Incidental Mutation 'IGL02407:Slfn2'
ID292135
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Slfn2
Ensembl Gene ENSMUSG00000072620
Gene Nameschlafen 2
SynonymsShlf2
Accession Numbers

MGI: 1313258

Is this an essential gene? Probably non essential (E-score: 0.054) question?
Stock #IGL02407
Quality Score
Status
Chromosome11
Chromosomal Location83065112-83070678 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to A at 83069576 bp
ZygosityHeterozygous
Amino Acid Change Threonine to Lysine at position 127 (T127K)
Ref Sequence ENSEMBL: ENSMUSP00000035562 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000038038]
Predicted Effect probably benign
Transcript: ENSMUST00000038038
AA Change: T127K

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000035562
Gene: ENSMUSG00000072620
AA Change: T127K

DomainStartEndE-ValueType
low complexity region 162 172 N/A INTRINSIC
Pfam:AlbA_2 231 365 4.5e-12 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000214134
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
Validation Efficiency
MGI Phenotype PHENOTYPE: Mice homozygous for an ENU-induced allele exhibit increased susceptibility to bacterial and viral infections, reduced T cell numbers, decreased T cell proliferation, and increased apoptosis of activated T cells. [provided by MGI curators]
Allele List at MGI

All alleles(1) : Chemically induced(1)

Other mutations in this stock
Total: 60 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406P16Rik A T 7: 34,256,484 N393K probably damaging Het
A2m G A 6: 121,668,616 W1040* probably null Het
Adgrv1 C A 13: 81,479,670 A3691S probably damaging Het
Als2cl T A 9: 110,889,227 Y345* probably null Het
Aplp2 A T 9: 31,158,527 Y496* probably null Het
Ash1l T C 3: 89,072,548 V2793A probably damaging Het
Bfsp1 A T 2: 143,826,933 D575E probably benign Het
Ceacam20 G T 7: 19,970,407 V128F probably benign Het
Cers4 A T 8: 4,520,306 K204* probably null Het
Cog1 T C 11: 113,654,026 Y345H probably benign Het
Col14a1 T C 15: 55,448,876 probably benign Het
Col19a1 A T 1: 24,312,372 probably null Het
Ctnnd2 T A 15: 30,966,768 M955K probably damaging Het
Cyp3a16 A T 5: 145,451,842 M275K probably damaging Het
Degs2 T G 12: 108,691,995 T242P probably damaging Het
Elac2 T C 11: 64,999,175 V612A probably benign Het
Elovl6 T A 3: 129,605,084 F45I probably damaging Het
Exoc1 A C 5: 76,545,346 N360H probably damaging Het
Fam221b A T 4: 43,666,309 S101T possibly damaging Het
Glyr1 A G 16: 5,036,948 F89L probably benign Het
Herc4 C A 10: 63,306,424 T668K probably damaging Het
Hibadh C T 6: 52,548,889 V259I possibly damaging Het
Hp1bp3 T A 4: 138,240,672 D397E probably damaging Het
Ift80 G T 3: 68,898,536 D724E probably benign Het
Igkv3-10 T C 6: 70,573,239 probably benign Het
Irf9 G T 14: 55,605,221 A75S possibly damaging Het
Kif13a C T 13: 46,785,293 V76M probably damaging Het
Krt4 T C 15: 101,921,305 I263V probably benign Het
Lgals8 A G 13: 12,454,818 W87R probably benign Het
Mccc2 G A 13: 99,991,308 P96L probably damaging Het
Megf11 A C 9: 64,680,249 D443A probably damaging Het
Nckap5l T C 15: 99,423,127 probably benign Het
Ndor1 A G 2: 25,249,269 V230A probably benign Het
Nif3l1 G T 1: 58,457,797 V294L possibly damaging Het
Olfr1285 T A 2: 111,408,578 noncoding transcript Het
Pcdhb13 T A 18: 37,443,075 Y169N probably damaging Het
Peg3 A G 7: 6,707,636 I1529T probably damaging Het
Piezo2 T A 18: 63,146,844 I219F probably damaging Het
Prpf38a G A 4: 108,567,639 R242W unknown Het
Prrc2a A T 17: 35,160,504 D255E unknown Het
Rapgef6 G T 11: 54,676,355 D1121Y possibly damaging Het
Ryr3 T A 2: 112,754,958 H2761L probably damaging Het
Sel1l A T 12: 91,843,268 probably benign Het
Slc30a9 A G 5: 67,352,722 D539G probably damaging Het
Slc38a9 A G 13: 112,690,243 S172G probably benign Het
Smurf1 A T 5: 144,884,724 M496K probably damaging Het
Srgap2 A T 1: 131,319,602 V564D probably damaging Het
Stk32a T C 18: 43,297,511 I162T probably benign Het
Tchhl1 A T 3: 93,471,327 N446I possibly damaging Het
Tmem64 T A 4: 15,266,584 H211Q probably damaging Het
Trim3 T C 7: 105,613,011 N586S probably benign Het
Trpm1 A G 7: 64,219,121 E507G probably damaging Het
Tyk2 G T 9: 21,109,227 probably benign Het
Ugt3a2 A T 15: 9,365,230 K310* probably null Het
Unc13a T A 8: 71,648,942 N1022Y probably damaging Het
Vmn1r172 A T 7: 23,659,803 N38Y probably damaging Het
Vmn2r100 A T 17: 19,521,508 I161F probably damaging Het
Zcchc17 A G 4: 130,349,315 M25T probably benign Het
Zfp563 G A 17: 33,104,821 R130Q probably benign Het
Zhx2 A G 15: 57,823,406 S724G probably benign Het
Other mutations in Slfn2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02141:Slfn2 APN 11 83069844 missense probably benign 0.32
IGL03303:Slfn2 APN 11 83069467 missense possibly damaging 0.82
elektra UTSW 11 83069600 missense probably damaging 1.00
elektra2 UTSW 11 83069564 missense probably benign 0.05
R2270:Slfn2 UTSW 11 83069935 missense probably damaging 0.99
R2392:Slfn2 UTSW 11 83065328 missense possibly damaging 0.91
R3436:Slfn2 UTSW 11 83069564 missense probably benign 0.05
R3437:Slfn2 UTSW 11 83069564 missense probably benign 0.05
R5849:Slfn2 UTSW 11 83069576 missense probably benign 0.00
R7612:Slfn2 UTSW 11 83070263 missense probably damaging 1.00
R7738:Slfn2 UTSW 11 83069973 missense probably damaging 1.00
Posted On2015-04-16