Mutagenetix > Incidental Mutations

Incidental Mutation 'R7018:Slc30a2'

545441

Institutional Source

Beutler Lab

Gene Symbol

Slc30a2

Ensembl Gene

ENSMUSG00000028836

Gene Name

solute carrier family 30 (zinc transporter), member 2

Synonyms

Znt2

MMRRC Submission

Accession Numbers

Is this an essential gene?

Probably non essential (E-score: 0.157) question?

Stock #

R7018 (G1)

Quality Score

225.009

Status

Validated

Chromosome

Chromosomal Location

134343181-134354484 bp(+) (GRCm38)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 134347415 bp

Zygosity

Heterozygous

Amino Acid Change

Arginine to Glutamine at position 161 (R161Q)

Ref Sequence

ENSEMBL: ENSMUSP00000101500 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000081094] [ENSMUST00000105872] [ENSMUST00000105873] [ENSMUST00000105874]

Predicted Effect

probably damaging
Transcript: ENSMUST00000081094
AA Change: R81Q

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

SMART Domains

Protein: ENSMUSP00000079875
Gene: ENSMUSG00000028836
AA Change: R81Q

Domain	Start	End	E-Value	Type
Pfam:Cation_efflux	1	280	6e-64	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000105872
AA Change: R81Q

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

SMART Domains

Protein: ENSMUSP00000101498
Gene: ENSMUSG00000028836
AA Change: R81Q

Domain	Start	End	E-Value	Type
Pfam:Cation_efflux	1	280	6e-64	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000105873
AA Change: R112Q

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

SMART Domains

Protein: ENSMUSP00000101499
Gene: ENSMUSG00000028836
AA Change: R112Q

Domain	Start	End	E-Value	Type
Pfam:Cation_efflux	74	311	3.1e-42	PFAM

Predicted Effect

probably damaging
Transcript: ENSMUST00000105874
AA Change: R161Q

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

SMART Domains

Protein: ENSMUSP00000101500
Gene: ENSMUSG00000028836
AA Change: R161Q

Domain	Start	End	E-Value	Type
Pfam:Cation_efflux	70	277	3.4e-51	PFAM

Meta Mutation Damage Score

0.8991

Coding Region Coverage

1x: 100.0%
3x: 99.9%
10x: 99.6%
20x: 98.7%

Validation Efficiency

100% (64/64)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a zinc transporter that acts as a homodimer. The encoded protein plays a role in secreting zinc into breast milk. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Aug 2015]

