Incidental Mutation 'R1415:Zfp787'
ID 262758
Institutional Source Beutler Lab
Gene Symbol Zfp787
Ensembl Gene ENSMUSG00000046792
Gene Name zinc finger protein 787
Synonyms 2210018M03Rik
MMRRC Submission 039471-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R1415 (G1)
Quality Score 91
Status Not validated
Chromosome 7
Chromosomal Location 6134490-6158996 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 6135694 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glycine to Cysteine at position 186 (G186C)
Ref Sequence ENSEMBL: ENSMUSP00000092468 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000094870] [ENSMUST00000207315]
AlphaFold Q8BIF9
Predicted Effect probably damaging
Transcript: ENSMUST00000094870
AA Change: G186C

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000092468
Gene: ENSMUSG00000046792
AA Change: G186C

DomainStartEndE-ValueType
low complexity region 41 65 N/A INTRINSIC
ZnF_C2H2 66 88 5.67e-5 SMART
ZnF_C2H2 94 116 9.58e-3 SMART
ZnF_C2H2 122 144 1.84e-4 SMART
ZnF_C2H2 150 172 1.3e-4 SMART
ZnF_C2H2 178 200 6.88e-4 SMART
low complexity region 245 277 N/A INTRINSIC
ZnF_C2H2 280 303 2.36e-2 SMART
ZnF_C2H2 317 339 4.72e-2 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000207315
Predicted Effect noncoding transcript
Transcript: ENSMUST00000208973
Coding Region Coverage
  • 1x: 98.9%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 27 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acacb T C 5: 114,303,982 (GRCm39) V135A probably benign Het
Adam21 C T 12: 81,606,321 (GRCm39) W480* probably null Het
Ccdc71 T A 9: 108,340,407 (GRCm39) Y73* probably null Het
Cfap44 T A 16: 44,301,752 (GRCm39) I1830N probably damaging Het
Dnajb11 T C 16: 22,689,371 (GRCm39) V264A probably benign Het
Fam135b T C 15: 71,328,777 (GRCm39) E1174G probably damaging Het
Fam83e G A 7: 45,376,135 (GRCm39) E283K probably damaging Het
Gigyf1 A G 5: 137,517,478 (GRCm39) probably null Het
Letm1 A T 5: 33,926,906 (GRCm39) N130K probably benign Het
Lrp1b T C 2: 40,519,676 (GRCm39) Y137C probably damaging Het
Map3k2 A G 18: 32,361,330 (GRCm39) I597V possibly damaging Het
Nek1 A G 8: 61,542,720 (GRCm39) E770G probably benign Het
Or4d2b A C 11: 87,780,473 (GRCm39) V83G possibly damaging Het
Or52n2b A G 7: 104,565,543 (GRCm39) I320T probably benign Het
Pank2 T A 2: 131,124,638 (GRCm39) Y68* probably null Het
Prl2c2 G C 13: 13,176,786 (GRCm39) T47R probably damaging Het
Secisbp2l C A 2: 125,582,285 (GRCm39) G1057V probably benign Het
Slc30a2 C T 4: 134,076,660 (GRCm39) T265M probably damaging Het
Smarca2 A G 19: 26,688,084 (GRCm39) E1239G probably null Het
Snx30 C T 4: 59,879,261 (GRCm39) R167C probably damaging Het
Tmem26 T C 10: 68,614,491 (GRCm39) F302S possibly damaging Het
Tpgs2 A G 18: 25,301,610 (GRCm39) L19S probably damaging Het
Trp53bp1 T G 2: 121,066,665 (GRCm39) E687A probably damaging Het
Ttc27 C T 17: 75,046,667 (GRCm39) H243Y probably benign Het
Wdfy4 A T 14: 32,763,137 (GRCm39) V2318D possibly damaging Het
Wdr59 G A 8: 112,225,228 (GRCm39) P141S probably damaging Het
Zbed6 C T 1: 133,585,556 (GRCm39) V594M possibly damaging Het
Other mutations in Zfp787
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02546:Zfp787 APN 7 6,135,297 (GRCm39) missense probably damaging 0.99
IGL02721:Zfp787 APN 7 6,135,463 (GRCm39) splice site probably null
cheater UTSW 7 6,136,039 (GRCm39) missense possibly damaging 0.93
R0063:Zfp787 UTSW 7 6,135,322 (GRCm39) splice site probably null
R1434:Zfp787 UTSW 7 6,135,234 (GRCm39) missense probably damaging 0.98
R2042:Zfp787 UTSW 7 6,135,763 (GRCm39) missense possibly damaging 0.72
R5657:Zfp787 UTSW 7 6,136,053 (GRCm39) missense probably damaging 1.00
R5919:Zfp787 UTSW 7 6,135,834 (GRCm39) missense probably damaging 0.98
R6306:Zfp787 UTSW 7 6,135,360 (GRCm39) missense probably damaging 1.00
R7273:Zfp787 UTSW 7 6,136,039 (GRCm39) missense possibly damaging 0.93
R7316:Zfp787 UTSW 7 6,158,523 (GRCm39) unclassified probably benign
R7396:Zfp787 UTSW 7 6,135,106 (GRCm39) makesense probably null
R7880:Zfp787 UTSW 7 6,135,190 (GRCm39) missense probably benign 0.00
R7979:Zfp787 UTSW 7 6,146,094 (GRCm39) missense probably damaging 0.97
R9412:Zfp787 UTSW 7 6,135,946 (GRCm39) missense probably damaging 0.98
R9527:Zfp787 UTSW 7 6,136,027 (GRCm39) missense probably damaging 0.99
R9713:Zfp787 UTSW 7 6,146,059 (GRCm39) critical splice donor site probably null
Z1177:Zfp787 UTSW 7 6,135,123 (GRCm39) missense probably damaging 0.98
Predicted Primers
Posted On 2015-02-04