Mutagenetix > Incidental Mutation

Incidental Mutation 'R2145:Fnip2'

233709

Institutional Source

Beutler Lab

Gene Symbol

Fnip2

Ensembl Gene

ENSMUSG00000061175

Gene Name

folliculin interacting protein 2

Synonyms

D630023B12Rik

MMRRC Submission

040148-MU

Accession Numbers

Essential gene?

Non essential (E-score: 0.000) question?

Stock #

R2145 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

79363281-79475103 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 79407739 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Serine to Threonine at position 281 (S281T)

Ref Sequence

ENSEMBL: ENSMUSP00000115275 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000076136] [ENSMUST00000133154]

AlphaFold

Q80TD3

Predicted Effect

probably damaging
Transcript: ENSMUST00000076136
AA Change: S251T

PolyPhen 2 Score 0.977 (Sensitivity: 0.76; Specificity: 0.96)

SMART Domains

Protein: ENSMUSP00000075497
Gene: ENSMUSG00000061175
AA Change: S251T

Domain	Start	End	E-Value	Type
Pfam:FNIP_N	42	168	4.3e-39	PFAM
low complexity region	240	261	N/A	INTRINSIC
Pfam:FNIP_M	289	528	5.9e-92	PFAM
low complexity region	557	571	N/A	INTRINSIC
low complexity region	748	755	N/A	INTRINSIC
Pfam:FNIP_C	920	1104	4.1e-73	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000130613

Predicted Effect

probably damaging
Transcript: ENSMUST00000133154
AA Change: S281T

PolyPhen 2 Score 0.993 (Sensitivity: 0.70; Specificity: 0.97)

SMART Domains

Protein: ENSMUSP00000115275
Gene: ENSMUSG00000061175
AA Change: S281T

Domain	Start	End	E-Value	Type
Pfam:FNIP_N	42	164	5.2e-34	PFAM
low complexity region	270	291	N/A	INTRINSIC
Pfam:FNIP_M	323	557	3.9e-93	PFAM
low complexity region	587	601	N/A	INTRINSIC
low complexity region	778	785	N/A	INTRINSIC
Pfam:FNIP_C	951	1134	2.3e-74	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000154645

