Incidental Mutation 'R1800:Slc39a6'
ID 203095
Institutional Source Beutler Lab
Gene Symbol Slc39a6
Ensembl Gene ENSMUSG00000024270
Gene Name solute carrier family 39 (metal ion transporter), member 6
Synonyms Ermelin, Zip6
MMRRC Submission 039830-MU
Accession Numbers
Essential gene? Possibly essential (E-score: 0.641) question?
Stock # R1800 (G1)
Quality Score 225
Status Not validated
Chromosome 18
Chromosomal Location 24712938-24736874 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 24718259 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glutamic Acid at position 599 (D599E)
Ref Sequence ENSEMBL: ENSMUSP00000064667 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000070726] [ENSMUST00000154205]
AlphaFold Q8C145
Predicted Effect probably damaging
Transcript: ENSMUST00000070726
AA Change: D599E

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000064667
Gene: ENSMUSG00000024270
AA Change: D599E

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
low complexity region 94 141 N/A INTRINSIC
low complexity region 187 198 N/A INTRINSIC
Pfam:Zip 332 753 3e-104 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000154205
AA Change: D315E

PolyPhen 2 Score 0.058 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000122151
Gene: ENSMUSG00000024270
AA Change: D315E

DomainStartEndE-ValueType
Pfam:Zip 48 433 2e-94 PFAM
Coding Region Coverage
  • 1x: 97.4%
  • 3x: 96.8%
  • 10x: 95.0%
  • 20x: 91.2%
Validation Efficiency
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. SLC39A6 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: Mice homozygous for a null allele do not display any gross skin abnormalities. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 92 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1110002E22Rik A G 3: 137,772,479 (GRCm39) K556R probably damaging Het
4933406P04Rik A T 10: 20,186,893 (GRCm39) probably benign Het
Acmsd C A 1: 127,687,493 (GRCm39) Y258* probably null Het
Adgrf5 A T 17: 43,761,973 (GRCm39) I1223F probably damaging Het
Afp C T 5: 90,638,655 (GRCm39) P6S probably benign Het
Agap2 C A 10: 126,927,540 (GRCm39) H1120Q probably damaging Het
Angpt1 A G 15: 42,375,800 (GRCm39) V152A probably damaging Het
Ankrd1 A T 19: 36,096,759 (GRCm39) F23I probably damaging Het
Armc12 T C 17: 28,757,869 (GRCm39) S334P possibly damaging Het
Arnt2 C A 7: 83,924,583 (GRCm39) D415Y probably damaging Het
Cacna1s G T 1: 136,004,592 (GRCm39) V131L probably benign Het
Cacna2d2 T C 9: 107,404,632 (GRCm39) V1141A possibly damaging Het
Cfap61 T C 2: 145,884,542 (GRCm39) L580P probably damaging Het
Chga A T 12: 102,522,164 (GRCm39) S23C probably damaging Het
Chrna5 A G 9: 54,912,159 (GRCm39) T320A probably damaging Het
Col17a1 G T 19: 47,639,301 (GRCm39) N1081K possibly damaging Het
Cox7b2 A T 5: 71,600,406 (GRCm39) C51S possibly damaging Het
Cstdc3 T A 16: 36,132,895 (GRCm39) D57E probably damaging Het
Cwc22 A T 2: 77,759,797 (GRCm39) D83E possibly damaging Het
D130043K22Rik A C 13: 25,067,877 (GRCm39) D871A probably damaging Het
Dab2 A T 15: 6,464,948 (GRCm39) M361L probably benign Het
Dnah11 A C 12: 117,880,523 (GRCm39) Y3866D probably damaging Het
Dnmbp A G 19: 43,890,159 (GRCm39) I536T probably benign Het
Ehmt1 A T 2: 24,774,302 (GRCm39) S43R probably damaging Het
Ercc5 T C 1: 44,212,540 (GRCm39) L666P probably benign Het
F5 A G 1: 164,010,403 (GRCm39) H378R probably damaging Het
Fat2 A T 11: 55,174,718 (GRCm39) N1998K probably damaging Het
