Incidental Mutation 'IGL03136:Tprg'
ID410549
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Tprg
Ensembl Gene ENSMUSG00000048399
Gene Nametransformation related protein 63 regulated
Synonyms
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.068) question?
Stock #IGL03136
Quality Score
Status
Chromosome16
Chromosomal Location25286817-25422344 bp(+) (GRCm38)
Type of Mutationsplice site
DNA Base Change (assembly) T to C at 25412762 bp
ZygosityHeterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000052585 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056087]
Predicted Effect probably benign
Transcript: ENSMUST00000056087
SMART Domains Protein: ENSMUSP00000052585
Gene: ENSMUSG00000048399

DomainStartEndE-ValueType
Pfam:hSac2 69 176 1.8e-31 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730522E02Rik A G 11: 25,769,122 L7S unknown Het
Abr C T 11: 76,425,295 W571* probably null Het
Adam18 A T 8: 24,641,836 C420S probably damaging Het
Akap5 G T 12: 76,329,875 E694* probably null Het
Bbs1 T C 19: 4,890,991 K565R probably benign Het
Brix1 A G 15: 10,478,766 F189S probably damaging Het
Cnot4 C A 6: 35,051,241 R480L probably damaging Het
Ctu2 A G 8: 122,479,201 probably benign Het
Dhcr7 A G 7: 143,847,366 H422R probably damaging Het
Dock1 A G 7: 135,168,389 M1793V probably benign Het
Dock7 A G 4: 99,003,791 F853L probably damaging Het
Fkbp15 G A 4: 62,340,229 probably benign Het
Ftsj3 C T 11: 106,253,813 D117N probably damaging Het
Gphn A G 12: 78,481,333 I142V possibly damaging Het
Hsd3b1 G A 3: 98,852,985 A230V probably damaging Het
Hydin G A 8: 110,418,524 A836T probably benign Het
Ift52 G T 2: 163,025,334 E71* probably null Het
Ms4a14 T C 19: 11,304,411 D261G possibly damaging Het
Nid1 G A 13: 13,500,499 V935I probably benign Het
Nrap T C 19: 56,342,255 K1008E possibly damaging Het
Nup210 A C 6: 91,028,861 V1340G probably benign Het
Olfr1442 T A 19: 12,674,967 I254N probably damaging Het
Olfr169 A T 16: 19,566,353 F177I probably damaging Het
Olfr974 T C 9: 39,943,036 Y259H probably damaging Het
Pcdhb15 C A 18: 37,475,014 T433N probably damaging Het
Pdcd6ip T A 9: 113,691,499 N139I probably damaging Het
Pgbd1 A G 13: 21,433,439 V80A possibly damaging Het
Pigw A G 11: 84,877,777 I242T probably benign Het
Prtg T G 9: 72,856,985 V580G possibly damaging Het
Ptpn13 T A 5: 103,543,463 N1065K possibly damaging Het
Qrich1 G A 9: 108,544,918 R577H probably damaging Het
Ryr3 G A 2: 112,675,974 probably benign Het
Selenoi T C 5: 30,257,727 Y197H probably damaging Het
Slc47a2 A G 11: 61,310,765 C343R probably benign Het
Smurf2 A T 11: 106,831,048 D527E probably benign Het
Spam1 C T 6: 24,797,011 probably benign Het
Stkld1 T C 2: 26,951,423 V460A probably benign Het
Tgoln1 G A 6: 72,614,113 R339W probably damaging Het
Treml1 T G 17: 48,364,851 probably benign Het
Ttc39b A T 4: 83,237,280 V497E probably damaging Het
Vmn1r223 A G 13: 23,249,763 T176A possibly damaging Het
Vmn2r75 A T 7: 86,148,703 I634N possibly damaging Het
Vps13c A G 9: 67,950,310 E2608G probably damaging Het
Zfp575 A G 7: 24,585,956 C87R probably damaging Het
Zfp790 T A 7: 29,829,895 Y668* probably null Het
Other mutations in Tprg
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02999:Tprg APN 16 25317468 missense probably damaging 1.00
R0383:Tprg UTSW 16 25422235 missense probably damaging 1.00
R0831:Tprg UTSW 16 25317469 missense probably damaging 1.00
R1217:Tprg UTSW 16 25412843 missense probably damaging 1.00
R1885:Tprg UTSW 16 25412891 missense probably benign 0.11
R1950:Tprg UTSW 16 25317348 missense possibly damaging 0.83
R2869:Tprg UTSW 16 25412840 missense probably damaging 1.00
R2869:Tprg UTSW 16 25412840 missense probably damaging 1.00
R5935:Tprg UTSW 16 25317261 start codon destroyed possibly damaging 0.89
R6122:Tprg UTSW 16 25422401 splice site probably null
R7423:Tprg UTSW 16 25422253 missense probably damaging 1.00
Posted On2016-08-02