Incidental Mutation 'R1927:Mfsd12'
ID214962
Institutional Source Beutler Lab
Gene Symbol Mfsd12
Ensembl Gene ENSMUSG00000034854
Gene Namemajor facilitator superfamily domain containing 12
SynonymsWdt1, F630110N24Rik
MMRRC Submission 039945-MU
Accession Numbers
Is this an essential gene? Possibly essential (E-score: 0.561) question?
Stock #R1927 (G1)
Quality Score225
Status Not validated
Chromosome10
Chromosomal Location81357491-81366225 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) G to T at 81362087 bp
ZygosityHeterozygous
Amino Acid Change Methionine to Isoleucine at position 296 (M296I)
Ref Sequence ENSEMBL: ENSMUSP00000036116 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000020456] [ENSMUST00000044844] [ENSMUST00000132368] [ENSMUST00000140901]
Predicted Effect probably benign
Transcript: ENSMUST00000020456
SMART Domains Protein: ENSMUSP00000020456
Gene: ENSMUSG00000020234

DomainStartEndE-ValueType
Pfam:DUF4531 23 204 1.3e-113 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000044844
AA Change: M296I

PolyPhen 2 Score 0.151 (Sensitivity: 0.92; Specificity: 0.87)
SMART Domains Protein: ENSMUSP00000036116
Gene: ENSMUSG00000034854
AA Change: M296I

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
Pfam:MFS_2 20 423 5.2e-43 PFAM
Pfam:MFS_1 154 416 6.8e-12 PFAM
transmembrane domain 441 463 N/A INTRINSIC
low complexity region 464 476 N/A INTRINSIC
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124512
Predicted Effect noncoding transcript
Transcript: ENSMUST00000130762
Predicted Effect probably benign
Transcript: ENSMUST00000131736
SMART Domains Protein: ENSMUSP00000123068
Gene: ENSMUSG00000020234

DomainStartEndE-ValueType
Pfam:DUF4531 1 128 2.6e-47 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000132368
SMART Domains Protein: ENSMUSP00000120259
Gene: ENSMUSG00000034854

DomainStartEndE-ValueType
low complexity region 2 13 N/A INTRINSIC
Pfam:MFS_2 20 102 3.7e-11 PFAM
low complexity region 118 124 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000140901
SMART Domains Protein: ENSMUSP00000114203
Gene: ENSMUSG00000020235

