Incidental Mutation 'R1627:Zfp763'
ID 172578
Institutional Source Beutler Lab
Gene Symbol Zfp763
Ensembl Gene ENSMUSG00000067430
Gene Name zinc finger protein 763
Synonyms 1700065O13Rik
MMRRC Submission 039664-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1627 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 33235838-33252355 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 33240758 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tryptophan to Arginine at position 24 (W24R)
Ref Sequence ENSEMBL: ENSMUSP00000084936 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000087654]
AlphaFold Q8BIC7
Predicted Effect probably damaging
Transcript: ENSMUST00000087654
AA Change: W24R

PolyPhen 2 Score 0.998 (Sensitivity: 0.27; Specificity: 0.99)
SMART Domains Protein: ENSMUSP00000084936
Gene: ENSMUSG00000067430
AA Change: W24R

DomainStartEndE-ValueType
KRAB 10 60 7.47e-14 SMART
ZnF_C2H2 223 245 2.53e-2 SMART
ZnF_C2H2 251 273 4.54e-4 SMART
ZnF_C2H2 279 301 1.69e-3 SMART
ZnF_C2H2 307 329 5.72e-1 SMART
ZnF_C2H2 335 357 1.64e-1 SMART
ZnF_C2H2 363 385 1.56e-2 SMART
ZnF_C2H2 391 413 1.82e-3 SMART
ZnF_C2H2 419 441 1.64e-1 SMART
ZnF_C2H2 447 469 5.9e-3 SMART
ZnF_C2H2 475 497 2.02e-1 SMART
ZnF_C2H2 503 525 7.15e-2 SMART
ZnF_C2H2 531 553 1.79e-2 SMART
ZnF_C2H2 559 581 5.14e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000124465
Coding Region Coverage
  • 1x: 99.0%
  • 3x: 98.0%
  • 10x: 95.3%
  • 20x: 89.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcg3 A G 5: 105,083,880 (GRCm39) M630T probably benign Het
Anpep T C 7: 79,491,759 (GRCm39) I81V probably benign Het
Bub1 A G 2: 127,650,933 (GRCm39) S627P probably benign Het
C1s1 T A 6: 124,514,439 (GRCm39) N139I probably damaging Het
Car6 A T 4: 150,277,035 (GRCm39) V152D probably damaging Het
Cdh19 C A 1: 110,847,375 (GRCm39) M411I probably benign Het
Cep95 A G 11: 106,700,531 (GRCm39) E322G probably damaging Het
Chek1 C A 9: 36,625,737 (GRCm39) V303L probably benign Het
Dctn1 T A 6: 83,172,064 (GRCm39) I818N probably damaging Het
Dscaml1 T C 9: 45,664,445 (GRCm39) S2107P probably damaging Het
Dusp14 A G 11: 83,939,597 (GRCm39) I148T probably damaging Het
Eps15 A G 4: 109,227,754 (GRCm39) D645G probably damaging Het
Etl4 A G 2: 20,806,390 (GRCm39) N1153S possibly damaging Het
Fer1l6 A G 15: 58,513,728 (GRCm39) D1541G probably benign Het
Gm14496 A G 2: 181,640,571 (GRCm39) S513G probably damaging Het
H2-D1 G T 17: 35,482,471 (GRCm39) A64S possibly damaging Het
Hsd17b2 T A 8: 118,428,909 (GRCm39) F59I possibly damaging Het
Itgb7 T G 15: 102,131,911 (GRCm39) Q224P probably damaging Het
Jak1 A G 4: 101,048,821 (GRCm39) probably null Het
Kdm1b G A 13: 47,217,707 (GRCm39) probably null Het
Lrp8 A G 4: 107,711,613 (GRCm39) I466V probably damaging Het
Mga A G 2: 119,795,043 (GRCm39) D2909G probably damaging Het
Nol8 T C 13: 49,814,980 (GRCm39) S345P probably benign Het
Nup210l T C 3: 90,051,476 (GRCm39) M540T probably benign Het
Obscn C T 11: 59,003,464 (GRCm39) R1370H probably benign Het
