Incidental Mutation 'R3034:Tma7'
ID 264787
Institutional Source Beutler Lab
Gene Symbol Tma7
Ensembl Gene ENSMUSG00000091537
Gene Name translational machinery associated 7
Synonyms Ccdc72, 1110017O22Rik
MMRRC Submission 040550-MU
Accession Numbers
Essential gene? Possibly non essential (E-score: 0.405) question?
Stock # R3034 (G1)
Quality Score 225
Status Validated
Chromosome 9
Chromosomal Location 108907056-108911449 bp(-) (GRCm39)
Type of Mutation intron
DNA Base Change (assembly) T to C at 108911274 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000142209 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000026735] [ENSMUST00000167504] [ENSMUST00000192801]
AlphaFold Q8K003
Predicted Effect probably benign
Transcript: ENSMUST00000026735
SMART Domains Protein: ENSMUSP00000026735
Gene: ENSMUSG00000025645

DomainStartEndE-ValueType
coiled coil region 109 162 N/A INTRINSIC
low complexity region 224 236 N/A INTRINSIC
low complexity region 274 286 N/A INTRINSIC
transmembrane domain 381 403 N/A INTRINSIC
Predicted Effect unknown
Transcript: ENSMUST00000167504
AA Change: K13E
SMART Domains Protein: ENSMUSP00000133026
Gene: ENSMUSG00000091537
AA Change: K13E

DomainStartEndE-ValueType
Pfam:TMA7 3 64 4.9e-33 PFAM
Predicted Effect noncoding transcript
Transcript: ENSMUST00000192442
Predicted Effect probably benign
Transcript: ENSMUST00000192801
Predicted Effect noncoding transcript
Transcript: ENSMUST00000193868
Meta Mutation Damage Score 0.2366 question?
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.6%
  • 10x: 97.2%
  • 20x: 94.7%
Validation Efficiency 100% (44/44)
Allele List at MGI
Other mutations in this stock
Total: 42 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Alox12e T C 11: 70,207,079 (GRCm39) I576V probably benign Het
Apol7a T G 15: 77,273,923 (GRCm39) I180L probably benign Het
Aptx T C 4: 40,694,994 (GRCm39) N114S probably benign Het
Bltp3a T A 17: 28,113,720 (GRCm39) D1297E probably damaging Het
Cd40 T A 2: 164,904,235 (GRCm39) S65R probably benign Het
Cdh23 C T 10: 60,244,789 (GRCm39) probably benign Het
Coro7 G A 16: 4,450,155 (GRCm39) R565W probably damaging Het
Cpt1a C T 19: 3,428,390 (GRCm39) T588M probably damaging Het
Defb23 A G 2: 152,301,189 (GRCm39) S128P possibly damaging Het
Dgki G A 6: 37,064,605 (GRCm39) H250Y probably damaging Het
Fgr T C 4: 132,725,807 (GRCm39) probably null Het
Fkbp15 T C 4: 62,225,129 (GRCm39) probably null Het
Gpr137c C T 14: 45,457,733 (GRCm39) S95L probably damaging Het
Kirrel1 T C 3: 86,990,746 (GRCm39) D692G possibly damaging Het
Krt1 C A 15: 101,759,068 (GRCm39) R32L unknown Het
Lama2 C T 10: 26,877,231 (GRCm39) E2652K probably benign Het
Mbl1 C A 14: 40,880,790 (GRCm39) S226Y probably damaging Het
Mrps28 T A 3: 8,988,675 (GRCm39) D61V probably benign Het
Mthfd1 A G 12: 76,336,244 (GRCm39) K299E probably benign Het
Myo1b A G 1: 51,812,406 (GRCm39) Y738H possibly damaging Het
Myo5c A G 9: 75,193,859 (GRCm39) T1205A probably benign Het
Nfatc2 C T 2: 168,376,940 (GRCm39) G317S probably damaging Het
Nln C T 13: 104,173,947 (GRCm39) V525I possibly damaging Het
Nrap T C 19: 56,352,437 (GRCm39) E549G probably damaging Het
Nwd2 T A 5: 63,957,446 (GRCm39) Y259N probably damaging Het
Oas3 T C 5: 120,909,121 (GRCm39) D275G probably damaging Het
Or14a256 A T 7: 86,264,970 (GRCm39) D294E possibly damaging Het
Ovch2 A G 7: 107,384,699 (GRCm39) S473P probably damaging Het
Pde8b T A 13: 95,359,275 (GRCm39) Y16F probably damaging Het
Pmfbp1 A T 8: 110,247,553 (GRCm39) probably null Het
Pmvk T C 3: 89,375,824 (GRCm39) V74A probably damaging Het
Rab36 G A 10: 74,880,328 (GRCm39) V63I probably damaging Het
Rbm26 T A 14: 105,390,881 (GRCm39) T202S unknown Het
Rheb C T 5: 25,008,721 (GRCm39) E166K probably damaging Het
Rnf5 A G 17: 34,822,332 (GRCm39) V39A possibly damaging Het
Scn7a T C 2: 66,513,152 (GRCm39) Y1168C probably damaging Het
Tas2r114 A G 6: 131,666,611 (GRCm39) I139T probably benign Het
Tmem181a T A 17: 6,330,901 (GRCm39) S13T possibly damaging Het
Tmem62 C T 2: 120,809,605 (GRCm39) probably benign Het
Trim71 T C 9: 114,341,912 (GRCm39) D790G probably damaging Het
Trp53tg5 T C 2: 164,313,219 (GRCm39) K152R probably benign Het
Zdbf2 C A 1: 63,343,364 (GRCm39) A581E probably damaging Het
Other mutations in Tma7
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02176:Tma7 APN 9 108,911,153 (GRCm39) intron probably benign
IGL03268:Tma7 APN 9 108,907,450 (GRCm39) intron probably benign
R2205:Tma7 UTSW 9 108,911,294 (GRCm39) intron probably benign
R6577:Tma7 UTSW 9 108,911,262 (GRCm39) intron probably benign
R7091:Tma7 UTSW 9 108,911,580 (GRCm39) unclassified probably benign
R7631:Tma7 UTSW 9 108,911,507 (GRCm39) unclassified probably benign
Predicted Primers PCR Primer
(F):5'- TCGATCTTCACTTACCCAGGGG -3'
(R):5'- TAAGTCCTGTTTCCGGCATAC -3'

Sequencing Primer
(F):5'- GCGGCCTTGGCTTTTAGCTC -3'
(R):5'- CATACGATCAGGGGCTGGTG -3'
Posted On 2015-02-05