Incidental Mutation 'R5997:Fam71f2'
ID480615
Institutional Source Beutler Lab
Gene Symbol Fam71f2
Ensembl Gene ENSMUSG00000079652
Gene Namefamily with sequence similarity 71, member F2
Synonyms
MMRRC Submission 044176-MU
Accession Numbers

Genbank: NM_001101486; MGI: 2141439

Is this an essential gene? Probably non essential (E-score: 0.061) question?
Stock #R5997 (G1)
Quality Score225.009
Status Validated
Chromosome6
Chromosomal Location29279593-29290680 bp(+) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 29290424 bp
ZygosityHeterozygous
Amino Acid Change Leucine to Stop codon at position 267 (L267*)
Ref Sequence ENSEMBL: ENSMUSP00000110941 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115286] [ENSMUST00000167131] [ENSMUST00000167608]
Predicted Effect probably null
Transcript: ENSMUST00000115286
AA Change: L267*
SMART Domains Protein: ENSMUSP00000110941
Gene: ENSMUSG00000079652
AA Change: L267*

DomainStartEndE-ValueType
Pfam:DUF3699 105 175 8.3e-28 PFAM
low complexity region 188 204 N/A INTRINSIC
low complexity region 212 228 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000167131
SMART Domains Protein: ENSMUSP00000132049
Gene: ENSMUSG00000079652

