inositol polyphosphate 5-phosphatase J

Synonyms

Pipp, Pib5pa

MMRRC Submission

040949-MU

Accession Numbers

Essential gene?

Possibly non essential (E-score: 0.474) question?

Stock #

R4012 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

3444375-3454821 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 3450185 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Leucine at position 615 (F615L)

Ref Sequence

ENSEMBL: ENSMUSP00000139302 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000044507] [ENSMUST00000044682] [ENSMUST00000110018] [ENSMUST00000110019] [ENSMUST00000154756] [ENSMUST00000183684]

AlphaFold

P59644

Predicted Effect

probably benign
Transcript: ENSMUST00000044507
AA Change: F615L

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)

SMART Domains

Protein: ENSMUSP00000046625
Gene: ENSMUSG00000034570
AA Change: F615L

Domain	Start	End	E-Value	Type
low complexity region	11	24	N/A	INTRINSIC
low complexity region	115	131	N/A	INTRINSIC
low complexity region	144	155	N/A	INTRINSIC
low complexity region	180	216	N/A	INTRINSIC
low complexity region	292	311	N/A	INTRINSIC
low complexity region	333	365	N/A	INTRINSIC
low complexity region	390	413	N/A	INTRINSIC
IPPc	418	733	4.41e-98	SMART
low complexity region	840	862	N/A	INTRINSIC
low complexity region	868	887	N/A	INTRINSIC
low complexity region	898	919	N/A	INTRINSIC
low complexity region	924	943	N/A	INTRINSIC
low complexity region	992	1002	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000044682

SMART Domains

Protein: ENSMUSP00000041571
Gene: ENSMUSG00000034579

Domain	Start	End	E-Value	Type
signal peptide	1	19	N/A	INTRINSIC
PA2c	139	259	1.58e-2	SMART
low complexity region	305	324	N/A	INTRINSIC
Pfam:Phospholip_A2_2	343	431	4e-9	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000110018

SMART Domains

Protein: ENSMUSP00000105645
Gene: ENSMUSG00000034570

Domain	Start	End	E-Value	Type
IPPc	2	301	4e-86	SMART
low complexity region	408	430	N/A	INTRINSIC
low complexity region	436	455	N/A	INTRINSIC
low complexity region	466	487	N/A	INTRINSIC
low complexity region	492	511	N/A	INTRINSIC
low complexity region	560	570	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000110019

SMART Domains

Protein: ENSMUSP00000105646
Gene: ENSMUSG00000034570

Domain	Start	End	E-Value	Type
IPPc	2	301	4e-86	SMART
low complexity region	408	430	N/A	INTRINSIC
low complexity region	436	455	N/A	INTRINSIC
low complexity region	466	487	N/A	INTRINSIC
low complexity region	492	511	N/A	INTRINSIC
low complexity region	560	570	N/A	INTRINSIC

Predicted Effect

unknown
Transcript: ENSMUST00000148939
AA Change: F243L

Predicted Effect

probably benign
Transcript: ENSMUST00000154756
AA Change: F615L

PolyPhen 2 Score 0.062 (Sensitivity: 0.94; Specificity: 0.84)

SMART Domains

Protein: ENSMUSP00000139302
Gene: ENSMUSG00000034570
AA Change: F615L

Domain	Start	End	E-Value	Type
low complexity region	11	24	N/A	INTRINSIC
low complexity region	115	131	N/A	INTRINSIC
low complexity region	144	155	N/A	INTRINSIC
low complexity region	180	216	N/A	INTRINSIC
low complexity region	292	311	N/A	INTRINSIC
low complexity region	333	365	N/A	INTRINSIC
low complexity region	390	413	N/A	INTRINSIC
IPPc	418	733	4.41e-98	SMART
low complexity region	870	880	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000183684

Meta Mutation Damage Score

0.0662

Coding Region Coverage

1x: 99.2%
3x: 98.5%
10x: 96.8%
20x: 93.0%

Validation Efficiency

100% (79/79)

