Incidental Mutation 'R6712:Mfsd9'
ID 529157
Institutional Source Beutler Lab
Gene Symbol Mfsd9
Ensembl Gene ENSMUSG00000041945
Gene Name major facilitator superfamily domain containing 9
Synonyms 4931419K03Rik
MMRRC Submission 044830-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.056) question?
Stock # R6712 (G1)
Quality Score 84.0076
Status Not validated
Chromosome 1
Chromosomal Location 40811200-40829817 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) T to C at 40825601 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000035727 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000039672] [ENSMUST00000131390]
AlphaFold Q8C0T7
Predicted Effect probably null
Transcript: ENSMUST00000039672
SMART Domains Protein: ENSMUSP00000035727
Gene: ENSMUSG00000041945

DomainStartEndE-ValueType
low complexity region 16 32 N/A INTRINSIC
Pfam:Sugar_tr 39 301 4.7e-8 PFAM
Pfam:MFS_1 39 419 1.8e-42 PFAM
low complexity region 436 447 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000131390
SMART Domains Protein: ENSMUSP00000137884
Gene: ENSMUSG00000041945

DomainStartEndE-ValueType
low complexity region 16 32 N/A INTRINSIC
low complexity region 36 46 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000144385
Predicted Effect noncoding transcript
Transcript: ENSMUST00000195134
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 96.1%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 33 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Akap8l G A 17: 32,551,862 (GRCm39) T443M probably damaging Het
Ankmy1 A T 1: 92,798,644 (GRCm39) V950D probably damaging Het
Cep350 T C 1: 155,733,852 (GRCm39) K3014E possibly damaging Het
Col5a3 C T 9: 20,690,329 (GRCm39) G1162R probably damaging Het
Dmxl2 A G 9: 54,318,908 (GRCm39) Y1586H probably damaging Het
Dnah11 A T 12: 118,014,457 (GRCm39) I2010N probably damaging Het
Dock10 T A 1: 80,514,583 (GRCm39) M1446L probably benign Het
Fcmr T C 1: 130,805,588 (GRCm39) L274P probably damaging Het
Foxn1 T G 11: 78,252,085 (GRCm39) D382A probably damaging Het
Gpr179 T C 11: 97,226,993 (GRCm39) R1721G possibly damaging Het
H2aj A G 6: 136,785,524 (GRCm39) I63V probably benign Het
Mis18a T C 16: 90,524,045 (GRCm39) E39G possibly damaging Het
Mmp27 A T 9: 7,572,177 (GRCm39) T126S probably damaging Het
Myo1c C T 11: 75,562,461 (GRCm39) P918S probably benign Het
Myo5a A C 9: 75,120,182 (GRCm39) D1635A probably benign Het
Ngdn T C 14: 55,253,645 (GRCm39) V11A probably benign Het
Nlrc4 A T 17: 74,753,831 (GRCm39) M184K probably damaging Het
Or10h28 T G 17: 33,488,242 (GRCm39) H181Q possibly damaging Het
Or52e15 A T 7: 104,645,625 (GRCm39) I162K possibly damaging Het
Peli2 C A 14: 48,488,051 (GRCm39) Q81K probably benign Het
Pfdn2 T A 1: 171,185,419 (GRCm39) I97K probably damaging Het
Pknox1 C A 17: 31,814,290 (GRCm39) T205K probably benign Het
Polh T C 17: 46,501,655 (GRCm39) S179G probably benign Het
Ppp4r4 G A 12: 103,562,702 (GRCm39) R557Q probably damaging Het
Sipa1 A T 19: 5,710,847 (GRCm39) D54E possibly damaging Het
Tmc8 C A 11: 117,675,639 (GRCm39) N185K probably benign Het
Tns1 C A 1: 74,118,460 (GRCm39) E57* probably null Het
Tyro3 G A 2: 119,635,335 (GRCm39) A209T probably null Het
Ube2f T A 1: 91,204,171 (GRCm39) C116S possibly damaging Het
Vmn1r231 T C 17: 21,109,992 (GRCm39) T308A possibly damaging Het
Wwc2 T A 8: 48,353,838 (GRCm39) M99L probably benign Het
Zfp516 C T 18: 82,975,433 (GRCm39) R544C probably damaging Het
Zfp764l1 A T 7: 126,991,482 (GRCm39) H168Q probably damaging Het
Other mutations in Mfsd9
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00946:Mfsd9 APN 1 40,812,940 (GRCm39) missense probably benign 0.22
IGL01453:Mfsd9 APN 1 40,829,638 (GRCm39) splice site probably benign
R0631:Mfsd9 UTSW 1 40,829,634 (GRCm39) splice site probably benign
R1644:Mfsd9 UTSW 1 40,812,958 (GRCm39) missense probably benign 0.39
R4204:Mfsd9 UTSW 1 40,820,670 (GRCm39) missense probably damaging 1.00
R4761:Mfsd9 UTSW 1 40,813,635 (GRCm39) missense possibly damaging 0.61
R4777:Mfsd9 UTSW 1 40,820,700 (GRCm39) missense possibly damaging 0.64
R5109:Mfsd9 UTSW 1 40,813,365 (GRCm39) missense probably damaging 0.98
R8776:Mfsd9 UTSW 1 40,812,915 (GRCm39) makesense probably null
R8776-TAIL:Mfsd9 UTSW 1 40,812,915 (GRCm39) makesense probably null
R8839:Mfsd9 UTSW 1 40,813,554 (GRCm39) missense probably benign
R9411:Mfsd9 UTSW 1 40,829,692 (GRCm39) missense probably damaging 0.98
R9478:Mfsd9 UTSW 1 40,812,941 (GRCm39) missense probably benign 0.00
R9499:Mfsd9 UTSW 1 40,813,152 (GRCm39) missense probably damaging 0.96
R9551:Mfsd9 UTSW 1 40,813,152 (GRCm39) missense probably damaging 0.96
Predicted Primers PCR Primer
(F):5'- TTGCAAAACGCCGTATGAGG -3'
(R):5'- ACAGCTCTTTGTCCTCATAGG -3'

Sequencing Primer
(F):5'- GGCCGTTGCTAAATAAACTTGGC -3'
(R):5'- GTCCTCATAGGTAGCCAATATTGC -3'
Posted On 2018-07-24