Incidental Mutation 'R7080:Tcstv5'
ID 549479
Institutional Source Beutler Lab
Gene Symbol Tcstv5
Ensembl Gene ENSMUSG00000078537
Gene Name Tcstv family member 5
Synonyms B020031M17Rik
MMRRC Submission 045174-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.072) question?
Stock # R7080 (G1)
Quality Score 181.009
Status Not validated
Chromosome 13
Chromosomal Location 120410893-120412342 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 120411270 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Glycine at position 112 (D112G)
Ref Sequence ENSEMBL: ENSMUSP00000137705 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000080505] [ENSMUST00000180768]
AlphaFold Q3UT11
Predicted Effect probably benign
Transcript: ENSMUST00000080505
AA Change: D112G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000111142
Gene: ENSMUSG00000078537
AA Change: D112G

DomainStartEndE-ValueType
Pfam:DUF1438 7 157 8.2e-93 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000180768
AA Change: D112G

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000137705
Gene: ENSMUSG00000078537
AA Change: D112G

DomainStartEndE-ValueType
Pfam:DUF1438 7 157 8.2e-93 PFAM
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.8%
  • 20x: 99.3%
Validation Efficiency 94% (47/50)
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abca2 A G 2: 25,336,116 (GRCm39) E2162G probably benign Het
Ackr4 A G 9: 103,976,761 (GRCm39) V62A probably damaging Het
Atox1 T A 11: 55,341,365 (GRCm39) K57* probably null Het
Atp6v1e1 G A 6: 120,799,350 (GRCm39) probably benign Het
Bmpr2 T C 1: 59,906,842 (GRCm39) V645A probably benign Het
Brwd1 T C 16: 95,810,730 (GRCm39) T1602A probably benign Het
Cdc42bpg T C 19: 6,365,219 (GRCm39) V692A probably damaging Het
Cdca2 T C 14: 67,935,551 (GRCm39) D388G probably damaging Het
Celsr1 G A 15: 85,816,652 (GRCm39) R1764C possibly damaging Het
Copz2 G T 11: 96,747,538 (GRCm39) V174L probably benign Het
Dnaaf1 T C 8: 120,309,335 (GRCm39) L141P probably damaging Het
Fam170a T A 18: 50,413,740 (GRCm39) probably null Het
Fshr A T 17: 89,404,539 (GRCm39) probably null Het
Gbx1 C T 5: 24,731,298 (GRCm39) A173T probably benign Het
Gm3604 G A 13: 62,518,109 (GRCm39) A83V probably damaging Het
Gpr19 A T 6: 134,847,419 (GRCm39) V88D probably damaging Het
Hnrnpd C T 5: 100,124,392 (GRCm39) probably null Het
Homez T C 14: 55,095,112 (GRCm39) S199G probably benign Het
Kit T C 5: 75,767,941 (GRCm39) I108T probably damaging Het
Lrrc34 A C 3: 30,688,705 (GRCm39) Y199D probably damaging Het
Mapk12 T C 15: 89,017,350 (GRCm39) D208G probably damaging Het
Mon1a A G 9: 107,778,985 (GRCm39) D403G probably damaging Het
Myo1d C T 11: 80,565,460 (GRCm39) E426K probably damaging Het
Nol11 G A 11: 107,070,878 (GRCm39) T307I probably damaging Het
Or10d5 A G 9: 39,861,444 (GRCm39) C208R probably damaging Het
Or52b4 A T 7: 102,184,172 (GRCm39) I73F possibly damaging Het
Or5aq1b A G 2: 86,902,083 (GRCm39) Y132H probably damaging Het
Or6d15 A T 6: 116,559,314 (GRCm39) F198I probably damaging Het
Or8k28 A T 2: 86,285,835 (GRCm39) L260* probably null Het
Pcdhb16 C T 18: 37,611,516 (GRCm39) Q159* probably null Het
Phf19 G A 2: 34,788,724 (GRCm39) probably null Het
Qrfpr C T 3: 36,234,198 (GRCm39) R381H probably benign Het
Rad51ap2 A G 12: 11,506,366 (GRCm39) D96G probably benign Het
Ranbp1 T C 16: 18,063,097 (GRCm39) D93G possibly damaging Het
Reep1 A G 6: 71,757,749 (GRCm39) D116G possibly damaging Het
Rinl T C 7: 28,496,101 (GRCm39) C361R probably damaging Het
Rps6kb1 T C 11: 86,397,666 (GRCm39) D393G probably damaging Het
Slc2a12 T C 10: 22,541,216 (GRCm39) V357A probably benign Het
Spryd3 T C 15: 102,026,627 (GRCm39) D348G probably benign Het
Syne2 G A 12: 76,099,501 (GRCm39) A569T probably benign Het
Thoc6 C T 17: 23,892,503 (GRCm39) R6Q probably null Het
Tyw3 G C 3: 154,299,426 (GRCm39) S94R probably benign Het
Unc13b C T 4: 43,171,926 (GRCm39) T918I unknown Het
Unc80 A T 1: 66,685,680 (GRCm39) H2268L possibly damaging Het
Urod C T 4: 116,849,838 (GRCm39) A187T probably damaging Het
Usp46 G T 5: 74,177,344 (GRCm39) N205K probably benign Het
Wapl T C 14: 34,414,313 (GRCm39) F392L probably benign Het
Zim1 T C 7: 6,680,305 (GRCm39) T453A possibly damaging Het
Other mutations in Tcstv5
AlleleSourceChrCoordTypePredicted EffectPPH Score
R4700:Tcstv5 UTSW 13 120,411,378 (GRCm39) missense probably benign 0.01
R5345:Tcstv5 UTSW 13 120,411,384 (GRCm39) missense probably damaging 0.98
R5762:Tcstv5 UTSW 13 120,411,501 (GRCm39) missense probably benign
R5968:Tcstv5 UTSW 13 120,411,618 (GRCm39) start gained probably benign
R6221:Tcstv5 UTSW 13 120,411,534 (GRCm39) missense probably damaging 0.99
R9438:Tcstv5 UTSW 13 120,411,363 (GRCm39) missense probably benign 0.01
RF010:Tcstv5 UTSW 13 120,411,582 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- GGCCAAAAGCTCTTTGAAGCC -3'
(R):5'- CCAGAGTACAAGGTGCTCCAAATC -3'

Sequencing Primer
(F):5'- AAGCTCTTTGAAGCCATGCC -3'
(R):5'- GGTGCTCCAAATCTGAGACACTTTG -3'
Posted On 2019-05-15