Incidental Mutation 'R2436:Slc16a9'
ID 249591
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 040397-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R2436 (G1)
Quality Score 167
Status Not validated
Chromosome 10
Chromosomal Location 70081106-70121781 bp(+) (GRCm39)
Type of Mutation frame shift
DNA Base Change (assembly) TCCCC to TCCCCC at 70091911 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000047912 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046807]
AlphaFold Q7TM99
Predicted Effect probably null
Transcript: ENSMUST00000046807
SMART Domains Protein: ENSMUSP00000047912
Gene: ENSMUSG00000037762

DomainStartEndE-ValueType
Pfam:MFS_1 15 319 6.5e-17 PFAM
Pfam:MFS_1 303 500 1.2e-13 PFAM
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.5%
  • 10x: 97.0%
  • 20x: 94.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 36 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adgrg7 A G 16: 56,582,308 (GRCm39) S277P possibly damaging Het
Arl6ip4 T C 5: 124,254,662 (GRCm39) S52P probably benign Het
Barx2 T C 9: 31,824,383 (GRCm39) H2R probably damaging Het
Calhm3 T C 19: 47,140,404 (GRCm39) T230A probably damaging Het
Card11 C T 5: 140,868,117 (GRCm39) V844M possibly damaging Het
Dnah6 C T 6: 73,126,156 (GRCm39) R1327Q probably benign Het
Dnai4 T C 4: 102,923,549 (GRCm39) I427V probably benign Het
Ehbp1 C A 11: 22,039,524 (GRCm39) probably null Het
Fgg T A 3: 82,921,496 (GRCm39) I393N possibly damaging Het
Foxq1 A T 13: 31,742,516 (GRCm39) probably benign Het
Hmgxb3 T C 18: 61,280,566 (GRCm39) T646A probably benign Het
Homer3 G A 8: 70,745,706 (GRCm39) E324K possibly damaging Het
Krt80 A G 15: 101,257,384 (GRCm39) F183L probably damaging Het
Map3k21 A T 8: 126,668,354 (GRCm39) K647* probably null Het
Mcm3ap A G 10: 76,325,891 (GRCm39) Y1067C probably damaging Het
Myh1 G T 11: 67,104,097 (GRCm39) Q921H probably benign Het
Nme8 A G 13: 19,862,029 (GRCm39) F200S probably damaging Het
Nploc4 T C 11: 120,309,143 (GRCm39) N153S possibly damaging Het
Or14c45 T C 7: 86,176,591 (GRCm39) F209L probably damaging Het
Or2ak6 T C 11: 58,592,952 (GRCm39) C142R probably damaging Het
Or4a73 A G 2: 89,421,117 (GRCm39) V114A probably benign Het
Or5k1 C T 16: 58,617,607 (GRCm39) V201I probably benign Het
Pipox T A 11: 77,782,943 (GRCm39) L86F probably damaging Het
Polr3h G T 15: 81,801,406 (GRCm39) L157I probably benign Het
Prex2 G A 1: 11,336,376 (GRCm39) V1525M possibly damaging Het
Rapgef2 A T 3: 78,996,079 (GRCm39) D561E possibly damaging Het
Sacs A T 14: 61,440,354 (GRCm39) D800V possibly damaging Het
Sbsn A T 7: 30,451,655 (GRCm39) L223F possibly damaging Het
Srrm3 G T 5: 135,864,030 (GRCm39) E43* probably null Het
Tcaf3 G A 6: 42,570,663 (GRCm39) A363V probably damaging Het
Tmem138 A G 19: 10,552,268 (GRCm39) F78S probably damaging Het
Tnfrsf17 G A 16: 11,137,676 (GRCm39) D138N probably damaging Het
Tubgcp6 C T 15: 88,986,568 (GRCm39) V1344I probably benign Het
Usp24 T A 4: 106,266,842 (GRCm39) L1875* probably null Het
Vmn2r109 C A 17: 20,774,798 (GRCm39) G186C probably damaging Het
Zfp541 A G 7: 15,810,373 (GRCm39) N137D 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
R1301:Slc16a9 UTSW 10 70,118,308 (GRCm39) missense probably benign 0.07
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'- GAAAGAGGTATTTTATCCCGAACTCTG -3'
(R):5'- AAGCCTTCCATGCTCTGTACG -3'

Sequencing Primer
(F):5'- GGTATTTTATCCCGAACTCTGTACTC -3'
(R):5'- CTCTGTACGGTATCAATGACACGG -3'
Posted On 2014-11-12