Meta Mutation Damage Score

0.0960

Coding Region Coverage

1x: 99.2%
3x: 98.7%
10x: 97.5%
20x: 95.6%

Validation Efficiency

97% (101/104)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a member of the folliculin-interacting protein family. The encoded protein binds to the tumor suppressor folliculin and to AMP-activated protein kinase (AMPK) and be involved in regulating the O6-methylguanine-induced apoptosis signaling pathway. This protein may also play a role cellular metabolism and nutrient sensing by regulating the AMPK-mechanistic target of rapamycin signaling pathway. A homologous binding partner of this protein, folliculin-interacting protein 1, has similar binding activities and may suggest functional redundancy within this protein family. Both folliculin-interacting proteins have also been shown to bind the molecular chaperone heat shock protein-90 (Hsp90) and they may function as a co-chaperones in the stabilization of tumor suppressor folliculin which is a target of Hsp90 chaperone activity. [provided by RefSeq, Sep 2016]
PHENOTYPE: Mice homozygous for a null allele have normal lifespans. Mice with combined loss of this gene and a single null allele of Fnip1 develop kidney cancer. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 104 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Abca15	A	G	7: 119,953,701 (GRCm39)	N535S	probably benign	Het
Abcc6	A	T	7: 45,648,165 (GRCm39)	L717Q	probably benign	Het
Abraxas2	C	A	7: 132,484,790 (GRCm39)	Q278K	probably benign	Het
Acap2	A	T	16: 30,924,342 (GRCm39)	D637E	probably benign	Het
AI661453	A	G	17: 47,777,023 (GRCm39)		probably benign	Het
Aoah	A	T	13: 21,024,266 (GRCm39)	E74V	probably damaging	Het
Aoc1l1	A	T	6: 48,953,629 (GRCm39)	D518V	probably damaging	Het
Appl1	A	G	14: 26,671,576 (GRCm39)	L292S	possibly damaging	Het
Astl	T	A	2: 127,189,109 (GRCm39)	V166E	probably damaging	Het
Bbs1	T	G	19: 4,953,735 (GRCm39)	K143Q	possibly damaging	Het
Bbx	T	C	16: 50,094,907 (GRCm39)		probably benign	Het
Birc6	A	T	17: 74,967,408 (GRCm39)	Q4103L	possibly damaging	Het
C1qtnf2	T	G	11: 43,381,811 (GRCm39)	F178V	probably damaging	Het
Camta2	A	G	11: 70,562,401 (GRCm39)	F999L	probably benign	Het
Cfap68	T	C	9: 50,676,174 (GRCm39)	Y32C	probably damaging	Het
Clcn7	A	G	17: 25,363,425 (GRCm39)	I34V	probably benign	Het
Cntn5	G	T	9: 9,748,420 (GRCm39)	P487Q	probably damaging	Het
Ctu2	T	A	8: 123,205,891 (GRCm39)	I213K	probably benign	Het
Des	C	A	1: 75,340,108 (GRCm39)		probably benign	Het
Dgcr8	A	T	16: 18,098,094 (GRCm39)	D432E	probably benign	Het
