Incidental Mutation 'R7609:Tsga10'
ID 628262
Institutional Source Beutler Lab
Gene Symbol Tsga10
Ensembl Gene ENSMUSG00000060771
Gene Name testis specific 10
Synonyms Mtsga10, 4933432N21Rik
MMRRC Submission 045714-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.097) question?
Stock # R7609 (G1)
Quality Score 69.0074
Status Validated
Chromosome 1
Chromosomal Location 37793857-37905510 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to T at 37843974 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000110552 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000041815] [ENSMUST00000088072] [ENSMUST00000114902] [ENSMUST00000151735]
AlphaFold Q6NY15
Predicted Effect probably null
Transcript: ENSMUST00000041815
SMART Domains Protein: ENSMUSP00000048859
Gene: ENSMUSG00000060771

DomainStartEndE-ValueType
low complexity region 5 17 N/A INTRINSIC
coiled coil region 24 85 N/A INTRINSIC
coiled coil region 110 249 N/A INTRINSIC
Blast:SPEC 294 391 5e-6 BLAST
Predicted Effect probably null
Transcript: ENSMUST00000088072
SMART Domains Protein: ENSMUSP00000085391
Gene: ENSMUSG00000060771

DomainStartEndE-ValueType
low complexity region 5 17 N/A INTRINSIC
coiled coil region 24 85 N/A INTRINSIC
coiled coil region 110 249 N/A INTRINSIC
Blast:SPEC 294 391 5e-6 BLAST
Predicted Effect probably null
Transcript: ENSMUST00000114902
SMART Domains Protein: ENSMUSP00000110552
Gene: ENSMUSG00000060771

DomainStartEndE-ValueType
low complexity region 5 17 N/A INTRINSIC
coiled coil region 24 85 N/A INTRINSIC
coiled coil region 110 249 N/A INTRINSIC
Blast:SPEC 294 391 5e-6 BLAST
Predicted Effect probably benign
Transcript: ENSMUST00000151735
SMART Domains Protein: ENSMUSP00000120554
Gene: ENSMUSG00000060771

