Incidental Mutation 'R5964:Slc45a3'
ID 471921
Institutional Source Beutler Lab
Gene Symbol Slc45a3
Ensembl Gene ENSMUSG00000026435
Gene Name solute carrier family 45, member 3
Synonyms 2210413P12Rik, Pcanap6, IPCA-6
MMRRC Submission 044149-MU
Accession Numbers

Genbank: NM_145977; MGI: 1922082  

Is this an essential gene? Non essential (E-score: 0.000) question?
Stock # R5964 (G1)
Quality Score 207
Status Validated
Chromosome 1
Chromosomal Location 131962967-131982969 bp(+) (GRCm38)
Type of Mutation missense
DNA Base Change (assembly) A to G at 131978073 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 278 (E278G)
Ref Sequence ENSEMBL: ENSMUSP00000136190 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000027695] [ENSMUST00000177943] [ENSMUST00000190322]
AlphaFold Q8K0H7
Predicted Effect probably damaging
Transcript: ENSMUST00000027695
AA Change: E278G

PolyPhen 2 Score 0.982 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000027695
Gene: ENSMUSG00000026435
AA Change: E278G

DomainStartEndE-ValueType
Pfam:MFS_1 18 306 1.2e-12 PFAM
Pfam:MFS_2 21 408 5.4e-11 PFAM
transmembrane domain 520 542 N/A INTRINSIC
Predicted Effect probably damaging
Transcript: ENSMUST00000177943
AA Change: E278G

PolyPhen 2 Score 0.982 (Sensitivity: 0.75; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136190
Gene: ENSMUSG00000026435
AA Change: E278G

DomainStartEndE-ValueType
Pfam:MFS_1 18 306 1.5e-12 PFAM
Pfam:MFS_2 19 239 2.4e-13 PFAM
transmembrane domain 320 342 N/A INTRINSIC
transmembrane domain 355 377 N/A INTRINSIC
transmembrane domain 382 404 N/A INTRINSIC
transmembrane domain 520 542 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000185387
Predicted Effect probably benign
Transcript: ENSMUST00000190322
SMART Domains Protein: ENSMUSP00000140767
Gene: ENSMUSG00000026435