Dlgap5	G	A	14: 47,633,380 (GRCm39)	R549*	probably null	Het
Dmac2l	A	G	12: 69,787,828 (GRCm39)	Q88R	probably damaging	Het
Dmxl2	T	C	9: 54,323,194 (GRCm39)	T1397A	probably damaging	Het
Dnmt1	T	A	9: 20,848,451 (GRCm39)		probably benign	Het
Dstyk	T	A	1: 132,391,113 (GRCm39)	M838K	probably damaging	Het
Dtwd1	C	A	2: 126,001,904 (GRCm39)	T208N	probably damaging	Het
Dvl1	G	A	4: 155,932,273 (GRCm39)	V28I	possibly damaging	Het
Dync1i2	T	A	2: 71,044,907 (GRCm39)		probably benign	Het
Fer1l6	T	A	15: 58,499,383 (GRCm39)	M1251K	probably benign	Het
Fmod	T	C	1: 133,968,256 (GRCm39)	Y99H	probably benign	Het
Fn1	A	T	1: 71,645,163 (GRCm39)	V1552D	probably damaging	Het
Glb1	A	G	9: 114,293,233 (GRCm39)	H536R	probably benign	Het
Glis2	T	A	16: 4,431,506 (GRCm39)	S344R	possibly damaging	Het
Gm4847	A	T	1: 166,462,472 (GRCm39)	S339R	probably benign	Het
Gpr155	A	G	2: 73,187,002 (GRCm39)	S44P	probably benign	Het
Gprin1	G	A	13: 54,886,445 (GRCm39)	P610S	probably damaging	Het
Gvin3	T	A	7: 106,202,215 (GRCm39)	H343L	possibly damaging	Het
H2-Ob	A	T	17: 34,461,554 (GRCm39)	M98L	probably benign	Het
H3c6	T	C	13: 23,746,530 (GRCm39)	T4A	probably benign	Het
Hmcn2	T	C	2: 31,223,943 (GRCm39)		probably benign	Het
Ikbke	C	A	1: 131,201,211 (GRCm39)	V176L	probably damaging	Het
Il13	T	C	11: 53,523,351 (GRCm39)	T85A	possibly damaging	Het
Inpp5k	A	T	11: 75,538,017 (GRCm39)		probably null	Het
Irgm2	T	C	11: 58,111,355 (GRCm39)	S361P	possibly damaging	Het
Itga11	C	T	9: 62,639,486 (GRCm39)		probably benign	Het
Kalrn	G	T	16: 33,829,632 (GRCm39)		probably benign	Het
Kcng1	C	A	2: 168,110,952 (GRCm39)	G71C	probably damaging	Het
Kcnq5	T	A	1: 21,575,573 (GRCm39)	D291V	probably damaging	Het
Klhl7	A	T	5: 24,305,861 (GRCm39)	M37L	probably benign	Het
Letm1	A	AG	5: 33,926,859 (GRCm39)		probably null	Het
Lhx6	C	T	2: 35,977,478 (GRCm39)	V325I	probably benign	Het
Lipc	A	G	9: 70,841,817 (GRCm39)	I9T	possibly damaging	Het
Lsmem1	GTACATACATACATACATACATACATACA	GTACATACATACATACATACATACATACATACA	12: 40,235,260 (GRCm39)		probably null	Het
Mast1	C	A	8: 85,648,107 (GRCm39)	G458V	probably damaging	Het
Mga	T	C	2: 119,794,638 (GRCm39)	V2565A	possibly damaging	Het
Mpzl2	C	G	9: 44,955,471 (GRCm39)	D127E	probably benign	Het
Mrtfb	T	C	16: 13,230,450 (GRCm39)	I1045T	probably damaging	Het
Myh3	T	A	11: 66,981,882 (GRCm39)	C793S	probably benign	Het
Nomo1	T	C	7: 45,715,928 (GRCm39)	L765P	probably damaging	Het
Nup210	A	G	6: 91,005,858 (GRCm39)	I1335T	possibly damaging	Het
Or52b3	T	C	7: 102,204,267 (GRCm39)		probably null	Het
Oxr1	T	A	15: 41,683,340 (GRCm39)	S254R	probably damaging	Het
