Incidental Mutation 'R8077:Prdm12'
ID629060
Institutional Source Beutler Lab
Gene Symbol Prdm12
Ensembl Gene ENSMUSG00000079466
Gene NamePR domain containing 12
SynonymsLOC381359
Accession Numbers
Is this an essential gene? Essential (E-score: 1.000) question?
Stock #R8077 (G1)
Quality Score225.009
Status Validated
Chromosome2
Chromosomal Location31640037-31655795 bp(+) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 31642304 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Glutamic Acid at position 109 (K109E)
Ref Sequence ENSEMBL: ENSMUSP00000109098 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000113470]
Predicted Effect probably damaging
Transcript: ENSMUST00000113470
AA Change: K109E

PolyPhen 2 Score 0.987 (Sensitivity: 0.73; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000109098
Gene: ENSMUSG00000079466
AA Change: K109E

DomainStartEndE-ValueType
SET 86 209 1.24e-4 SMART
ZnF_C2H2 243 265 5.5e-3 SMART
ZnF_C2H2 271 293 1.82e-3 SMART
ZnF_C2H2 299 323 2.17e-1 SMART
low complexity region 329 362 N/A INTRINSIC
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.8%
  • 20x: 95.4%
Validation Efficiency 100% (60/60)
Allele List at MGI
Other mutations in this stock
Total: 61 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700093K21Rik A T 11: 23,517,237 V132E probably benign Het
4930563M21Rik C T 9: 55,987,966 V315M probably damaging Het
9430007A20Rik T C 4: 144,528,556 I182T probably benign Het
Alb G C 5: 90,467,355 R242P probably damaging Het
Amotl1 A T 9: 14,550,502 V805D probably damaging Het
Arhgef3 T C 14: 27,385,924 L179P probably damaging Het
Atp8b3 G A 10: 80,531,024 L247F possibly damaging Het
Ccdc191 T C 16: 43,915,605 probably null Het
Celsr3 A G 9: 108,828,331 H671R probably benign Het
Cemip C A 7: 84,003,408 probably benign Het
Cfap97 G T 8: 46,170,445 V291F possibly damaging Het
Clca2 A G 3: 145,071,527 V861A possibly damaging Het
Cln8 A T 8: 14,894,950 D88V probably damaging Het
Col18a1 C A 10: 77,080,851 G330V unknown Het
Dis3 C T 14: 99,090,035 R344Q probably benign Het
Esyt2 T A 12: 116,342,228 S359R possibly damaging Het
Fbxo41 A T 6: 85,473,229 L844Q probably damaging Het
Fn1 G A 1: 71,612,602 T1372M probably damaging Het
Gbp5 G A 3: 142,507,739 R472H probably benign Het
Gm156 A G 6: 129,766,695 Y209H probably benign Het
Gm21964 C T 8: 110,110,103 T207M probably damaging Het
Gm4559 C T 7: 142,273,816 R183K unknown Het
Gm9507 T A 10: 77,811,770 E25V unknown Het
Gm9573 TCAGTGGTGGTCAGGATGGGGGTAGAGCCTGAGCCACTCCTGGATGCAGTGGTGGTCAGG TCAGTGGTGGTCAGG 17: 35,619,736 probably benign Het
Golgb1 A G 16: 36,918,633 I2486V probably damaging Het
Ifitm10 A T 7: 142,370,967 V45D probably damaging Het
Ift80 A G 3: 68,916,145 Y595H probably benign Het
Itga8 C T 2: 12,242,433 V326I probably benign Het
Kif14 A T 1: 136,471,448 H449L possibly damaging Het
Ldlrad1 G A 4: 107,209,491 A8T probably benign Het
Lrrc8b C A 5: 105,480,017 S76R possibly damaging Het
Lrrn1 T C 6: 107,568,822 L527P probably damaging Het
Luc7l T C 17: 26,255,073 V35A probably damaging Het
Luzp1 T G 4: 136,543,091 V875G probably damaging Het
Mcf2l G T 8: 12,998,494 probably null Het
Mcoln2 T C 3: 146,190,414 M497T probably damaging Het
Mrgprb4 A T 7: 48,198,455 S242T probably benign Het
Nipbl T A 15: 8,311,250 R1995S possibly damaging Het
Nup35 A G 2: 80,638,936 probably null Het
Olfr1394 A G 11: 49,160,485 D157G probably damaging Het
Olfr420 A G 1: 174,151,845 probably benign Het
Olfr45 C T 7: 140,691,133 S76F probably benign Het
Ptch1 A T 13: 63,540,812 L444Q probably damaging Het
Qtrt1 C T 9: 21,420,096 R374* probably null Het
Rnase11 T C 14: 51,049,941 D52G probably damaging Het
Rps6 A G 4: 86,855,921 S148P probably benign Het
Rrm2b T C 15: 37,946,800 K86E possibly damaging Het
Sh2d1b2 A G 1: 170,248,173 K59E possibly damaging Het
Six6 T A 12: 72,940,326 W91R probably damaging Het
Slc23a2 C A 2: 132,089,172 A136S possibly damaging Het
Slc9a5 G A 8: 105,359,380 R593H probably damaging Het
Smbd1 T C 16: 32,810,434 M1V probably null Het
Ssbp4 T C 8: 70,598,997 Y239C probably damaging Het
Stox1 T C 10: 62,665,566 E405G probably damaging Het
Tmem192 A G 8: 64,965,544 I194V probably benign Het
Tns3 A T 11: 8,445,667 C1246S probably damaging Het
Ugt1a6a A T 1: 88,138,853 Q127L probably benign Het
Ush2a A G 1: 188,542,828 I1833V probably benign Het
Vmn2r66 A T 7: 85,006,885 Y308N probably benign Het
Vti1a T G 19: 55,576,485 L191R probably benign Het
Zbtb38 A T 9: 96,688,100 N310K probably benign Het
Other mutations in Prdm12
AlleleSourceChrCoordTypePredicted EffectPPH Score
R0674:Prdm12 UTSW 2 31643912 missense probably benign 0.23
R1424:Prdm12 UTSW 2 31643811 missense probably damaging 1.00
R1434:Prdm12 UTSW 2 31640307 missense possibly damaging 0.73
R1495:Prdm12 UTSW 2 31640193 missense probably damaging 1.00
R1509:Prdm12 UTSW 2 31654174 missense probably damaging 1.00
R2135:Prdm12 UTSW 2 31640313 missense possibly damaging 0.73
R2432:Prdm12 UTSW 2 31651852 missense probably benign 0.02
R3801:Prdm12 UTSW 2 31651947 missense probably damaging 0.96
R6092:Prdm12 UTSW 2 31643877 missense probably damaging 1.00
R6311:Prdm12 UTSW 2 31654309 missense probably benign 0.14
R6511:Prdm12 UTSW 2 31640309 missense probably damaging 0.99
R7252:Prdm12 UTSW 2 31642374 missense possibly damaging 0.92
R7292:Prdm12 UTSW 2 31643850 missense probably damaging 1.00
R7686:Prdm12 UTSW 2 31640217 missense probably damaging 0.96
R7747:Prdm12 UTSW 2 31653871 intron probably null
R7872:Prdm12 UTSW 2 31640219 missense probably damaging 1.00
X0023:Prdm12 UTSW 2 31640280 missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ATTTGCCACTGGAGAGAGTTGG -3'
(R):5'- GCCAGACAGAGTTCCTTTCTGC -3'

Sequencing Primer
(F):5'- GCTGCTTGTGCTCGCAG -3'
(R):5'- TTCTGCCGCCAGTGGATAC -3'
Posted On2020-06-30