Mutagenetix > Incidental Mutation

Incidental Mutation 'R4933:Sult3a1'

380727

Institutional Source

Beutler Lab

Gene Symbol

Sult3a1

Ensembl Gene

ENSMUSG00000069668

Gene Name

sulfotransferase family 3A, member 1

Synonyms

Sultx2

MMRRC Submission

042533-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.181) question?

Stock #

R4933 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

33857721-33879532 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

T to A at 33866554 bp (GRCm38)

Zygosity

Heterozygous

Amino Acid Change

Isoleucine to Asparagine at position 59 (I59N)

Ref Sequence

ENSEMBL: ENSMUSP00000151228 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000092597] [ENSMUST00000218204]

AlphaFold

no structure available at present

Predicted Effect

probably damaging
Transcript: ENSMUST00000092597
AA Change: I59N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

SMART Domains

Protein: ENSMUSP00000090259
Gene: ENSMUSG00000069668
AA Change: I59N

Domain	Start	End	E-Value	Type
Pfam:Sulfotransfer_1	36	283	1.8e-81	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000218204
AA Change: I59N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)

Meta Mutation Damage Score

0.6467

Coding Region Coverage

1x: 99.0%
3x: 98.1%
10x: 95.4%
20x: 89.3%

Validation Efficiency

97% (73/75)

Allele List at MGI

Other mutations in this stock

Total: 55 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
2610021A01Rik	A	G	7: 41,626,802 (GRCm38)	E643G	probably damaging	Het
4430402I18Rik	G	T	19: 28,941,775 (GRCm38)	H195N	possibly damaging	Het
Abca2	T	C	2: 25,444,827 (GRCm38)	V1937A	probably benign	Het
Acot10	A	T	15: 20,666,330 (GRCm38)	N108K	possibly damaging	Het
Agtpbp1	A	T	13: 59,500,572 (GRCm38)	M478K	probably benign	Het
Akirin1	G	A	4: 123,736,858 (GRCm38)	S191F	probably damaging	Het
Aurkb	T	C	11: 69,048,144 (GRCm38)		probably benign	Het
Cabyr	T	C	18: 12,744,492 (GRCm38)		probably benign	Het
Ccp110	A	G	7: 118,725,319 (GRCm38)	E688G	probably damaging	Het
Champ1	T	A	8: 13,879,137 (GRCm38)	S432T	probably benign	Het
Crybg1	T	A	10: 43,999,213 (GRCm38)	N633I	probably damaging	Het
Dagla	A	T	19: 10,269,715 (GRCm38)		probably null	Het
Dkkl1	A	T	7: 45,211,525 (GRCm38)	L10Q	probably null	Het
Dnah8	G	A	17: 30,748,568 (GRCm38)	D2585N	probably benign	Het
E430018J23Rik	A	G	7: 127,393,349 (GRCm38)	Y30H	probably damaging	Het
Fndc7	G	T	3: 108,876,670 (GRCm38)	Q208K	probably benign	Het
Gins4	A	T	8: 23,234,780 (GRCm38)	C53S	probably damaging	Het
Gja8	T	A	3: 96,919,035 (GRCm38)		probably benign	Het
Golph3l	T	A	3: 95,617,423 (GRCm38)	N328K	probably benign	Het
Haus6	A	C	4: 86,585,287 (GRCm38)		probably benign	Het
Hdac5	A	G	11: 102,200,563 (GRCm38)		probably benign	Het
Ide	A	G	19: 37,277,756 (GRCm38)	Y883H	unknown	Het
Igf2r	A	G	17: 12,691,877 (GRCm38)		probably null	Het
Kdm3b	T	C	18: 34,810,393 (GRCm38)	Y723H	probably damaging	Het
Kif21b	G	A	1: 136,151,325 (GRCm38)		probably null	Het
Lancl1	A	T	1: 67,021,034 (GRCm38)	N77K	probably benign	Het
Lyst	G	A	13: 13,759,378 (GRCm38)	V3554I	probably benign	Het
Lyst	T	A	13: 13,637,764 (GRCm38)	N920K	probably damaging	Het
Map1a	G	A	2: 121,305,905 (GRCm38)	A2163T	probably damaging	Het
Mapk7	G	T	11: 61,493,908 (GRCm38)		probably benign	Het
Myo10	C	A	15: 25,781,118 (GRCm38)	Q154K	probably damaging	Het
Olfr13	C	T	6: 43,174,321 (GRCm38)	L112F	probably benign	Het
Olfr132	A	G	17: 38,130,550 (GRCm38)	I214T	probably damaging	Het
Pcdhgb2	G	A	18: 37,692,214 (GRCm38)	V753M	probably benign	Het
Pnn	T	A	12: 59,070,227 (GRCm38)	L195Q	probably damaging	Het
Pot1a	A	G	6: 25,771,541 (GRCm38)	V227A	possibly damaging	Het
Ppp1r21	T	A	17: 88,547,621 (GRCm38)	D109E	probably benign	Het
Prr15l	G	A	11: 96,934,762 (GRCm38)	G73S	probably damaging	Het
Rnf148	A	G	6: 23,654,340 (GRCm38)	F219S	probably benign	Het
Rnpep	C	A	1: 135,267,026 (GRCm38)		probably benign	Het
Ryr1	T	C	7: 29,104,298 (GRCm38)	T643A	probably damaging	Het
Ryr2	A	T	13: 11,945,945 (GRCm38)	C36S	probably damaging	Het
Shc3	G	T	13: 51,442,769 (GRCm38)	T406N	probably benign	Het
Slit3	G	T	11: 35,688,593 (GRCm38)	G1199V	probably damaging	Het
Sptbn5	G	A	2: 120,050,120 (GRCm38)		noncoding transcript	Het
St8sia6	T	C	2: 13,665,442 (GRCm38)	N236D	probably damaging	Het
Stpg1	A	T	4: 135,506,416 (GRCm38)	Q3L	probably benign	Het
Svs1	T	C	6: 48,987,492 (GRCm38)	S145P	probably damaging	Het
Vmn1r208	T	G	13: 22,772,788 (GRCm38)	I180L	probably benign	Het
Vmn2r51	A	T	7: 10,098,320 (GRCm38)	N446K	probably damaging	Het
Vmn2r63	A	T	7: 42,903,978 (GRCm38)	I618N	probably damaging	Het
Wrn	T	C	8: 33,322,343 (GRCm38)	N182S	probably benign	Het
Zfp296	G	T	7: 19,579,712 (GRCm38)	C164F	possibly damaging	Het
Zmynd8	A	G	2: 165,834,951 (GRCm38)	V249A	possibly damaging	Het
Zswim2	A	G	2: 83,925,227 (GRCm38)	L110P	probably damaging	Het

