Mutagenetix > Incidental Mutation

Incidental Mutation 'R7767:Inppl1'

598300

Institutional Source

Beutler Lab

Gene Symbol

Inppl1

Ensembl Gene

ENSMUSG00000032737

Gene Name

inositol polyphosphate phosphatase-like 1

Synonyms

SHIP2

MMRRC Submission

045823-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.842) question?

Stock #

R7767 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

101471839-101487419 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 101473545 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Valine to Alanine at position 1035 (V1035A)

Ref Sequence

ENSEMBL: ENSMUSP00000048057 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000008090] [ENSMUST00000035836] [ENSMUST00000165052] [ENSMUST00000185929]

AlphaFold

Q6P549

Predicted Effect

probably benign
Transcript: ENSMUST00000008090

SMART Domains

Protein: ENSMUSP00000008090
Gene: ENSMUSG00000007946

Domain	Start	End	E-Value	Type
low complexity region	40	51	N/A	INTRINSIC
HOX	90	152	5.75e-27	SMART
low complexity region	183	223	N/A	INTRINSIC
low complexity region	225	244	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000035836
AA Change: V1035A

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000048057
Gene: ENSMUSG00000032737
AA Change: V1035A

Domain	Start	End	E-Value	Type
SH2	19	108	1.21e-26	SMART
low complexity region	116	137	N/A	INTRINSIC
low complexity region	156	175	N/A	INTRINSIC
Blast:IPPc	250	349	5e-14	BLAST
IPPc	423	736	3.98e-137	SMART
low complexity region	934	957	N/A	INTRINSIC
low complexity region	997	1013	N/A	INTRINSIC
low complexity region	1036	1047	N/A	INTRINSIC
low complexity region	1049	1068	N/A	INTRINSIC
low complexity region	1089	1102	N/A	INTRINSIC
SAM	1192	1257	2.47e-8	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000165052
AA Change: V1035A

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000132883
Gene: ENSMUSG00000032737
AA Change: V1035A

Domain	Start	End	E-Value	Type
SH2	19	108	1.21e-26	SMART
low complexity region	116	137	N/A	INTRINSIC
low complexity region	156	175	N/A	INTRINSIC
Blast:IPPc	250	349	5e-14	BLAST
IPPc	423	736	3.98e-137	SMART
low complexity region	934	957	N/A	INTRINSIC
low complexity region	997	1013	N/A	INTRINSIC
low complexity region	1036	1047	N/A	INTRINSIC
low complexity region	1049	1068	N/A	INTRINSIC
low complexity region	1089	1102	N/A	INTRINSIC
SAM	1192	1257	2.47e-8	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000185929
AA Change: V1035A

PolyPhen 2 Score 0.026 (Sensitivity: 0.95; Specificity: 0.81)

SMART Domains

Protein: ENSMUSP00000139910
Gene: ENSMUSG00000032737
AA Change: V1035A

Domain	Start	End	E-Value	Type
SH2	19	108	7.6e-29	SMART
low complexity region	116	137	N/A	INTRINSIC
low complexity region	156	175	N/A	INTRINSIC
Blast:IPPc	250	349	4e-14	BLAST
IPPc	423	736	1.9e-139	SMART
low complexity region	934	957	N/A	INTRINSIC
low complexity region	997	1013	N/A	INTRINSIC
low complexity region	1036	1047	N/A	INTRINSIC
low complexity region	1049	1068	N/A	INTRINSIC
low complexity region	1089	1102	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000210116

