Incidental Mutation 'R5822:Pramel18'
ID 449970
Institutional Source Beutler Lab
Gene Symbol Pramel18
Ensembl Gene ENSMUSG00000037028
Gene Name PRAME like 18
Synonyms Gm12800
MMRRC Submission 044052-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.077) question?
Stock # R5822 (G1)
Quality Score 225
Status Validated
Chromosome 4
Chromosomal Location 101766318-101769105 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 101767440 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Valine at position 230 (M230V)
Ref Sequence ENSEMBL: ENSMUSP00000075380 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000075999]
AlphaFold B1AUV4
Predicted Effect probably damaging
Transcript: ENSMUST00000075999
AA Change: M230V

PolyPhen 2 Score 0.999 (Sensitivity: 0.14; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000075380
Gene: ENSMUSG00000037028
AA Change: M230V

DomainStartEndE-ValueType
SCOP:d1a4ya_ 206 410 9e-11 SMART
Meta Mutation Damage Score 0.1745 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.2%
  • 20x: 94.8%
Validation Efficiency 96% (54/56)
Allele List at MGI
Other mutations in this stock
Total: 51 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4930553M12Rik T C 4: 88,786,596 (GRCm39) I7M unknown Het
Abca8a C T 11: 109,921,705 (GRCm39) E1450K probably damaging Het
B4galnt2 T C 11: 95,756,985 (GRCm39) Y482C probably damaging Het
Bud23 A G 5: 135,092,775 (GRCm39) F9L probably damaging Het
Cacna1s A T 1: 136,039,816 (GRCm39) E1214V probably damaging Het
Cdh20 T C 1: 104,861,823 (GRCm39) M1T probably null Het
Chkb T C 15: 89,313,715 (GRCm39) E30G probably benign Het
Crp A C 1: 172,525,635 (GRCm39) probably benign Het
Cyp11b1 T C 15: 74,708,670 (GRCm39) R375G probably null Het
Ddx11 C T 17: 66,436,976 (GRCm39) S90L probably benign Het
Flnc A C 6: 29,459,429 (GRCm39) I2510L probably damaging Het
Ftdc1 C A 16: 58,436,075 (GRCm39) probably null Het
Fyb1 T A 15: 6,692,707 (GRCm39) probably benign Het
Gbp3 C T 3: 142,272,239 (GRCm39) P247L probably benign Het
Ggn C T 7: 28,871,981 (GRCm39) P454S probably damaging Het
Herc1 T A 9: 66,352,894 (GRCm39) S2127T probably benign Het
Ipo11 A G 13: 106,984,926 (GRCm39) probably benign Het
Kcnh7 G A 2: 62,546,582 (GRCm39) R1000W probably benign Het
Kdm5b A T 1: 134,516,511 (GRCm39) probably benign Het
Klc3 C T 7: 19,129,724 (GRCm39) probably null Het
Lst1 A T 17: 35,407,359 (GRCm39) M3K unknown Het
Madd C T 2: 90,982,878 (GRCm39) R1355Q probably damaging Het
Map3k10 A G 7: 27,356,159 (GRCm39) L920P probably damaging Het
Mdga2 A G 12: 66,702,109 (GRCm39) V423A probably damaging Het
Mogat2 T C 7: 98,869,112 (GRCm39) D302G possibly damaging Het
Nkapl A C 13: 21,652,593 (GRCm39) S7A unknown Het
Npas2 A G 1: 39,386,647 (GRCm39) S639G probably benign Het
Nr1h5 T G 3: 102,856,644 (GRCm39) H260P probably damaging Het
Or2g25 T C 17: 37,971,122 (GRCm39) Y34C probably damaging Het
Or2t49 A T 11: 58,392,464 (GRCm39) L306Q possibly damaging Het
Or4c35 T C 2: 89,808,787 (GRCm39) S222P probably damaging Het
