Incidental Mutation 'R6400:Tcte2'
Institutional Source Beutler Lab
Gene Symbol Tcte2
Ensembl Gene ENSMUSG00000038347
Gene Namet-complex-associated testis expressed 2
MMRRC Submission
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.063) question?
Stock #R6400 (G1)
Quality Score225.009
Status Validated
Chromosomal Location13482553-13761825 bp(-) (GRCm38)
Type of Mutationintron
DNA Base Change (assembly) T to A at 13722452 bp
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000114746 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053376] [ENSMUST00000127032] [ENSMUST00000128194] [ENSMUST00000130033] [ENSMUST00000142863] [ENSMUST00000143162] [ENSMUST00000148430]
Predicted Effect probably benign
Transcript: ENSMUST00000053376
SMART Domains Protein: ENSMUSP00000059081
Gene: ENSMUSG00000038347

low complexity region 42 55 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000127032
AA Change: S108C
Predicted Effect probably benign
Transcript: ENSMUST00000128194
Predicted Effect probably benign
Transcript: ENSMUST00000130033
Predicted Effect noncoding transcript
Transcript: ENSMUST00000135850
Predicted Effect probably benign
Transcript: ENSMUST00000142863
Predicted Effect probably benign
Transcript: ENSMUST00000143162
Predicted Effect probably benign
Transcript: ENSMUST00000148430
Meta Mutation Damage Score 0.0898 question?
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.8%
  • 10x: 99.0%
  • 20x: 96.2%
Validation Efficiency 100% (32/32)
Allele List at MGI
Other mutations in this stock
Total: 31 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc9 A G 6: 142,692,709 *160Q probably null Het
Aen G A 7: 78,907,394 G330E probably benign Het
Akap8l G A 17: 32,336,320 R262C probably damaging Het
Cbx8 G A 11: 119,038,868 Q300* probably null Het
Cd274 C T 19: 29,385,408 T290M probably damaging Het
Cd36 A C 5: 17,814,723 S127A probably damaging Het
Celf3 A G 3: 94,480,286 Y55C probably damaging Het
Clec1a A T 6: 129,435,353 probably null Het
Cog2 A T 8: 124,550,306 I684F probably damaging Het
Cyp2c65 C T 19: 39,061,114 L29F possibly damaging Het
Dnajc14 A G 10: 128,807,490 E427G probably damaging Het
Dytn A T 1: 63,641,176 L408* probably null Het
Flg A G 3: 93,279,921 T227A probably benign Het
Heatr4 T A 12: 83,955,010 K887M probably null Het
Hoxb1 C T 11: 96,365,992 Q56* probably null Het
Kcnh7 T A 2: 62,739,344 N736I probably damaging Het
Lgr4 T C 2: 109,991,133 V120A probably damaging Het
Ltbp1 A G 17: 75,151,402 Y326C possibly damaging Het
Map3k1 A T 13: 111,755,725 S999T probably damaging Het
Med12l T C 3: 59,247,911 F1171L probably damaging Het
Muc5b T C 7: 141,858,665 S1783P unknown Het
Nbr1 T C 11: 101,565,774 L159P probably damaging Het
Nme9 T C 9: 99,469,707 F248S possibly damaging Het
Olfr1265 C T 2: 90,037,395 L159F probably benign Het
Olfr420 T C 1: 174,159,264 S164P probably damaging Het
Rasgrf1 C T 9: 89,991,630 T664I probably damaging Het
Setx A G 2: 29,130,274 D91G probably damaging Het
Stim1 A G 7: 102,430,950 R514G probably null Het
Svep1 C A 4: 58,049,169 G3446V probably damaging Het
Trmt10b A G 4: 45,308,562 K239E probably damaging Het
Wdr70 A T 15: 8,042,841 S189T probably benign Het
Other mutations in Tcte2
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01475:Tcte2 APN 17 13717562 intron probably benign
R1573:Tcte2 UTSW 17 13717637 splice site probably benign
R2442:Tcte2 UTSW 17 13714077 missense possibly damaging 0.83
R4561:Tcte2 UTSW 17 13722602 intron probably benign
R4868:Tcte2 UTSW 17 13728008 missense probably damaging 1.00
R6610:Tcte2 UTSW 17 13727988 nonsense probably null
Predicted Primers PCR Primer

Sequencing Primer
Posted On2018-05-04