Coding Region Coverage

1x: 100.0%
3x: 100.0%
10x: 99.8%
20x: 99.3%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is an SH2-containing 5'-inositol phosphatase that is involved in the regulation of insulin function. The encoded protein also plays a role in the regulation of epidermal growth factor receptor turnover and actin remodelling. Additionally, this gene supports metastatic growth in breast cancer and is a valuable biomarker for breast cancer. [provided by RefSeq, Jan 2009]
PHENOTYPE: Homozygous mice display decreased postnatal growth, decreased circulating levels of leptin, free fatty acids, triglycerides, and total cholesterol, and resistance to diet-induced obesity. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 77 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Aox4	C	A	1: 58,274,366 (GRCm39)	S384Y	probably damaging	Het
Arhgef15	T	C	11: 68,844,673 (GRCm39)	E308G	probably damaging	Het
Asb15	A	G	6: 24,559,281 (GRCm39)	D142G	probably benign	Het
Atg13	A	G	2: 91,509,711 (GRCm39)	S394P	probably damaging	Het
Atp10a	G	C	7: 58,308,597 (GRCm39)	W132S	probably damaging	Het
Bltp1	G	T	3: 36,974,436 (GRCm39)		probably null	Het
Bod1l	T	A	5: 41,974,099 (GRCm39)	N2405I	probably benign	Het
Capsl	C	T	15: 9,462,770 (GRCm39)	R137C	probably damaging	Het
Cd109	T	A	9: 78,617,441 (GRCm39)	M1313K	probably damaging	Het
Chst13	G	A	6: 90,286,566 (GRCm39)	A132V	possibly damaging	Het
Cobl	T	C	11: 12,362,117 (GRCm39)		probably benign	Het
Coq9	A	T	8: 95,577,214 (GRCm39)	E193V	probably benign	Het
Cpd	T	A	11: 76,704,385 (GRCm39)	I410F	probably benign	Het
Cyth3	T	G	5: 143,693,229 (GRCm39)	V351G	probably damaging	Het
Dcdc2c	T	C	12: 28,520,256 (GRCm39)	K607E		Het
Dcp1a	T	C	14: 30,201,775 (GRCm39)		probably null	Het
Dennd3	A	G	15: 73,394,079 (GRCm39)	I35V	probably benign	Het
Dlgap4	C	T	2: 156,587,973 (GRCm39)	R606W	probably damaging	Het
Dnhd1	A	G	7: 105,343,817 (GRCm39)	I1720M	probably benign	Het
Erbin	A	G	13: 103,995,907 (GRCm39)	L265P	probably damaging	Het
Ern1	T	C	11: 106,291,134 (GRCm39)	D847G	probably damaging	Het
Esyt3	T	G	9: 99,207,024 (GRCm39)	S342R	probably benign	Het
Exoc2	A	T	13: 31,060,752 (GRCm39)	I584K	probably benign	Het
Fam240a	T	C	9: 110,744,090 (GRCm39)	R50G	probably damaging	Het
Glis3	A	T	19: 28,241,360 (GRCm39)	M858K	probably benign	Het
Gls2	C	T	10: 128,030,998 (GRCm39)	R86C	unknown	Het
Gm10972	C	A	3: 94,550,901 (GRCm39)	Y25*	probably null	Het
H2-T10	A	T	17: 36,428,622 (GRCm39)	M350K	probably benign	Het
Has1	A	T	17: 18,070,792 (GRCm39)	V43D	probably damaging	Het
Herc2	T	A	7: 55,878,275 (GRCm39)	S4609R	probably benign	Het
Hmgcs2	A	C	3: 98,198,582 (GRCm39)	T162P	probably damaging	Het
Hspg2	G	T	4: 137,239,177 (GRCm39)	C368F	probably damaging	Het
