Incidental Mutation 'R7154:Ttc30b'
ID557124
Institutional Source Beutler Lab
Gene Symbol Ttc30b
Ensembl Gene ENSMUSG00000075273
Gene Nametetratricopeptide repeat domain 30B
Synonyms
MMRRC Submission
Accession Numbers
Is this an essential gene? Non essential (E-score: 0.000) question?
Stock #R7154 (G1)
Quality Score225.009
Status Validated
Chromosome2
Chromosomal Location75935849-75938585 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) C to T at 75938061 bp
ZygosityHeterozygous
Amino Acid Change Arginine to Histidine at position 116 (R116H)
Ref Sequence ENSEMBL: ENSMUSP00000097576 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099996]
Predicted Effect possibly damaging
Transcript: ENSMUST00000099996
AA Change: R116H

PolyPhen 2 Score 0.880 (Sensitivity: 0.82; Specificity: 0.94)
SMART Domains Protein: ENSMUSP00000097576
Gene: ENSMUSG00000075273
AA Change: R116H

DomainStartEndE-ValueType
TPR 45 78 1.1e-1 SMART
TPR 153 186 3.89e1 SMART
TPR 187 220 6.24e1 SMART
TPR 423 456 7.49e1 SMART
Blast:TPR 457 491 3e-10 BLAST
low complexity region 514 528 N/A INTRINSIC
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.1%
Validation Efficiency 100% (67/67)
Allele List at MGI
Other mutations in this stock
Total: 67 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
8030423J24Rik T C 13: 70,884,225 F139L unknown Het
Adgre1 G A 17: 57,444,087 probably null Het
Agap2 A G 10: 127,091,655 D1135G probably benign Het
Akp3 T C 1: 87,125,224 L45P probably damaging Het
Arfgap3 A T 15: 83,336,704 W71R probably damaging Het
Asic3 G A 5: 24,413,662 probably benign Het
Asph A T 4: 9,630,930 N139K possibly damaging Het
Atr T A 9: 95,865,045 C127S probably benign Het
Auts2 A T 5: 131,451,893 S255T Het
Bcl6 G A 16: 23,966,226 R675* probably null Het
Cacnb1 A G 11: 98,005,133 L443P probably damaging Het
Cbfa2t3 G A 8: 122,638,144 Q300* probably null Het
Ccer1 A T 10: 97,694,339 D288V unknown Het
Col18a1 G A 10: 77,072,965 P611S probably benign Het
Cpa6 T A 1: 10,337,469 D281V possibly damaging Het
Cyp2e1 A G 7: 140,770,137 Y245C probably damaging Het
Cyp4a31 T C 4: 115,574,766 probably null Het
Entpd1 T C 19: 40,724,986 Y188H probably damaging Het
Epb42 T C 2: 121,033,362 D111G probably benign Het
Espl1 A G 15: 102,324,049 D2064G probably damaging Het
Fat3 A C 9: 15,996,864 V2614G probably damaging Het
Fos A T 12: 85,474,157 M40L probably benign Het
Frmd4b T A 6: 97,306,746 E434V probably damaging Het
Galnt6 A T 15: 100,693,464 D586E probably benign Het
Gapvd1 T C 2: 34,725,063 K474R probably damaging Het
Gimap8 T A 6: 48,656,188 F314I probably damaging Het
Gm10696 A G 3: 94,176,219 I95T probably benign Het
Gm11639 T A 11: 104,699,140 probably null Het
Gm14393 T G 2: 175,061,783 K110N probably damaging Het
Gm4131 C A 14: 62,480,933 A75S probably damaging Het
Heatr6 G A 11: 83,777,241 V854I probably benign Het
Hic2 T A 16: 17,258,942 M545K possibly damaging Het
Ip6k1 A G 9: 108,045,662 Y331C probably damaging Het
Kalrn C T 16: 34,212,157 probably null Het
