Incidental Mutation 'R1301:Slc16a9'
ID 158377
Institutional Source Beutler Lab
Gene Symbol Slc16a9
Ensembl Gene ENSMUSG00000037762
Gene Name solute carrier family 16 (monocarboxylic acid transporters), member 9
Synonyms 4930425B13Rik, 1200003C15Rik
MMRRC Submission 039367-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1301 (G1)
Quality Score 225
Status Validated
Chromosome 10
Chromosomal Location 70081106-70121781 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 70118308 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 209 (D209G)
Ref Sequence ENSEMBL: ENSMUSP00000047912 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046807]
AlphaFold Q7TM99
Predicted Effect probably benign
Transcript: ENSMUST00000046807
AA Change: D209G

PolyPhen 2 Score 0.067 (Sensitivity: 0.94; Specificity: 0.84)
SMART Domains Protein: ENSMUSP00000047912
Gene: ENSMUSG00000037762
AA Change: D209G

DomainStartEndE-ValueType
Pfam:MFS_1 15 319 6.5e-17 PFAM
Pfam:MFS_1 303 500 1.2e-13 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000064271
Predicted Effect noncoding transcript
Transcript: ENSMUST00000155933
Predicted Effect noncoding transcript
Transcript: ENSMUST00000161841
Meta Mutation Damage Score 0.1402 question?
Coding Region Coverage
  • 1x: 98.7%
  • 3x: 97.5%
  • 10x: 93.3%
  • 20x: 82.6%
Validation Efficiency 96% (67/70)
Allele List at MGI
Other mutations in this stock
Total: 56 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl4fm2 T A 4: 144,291,635 (GRCm39) I24L probably benign Het
Ano1 A G 7: 144,187,426 (GRCm39) W447R possibly damaging Het
Blm T A 7: 80,105,165 (GRCm39) K103* probably null Het
Camta2 A G 11: 70,567,230 (GRCm39) I675T probably benign Het
Catsperz G A 19: 6,902,450 (GRCm39) R15C probably damaging Het
Chd1l T C 3: 97,510,964 (GRCm39) probably benign Het
Corin C A 5: 72,462,276 (GRCm39) E844D possibly damaging Het
Cyb5rl T G 4: 106,938,104 (GRCm39) M127R probably damaging Het
Dcdc2a A T 13: 25,286,569 (GRCm39) N164I possibly damaging Het
Dnah6 A G 6: 73,185,528 (GRCm39) probably null Het
Emilin2 T C 17: 71,562,960 (GRCm39) probably benign Het
Epb41l2 T A 10: 25,319,800 (GRCm39) V211D probably damaging Het
Fbxo47 C T 11: 97,759,427 (GRCm39) M166I probably benign Het
Golm1 T C 13: 59,786,187 (GRCm39) D335G probably damaging Het
Gpn1 T A 5: 31,660,773 (GRCm39) M188K probably damaging Het
Gpr84 T A 15: 103,217,646 (GRCm39) S144C probably damaging Het
Grm8 G T 6: 27,981,200 (GRCm39) Q237K possibly damaging Het
Gsdmd C A 15: 75,738,908 (GRCm39) probably null Het
Hmgcr G A 13: 96,795,528 (GRCm39) T347I probably damaging Het
Hsd17b7 T A 1: 169,788,774 (GRCm39) probably benign Het
Hsd3b9 G A 3: 98,354,182 (GRCm39) Q106* probably null Het
Klhl7 T G 5: 24,364,489 (GRCm39) W508G probably damaging Het
Lrp2 C A 2: 69,258,948 (GRCm39) D4581Y probably damaging Het
Lrrc7 T C 3: 157,840,968 (GRCm39) N1357D probably benign Het
Macf1 T C 4: 123,380,451 (GRCm39) probably benign Het
Mroh7 T C 4: 106,577,692 (GRCm39) T329A probably damaging Het
