Mutagenetix > Incidental Mutation

Incidental Mutation 'R5053:As3mt'

394783

Institutional Source

Beutler Lab

Gene Symbol

As3mt

Ensembl Gene

ENSMUSG00000003559

Gene Name

arsenite methyltransferase

Synonyms

Cyt19, 2310045H08Rik

MMRRC Submission

042643-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.070) question?

Stock #

R5053 (G1)

Quality Score

225

Status

Not validated

Chromosome

Chromosomal Location

46695897-46729538 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

A to G at 46697493 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Tyrosine to Cysteine at position 87 (Y87C)

Ref Sequence

ENSEMBL: ENSMUSP00000003655 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000003655]

AlphaFold

Q91WU5

Predicted Effect

probably damaging
Transcript: ENSMUST00000003655
AA Change: Y87C

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

SMART Domains

Protein: ENSMUSP00000003655
Gene: ENSMUSG00000003559
AA Change: Y87C

Domain	Start	End	E-Value	Type
Pfam:Methyltransf_23	34	227	2.5e-14	PFAM
Pfam:PCMT	64	183	7.7e-9	PFAM
Pfam:Ubie_methyltran	64	196	8.9e-16	PFAM
Pfam:PrmA	65	193	1.8e-6	PFAM
Pfam:Methyltransf_31	70	243	2e-36	PFAM
Pfam:Methyltransf_18	71	187	9.7e-14	PFAM
Pfam:Methyltransf_25	75	180	2.8e-15	PFAM
Pfam:Methyltransf_12	76	182	2.9e-14	PFAM
Pfam:Methyltransf_11	76	184	2.7e-19	PFAM
low complexity region	297	310	N/A	INTRINSIC

Coding Region Coverage

1x: 99.3%
3x: 98.3%
10x: 95.9%
20x: 90.6%

Validation Efficiency

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] AS3MT catalyzes the transfer of a methyl group from S-adenosyl-L-methionine (AdoMet) to trivalent arsenical and may play a role in arsenic metabolism (Lin et al., 2002 [PubMed 11790780]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Mice homozygous for a null allele have abnormalities in arsenic methylation and in the distribution/retention of orally administered arsenate. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Acvrl1	A	T	15: 101,035,250 (GRCm39)	I259F	probably damaging	Het
Adgrf2	A	G	17: 43,021,334 (GRCm39)	S497P	probably damaging	Het
Adsl	T	C	15: 80,844,651 (GRCm39)	C180R	probably damaging	Het
Ahctf1	A	G	1: 179,614,349 (GRCm39)	I448T	possibly damaging	Het
Alg9	G	T	9: 50,699,472 (GRCm39)	G200W	probably damaging	Het
Amhr2	G	A	15: 102,355,693 (GRCm39)	V213I	probably damaging	Het
Ankrd44	A	T	1: 54,774,248 (GRCm39)	L200*	probably null	Het
Bcl11a	C	A	11: 24,114,068 (GRCm39)	F470L	probably benign	Het
Cacna2d2	A	T	9: 107,392,063 (GRCm39)	Y468F	probably damaging	Het
Cep250	A	G	2: 155,804,848 (GRCm39)	D71G	possibly damaging	Het
Clca4b	T	C	3: 144,616,882 (GRCm39)	T923A	probably benign	Het
Clec16a	T	C	16: 10,394,461 (GRCm39)	L273P	probably damaging	Het
Comtd1	T	C	14: 21,897,764 (GRCm39)	D123G	probably damaging	Het
Cpa5	A	T	6: 30,623,271 (GRCm39)	E144V	probably damaging	Het
Cyp2c37	G	A	19: 39,990,331 (GRCm39)	S343N	probably benign	Het
Dennd6a	C	A	14: 26,329,738 (GRCm39)	T103K	probably damaging	Het
Ect2l	A	G	10: 18,016,093 (GRCm39)	L733P	probably damaging	Het
Erg	T	A	16: 95,325,393 (GRCm39)	H11L	probably benign	Het
Ero1b	T	C	13: 12,614,795 (GRCm39)	L253P	probably damaging	Het
Etfbkmt	T	A	6: 149,048,766 (GRCm39)	L135*	probably null	Het
Frmd4a	A	T	2: 4,608,732 (GRCm39)	T867S	probably damaging	Het
Gm815	C	T	19: 26,863,813 (GRCm39)	A18V	unknown	Het
Gna12	C	A	5: 140,746,482 (GRCm39)	R321L	probably benign	Het
Herc1	A	T	9: 66,377,608 (GRCm39)	K3458M	possibly damaging	Het
Irs1	A	G	1: 82,264,643 (GRCm39)	L1191P	probably benign	Het
Kcp	G	T	6: 29,496,957 (GRCm39)	Q551K	probably benign	Het
Klhl11	C	T	11: 100,363,026 (GRCm39)	V177M	probably damaging	Het
Klk14	G	A	7: 43,341,501 (GRCm39)	C51Y	probably damaging	Het
Llcfc1	A	G	6: 41,662,269 (GRCm39)	H91R	possibly damaging	Het
Lmnb2	A	T	10: 80,740,489 (GRCm39)	M223K	probably damaging	Het
Mbd6	C	T	10: 127,122,310 (GRCm39)	V173I	probably benign	Het
Mme	T	A	3: 63,272,270 (GRCm39)	V623E	probably damaging	Het
Ndc1	T	C	4: 107,231,415 (GRCm39)	S119P	probably damaging	Het
Nfs1	A	C	2: 155,968,318 (GRCm39)	C383G	probably damaging	Het
Nphp4	A	G	4: 152,628,919 (GRCm39)		probably null	Het
Oca2	C	A	7: 55,973,328 (GRCm39)	Q411K	probably benign	Het
Or10ab4	A	G	7: 107,654,741 (GRCm39)	H184R	probably benign	Het
Or11h23	T	A	14: 50,947,968 (GRCm39)	Y60*	probably null	Het
Or1ad1	G	A	11: 50,876,137 (GRCm39)	G203D	probably damaging	Het
Or4c15	C	A	2: 88,760,597 (GRCm39)	V21F	probably benign	Het
Or8k25	A	G	2: 86,243,682 (GRCm39)	F238S	probably damaging	Het
Pcdh7	A	T	5: 57,878,943 (GRCm39)	T493S	probably damaging	Het
Phf20	T	C	2: 156,115,782 (GRCm39)	S368P	probably benign	Het
Pla2g2e	T	G	4: 138,607,686 (GRCm39)	V22G	possibly damaging	Het
Plxna1	A	T	6: 89,299,442 (GRCm39)	H1736Q	probably damaging	Het
Prlr	C	A	15: 10,325,471 (GRCm39)	Q215K	probably benign	Het
Prpf6	T	C	2: 181,291,246 (GRCm39)	V687A	probably benign	Het
Ptprq	T	A	10: 107,399,063 (GRCm39)	T1951S	probably damaging	Het
Sec31a	G	T	5: 100,541,073 (GRCm39)	Q345K	possibly damaging	Het
Serpina3k	T	C	12: 104,309,473 (GRCm39)		probably null	Het
Sertad3	T	A	7: 27,175,947 (GRCm39)	V127E	probably benign	Het
Sf3b1	A	T	1: 55,036,336 (GRCm39)	N912K	probably benign	Het
Shq1	A	G	6: 100,632,220 (GRCm39)	L202P	probably damaging	Het
Sp8	C	T	12: 118,813,339 (GRCm39)	T398M	probably damaging	Het
Tmem150c	A	T	5: 100,231,599 (GRCm39)	D125E	probably benign	Het
Trim3	G	T	7: 105,266,968 (GRCm39)	D470E	probably damaging	Het
Ubap1	T	A	4: 41,387,315 (GRCm39)	C88*	probably null	Het
Unc79	T	A	12: 103,071,007 (GRCm39)	D1124E	probably damaging	Het
Usf3	T	C	16: 44,037,550 (GRCm39)	S677P	probably benign	Het
Vmn1r76	T	C	7: 11,664,241 (GRCm39)		probably null	Het
Zfp819	C	T	7: 43,266,570 (GRCm39)	T275I	probably damaging	Het
Zranb2	T	A	3: 157,246,796 (GRCm39)	D161E	probably damaging	Het

