Mutagenetix > Incidental Mutations

Incidental Mutation 'R0193:Rufy1'

23232

Institutional Source

Beutler Lab

Gene Symbol

Rufy1

Ensembl Gene

ENSMUSG00000020375

Gene Name

RUN and FYVE domain containing 1

Synonyms

ZFYVE12, 3000002E04Rik, Rabip4

MMRRC Submission

038452-MU

Accession Numbers

Is this an essential gene?

Possibly non essential (E-score: 0.424) question?

Stock #

R0193 (G1)

Quality Score

225

Status

Validated (trace)

Chromosome

Chromosomal Location

50389286-50431125 bp(-) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to T at 50389852 bp

Zygosity

Heterozygous

Amino Acid Change

Threonine to Asparagine at position 701 (T701N)

Ref Sequence

ENSEMBL: ENSMUSP00000020643 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000020643] [ENSMUST00000069304] [ENSMUST00000077817] [ENSMUST00000109142]

Predicted Effect

probably benign
Transcript: ENSMUST00000020643
AA Change: T701N

PolyPhen 2 Score 0.122 (Sensitivity: 0.93; Specificity: 0.86)

SMART Domains

Protein: ENSMUSP00000020643
Gene: ENSMUSG00000020375
AA Change: T701N

Domain	Start	End	E-Value	Type
low complexity region	15	32	N/A	INTRINSIC
low complexity region	83	111	N/A	INTRINSIC
RUN	211	273	1.21e-21	SMART
coiled coil region	324	384	N/A	INTRINSIC
coiled coil region	409	621	N/A	INTRINSIC
FYVE	638	705	1.24e-24	SMART

Predicted Effect

probably benign
Transcript: ENSMUST00000069304

SMART Domains

Protein: ENSMUSP00000070503
Gene: ENSMUSG00000007850

Domain	Start	End	E-Value	Type
RRM	12	86	3.77e-10	SMART
RRM	112	184	2.59e-8	SMART
low complexity region	236	254	N/A	INTRINSIC
RRM	290	360	1.45e-11	SMART
low complexity region	383	401	N/A	INTRINSIC
low complexity region	413	433	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000077817

SMART Domains

Protein: ENSMUSP00000076989
Gene: ENSMUSG00000007850

Domain	Start	End	E-Value	Type
RRM	12	86	3.77e-10	SMART
RRM	112	184	2.59e-8	SMART
low complexity region	236	254	N/A	INTRINSIC
RRM	290	360	1.45e-11	SMART
low complexity region	383	401	N/A	INTRINSIC
low complexity region	413	437	N/A	INTRINSIC
low complexity region	451	472	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000109142

SMART Domains

Protein: ENSMUSP00000104770
Gene: ENSMUSG00000007850

Domain	Start	End	E-Value	Type
RRM	12	86	3.77e-10	SMART
RRM	112	184	2.59e-8	SMART
low complexity region	236	254	N/A	INTRINSIC
RRM	290	360	1.45e-11	SMART
low complexity region	383	401	N/A	INTRINSIC
low complexity region	413	433	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000123371

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000126737

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000134230

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000135508

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000140056

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000151537

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000156642

Meta Mutation Damage Score

0.1203

Coding Region Coverage

1x: 98.9%
3x: 98.0%
10x: 94.7%
20x: 85.3%

Validation Efficiency

95% (186/196)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a protein that contains a RUN domain and a FYVE-type zinc finger domain. The encoded protein binds to phosphatidylinositol-3-phosphate (PI3P) and plays a role in early endosomal trafficking, tethering and fusion through interactions with small GTPases including Rab4, Rab5 and Rab14. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]

