Incidental Mutation 'R5722:Zfp790'
ID 452259
Institutional Source Beutler Lab
Gene Symbol Zfp790
Ensembl Gene ENSMUSG00000011427
Gene Name zinc finger protein 790
Synonyms 6330581L23Rik
MMRRC Submission 043340-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.053) question?
Stock # R5722 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 29515539-29530430 bp(+) (GRCm39)
Type of Mutation nonsense
DNA Base Change (assembly) C to A at 29529514 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Stop codon at position 733 (S733*)
Ref Sequence ENSEMBL: ENSMUSP00000136932 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000032796] [ENSMUST00000108223] [ENSMUST00000178162]
AlphaFold Q80ZX2
Predicted Effect probably null
Transcript: ENSMUST00000032796
AA Change: S733*
SMART Domains Protein: ENSMUSP00000032796
Gene: ENSMUSG00000011427
AA Change: S733*

DomainStartEndE-ValueType
KRAB 5 65 3e-27 SMART
ZnF_C2H2 224 246 2.95e-3 SMART
ZnF_C2H2 252 274 2.53e-2 SMART
ZnF_C2H2 280 302 5.5e-3 SMART
ZnF_C2H2 308 330 2.75e-3 SMART
ZnF_C2H2 336 358 2.12e-4 SMART
ZnF_C2H2 364 386 1.03e-2 SMART
Pfam:zf-C2H2_6 391 403 2.4e-1 PFAM
ZnF_C2H2 448 470 9.56e1 SMART
ZnF_C2H2 476 498 7.26e-3 SMART
ZnF_C2H2 504 526 2.57e-3 SMART
ZnF_C2H2 532 554 6.42e-4 SMART
ZnF_C2H2 640 662 1.12e-3 SMART
ZnF_C2H2 668 690 2.12e-4 SMART
ZnF_C2H2 696 718 1.98e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000108223
SMART Domains Protein: ENSMUSP00000103858
Gene: ENSMUSG00000050855

DomainStartEndE-ValueType
KRAB 6 67 2.42e-22 SMART
Predicted Effect probably null
Transcript: ENSMUST00000178162
AA Change: S733*
SMART Domains Protein: ENSMUSP00000136932
Gene: ENSMUSG00000011427
AA Change: S733*