Kxd1 T C 8: 70,515,434 K88E probably damaging Het
Lrrc37a A C 11: 103,502,856 V581G probably benign Het
Mex3d A T 10: 80,386,750 V224E Het
Mtx2 T A 2: 74,876,418 C246S probably damaging Het
Mybbp1a A G 11: 72,447,642 probably null Het
Myh6 A G 14: 54,960,307 I458T probably benign Het
Ndufs6 A G 13: 73,320,292 V96A possibly damaging Het
Nemf A T 12: 69,316,741 probably null Het
Notch1 T C 2: 26,459,938 S2397G probably benign Het
Olfr1229 A G 2: 89,282,860 I91T probably damaging Het
Olfr522 T C 7: 140,162,084 I289V probably benign Het
Osbpl1a T C 18: 12,768,592 E619G probably benign Het
Pfkl T C 10: 78,001,455 R95G probably benign Het
Plat T A 8: 22,778,505 I391K possibly damaging Het
Ppp1r21 A G 17: 88,554,886 H244R probably damaging Het
Rapgef3 G C 15: 97,753,877 H578Q probably benign Het
Rnf145 C A 11: 44,524,995 N12K probably damaging Het
Sfxn5 C T 6: 85,332,423 C100Y unknown Het
Sh3rf1 T A 8: 61,372,714 L581Q possibly damaging Het
Sipa1l2 T C 8: 125,468,339 K887E probably benign Het
Stard9 C A 2: 120,701,314 T2684N probably benign Het
Stard9 A C 2: 120,704,542 Q3760P probably benign Het
Stpg2 A G 3: 139,215,295 E87G probably benign Het
Syne2 A G 12: 76,059,457 Q792R possibly damaging Het
Taf7 T C 18: 37,642,548 D322G possibly damaging Het
Tbc1d1 A G 5: 64,173,813 S112G possibly damaging Het
Tbx3 A G 5: 119,672,028 M5V possibly damaging Het
Tmem45b A T 9: 31,428,032 I215N possibly damaging Het
Tpd52 G A 3: 8,963,856 Q43* probably null Het
Trpa1 T A 1: 14,882,233 N858I possibly damaging Het
Ttll5 A G 12: 85,925,764 D767G probably damaging Het
Vmn2r3 G A 3: 64,287,311 T62I probably benign Het
Wdr59 A T 8: 111,458,735 N874K Het
Other mutations in Ttc30b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01525:Ttc30b APN 2 75936882 missense probably damaging 1.00
IGL02565:Ttc30b APN 2 75937903 missense probably benign 0.03
IGL02891:Ttc30b APN 2 75937060 missense possibly damaging 0.88
R0383:Ttc30b UTSW 2 75938242 missense probably damaging 1.00
R0542:Ttc30b UTSW 2 75936711 missense probably damaging 0.98
R1470:Ttc30b UTSW 2 75937811 missense probably benign
R1470:Ttc30b UTSW 2 75937811 missense probably benign
R1656:Ttc30b UTSW 2 75937416 missense probably benign 0.26
R1951:Ttc30b UTSW 2 75937242 missense probably damaging 1.00
R1959:Ttc30b UTSW 2 75937099 missense probably benign 0.06
R1994:Ttc30b UTSW 2 75938058 missense probably damaging 1.00
R2132:Ttc30b UTSW 2 75936785 missense probably damaging 1.00
R4968:Ttc30b UTSW 2 75938047 missense probably benign 0.00
R6110:Ttc30b UTSW 2 75937800 missense probably damaging 1.00
R6502:Ttc30b UTSW 2 75937104 missense possibly damaging 0.87
R7182:Ttc30b UTSW 2 75937949 nonsense probably null
R7269:Ttc30b UTSW 2 75937494 missense probably damaging 1.00
Z1088:Ttc30b UTSW 2 75937982 missense probably benign
Predicted Primers PCR Primer
(F):5'- AGGCAGCTTCATAGTGTCCCTC -3'
(R):5'- CAGTGGTGTACAGGCTCATC -3'

Sequencing Primer
(F):5'- CTCTTTGTAGAGCAGACAACCTAGG -3'
(R):5'- TACTACCGCCTGCAGGAGTTC -3'
Posted On2019-06-26