DomainStartEndE-ValueType
low complexity region 5 17 N/A INTRINSIC
coiled coil region 24 85 N/A INTRINSIC
coiled coil region 110 229 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 96% (69/72)
Allele List at MGI
Other mutations in this stock
Total: 71 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930563M21Rik T C 9: 55,896,744 (GRCm39) Y288C probably benign Het
Acta2 G A 19: 34,229,931 (GRCm39) T8I probably benign Het
Agl C A 3: 116,600,928 (GRCm39) R24I possibly damaging Het
Aldoart2 A G 12: 55,612,833 (GRCm39) T253A probably benign Het
Ankrd39 G A 1: 36,578,546 (GRCm39) R160W probably damaging Het
Aspscr1 C T 11: 120,568,348 (GRCm39) T57M probably damaging Het
Baz2b A G 2: 59,792,817 (GRCm39) L437S probably benign Het
Bcl9l T A 9: 44,417,044 (GRCm39) L331Q probably damaging Het
Cdhr4 C A 9: 107,874,482 (GRCm39) P546T probably damaging Het
Cfap61 T C 2: 145,954,453 (GRCm39) C231R unknown Het
Cnih4 T C 1: 180,983,467 (GRCm39) L61P probably damaging Het
Dtx4 A G 19: 12,469,645 (GRCm39) Y161H probably damaging Het
Epha7 C T 4: 28,871,937 (GRCm39) S422L probably benign Het
Ercc6 A G 14: 32,288,318 (GRCm39) H830R probably benign Het
Exoc7 T C 11: 116,180,085 (GRCm39) N673S possibly damaging Het
Gm12185 T C 11: 48,806,850 (GRCm39) S114G possibly damaging Het
Hsfy2 A T 1: 56,676,310 (GRCm39) F76I probably benign Het
Igsf9b A G 9: 27,257,186 (GRCm39) D1413G probably benign Het
Klk1b8 G A 7: 43,451,603 (GRCm39) C198Y probably damaging Het
Lama3 G T 18: 12,664,891 (GRCm39) probably null Het
Lce3f A T 3: 92,900,403 (GRCm39) S75C unknown Het
Ldhal6b T C 17: 5,468,266 (GRCm39) M223V probably benign Het
Magoh T C 4: 107,744,409 (GRCm39) V126A possibly damaging Het
Mc1r A T 8: 124,135,032 (GRCm39) I262F probably damaging Het
Mecom A G 3: 30,010,591 (GRCm39) I629T probably damaging Het
Mkrn2os A G 6: 115,563,687 (GRCm39) V116A possibly damaging Het
Mtcl3 A T 10: 29,024,224 (GRCm39) D380V probably damaging Het
Muc5b T A 7: 141,415,466 (GRCm39) V2804D possibly damaging Het
Myo15a T C 11: 60,379,637 (GRCm39) V279A Het
Nhlrc2 A G 19: 56,583,328 (GRCm39) I600V probably benign Het
Nipbl T C 15: 8,335,356 (GRCm39) Q2183R probably benign Het
Obscn C T 11: 58,891,125 (GRCm39) E7136K unknown Het
Or10ag56 T C 2: 87,139,853 (GRCm39) V260A probably benign Het
Or5p4 T A 7: 107,680,753 (GRCm39) F251I probably damaging Het
Or8c9 A C 9: 38,241,520 (GRCm39) L209F possibly damaging Het
Or8g37 C T 9: 39,731,583 (GRCm39) T216I probably benign Het
Otop3 T C 11: 115,230,546 (GRCm39) I141T possibly damaging Het
Pde4dip C A 3: 97,622,881 (GRCm39) V1443F possibly damaging Het
Pdgfra T C 5: 75,327,382 (GRCm39) V193A probably benign Het
Phf3 T C 1: 30,844,582 (GRCm39) Y1459C probably benign Het
Pias4 A T 10: 80,993,860 (GRCm39) probably null Het
Plcg2 A G 8: 118,284,852 (GRCm39) N159S probably benign Het
Plekha7 T C 7: 115,763,681 (GRCm39) D307G probably benign Het
Ptprd T C 4: 75,990,240 (GRCm39) K491E probably benign Het
Rbpjl A T 2: 164,247,734 (GRCm39) R62S probably benign Het
Rgs11 T C 17: 26,426,415 (GRCm39) S245P probably damaging Het
Ripor3 G A 2: 167,826,490 (GRCm39) A685V possibly damaging Het
Rnase9 G A 14: 51,276,940 (GRCm39) P13S possibly damaging Het
Saxo5 A T 8: 3,526,057 (GRCm39) H70L probably benign Het
Scin C T 12: 40,174,588 (GRCm39) C165Y probably damaging Het
Senp7 T C 16: 55,932,000 (GRCm39) W100R probably benign Het
Slc26a2 T C 18: 61,331,532 (GRCm39) D633G probably benign Het
Slc4a4 C T 5: 89,283,545 (GRCm39) P446S probably damaging Het
Spag17 T A 3: 100,002,911 (GRCm39) C1878* probably null Het
Ssc5d A G 7: 4,930,575 (GRCm39) E129G possibly damaging Het
Supt6 T C 11: 78,117,777 (GRCm39) N480D probably benign Het
Tbk1 A G 10: 121,388,406 (GRCm39) L590S probably damaging Het