Other mutations in As3mt

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL00486:As3mt	APN	19	46,708,864 (GRCm39)	missense	probably benign	0.06
IGL00903:As3mt	APN	19	46,700,673 (GRCm39)	missense	probably benign	0.04
IGL02190:As3mt	APN	19	46,708,384 (GRCm39)	missense	probably benign	0.38
IGL03088:As3mt	APN	19	46,696,233 (GRCm39)	missense	probably damaging	1.00
PIT4791001:As3mt	UTSW	19	46,708,788 (GRCm39)	missense	probably damaging	1.00
R1797:As3mt	UTSW	19	46,713,373 (GRCm39)	missense	possibly damaging	0.92
R2157:As3mt	UTSW	19	46,696,231 (GRCm39)	missense	probably benign	0.36
R3113:As3mt	UTSW	19	46,703,717 (GRCm39)	splice site	probably benign
R3816:As3mt	UTSW	19	46,696,216 (GRCm39)	missense	probably benign	0.32
R4819:As3mt	UTSW	19	46,695,968 (GRCm39)	unclassified	probably benign
R5333:As3mt	UTSW	19	46,696,635 (GRCm39)	missense	probably null	0.97
R6003:As3mt	UTSW	19	46,696,567 (GRCm39)	missense	possibly damaging	0.85
R6269:As3mt	UTSW	19	46,708,391 (GRCm39)	missense	probably damaging	1.00
R6281:As3mt	UTSW	19	46,713,362 (GRCm39)	missense	possibly damaging	0.56
R6317:As3mt	UTSW	19	46,713,410 (GRCm39)	missense	probably benign	0.01
R6803:As3mt	UTSW	19	46,698,020 (GRCm39)	missense	probably benign	0.01
R7346:As3mt	UTSW	19	46,708,891 (GRCm39)	missense	probably damaging	1.00
R8061:As3mt	UTSW	19	46,728,982 (GRCm39)	missense	probably damaging	1.00
R8331:As3mt	UTSW	19	46,697,445 (GRCm39)	missense	probably damaging	1.00
R9545:As3mt	UTSW	19	46,696,233 (GRCm39)	missense	probably damaging	0.97
R9697:As3mt	UTSW	19	46,708,420 (GRCm39)	missense	probably benign	0.00

Predicted Primers

PCR Primer
(F):5'- TGCCTACAATGCTGCTAGGG -3'
(R):5'- GTGCCACTGTTGTCACAAGC -3'

Sequencing Primer
(F):5'- AGACGTGGCCCTGTTGAG -3'
(R):5'- TGTCACAAGCTCATCTACCAGGTTAG -3'

Posted On

2016-06-15