Incidental Mutation 'R7627:Zfp160'
ID 589521
Institutional Source Beutler Lab
Gene Symbol Zfp160
Ensembl Gene ENSMUSG00000067942
Gene Name zinc finger protein 160
Synonyms 6720480D16Rik, 6720480D16Rik
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R7627 (G1)
Quality Score 225.009
Status Not validated
Chromosome 17
Chromosomal Location 21229203-21249119 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 21247270 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Proline at position 607 (S607P)
Ref Sequence ENSEMBL: ENSMUSP00000086191 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088811] [ENSMUST00000231482] [ENSMUST00000232320] [ENSMUST00000232354] [ENSMUST00000232473] [ENSMUST00000232663]
AlphaFold E9Q459
Predicted Effect probably damaging
Transcript: ENSMUST00000088811
AA Change: S607P

PolyPhen 2 Score 0.994 (Sensitivity: 0.69; Specificity: 0.97)
SMART Domains Protein: ENSMUSP00000086191
Gene: ENSMUSG00000067942
AA Change: S607P

DomainStartEndE-ValueType
KRAB 8 68 1.91e-29 SMART
low complexity region 100 110 N/A INTRINSIC
ZnF_C2H2 146 168 1.69e-3 SMART
ZnF_C2H2 174 196 2.91e-2 SMART
ZnF_C2H2 202 224 1.4e-4 SMART
ZnF_C2H2 230 252 3.89e-3 SMART
ZnF_C2H2 258 280 1.72e-4 SMART
ZnF_C2H2 286 308 4.94e-5 SMART
ZnF_C2H2 314 336 2.12e-4 SMART
ZnF_C2H2 342 364 1.12e-3 SMART
ZnF_C2H2 370 392 1.2e-3 SMART
ZnF_C2H2 398 420 6.42e-4 SMART
ZnF_C2H2 426 448 9.08e-4 SMART
ZnF_C2H2 454 476 1.84e-4 SMART
ZnF_C2H2 482 504 1.5e-4 SMART
ZnF_C2H2 510 532 3.44e-4 SMART
ZnF_C2H2 538 560 1.12e-3 SMART
ZnF_C2H2 566 588 2.27e-4 SMART
ZnF_C2H2 594 616 1.04e-3 SMART
ZnF_C2H2 622 644 1.13e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000231482
Predicted Effect probably benign
Transcript: ENSMUST00000232320
Predicted Effect probably benign
Transcript: ENSMUST00000232354
Predicted Effect probably benign
Transcript: ENSMUST00000232473
Predicted Effect probably benign
Transcript: ENSMUST00000232663
Coding Region Coverage
  • 1x: 100.0%
  • 3x: 100.0%
  • 10x: 99.7%
  • 20x: 99.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9230112D13Rik T A 14: 34,234,055 (GRCm39) I79L unknown Het
Acta2 G A 19: 34,229,931 (GRCm39) T8I probably benign Het
Acvrl1 G A 15: 101,033,747 (GRCm39) R143Q probably benign Het
Adam22 A G 5: 8,417,933 (GRCm39) S8P probably benign Het
Ankrd11 A G 8: 123,617,690 (GRCm39) I2054T possibly damaging Het
Cactin CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG CCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAGTCGGAG 10: 81,157,152 (GRCm39) probably benign Het
Cad T A 5: 31,217,508 (GRCm39) L354Q probably damaging Het
Ccdc15 A T 9: 37,253,698 (GRCm39) C184S unknown Het
Ccl8 A G 11: 82,006,865 (GRCm39) D26G probably benign Het
Ccsap T C 8: 124,569,097 (GRCm39) Y248C probably damaging Het
Col5a1 T G 2: 27,840,665 (GRCm39) Y271* probably null Het
Dnmt3b A G 2: 153,519,500 (GRCm39) N695S probably benign Het
Dync1li2 A G 8: 105,156,140 (GRCm39) C234R probably benign Het
Dync2h1 A T 9: 7,101,111 (GRCm39) D2758E probably benign Het
Eif2ak3 A T 6: 70,869,919 (GRCm39) T869S probably benign Het
Foxn4 G T 5: 114,398,495 (GRCm39) P175H possibly damaging Het
Gbp5 T G 3: 142,206,319 (GRCm39) M1R probably null Het
Glp2r G T 11: 67,637,589 (GRCm39) L30I unknown Het
Gls A T 1: 52,205,425 (GRCm39) D639E probably benign Het
Gm5145 G T 17: 20,790,654 (GRCm39) E11* probably null Het
Gm9772 T A 17: 22,226,160 (GRCm39) K41N probably damaging Het
Gnat3 A T 5: 18,204,746 (GRCm39) D133V Het
Gse1 C A 8: 121,299,516 (GRCm39) P849T unknown Het
H2ac15 C A 13: 21,937,916 (GRCm39) V28L probably benign Het
Hoxb9 A G 11: 96,165,521 (GRCm39) T197A probably damaging Het
Krt39 A G 11: 99,405,575 (GRCm39) S442P possibly damaging Het
Leng9 A G 7: 4,151,617 (GRCm39) L353P probably damaging Het