DomainStartEndE-ValueType
KRAB 5 65 3e-27 SMART
ZnF_C2H2 224 246 2.95e-3 SMART
ZnF_C2H2 252 274 2.53e-2 SMART
ZnF_C2H2 280 302 5.5e-3 SMART
ZnF_C2H2 308 330 2.75e-3 SMART
ZnF_C2H2 336 358 2.12e-4 SMART
ZnF_C2H2 364 386 1.03e-2 SMART
ZnF_C2H2 448 470 9.56e1 SMART
ZnF_C2H2 476 498 7.26e-3 SMART
ZnF_C2H2 504 526 2.57e-3 SMART
ZnF_C2H2 532 554 6.42e-4 SMART
ZnF_C2H2 640 662 1.12e-3 SMART
ZnF_C2H2 668 690 2.12e-4 SMART
ZnF_C2H2 696 718 1.98e-4 SMART
Coding Region Coverage
  • 1x: 99.1%
  • 3x: 98.3%
  • 10x: 96.5%
  • 20x: 93.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Actl6a G A 3: 32,772,194 (GRCm39) R164H probably damaging Het
Afg3l2 A G 18: 67,573,269 (GRCm39) Y178H probably benign Het
Agtr1a A G 13: 30,566,016 (GRCm39) *360W probably null Het
Arfgef1 A G 1: 10,209,109 (GRCm39) V1830A probably benign Het
Asic2 A T 11: 81,858,806 (GRCm39) S69T probably benign Het
Axin1 A T 17: 26,401,531 (GRCm39) N368Y probably damaging Het
Brme1 A G 8: 84,898,473 (GRCm39) E537G probably damaging Het
Ces1d G A 8: 93,904,756 (GRCm39) P328L probably benign Het
Cndp2 T A 18: 84,686,203 (GRCm39) K461* probably null Het
Cntnap5c A T 17: 58,620,852 (GRCm39) H977L probably benign Het
Fkbpl G A 17: 34,864,303 (GRCm39) A24T probably benign Het
Glg1 T C 8: 111,896,194 (GRCm39) T177A possibly damaging Het
Gm7168 T C 17: 14,169,824 (GRCm39) V397A probably benign Het
Hif1a T A 12: 73,988,533 (GRCm39) D535E probably benign Het
Hjurp GT GTT 1: 88,194,246 (GRCm39) probably null Het
Ice1 T C 13: 70,763,219 (GRCm39) E173G possibly damaging Het
Ighmbp2 A G 19: 3,329,909 (GRCm39) V115A probably damaging Het
Irf2 A T 8: 47,271,831 (GRCm39) E101D possibly damaging Het
Kat8 G A 7: 127,523,988 (GRCm39) E343K probably damaging Het
Kyat1 C T 2: 30,078,123 (GRCm39) C127Y probably damaging Het
Mrgpra4 T C 7: 47,630,755 (GRCm39) H282R probably benign Het
Npsr1 C A 9: 24,225,096 (GRCm39) P368Q probably damaging Het
Nwd1 G A 8: 73,401,872 (GRCm39) V839M probably damaging Het
Or51a43 T A 7: 103,717,930 (GRCm39) M103L probably damaging Het
Or6n2 G T 1: 173,897,436 (GRCm39) D191Y probably damaging Het
P4ha3 A G 7: 99,955,198 (GRCm39) D351G probably benign Het
Pard3b T A 1: 62,479,160 (GRCm39) probably null Het
Pgap6 CGGGG CGGGGG 17: 26,339,536 (GRCm39) probably null Het
Pik3c2b G T 1: 133,031,574 (GRCm39) G1505W probably damaging Het
Plppr5 A T 3: 117,414,714 (GRCm39) I112L probably benign Het
Potefam1 T A 2: 111,034,468 (GRCm39) T355S probably benign Het
Ptprq A G 10: 107,522,226 (GRCm39) I575T possibly damaging Het
Ranbp3l A G 15: 9,029,656 (GRCm39) E46G probably damaging Het
Rbm46 A G 3: 82,772,640 (GRCm39) V164A possibly damaging Het
Sap25 A G 5: 137,639,713 (GRCm39) E13G probably benign Het
Setbp1 A T 18: 78,899,860 (GRCm39) V1269E possibly damaging Het
Smgc T A 15: 91,726,109 (GRCm39) S18R possibly damaging Het
Snrk T C 9: 121,993,072 (GRCm39) I345T probably benign Het
Sp4 T A 12: 118,262,976 (GRCm39) I357F possibly damaging Het
Sra1 A G 18: 36,808,031 (GRCm39) L399P probably damaging Het
Stat6 A G 10: 127,494,242 (GRCm39) T658A probably benign Het
Sv2a G A 3: 96,092,339 (GRCm39) R13H probably benign Het
Thoc3 G T 13: 54,608,014 (GRCm39) T310N probably damaging Het
Tox3 A C 8: 91,074,489 (GRCm39) probably null Het
Trpc6 A G 9: 8,680,550 (GRCm39) E848G possibly damaging Het
Ttn T A 2: 76,538,590 (GRCm39) T34703S possibly damaging Het
Ttn T C 2: 76,776,312 (GRCm39) I1577V probably damaging Het
Ubqln3 G A 7: 103,790,674 (GRCm39) P472L probably benign Het
Ugt2b36 C T 5: 87,240,297 (GRCm39) W29* probably null Het
Wdr17 C T 8: 55,113,806 (GRCm39) probably null Het
Other mutations in Zfp790
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00229:Zfp790 APN 7 29,527,988 (GRCm39) missense probably benign 0.32
IGL00979:Zfp790 APN 7 29,529,034 (GRCm39) missense probably benign 0.00
IGL02286:Zfp790 APN 7 29,529,160 (GRCm39) missense possibly damaging 0.53
IGL03136:Zfp790 APN 7 29,529,320 (GRCm39) nonsense probably null
R0021:Zfp790 UTSW 7 29,525,113 (GRCm39) unclassified probably benign
R0077:Zfp790 UTSW 7 29,524,300 (GRCm39) missense probably damaging 0.98
R1477:Zfp790 UTSW 7 29,522,525 (GRCm39) start gained probably benign
R1572:Zfp790 UTSW 7 29,527,564 (GRCm39) missense probably benign 0.33
R2015:Zfp790 UTSW 7 29,528,286 (GRCm39) missense probably benign 0.29
R4941:Zfp790 UTSW 7 29,528,916 (GRCm39) missense possibly damaging 0.83
R5019:Zfp790 UTSW 7 29,529,192 (GRCm39) missense probably benign 0.00
R5159:Zfp790 UTSW 7 29,529,192 (GRCm39) missense probably benign 0.00
R5160:Zfp790 UTSW 7 29,529,192 (GRCm39) missense probably benign 0.00
R5954:Zfp790 UTSW 7 29,528,929 (GRCm39) missense probably damaging 1.00
R6025:Zfp790 UTSW 7 29,528,970 (GRCm39) missense possibly damaging 0.71
R6312:Zfp790 UTSW 7 29,527,647 (GRCm39) missense probably damaging 1.00
R7392:Zfp790 UTSW 7 29,528,050 (GRCm39) missense possibly damaging 0.52
R7623:Zfp790 UTSW 7 29,525,130 (GRCm39) nonsense probably null
R8036:Zfp790 UTSW 7 29,528,346 (GRCm39) missense possibly damaging 0.92
R8175:Zfp790 UTSW 7 29,529,205 (GRCm39) missense possibly damaging 0.96
R8898:Zfp790 UTSW 7 29,522,525 (GRCm39) start gained probably benign
R8988:Zfp790 UTSW 7 29,527,593 (GRCm39) missense probably benign
R9176:Zfp790 UTSW 7 29,529,387 (GRCm39) missense probably benign 0.04
R9404:Zfp790 UTSW 7 29,525,185 (GRCm39) missense probably benign
R9519:Zfp790 UTSW 7 29,522,567 (GRCm39) missense unknown
Z1186:Zfp790 UTSW 7 29,529,109 (GRCm39) missense possibly damaging 0.53
Z1186:Zfp790 UTSW 7 29,529,258 (GRCm39) missense possibly damaging 0.92
Z1186:Zfp790 UTSW 7 29,529,208 (GRCm39) missense possibly damaging 0.72
Predicted Primers PCR Primer
(F):5'- GGCATTCACATGATACAGACCTC -3'
(R):5'- AGACCCAGAAATAGGCTTTTCC -3'

Sequencing Primer
(F):5'- GACCTCAAGGCAGTTCATATTCGG -3'
(R):5'- CAAGCCCTCCACCTTAACTTAATTTC -3'
Posted On 2017-01-03