Allele List at MGI

Other mutations in this stock

Total: 62 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
Apcdd1	G	T	18: 62,937,049	R129L	probably damaging	Het
Arhgef28	C	T	13: 97,965,435	V844I	probably damaging	Het
Arhgef5	T	C	6: 43,288,731	V1569A	probably damaging	Het
Atr	T	A	9: 95,866,694	S431T	probably benign	Het
Cdh11	T	C	8: 102,634,321	D795G	possibly damaging	Het
Crygf	T	C	1: 65,927,971	S85P	probably benign	Het
Diexf	A	G	1: 193,114,855	I563T	probably benign	Het
Dip2c	T	A	13: 9,659,278	Y1385N	probably damaging	Het
Dnah14	G	A	1: 181,626,944	V840I	possibly damaging	Het
Dsg1a	T	C	18: 20,328,738	F299L	possibly damaging	Het
Fgfr4	A	T	13: 55,166,200	S576C	probably damaging	Het
Frmd8	T	C	19: 5,869,518	D167G	probably damaging	Het
Gm5105	G	A	3: 138,049,558	T89I	unknown	Het
Grhl1	C	T	12: 24,575,997	S35L	possibly damaging	Het
Gsn	A	G	2: 35,293,506	E242G	probably benign	Het
Hcrtr1	A	G	4: 130,135,868	I140T	probably damaging	Het
Ifnlr1	T	C	4: 135,703,824	Y208H	possibly damaging	Het
Ighv1-58	T	C	12: 115,312,365	Y51C	probably damaging	Het
Iqcj	T	A	3: 68,041,247	Y21*	probably null	Het
Kcnc4	T	C	3: 107,458,862	Y10C	probably benign	Het
Kcnk7	G	T	19: 5,706,132	G129W	probably damaging	Het
Kcnq2	T	A	2: 181,081,724	R620*	probably null	Het
Klk13	C	A	7: 43,726,702	P267Q	probably benign	Het
Krt1	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC	15: 101,850,378		probably benign	Het
L3mbtl4	G	A	17: 68,486,943	R314H	probably damaging	Het
Lamc2	T	A	1: 153,136,742	M729L	probably benign	Het
Lyst	T	G	13: 13,743,459		probably null	Het
Med13l	G	A	5: 118,751,986	R1909H	probably damaging	Het
Mstn	T	A	1: 53,064,084	L193Q	possibly damaging	Het
Mylk	T	C	16: 35,000,426	V125A	possibly damaging	Het
Nalcn	T	A	14: 123,409,821	M547L	probably damaging	Het
Nckap5	A	G	1: 126,025,048	S1256P	probably damaging	Het
Nkain1	T	C	4: 130,532,118	Y189C	probably damaging	Het
Olfr1164	T	A	2: 88,093,256	I227F	probably benign	Het
Olfr193	A	G	16: 59,110,607	M1T	probably null	Het
Olfr490	T	G	7: 108,286,344	I261L	probably benign	Het
Olfr761	A	T	17: 37,952,502	I174N	probably damaging	Het
Oosp3	T	A	19: 11,699,419	D47E	probably benign	Het
Pcdh15	G	T	10: 74,466,354	G942W	probably damaging	Het
Pcyox1l	C	A	18: 61,707,554		probably benign	Het
Peg3	T	C	7: 6,708,839	E1128G	possibly damaging	Het
Pkd1l3	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA	8: 109,624,195		probably benign	Het
Plscr1	T	A	9: 92,264,662	V119D	probably damaging	Het
Prss56	A	T	1: 87,185,948	D258V	possibly damaging	Het
Ptpn23	T	G	9: 110,385,816	K85Q	possibly damaging	Het
Ranbp3l	C	A	15: 9,007,285	S7Y	probably benign	Het
Rnf31	T	C	14: 55,592,233	L85P	probably damaging	Het
Rptn	T	C	3: 93,397,900	C847R	possibly damaging	Het
Six4	T	A	12: 73,108,953	E413D	probably benign	Het
Sned1	T	C	1: 93,284,421	V1115A	probably damaging	Het
Spen	T	C	4: 141,493,444	K401E	unknown	Het
Srbd1	T	A	17: 86,136,415	R128W	possibly damaging	Het
Strc	A	T	2: 121,369,058	I1300N	probably damaging	Het
Susd1	T	G	4: 59,390,627	T230P	probably benign	Het
Thumpd2	G	T	17: 81,055,897	S47*	probably null	Het
Tmprss11a	C	T	5: 86,428,570	V141I	probably damaging	Het
Tmprss15	T	C	16: 79,024,853	Y438C	possibly damaging	Het
Tnfrsf1a	T	C	6: 125,356,951	S56P	probably damaging	Het
Ttc39d	T	C	17: 80,216,181	W90R	probably benign	Het
Vmn2r111	T	C	17: 22,559,051	N549S	possibly damaging	Het
Wdr20rt	A	T	12: 65,225,762		probably null	Het
Zfp646	C	A	7: 127,882,322	Q1224K	probably benign	Het

Other mutations in Slc30a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01321:Slc30a2	APN	4	134343300	missense	probably damaging	0.96
IGL01822:Slc30a2	APN	4	134348637	missense	probably damaging	0.98
IGL02808:Slc30a2	APN	4	134344049	missense	possibly damaging	0.65
R1415:Slc30a2	UTSW	4	134349349	missense	probably damaging	1.00
R2279:Slc30a2	UTSW	4	134348546	missense	probably benign
R4151:Slc30a2	UTSW	4	134344048	missense	probably benign	0.00
R4278:Slc30a2	UTSW	4	134346049	missense	probably null	1.00
R4783:Slc30a2	UTSW	4	134344006	critical splice acceptor site	probably null
R5823:Slc30a2	UTSW	4	134345978	missense	probably damaging	0.98
R7017:Slc30a2	UTSW	4	134347415	missense	probably damaging	1.00
R7021:Slc30a2	UTSW	4	134347415	missense	probably damaging	1.00
R7034:Slc30a2	UTSW	4	134347342	missense	possibly damaging	0.80
R7053:Slc30a2	UTSW	4	134347415	missense	probably damaging	1.00
R7056:Slc30a2	UTSW	4	134347415	missense	probably damaging	1.00
R7057:Slc30a2	UTSW	4	134347415	missense	probably damaging	1.00
R7067:Slc30a2	UTSW	4	134344218	critical splice donor site	probably null
R7138:Slc30a2	UTSW	4	134344118	missense	probably benign	0.00
R7275:Slc30a2	UTSW	4	134349270	splice site	probably null
R7289:Slc30a2	UTSW	4	134344213	missense	possibly damaging	0.69
R8015:Slc30a2	UTSW	4	134347450	missense	probably benign	0.01
R8359:Slc30a2	UTSW	4	134349379	missense	probably damaging	0.98
Z1176:Slc30a2	UTSW	4	134344089	missense	probably benign	0.00
Z1177:Slc30a2	UTSW	4	134347455	frame shift	probably null

Predicted Primers

PCR Primer
(F):5'- GTACCCAGACATCGTTGGTG -3'
(R):5'- AGCACAGACTCCTTCCCTTG -3'

Sequencing Primer
(F):5'- GAGACCCAGGCCCTGACTTTAC -3'
(R):5'- CCTTCCCTTGGGAGCTGATG -3'

Posted On

2019-05-13