Mutagenetix > Incidental Mutation

Incidental Mutation 'R6256:Sult6b1'

506147

Institutional Source

Beutler Lab

Gene Symbol

Sult6b1

Ensembl Gene

ENSMUSG00000038045

Gene Name

sulfotransferase family, cytosolic, 6B, member 1

Synonyms

2410078J06Rik

MMRRC Submission

044373-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.069) question?

Stock #

R6256 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

79192314-79214421 bp(-) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to T at 79214343 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Phenylalanine to Isoleucine at position 27 (F27I)

Ref Sequence

ENSEMBL: ENSMUSP00000132823 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000042683] [ENSMUST00000159710] [ENSMUST00000169544]

AlphaFold

P0CC03

Predicted Effect

probably benign
Transcript: ENSMUST00000042683

SMART Domains

Protein: ENSMUSP00000038282
Gene: ENSMUSG00000038045

Domain	Start	End	E-Value	Type
Pfam:Sulfotransfer_1	17	252	2.6e-57	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000159710

Predicted Effect

probably benign
Transcript: ENSMUST00000169544
AA Change: F27I

PolyPhen 2 Score 0.047 (Sensitivity: 0.94; Specificity: 0.83)

SMART Domains

Protein: ENSMUSP00000132823
Gene: ENSMUSG00000038045
AA Change: F27I

Domain	Start	End	E-Value	Type
Pfam:Sulfotransfer_1	55	290	2.1e-57	PFAM

Coding Region Coverage

1x: 99.9%
3x: 99.6%
10x: 97.9%
20x: 93.5%

Validation Efficiency

99% (74/75)

Allele List at MGI

Other mutations in this stock

Total: 46 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1700030K09Rik	A	T	8: 73,205,272 (GRCm39)	Q361L	probably damaging	Het
Abca7	A	G	10: 79,838,456 (GRCm39)	T577A	probably damaging	Het
Acad12	A	T	5: 121,752,149 (GRCm39)	V54E	probably benign	Het
Ago4	A	G	4: 126,414,019 (GRCm39)	Y91H	probably damaging	Het
Akr1b10	T	C	6: 34,364,623 (GRCm39)	V28A	probably damaging	Het
Ccdc33	T	A	9: 58,009,201 (GRCm39)		probably null	Het
Ccdc7a	T	C	8: 129,662,074 (GRCm39)		probably null	Het
Ces1f	A	T	8: 93,992,422 (GRCm39)	V343E	probably damaging	Het
Cftr	T	C	6: 18,274,660 (GRCm39)	L896P	probably damaging	Het
Csmd3	G	A	15: 47,533,125 (GRCm39)	P2375S	probably damaging	Het
Dnajb14	C	T	3: 137,614,124 (GRCm39)	A345V	probably damaging	Het
Dnajb14	G	C	3: 137,614,123 (GRCm39)	A345P	probably damaging	Het
Dnase1	G	A	16: 3,855,485 (GRCm39)	R24K	probably benign	Het
Dnmbp	C	T	19: 43,840,720 (GRCm39)	V560M	probably damaging	Het
Dop1b	T	A	16: 93,604,102 (GRCm39)	I1981N	possibly damaging	Het
Eif3a	A	C	19: 60,759,464 (GRCm39)	S770A	possibly damaging	Het
Fbxl7	A	T	15: 26,553,088 (GRCm39)	C60S	probably benign	Het
Fras1	A	T	5: 96,881,702 (GRCm39)	D2478V	possibly damaging	Het
Hrnr	A	G	3: 93,229,918 (GRCm39)	D52G	probably damaging	Het
Jmjd1c	T	A	10: 67,056,187 (GRCm39)	L823M	probably damaging	Het
Kdm1a	G	T	4: 136,295,911 (GRCm39)	C172*	probably null	Het
Kdm6b	C	T	11: 69,297,555 (GRCm39)	E295K	probably damaging	Het
Mepe	A	T	5: 104,484,940 (GRCm39)	M27L	probably benign	Het
Mogat2	A	T	7: 98,869,102 (GRCm39)	H305Q	probably damaging	Het
Mst1r	T	A	9: 107,794,465 (GRCm39)	Y1215N	probably damaging	Het
Muc5ac	A	T	7: 141,343,532 (GRCm39)	H48L	possibly damaging	Het
Myo7b	T	C	18: 32,116,748 (GRCm39)	D953G	probably damaging	Het
Ocel1	T	C	8: 71,824,472 (GRCm39)		probably benign	Het
Pcdhb6	A	G	18: 37,468,978 (GRCm39)	D633G	probably damaging	Het
Ppm1l	A	G	3: 69,405,230 (GRCm39)	I176V	probably benign	Het
Sall3	C	T	18: 81,013,076 (GRCm39)	R1120H	possibly damaging	Het
Sbf1	G	A	15: 89,185,070 (GRCm39)	P1018S	probably benign	Het
Setbp1	T	C	18: 78,900,472 (GRCm39)	Y1065C	probably damaging	Het
Slc25a2	T	C	18: 37,770,776 (GRCm39)		probably null	Het
Slc4a2	C	A	5: 24,640,888 (GRCm39)	T729K	probably damaging	Het
Sptlc2	T	C	12: 87,402,305 (GRCm39)	E207G	probably damaging	Het
Syf2	A	T	4: 134,661,889 (GRCm39)	K84N	probably damaging	Het
Tmem209	A	T	6: 30,497,166 (GRCm39)	N183K	probably benign	Het
Tmem232	G	T	17: 65,785,397 (GRCm39)	Q188K	possibly damaging	Het
Tomm70a	A	T	16: 56,973,055 (GRCm39)	T598S	probably benign	Het
Ttll13	A	G	7: 79,908,052 (GRCm39)	T556A	probably benign	Het
Vmn2r120	A	T	17: 57,831,700 (GRCm39)	L363*	probably null	Het
Xpo6	G	T	7: 125,707,791 (GRCm39)	Q872K	probably damaging	Het
Xrra1	A	C	7: 99,563,671 (GRCm39)	S553R	probably damaging	Het
Zfy1	A	T	Y: 738,765 (GRCm39)	V147E	unknown	Homo
Zfy2	T	C	Y: 2,116,267 (GRCm39)	I258V	probably benign	Homo

