Incidental Mutation 'R2181:Zfp764'
ID237189
Institutional Source Beutler Lab
Gene Symbol Zfp764
Ensembl Gene ENSMUSG00000045757
Gene Namezinc finger protein 764
Synonyms
MMRRC Submission 040183-MU
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.070) question?
Stock #R2181 (G1)
Quality Score225
Status Not validated
Chromosome7
Chromosomal Location127403668-127406822 bp(-) (GRCm38)
Type of Mutationmissense
DNA Base Change (assembly) A to G at 127406499 bp
ZygosityHeterozygous
Amino Acid Change Tryptophan to Arginine at position 36 (W36R)
Ref Sequence ENSEMBL: ENSMUSP00000052944 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059199]
Predicted Effect probably damaging
Transcript: ENSMUST00000059199
AA Change: W36R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000052944
Gene: ENSMUSG00000045757
AA Change: W36R

DomainStartEndE-ValueType
KRAB 22 82 7.33e-31 SMART
low complexity region 102 115 N/A INTRINSIC
ZnF_C2H2 152 174 4.47e-3 SMART
ZnF_C2H2 180 202 1.47e-3 SMART
ZnF_C2H2 208 230 4.3e-5 SMART
ZnF_C2H2 236 258 6.78e-3 SMART
ZnF_C2H2 264 286 1.47e-3 SMART
ZnF_C2H2 292 315 1.45e-2 SMART
ZnF_C2H2 321 343 6.52e-5 SMART
ZnF_C2H2 349 371 6.67e-2 SMART
ZnF_C2H2 377 399 1.67e-2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000139118
Predicted Effect noncoding transcript
Transcript: ENSMUST00000205429
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.6%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700037C18Rik C T 16: 3,907,086 S43N possibly damaging Het
Abcb5 T G 12: 118,867,946 I1224L possibly damaging Het
Adgra2 G A 8: 27,121,673 G1002S probably damaging Het
Arhgap28 T C 17: 67,896,117 T114A probably damaging Het
Colec12 T A 18: 9,846,828 S75T probably damaging Het
Cyp2c67 A G 19: 39,609,097 C486R possibly damaging Het
Ecm2 T A 13: 49,530,289 L581Q probably damaging Het
Faxc T A 4: 21,931,591 S10T probably benign Het
Frem2 A G 3: 53,574,587 I1893T possibly damaging Het
Gabrr3 T A 16: 59,448,009 D328E probably damaging Het
Gbp7 A G 3: 142,544,030 I421V possibly damaging Het
Gorasp1 A G 9: 119,928,356 S317P probably damaging Het
Htr6 A G 4: 139,074,425 S113P probably damaging Het
Ift74 A G 4: 94,632,714 E168G probably damaging Het
Kdm6b A T 11: 69,401,126 Y1443* probably null Het
Mmp28 A C 11: 83,442,717 V466G possibly damaging Het
Nbea A T 3: 56,029,939 S750R possibly damaging Het
Nbeal1 T C 1: 60,278,780 F1959L probably damaging Het
Nelfa T C 5: 33,900,509 N314D probably benign Het
Numbl T A 7: 27,268,921 probably null Het
Olfr1370 G T 13: 21,073,224 P26T probably damaging Het
Olfr1467 G T 19: 13,365,074 V149F probably benign Het
Olfr272 T A 4: 52,911,524 K90M probably damaging Het
Olfr346 G A 2: 36,688,334 D111N probably damaging Het
Olfr678 T C 7: 105,070,211 V248A possibly damaging Het
Penk T C 4: 4,134,041 probably null Het
Pglyrp2 A G 17: 32,418,962 S31P probably damaging Het
Pigg T C 5: 108,336,500 S538P probably damaging Het
Pld2 A G 11: 70,542,989 T252A possibly damaging Het
Ppp2r5e T C 12: 75,462,324 I394V probably benign Het
Sh3rf1 G T 8: 61,363,238 V510F probably damaging Het
Slc4a2 A G 5: 24,435,653 H677R possibly damaging Het
Stam2 A T 2: 52,703,144 H345Q probably benign Het
Tmtc3 T C 10: 100,448,973 N600S probably benign Het
Trappc8 A G 18: 20,819,222 probably null Het
Vmn1r72 A T 7: 11,669,668 C284* probably null Het
Vmn2r76 T C 7: 86,225,535 I745V probably benign Het
Zfhx4 A C 3: 5,403,332 D2850A probably damaging Het
Zfp804b G A 5: 6,771,674 T463I probably damaging Het
Zfp811 T G 17: 32,797,721 K448N probably damaging Het
Other mutations in Zfp764
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00948:Zfp764 APN 7 127405204 missense possibly damaging 0.93
PIT4514001:Zfp764 UTSW 7 127404741 missense probably benign 0.26
R0528:Zfp764 UTSW 7 127404879 missense possibly damaging 0.92
R0619:Zfp764 UTSW 7 127406541 missense probably benign 0.08
R1183:Zfp764 UTSW 7 127406247 missense probably damaging 1.00
R1770:Zfp764 UTSW 7 127405567 nonsense probably null
R1878:Zfp764 UTSW 7 127405042 missense probably benign 0.04
R1885:Zfp764 UTSW 7 127405039 missense probably benign
R4780:Zfp764 UTSW 7 127404771 missense probably benign 0.13
R5242:Zfp764 UTSW 7 127405369 missense probably benign
R5493:Zfp764 UTSW 7 127404933 missense probably benign 0.00
R7109:Zfp764 UTSW 7 127404715 missense possibly damaging 0.92
R7214:Zfp764 UTSW 7 127405278 missense probably benign 0.05
R8047:Zfp764 UTSW 7 127406240 missense not run
Predicted Primers PCR Primer
(F):5'- ACTTCTGTCCTGCACATGGC -3'
(R):5'- CCGTGAACTGAGAAGGCAATC -3'

Sequencing Primer
(F):5'- ACCTCTGGATCCTGTGCACAG -3'
(R):5'- CTGAGAAGGCAATCCCAGGC -3'
Posted On2014-10-02