Incidental Mutation 'IGL01662:Mfsd4b2'
ID 103217
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Mfsd4b2
Ensembl Gene ENSMUSG00000039339
Gene Name major facilitator superfamily domain containing 4B2
Synonyms 2010001E11Rik, Mfsd4b2, Mfsd4b2-ps
Accession Numbers
Essential gene? Probably non essential (E-score: 0.093) question?
Stock # IGL01662
Quality Score
Status
Chromosome 10
Chromosomal Location 39796956-39802945 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to G at 39798193 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000040384 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000045526]
AlphaFold no structure available at present
Predicted Effect probably benign
Transcript: ENSMUST00000045526
SMART Domains Protein: ENSMUSP00000040384
Gene: ENSMUSG00000039339

DomainStartEndE-ValueType
Pfam:MFS_1 1 322 3.9e-11 PFAM
transmembrane domain 335 357 N/A INTRINSIC
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsm5 A T 7: 119,137,511 (GRCm39) I402F probably damaging Het
Acvr2b T C 9: 119,261,570 (GRCm39) Y388H probably damaging Het
Adh1 G A 3: 137,988,512 (GRCm39) D162N possibly damaging Het
C6 G T 15: 4,822,236 (GRCm39) R585I probably damaging Het
Ccdc169 T A 3: 55,070,732 (GRCm39) probably null Het
Cdh13 T A 8: 119,401,916 (GRCm39) M106K probably damaging Het
Cep78 C T 19: 15,938,359 (GRCm39) E530K probably damaging Het
Cyfip1 T A 7: 55,546,487 (GRCm39) L533Q probably damaging Het
Etl4 T C 2: 20,811,460 (GRCm39) V1181A probably benign Het
Galnt7 T G 8: 57,984,769 (GRCm39) probably benign Het
Gm11595 G A 11: 99,663,498 (GRCm39) R61C unknown Het
Gucy1a1 T A 3: 82,016,560 (GRCm39) I143F possibly damaging Het
Hmcn1 T C 1: 150,613,050 (GRCm39) N1410D possibly damaging Het
Ltbp2 G A 12: 84,856,020 (GRCm39) T741I probably benign Het
Mdc1 T C 17: 36,163,397 (GRCm39) S982P probably benign Het
Mrgprb5 T G 7: 47,818,172 (GRCm39) I188L probably benign Het
Naip6 T A 13: 100,436,862 (GRCm39) S554C probably damaging Het
Nav2 A G 7: 49,220,957 (GRCm39) N1715D probably damaging Het
Nav3 A T 10: 109,605,119 (GRCm39) S985T possibly damaging Het
Nme7 A G 1: 164,155,866 (GRCm39) Q22R probably benign Het
Or52i2 T C 7: 102,319,927 (GRCm39) W267R probably damaging Het
Otulinl C T 15: 27,658,151 (GRCm39) D290N probably damaging Het
Pabir1 A G 19: 24,453,948 (GRCm39) V258A probably benign Het
Ppp1r9a A G 6: 5,115,322 (GRCm39) E815G probably damaging Het
Ppp2r2c T A 5: 37,083,744 (GRCm39) I95N probably damaging Het
Ppp4r4 G A 12: 103,569,225 (GRCm39) E717K possibly damaging Het
Prdm2 A G 4: 142,860,138 (GRCm39) S1051P possibly damaging Het
Rnf214 T C 9: 45,811,084 (GRCm39) D193G probably damaging Het
Sirpb1b G T 3: 15,608,244 (GRCm39) T167K probably damaging Het
Slc16a3 C A 11: 120,847,532 (GRCm39) S240* probably null Het
Snx14 T A 9: 88,267,891 (GRCm39) probably benign Het
Sorbs2 A G 8: 46,256,866 (GRCm39) probably benign Het
Stk-ps2 A T 1: 46,068,522 (GRCm39) noncoding transcript Het
Taar7b A T 10: 23,875,874 (GRCm39) D13V probably benign Het
Trp53bp1 T C 2: 121,066,506 (GRCm39) E740G probably damaging Het
Unc79 C T 12: 103,115,279 (GRCm39) A2054V possibly damaging Het
Zfp106 A G 2: 120,354,034 (GRCm39) V211A probably benign Het
Zfp112 A G 7: 23,825,379 (GRCm39) H449R probably benign Het
Other mutations in Mfsd4b2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00231:Mfsd4b2 APN 10 39,801,057 (GRCm39) splice site probably benign
IGL01546:Mfsd4b2 APN 10 39,797,471 (GRCm39) missense probably damaging 1.00
IGL02151:Mfsd4b2 APN 10 39,797,687 (GRCm39) missense probably damaging 1.00
R1928:Mfsd4b2 UTSW 10 39,797,458 (GRCm39) missense probably damaging 1.00
R2851:Mfsd4b2 UTSW 10 39,798,119 (GRCm39) missense probably benign 0.07
R3777:Mfsd4b2 UTSW 10 39,797,527 (GRCm39) missense possibly damaging 0.54
R5055:Mfsd4b2 UTSW 10 39,799,773 (GRCm39) missense possibly damaging 0.79
R5257:Mfsd4b2 UTSW 10 39,798,017 (GRCm39) missense probably benign 0.00
R5258:Mfsd4b2 UTSW 10 39,798,017 (GRCm39) missense probably benign 0.00
R5563:Mfsd4b2 UTSW 10 39,798,038 (GRCm39) missense probably benign 0.15
R5728:Mfsd4b2 UTSW 10 39,799,791 (GRCm39) missense possibly damaging 0.47
R5888:Mfsd4b2 UTSW 10 39,798,031 (GRCm39) missense probably benign 0.00
R6147:Mfsd4b2 UTSW 10 39,797,573 (GRCm39) missense probably benign
R6362:Mfsd4b2 UTSW 10 39,797,605 (GRCm39) missense probably damaging 1.00
R7462:Mfsd4b2 UTSW 10 39,797,877 (GRCm39) missense probably benign 0.03
R7801:Mfsd4b2 UTSW 10 39,799,777 (GRCm39) missense probably benign 0.00
R8126:Mfsd4b2 UTSW 10 39,797,984 (GRCm39) missense probably benign
R8158:Mfsd4b2 UTSW 10 39,798,064 (GRCm39) missense probably benign 0.35
R8677:Mfsd4b2 UTSW 10 39,799,805 (GRCm39) missense probably benign 0.00
R9013:Mfsd4b2 UTSW 10 39,798,062 (GRCm39) missense probably benign 0.05
Z1176:Mfsd4b2 UTSW 10 39,797,596 (GRCm39) missense probably benign 0.05
Posted On 2014-01-21