Mutagenetix > Incidental Mutation

Incidental Mutation 'R0458:Snx6'

41328

Institutional Source

Beutler Lab

Gene Symbol

Snx6

Ensembl Gene

ENSMUSG00000005656

Gene Name

sorting nexin 6

Synonyms

2010006G21Rik, 2610032J07Rik, 2810425K19Rik

MMRRC Submission

038658-MU

Accession Numbers

Essential gene?

Probably essential (E-score: 0.832) question?

Stock #

R0458 (G1)

Quality Score

213

Status

Validated

Chromosome

Chromosomal Location

54793124-54842464 bp(-) (GRCm39)

Type of Mutation

nonsense

DNA Base Change (assembly)

G to T at 54814921 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Stop codon at position 17 (Y17*)

Ref Sequence

ENSEMBL: ENSMUSP00000151488 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000005798] [ENSMUST00000218934] [ENSMUST00000219781]

AlphaFold

Q6P8X1

Predicted Effect

probably null
Transcript: ENSMUST00000005798
AA Change: Y133*

SMART Domains

Protein: ENSMUSP00000005798
Gene: ENSMUSG00000005656
AA Change: Y133*

Domain	Start	End	E-Value	Type
Pfam:PX	29	170	2.8e-21	PFAM
Pfam:Vps5	184	399	2e-16	PFAM

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218066

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000218337

Predicted Effect

probably null
Transcript: ENSMUST00000218934
AA Change: Y17*

Predicted Effect

probably benign
Transcript: ENSMUST00000219781

Meta Mutation Damage Score

0.9755

Coding Region Coverage

1x: 99.7%
3x: 98.9%
10x: 97.0%
20x: 94.3%

Validation Efficiency

100% (79/79)

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 sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein associates with the long isoform of the leptin receptor, the transforming growth factor-beta family of receptor serine-threonine kinases, and with receptor tyrosine kinases for platelet-derived growth factor, insulin, and epidermal growth factor. This protein may form oligomeric complexes with family member proteins through interactions of both the PX domain and the coiled coil regions of the molecules. Translocation of this protein from the cytoplasm to the nucleus occurs after binding to proviral integration site 1 protein. This gene results in two transcripts encoding two distinct isoforms. [provided by RefSeq, Jul 2008]