DomainStartEndE-ValueType
Pfam:DUF3699 46 119 7.1e-29 PFAM
low complexity region 130 146 N/A INTRINSIC
low complexity region 154 170 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000167608
Meta Mutation Damage Score 0.9754 question?
Coding Region Coverage
  • 1x: 99.8%
  • 3x: 99.4%
  • 10x: 97.1%
  • 20x: 90.5%
Validation Efficiency 100% (78/78)
Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock
Total: 78 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700061G19Rik A T 17: 56,876,373 D38V probably benign Het
Abcb9 A T 5: 124,089,815 V121E possibly damaging Het
Adamts20 T A 15: 94,379,747 Y278F probably damaging Het
Adcy7 A T 8: 88,326,392 D972V probably benign Het
Adgrf3 C A 5: 30,198,362 probably null Het
Ahdc1 G T 4: 133,063,895 G816C probably benign Het
Aifm3 A G 16: 17,502,130 K283E probably benign Het
Akap6 T C 12: 52,937,233 probably null Het
Ank1 T C 8: 23,099,662 L593P probably damaging Het
Apol11b T A 15: 77,635,497 T128S probably benign Het
C1qtnf7 C A 5: 43,616,085 T235K probably damaging Het
Camk2a A T 18: 60,977,957 I73F probably damaging Het
Cd109 G T 9: 78,705,062 V1244F possibly damaging Het
Cep164 A G 9: 45,769,463 L1240S possibly damaging Het
Cnga1 T A 5: 72,604,575 D532V probably damaging Het
Cyp4a14 A T 4: 115,496,100 L5* probably null Het
Cyp4a30b A T 4: 115,459,391 K405* probably null Het
Dchs1 T C 7: 105,754,095 D3080G probably benign Het
Ddx1 T C 12: 13,237,799 D168G probably damaging Het
Dhx57 T G 17: 80,245,806 K1231Q probably damaging Het
Dnah14 A G 1: 181,770,105 N3640D probably benign Het
Dock4 T A 12: 40,755,834 L935Q probably damaging Het
Dus2 A T 8: 106,046,066 R269S probably benign Het
E230025N22Rik G A 18: 36,689,108 R201C possibly damaging Het
Erbb3 G A 10: 128,583,185 T269M probably damaging Het
Fbxo43 T C 15: 36,162,093 R323G probably damaging Het
Fktn A G 4: 53,735,061 H233R probably benign Het
Ftsj3 A T 11: 106,252,251 D412E probably damaging Het
Fzd7 A T 1: 59,484,544 M529L probably benign Het
Fzr1 T A 10: 81,370,826 probably null Het
Ganc T G 2: 120,430,605 V257G possibly damaging Het
Gm4131 T C 14: 62,464,758 K254E probably damaging Het
Gm6583 C T 5: 112,355,008 V277M possibly damaging Het
Gm7347 G T 5: 26,057,249 Y91* probably null Het
Gm9857 G A 3: 108,940,165 probably benign Het
Grpel1 T C 5: 36,465,248 S19P probably benign Het
Gtf3c4 T C 2: 28,833,711 K670E possibly damaging Het
Hist1h2bf G A 13: 23,574,103 probably benign Het
Hmcn1 G T 1: 150,704,173 Q1938K possibly damaging Het
Hnrnpk T C 13: 58,399,157 D71G probably damaging Het
Hspa4l G A 3: 40,767,979 R311H probably damaging Het
Igkv3-5 T A 6: 70,663,704 F56L probably benign Het
Igkv6-20 T A 6: 70,335,914 T92S possibly damaging Het
Krt8 C T 15: 102,000,594 V200I possibly damaging Het
Lamb2 A T 9: 108,480,388 T66S possibly damaging Het
Lamp3 A G 16: 19,701,028 L135S probably benign Het
Lrguk A G 6: 34,129,143 Y701C probably damaging Het
Mcc G T 18: 44,449,321 L588M probably damaging Het
Mcidas T A 13: 112,998,586 L234Q probably damaging Het
Mtmr14 T A 6: 113,280,614 L208Q probably damaging Het
Myof A G 19: 37,905,299 F1139L possibly damaging Het
Nlrp14 C A 7: 107,182,496 T300K probably benign Het
Olfr1474 A G 19: 13,471,506 I179V probably benign Het
Olfr165 T A 16: 19,407,944 H24L probably benign Het
Olfr716 A T 7: 107,147,328 E4V possibly damaging Het
Olfr890 A T 9: 38,143,801 Y217F probably damaging Het
Orc2 A G 1: 58,472,388 I354T probably damaging Het
Pard3b G T 1: 62,076,409 S140I probably damaging Het
Pcgf5 A G 19: 36,434,603 D49G probably benign Het
Pcsk6 T C 7: 65,959,293 F388S probably damaging Het
Prokr2 A C 2: 132,381,442 I60S probably damaging Het
Rab33b A G 3: 51,484,479 T50A possibly damaging Het
Rbms3 T C 9: 116,719,389 D61G probably damaging Het
Rhcg T A 7: 79,600,514 K274* probably null Het
Rnf112 C T 11: 61,451,022 V319M possibly damaging Het
Rnf44 A T 13: 54,682,800 S265T possibly damaging Het
Sf3a3 A G 4: 124,722,058 D168G probably damaging Het
Sik2 A G 9: 50,895,342 probably null Het
Slco1a5 T A 6: 142,253,113 L275F probably benign Het
Smtnl1 T C 2: 84,815,378 H383R probably damaging Het
Spns3 T G 11: 72,539,078 T175P probably damaging Het
Togaram1 A G 12: 64,995,538 T1174A probably benign Het
Tradd C T 8: 105,260,645 E10K possibly damaging Het
Ttc7b A T 12: 100,373,560 Y579N probably damaging Het
Uncx G A 5: 139,547,589 G470R probably damaging Het
Vav3 T A 3: 109,501,461 M177K probably damaging Het
Wfs1 A T 5: 36,967,750 I599N probably damaging Het
Zfp454 G A 11: 50,873,622 H217Y probably damaging Het
Other mutations in Fam71f2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01732:Fam71f2 APN 6 29285980 missense probably damaging 1.00
3-1:Fam71f2 UTSW 6 29290490 missense possibly damaging 0.94
R0389:Fam71f2 UTSW 6 29281392 missense possibly damaging 0.92
R1348:Fam71f2 UTSW 6 29283285 missense probably benign
R1661:Fam71f2 UTSW 6 29285938 missense probably damaging 1.00
R1982:Fam71f2 UTSW 6 29285922 missense probably benign 0.35
R4553:Fam71f2 UTSW 6 29287706 missense probably benign 0.45
R5197:Fam71f2 UTSW 6 29281222 start gained probably benign
R5211:Fam71f2 UTSW 6 29286099 nonsense probably null
R5918:Fam71f2 UTSW 6 29285943 missense probably null 0.99
R7316:Fam71f2 UTSW 6 29286102 missense probably benign 0.00
R7480:Fam71f2 UTSW 6 29281436 intron probably null
Predicted Primers PCR Primer
(F):5'- ACTGGCAGACAAATATGTGCTC -3'
(R):5'- TCGCTCCCATGGTTACTTGG -3'

Sequencing Primer
(F):5'- GAGACATTGTTCCAGCCCTTAAGTG -3'
(R):5'- TTACTTGGCCCACTGCAGGAAG -3'
Posted On2017-06-26