Incidental Mutation 'IGL01019:Zfp160'
ID 54056
Institutional Source Australian Phenomics Network (link to record)
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 # IGL01019
Quality Score
Status
Chromosome 17
Chromosomal Location 21229203-21249119 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 21241088 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 52 (M52K)
Ref Sequence ENSEMBL: ENSMUSP00000155916 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000088811] [ENSMUST00000231482] [ENSMUST00000232320] [ENSMUST00000232354] [ENSMUST00000232473] [ENSMUST00000232595] [ENSMUST00000232663]
AlphaFold E9Q459
Predicted Effect probably benign
Transcript: ENSMUST00000088811
AA Change: M88K

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
SMART Domains Protein: ENSMUSP00000086191
Gene: ENSMUSG00000067942
AA Change: M88K

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 possibly damaging
Transcript: ENSMUST00000231482
AA Change: M52K

PolyPhen 2 Score 0.677 (Sensitivity: 0.86; Specificity: 0.92)
Predicted Effect probably benign
Transcript: ENSMUST00000232320
AA Change: M88K

PolyPhen 2 Score 0.073 (Sensitivity: 0.93; Specificity: 0.84)
Predicted Effect probably benign
Transcript: ENSMUST00000232354
AA Change: M88K

PolyPhen 2 Score 0.015 (Sensitivity: 0.96; Specificity: 0.79)
Predicted Effect possibly damaging
Transcript: ENSMUST00000232473
AA Change: M52K

PolyPhen 2 Score 0.677 (Sensitivity: 0.86; Specificity: 0.92)
Predicted Effect probably benign
Transcript: ENSMUST00000232595
AA Change: M88K

PolyPhen 2 Score 0.028 (Sensitivity: 0.95; Specificity: 0.81)
Predicted Effect probably benign
Transcript: ENSMUST00000232663
AA Change: M88K

PolyPhen 2 Score 0.144 (Sensitivity: 0.92; Specificity: 0.86)
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930022D16Rik T C 11: 109,308,737 (GRCm39) probably benign Het
Aatk T C 11: 119,903,101 (GRCm39) S375G probably benign Het
Abcg8 T C 17: 84,999,423 (GRCm39) M173T probably benign Het
B3galt2 A C 1: 143,522,495 (GRCm39) R210S probably benign Het
Bltp1 G T 3: 37,061,133 (GRCm39) probably null Het
Capn5 C T 7: 97,784,971 (GRCm39) A168T probably damaging Het
Cbx7 C T 15: 79,814,829 (GRCm39) G24D probably damaging Het
Ccdc7a A T 8: 129,788,099 (GRCm39) S77T probably benign Het
Cd200r2 T A 16: 44,729,832 (GRCm39) probably benign Het
Cdh11 T C 8: 103,406,377 (GRCm39) H32R probably benign Het
Chdh A T 14: 29,753,289 (GRCm39) N66I probably benign Het
Clca3a2 G A 3: 144,519,388 (GRCm39) Q263* probably null Het
Dcc T C 18: 71,942,161 (GRCm39) I319V probably benign Het
Depdc5 G T 5: 33,050,745 (GRCm39) M170I probably damaging Het
Dop1b T A 16: 93,607,117 (GRCm39) L2140Q probably benign Het
Frem3 G A 8: 81,341,763 (GRCm39) G1352E probably benign Het
Fsd1l T A 4: 53,694,742 (GRCm39) C389S probably damaging Het
Grin2c C T 11: 115,148,936 (GRCm39) A221T possibly damaging Het
Gstz1 C A 12: 87,210,575 (GRCm39) P153T probably damaging Het
Itgb2 T C 10: 77,378,237 (GRCm39) S22P possibly damaging Het
Krt87 G T 15: 101,336,312 (GRCm39) Q114K possibly damaging Het
Krtap5-4 A C 7: 141,857,647 (GRCm39) S106R unknown Het
Lats1 T C 10: 7,581,435 (GRCm39) V740A probably damaging Het
Mcm9 C A 10: 53,506,041 (GRCm39) G78C probably damaging Het
Mn1 G A 5: 111,569,413 (GRCm39) E1128K possibly damaging Het
Myo1f G A 17: 33,811,977 (GRCm39) R592H possibly damaging Het
Nfat5 G T 8: 108,094,146 (GRCm39) A277S probably damaging Het
Nfkbia T A 12: 55,537,327 (GRCm39) Y254F probably damaging Het
Nr3c2 A T 8: 77,635,843 (GRCm39) N315Y probably damaging Het
Otof T C 5: 30,562,560 (GRCm39) M258V probably benign Het
Panx3 C T 9: 37,572,767 (GRCm39) C261Y probably damaging Het
Pdia2 C A 17: 26,417,896 (GRCm39) G38W probably damaging Het
Psg19 G T 7: 18,527,971 (GRCm39) Y257* probably null Het
Ptpre A T 7: 135,280,054 (GRCm39) K586* probably null Het
Reps1 A G 10: 18,000,643 (GRCm39) R752G probably damaging Het
Rpgrip1 T A 14: 52,368,633 (GRCm39) D277E possibly damaging Het
Rpl21-ps6 A G 17: 56,222,671 (GRCm39) noncoding transcript Het
Serpinf2 T A 11: 75,327,333 (GRCm39) E198V possibly damaging Het
Sh3tc1 A G 5: 35,860,719 (GRCm39) L1046P probably damaging Het
Snw1 T C 12: 87,497,711 (GRCm39) E426G probably benign Het
Sord T A 2: 122,094,564 (GRCm39) N317K probably benign Het
Taar3 A T 10: 23,826,330 (GRCm39) D292V probably damaging Het
Tdrd3 C A 14: 87,709,618 (GRCm39) T94K probably damaging Het
Ttn C A 2: 76,687,165 (GRCm39) E736* probably null Het
Usp32 A G 11: 84,930,091 (GRCm39) V562A probably damaging Het
Vmn1r169 T G 7: 23,276,611 (GRCm39) M1R probably null Het
Vmn2r3 C T 3: 64,167,304 (GRCm39) C609Y probably damaging Het
Vmn2r69 T C 7: 85,055,739 (GRCm39) T800A probably benign Het
Vmn2r72 G A 7: 85,387,542 (GRCm39) T674I probably benign Het
Zfp607a T A 7: 27,578,042 (GRCm39) C371S probably damaging Het
Other mutations in Zfp160
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00714:Zfp160 APN 17 21,246,964 (GRCm39) missense probably benign
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
R7627:Zfp160 UTSW 17 21,247,270 (GRCm39) missense probably damaging 0.99
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
Posted On 2013-06-28