Allele List at MGI

Other mutations in this stock

Total: 76 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4933407L21Rik	A	G	1: 85,856,747 (GRCm39)	E8G	unknown	Het
9130008F23Rik	T	C	17: 41,191,127 (GRCm39)	T101A	probably benign	Het
Abcb8	C	T	5: 24,611,231 (GRCm39)	T455I	probably benign	Het
Abcb9	C	A	5: 124,220,209 (GRCm39)		probably null	Het
Akp3	T	G	1: 87,054,259 (GRCm39)	Y265*	probably null	Het
Atp6v1b1	A	T	6: 83,729,390 (GRCm39)	D109V	probably damaging	Het
Aurka	C	A	2: 172,212,366 (GRCm39)	E4*	probably null	Het
Cacna1g	T	A	11: 94,300,266 (GRCm39)	Q2168L	probably damaging	Het
Cdc45	T	A	16: 18,600,722 (GRCm39)		probably benign	Het
Cfap61	T	C	2: 145,850,837 (GRCm39)	V325A	probably benign	Het
Clasp2	T	A	9: 113,735,292 (GRCm39)		probably null	Het
Crim1	T	A	17: 78,620,655 (GRCm39)	I365N	probably damaging	Het
Dcaf8	A	G	1: 172,001,610 (GRCm39)	N269S	probably benign	Het
Dnaaf5	T	C	5: 139,147,633 (GRCm39)	V399A	possibly damaging	Het
Ear2	A	G	14: 44,340,705 (GRCm39)	Y121C	probably damaging	Het
Eef2k	T	C	7: 120,502,513 (GRCm39)	Y692H	probably damaging	Het
Elavl2	A	T	4: 91,197,104 (GRCm39)		probably benign	Het
Epn2	C	A	11: 61,437,281 (GRCm39)	R97L	possibly damaging	Het
Fam243	T	C	16: 92,117,995 (GRCm39)	I98V	probably benign	Het
Fzd6	G	A	15: 38,894,676 (GRCm39)	A281T	probably damaging	Het
Garem2	T	A	5: 30,319,180 (GRCm39)	I214N	probably damaging	Het
Glg1	A	G	8: 111,887,238 (GRCm39)		probably benign	Het
Golm1	T	C	13: 59,812,178 (GRCm39)	E48G	probably damaging	Het
Gpaa1	G	T	15: 76,216,233 (GRCm39)	R12L	probably benign	Het
Gstm1	T	A	3: 107,924,679 (GRCm39)	T34S	probably benign	Het
Gtf3c1	G	A	7: 125,243,306 (GRCm39)	P1766L	possibly damaging	Het
Herc1	A	T	9: 66,383,663 (GRCm39)	Q3709L	probably benign	Het
Hoxa13	CCG	CCGCG	6: 52,237,618 (GRCm39)		probably null	Het
Icam1	A	G	9: 20,939,157 (GRCm39)		probably null	Het
Itga9	T	C	9: 118,510,096 (GRCm39)		probably null	Het
Kif15	T	C	9: 122,838,424 (GRCm39)	F1121L	probably benign	Het
Klhl30	T	A	1: 91,288,718 (GRCm39)		probably benign	Het
Ldlrad1	T	C	4: 107,073,387 (GRCm39)	C141R	probably damaging	Het
Lemd2	T	C	17: 27,409,627 (GRCm39)	D508G	probably damaging	Het
Lilra5	A	C	7: 4,241,218 (GRCm39)	T52P	probably benign	Het
Lrtm2	G	A	6: 119,294,229 (GRCm39)	P301S	probably damaging	Het
Mcoln2	A	G	3: 145,855,768 (GRCm39)		probably benign	Het
Mkrn2os	A	G	6: 115,563,631 (GRCm39)	S135P	probably damaging	Het
Mlxipl	T	C	5: 135,162,224 (GRCm39)	V607A	probably benign	Het
Mmadhc	T	C	2: 50,171,173 (GRCm39)	Y213C	probably benign	Het
Mpo	C	A	11: 87,687,123 (GRCm39)	A223E	probably benign	Het
Mthfd2l	C	G	5: 91,168,036 (GRCm39)	I310M	probably damaging	Het
Muc5b	C	A	7: 141,418,709 (GRCm39)	A3885D	probably benign	Het
Mvp	A	G	7: 126,597,663 (GRCm39)	W152R	probably damaging	Het
Nmur2	A	T	11: 55,931,394 (GRCm39)	F106I	possibly damaging	Het
Nr3c2	T	A	8: 77,636,167 (GRCm39)	F423I	probably damaging	Het
Or1l8	A	G	2: 36,817,349 (GRCm39)	V259A	probably damaging	Het
Or5m5	A	G	2: 85,814,600 (GRCm39)	S139G	probably benign	Het
Or8c16	G	A	9: 38,130,344 (GRCm39)	C75Y	probably damaging	Het
Or9q1	G	T	19: 13,805,593 (GRCm39)	H56N	probably benign	Het
Pappa	A	G	4: 65,074,119 (GRCm39)	I224M	probably damaging	Het
Prex1	A	C	2: 166,427,743 (GRCm39)	S800A	probably damaging	Het
Prkaca	T	C	8: 84,721,911 (GRCm39)		probably benign	Het
Ptpru	A	T	4: 131,526,986 (GRCm39)	V662E	possibly damaging	Het
Rabep1	T	A	11: 70,777,824 (GRCm39)		probably null	Het
Rbms2	C	T	10: 127,987,058 (GRCm39)	C50Y	probably damaging	Het
Rd3	C	T	1: 191,709,414 (GRCm39)	P25S	probably damaging	Het
Rnf148	T	G	6: 23,654,256 (GRCm39)	I247L	probably benign	Het
Sf3b3	A	G	8: 111,538,768 (GRCm39)		probably benign	Het
Slc35c1	A	T	2: 92,284,858 (GRCm39)	F252Y	probably damaging	Het
Slc38a11	T	C	2: 65,193,813 (GRCm39)		probably null	Het
Sox6	C	A	7: 115,089,029 (GRCm39)	R611L	probably damaging	Het
Spata13	G	A	14: 60,929,492 (GRCm39)	R350H	probably damaging	Het
Sppl2a	G	T	2: 126,746,879 (GRCm39)	A483D	probably damaging	Het
Stat1	C	T	1: 52,188,211 (GRCm39)		probably benign	Het
Tab2	A	T	10: 7,795,319 (GRCm39)	Y314N	probably damaging	Het
Tor1aip1	T	C	1: 155,906,153 (GRCm39)	N213S	probably damaging	Het
Trim39	T	C	17: 36,572,404 (GRCm39)	K300E	probably damaging	Het
Tubal3	T	C	13: 3,983,137 (GRCm39)	S306P	probably damaging	Het
Ufm1	A	G	3: 53,768,655 (GRCm39)	L33P	probably damaging	Het
Washc4	G	A	10: 83,382,663 (GRCm39)	V26I	possibly damaging	Het
Wfs1	A	G	5: 37,126,013 (GRCm39)	Y293H	probably damaging	Het
Zbtb41	T	C	1: 139,351,214 (GRCm39)	V109A	probably damaging	Het
Zfp667	T	C	7: 6,307,844 (GRCm39)	S171P	probably benign	Het
Zkscan5	T	A	5: 145,142,281 (GRCm39)	H59Q	probably damaging	Het
Zswim8	C	T	14: 20,768,965 (GRCm39)	R1128W	probably damaging	Het

