Incidental Mutation 'R8247:Zfp367'
ID 640729
Institutional Source Beutler Lab
Gene Symbol Zfp367
Ensembl Gene ENSMUSG00000044934
Gene Name zinc finger protein 367
Synonyms 8030486J21Rik, ZFF29a, ZFF29b
MMRRC Submission 067674-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R8247 (G1)
Quality Score 117.008
Status Not validated
Chromosome 13
Chromosomal Location 64280836-64301013 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 64300482 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 108 (S108P)
Ref Sequence ENSEMBL: ENSMUSP00000050854 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059817] [ENSMUST00000117241]
AlphaFold Q0VDT2
Predicted Effect probably benign
Transcript: ENSMUST00000059817
AA Change: S108P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000050854
Gene: ENSMUSG00000044934
AA Change: S108P

DomainStartEndE-ValueType
low complexity region 5 14 N/A INTRINSIC
low complexity region 37 59 N/A INTRINSIC
low complexity region 77 94 N/A INTRINSIC
low complexity region 105 113 N/A INTRINSIC
ZnF_C2H2 157 179 3.44e-4 SMART
ZnF_C2H2 185 209 2.4e-3 SMART
coiled coil region 299 332 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000117241
AA Change: S108P

PolyPhen 2 Score 0.000 (Sensitivity: 1.00; Specificity: 0.00)
SMART Domains Protein: ENSMUSP00000113331
Gene: ENSMUSG00000044934
AA Change: S108P

