Incidental Mutation 'R5197:Fam71f2'
ID400345
Institutional Source Beutler Lab
Gene Symbol Fam71f2
Ensembl Gene ENSMUSG00000079652
Gene Namefamily with sequence similarity 71, member F2
Synonyms
MMRRC Submission 042773-MU
Accession Numbers

Genbank: NM_001101486; MGI: 2141439

Is this an essential gene? Probably non essential (E-score: 0.061) question?
Stock #R5197 (G1)
Quality Score225
Status Not validated
Chromosome6
Chromosomal Location29279593-29290680 bp(+) (GRCm38)
Type of Mutationstart gained
DNA Base Change (assembly) G to T at 29281222 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000125895 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115286] [ENSMUST00000167131] [ENSMUST00000167608]
Predicted Effect probably benign
Transcript: ENSMUST00000115286
SMART Domains Protein: ENSMUSP00000110941
Gene: ENSMUSG00000079652

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
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.3%
  • 20x: 95.5%
Validation Efficiency 99% (67/68)
Allele List at MGI

All alleles(4) : Gene trapped(4)

Other mutations in this stock
Total: 64 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acsbg1 T C 9: 54,622,582 E247G possibly damaging Het
Adgra3 A G 5: 49,960,754 F1151L probably benign Het
Afg3l2 G T 18: 67,421,259 L458M probably damaging Het
Aldh4a1 A C 4: 139,648,301 probably benign Het
Anln A T 9: 22,352,781 probably null Het
Aste1 T C 9: 105,405,054 S74P probably damaging Het
Atp6v0e2 G A 6: 48,540,117 R77H probably benign Het
Brpf1 A G 6: 113,319,941 D962G possibly damaging Het
Btbd2 T C 10: 80,646,419 D249G probably damaging Het
Catsper3 T C 13: 55,808,176 probably null Het
Cfap43 A G 19: 47,897,372 L268P probably damaging Het
Cftr T C 6: 18,255,414 V540A probably benign Het
Col22a1 C T 15: 72,009,406 G32D probably damaging Het
Col5a2 G T 1: 45,393,081 P804Q probably benign Het
Cyp2d41-ps A G 15: 82,778,780 noncoding transcript Het
Cyp39a1 T G 17: 43,746,538 L423V possibly damaging Het
Elmo1 T G 13: 20,564,437 V484G probably benign Het
Eps8 C A 6: 137,490,290 Q656H probably damaging Het
Eps8 T C 6: 137,490,291 Q656R possibly damaging Het
Fshb T C 2: 107,057,509 D55G possibly damaging Het
Gm13089 A C 4: 143,698,062 C270W possibly damaging Het
Herc1 C A 9: 66,448,504 Q2346K probably damaging Het
Hist1h3d T A 13: 23,576,130 L110Q probably damaging Het
Htr3b T C 9: 48,945,515 D221G probably benign Het
Ift74 T A 4: 94,662,596 D328E probably benign Het
Kif21b A T 1: 136,144,625 K23M probably damaging Het
Lgr6 C T 1: 134,994,010 A199T probably damaging Het
Lipc T A 9: 70,798,391 E470V probably benign Het
Lrrc4 G T 6: 28,830,143 T68K probably damaging Het
Lrrc63 T A 14: 75,084,882 H594L possibly damaging Het
Mfsd14a A T 3: 116,648,501 probably benign Het
Mob2 T C 7: 142,009,537 probably null Het
Nckap5 T A 1: 126,222,673 H105L possibly damaging Het
Ngef C A 1: 87,509,368 G133* probably null Het
Olfr1 AGCGGTCGTAGGC AGC 11: 73,395,654 probably null Het
Olfr1000 T C 2: 85,608,447 I154M probably benign Het
Olfr113 T G 17: 37,575,220 I68L probably benign Het
Olfr1477 G T 19: 13,502,384 V14F possibly damaging Het
Olfr31 T A 14: 14,328,462 M117K probably damaging Het
Olfr593 G A 7: 103,212,000 V47I probably benign Het
Pard3 A G 8: 127,073,290 probably null Het
Pgm1 C T 5: 64,105,832 A274V possibly damaging Het
Ppp1r9a T A 6: 5,156,177 S1144R probably damaging Het
Prkcq C T 2: 11,299,416 P590L probably damaging Het
Psmd13 T A 7: 140,894,461 probably null Het
Rab3gap1 T A 1: 127,889,194 D63E probably benign Het
Rag2 C A 2: 101,630,740 T465K probably damaging Het
Rnase6 A G 14: 51,130,213 M21V unknown Het
Rufy4 T C 1: 74,147,663 C537R probably damaging Het
Ryr2 A T 13: 11,638,430 probably null Het
Sash1 T G 10: 8,740,225 R624S probably damaging Het
Slc1a2 A G 2: 102,756,115 I355V probably benign Het
Srrm2 T C 17: 23,817,384 S1097P probably benign Het
Sugct C T 13: 17,323,276 A271T probably damaging Het
Tdrd7 T C 4: 46,034,350 V1065A probably damaging Het
Tmprss6 T A 15: 78,454,189 Y307F probably damaging Het
Tram1 T C 1: 13,571,902 N216S probably benign Het
Ttk T C 9: 83,839,341 V93A probably benign Het
Ubr4 A G 4: 139,468,097 Y1210C probably damaging Het
Wdr7 A G 18: 63,738,866 K364E probably benign Het
Xrcc2 G T 5: 25,692,658 H98N probably benign Het
Zdhhc11 A G 13: 73,965,569 I77V probably benign Het
Zfp54 C T 17: 21,434,180 S312L probably benign Het
Zfp647 G A 15: 76,912,085 P125L 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
R5211:Fam71f2 UTSW 6 29286099 nonsense probably null
R5918:Fam71f2 UTSW 6 29285943 missense probably null 0.99
R5997:Fam71f2 UTSW 6 29290424 nonsense probably null
R7316:Fam71f2 UTSW 6 29286102 missense probably benign 0.00
Predicted Primers
Posted On2016-07-06