Mutagenetix > Incidental Mutation

Incidental Mutation 'R7057:Slc30a2'

547972

Institutional Source

Beutler Lab

Gene Symbol

Slc30a2

Ensembl Gene

ENSMUSG00000028836

Gene Name

solute carrier family 30 (zinc transporter), member 2

Synonyms

Znt2

MMRRC Submission

045154-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.158) question?

Stock #

R7057 (G1)

Quality Score

225.009

Status

Not validated

Chromosome

Chromosomal Location

134070492-134081795 bp(+) (GRCm39)

Type of Mutation

missense

DNA Base Change (assembly)

G to A at 134074726 bp (GRCm39)

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]

AlphaFold

Q2HJ10

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: 100.0%
10x: 99.8%
20x: 99.2%

Validation Efficiency

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: 67 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
1810009J06Rik	T	A	6: 40,945,181 (GRCm39)	V220D	probably benign	Het
Ankrd1	T	C	19: 36,095,633 (GRCm39)	E113G	possibly damaging	Het
Aqp12	T	C	1: 92,939,718 (GRCm39)	L249P	probably damaging	Het
Atg4a-ps	A	G	3: 103,553,296 (GRCm39)	F15S	possibly damaging	Het
Bub1	T	A	2: 127,671,447 (GRCm39)	M46L	probably benign	Het
C1ra	G	A	6: 124,494,684 (GRCm39)	E316K	probably benign	Het
C2cd4d	A	G	3: 94,270,800 (GRCm39)	H22R	probably benign	Het
Ccdc157	A	G	11: 4,094,586 (GRCm39)	V480A	probably benign	Het
Cdc42ep3	G	A	17: 79,642,952 (GRCm39)		probably benign	Het
Cela1	T	A	15: 100,580,774 (GRCm39)	T161S	possibly damaging	Het
Chtf18	G	T	17: 25,940,100 (GRCm39)	A697E	possibly damaging	Het
Cr2	T	C	1: 194,833,918 (GRCm39)	D957G	possibly damaging	Het
Cyp2c40	A	G	19: 39,796,063 (GRCm39)	V60A	probably damaging	Het
Dazl	CCATGATGGCGGC	CC	17: 50,600,434 (GRCm39)		probably null	Het
Dock2	A	T	11: 34,177,684 (GRCm39)	L1824Q	probably benign	Het
Dock2	T	C	11: 34,586,044 (GRCm39)	Y546C	probably benign	Het
Focad	G	A	4: 88,192,342 (GRCm39)	C557Y	unknown	Het
Ftmt	T	A	18: 52,465,180 (GRCm39)	N165K	probably benign	Het
Gen1	A	C	12: 11,292,419 (GRCm39)	S457A	probably benign	Het
Gja1	T	G	10: 56,264,129 (GRCm39)	S163A	probably benign	Het
Gm8267	T	C	14: 44,959,481 (GRCm39)	I194M	probably damaging	Het
Golga3	T	A	5: 110,336,529 (GRCm39)	S389R	probably damaging	Het
Gpc5	C	A	14: 115,370,654 (GRCm39)	Q87K	possibly damaging	Het
Hmcn2	G	A	2: 31,312,661 (GRCm39)	A3420T	probably damaging	Het
Htt	A	G	5: 34,979,067 (GRCm39)	S817G	probably null	Het
Hus1b	C	T	13: 31,131,533 (GRCm39)	C42Y	possibly damaging	Het
Iars2	A	G	1: 185,021,564 (GRCm39)	F913L	probably benign	Het
Kcna4	A	G	2: 107,125,665 (GRCm39)	E133G	probably damaging	Het
Klhl36	T	C	8: 120,603,536 (GRCm39)	L597P	probably benign	Het
Ltv1	T	C	10: 13,056,646 (GRCm39)	E299G	possibly damaging	Het
Mmp12	A	G	9: 7,357,840 (GRCm39)	Y348C	probably damaging	Het
Mmp12	G	A	9: 7,369,173 (GRCm39)	V270I	probably benign	Het
Mmp2	A	G	8: 93,558,333 (GRCm39)	D134G	probably damaging	Het
Mrpl15	A	T	1: 4,846,865 (GRCm39)	M237K	probably benign	Het
Ms4a6b	G	T	19: 11,504,253 (GRCm39)	V177F	possibly damaging	Het
Muc16	A	G	9: 18,557,375 (GRCm39)	S2973P	unknown	Het
Or1e30	A	C	11: 73,677,974 (GRCm39)	D70A	possibly damaging	Het
Or4c114	A	C	2: 88,904,808 (GRCm39)	I209S	possibly damaging	Het
Or5b120	G	T	19: 13,480,243 (GRCm39)	D179Y	probably damaging	Het
Or5b12b	A	T	19: 12,862,006 (GRCm39)	I254F	probably damaging	Het
Or8b48	A	T	9: 38,493,050 (GRCm39)	H159L	probably damaging	Het
Pikfyve	T	A	1: 65,286,364 (GRCm39)	I1201K	probably benign	Het
Plekhn1	T	G	4: 156,318,374 (GRCm39)	M83L	probably damaging	Het
Pnlip	G	T	19: 58,664,695 (GRCm39)	D212Y	probably damaging	Het
Pomt2	T	C	12: 87,174,152 (GRCm39)	N417S	probably damaging	Het
Pxylp1	T	A	9: 96,707,103 (GRCm39)	M360L	probably benign	Het
Rbak	G	A	5: 143,159,682 (GRCm39)	T457I	possibly damaging	Het
Runx2	A	T	17: 45,125,424 (GRCm39)	W31R	probably null	Het
Sec16a	T	A	2: 26,315,277 (GRCm39)	I1795F	probably damaging	Het
Sik2	A	T	9: 50,909,861 (GRCm39)	I64N	probably damaging	Het
Slc26a8	T	C	17: 28,857,371 (GRCm39)	E924G	possibly damaging	Het
Slc45a4	C	A	15: 73,459,487 (GRCm39)	D174Y	probably damaging	Het
Slc6a6	A	C	6: 91,718,248 (GRCm39)	E354A	probably damaging	Het
Slc8a1	A	T	17: 81,956,524 (GRCm39)	S171R	probably damaging	Het
Srgap1	T	C	10: 121,640,858 (GRCm39)	I669M	probably benign	Het
Stk39	C	A	2: 68,240,471 (GRCm39)	A87S	possibly damaging	Het
Tasor	A	T	14: 27,183,608 (GRCm39)	N689I	probably damaging	Het
Tbx18	C	A	9: 87,587,317 (GRCm39)	S600I	possibly damaging	Het
Tesc	A	C	5: 118,193,025 (GRCm39)	K114Q	probably damaging	Het
Tll1	T	C	8: 64,554,915 (GRCm39)	D256G	probably damaging	Het
Tmem35b	T	A	4: 127,021,679 (GRCm39)	I45K	probably benign	Het
Tnks	T	C	8: 35,307,168 (GRCm39)	D1127G	probably damaging	Het
Trpm8	A	T	1: 88,289,802 (GRCm39)	D920V	probably null	Het
U2af1	A	T	17: 31,867,831 (GRCm39)	D79E	probably benign	Het
Zfp704	T	C	3: 9,535,977 (GRCm39)	D331G	probably damaging	Het
Znrf3	G	T	11: 5,232,442 (GRCm39)	P261Q	probably benign	Het
Zscan4b	A	T	7: 10,635,636 (GRCm39)	C202*	probably null	Het