MGI Phenotype

PHENOTYPE: Mice homozygous for a null allele are viable, fertile, and show normal mammary gland development and no spontaneous mammary tumors. However, in an oncogene-driven breast cancer mouse model, mice show increased mammary hyperplasia and tumor growth paradoxically associated with reduced lung metastases. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 79 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Adnp2	G	T	18: 80,174,036 (GRCm39)	F124L	probably benign	Het
Aicda	A	G	6: 122,536,449 (GRCm39)	K10E	probably benign	Het
Als2	A	G	1: 59,226,575 (GRCm39)	C910R	probably benign	Het
Ankrd11	T	A	8: 123,619,156 (GRCm39)	K1565N	probably damaging	Het
Apol7b	T	C	15: 77,308,909 (GRCm39)	D63G	probably damaging	Het
Arhgef4	T	C	1: 34,764,187 (GRCm39)	C1148R	possibly damaging	Het
Atg16l1	A	G	1: 87,694,629 (GRCm39)	D102G	probably damaging	Het
Babam2	T	C	5: 32,158,782 (GRCm39)	V244A	probably damaging	Het
Brd10	T	G	19: 29,720,990 (GRCm39)	K622N	probably damaging	Het
Cars1	G	A	7: 143,113,411 (GRCm39)	A668V	possibly damaging	Het
Ccdc168	T	C	1: 44,100,129 (GRCm39)	D323G	possibly damaging	Het
Ccdc185	T	A	1: 182,576,453 (GRCm39)	S79C	possibly damaging	Het
Ccdc88b	G	C	19: 6,826,359 (GRCm39)	R1119G	probably damaging	Het
Cebpz	A	T	17: 79,231,896 (GRCm39)	V810E	probably damaging	Het
Cep120	T	C	18: 53,871,654 (GRCm39)	T73A	probably damaging	Het
Chat	C	A	14: 32,145,269 (GRCm39)	C380F	possibly damaging	Het
Cltc	T	C	11: 86,648,087 (GRCm39)	Q10R	probably benign	Het
Cripto	C	T	9: 110,769,781 (GRCm39)	M169I	probably benign	Het
Cst8	T	C	2: 148,646,622 (GRCm39)		probably benign	Het
Cts3	C	T	13: 61,715,868 (GRCm39)		probably null	Het
Cyp4a29	T	A	4: 115,105,707 (GRCm39)	D136E	probably benign	Het
Dmxl2	A	C	9: 54,286,297 (GRCm39)		probably null	Het
Dsg4	T	A	18: 20,584,919 (GRCm39)	V211E	possibly damaging	Het
Efcab5	C	T	11: 77,008,656 (GRCm39)	V957I	probably damaging	Het
Eif4g2	A	T	7: 110,673,358 (GRCm39)	L807Q	possibly damaging	Het
Epha4	A	G	1: 77,366,731 (GRCm39)		probably benign	Het
Epm2aip1	A	T	9: 111,101,458 (GRCm39)	I144F	probably benign	Het
Erbb4	C	T	1: 68,599,735 (GRCm39)	R114H	probably damaging	Het
Fabp3	C	T	4: 130,206,180 (GRCm39)	T57I	probably benign	Het
Fam170a	C	T	18: 50,415,038 (GRCm39)	A228V	probably damaging	Het
Foxred1	A	T	9: 35,117,571 (GRCm39)	M254K	possibly damaging	Het
Gm1527	T	A	3: 28,952,969 (GRCm39)	C90S	probably benign	Het
Gpr137b	T	C	13: 13,533,947 (GRCm39)	T370A	probably benign	Het
Gtf2e2	A	G	8: 34,245,993 (GRCm39)		probably benign	Het
Hgsnat	A	T	8: 26,445,817 (GRCm39)	L359*	probably null	Het
Hhip	A	T	8: 80,719,223 (GRCm39)	C435S	probably damaging	Het