Other mutations in Sult6b1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01479:Sult6b1	APN	17	79,213,005 (GRCm39)	missense	probably benign	0.00
IGL02065:Sult6b1	APN	17	79,196,504 (GRCm39)	missense	probably damaging	0.99
R0522:Sult6b1	UTSW	17	79,212,958 (GRCm39)	missense	probably damaging	0.97
R1911:Sult6b1	UTSW	17	79,196,393 (GRCm39)	missense	possibly damaging	0.81
R3546:Sult6b1	UTSW	17	79,214,336 (GRCm39)	missense	probably benign	0.00
R4105:Sult6b1	UTSW	17	79,214,291 (GRCm39)	missense	probably damaging	1.00
R4107:Sult6b1	UTSW	17	79,214,291 (GRCm39)	missense	probably damaging	1.00
R4108:Sult6b1	UTSW	17	79,214,291 (GRCm39)	missense	probably damaging	1.00
R5063:Sult6b1	UTSW	17	79,213,005 (GRCm39)	missense	probably benign	0.00
R5478:Sult6b1	UTSW	17	79,202,101 (GRCm39)	splice site	probably null
R5845:Sult6b1	UTSW	17	79,202,059 (GRCm39)	missense	probably damaging	1.00
R6374:Sult6b1	UTSW	17	79,214,360 (GRCm39)	missense	probably benign	0.04
R7128:Sult6b1	UTSW	17	79,202,070 (GRCm39)	missense	probably damaging	1.00
R7357:Sult6b1	UTSW	17	79,202,059 (GRCm39)	missense	probably damaging	1.00
R7903:Sult6b1	UTSW	17	79,198,279 (GRCm39)	missense	probably benign	0.31

Predicted Primers

PCR Primer
(F):5'- TGGAAACGAACCTCCTCCTTC -3'
(R):5'- TTGCCAGGAGGATATTCAAACAGG -3'

Sequencing Primer
(F):5'- GAACCTCCTCCTTCCCACC -3'
(R):5'- TGAATGAGAATGGTTGATTGTTTTCC -3'

Posted On

2018-02-28