Fbxo28 T C 1: 182,169,099 (GRCm39) D13G unknown Het
Fras1 T C 5: 96,857,741 (GRCm39) S2012P probably benign Het
Gm5624 T A 14: 44,799,302 (GRCm39) N41I probably damaging Het
Gm8104 A G 14: 42,959,028 (GRCm39) I73V possibly damaging Het
Gpr141b T C 13: 19,913,849 (GRCm39) noncoding transcript Het
Gpr68 G A 12: 100,845,167 (GRCm39) P126S probably damaging Het
Gucy1a2 A T 9: 3,582,685 (GRCm39) T156S possibly damaging Het
Hacl1 T A 14: 31,336,221 (GRCm39) Y429F probably damaging Het
Haus3 A C 5: 34,320,916 (GRCm39) L510R probably damaging Het
Helq C T 5: 100,921,990 (GRCm39) G738D probably benign Het
Hsd3b2 G C 3: 98,619,553 (GRCm39) P131A probably damaging Het
Il22ra1 G T 4: 135,475,471 (GRCm39) C247F probably benign Het
Ivl T C 3: 92,479,891 (GRCm39) E58G unknown Het
Kcnk9 G T 15: 72,417,948 (GRCm39) Q61K probably benign Het
Kremen1 CGGG CGGGGGG 11: 5,151,791 (GRCm39) probably benign Het
Loxhd1 G T 18: 77,490,198 (GRCm39) A1314S probably damaging Het
Lratd1 T C 12: 14,200,226 (GRCm39) Y167C probably damaging Het
Lrba A G 3: 86,259,175 (GRCm39) I1397V probably benign Het
Lrig3 T A 10: 125,832,920 (GRCm39) probably null Het
Lrrc36 A G 8: 106,176,397 (GRCm39) D378G probably damaging Het
Lrrc49 G A 9: 60,505,474 (GRCm39) T527I probably damaging Het
Map4k4 C A 1: 40,062,620 (GRCm39) T1195K probably damaging Het
Mrps33 G A 6: 39,779,429 (GRCm39) R89C probably damaging Het
Mtor T C 4: 148,547,349 (GRCm39) V444A probably benign Het
Myh2 A G 11: 67,079,764 (GRCm39) E1046G probably damaging Het
Myo15b G T 11: 115,771,335 (GRCm39) probably null Het
Myo5c T C 9: 75,153,446 (GRCm39) Y111H probably damaging Het
Ncoa4-ps A T 12: 119,225,506 (GRCm39) noncoding transcript Het
Ndufv2 G C 17: 66,390,481 (GRCm39) T163R probably damaging Het
Nf1 A G 11: 79,444,794 (GRCm39) N373S possibly damaging Het
Nwd2 A G 5: 63,962,917 (GRCm39) M834V probably benign Het
Ogfod2 T C 5: 124,253,019 (GRCm39) V343A probably damaging Het
Or11g2 C T 14: 50,856,143 (GRCm39) L155F probably benign Het
Or11j4 C A 14: 50,630,786 (GRCm39) S191* probably null Het
Or3a1b A T 11: 74,012,234 (GRCm39) T40S probably benign Het
Or4c115 T A 2: 88,928,050 (GRCm39) T74S probably benign Het
Or51ag1 T C 7: 103,155,248 (GRCm39) I302V possibly damaging Het
Or52ab2 T A 7: 102,969,621 (GRCm39) M1K probably null Het
Or8g34 A T 9: 39,373,410 (GRCm39) I228F probably damaging Het
Parp1 T A 1: 180,428,091 (GRCm39) probably null Het
Ppp3ca A T 3: 136,640,792 (GRCm39) I448F probably damaging Het
Prss44 T C 9: 110,646,272 (GRCm39) V333A probably damaging Het
Pxk C T 14: 8,151,507 (GRCm38) R441* probably null Het
Rars1 A C 11: 35,716,822 (GRCm39) D231E probably benign Het
Rfc1 T C 5: 65,421,722 (GRCm39) Y1059C probably damaging Het
Rilpl1 T A 5: 124,652,719 (GRCm39) I2F probably damaging Het
Sarm1 G T 11: 78,381,820 (GRCm39) A221E possibly damaging Het
Serpina3f A G 12: 104,183,665 (GRCm39) T176A probably damaging Het
Slc22a20 T C 19: 6,035,695 (GRCm39) E131G probably benign Het
Slc26a11 T C 11: 119,263,979 (GRCm39) V343A probably damaging Het
Slc2a4 A G 11: 69,837,133 (GRCm39) I9T probably benign Het
Slc5a6 G T 5: 31,198,020 (GRCm39) S285* probably null Het
Spata9 A G 13: 76,125,760 (GRCm39) H81R probably benign Het
St7l A G 3: 104,826,812 (GRCm39) E436G probably damaging Het
Tecrl A G 5: 83,427,077 (GRCm39) I357T probably damaging Het
Thop1 C T 10: 80,909,043 (GRCm39) R25C probably damaging Het
Tmprss12 A G 15: 100,190,428 (GRCm39) E266G probably benign Het
