Incidental Mutation 'R7166:Zfp960'
ID 557960
Institutional Source Beutler Lab
Gene Symbol Zfp960
Ensembl Gene ENSMUSG00000096696
Gene Name zinc finger protein 960
Synonyms BC018101
MMRRC Submission 045227-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.206) question?
Stock # R7166 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 17284375-17309890 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 17308761 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 492 (C492S)
Ref Sequence ENSEMBL: ENSMUSP00000123102 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000127027]
AlphaFold L7N267
Predicted Effect probably damaging
Transcript: ENSMUST00000127027
AA Change: C492S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000123102
Gene: ENSMUSG00000096696
AA Change: C492S

DomainStartEndE-ValueType
KRAB 13 82 4.42e-16 SMART
ZnF_C2H2 158 180 3.95e-4 SMART
ZnF_C2H2 186 208 4.4e-2 SMART
ZnF_C2H2 238 260 2.95e-3 SMART
ZnF_C2H2 266 288 6.32e-3 SMART
ZnF_C2H2 294 316 8.94e-3 SMART
ZnF_C2H2 322 344 2.53e-2 SMART
ZnF_C2H2 350 372 3.21e-4 SMART
ZnF_C2H2 378 400 3.89e-3 SMART
ZnF_C2H2 406 428 2.2e-2 SMART
ZnF_C2H2 434 456 7.9e-4 SMART
ZnF_C2H2 462 484 7.9e-4 SMART
ZnF_C2H2 490 512 7.78e-3 SMART
ZnF_C2H2 518 540 3.95e-4 SMART
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency 98% (52/53)
Allele List at MGI
Other mutations in this stock
Total: 53 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ambn T C 5: 88,615,387 (GRCm39) L272P possibly damaging Het
Ash2l C A 8: 26,317,348 (GRCm39) G335V probably damaging Het
Atp13a1 T A 8: 70,251,966 (GRCm39) probably null Het
Atp13a2 G A 4: 140,734,295 (GRCm39) R1139Q possibly damaging Het
Atxn2 T A 5: 121,934,460 (GRCm39) N886K possibly damaging Het
Celsr3 G T 9: 108,720,150 (GRCm39) C2512F probably damaging Het
Cfap221 A G 1: 119,875,843 (GRCm39) V449A probably benign Het
Cfhr2 A T 1: 139,758,839 (GRCm39) C70* probably null Het
Chfr C A 5: 110,306,671 (GRCm39) P472Q probably benign Het
Crybg2 G A 4: 133,788,193 (GRCm39) R22Q probably damaging Het
Eef2k T C 7: 120,483,995 (GRCm39) F244L probably damaging Het
Efcab11 A T 12: 99,849,614 (GRCm39) M23K Het
Eif4a3l2 A G 6: 116,528,329 (GRCm39) I69V probably benign Het
Ercc8 T A 13: 108,305,967 (GRCm39) M114K possibly damaging Het
Fam217a T C 13: 35,094,298 (GRCm39) Y487C probably benign Het
Farsb T C 1: 78,447,821 (GRCm39) N205S probably benign Het
Glra1 A G 11: 55,405,904 (GRCm39) F370S probably benign Het
Gm12258 T A 11: 58,749,299 (GRCm39) M158K Het
Gm14305 T A 2: 176,412,736 (GRCm39) H209Q probably damaging Het
Gm4924 A T 10: 82,214,035 (GRCm39) Q611L unknown Het
H4c11 A G 13: 21,919,321 (GRCm39) H19R unknown Het
Haus6 T C 4: 86,501,924 (GRCm39) E649G possibly damaging Het
Hlcs C T 16: 94,063,585 (GRCm39) D345N possibly damaging Het
Htt C A 5: 35,010,238 (GRCm39) Q1564K probably benign Het
Itpr1 G A 6: 108,355,151 (GRCm39) V481I probably benign Het
Jak3 T C 8: 72,134,960 (GRCm39) I531T probably damaging Het
Kng1 T A 16: 22,898,428 (GRCm39) H609Q probably benign Het