Tmem63a T A 1: 180,780,539 (GRCm39) probably null Het
Tpsg1 G T 17: 25,592,184 (GRCm39) G86V probably damaging Het
Trio A G 15: 27,912,728 (GRCm39) S109P unknown Het
Ttn A T 2: 76,626,107 (GRCm39) L14984* probably null Het
Tyr T C 7: 87,133,092 (GRCm39) T325A probably benign Het
U2surp A T 9: 95,367,732 (GRCm39) probably null Het
Uba6 C A 5: 86,294,934 (GRCm39) K368N probably benign Het
Upb1 A G 10: 75,272,035 (GRCm39) T283A probably benign Het
Urb1 CACTTAC CAC 16: 90,569,461 (GRCm39) probably benign Het
Vmn1r31 A G 6: 58,449,455 (GRCm39) Y137H probably damaging Het
Wdtc1 T C 4: 133,023,748 (GRCm39) K541R probably damaging Het
Wrn A G 8: 33,800,741 (GRCm39) I624T possibly damaging Het
Zfp804b T A 5: 6,820,066 (GRCm39) D999V possibly damaging Het
Zmym4 T A 4: 126,819,588 (GRCm39) H105L probably benign Het
Other mutations in Tsga10
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00573:Tsga10 APN 1 37,846,151 (GRCm39) missense probably damaging 0.99
IGL00579:Tsga10 APN 1 37,874,534 (GRCm39) missense probably damaging 1.00
IGL00837:Tsga10 APN 1 37,840,992 (GRCm39) splice site probably benign
IGL01577:Tsga10 APN 1 37,874,538 (GRCm39) missense possibly damaging 0.85
IGL01727:Tsga10 APN 1 37,874,355 (GRCm39) missense probably damaging 1.00
IGL02037:Tsga10 APN 1 37,846,098 (GRCm39) missense probably benign 0.05
IGL02510:Tsga10 APN 1 37,800,066 (GRCm39) missense possibly damaging 0.89
R0346:Tsga10 UTSW 1 37,879,600 (GRCm39) missense possibly damaging 0.65
R0789:Tsga10 UTSW 1 37,840,868 (GRCm39) missense possibly damaging 0.87
R0961:Tsga10 UTSW 1 37,800,509 (GRCm39) critical splice donor site probably null
R1370:Tsga10 UTSW 1 37,874,534 (GRCm39) missense probably damaging 1.00
R1440:Tsga10 UTSW 1 37,858,680 (GRCm39) missense probably damaging 1.00
R1827:Tsga10 UTSW 1 37,874,661 (GRCm39) missense probably damaging 1.00
R2504:Tsga10 UTSW 1 37,854,758 (GRCm39) missense probably damaging 1.00
R3104:Tsga10 UTSW 1 37,840,872 (GRCm39) missense probably damaging 1.00
R3105:Tsga10 UTSW 1 37,840,872 (GRCm39) missense probably damaging 1.00
R3106:Tsga10 UTSW 1 37,840,872 (GRCm39) missense probably damaging 1.00
R3824:Tsga10 UTSW 1 37,873,278 (GRCm39) missense possibly damaging 0.73
R3825:Tsga10 UTSW 1 37,873,278 (GRCm39) missense possibly damaging 0.73
R4560:Tsga10 UTSW 1 37,846,163 (GRCm39) missense probably benign 0.00
R4773:Tsga10 UTSW 1 37,874,606 (GRCm39) missense probably damaging 1.00
R4927:Tsga10 UTSW 1 37,840,931 (GRCm39) missense probably damaging 1.00
R5036:Tsga10 UTSW 1 37,823,049 (GRCm39) missense possibly damaging 0.65
R5326:Tsga10 UTSW 1 37,800,598 (GRCm39) missense probably damaging 1.00
R5345:Tsga10 UTSW 1 37,802,392 (GRCm39) missense probably damaging 1.00
R5503:Tsga10 UTSW 1 37,800,028 (GRCm39) makesense probably null
R5542:Tsga10 UTSW 1 37,800,598 (GRCm39) missense probably damaging 1.00
R5793:Tsga10 UTSW 1 37,874,540 (GRCm39) missense probably damaging 1.00
R6340:Tsga10 UTSW 1 37,874,266 (GRCm39) intron probably benign
R7096:Tsga10 UTSW 1 37,879,695 (GRCm39) missense probably damaging 0.98
R7130:Tsga10 UTSW 1 37,822,965 (GRCm39) missense probably damaging 1.00
R7401:Tsga10 UTSW 1 37,873,268 (GRCm39) missense probably null 1.00
R7649:Tsga10 UTSW 1 37,874,229 (GRCm39) missense unknown
R7773:Tsga10 UTSW 1 37,874,323 (GRCm39) missense unknown
R8242:Tsga10 UTSW 1 37,846,182 (GRCm39) missense probably benign 0.28
R8379:Tsga10 UTSW 1 37,840,959 (GRCm39) missense probably benign 0.00
R9205:Tsga10 UTSW 1 37,880,359 (GRCm39) start gained probably benign
R9252:Tsga10 UTSW 1 37,873,364 (GRCm39) missense probably benign 0.35
Predicted Primers PCR Primer
(F):5'- GATTCGTGTCCTGGACCTTC -3'
(R):5'- CACTCCTTACCACAGTTGAAGC -3'

Sequencing Primer
(F):5'- GGACCTTCTGCTTTATGTCACTGAG -3'
(R):5'- GCCAAAATACTATCCTGTTG -3'
Posted On 2020-02-20