Ighv11-1	A	G	12: 113,945,722 (GRCm39)	S44P	probably damaging	Het
Kmt2a	C	T	9: 44,730,295 (GRCm39)	V3341I	unknown	Het
Lrp1b	T	C	2: 40,691,517 (GRCm39)	N3434S		Het
Lrriq1	G	C	10: 103,051,815 (GRCm39)	S312R	probably damaging	Het
Map1a	G	A	2: 121,132,517 (GRCm39)	S1111N	probably damaging	Het
Myo15a	T	C	11: 60,392,922 (GRCm39)	V1029A		Het
Nol11	T	C	11: 107,069,908 (GRCm39)	H314R	possibly damaging	Het
Nphs1	A	T	7: 30,162,733 (GRCm39)	D404V	probably damaging	Het
Odr4	A	G	1: 150,247,788 (GRCm39)	V387A	probably benign	Het
Or51r1	A	T	7: 102,220,971 (GRCm39)		probably benign	Het
Pabpc2	T	C	18: 39,907,607 (GRCm39)	Y291H	possibly damaging	Het
Pcdh15	G	A	10: 74,322,088 (GRCm39)	A1020T	probably benign	Het
Pla2g4f	A	C	2: 120,135,490 (GRCm39)	S395A	possibly damaging	Het
Ppp1r18	A	G	17: 36,178,176 (GRCm39)	Q17R	probably damaging	Het
Prokr2	A	T	2: 132,215,996 (GRCm39)	V155D	probably damaging	Het
Pwwp2a	T	G	11: 43,596,696 (GRCm39)	C620W	probably damaging	Het
Rabepk	T	C	2: 34,675,605 (GRCm39)	D175G	probably damaging	Het
Rad54l	T	C	4: 115,956,866 (GRCm39)	Y485C	probably damaging	Het
Rasef	A	G	4: 73,652,771 (GRCm39)	S577P	probably damaging	Het
Rgma	C	A	7: 73,067,752 (GRCm39)	L446I	unknown	Het
Rnf212b	T	C	14: 55,079,825 (GRCm39)	S182P	probably damaging	Het
Rnf6	C	A	5: 146,147,986 (GRCm39)	R344I	probably damaging	Het
Rnf6	T	A	5: 146,147,987 (GRCm39)	R344*	probably null	Het
Sgo1	A	G	17: 53,986,639 (GRCm39)	I184T	possibly damaging	Het
Sgpl1	A	T	10: 60,953,502 (GRCm39)	I78N	possibly damaging	Het
Snx13	T	A	12: 35,157,483 (GRCm39)	Y510N	probably damaging	Het
Sptbn2	G	A	19: 4,784,171 (GRCm39)	E638K	possibly damaging	Het
Sspo	A	G	6: 48,428,316 (GRCm39)	T349A	probably damaging	Het
Sv2c	C	T	13: 96,126,223 (GRCm39)	S343N	probably damaging	Het
Syne1	C	A	10: 5,283,560 (GRCm39)	V1502F	possibly damaging	Het
Syne1	T	A	10: 5,283,632 (GRCm39)	I1478F	possibly damaging	Het
Tmem121	C	T	12: 113,151,992 (GRCm39)	A70V	probably damaging	Het
Tmem215	A	G	4: 40,474,042 (GRCm39)	I40V	possibly damaging	Het
Trim25	A	G	11: 88,899,943 (GRCm39)		probably null	Het
Trio	A	G	15: 27,889,504 (GRCm39)	V534A	unknown	Het
Tyr	T	A	7: 87,142,218 (GRCm39)	E114V	probably benign	Het
Ush2a	A	T	1: 188,285,457 (GRCm39)	T1998S	probably benign	Het
Usp40	G	T	1: 87,909,900 (GRCm39)	A518E	probably benign	Het
Usp48	T	A	4: 137,331,956 (GRCm39)		probably null	Het
Vash1	T	A	12: 86,733,767 (GRCm39)	F152L	probably damaging	Het
Vsig10l	C	A	7: 43,113,141 (GRCm39)	P31Q	probably damaging	Het
Xab2	C	T	8: 3,669,018 (GRCm39)	E43K	probably benign	Het
Zfp423	G	A	8: 88,507,512 (GRCm39)	S944F	probably damaging	Het
Zp2	A	T	7: 119,736,392 (GRCm39)	D350E	probably benign	Het
Zscan4e	T	G	7: 11,041,461 (GRCm39)	Q165P	probably damaging	Het

