Incidental Mutation 'R0761:Mfap3l'
ID 70091
Institutional Source Beutler Lab
Gene Symbol Mfap3l
Ensembl Gene ENSMUSG00000031647
Gene Name microfibrillar-associated protein 3-like
Synonyms 5430405D20Rik, NYD-sp9, 4933428A15Rik
MMRRC Submission 038941-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.066) question?
Stock # R0761 (G1)
Quality Score 225
Status Validated
Chromosome 8
Chromosomal Location 61085861-61129763 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to T at 61124615 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Leucine at position 286 (V286L)
Ref Sequence ENSEMBL: ENSMUSP00000124330 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000034066] [ENSMUST00000160719] [ENSMUST00000161421] [ENSMUST00000161702]
AlphaFold Q9D3X9
Predicted Effect possibly damaging
Transcript: ENSMUST00000034066
AA Change: V286L

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000034066
Gene: ENSMUSG00000031647
AA Change: V286L

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
IGc2 59 132 5.65e-12 SMART
transmembrane domain 150 172 N/A INTRINSIC
low complexity region 343 374 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000160719
AA Change: V286L

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000125139
Gene: ENSMUSG00000031647
AA Change: V286L

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
IGc2 59 132 5.65e-12 SMART
transmembrane domain 150 172 N/A INTRINSIC
low complexity region 343 374 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000161421
AA Change: V183L

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000124136
Gene: ENSMUSG00000031647
AA Change: V183L

DomainStartEndE-ValueType
SCOP:d1biha4 1 39 1e-9 SMART
Blast:IG 1 40 1e-18 BLAST
transmembrane domain 47 69 N/A INTRINSIC
low complexity region 240 271 N/A INTRINSIC
Predicted Effect possibly damaging
Transcript: ENSMUST00000161702
AA Change: V286L

PolyPhen 2 Score 0.875 (Sensitivity: 0.83; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000124330
Gene: ENSMUSG00000031647
AA Change: V286L