Allele List at MGI

Other mutations in this stock

Total: 91 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
9330182L06Rik	A	T	5: 9,422,359	Q352L	probably damaging	Het
Adgrb1	T	C	15: 74,572,156	S96P	probably damaging	Het
Akr1c20	A	G	13: 4,511,293		probably benign	Het
Atp2a3	G	T	11: 72,972,220	V99L	possibly damaging	Het
Atp6v0a1	T	A	11: 101,048,482	I691N	possibly damaging	Het
Atp8b1	C	T	18: 64,561,636	R525Q	probably benign	Het
Aurkb	A	G	11: 69,048,544	D151G	probably damaging	Het
Bank1	A	T	3: 136,066,518		probably benign	Het
Bcl9l	T	C	9: 44,507,406	L847P	probably damaging	Het
Bscl2	T	A	19: 8,847,429	M292K	probably benign	Het
Cacna1c	C	T	6: 118,602,402		probably benign	Het
Cadps2	T	C	6: 23,599,440	K260R	probably benign	Het
Cc2d2a	T	C	5: 43,736,118	S1419P	probably damaging	Het
Ccdc180	G	A	4: 45,914,803	E145K	probably benign	Het
Ccdc58	T	C	16: 36,082,814	S59P	probably damaging	Het
Ccno	C	T	13: 112,988,884		probably benign	Het
Cd300a	A	G	11: 114,893,376	D70G	probably benign	Het
Cenpc1	T	C	5: 86,032,403	D670G	probably benign	Het
Cenpl	A	G	1: 161,085,988	I323V	probably damaging	Het
Cfap44	A	G	16: 44,449,210		probably null	Het
Cfap74	C	T	4: 155,426,115	R386C	probably benign	Het
Cic	C	A	7: 25,287,141	S1299Y	probably damaging	Het
Cic	T	A	7: 25,287,140	S1299T	probably damaging	Het
Clcnkb	T	C	4: 141,412,316	E125G	possibly damaging	Het
Clstn1	G	A	4: 149,634,796	V361M	probably damaging	Het
Coro7	G	A	16: 4,627,504		probably benign	Het
Dchs1	C	T	7: 105,764,983	R875H	probably benign	Het
Eif3j1	A	C	2: 122,052,027	M239L	probably benign	Het
Eif4g3	G	T	4: 138,146,376		probably benign	Het
Erbb4	T	C	1: 68,043,960		probably benign	Het
Erlin2	T	G	8: 27,031,764	V164G	possibly damaging	Het
Fbxo43	G	T	15: 36,161,883	Q393K	probably benign	Het
Fcgr4	A	T	1: 171,025,760	N178I	possibly damaging	Het
Grid2	A	G	6: 64,063,953	N293S	possibly damaging	Het
H2-M1	C	T	17: 36,671,332	V126I	probably benign	Het
Htr1f	T	A	16: 64,926,749	Y60F	probably damaging	Het
Ilf2	A	G	3: 90,481,339		probably null	Het
Impg2	A	T	16: 56,265,049	K931*	probably null	Het
Ints1	T	C	5: 139,751,730	E2176G	probably damaging	Het
Iqsec2	T	C	X: 152,223,403	V1319A	probably benign	Het
Iqsec3	G	T	6: 121,410,724	D685E	probably damaging	Het
Itgbl1	G	A	14: 123,846,546	V279I	probably benign	Het
Kdm4b	C	T	17: 56,393,952	A541V	probably benign	Het
Kif14	A	T	1: 136,468,438	T161S	probably benign	Het
Krt86	T	C	15: 101,479,363		probably benign	Het
Kyat1	C	T	2: 30,187,186		probably null	Het
Limch1	T	C	5: 67,027,539	W791R	probably damaging	Het
Map3k11	T	A	19: 5,695,846	M396K	probably damaging	Het
Mat2a	A	G	6: 72,436,195		probably null	Het
Mbnl2	A	G	14: 120,379,237	I88V	possibly damaging	Het
Mib2	T	C	4: 155,655,673	T708A	probably benign	Het
Mkks	T	C	2: 136,877,606		probably null	Het
Mtss1	T	C	15: 58,944,017	M565V	probably damaging	Het
Myoc	A	G	1: 162,649,035	N436S	probably damaging	Het
Myod1	T	A	7: 46,377,112	V147E	probably damaging	Het
Ngef	A	G	1: 87,509,334	L144P	probably benign	Het
Ngrn	C	T	7: 80,261,930	R92W	probably damaging	Het
Nup153	G	A	13: 46,709,654	T349I	probably benign	Het
Olfr1211	T	A	2: 88,930,283	I11L	probably benign	Het
Olfr600	G	T	7: 103,346,204	S241R	possibly damaging	Het
Pigl	A	G	11: 62,503,748	I135M	probably damaging	Het
Pitpnm3	A	G	11: 72,070,492		probably benign	Het
Pkhd1	A	T	1: 20,358,917	F2420I	probably damaging	Het
Polr2b	C	T	5: 77,320,076	T119M	probably damaging	Het
Prr29	A	G	11: 106,376,896	Y130C	probably damaging	Het
Rab11fip3	T	C	17: 25,990,999	I1048V	probably damaging	Het
Rab12	G	A	17: 66,500,362	T124I	probably damaging	Het
Rab44	A	G	17: 29,140,307	S490G	probably benign	Het
Rasa3	A	G	8: 13,570,233		probably null	Het
Rhbdl3	C	T	11: 80,353,574	S369L	possibly damaging	Het
Rimbp2	A	T	5: 128,788,356	S643T	probably benign	Het
Rin1	T	G	19: 5,052,652	S396R	probably damaging	Het
Rpusd3	C	T	6: 113,419,237	G28S	probably damaging	Het
Rtl9	T	A	X: 143,100,278	S229T	probably damaging	Het
Scn4a	A	T	11: 106,320,538	L1551*	probably null	Het
Sec24b	T	C	3: 129,988,984	N1119S	probably null	Het
Serbp1	T	A	6: 67,272,884	*75R	probably null	Het
Setx	C	T	2: 29,179,673	P2497S	probably benign	Het
Slc26a11	A	T	11: 119,359,314	I132F	probably damaging	Het
Slc4a1	A	G	11: 102,352,684	V707A	possibly damaging	Het
Slfn1	A	G	11: 83,121,843	I262V	probably damaging	Het
Tmem168	T	A	6: 13,583,313	D523V	possibly damaging	Het
Traf7	G	T	17: 24,510,551	Q469K	probably benign	Het
Trdmt1	C	A	2: 13,544,617	V6F	probably damaging	Het
Tsacc	A	T	3: 88,287,088		probably benign	Het
Vmn2r5	A	G	3: 64,491,530	I589T	possibly damaging	Het
Vmn2r7	T	C	3: 64,691,039	D699G	probably damaging	Het
Vmn2r82	T	C	10: 79,381,295	V487A	probably damaging	Het
Zfp287	A	T	11: 62,715,029	S351T	probably benign	Het
Zfp651	T	C	9: 121,767,666	V696A	probably damaging	Het
Zfp654	T	C	16: 64,785,688	H176R	possibly damaging	Het