Other mutations in Sult3a1

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01984:Sult3a1	APN	10	33,879,209 (GRCm38)	nonsense	probably null
IGL02269:Sult3a1	APN	10	33,879,263 (GRCm38)	missense	probably benign	0.25
IGL02302:Sult3a1	APN	10	33,866,575 (GRCm38)	missense	possibly damaging	0.81
IGL02947:Sult3a1	APN	10	33,864,050 (GRCm38)	missense	possibly damaging	0.92
IGL02966:Sult3a1	APN	10	33,877,273 (GRCm38)	splice site	probably benign
IGL03271:Sult3a1	APN	10	33,864,001 (GRCm38)	missense	probably benign
IGL03367:Sult3a1	APN	10	33,877,346 (GRCm38)	missense	probably benign	0.01
R0539:Sult3a1	UTSW	10	33,866,523 (GRCm38)	missense	probably damaging	1.00
R0627:Sult3a1	UTSW	10	33,864,014 (GRCm38)	missense	probably benign	0.00
R0838:Sult3a1	UTSW	10	33,879,288 (GRCm38)	missense	probably damaging	0.99
R1538:Sult3a1	UTSW	10	33,870,170 (GRCm38)	missense	probably benign	0.29
R1604:Sult3a1	UTSW	10	33,866,620 (GRCm38)	missense	probably damaging	1.00
R1622:Sult3a1	UTSW	10	33,870,250 (GRCm38)	missense	probably benign	0.39
R3031:Sult3a1	UTSW	10	33,877,349 (GRCm38)	missense	possibly damaging	0.70
R5943:Sult3a1	UTSW	10	33,866,641 (GRCm38)	missense	probably damaging	0.99
R6440:Sult3a1	UTSW	10	33,870,202 (GRCm38)	missense	possibly damaging	0.46
R7140:Sult3a1	UTSW	10	33,877,287 (GRCm38)	missense	probably damaging	1.00
R7356:Sult3a1	UTSW	10	33,866,583 (GRCm38)	missense	probably benign	0.25
R8342:Sult3a1	UTSW	10	33,866,521 (GRCm38)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- TCCAGCCTTATGTACTTGAGTG -3'
(R):5'- GACTAAGCTTATGACATACTTTGGC -3'

Sequencing Primer
(F):5'- GGAAATGATAACTGAGCGTATCC -3'
(R):5'- TGTGGGAACTGAAGATGC -3'

Posted On

2016-04-15