Incidental Mutation 'R4515:Txn2'
ID 332881
Institutional Source Beutler Lab
Gene Symbol Txn2
Ensembl Gene ENSMUSG00000005354
Gene Name thioredoxin 2
Synonyms Trx2, 2510006J11Rik
MMRRC Submission 041589-MU
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock # R4515 (G1)
Quality Score 190
Status Validated
Chromosome 15
Chromosomal Location 77915047-77929006 bp(-) (GRCm38)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 77915443 bp (GRCm38)
Zygosity Heterozygous
Amino Acid Change
Gene Model predicted gene model for transcript(s): [ENSMUST00000005487] [ENSMUST00000109748] [ENSMUST00000174529]
AlphaFold P97493
Predicted Effect probably benign
Transcript: ENSMUST00000005487
SMART Domains Protein: ENSMUSP00000005487
Gene: ENSMUSG00000005354

Pfam:Thioredoxin 61 164 7.8e-31 PFAM
Pfam:Thioredoxin_7 72 141 5.1e-9 PFAM
Pfam:Thioredoxin_2 74 161 2.4e-9 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000109748
SMART Domains Protein: ENSMUSP00000105370
Gene: ENSMUSG00000005354

Pfam:Thioredoxin 61 164 2.6e-30 PFAM
Pfam:Thioredoxin_2 74 161 1.7e-8 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173561
Predicted Effect probably benign
Transcript: ENSMUST00000173631
SMART Domains Protein: ENSMUSP00000134682
Gene: ENSMUSG00000005354

Pfam:Thioredoxin 25 128 8.1e-31 PFAM
Pfam:Thioredoxin_2 38 125 4.8e-9 PFAM
Predicted Effect probably null
Transcript: ENSMUST00000174468
SMART Domains Protein: ENSMUSP00000133548
Gene: ENSMUSG00000005354

Pfam:Thioredoxin 1 57 1.7e-18 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000174529
SMART Domains Protein: ENSMUSP00000133605
Gene: ENSMUSG00000005354