Mamdc2 A T 19: 23,288,355 (GRCm39) M561K probably damaging Het
Mamdc4 A G 2: 25,458,225 (GRCm39) V395A probably damaging Het
Mrpl32 G A 13: 14,787,498 (GRCm39) R36C probably benign Het
Or6b2b A T 1: 92,419,107 (GRCm39) Y123* probably null Het
Or7e168 A G 9: 19,719,947 (GRCm39) D111G probably damaging Het
Papss1 T A 3: 131,290,873 (GRCm39) D205E probably benign Het
Pdlim2 T C 14: 70,408,924 (GRCm39) D151G probably benign Het
Pdxp T C 15: 78,798,339 (GRCm39) V57A probably damaging Het
Plec T A 15: 76,061,594 (GRCm39) E2781V probably damaging Het
Prr7 GCGCCGCCGCACGCGCACCCGCACCCACACCATCACGCACTGCCGCACCCACCGCCGCCGCAC GCGCCGCCGCAC 13: 55,620,147 (GRCm39) probably benign Het
Rnf32 G A 5: 29,402,948 (GRCm39) probably benign Het
Ryr2 A G 13: 11,776,213 (GRCm39) V1108A possibly damaging Het
Slc4a8 A G 15: 100,686,104 (GRCm39) H276R probably benign Het
Slco1a7 C T 6: 141,690,271 (GRCm39) V161I probably damaging Het
Spta1 T A 1: 174,032,944 (GRCm39) D1000E probably damaging Het
Sva C A 6: 42,019,598 (GRCm39) Q153K unknown Het
Tmprss11d T C 5: 86,457,365 (GRCm39) Y236C possibly damaging Het
Zfp82 C A 7: 29,756,147 (GRCm39) G312W probably damaging Het
Other mutations in Zfp160
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00714:Zfp160 APN 17 21,246,964 (GRCm39) missense probably benign
IGL01019:Zfp160 APN 17 21,241,088 (GRCm39) missense possibly damaging 0.68
IGL02430:Zfp160 APN 17 21,245,792 (GRCm39) missense possibly damaging 0.76
R0412:Zfp160 UTSW 17 21,247,139 (GRCm39) missense probably damaging 0.97
R0600:Zfp160 UTSW 17 21,247,268 (GRCm39) missense probably benign 0.00
R2146:Zfp160 UTSW 17 21,247,244 (GRCm39) missense probably benign 0.13
R2157:Zfp160 UTSW 17 21,241,090 (GRCm39) missense probably benign 0.23
R2411:Zfp160 UTSW 17 21,246,007 (GRCm39) missense possibly damaging 0.94
R2904:Zfp160 UTSW 17 21,245,911 (GRCm39) missense probably benign 0.00
R4249:Zfp160 UTSW 17 21,246,000 (GRCm39) missense probably benign 0.11
R4896:Zfp160 UTSW 17 21,240,343 (GRCm39) missense probably benign 0.00
R5106:Zfp160 UTSW 17 21,247,023 (GRCm39) missense probably damaging 0.99
R5342:Zfp160 UTSW 17 21,240,995 (GRCm39) missense possibly damaging 0.95
R5352:Zfp160 UTSW 17 21,247,114 (GRCm39) missense probably benign 0.02
R6193:Zfp160 UTSW 17 21,247,124 (GRCm39) missense probably benign 0.24
R6230:Zfp160 UTSW 17 21,246,707 (GRCm39) missense probably benign 0.38
R6753:Zfp160 UTSW 17 21,240,996 (GRCm39) missense probably benign 0.02
R6928:Zfp160 UTSW 17 21,261,724 (GRCm39) missense probably benign 0.04
R7040:Zfp160 UTSW 17 21,246,794 (GRCm39) missense probably damaging 1.00
R7255:Zfp160 UTSW 17 21,245,749 (GRCm39) missense probably benign 0.18
R7497:Zfp160 UTSW 17 21,246,455 (GRCm39) missense probably benign 0.08
R7510:Zfp160 UTSW 17 21,246,655 (GRCm39) missense probably benign 0.00
R7540:Zfp160 UTSW 17 21,245,922 (GRCm39) nonsense probably null
R8169:Zfp160 UTSW 17 21,247,298 (GRCm39) missense probably damaging 0.97
R8240:Zfp160 UTSW 17 21,246,350 (GRCm39) missense probably damaging 0.99
R8330:Zfp160 UTSW 17 21,246,313 (GRCm39) missense probably damaging 1.00
R8367:Zfp160 UTSW 17 21,245,804 (GRCm39) missense probably benign 0.22
R8802:Zfp160 UTSW 17 21,246,867 (GRCm39) missense probably damaging 1.00
R9183:Zfp160 UTSW 17 21,240,354 (GRCm39) missense possibly damaging 0.84
R9556:Zfp160 UTSW 17 21,247,031 (GRCm39) missense probably benign 0.03
R9695:Zfp160 UTSW 17 21,245,746 (GRCm39) missense possibly damaging 0.53
Z1177:Zfp160 UTSW 17 21,247,152 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GTACTCAAGTTTGACTACTCATCAG -3'
(R):5'- AACTCATGATGGGTGTTTATCGTC -3'

Sequencing Primer
(F):5'- AGTTTGACTACTCATCAGGCAATCC -3'
(R):5'- ATTCCTGGATATTATGCAAGAAGTG -3'
Posted On 2019-10-24