Other mutations in Snx6

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01340:Snx6	APN	12	54,801,094 (GRCm39)	missense	probably damaging	0.99
IGL02682:Snx6	APN	12	54,801,130 (GRCm39)	missense	probably damaging	1.00
IGL02995:Snx6	APN	12	54,842,295 (GRCm39)	splice site	probably benign
IGL03240:Snx6	APN	12	54,830,228 (GRCm39)	missense	probably damaging	0.98
IGL03353:Snx6	APN	12	54,812,469 (GRCm39)	splice site	probably benign
PIT4362001:Snx6	UTSW	12	54,814,815 (GRCm39)	missense	possibly damaging	0.80
R0610:Snx6	UTSW	12	54,798,574 (GRCm39)	missense	probably damaging	1.00
R0689:Snx6	UTSW	12	54,810,441 (GRCm39)	missense	probably benign	0.00
R1818:Snx6	UTSW	12	54,830,259 (GRCm39)	missense	possibly damaging	0.95
R1819:Snx6	UTSW	12	54,830,259 (GRCm39)	missense	possibly damaging	0.95
R4946:Snx6	UTSW	12	54,817,528 (GRCm39)	missense	probably damaging	1.00
R5275:Snx6	UTSW	12	54,830,807 (GRCm39)	missense	probably damaging	1.00
R5373:Snx6	UTSW	12	54,817,513 (GRCm39)	missense	probably damaging	0.99
R5374:Snx6	UTSW	12	54,817,513 (GRCm39)	missense	probably damaging	0.99
R5497:Snx6	UTSW	12	54,803,846 (GRCm39)	missense	probably damaging	0.98
R5907:Snx6	UTSW	12	54,801,104 (GRCm39)	missense	probably damaging	1.00
R5947:Snx6	UTSW	12	54,817,549 (GRCm39)	nonsense	probably null
R6178:Snx6	UTSW	12	54,807,249 (GRCm39)	missense	probably damaging	0.99
R6287:Snx6	UTSW	12	54,793,813 (GRCm39)	missense	possibly damaging	0.75
R6321:Snx6	UTSW	12	54,798,798 (GRCm39)	missense	probably damaging	1.00
R6878:Snx6	UTSW	12	54,810,386 (GRCm39)	splice site	probably null
R7055:Snx6	UTSW	12	54,830,864 (GRCm39)	missense	probably damaging	1.00
R8227:Snx6	UTSW	12	54,798,756 (GRCm39)	missense	possibly damaging	0.82
R8899:Snx6	UTSW	12	54,812,423 (GRCm39)	missense	probably benign	0.06
R9606:Snx6	UTSW	12	54,814,811 (GRCm39)	missense	probably benign	0.30

Predicted Primers

PCR Primer
(F):5'- CCCTCTGACTCTAAAGCATCCCGTG -3'
(R):5'- AACAAAACTTGTGTGCTGCTCTGTG -3'

Sequencing Primer
(F):5'- AGGACAGTGCTCCTCCC -3'
(R):5'- GCATGAGGCTTTCTCAGAAATG -3'

Posted On

2013-05-23