DomainStartEndE-ValueType
signal peptide 1 28 N/A INTRINSIC
IGc2 59 132 5.65e-12 SMART
transmembrane domain 150 172 N/A INTRINSIC
low complexity region 343 374 N/A INTRINSIC
Meta Mutation Damage Score 0.1795 question?
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 94.7%
Validation Efficiency 100% (51/51)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2610008E11Rik T C 10: 78,903,833 (GRCm39) Y133C probably benign Het
Adcy5 G A 16: 35,091,195 (GRCm39) probably benign Het
Asb17 A G 3: 153,550,052 (GRCm39) K28R probably damaging Het
Bbs10 G T 10: 111,135,244 (GRCm39) C119F probably damaging Het
Camk2g G A 14: 20,816,280 (GRCm39) Q119* probably null Het
Cdh18 A T 15: 23,226,838 (GRCm39) I46L possibly damaging Het
Cimip2a T C 2: 25,110,135 (GRCm39) probably benign Het
Clmn T A 12: 104,747,817 (GRCm39) N577Y probably damaging Het
Col1a2 G A 6: 4,518,822 (GRCm39) probably benign Het
Crocc T C 4: 140,774,387 (GRCm39) E63G probably benign Het
Crocc T C 4: 140,757,087 (GRCm39) T965A probably benign Het
Cryzl2 A G 1: 157,293,294 (GRCm39) I132V probably benign Het
Csgalnact2 T C 6: 118,103,073 (GRCm39) probably benign Het
Ctr9 T C 7: 110,645,479 (GRCm39) S569P probably damaging Het
Cul3 A G 1: 80,255,203 (GRCm39) probably benign Het
Dcp2 G A 18: 44,543,300 (GRCm39) S286N probably benign Het
Dgkz C T 2: 91,775,696 (GRCm39) R189H probably benign Het
Dst A G 1: 34,221,848 (GRCm39) T2551A probably benign Het
Kcna4 T A 2: 107,126,417 (GRCm39) S384T probably benign Het
Klhl17 T C 4: 156,317,204 (GRCm39) probably null Het
Kmt2e C A 5: 23,708,032 (GRCm39) S1865* probably null Het
L3mbtl1 G A 2: 162,807,967 (GRCm39) R534H probably damaging Het
Lmnb2 A T 10: 80,742,088 (GRCm39) M1K probably null Het
Lrp1b T C 2: 41,075,947 (GRCm39) D1784G probably damaging Het
Lrrc34 A G 3: 30,685,425 (GRCm39) probably null Het
Megf10 C A 18: 57,421,048 (GRCm39) Y895* probably null Het
Mesd G T 7: 83,544,951 (GRCm39) A143S probably damaging Het
Mroh2a G A 1: 88,171,672 (GRCm39) R770Q probably damaging Het
Nek1 T A 8: 61,542,489 (GRCm39) D717E probably benign Het
Nudt12 A T 17: 59,318,064 (GRCm39) D60E probably benign Het
Nup205 C T 6: 35,173,363 (GRCm39) probably benign Het
Or11g27 T C 14: 50,771,159 (GRCm39) S97P possibly damaging Het
Or2j3 A T 17: 38,616,282 (GRCm39) H23Q probably benign Het
Or4a75 T C 2: 89,448,179 (GRCm39) D119G probably damaging Het
Or5w19 C T 2: 87,698,880 (GRCm39) P182S possibly damaging Het
Pacs2 T A 12: 113,023,688 (GRCm39) probably benign Het
Pcdha9 T A 18: 37,133,016 (GRCm39) L695* probably null Het
Pira12 A T 7: 3,896,978 (GRCm39) probably null Het
Pkd1l1 A G 11: 8,804,375 (GRCm39) S1739P probably damaging Het
Polr1e C A 4: 45,027,392 (GRCm39) D207E probably damaging Het
Polr3f T A 2: 144,376,327 (GRCm39) V142E probably damaging Het
Psma6 T A 12: 55,459,127 (GRCm39) W170R possibly damaging Het
Rev3l T C 10: 39,750,191 (GRCm39) Y3114H probably benign Het
Rps6ka5 C T 12: 100,537,141 (GRCm39) A530T probably damaging Het
Simc1 T C 13: 54,674,387 (GRCm39) Y912H probably damaging Het
Tnfrsf1b T C 4: 144,942,670 (GRCm39) D371G possibly damaging Het
Trank1 T C 9: 111,195,681 (GRCm39) V1235A probably damaging Het
Ttn T C 2: 76,577,102 (GRCm39) E24597G probably damaging Het
Ubr2 G A 17: 47,294,242 (GRCm39) P297L probably damaging Het
Unc5d A T 8: 29,186,560 (GRCm39) probably null Het
Xpo4 A G 14: 57,850,840 (GRCm39) F355L probably damaging Het
Other mutations in Mfap3l
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00587:Mfap3l APN 8 61,124,943 (GRCm39) missense probably benign 0.28
IGL00958:Mfap3l APN 8 61,124,516 (GRCm39) missense probably benign 0.00
IGL01995:Mfap3l APN 8 61,124,498 (GRCm39) missense possibly damaging 0.59
R1888:Mfap3l UTSW 8 61,124,424 (GRCm39) missense possibly damaging 0.94
R1888:Mfap3l UTSW 8 61,124,424 (GRCm39) missense possibly damaging 0.94
R4646:Mfap3l UTSW 8 61,124,184 (GRCm39) missense probably damaging 1.00
R5286:Mfap3l UTSW 8 61,109,903 (GRCm39) missense probably benign 0.19
R5637:Mfap3l UTSW 8 61,109,821 (GRCm39) missense probably damaging 0.98
R6216:Mfap3l UTSW 8 61,124,841 (GRCm39) missense probably damaging 0.97
R7124:Mfap3l UTSW 8 61,124,303 (GRCm39) missense probably damaging 0.97
R7597:Mfap3l UTSW 8 61,124,315 (GRCm39) missense possibly damaging 0.95
R8745:Mfap3l UTSW 8 61,124,958 (GRCm39) missense possibly damaging 0.87
R9118:Mfap3l UTSW 8 61,109,716 (GRCm39) missense probably damaging 0.99
R9296:Mfap3l UTSW 8 61,124,615 (GRCm39) missense possibly damaging 0.88
R9531:Mfap3l UTSW 8 61,109,787 (GRCm39) missense probably damaging 0.99
Predicted Primers PCR Primer
(F):5'- TGAGATTGCTAAACGCATCCCCATC -3'
(R):5'- TGTCACATGTCACTGCTGGCTC -3'

Sequencing Primer
(F):5'- ACTTGCCAAAGTGACTCAGTTC -3'
(R):5'- TCTGGTGCCTCTACAGGAGAC -3'
Posted On 2013-09-30