Pfam:Thioredoxin 1 62 5.6e-19 PFAM
Pfam:Thioredoxin_7 3 80 1.5e-8 PFAM
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.5%
  • 3x: 98.7%
  • 10x: 97.1%
  • 20x: 94.6%
Validation Efficiency 96% (65/68)
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This nuclear gene encodes a mitochondrial member of the thioredoxin family, a group of small multifunctional redox-active proteins. The encoded protein may play important roles in the regulation of the mitochondrial membrane potential and in protection against oxidant-induced apoptosis. [provided by RefSeq, Jul 2008]
PHENOTYPE: Mice homozygous for mutations that inactivate the gene exhibit exencephaly and embyronic lethality. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A430033K04Rik G T 5: 138,647,744 K630N probably damaging Het
Acss2 C A 2: 155,556,363 L335I probably benign Het
Alg6 A T 4: 99,752,786 probably benign Het
Atp8b3 C T 10: 80,523,847 M984I probably benign Het
Bsn G T 9: 108,104,078 probably null Het
Ccdc88a T C 11: 29,482,651 I1219T probably benign Het
Cdhr4 G A 9: 107,992,951 E52K probably benign Het
Ces1a T A 8: 93,020,904 N500Y probably damaging Het
Chd3 G T 11: 69,349,877 R1579S probably benign Het
Chrnb3 T C 8: 27,385,090 L39P probably damaging Het
Ckm A G 7: 19,420,284 K319E probably damaging Het
Cnot6 C T 11: 49,702,536 probably null Het
Copg1 A G 6: 87,907,546 probably benign Het
Dbn1 A T 13: 55,476,229 I350N possibly damaging Het
Dnah2 A G 11: 69,465,631 S2135P possibly damaging Het
Dsg2 C A 18: 20,601,387 D807E probably benign Het
Fam122c G A X: 53,293,499 R94H possibly damaging Het
Foxi1 A G 11: 34,207,972 F18L probably damaging Het
Galnt3 C A 2: 66,093,610 R438L probably damaging Het
Glod4 T A 11: 76,243,571 D25V probably damaging Het
Gm11492 A G 11: 87,568,057 H419R probably benign Het
Gm9008 C T 6: 76,496,809 V275I probably benign Het
Golga4 T A 9: 118,559,008 S1733T probably benign Het
H2-M10.3 C T 17: 36,367,830 probably null Het
Hemgn T C 4: 46,396,477 E253G probably damaging Het
Itsn1 G A 16: 91,899,649 V47M probably damaging Het
Kif5b A G 18: 6,208,257 V947A probably benign Het
Kif9 A G 9: 110,489,867 H133R probably benign Het
Lce1l T C 3: 92,850,474 T26A unknown Het
Macf1 T C 4: 123,493,988 E1172G probably damaging Het
Nkx3-2 C T 5: 41,763,938 V3M probably damaging Het
Nr2e1 G A 10: 42,578,191 T49I probably benign Het
Oc90 A G 15: 65,892,393 L138P probably damaging Het
Olfr834 T G 9: 18,987,982 probably null Het
Olfr954 C T 9: 39,462,231 R264* probably null Het
Orc4 G A 2: 48,937,489 P31S probably benign Het
Paqr3 T A 5: 97,103,361 N168I possibly damaging Het
Pcdhac1 T A 18: 37,091,379 I415N probably damaging Het
Pdik1l T C 4: 134,278,896 N75S probably damaging Het
Pik3r4 A G 9: 105,672,725 H1005R probably damaging Het
Plekhn1 T C 4: 156,225,531 S109G probably damaging Het
Prkch A G 12: 73,702,838 T402A possibly damaging Het
Ptger4 C A 15: 5,242,379 R253L probably damaging Het
Rabac1 A T 7: 24,970,160 Y173* probably null Het
Rapsn G A 2: 91,043,212 V288M possibly damaging Het
Sec31a A G 5: 100,365,958 S993P probably damaging Het
Serpina9 T A 12: 104,001,294 M281L probably benign Het
Serpine1 G A 5: 137,069,468 A117V probably damaging Het
Sh3tc2 A G 18: 61,987,693 probably null Het
Sipa1l2 T C 8: 125,492,226 D124G probably benign Het
Slc6a12 T A 6: 121,353,530 probably null Het
Stk11 A G 10: 80,116,601 probably benign Het
Tcaf3 A G 6: 42,589,996 Y720H probably damaging Het
Tmem38a C T 8: 72,572,161 P20S possibly damaging Het
Tmprss11a C T 5: 86,420,196 R224K probably damaging Het
Tmprss15 C T 16: 78,957,356 S988N probably benign Het
Ugt1a10 T A 1: 88,056,197 V239E probably damaging Het
Vmn2r102 A G 17: 19,681,213 Y534C probably damaging Het
Vmn2r78 A T 7: 86,954,258 D548V probably damaging Het
Other mutations in Txn2
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0611:Txn2 UTSW 15 77927717 missense probably damaging 1.00
R0919:Txn2 UTSW 15 77927749 missense probably damaging 1.00
R2504:Txn2 UTSW 15 77926670 intron probably benign
R3700:Txn2 UTSW 15 77927776 missense possibly damaging 0.69
R5897:Txn2 UTSW 15 77924526 missense probably benign 0.43
R6879:Txn2 UTSW 15 77919722 intron probably benign
R7101:Txn2 UTSW 15 77926678 missense unknown
R7215:Txn2 UTSW 15 77927686 splice site probably null
R9215:Txn2 UTSW 15 77919765 missense unknown
R9719:Txn2 UTSW 15 77928089 unclassified probably benign
Predicted Primers PCR Primer

Sequencing Primer
Posted On 2015-08-18