Mdn1 T A 4: 32,746,446 (GRCm39) S4131T probably damaging Het
Npnt A G 3: 132,653,889 (GRCm39) S31P probably damaging Het
Or1r1 A T 11: 73,875,121 (GRCm39) F104L possibly damaging Het
Or4c100 A T 2: 88,355,990 (GRCm39) Q21L possibly damaging Het
Or8h8 T A 2: 86,753,092 (GRCm39) K261N probably damaging Het
Paxx A T 2: 25,350,238 (GRCm39) L123Q probably damaging Het
Prdm13 C T 4: 21,683,528 (GRCm39) R144Q unknown Het
Rab2b C A 14: 52,516,802 (GRCm39) probably benign Het
Rnf207 A G 4: 152,396,237 (GRCm39) I509T probably damaging Het
Ropn1l T C 15: 31,453,655 (GRCm39) Q12R Het
Ryr3 T G 2: 112,705,373 (GRCm39) Y847S probably damaging Het
Slc1a6 A T 10: 78,648,646 (GRCm39) T456S possibly damaging Het
Slc26a2 A T 18: 61,331,901 (GRCm39) M510K possibly damaging Het
Slc5a9 T C 4: 111,741,036 (GRCm39) T537A probably benign Het
Slc9b2 T C 3: 135,031,939 (GRCm39) Y132H unknown Het
Sltm T C 9: 70,492,132 (GRCm39) L725S probably damaging Het
Spz1 A G 13: 92,712,435 (GRCm39) C14R probably benign Het
Srrm4 T A 5: 116,609,301 (GRCm39) Q172L unknown Het
Synj2bp T C 12: 81,551,289 (GRCm39) D92G probably benign Het
Tmem169 A C 1: 72,340,229 (GRCm39) T220P probably benign Het
Ttn T A 2: 76,718,372 (GRCm39) I7270F unknown Het
Txndc16 T G 14: 45,420,611 (GRCm39) N137H probably benign Het
Ubr5 A G 15: 37,976,389 (GRCm39) Y2499H Het
Ugt2b38 T C 5: 87,558,305 (GRCm39) D452G probably damaging Het
Zfp12 T A 5: 143,231,257 (GRCm39) I560N possibly damaging Het
Zfp60 A G 7: 27,448,937 (GRCm39) K535R possibly damaging Het
Other mutations in Zfp960
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1026:Zfp960 UTSW 17 17,308,518 (GRCm39) missense probably damaging 1.00
R1511:Zfp960 UTSW 17 17,308,518 (GRCm39) missense probably damaging 1.00
R2141:Zfp960 UTSW 17 17,308,146 (GRCm39) missense probably benign 0.09
R3729:Zfp960 UTSW 17 17,308,633 (GRCm39) missense probably damaging 1.00
R3730:Zfp960 UTSW 17 17,308,633 (GRCm39) missense probably damaging 1.00
R3731:Zfp960 UTSW 17 17,308,633 (GRCm39) missense probably damaging 1.00
R4799:Zfp960 UTSW 17 17,308,698 (GRCm39) missense probably damaging 1.00
R5418:Zfp960 UTSW 17 17,307,805 (GRCm39) missense probably damaging 1.00
R5513:Zfp960 UTSW 17 17,307,996 (GRCm39) missense possibly damaging 0.64
R6309:Zfp960 UTSW 17 17,308,639 (GRCm39) missense probably benign 0.08
R6836:Zfp960 UTSW 17 17,308,434 (GRCm39) missense probably damaging 1.00
R7528:Zfp960 UTSW 17 17,307,825 (GRCm39) missense possibly damaging 0.84
R7576:Zfp960 UTSW 17 17,308,227 (GRCm39) missense probably benign 0.05
R8063:Zfp960 UTSW 17 17,308,623 (GRCm39) missense probably benign 0.03
R8263:Zfp960 UTSW 17 17,308,202 (GRCm39) nonsense probably null
R8354:Zfp960 UTSW 17 17,308,461 (GRCm39) missense probably benign 0.00
R8454:Zfp960 UTSW 17 17,308,461 (GRCm39) missense probably benign 0.00
R9750:Zfp960 UTSW 17 17,307,898 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- CGTCACAGCACTCTTCAAAGACAT -3'
(R):5'- GTACTGTGACCTGCAAAGGCTT -3'

Sequencing Primer
(F):5'- AGCCTTTGCATGTCACAGATAC -3'
(R):5'- GCCACATTGATTACATTCATACGGG -3'
Posted On 2019-06-26