Other mutations in Slc30a2

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL01321:Slc30a2	APN	4	134,070,611 (GRCm39)	missense	probably damaging	0.96
IGL01822:Slc30a2	APN	4	134,075,948 (GRCm39)	missense	probably damaging	0.98
IGL02808:Slc30a2	APN	4	134,071,360 (GRCm39)	missense	possibly damaging	0.65
R1415:Slc30a2	UTSW	4	134,076,660 (GRCm39)	missense	probably damaging	1.00
R2279:Slc30a2	UTSW	4	134,075,857 (GRCm39)	missense	probably benign
R4151:Slc30a2	UTSW	4	134,071,359 (GRCm39)	missense	probably benign	0.00
R4278:Slc30a2	UTSW	4	134,073,360 (GRCm39)	missense	probably null	1.00
R4783:Slc30a2	UTSW	4	134,071,317 (GRCm39)	critical splice acceptor site	probably null
R5823:Slc30a2	UTSW	4	134,073,289 (GRCm39)	missense	probably damaging	0.98
R7017:Slc30a2	UTSW	4	134,074,726 (GRCm39)	missense	probably damaging	1.00
R7018:Slc30a2	UTSW	4	134,074,726 (GRCm39)	missense	probably damaging	1.00
R7021:Slc30a2	UTSW	4	134,074,726 (GRCm39)	missense	probably damaging	1.00
R7034:Slc30a2	UTSW	4	134,074,653 (GRCm39)	missense	possibly damaging	0.80
R7053:Slc30a2	UTSW	4	134,074,726 (GRCm39)	missense	probably damaging	1.00
R7056:Slc30a2	UTSW	4	134,074,726 (GRCm39)	missense	probably damaging	1.00
R7067:Slc30a2	UTSW	4	134,071,529 (GRCm39)	critical splice donor site	probably null
R7138:Slc30a2	UTSW	4	134,071,429 (GRCm39)	missense	probably benign	0.00
R7275:Slc30a2	UTSW	4	134,076,581 (GRCm39)	splice site	probably null
R7289:Slc30a2	UTSW	4	134,071,524 (GRCm39)	missense	possibly damaging	0.69
R8015:Slc30a2	UTSW	4	134,074,761 (GRCm39)	missense	probably benign	0.01
R8359:Slc30a2	UTSW	4	134,076,690 (GRCm39)	missense	probably damaging	0.98
Z1176:Slc30a2	UTSW	4	134,071,400 (GRCm39)	missense	probably benign	0.00
Z1177:Slc30a2	UTSW	4	134,074,766 (GRCm39)	frame shift	probably null

Predicted Primers

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

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

Posted On

2019-05-13