Incidental Mutation 'R9334:Tnfsf10'
ID 706976
Institutional Source Beutler Lab
Gene Symbol Tnfsf10
Ensembl Gene ENSMUSG00000039304
Gene Name tumor necrosis factor (ligand) superfamily, member 10
Synonyms APO-2L, A330042I21Rik, Trail
MMRRC Submission
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R9334 (G1)
Quality Score 225.009
Status Not validated
Chromosome 3
Chromosomal Location 27371226-27393814 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 27389496 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 186 (Y186N)
Ref Sequence ENSEMBL: ENSMUSP00000040271 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000046383] [ENSMUST00000174840]
AlphaFold P50592
Predicted Effect probably damaging
Transcript: ENSMUST00000046383
AA Change: Y186N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000040271
Gene: ENSMUSG00000039304
AA Change: Y186N

DomainStartEndE-ValueType
transmembrane domain 20 42 N/A INTRINSIC
TNF 146 290 5.35e-37 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000174840
AA Change: Y186N

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000133917
Gene: ENSMUSG00000039304
AA Change: Y186N

DomainStartEndE-ValueType
transmembrane domain 15 37 N/A INTRINSIC
Pfam:TNF 156 226 7.1e-17 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.5%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is a cytokine that belongs to the tumor necrosis factor (TNF) ligand family. This protein preferentially induces apoptosis in transformed and tumor cells, but does not appear to kill normal cells although it is expressed at a significant level in most normal tissues. This protein binds to several members of TNF receptor superfamily including TNFRSF10A/TRAILR1, TNFRSF10B/TRAILR2, TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and possibly also to TNFRSF11B/OPG. The activity of this protein may be modulated by binding to the decoy receptors TNFRSF10C/TRAILR3, TNFRSF10D/TRAILR4, and TNFRSF11B/OPG that cannot induce apoptosis. The binding of this protein to its receptors has been shown to trigger the activation of MAPK8/JNK, caspase 8, and caspase 3. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2010]
PHENOTYPE: Homozygotes for a null allele show thymus hyperplasia, abnormal negative T cell selection, increased susceptibility to autoimmune diseases and to tumor initiation and metastasis, and resistance to induced hepatitis. Homozygotes for another null allele are unable to control A20 lymphoma progression. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actr1b A T 1: 36,739,251 (GRCm39) I346N probably damaging Het
Adam6b A C 12: 113,454,768 (GRCm39) E528D probably damaging Het
Ang A G 14: 51,339,017 (GRCm39) M53V possibly damaging Het
Ankrd26 G A 6: 118,509,262 (GRCm39) A601V probably benign Het
Atp6v0d2 A G 4: 19,890,695 (GRCm39) L155P probably damaging Het
Cacna1a T C 8: 85,296,594 (GRCm39) V1204A probably damaging Het
Car4 A G 11: 84,855,415 (GRCm39) I183V probably benign Het
Ccdc149 G T 5: 52,578,171 (GRCm39) A87E possibly damaging Het
Ccdc88b A G 19: 6,833,541 (GRCm39) M208T possibly damaging Het
Ccnt2 T C 1: 127,723,046 (GRCm39) L162S probably damaging Het
Cd27 A G 6: 125,213,718 (GRCm39) probably null Het
Cfap44 C A 16: 44,239,654 (GRCm39) T567K probably damaging Het
Cpne5 C T 17: 29,423,673 (GRCm39) V152M probably benign Het
Cyp2u1 C T 3: 131,092,065 (GRCm39) V152M probably damaging Het
Dnajc13 A T 9: 104,051,659 (GRCm39) F1733I probably benign Het
Dop1a A G 9: 86,403,027 (GRCm39) Y1409C probably damaging Het
Ecm2 T C 13: 49,677,815 (GRCm39) M367T probably benign Het
Eif4g2 A G 7: 110,674,031 (GRCm39) S658P possibly damaging Het
Exoc3l4 T C 12: 111,397,117 (GRCm39) L666P probably damaging Het
Fbxl4 G A 4: 22,376,778 (GRCm39) M71I probably damaging Het
Fbxw10 T C 11: 62,765,910 (GRCm39) S727P possibly damaging Het
Fem1b A T 9: 62,703,604 (GRCm39) L552* probably null Het
Filip1 A T 9: 79,725,739 (GRCm39) V960D probably benign Het
Glipr1l3 A T 10: 111,979,948 (GRCm39) M198K probably benign Het
Gm19410 T A 8: 36,270,722 (GRCm39) C1216* probably null Het
Gmps T A 3: 63,889,864 (GRCm39) V81E probably damaging Het
Gpr150 G T 13: 76,204,103 (GRCm39) Q281K probably benign Het
Grsf1 A G 5: 88,820,469 (GRCm39) V221A probably damaging Het
Gsc T A 12: 104,439,353 (GRCm39) I8F probably damaging Het