Or7a36 C T 10: 78,820,023 (GRCm39) T133I possibly damaging Het
Or8a1b T C 9: 37,623,087 (GRCm39) M163V probably benign Het
Pan2 T C 10: 128,156,249 (GRCm39) L1142P probably damaging Het
Pdik1l C T 4: 134,014,474 (GRCm39) E11K possibly damaging Het
Ppp1r15a A G 7: 45,172,727 (GRCm39) V555A probably damaging Het
Ppp6c G A 2: 39,090,064 (GRCm39) Q81* probably null Het
Ptprz1 A T 6: 23,001,444 (GRCm39) Y1178F probably benign Het
Relch G A 1: 105,646,581 (GRCm39) V660M probably damaging Het
Rictor G A 15: 6,823,487 (GRCm39) E1555K probably benign Het
Rims2 T A 15: 39,339,886 (GRCm39) L860Q probably damaging Het
Sdr39u1 A G 14: 56,135,196 (GRCm39) V249A probably benign Het
Serhl T C 15: 83,000,528 (GRCm39) V305A probably benign Het
Slc5a11 T C 7: 122,851,654 (GRCm39) I201T probably damaging Het
Stk32a A T 18: 43,446,552 (GRCm39) E334V probably benign Het
Tmem217 A G 17: 29,745,529 (GRCm39) L67P probably damaging Het
Tnnt1 A T 7: 4,519,345 (GRCm39) L12* probably null Het
Trim80 C T 11: 115,338,747 (GRCm39) R526C probably damaging Het
Unc5b A T 10: 60,608,306 (GRCm39) F635I possibly damaging Het
Utp20 T G 10: 88,653,147 (GRCm39) N311T probably benign Het
Zfp276 A G 8: 123,982,457 (GRCm39) T74A probably benign Het
Other mutations in Pramel18
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02430:Pramel18 APN 4 101,767,477 (GRCm39) missense probably benign 0.02
IGL02683:Pramel18 APN 4 101,767,551 (GRCm39) missense probably benign 0.00
IGL03403:Pramel18 APN 4 101,767,125 (GRCm39) missense probably benign 0.40
R0833:Pramel18 UTSW 4 101,767,294 (GRCm39) missense probably damaging 0.97
R1054:Pramel18 UTSW 4 101,766,361 (GRCm39) missense probably benign 0.00
R1953:Pramel18 UTSW 4 101,767,312 (GRCm39) missense probably benign
R2216:Pramel18 UTSW 4 101,767,257 (GRCm39) missense probably damaging 0.99
R3746:Pramel18 UTSW 4 101,767,073 (GRCm39) missense possibly damaging 0.63
R3747:Pramel18 UTSW 4 101,767,073 (GRCm39) missense possibly damaging 0.63
R3750:Pramel18 UTSW 4 101,767,073 (GRCm39) missense possibly damaging 0.63
R4931:Pramel18 UTSW 4 101,766,367 (GRCm39) missense possibly damaging 0.47
R5102:Pramel18 UTSW 4 101,766,436 (GRCm39) missense probably damaging 1.00
R5586:Pramel18 UTSW 4 101,767,317 (GRCm39) missense probably benign 0.00
R6395:Pramel18 UTSW 4 101,767,189 (GRCm39) missense probably benign
R6904:Pramel18 UTSW 4 101,767,291 (GRCm39) missense possibly damaging 0.86
R7544:Pramel18 UTSW 4 101,768,599 (GRCm39) missense possibly damaging 0.56
R7768:Pramel18 UTSW 4 101,769,010 (GRCm39) missense probably benign
R8342:Pramel18 UTSW 4 101,767,581 (GRCm39) missense probably benign 0.01
R8917:Pramel18 UTSW 4 101,768,935 (GRCm39) missense probably benign 0.09
Z1088:Pramel18 UTSW 4 101,766,315 (GRCm39) splice site probably null
Z1088:Pramel18 UTSW 4 101,767,383 (GRCm39) missense probably benign 0.00
Predicted Primers PCR Primer
(F):5'- TTCTACAATGGGCCCAGCAG -3'
(R):5'- AGAAACAGGTCCCCATCTTTCC -3'

Sequencing Primer
(F):5'- CCCAGCAGAGAAACGAGTATGTG -3'
(R):5'- AACAAGTGTTTCATGTGGTCCC -3'
Posted On 2016-12-20