Hoxa13	T	C	6: 52,236,107 (GRCm39)	D310G	possibly damaging	Het
Hspa14	T	C	2: 3,513,675 (GRCm39)	Y18C	probably damaging	Het
Ighg1	A	G	12: 113,293,270 (GRCm39)	V140A	probably damaging	Het
Ighv1-58	A	T	12: 115,275,930 (GRCm39)	Y69*	probably null	Het
Kcna1	T	A	6: 126,619,873 (GRCm39)	Y149F	probably benign	Het
Kcnj6	A	T	16: 94,625,877 (GRCm39)		probably null	Het
Krtap4-1	G	T	11: 99,518,637 (GRCm39)	C124*	probably null	Het
Lama1	T	A	17: 68,119,368 (GRCm39)	L2615*	probably null	Het
Lcp2	A	T	11: 34,018,439 (GRCm39)	I72F	probably damaging	Het
Med1	T	A	11: 98,062,532 (GRCm39)	I189F	possibly damaging	Het
Meioc	C	T	11: 102,566,654 (GRCm39)	R757C	probably damaging	Het
Mtr	T	A	13: 12,204,283 (GRCm39)	H1171L	probably damaging	Het
Mtr	G	C	13: 12,204,284 (GRCm39)	H1171D	probably damaging	Het
Naa12	A	G	18: 80,255,339 (GRCm39)	D211G	probably benign	Het
Nlrc5	A	G	8: 95,202,620 (GRCm39)	Y240C	possibly damaging	Het
Nsun4	T	A	4: 115,908,259 (GRCm39)	H767L	possibly damaging	Het
Pcdha1	T	A	18: 37,064,189 (GRCm39)	N284K	probably benign	Het
Pcdhgb8	A	C	18: 37,896,414 (GRCm39)	S495R	probably benign	Het
Pramel1	T	A	4: 143,123,260 (GRCm39)	I79N	possibly damaging	Het
Prdm6	A	T	18: 53,673,390 (GRCm39)	E183D	possibly damaging	Het
Prex2	T	C	1: 11,254,740 (GRCm39)	F1125L	probably benign	Het
Prkg2	T	C	5: 99,127,674 (GRCm39)	I346V	possibly damaging	Het
Ptprz1	A	G	6: 23,002,584 (GRCm39)	D1558G	probably damaging	Het
Pttg1ip2	A	C	5: 5,528,955 (GRCm39)	L20R	probably damaging	Het
Qng1	T	A	13: 58,529,800 (GRCm39)	K271*	probably null	Het
Rab11fip3	GCTCGTCT	GCT	17: 26,287,002 (GRCm39)		probably null	Het
Rin2	C	T	2: 145,702,366 (GRCm39)	T354I	probably benign	Het
S100a6	A	G	3: 90,521,508 (GRCm39)	D50G	probably damaging	Het
Shroom3	T	A	5: 93,096,342 (GRCm39)		probably benign	Het
Sipa1l1	G	A	12: 82,388,556 (GRCm39)	V261M	possibly damaging	Het
Slc5a4b	T	A	10: 75,910,826 (GRCm39)	I337F	probably damaging	Het
Smarcc1	A	G	9: 109,961,273 (GRCm39)	Y30C	possibly damaging	Het
Swap70	A	G	7: 109,880,512 (GRCm39)	K576E	possibly damaging	Het
Syt6	A	G	3: 103,532,809 (GRCm39)		probably benign	Het
Szt2	T	C	4: 118,241,097 (GRCm39)	I1726V	probably benign	Het
Thoc1	A	G	18: 9,987,651 (GRCm39)	K453E	possibly damaging	Het
Tmem38b	A	G	4: 53,854,409 (GRCm39)	I214V	probably benign	Het
Tonsl	A	T	15: 76,521,244 (GRCm39)	I354N	probably damaging	Het
Trappc9	T	C	15: 72,903,472 (GRCm39)	I303V	possibly damaging	Het
Trim66	A	G	7: 109,057,338 (GRCm39)	S1032P	probably damaging	Het
Tsc22d4	T	C	5: 137,756,590 (GRCm39)	V6A	probably benign	Het
Ubtd2	A	G	11: 32,449,260 (GRCm39)	K36E	probably benign	Het
Zkscan2	T	C	7: 123,097,883 (GRCm39)	E171G	possibly damaging	Het