DomainStartEndE-ValueType
low complexity region 5 14 N/A INTRINSIC
low complexity region 37 59 N/A INTRINSIC
low complexity region 77 94 N/A INTRINSIC
low complexity region 105 113 N/A INTRINSIC
ZnF_C2H2 157 179 3.44e-4 SMART
ZnF_C2H2 185 209 2.4e-3 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.9%
Validation Efficiency 99% (69/70)
Allele List at MGI
Other mutations in this stock
Total: 70 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
5730596B20Rik T C 6: 52,155,942 (GRCm39) S3P unknown Het
Abca15 A T 7: 119,936,445 (GRCm39) Y170F possibly damaging Het
Alpl C T 4: 137,473,764 (GRCm39) V313M probably damaging Het
Ankrd44 T C 1: 54,792,102 (GRCm39) H311R probably damaging Het
Atm A T 9: 53,361,870 (GRCm39) L2749Q Het
Bicd2 C T 13: 49,533,462 (GRCm39) R683W probably damaging Het
Brat1 C A 5: 140,698,893 (GRCm39) P342T possibly damaging Het
Camta1 T A 4: 151,159,721 (GRCm39) T482S probably damaging Het
Carhsp1 A G 16: 8,481,535 (GRCm39) V67A probably damaging Het
Carmil1 T A 13: 24,282,998 (GRCm39) N512I probably damaging Het
Ccdc126 C T 6: 49,316,775 (GRCm39) T85M probably damaging Het
Cd274 C T 19: 29,362,795 (GRCm39) Q286* probably null Het
Cep192 T A 18: 67,974,188 (GRCm39) I1097N probably benign Het
Cimip4 A C 15: 78,262,992 (GRCm39) S221A probably benign Het
Clvs1 A T 4: 9,281,885 (GRCm39) N110Y possibly damaging Het
Cntln A G 4: 85,019,017 (GRCm39) T102A probably benign Het
Cp A C 3: 20,020,570 (GRCm39) I188L possibly damaging Het
Crh A G 3: 19,748,291 (GRCm39) L117P probably benign Het
Dcaf1 A T 9: 106,731,427 (GRCm39) I635F possibly damaging Het
Dennd2c A G 3: 103,059,637 (GRCm39) D521G probably damaging Het
E2f2 C T 4: 135,900,126 (GRCm39) T12M possibly damaging Het
Eid2 G A 7: 27,967,972 (GRCm39) R198H probably damaging Het
Exosc4 G T 15: 76,213,279 (GRCm39) C74F probably damaging Het
Fanca A T 8: 124,010,694 (GRCm39) probably benign Het
Ganc A T 2: 120,267,181 (GRCm39) Q499L probably null Het
Gfy T C 7: 44,827,710 (GRCm39) T129A possibly damaging Het
Gli3 G T 13: 15,901,360 (GRCm39) M1582I possibly damaging Het
Gm4744 A G 6: 40,926,402 (GRCm39) S63P Het
Htr2b T C 1: 86,027,817 (GRCm39) T230A probably benign Het
Iqcb1 T A 16: 36,678,836 (GRCm39) N383K probably benign Het
Lpcat1 A T 13: 73,662,071 (GRCm39) I471F probably damaging Het
Lrch3 T G 16: 32,829,713 (GRCm39) L781* probably null Het
Lrif1 T A 3: 106,641,692 (GRCm39) S3T probably damaging Het
Lrp2 T A 2: 69,261,431 (GRCm39) R4503S possibly damaging Het
Lrrc8c T C 5: 105,756,310 (GRCm39) I695T probably damaging Het
Mak G A 13: 41,193,146 (GRCm39) T473M possibly damaging Het
Map2k5 A T 9: 63,279,019 (GRCm39) Y62N probably damaging Het
Mbd3l2 T C 9: 18,356,299 (GRCm39) L208P probably damaging Het
Myo18b T C 5: 112,840,062 (GRCm39) E2577G probably damaging Het
Nfia A T 4: 97,953,644 (GRCm39) T461S probably benign Het
Oaz3 A G 3: 94,343,741 (GRCm39) Y41H probably damaging Het
Or10ab5 T A 7: 108,245,370 (GRCm39) I138F probably damaging Het
Or1p1 C A 11: 74,180,315 (GRCm39) T281K noncoding transcript Het
Or2ad1 A G 13: 21,326,295 (GRCm39) S311P probably benign Het
Or51m1 T C 7: 103,578,783 (GRCm39) V251A possibly damaging Het
Pin1rt1 T C 2: 104,544,892 (GRCm39) E80G probably damaging Het
Pmpcb T C 5: 21,961,852 (GRCm39) Y457H probably damaging Het
Polr2b T C 5: 77,468,062 (GRCm39) S121P possibly damaging Het
Ppm1e C T 11: 87,122,101 (GRCm39) G619R probably benign Het
Pramel5 T A 4: 143,999,395 (GRCm39) M231L probably damaging Het
Prex2 G T 1: 11,270,194 (GRCm39) C1293F probably benign Het
Psg20 A G 7: 18,416,562 (GRCm39) F185L probably benign Het
Psg28 A G 7: 18,156,864 (GRCm39) V457A probably benign Het
Pxmp2 A G 5: 110,422,445 (GRCm39) L188P probably damaging Het
Scd3 A T 19: 44,227,003 (GRCm39) N279I possibly damaging Het
Scg2 T G 1: 79,414,236 (GRCm39) K162N possibly damaging Het
Sipa1l2 T C 8: 126,149,372 (GRCm39) E1629G probably benign Het
Slc27a2 T A 2: 126,395,515 (GRCm39) F147L probably benign Het
Smco1 T C 16: 32,092,557 (GRCm39) V76A probably benign Het
Spic T C 10: 88,511,923 (GRCm39) K111R probably damaging Het
Spidr A G 16: 15,786,390 (GRCm39) probably null Het
Sptbn1 T A 11: 30,063,906 (GRCm39) I1971F possibly damaging Het
Stard8 C T X: 98,109,570 (GRCm39) S155L probably benign Het
Tiam1 G A 16: 89,695,037 (GRCm39) T140M probably benign Het
Ttc28 G A 5: 111,381,207 (GRCm39) D1240N probably benign Het
Ufl1 T C 4: 25,250,606 (GRCm39) E749G probably benign Het
Vmn1r168 G T 7: 23,240,487 (GRCm39) V115F possibly damaging Het
Wars2 G A 3: 99,094,965 (GRCm39) V87I probably benign Het
Zdhhc14 T A 17: 5,736,031 (GRCm39) C170S probably damaging Het
Zfp113 C T 5: 138,143,296 (GRCm39) C318Y possibly damaging Het
Other mutations in Zfp367
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01147:Zfp367 APN 13 64,283,253 (GRCm39) missense probably damaging 1.00
IGL03151:Zfp367 APN 13 64,293,445 (GRCm39) missense probably damaging 1.00
IGL03267:Zfp367 APN 13 64,292,097 (GRCm39) splice site probably benign
fisher UTSW 13 64,293,457 (GRCm39) missense probably damaging 1.00
Otter UTSW 13 64,292,069 (GRCm39) nonsense probably null
R4608:Zfp367 UTSW 13 64,283,238 (GRCm39) missense probably damaging 1.00
R6180:Zfp367 UTSW 13 64,283,204 (GRCm39) missense probably damaging 1.00
R6531:Zfp367 UTSW 13 64,292,064 (GRCm39) missense probably damaging 1.00
R7727:Zfp367 UTSW 13 64,293,457 (GRCm39) missense probably damaging 1.00
R8754:Zfp367 UTSW 13 64,292,069 (GRCm39) nonsense probably null
R9557:Zfp367 UTSW 13 64,300,586 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- ACAGCAGTGCAAGGCATCTG -3'
(R):5'- TACTGGTATCGGTCATCAGGAC -3'

Sequencing Primer
(F):5'- TGCAAGGCATCTGGACAC -3'
(R):5'- TCATCAGGACCACGCCG -3'
Posted On 2020-07-28