DomainStartEndE-ValueType
Pfam:MFS_2 20 218 3.3e-9 PFAM
Pfam:MFS_1 51 219 1.7e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000191034
Meta Mutation Damage Score 0.1110 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.5%
  • 10x: 97.5%
  • 20x: 92.2%
Validation Efficiency 96% (87/91)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adam15 G A 3: 89,343,567 Q581* probably null Het
Agl A G 3: 116,793,774 V44A probably damaging Het
Alpk3 T A 7: 81,092,260 D608E possibly damaging Het
Aspm C A 1: 139,455,227 probably benign Het
Bbs2 T C 8: 94,068,367 N692S probably benign Het
Bend4 A G 5: 67,417,818 I240T probably benign Het
Casp8 G T 1: 58,833,736 R277L possibly damaging Het
Ccdc61 A T 7: 18,900,940 I123N probably damaging Het
Ccr9 T G 9: 123,779,434 I60M probably benign Het
Cd163 T A 6: 124,326,572 W1066R probably benign Het
Cd226 A T 18: 89,207,183 H68L probably benign Het
Cdkn3 T A 14: 46,767,217 C79S probably null Het
Cnnm1 A T 19: 43,469,723 E658V probably benign Het
Cog7 T C 7: 121,956,029 R304G probably damaging Het
Cpt1a T A 19: 3,365,760 V286E possibly damaging Het
Creg2 C A 1: 39,624,954 R212L probably benign Het
Cyp26a1 T G 19: 37,699,962 S311A probably damaging Het
Cyp2b10 T C 7: 25,926,223 Y484H probably benign Het
Cyp3a44 T A 5: 145,788,467 Y308F possibly damaging Het
Dlg5 A G 14: 24,164,089 V744A probably benign Het
Dlgap2 T A 8: 14,727,128 Y124* probably null Het
Dnah3 T C 7: 119,922,880 D4030G probably benign Het
Dnah5 A G 15: 28,458,584 T4456A possibly damaging Het
Dtx2 T A 5: 136,023,699 V347D probably benign Het
Gigyf2 C T 1: 87,407,167 T294M probably damaging Het
Gli3 C G 13: 15,726,162 S1378* probably null Het
Gm884 A G 11: 103,542,120 S1232P possibly damaging Het
Gnao1 G A 8: 93,966,999 D337N probably benign Het
Gp2 T A 7: 119,449,129 Q422L probably benign Het
Ifit1 T A 19: 34,648,469 M335K possibly damaging Het
Ism1 T C 2: 139,678,757 S30P probably benign Het
Itgax A G 7: 128,140,447 D677G probably damaging Het
Kansl1l G A 1: 66,725,922 A442V probably damaging Het
Kif13a T C 13: 46,771,524 I311M probably damaging Het
Lsm14b T A 2: 180,031,425 S84R probably benign Het
Lzts3 A G 2: 130,636,288 Y297H probably damaging Het
Map4k3 A G 17: 80,644,762 I205T probably damaging Het
Matn2 A T 15: 34,410,165 N501I probably damaging Het
Mctp2 T C 7: 72,103,177 E776G probably damaging Het
Mex3d A T 10: 80,382,587 N265K probably damaging Het
Myo5a A G 9: 75,203,833 T1534A probably benign Het
Ncoa7 T C 10: 30,704,636 M35V probably damaging Het
Nek4 G A 14: 30,957,079 probably null Het
Ngrn T C 7: 80,261,933 probably null Het
Nlrp1a T A 11: 71,123,020 Q468L probably benign Het
Olfr1450 A C 19: 12,954,531 Q314P probably benign Het
Olfr743 T A 14: 50,534,198 M262K probably damaging Het
Phtf2 T C 5: 20,775,934 D433G probably damaging Het
Prdm13 G A 4: 21,683,852 Q140* probably null Het
Prtg G A 9: 72,892,254 G778E probably benign Het
Pum3 T C 19: 27,420,051 E308G probably damaging Het
Pwp1 T G 10: 85,882,886 F306V probably damaging Het
Rab24 A T 13: 55,321,576 Y27N probably damaging Het
Rnf215 T C 11: 4,135,898 F126L probably benign Het
Samd13 A T 3: 146,680,696 probably benign Het
Serac1 T A 17: 6,065,049 H213L probably benign Het
Slit3 C T 11: 35,700,236 R1292C probably damaging Het
Slx4 A T 16: 4,000,951 probably null Het
Smarca4 C A 9: 21,647,430 T631K probably benign Het
Snx16 C T 3: 10,434,481 R163Q possibly damaging Het
Stk40 T C 4: 126,128,895 V140A probably damaging Het
Tcf12 A T 9: 71,868,240 D409E probably damaging Het
Tgfbr2 G T 9: 116,110,255 T168K possibly damaging Het
Ticam1 G T 17: 56,271,703 H131N probably damaging Het
Ttn C A 2: 76,713,511 E31298* probably null Het
Ttn C A 2: 76,829,888 R7458I possibly damaging Het
Usp7 A G 16: 8,712,102 V133A possibly damaging Het
Wbp1l C T 19: 46,654,180 R191* probably null Het
Wdfy4 T C 14: 33,106,011 E1118G probably damaging Het
Zfp81 G C 17: 33,336,845 P3A probably damaging Het
Znhit6 A G 3: 145,576,933 K21R possibly damaging Het
Other mutations in Slc45a3
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00962:Slc45a3 APN 1 131977527 missense probably damaging 0.98
IGL01626:Slc45a3 APN 1 131978987 missense possibly damaging 0.73
IGL01677:Slc45a3 APN 1 131978970 missense probably damaging 0.99
F6893:Slc45a3 UTSW 1 131981337 missense probably benign
R0122:Slc45a3 UTSW 1 131977740 missense probably damaging 1.00
R0402:Slc45a3 UTSW 1 131977527 missense possibly damaging 0.85
R1596:Slc45a3 UTSW 1 131981529 missense probably damaging 1.00
R1647:Slc45a3 UTSW 1 131977524 missense probably damaging 1.00
R1752:Slc45a3 UTSW 1 131977521 missense probably damaging 1.00
R1771:Slc45a3 UTSW 1 131976956 missense possibly damaging 0.51
R1776:Slc45a3 UTSW 1 131976956 missense possibly damaging 0.51
R2071:Slc45a3 UTSW 1 131977632 missense probably damaging 1.00
R2939:Slc45a3 UTSW 1 131977899 missense probably damaging 1.00
R4230:Slc45a3 UTSW 1 131981661 missense probably damaging 0.96
R4876:Slc45a3 UTSW 1 131981547 missense possibly damaging 0.48
R4906:Slc45a3 UTSW 1 131981577 missense probably damaging 1.00
R5265:Slc45a3 UTSW 1 131978194 missense possibly damaging 0.46
R6849:Slc45a3 UTSW 1 131977964 missense probably damaging 1.00
R7483:Slc45a3 UTSW 1 131976811 start gained probably benign
R8104:Slc45a3 UTSW 1 131977016 missense probably benign 0.29
R8322:Slc45a3 UTSW 1 131977785 missense probably damaging 0.99
R8333:Slc45a3 UTSW 1 131978190 missense probably damaging 1.00
R9011:Slc45a3 UTSW 1 131977976 missense probably benign 0.02
R9035:Slc45a3 UTSW 1 131981449 frame shift probably null
R9101:Slc45a3 UTSW 1 131977437 missense possibly damaging 0.51
Predicted Primers PCR Primer
(F):5'- AGCCACTCTGTTTGTGACGG -3'
(R):5'- TTTCCTTTACTGACGGGGAGC -3'

Sequencing Primer
(F):5'- TTTGTGACGGAGGAGGCAGTAC -3'
(R):5'- AGTCACCCAGGGTAGAGTCAC -3'
Posted On 2017-03-31