Mroh9 C T 1: 162,871,552 (GRCm39) probably null Het
Mta2 A G 19: 8,926,550 (GRCm39) probably benign Het
Myo3a A T 2: 22,271,906 (GRCm39) probably benign Het
Nrip2 A G 6: 128,384,352 (GRCm39) D153G probably benign Het
Nup133 T C 8: 124,644,156 (GRCm39) probably benign Het
Nup210 C T 6: 91,019,329 (GRCm39) V259M possibly damaging Het
Or10ak14 C T 4: 118,610,816 (GRCm39) M308I probably benign Het
Or5b112 A T 19: 13,319,211 (GRCm39) I30F probably benign Het
Or9i14 A T 19: 13,792,726 (GRCm39) V76D probably damaging Het
Otog C T 7: 45,939,113 (GRCm39) R2048C probably damaging Het
Pacc1 T C 1: 191,080,632 (GRCm39) V284A probably damaging Het
Paqr7 T C 4: 134,235,124 (GRCm39) L327P probably damaging Het
Parl A G 16: 20,105,676 (GRCm39) S249P probably damaging Het
Phc1 A G 6: 122,302,833 (GRCm39) I230T probably benign Het
Pitpnm1 T G 19: 4,160,831 (GRCm39) probably null Het
Plpp1 A G 13: 112,971,477 (GRCm39) Y48C probably damaging Het
Pxdc1 A G 13: 34,812,870 (GRCm39) F194L probably benign Het
Rp1 A T 1: 4,416,159 (GRCm39) V1651D possibly damaging Het
Serpinb1c T A 13: 33,080,943 (GRCm39) R47* probably null Het
Sis T C 3: 72,853,915 (GRCm39) T521A possibly damaging Het
Slc26a4 A T 12: 31,575,567 (GRCm39) C706* probably null Het
Slc37a2 A G 9: 37,148,177 (GRCm39) V325A probably benign Het
Speg T A 1: 75,378,145 (GRCm39) D784E probably damaging Het
Sycp1 T C 3: 102,827,938 (GRCm39) I270V probably benign Het
Tatdn2 T A 6: 113,681,076 (GRCm39) F309I probably damaging Het
Tmem67 T C 4: 12,089,400 (GRCm39) probably benign Het
Trpm1 T A 7: 63,852,801 (GRCm39) probably null Het
Wrn T C 8: 33,782,714 (GRCm39) R496G probably damaging Het
Zfhx2 A G 14: 55,300,854 (GRCm39) V2299A probably benign Het
Zfp819 T A 7: 43,266,524 (GRCm39) S260T possibly damaging Het
Other mutations in Slc16a9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00159:Slc16a9 APN 10 70,118,529 (GRCm39) missense probably benign 0.04
IGL01725:Slc16a9 APN 10 70,119,815 (GRCm39) missense probably benign
IGL02963:Slc16a9 APN 10 70,102,966 (GRCm39) missense probably damaging 1.00
PIT4810001:Slc16a9 UTSW 10 70,119,762 (GRCm39) nonsense probably null
R2436:Slc16a9 UTSW 10 70,091,911 (GRCm39) frame shift probably null
R4036:Slc16a9 UTSW 10 70,110,786 (GRCm39) missense probably damaging 1.00
R4591:Slc16a9 UTSW 10 70,118,710 (GRCm39) missense probably damaging 1.00
R5377:Slc16a9 UTSW 10 70,118,958 (GRCm39) missense probably damaging 1.00
R5868:Slc16a9 UTSW 10 70,118,320 (GRCm39) missense probably benign 0.01
R7313:Slc16a9 UTSW 10 70,119,000 (GRCm39) missense probably damaging 1.00
R9044:Slc16a9 UTSW 10 70,110,797 (GRCm39) missense probably benign 0.06
R9789:Slc16a9 UTSW 10 70,118,340 (GRCm39) missense possibly damaging 0.93
Z1176:Slc16a9 UTSW 10 70,119,856 (GRCm39) missense probably benign 0.15
Predicted Primers PCR Primer
(F):5'- TGGGTCTATTCATCTACGCAGCTCTG -3'
(R):5'- AGCAGCGATGGTGGAAATCCTC -3'

Sequencing Primer
(F):5'- GCAGAGGATGCTGATTGAATTCTATG -3'
(R):5'- ATGGTGGAAATCCTCCGATG -3'
Posted On 2014-02-18