Pan3	A	G	5: 147,466,908 (GRCm39)	I592V	possibly damaging	Het
Pask	C	T	1: 93,249,019 (GRCm39)	A794T	probably benign	Het
Pex2	T	C	3: 5,626,650 (GRCm39)	E53G	probably damaging	Het
Pfkfb2	T	C	1: 130,626,460 (GRCm39)	T438A	probably benign	Het
Phactr4	T	C	4: 132,098,095 (GRCm39)	E391G	probably damaging	Het
Pira2	A	T	7: 3,847,344 (GRCm39)	L115Q	probably damaging	Het
Pkhd1l1	A	T	15: 44,376,273 (GRCm39)		probably null	Het
Pnlip	A	G	19: 58,664,876 (GRCm39)	S235G	probably benign	Het
Prkd1	A	G	12: 50,536,694 (GRCm39)	V130A	possibly damaging	Het
Ptpn13	A	G	5: 103,703,999 (GRCm39)	T1344A	probably benign	Het
Ptprc	T	C	1: 138,001,419 (GRCm39)	Y780C	probably damaging	Het
Pxn	T	A	5: 115,690,815 (GRCm39)		probably benign	Het
Rap1gap2	G	A	11: 74,316,802 (GRCm39)	T245M	probably damaging	Het
Rc3h1	G	T	1: 160,757,827 (GRCm39)	K48N	probably damaging	Het
Rfwd3	T	C	8: 112,009,245 (GRCm39)	I444V	probably benign	Het
Rictor	C	T	15: 6,794,588 (GRCm39)	R293C	probably damaging	Het
Rif1	T	A	2: 52,001,412 (GRCm39)	I1622N	possibly damaging	Het
Rnf213	T	C	11: 119,306,019 (GRCm39)	V609A	probably benign	Het
Scgb1b2	G	T	7: 30,991,188 (GRCm39)		probably benign	Het
Serac1	A	T	17: 6,101,060 (GRCm39)	I448N	probably damaging	Het
Sh3kbp1	C	A	X: 158,607,492 (GRCm39)	T200K	probably benign	Het
Sned1	T	A	1: 93,199,406 (GRCm39)	F495L	probably damaging	Het
Socs7	T	C	11: 97,263,950 (GRCm39)	F281L	probably benign	Het
Spta1	C	T	1: 174,040,180 (GRCm39)	L1214F	probably benign	Het
Ssu72	A	G	4: 155,789,900 (GRCm39)	E21G	probably damaging	Het
Syngr4	A	G	7: 45,536,464 (GRCm39)	V186A	probably benign	Het
Tars3	G	A	7: 65,305,539 (GRCm39)	M254I	possibly damaging	Het
Tmem130	C	A	5: 144,680,595 (GRCm39)	V270L	probably benign	Het
Trim66	A	T	7: 109,074,320 (GRCm39)	I647N	probably damaging	Het
Tspyl2	A	T	X: 151,121,890 (GRCm39)	D572E	probably benign	Het
Unc45b	G	A	11: 82,808,580 (GRCm39)	R222H	probably benign	Het
Uxs1	T	C	1: 43,866,783 (GRCm39)	Y29C	probably damaging	Het
Virma	T	A	4: 11,548,726 (GRCm39)		probably benign	Het
Vmn1r202	C	T	13: 22,685,953 (GRCm39)	G155S	possibly damaging	Het
Vmn2r24	T	A	6: 123,755,972 (GRCm39)	F15I	probably benign	Het
Wdr64	A	G	1: 175,594,661 (GRCm39)	T471A	probably benign	Het
Zfa-ps	T	A	10: 52,419,373 (GRCm39)		noncoding transcript	Het
Zfp260	A	G	7: 29,804,765 (GRCm39)	K222E	probably damaging	Het
Zfp300	A	G	X: 20,948,190 (GRCm39)	S525P	possibly damaging	Het
Zfp821	A	G	8: 110,450,979 (GRCm39)	D324G	probably damaging	Het
Zfp934	T	C	13: 62,665,648 (GRCm39)	D331G	probably damaging	Het
Zscan29	T	C	2: 121,000,587 (GRCm39)	R7G	probably damaging	Het

