Incidental Mutation 'R9412:Zfp787'
ID 711848
Institutional Source Beutler Lab
Gene Symbol Zfp787
Ensembl Gene ENSMUSG00000046792
Gene Name zinc finger protein 787
Synonyms 2210018M03Rik
MMRRC Submission
Accession Numbers
Essential gene? Probably non essential (E-score: 0.087) question?
Stock # R9412 (G1)
Quality Score 225.009
Status Not validated
Chromosome 7
Chromosomal Location 6134490-6158996 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 6135946 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Alanine at position 102 (T102A)
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: T102A

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000092468
Gene: ENSMUSG00000046792
AA Change: T102A

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
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 99.9%
  • 10x: 99.7%
  • 20x: 98.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 46 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700029H14Rik T A 8: 13,604,695 (GRCm39) T203S possibly damaging Het
2700049A03Rik G A 12: 71,235,457 (GRCm39) E1136K possibly damaging Het
Abca6 C A 11: 110,103,059 (GRCm39) R844L probably damaging Het
Abcb9 C T 5: 124,221,753 (GRCm39) R207Q probably benign Het
Abcd4 T C 12: 84,655,581 (GRCm39) R343G probably damaging Het
Arhgap45 T A 10: 79,855,564 (GRCm39) M1K probably null Het
Art3 A G 5: 92,541,013 (GRCm39) Y252C probably damaging Het
Ascc3 T C 10: 50,525,230 (GRCm39) M475T probably benign Het
Atxn2 C T 5: 121,940,201 (GRCm39) P992L possibly damaging Het
Dclk3 G A 9: 111,311,819 (GRCm39) probably null Het
Ddx21 T C 10: 62,429,881 (GRCm39) T288A possibly damaging Het
Fat3 T C 9: 15,908,703 (GRCm39) D2433G probably damaging Het
Flnc G A 6: 29,441,484 (GRCm39) R422Q probably benign Het
Fmnl2 G T 2: 53,007,016 (GRCm39) R776L unknown Het
Fndc1 T A 17: 7,991,198 (GRCm39) T833S unknown Het
Igf1r T A 7: 67,857,001 (GRCm39) Y988N probably damaging Het
Ints2 T C 11: 86,117,589 (GRCm39) Y711C probably damaging Het
Irx5 A G 8: 93,086,351 (GRCm39) K145E probably damaging Het
Kdm5a A G 6: 120,365,991 (GRCm39) Y377C probably damaging Het
Lrp1 T A 10: 127,409,287 (GRCm39) T1611S probably damaging Het
Lrrc28 T A 7: 67,181,512 (GRCm39) E241V probably damaging Het
Med23 T C 10: 24,778,019 (GRCm39) F789S probably damaging Het
Ncapd3 C T 9: 26,967,451 (GRCm39) Q596* probably null Het
Nrde2 C A 12: 100,096,681 (GRCm39) E1040* probably null Het
Or2n1d A T 17: 38,646,320 (GRCm39) T91S possibly damaging Het
Pcdh15 CAGAGA CAGA 10: 74,481,663 (GRCm39) probably null Het
Pcm1 T G 8: 41,740,788 (GRCm39) N972K probably damaging Het
Peg10 C CTCT 6: 4,756,453 (GRCm39) probably benign Het
Pla2g4a T C 1: 149,755,772 (GRCm39) T222A probably damaging Het
Ptchd3 A T 11: 121,732,779 (GRCm39) K556N possibly damaging Het
Relch A G 1: 105,662,288 (GRCm39) T936A probably benign Het
Scap T C 9: 110,207,673 (GRCm39) C461R possibly damaging Het
Scgb1b10 T A 7: 31,800,627 (GRCm39) L72* probably null Het
Serpinb6c C A 13: 34,081,371 (GRCm39) A93S probably benign Het
Serpinb9c C A 13: 33,334,231 (GRCm39) L298F probably damaging Het
Slf2 A T 19: 44,930,460 (GRCm39) E512D probably benign Het
Snapc3 C T 4: 83,354,570 (GRCm39) H194Y probably benign Het
Suox T A 10: 128,507,758 (GRCm39) D90V possibly damaging Het
Supt20 TCAGCAGCAGCAGCAGCAGCAGCA TCAGCAGCAGCAGCAGCAGCA 3: 54,635,069 (GRCm39) probably benign Het
Tert C T 13: 73,797,046 (GRCm39) R1095W probably benign Het
Tut4 A T 4: 108,414,561 (GRCm39) H46L Het
Unc13c T C 9: 73,839,772 (GRCm39) I360V probably benign Het
Uqcc1 A G 2: 155,693,329 (GRCm39) C235R probably benign Het
Vmn2r9 T A 5: 108,991,484 (GRCm39) I626F probably damaging Het
Vmn2r90 T G 17: 17,954,213 (GRCm39) C792W probably damaging Het
Zfp57 C T 17: 37,320,814 (GRCm39) P223S probably benign 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
R1415:Zfp787 UTSW 7 6,135,694 (GRCm39) missense probably damaging 1.00
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
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 PCR Primer
(F):5'- CTTGCTCTGTGTGAAGCTGC -3'
(R):5'- CCTCATCATGGATGACGATGAC -3'

Sequencing Primer
(F):5'- GTGTGAAGCTGCGGCCG -3'
(R):5'- ATGACGTCCCCAGCTGG -3'
Posted On 2022-05-16