Tpgs1 T A 10: 79,511,344 (GRCm39) V162D possibly damaging Het
Trpa1 C T 1: 14,944,648 (GRCm39) R1032Q probably benign Het
Tspan12 A G 6: 21,795,699 (GRCm39) Y164H probably damaging Het
Ubr4 T C 4: 139,135,274 (GRCm39) Y869H probably damaging Het
Vmn1r21 A G 6: 57,820,799 (GRCm39) I215T probably benign Het
Zan A T 5: 137,384,713 (GRCm39) S5104T unknown Het
Zfp318 T C 17: 46,722,980 (GRCm39) V1661A probably benign Het
Zfp365 C T 10: 67,724,772 (GRCm39) R372K probably damaging Het
Other mutations in Slc39a6
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00943:Slc39a6 APN 18 24,722,802 (GRCm39) critical splice donor site probably null
IGL01412:Slc39a6 APN 18 24,718,413 (GRCm39) missense probably damaging 1.00
IGL02182:Slc39a6 APN 18 24,734,347 (GRCm39) missense probably damaging 0.99
IGL02332:Slc39a6 APN 18 24,722,880 (GRCm39) missense probably benign 0.22
IGL02648:Slc39a6 APN 18 24,715,424 (GRCm39) missense probably damaging 1.00
Lobar UTSW 18 24,729,386 (GRCm39) nonsense probably null
R0066:Slc39a6 UTSW 18 24,732,326 (GRCm39) missense probably damaging 1.00
R0066:Slc39a6 UTSW 18 24,732,326 (GRCm39) missense probably damaging 1.00
R0729:Slc39a6 UTSW 18 24,734,527 (GRCm39) missense probably benign 0.00
R1128:Slc39a6 UTSW 18 24,718,349 (GRCm39) missense probably damaging 1.00
R1621:Slc39a6 UTSW 18 24,733,946 (GRCm39) missense probably benign 0.08
R1799:Slc39a6 UTSW 18 24,718,524 (GRCm39) missense probably benign 0.00
R1885:Slc39a6 UTSW 18 24,734,539 (GRCm39) splice site probably null
R4159:Slc39a6 UTSW 18 24,730,885 (GRCm39) missense possibly damaging 0.88
R4809:Slc39a6 UTSW 18 24,718,531 (GRCm39) nonsense probably null
R4903:Slc39a6 UTSW 18 24,730,925 (GRCm39) missense probably damaging 1.00
R4994:Slc39a6 UTSW 18 24,729,351 (GRCm39) missense probably damaging 1.00
R5352:Slc39a6 UTSW 18 24,734,093 (GRCm39) missense probably benign 0.00
R5398:Slc39a6 UTSW 18 24,730,936 (GRCm39) missense probably damaging 1.00
R5832:Slc39a6 UTSW 18 24,734,669 (GRCm39) missense possibly damaging 0.81
R6182:Slc39a6 UTSW 18 24,734,013 (GRCm39) missense probably benign 0.16
R6853:Slc39a6 UTSW 18 24,732,376 (GRCm39) missense possibly damaging 0.71
R7226:Slc39a6 UTSW 18 24,717,084 (GRCm39) missense probably damaging 1.00
R7252:Slc39a6 UTSW 18 24,734,442 (GRCm39) missense possibly damaging 0.64
R7263:Slc39a6 UTSW 18 24,734,260 (GRCm39) missense probably benign
R7328:Slc39a6 UTSW 18 24,733,987 (GRCm39) missense probably benign 0.00
R7388:Slc39a6 UTSW 18 24,717,106 (GRCm39) missense probably damaging 1.00
R7395:Slc39a6 UTSW 18 24,718,332 (GRCm39) missense probably damaging 1.00
R8393:Slc39a6 UTSW 18 24,732,331 (GRCm39) missense possibly damaging 0.89
R8695:Slc39a6 UTSW 18 24,736,811 (GRCm39) unclassified probably benign
R8889:Slc39a6 UTSW 18 24,729,386 (GRCm39) nonsense probably null
R8892:Slc39a6 UTSW 18 24,729,386 (GRCm39) nonsense probably null
R9172:Slc39a6 UTSW 18 24,715,399 (GRCm39) missense probably damaging 0.99
R9178:Slc39a6 UTSW 18 24,733,970 (GRCm39) missense probably damaging 0.99
R9215:Slc39a6 UTSW 18 24,732,323 (GRCm39) missense probably benign 0.04
R9349:Slc39a6 UTSW 18 24,718,493 (GRCm39) missense probably benign
X0065:Slc39a6 UTSW 18 24,718,432 (GRCm39) missense possibly damaging 0.95
Z1176:Slc39a6 UTSW 18 24,718,372 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTAGCCCATATTTCCTGAGCAC -3'
(R):5'- AATGAATATGTGCCCAGGGG -3'

Sequencing Primer
(F):5'- CCTGAGCACTTCATTATTAGAAAGC -3'
(R):5'- GCTGCAAGAACAAGTGCCATTC -3'
Posted On 2014-06-23