Homer2 A T 7: 81,261,078 (GRCm39) C284* probably null Het
Hrg T A 16: 22,780,061 (GRCm39) H446Q unknown Het
Jag1 C T 2: 136,943,593 (GRCm39) R201H probably damaging Het
Kctd15 C T 7: 34,341,483 (GRCm39) R148H possibly damaging Het
Klhdc7a G A 4: 139,693,493 (GRCm39) R485C probably benign Het
Ldhd T A 8: 112,353,980 (GRCm39) I407F probably benign Het
Lgals12 G A 19: 7,578,086 (GRCm39) R192C probably benign Het
Lmf2 G A 15: 89,239,577 (GRCm39) L26F probably damaging Het
Lum A T 10: 97,404,347 (GRCm39) I81F probably damaging Het
Map1b G T 13: 99,568,148 (GRCm39) D1524E unknown Het
Marveld3 A G 8: 110,675,036 (GRCm39) L260S probably damaging Het
Mms19 C T 19: 41,942,203 (GRCm39) R555H probably benign Het
Mrpl37 G A 4: 106,921,605 (GRCm39) T208I probably benign Het
Mug1 A T 6: 121,838,490 (GRCm39) T498S probably benign Het
Myo3b T C 2: 70,047,360 (GRCm39) C289R probably damaging Het
Myo7a A T 7: 97,716,369 (GRCm39) F1459Y probably damaging Het
Neurl4 C A 11: 69,796,792 (GRCm39) R518S probably damaging Het
Nmnat2 T G 1: 152,949,585 (GRCm39) V43G probably damaging Het
Or2b11 T C 11: 59,462,272 (GRCm39) Y98C probably damaging Het
Or2n1b T A 17: 38,459,840 (GRCm39) F120L probably benign Het
Or6c6c A G 10: 129,541,683 (GRCm39) N312S probably benign Het
Otog A G 7: 45,909,353 (GRCm39) T608A possibly damaging Het
Pck2 G A 14: 55,785,283 (GRCm39) R482Q probably damaging Het
Pcx G A 19: 4,670,532 (GRCm39) M1013I probably benign Het
Pex13 A G 11: 23,605,630 (GRCm39) M200T probably benign Het
Pigt CCGTGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCATGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCC CCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGTGCCCGTGGTGTACCCCCTCTCTAGTCCTGTGAGCCCGTGGTGTACCCCCTCTCTAGTCCGGCGCGCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCATGGTGTGCCCCCTCTCTAGTCCGGCGCTCCCGTGGTGTGCCCCCTCTCTAGTCCGGCGAGCCCGTGGTGTGCCCCCTCTCTAGTCC 2: 164,349,420 (GRCm39) probably null Het
Pramel32 A T 4: 88,548,186 (GRCm39) I73K probably damaging Het
Ptpn4 T C 1: 119,730,114 (GRCm39) H26R probably benign Het
Ralgps2 T A 1: 156,715,599 (GRCm39) E72V probably damaging Het
Relch T A 1: 105,654,179 (GRCm39) F873L possibly damaging Het
Scube1 A T 15: 83,512,264 (GRCm39) C396S possibly damaging Het
Sec23b T A 2: 144,410,550 (GRCm39) N283K possibly damaging Het
Setx T A 2: 29,044,032 (GRCm39) Y1800* probably null Het
Sgce G T 6: 4,707,205 (GRCm39) S213R probably damaging Het
Skic3 C A 13: 76,281,076 (GRCm39) T704N possibly damaging Het
Slc36a2 T C 11: 55,075,865 (GRCm39) probably benign Het
Sult5a1 A T 8: 123,875,146 (GRCm39) D129E probably damaging Het
Tacr1 A T 6: 82,380,913 (GRCm39) H108L probably damaging Het
Unc80 T C 1: 66,688,919 (GRCm39) S2428P possibly damaging Het
Vwf G A 6: 125,654,909 (GRCm39) R2535H Het
Zfp532 A G 18: 65,756,128 (GRCm39) I20M probably damaging Het
Other mutations in Tnfsf10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02155:Tnfsf10 APN 3 27,389,380 (GRCm39) missense possibly damaging 0.71
IGL03071:Tnfsf10 APN 3 27,389,769 (GRCm39) missense probably damaging 1.00
IGL03157:Tnfsf10 APN 3 27,380,106 (GRCm39) missense possibly damaging 0.77
IGL03226:Tnfsf10 APN 3 27,389,597 (GRCm39) nonsense probably null
R4051:Tnfsf10 UTSW 3 27,389,503 (GRCm39) missense probably damaging 1.00
R4679:Tnfsf10 UTSW 3 27,389,728 (GRCm39) missense probably damaging 0.99
R5799:Tnfsf10 UTSW 3 27,389,742 (GRCm39) missense probably damaging 1.00
R6101:Tnfsf10 UTSW 3 27,389,698 (GRCm39) missense probably damaging 1.00
R6105:Tnfsf10 UTSW 3 27,389,698 (GRCm39) missense probably damaging 1.00
R6882:Tnfsf10 UTSW 3 27,380,182 (GRCm39) missense possibly damaging 0.95
R7362:Tnfsf10 UTSW 3 27,389,497 (GRCm39) missense probably damaging 1.00
R7873:Tnfsf10 UTSW 3 27,389,808 (GRCm39) missense probably benign 0.05
R8819:Tnfsf10 UTSW 3 27,389,451 (GRCm39) missense probably benign 0.07
R9034:Tnfsf10 UTSW 3 27,389,379 (GRCm39) missense probably benign 0.00
R9035:Tnfsf10 UTSW 3 27,389,379 (GRCm39) missense probably benign 0.00
R9125:Tnfsf10 UTSW 3 27,380,028 (GRCm39) intron probably benign
R9193:Tnfsf10 UTSW 3 27,371,407 (GRCm39) missense possibly damaging 0.90
Predicted Primers PCR Primer
(F):5'- ATTGTGTGCAAGCCCAATG -3'
(R):5'- ACCAACAGCTGTTTCTGGCG -3'

Sequencing Primer
(F):5'- GGTATCTCCTCATTCGATGTAAACG -3'
(R):5'- TTCTGGCGCTCTTCATGAG -3'
Posted On 2022-04-18