DomainStartEndE-ValueType
Blast:WD40 172 213 1e-19 BLAST
WD40 218 257 1.2e-2 SMART
WD40 260 297 6.79e-2 SMART
WD40 302 341 3.99e-8 SMART
WD40 344 386 2.84e-4 SMART
WD40 389 429 1.98e1 SMART
WD40 432 471 1.11e-6 SMART
Coding Region Coverage
  • 1x: 97.5%
  • 3x: 96.9%
  • 10x: 95.3%
  • 20x: 92.5%
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for a null allele exhibit a grey (grizzled) coat. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A2m T C 6: 121,636,379 S31P probably damaging Het
Abca12 G T 1: 71,244,840 H2524Q probably damaging Het
Acsl5 T C 19: 55,278,154 V135A probably benign Het
Actl11 T G 9: 107,929,537 L353R possibly damaging Het
Adcy6 G T 15: 98,598,498 probably null Het
B230104I21Rik A G 4: 154,341,237 I697T probably damaging Het
BC061237 G A 14: 44,501,243 R33K possibly damaging Het
Brf1 C A 12: 113,000,344 V5F possibly damaging Het
Chmp2a C T 7: 13,033,936 A21T possibly damaging Het
Cwh43 A G 5: 73,453,074 N607S probably benign Het
Ddhd2 G A 8: 25,741,661 L445F possibly damaging Het
Dicer1 C A 12: 104,702,884 D1180Y possibly damaging Het
Dock5 A T 14: 67,846,062 S133T possibly damaging Het
Dyx1c1 A T 9: 72,960,627 I57L probably damaging Het
Efs A T 14: 54,917,163 C540S possibly damaging Het
Ehd4 C T 2: 120,091,492 G428S probably benign Het
Eml1 C T 12: 108,538,217 R812* probably null Het
Enpp1 C T 10: 24,654,888 D557N possibly damaging Het
Fn3krp A G 11: 121,424,977 T65A probably damaging Het
Galnt5 A G 2: 57,998,603 R72G probably benign Het
Gfod1 C T 13: 43,200,860 R213H possibly damaging Het
Gm10518 A G 1: 179,803,645 probably benign Het
Gm5431 A G 11: 48,889,255 F558S probably damaging Het
Got1 C T 19: 43,515,680 probably null Het
Gucy2g C T 19: 55,237,759 V242I probably benign Het
Hdgfl2 T A 17: 56,099,874 V606E possibly damaging Het
Hoxa3 T C 6: 52,169,999 probably benign Het
Iqub T A 6: 24,491,671 I339L probably benign Het
Kdm4c C T 4: 74,345,483 T668I probably benign Het
Klhl32 T C 4: 24,617,474 I592V probably benign Het
Mfsd4b4 C T 10: 39,892,441 A219T probably damaging Het
Mrpl52 T C 14: 54,426,957 S9P possibly damaging Het
Nbr1 A G 11: 101,567,214 Y273C possibly damaging Het
Ncf4 G T 15: 78,260,646 G217V probably damaging Het
Neo1 T C 9: 58,990,385 E96G probably benign Het
Nid2 T A 14: 19,768,276 N279K probably damaging Het
Nr5a2 A G 1: 136,944,994 Y56H probably damaging Het
Ntn4 C T 10: 93,707,353 R314W probably damaging Het
Nynrin A G 14: 55,863,592 T280A probably benign Het
Olfr1364 A G 13: 21,574,256 F67L probably benign Het
Olfr1367 T A 13: 21,346,946 I6N probably benign Het
Olfr1463 T C 19: 13,235,029 Y260H probably damaging Het
Olfr545 A G 7: 102,494,059 S239P possibly damaging Het
Olfr97 A G 17: 37,231,543 Y276H probably damaging Het
Otog G A 7: 46,246,283 C107Y probably damaging Het
Ptprn A G 1: 75,254,122 V565A probably benign Het
Rbm6 T G 9: 107,852,903 D182A probably damaging Het
Rhbg A G 3: 88,244,552 F400L probably benign Het
Rpl22l1 T A 3: 28,806,589 N33K possibly damaging Het
Rtp1 T A 16: 23,431,209 I108N probably damaging Het
Sema6b A T 17: 56,132,797 F15I probably benign Het
Sirpa C T 2: 129,616,376 T304I possibly damaging Het
Slc22a29 A G 19: 8,207,066 I257T probably benign Het
Slc41a1 T C 1: 131,841,200 I256T probably damaging Het
Smg6 A G 11: 75,142,848 K1208R probably damaging Het
Sorcs1 G T 19: 50,222,195 P744Q probably damaging Het
Sptbn5 T C 2: 120,070,462 T213A probably benign Het
St18 A G 1: 6,802,712 T224A probably benign Het
Stat3 T C 11: 100,894,829 N465S probably damaging Het
Stmn2 T A 3: 8,545,576 M40K probably benign Het
Tespa1 A G 10: 130,348,239 D63G probably benign Het
Thrb T A 14: 18,008,674 C133S probably damaging Het
Tmem25 C T 9: 44,796,483 V172M possibly damaging Het
Tns2 C T 15: 102,108,934 R281C probably damaging Het
Trhde T A 10: 114,800,849 Y151F probably damaging Het
Trp53bp2 A G 1: 182,452,664 T912A probably damaging Het
Unc79 C A 12: 103,169,692 A2269E probably damaging Het
Zfp507 C T 7: 35,793,725 R631Q probably damaging Het
Zfp758 T G 17: 22,375,842 S436R probably damaging Het
Zfp791 G T 8: 85,110,683 T184K probably benign Het
Znrf3 A G 11: 5,281,062 V817A probably benign Het
Other mutations in Mfsd12
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01556:Mfsd12 APN 10 81363024 missense probably damaging 0.98
IGL01928:Mfsd12 APN 10 81365788 unclassified probably benign
P0038:Mfsd12 UTSW 10 81362218 missense probably benign 0.02
R0048:Mfsd12 UTSW 10 81362814 missense possibly damaging 0.77
R0048:Mfsd12 UTSW 10 81362814 missense possibly damaging 0.77
R0152:Mfsd12 UTSW 10 81357799 missense probably damaging 1.00
R0317:Mfsd12 UTSW 10 81357799 missense probably damaging 1.00
R0565:Mfsd12 UTSW 10 81361409 missense probably benign 0.00
R1283:Mfsd12 UTSW 10 81361435 missense probably benign 0.00
R1983:Mfsd12 UTSW 10 81362256 splice site probably null
R1994:Mfsd12 UTSW 10 81357681 missense probably damaging 1.00
R1995:Mfsd12 UTSW 10 81357681 missense probably damaging 1.00
R2055:Mfsd12 UTSW 10 81360229 missense probably damaging 1.00
R2197:Mfsd12 UTSW 10 81357734 missense probably damaging 1.00
R3120:Mfsd12 UTSW 10 81361215 missense probably benign 0.00
R4162:Mfsd12 UTSW 10 81361097 critical splice acceptor site probably null
R4163:Mfsd12 UTSW 10 81361097 critical splice acceptor site probably null
R4417:Mfsd12 UTSW 10 81364703 unclassified probably benign
R5622:Mfsd12 UTSW 10 81363627 missense probably null 0.98
R6407:Mfsd12 UTSW 10 81362233 splice site probably null
R7759:Mfsd12 UTSW 10 81363593 missense probably benign 0.10
R7780:Mfsd12 UTSW 10 81357884 missense probably benign 0.19
Predicted Primers PCR Primer
(F):5'- AGTCAATACTATGGAAGCCCTCAG -3'
(R):5'- AGCACCTGTCACTCACATTC -3'

Sequencing Primer
(F):5'- GCTTGTTTCTAAATCTCTAACTGGTG -3'
(R):5'- CTATGCGCCGGTTGACTG -3'
Posted On2014-07-14