Mutagenetix > Incidental Mutation

Incidental Mutation 'R4726:Slc39a14'

358488

Institutional Source

Beutler Lab

Gene Symbol

Slc39a14

Ensembl Gene

ENSMUSG00000022094

Gene Name

solute carrier family 39 (zinc transporter), member 14

Synonyms

Zip14, G630015O18Rik

MMRRC Submission

041989-MU

Accession Numbers

Essential gene?

Probably non essential (E-score: 0.135) question?

Stock #

R4726 (G1)

Quality Score

225

Status

Validated

Chromosome

Chromosomal Location

70540918-70588874 bp(-) (GRCm39)

Type of Mutation

critical splice donor site (2 bp from exon)

DNA Base Change (assembly)

A to G at 70551048 bp (GRCm39)

Zygosity

Heterozygous

Amino Acid Change

Ref Sequence

ENSEMBL: ENSMUSP00000066108 (fasta)

Gene Model

predicted gene model for transcript(s): [ENSMUST00000022688] [ENSMUST00000068044] [ENSMUST00000127000] [ENSMUST00000143153] [ENSMUST00000151011] [ENSMUST00000152442] [ENSMUST00000152067]

AlphaFold

Q75N73

Predicted Effect

probably benign
Transcript: ENSMUST00000022688

SMART Domains

Protein: ENSMUSP00000022688
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
Pfam:Zip	149	480	4.4e-72	PFAM

Predicted Effect

probably null
Transcript: ENSMUST00000068044

SMART Domains

Protein: ENSMUSP00000066108
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
Pfam:Zip	149	480	5.4e-73	PFAM

Predicted Effect

probably benign
Transcript: ENSMUST00000127000

SMART Domains

Protein: ENSMUSP00000117792
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000143153

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000145040

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000146453

Predicted Effect

probably benign
Transcript: ENSMUST00000151011

SMART Domains

Protein: ENSMUSP00000118319
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000152202

Predicted Effect

noncoding transcript
Transcript: ENSMUST00000155825

Predicted Effect

probably benign
Transcript: ENSMUST00000152442

SMART Domains

Protein: ENSMUSP00000117010
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC

Predicted Effect

probably benign
Transcript: ENSMUST00000152067

SMART Domains

Protein: ENSMUSP00000119040
Gene: ENSMUSG00000022094

Domain	Start	End	E-Value	Type
signal peptide	1	28	N/A	INTRINSIC
Pfam:Zip	149	480	3.3e-69	PFAM

Meta Mutation Damage Score

0.9485

Coding Region Coverage

1x: 99.2%
3x: 98.6%
10x: 97.1%
20x: 94.8%

Validation Efficiency

99% (74/75)

MGI Phenotype

FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] Zinc is an essential cofactor for hundreds of enzymes. It is involved in protein, nucleic acid, carbohydrate, and lipid metabolism, as well as in the control of gene transcription, growth, development, and differentiation. SLC39A14 belongs to a subfamily of proteins that show structural characteristics of zinc transporters (Taylor and Nicholson, 2003 [PubMed 12659941]).[supplied by OMIM, Mar 2008]
PHENOTYPE: Homozygotes for a null allele show dwarfism, scoliosis, osteopenia, short long bones, altered gluconeogenesis and chondrocyte differentiation, low plasma IGF-I and liver zinc levels. Homozygotes for another null allele show reduced liver zinc levels and hepatocyte proliferation after hepatectomy. [provided by MGI curators]