Other mutations in Inpp5j

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00231:Inpp5j	APN	11	3,450,009 (GRCm39)	splice site	probably benign
IGL00435:Inpp5j	APN	11	3,452,255 (GRCm39)	missense	probably benign	0.00
IGL00509:Inpp5j	APN	11	3,451,595 (GRCm39)	missense	possibly damaging	0.94
IGL00916:Inpp5j	APN	11	3,452,389 (GRCm39)	missense	probably damaging	1.00
IGL00975:Inpp5j	APN	11	3,452,176 (GRCm39)	missense	probably damaging	1.00
IGL01523:Inpp5j	APN	11	3,445,932 (GRCm39)	splice site	probably null
IGL02472:Inpp5j	APN	11	3,445,338 (GRCm39)	unclassified	probably benign
IGL02512:Inpp5j	APN	11	3,449,661 (GRCm39)	missense	probably damaging	1.00
IGL02897:Inpp5j	APN	11	3,450,619 (GRCm39)	missense	probably damaging	1.00
IGL03408:Inpp5j	APN	11	3,452,809 (GRCm39)	missense	possibly damaging	0.95
R0048:Inpp5j	UTSW	11	3,451,417 (GRCm39)	missense	probably damaging	0.97
R0440:Inpp5j	UTSW	11	3,451,150 (GRCm39)	missense	possibly damaging	0.95
R0455:Inpp5j	UTSW	11	3,453,122 (GRCm39)	missense	possibly damaging	0.66
R0483:Inpp5j	UTSW	11	3,449,738 (GRCm39)	missense	probably damaging	1.00
R0554:Inpp5j	UTSW	11	3,449,644 (GRCm39)	missense	probably damaging	1.00
R0639:Inpp5j	UTSW	11	3,451,147 (GRCm39)	missense	probably benign	0.29
R0673:Inpp5j	UTSW	11	3,451,147 (GRCm39)	missense	probably benign	0.29
R0926:Inpp5j	UTSW	11	3,451,439 (GRCm39)	splice site	probably benign
R1114:Inpp5j	UTSW	11	3,444,814 (GRCm39)	missense	possibly damaging	0.57
R1132:Inpp5j	UTSW	11	3,452,305 (GRCm39)	missense	possibly damaging	0.90
R1463:Inpp5j	UTSW	11	3,451,147 (GRCm39)	missense	probably benign	0.03
R1757:Inpp5j	UTSW	11	3,454,738 (GRCm39)	missense	possibly damaging	0.49
R1978:Inpp5j	UTSW	11	3,452,150 (GRCm39)	missense	probably damaging	1.00
R3078:Inpp5j	UTSW	11	3,453,124 (GRCm39)	splice site	probably null
R3831:Inpp5j	UTSW	11	3,450,229 (GRCm39)	missense	probably damaging	1.00
R4183:Inpp5j	UTSW	11	3,451,134 (GRCm39)	missense	probably damaging	0.99
R4209:Inpp5j	UTSW	11	3,451,107 (GRCm39)	missense	probably damaging	1.00
R4210:Inpp5j	UTSW	11	3,451,107 (GRCm39)	missense	probably damaging	1.00
R4211:Inpp5j	UTSW	11	3,451,107 (GRCm39)	missense	probably damaging	1.00
R4477:Inpp5j	UTSW	11	3,451,625 (GRCm39)	missense	probably damaging	1.00
R4729:Inpp5j	UTSW	11	3,445,025 (GRCm39)	missense	probably damaging	0.99
R4840:Inpp5j	UTSW	11	3,449,676 (GRCm39)	missense	probably damaging	1.00
R5025:Inpp5j	UTSW	11	3,450,664 (GRCm39)	missense	probably damaging	1.00
R5151:Inpp5j	UTSW	11	3,452,270 (GRCm39)	missense	probably damaging	1.00
R5195:Inpp5j	UTSW	11	3,449,889 (GRCm39)	critical splice donor site	probably null
R5623:Inpp5j	UTSW	11	3,444,766 (GRCm39)	missense	probably damaging	0.96
R6262:Inpp5j	UTSW	11	3,452,615 (GRCm39)	missense	probably benign	0.02
R6448:Inpp5j	UTSW	11	3,445,387 (GRCm39)	missense	probably damaging	0.99
R6465:Inpp5j	UTSW	11	3,452,293 (GRCm39)	missense	possibly damaging	0.84
R6723:Inpp5j	UTSW	11	3,450,640 (GRCm39)	missense	probably damaging	0.99
R6895:Inpp5j	UTSW	11	3,445,557 (GRCm39)	splice site	probably null
R7060:Inpp5j	UTSW	11	3,450,133 (GRCm39)	splice site	probably null
R7346:Inpp5j	UTSW	11	3,451,065 (GRCm39)	missense	probably damaging	1.00
R8026:Inpp5j	UTSW	11	3,445,171 (GRCm39)	missense
R8360:Inpp5j	UTSW	11	3,449,767 (GRCm39)	missense	probably damaging	0.99
R9706:Inpp5j	UTSW	11	3,449,960 (GRCm39)	missense	possibly damaging	0.95
T0975:Inpp5j	UTSW	11	3,452,527 (GRCm39)	missense	possibly damaging	0.69
Z1176:Inpp5j	UTSW	11	3,452,484 (GRCm39)	nonsense	probably null
Z1177:Inpp5j	UTSW	11	3,452,191 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- AAAGTTAAGGGGCCCTTCCTG -3'
(R):5'- CACCCATTGGCACTTCTAAAGG -3'

Sequencing Primer
(F):5'- CCTTTCAAGATGGGCCAAGTG -3'
(R):5'- CCATTGGCACTTCTAAAGGGTTGG -3'

Posted On

2015-04-29