Or2ad1 A G 13: 21,327,125 (GRCm39) F34S probably damaging Het
Pbx3 A G 2: 34,065,965 (GRCm39) V375A probably benign Het
Ppp1r9a T C 6: 4,906,168 (GRCm39) V241A possibly damaging Het
Psmd6 C T 14: 14,112,539 (GRCm38) V354M probably damaging Het
Rab2a T C 4: 8,578,481 (GRCm39) F94L probably damaging Het
Rev1 T C 1: 38,094,571 (GRCm39) D949G probably damaging Het
Ric8a A G 7: 140,438,091 (GRCm39) D110G probably damaging Het
Rlf A T 4: 121,007,197 (GRCm39) D594E probably benign Het
Septin1 C A 7: 126,817,230 (GRCm39) probably null Het
Slco5a1 G C 1: 13,060,607 (GRCm39) P38R probably damaging Het
Snx33 C A 9: 56,833,241 (GRCm39) R276L probably damaging Het
Taf11 A T 17: 28,124,253 (GRCm39) D101E probably benign Het
Ttn A G 2: 76,764,564 (GRCm39) S3168P probably damaging Het
Uggt2 T C 14: 119,295,075 (GRCm39) E41G possibly damaging Het
Vmn2r80 A G 10: 79,030,249 (GRCm39) R692G probably damaging Het
Other mutations in Zfp763
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02638:Zfp763 APN 17 33,238,908 (GRCm39) missense probably benign 0.41
IGL03291:Zfp763 APN 17 33,238,860 (GRCm39) missense probably damaging 0.96
R0346:Zfp763 UTSW 17 33,238,721 (GRCm39) missense probably benign 0.26
R0675:Zfp763 UTSW 17 33,238,774 (GRCm39) missense possibly damaging 0.92
R0683:Zfp763 UTSW 17 33,237,892 (GRCm39) missense probably damaging 1.00
R1494:Zfp763 UTSW 17 33,240,477 (GRCm39) missense probably damaging 0.99
R1521:Zfp763 UTSW 17 33,252,276 (GRCm39) start codon destroyed probably benign 0.03
R1607:Zfp763 UTSW 17 33,238,881 (GRCm39) missense probably benign 0.08
R1714:Zfp763 UTSW 17 33,238,591 (GRCm39) missense probably damaging 0.99
R1993:Zfp763 UTSW 17 33,237,413 (GRCm39) missense probably damaging 1.00
R2109:Zfp763 UTSW 17 33,238,752 (GRCm39) missense probably benign
R4420:Zfp763 UTSW 17 33,237,455 (GRCm39) missense probably benign 0.43
R4612:Zfp763 UTSW 17 33,237,922 (GRCm39) missense probably benign 0.05
R5114:Zfp763 UTSW 17 33,237,949 (GRCm39) missense probably damaging 0.99
R5426:Zfp763 UTSW 17 33,238,569 (GRCm39) missense probably benign
R5503:Zfp763 UTSW 17 33,238,507 (GRCm39) missense possibly damaging 0.95
R5534:Zfp763 UTSW 17 33,240,768 (GRCm39) missense probably damaging 0.97
R6133:Zfp763 UTSW 17 33,237,675 (GRCm39) missense possibly damaging 0.75
R7141:Zfp763 UTSW 17 33,237,769 (GRCm39) missense probably damaging 0.97
R7365:Zfp763 UTSW 17 33,252,352 (GRCm39) start gained probably benign
R7430:Zfp763 UTSW 17 33,238,506 (GRCm39) missense possibly damaging 0.68
R7552:Zfp763 UTSW 17 33,237,625 (GRCm39) missense probably benign
R8277:Zfp763 UTSW 17 33,252,294 (GRCm39) start gained probably benign
R8446:Zfp763 UTSW 17 33,238,473 (GRCm39) missense probably benign 0.28
R8964:Zfp763 UTSW 17 33,240,710 (GRCm39) missense probably benign 0.25
R9662:Zfp763 UTSW 17 33,240,787 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- TGTAGTGTGATTTGACCTGCTCCTTCA -3'
(R):5'- GCCTTGTCTGTGATCTGCTTGTCTAAGA -3'

Sequencing Primer
(F):5'- tcaccatcatgtcccctttc -3'
(R):5'- atccgccttcctctgcc -3'
Posted On 2014-04-24