Allele List at MGI

Other mutations in this stock

Total: 71 list
Gene	Ref	Var	Chr/Loc	Mutation	Predicted Effect	Zygosity
4930583I09Rik	T	C	17: 65,141,448 (GRCm39)	S52G	probably null	Het
Abcc2	T	C	19: 43,820,553 (GRCm39)	S1351P	probably benign	Het
Acp2	T	A	2: 91,034,622 (GRCm39)	L87Q	probably damaging	Het
Adgrl3	C	A	5: 81,794,425 (GRCm39)	T550K	possibly damaging	Het
Amotl2	A	G	9: 102,601,018 (GRCm39)	R329G	probably benign	Het
Angel1	T	C	12: 86,768,649 (GRCm39)	N278S	probably damaging	Het
Ankrd12	A	C	17: 66,277,319 (GRCm39)	M1985R	probably damaging	Het
Apob	T	A	12: 8,040,267 (GRCm39)	F535I	probably damaging	Het
Art3	A	G	5: 92,559,002 (GRCm39)	K313R	probably benign	Het
Asxl2	C	T	12: 3,551,872 (GRCm39)	H1205Y	possibly damaging	Het
Bsph1	A	T	7: 13,206,920 (GRCm39)	M99L	probably benign	Het
Ccdc153	T	C	9: 44,154,963 (GRCm39)		probably null	Het
Cdh16	A	T	8: 105,342,664 (GRCm39)	M28K	probably damaging	Het
Cdhr2	T	C	13: 54,866,352 (GRCm39)	F353L	probably damaging	Het
Chrna2	G	T	14: 66,386,345 (GRCm39)	V164L	possibly damaging	Het
Cip2a	A	G	16: 48,834,433 (GRCm39)	T672A	probably benign	Het
Ckmt1	T	C	2: 121,191,712 (GRCm39)		probably null	Het
Col25a1	A	T	3: 130,313,430 (GRCm39)	E280V	possibly damaging	Het
Dnajc12	A	G	10: 63,233,087 (GRCm39)	D76G	probably damaging	Het
Drd3	G	T	16: 43,643,164 (GRCm39)	E467*	probably null	Het
Ecpas	A	G	4: 58,844,191 (GRCm39)	V525A	probably damaging	Het
Ehbp1l1	C	A	19: 5,769,204 (GRCm39)	A700S	possibly damaging	Het
Gab1	T	C	8: 81,515,682 (GRCm39)	D212G	possibly damaging	Het
Gm26996	A	G	6: 130,557,134 (GRCm39)		noncoding transcript	Het
Gm28113	A	G	15: 75,198,577 (GRCm39)		noncoding transcript	Het
Has3	T	C	8: 107,604,718 (GRCm39)	F308S	probably damaging	Het
Ifit3b	T	A	19: 34,588,860 (GRCm39)	I12N	probably benign	Het
Ifna4	C	A	4: 88,760,519 (GRCm39)	T141K	probably benign	Het
Ints3	A	G	3: 90,301,084 (GRCm39)	S840P	probably damaging	Het
Itih4	T	C	14: 30,611,792 (GRCm39)	V132A	probably damaging	Het
Itprid2	T	A	2: 79,493,101 (GRCm39)	I1216N	probably damaging	Het
Kcnj10	A	G	1: 172,196,639 (GRCm39)	Y51C	probably damaging	Het
Klk1b24	G	A	7: 43,839,820 (GRCm39)	V60I	probably damaging	Het
Klra14-ps	C	A	6: 130,134,626 (GRCm39)		noncoding transcript	Het
Krt6b	A	G	15: 101,586,520 (GRCm39)	I323T	probably damaging	Het
Lilra5	A	C	7: 4,240,957 (GRCm39)	Q17P	probably benign	Het
Lrrc7	GAAGTTGTTTGGAGATTCTTATCTTA	GA	3: 158,024,045 (GRCm39)		probably benign	Het
Map3k4	T	C	17: 12,451,851 (GRCm39)	N1479S	possibly damaging	Het
Mbd3l2	A	T	9: 18,356,256 (GRCm39)	I194F	probably damaging	Het
Megf10	T	C	18: 57,420,864 (GRCm39)	I834T	probably benign	Het
Mterf4	G	A	1: 93,229,471 (GRCm39)	T251M	probably damaging	Het
Mtmr3	A	T	11: 4,457,634 (GRCm39)	D170E	probably damaging	Het
Myom3	C	T	4: 135,534,586 (GRCm39)		probably null	Het
Nemp1	G	A	10: 127,530,462 (GRCm39)	V305I	probably benign	Het
Nlrp1b	G	T	11: 71,072,232 (GRCm39)	T537K	probably benign	Het
Npdc1	G	A	2: 25,298,957 (GRCm39)	D284N	probably damaging	Het
Or5b3	T	A	19: 13,388,469 (GRCm39)	C179S	probably damaging	Het
Or6c206	A	G	10: 129,097,045 (GRCm39)	T72A	possibly damaging	Het
Or8k28	A	G	2: 86,286,580 (GRCm39)	F12L	possibly damaging	Het
Pias1	A	G	9: 62,827,771 (GRCm39)	V212A	probably damaging	Het
Plscr1	T	A	9: 92,145,221 (GRCm39)	V77D	probably damaging	Het
Plxna1	T	C	6: 89,299,798 (GRCm39)	N1657S	probably damaging	Het
Ptprf	A	G	4: 118,069,414 (GRCm39)	V1551A	possibly damaging	Het
Ptprn2	C	A	12: 117,211,393 (GRCm39)	Y857*	probably null	Het
Puf60	A	T	15: 75,944,183 (GRCm39)		probably null	Het
Rnf20	C	T	4: 49,654,579 (GRCm39)	R879*	probably null	Het
Robo1	G	A	16: 72,768,931 (GRCm39)	A499T	probably damaging	Het
Smarcad1	A	T	6: 65,052,025 (GRCm39)	H6L	probably damaging	Het
Smg5	A	G	3: 88,243,758 (GRCm39)	S10G	possibly damaging	Het
Stk39	T	A	2: 68,093,647 (GRCm39)	D488V	probably damaging	Het
Stx19	A	G	16: 62,642,495 (GRCm39)	N104D	probably benign	Het
Tcstv1b	A	T	13: 120,635,173 (GRCm39)	S152C	possibly damaging	Het
Tmem222	T	C	4: 133,004,975 (GRCm39)	M21V	probably benign	Het
Trim43b	T	A	9: 88,971,538 (GRCm39)	N205I	possibly damaging	Het
Ubr4	C	A	4: 139,209,890 (GRCm39)	H5017N	possibly damaging	Het
Vmn2r93	A	G	17: 18,536,960 (GRCm39)	T548A	probably damaging	Het
Vps8	G	A	16: 21,267,154 (GRCm39)		probably null	Het
Wasl	A	G	6: 24,633,110 (GRCm39)	V176A	probably benign	Het
Wbp2nl	T	A	15: 82,190,255 (GRCm39)	V61E	probably damaging	Het
Zfp959	T	A	17: 56,205,260 (GRCm39)		probably null	Het
Zmiz1	T	C	14: 25,644,098 (GRCm39)		probably null	Het