Other mutations in Fnip2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00326:Fnip2	APN	3	79,388,828 (GRCm39)	missense	probably benign
IGL00339:Fnip2	APN	3	79,422,462 (GRCm39)	missense	probably benign	0.12
IGL00340:Fnip2	APN	3	79,425,368 (GRCm39)	splice site	probably benign
IGL00434:Fnip2	APN	3	79,419,796 (GRCm39)	splice site	probably benign
IGL01134:Fnip2	APN	3	79,419,810 (GRCm39)	nonsense	probably null
IGL02732:Fnip2	APN	3	79,373,004 (GRCm39)	missense	probably damaging	1.00
IGL03327:Fnip2	APN	3	79,425,388 (GRCm39)	missense	probably damaging	0.98
IGL03402:Fnip2	APN	3	79,388,583 (GRCm39)	missense	possibly damaging	0.92
R0314:Fnip2	UTSW	3	79,388,496 (GRCm39)	missense	probably damaging	1.00
R0318:Fnip2	UTSW	3	79,419,685 (GRCm39)	missense	probably damaging	1.00
R0699:Fnip2	UTSW	3	79,388,446 (GRCm39)	missense	probably benign	0.00
R1188:Fnip2	UTSW	3	79,369,469 (GRCm39)	missense	probably damaging	1.00
R1290:Fnip2	UTSW	3	79,373,000 (GRCm39)	missense	probably damaging	1.00
R1406:Fnip2	UTSW	3	79,415,398 (GRCm39)	missense	possibly damaging	0.85
R1406:Fnip2	UTSW	3	79,415,398 (GRCm39)	missense	possibly damaging	0.85
R1535:Fnip2	UTSW	3	79,389,072 (GRCm39)	missense	probably damaging	1.00
R1618:Fnip2	UTSW	3	79,415,475 (GRCm39)	missense	possibly damaging	0.70
R1661:Fnip2	UTSW	3	79,422,456 (GRCm39)	missense	probably benign
R1665:Fnip2	UTSW	3	79,422,456 (GRCm39)	missense	probably benign
R1965:Fnip2	UTSW	3	79,400,779 (GRCm39)	missense	probably benign	0.31
R1966:Fnip2	UTSW	3	79,400,779 (GRCm39)	missense	probably benign	0.31
R1976:Fnip2	UTSW	3	79,388,238 (GRCm39)	missense	probably benign	0.02
R2004:Fnip2	UTSW	3	79,419,632 (GRCm39)	splice site	probably benign
R2054:Fnip2	UTSW	3	79,479,772 (GRCm39)	unclassified	probably benign
R2400:Fnip2	UTSW	3	79,386,941 (GRCm39)	missense	probably benign	0.03
R2679:Fnip2	UTSW	3	79,388,233 (GRCm39)	missense	probably benign	0.13
R3157:Fnip2	UTSW	3	79,474,901 (GRCm39)	missense	probably damaging	1.00
R3851:Fnip2	UTSW	3	79,369,464 (GRCm39)	missense	probably damaging	1.00
R3910:Fnip2	UTSW	3	79,386,812 (GRCm39)	missense	possibly damaging	0.83
R3911:Fnip2	UTSW	3	79,386,812 (GRCm39)	missense	possibly damaging	0.83
R3912:Fnip2	UTSW	3	79,386,812 (GRCm39)	missense	possibly damaging	0.83
R4035:Fnip2	UTSW	3	79,386,808 (GRCm39)	missense	probably benign	0.00
R4166:Fnip2	UTSW	3	79,369,442 (GRCm39)	missense	probably damaging	1.00
R4537:Fnip2	UTSW	3	79,373,021 (GRCm39)	missense	probably damaging	0.98
R4732:Fnip2	UTSW	3	79,388,959 (GRCm39)	missense	probably damaging	1.00
R4733:Fnip2	UTSW	3	79,388,959 (GRCm39)	missense	probably damaging	1.00
R4774:Fnip2	UTSW	3	79,373,028 (GRCm39)	nonsense	probably null
R4923:Fnip2	UTSW	3	79,396,701 (GRCm39)	critical splice acceptor site	probably null
R5043:Fnip2	UTSW	3	79,400,174 (GRCm39)	nonsense	probably null
R5160:Fnip2	UTSW	3	79,396,298 (GRCm39)	missense	probably damaging	1.00
R5162:Fnip2	UTSW	3	79,389,084 (GRCm39)	missense	probably damaging	1.00
R5196:Fnip2	UTSW	3	79,479,845 (GRCm39)	unclassified	probably benign
R5283:Fnip2	UTSW	3	79,373,015 (GRCm39)	missense	probably damaging	1.00
R5364:Fnip2	UTSW	3	79,388,475 (GRCm39)	missense	probably benign	0.00
R5402:Fnip2	UTSW	3	79,388,250 (GRCm39)	missense	possibly damaging	0.89
R6340:Fnip2	UTSW	3	79,415,152 (GRCm39)	missense	probably damaging	1.00
R6459:Fnip2	UTSW	3	79,388,941 (GRCm39)	missense	possibly damaging	0.93
R6592:Fnip2	UTSW	3	79,389,015 (GRCm39)	missense	probably benign	0.26
R6616:Fnip2	UTSW	3	79,388,189 (GRCm39)	missense	probably benign	0.00
R6933:Fnip2	UTSW	3	79,425,418 (GRCm39)	missense	probably benign	0.28
R6962:Fnip2	UTSW	3	79,396,610 (GRCm39)	missense	probably damaging	1.00
R6971:Fnip2	UTSW	3	79,388,428 (GRCm39)	nonsense	probably null
R7050:Fnip2	UTSW	3	79,413,577 (GRCm39)	missense	probably damaging	0.99
R7097:Fnip2	UTSW	3	79,388,313 (GRCm39)	missense	probably benign
R7315:Fnip2	UTSW	3	79,413,512 (GRCm39)	critical splice donor site	probably null
R7714:Fnip2	UTSW	3	79,425,421 (GRCm39)	missense	probably damaging	1.00
R7782:Fnip2	UTSW	3	79,415,430 (GRCm39)	missense	probably benign	0.00
R8381:Fnip2	UTSW	3	79,373,000 (GRCm39)	missense	probably damaging	1.00
R8479:Fnip2	UTSW	3	79,419,862 (GRCm39)	missense	probably damaging	1.00
R8485:Fnip2	UTSW	3	79,388,844 (GRCm39)	missense	probably benign	0.35
R9344:Fnip2	UTSW	3	79,407,717 (GRCm39)	missense	possibly damaging	0.87
R9753:Fnip2	UTSW	3	79,415,411 (GRCm39)	missense	probably benign	0.27

Predicted Primers

PCR Primer
(F):5'- GGTCTTCTTTCCCTGACAACAG -3'
(R):5'- CATGAGTTTGTGTCACCTTACG -3'

Sequencing Primer
(F):5'- CTGACAACAGGCAAGGATAAGC -3'
(R):5'- TCTGATTTGGCTAGGAACCCCAG -3'

Posted On

2014-10-01