Other mutations in Rufy1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01131:Rufy1	APN	11	50392023	missense	probably damaging	1.00
IGL01640:Rufy1	APN	11	50390378	unclassified	probably benign
IGL01829:Rufy1	APN	11	50416244	nonsense	probably null
IGL02559:Rufy1	APN	11	50420483	missense	probably damaging	1.00
IGL03409:Rufy1	APN	11	50406483	missense	probably benign	0.00
R0053:Rufy1	UTSW	11	50401465	missense	probably benign	0.10
R0053:Rufy1	UTSW	11	50401465	missense	probably benign	0.10
R1028:Rufy1	UTSW	11	50414598	splice site	probably null
R1591:Rufy1	UTSW	11	50394928	missense	probably damaging	1.00
R1818:Rufy1	UTSW	11	50414572	missense	probably benign	0.43
R1952:Rufy1	UTSW	11	50406406	missense	probably benign	0.01
R2228:Rufy1	UTSW	11	50397784	splice site	probably null
R2982:Rufy1	UTSW	11	50419708	missense	possibly damaging	0.77
R4837:Rufy1	UTSW	11	50401493	missense	probably damaging	0.96
R4874:Rufy1	UTSW	11	50406450	missense	possibly damaging	0.80
R4959:Rufy1	UTSW	11	50401488	missense	probably benign
R4968:Rufy1	UTSW	11	50410607	missense	probably benign	0.01
R5204:Rufy1	UTSW	11	50406434	missense	probably damaging	1.00
R5426:Rufy1	UTSW	11	50421734	missense	probably damaging	1.00
R5966:Rufy1	UTSW	11	50401488	missense	probably benign
R6129:Rufy1	UTSW	11	50417248	missense	probably damaging	0.99
R6930:Rufy1	UTSW	11	50398380	missense	probably benign	0.05
R7073:Rufy1	UTSW	11	50404463	missense	probably benign	0.05
R7462:Rufy1	UTSW	11	50407828	missense	possibly damaging	0.93
R7646:Rufy1	UTSW	11	50410609	missense	probably damaging	1.00
R7951:Rufy1	UTSW	11	50430909	missense	probably benign
R7971:Rufy1	UTSW	11	50421671	missense	probably damaging	1.00
R8308:Rufy1	UTSW	11	50406406	missense	probably benign	0.01

Predicted Primers

PCR Primer
(F):5'- TTGGCATTCTCTTCCGAGGCTGAC -3'
(R):5'- CCTTGCCCGAGTTCTCTAATGACTG -3'

Sequencing Primer
(F):5'- ACAGCCTGGTGAAGGTTTC -3'
(R):5'- CAGCAGGACCAATTGTTTGACTG -3'

Posted On

2013-04-16