Other mutations in Slc39a14

Allele	Source	Chr	Coord	Type	Predicted Effect	PPH Score
IGL02183:Slc39a14	APN	14	70,544,134 (GRCm39)	missense	possibly damaging	0.91
IGL02348:Slc39a14	APN	14	70,553,885 (GRCm39)	critical splice donor site	probably null
IGL03108:Slc39a14	APN	14	70,556,368 (GRCm39)	missense	probably damaging	0.98
IGL03391:Slc39a14	APN	14	70,547,291 (GRCm39)	missense	probably damaging	1.00
R1741:Slc39a14	UTSW	14	70,556,193 (GRCm39)	missense	probably damaging	1.00
R2437:Slc39a14	UTSW	14	70,553,885 (GRCm39)	critical splice donor site	probably null
R4808:Slc39a14	UTSW	14	70,553,250 (GRCm39)	missense	probably damaging	1.00
R4911:Slc39a14	UTSW	14	70,547,371 (GRCm39)	missense	probably benign	0.00
R4957:Slc39a14	UTSW	14	70,553,260 (GRCm39)	missense	probably damaging	0.99
R5815:Slc39a14	UTSW	14	70,544,194 (GRCm39)	missense	probably damaging	1.00
R6393:Slc39a14	UTSW	14	70,547,262 (GRCm39)	missense	probably benign	0.02
R6464:Slc39a14	UTSW	14	70,544,177 (GRCm39)	missense	probably damaging	0.98
R6466:Slc39a14	UTSW	14	70,547,335 (GRCm39)	missense	probably damaging	1.00
R6757:Slc39a14	UTSW	14	70,548,333 (GRCm39)	missense	probably damaging	1.00
R6969:Slc39a14	UTSW	14	70,546,275 (GRCm39)	missense	probably damaging	0.99
R7569:Slc39a14	UTSW	14	70,547,276 (GRCm39)	missense	possibly damaging	0.66
R7711:Slc39a14	UTSW	14	70,551,124 (GRCm39)	missense	probably damaging	1.00
R7830:Slc39a14	UTSW	14	70,547,566 (GRCm39)	missense	probably benign	0.00
R8075:Slc39a14	UTSW	14	70,546,247 (GRCm39)	missense	possibly damaging	0.87
R9171:Slc39a14	UTSW	14	70,547,687 (GRCm39)	missense	probably benign	0.01
R9371:Slc39a14	UTSW	14	70,547,569 (GRCm39)	missense	probably benign
R9576:Slc39a14	UTSW	14	70,556,235 (GRCm39)	missense	probably benign
R9653:Slc39a14	UTSW	14	70,547,248 (GRCm39)	missense	probably damaging	1.00

Predicted Primers

PCR Primer
(F):5'- CTCGTCCATGTGTGGGGTCT -3'
(R):5'- ACCCACAATTCTCCTGTCCA -3'

Sequencing Primer
(F):5'- TAAGGATGGGATTTTAACCTAGCCC -3'
(R):5'- GGTGGTTGCCTTGCTCCC -3'

Posted On

2015-11-11