Other mutations in Inppl1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00899:Inppl1	APN	7	101,478,365 (GRCm39)	missense	probably damaging	1.00
IGL01633:Inppl1	APN	7	101,483,041 (GRCm39)	nonsense	probably null
IGL01678:Inppl1	APN	7	101,481,803 (GRCm39)	missense	probably benign	0.09
IGL02420:Inppl1	APN	7	101,481,526 (GRCm39)	unclassified	probably benign
IGL02423:Inppl1	APN	7	101,481,450 (GRCm39)	missense	probably benign	0.02
IGL02965:Inppl1	APN	7	101,477,478 (GRCm39)	missense	possibly damaging	0.87
IGL03329:Inppl1	APN	7	101,473,587 (GRCm39)	missense	possibly damaging	0.48
ditzel	UTSW	7	101,476,663 (GRCm39)	nonsense	probably null
PIT4362001:Inppl1	UTSW	7	101,475,220 (GRCm39)	missense	probably benign	0.34
R0310:Inppl1	UTSW	7	101,477,706 (GRCm39)	splice site	probably benign
R0355:Inppl1	UTSW	7	101,476,664 (GRCm39)	missense	probably damaging	1.00
R0394:Inppl1	UTSW	7	101,477,402 (GRCm39)	splice site	probably benign
R0547:Inppl1	UTSW	7	101,480,210 (GRCm39)	missense	probably benign	0.02
R0578:Inppl1	UTSW	7	101,480,795 (GRCm39)	missense	probably damaging	1.00
R1506:Inppl1	UTSW	7	101,473,174 (GRCm39)	missense	probably benign	0.01
R1526:Inppl1	UTSW	7	101,482,153 (GRCm39)	missense	probably benign	0.02
R1901:Inppl1	UTSW	7	101,472,584 (GRCm39)	missense	possibly damaging	0.85
R2381:Inppl1	UTSW	7	101,478,439 (GRCm39)	missense	probably damaging	1.00
R3690:Inppl1	UTSW	7	101,481,275 (GRCm39)	missense	probably damaging	0.99
R4911:Inppl1	UTSW	7	101,481,516 (GRCm39)	missense	possibly damaging	0.94
R5637:Inppl1	UTSW	7	101,478,055 (GRCm39)	missense	probably benign	0.08
R6227:Inppl1	UTSW	7	101,473,506 (GRCm39)	missense	possibly damaging	0.88
R6409:Inppl1	UTSW	7	101,478,168 (GRCm39)	missense	probably damaging	1.00
R6678:Inppl1	UTSW	7	101,481,477 (GRCm39)	missense	probably damaging	0.99
R6752:Inppl1	UTSW	7	101,481,749 (GRCm39)	nonsense	probably null
R7095:Inppl1	UTSW	7	101,476,663 (GRCm39)	nonsense	probably null
R7196:Inppl1	UTSW	7	101,477,993 (GRCm39)	missense	probably benign	0.05
R7421:Inppl1	UTSW	7	101,482,144 (GRCm39)	missense	probably damaging	0.99
R7575:Inppl1	UTSW	7	101,477,689 (GRCm39)	missense	probably damaging	1.00
R7664:Inppl1	UTSW	7	101,479,304 (GRCm39)	missense	probably damaging	0.97
R8131:Inppl1	UTSW	7	101,479,268 (GRCm39)	missense	possibly damaging	0.50
R8206:Inppl1	UTSW	7	101,472,783 (GRCm39)	missense	possibly damaging	0.52
R8492:Inppl1	UTSW	7	101,475,985 (GRCm39)	missense	probably damaging	1.00
R8559:Inppl1	UTSW	7	101,478,834 (GRCm39)	nonsense	probably null
R8707:Inppl1	UTSW	7	101,478,903 (GRCm39)	missense
R8876:Inppl1	UTSW	7	101,472,750 (GRCm39)	missense	possibly damaging	0.71
R8921:Inppl1	UTSW	7	101,472,593 (GRCm39)	missense	possibly damaging	0.92
R9021:Inppl1	UTSW	7	101,480,915 (GRCm39)	missense	probably damaging	0.96
R9113:Inppl1	UTSW	7	101,475,231 (GRCm39)	missense	probably benign	0.05

Predicted Primers

PCR Primer
(F):5'- TTGCAGTACCGAACAAGACC -3'
(R):5'- TCCAGGCTGAAGTCAGAAGG -3'

Sequencing Primer
(F):5'- AGACCGGTCATCCCCACTTG -3'
(R):5'- CTGAAGTCAGAAGGGACATCTG -3'

Posted On

2019-11-26