Incidental Mutation 'IGL02894:Zfp955a'
ID363321
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp955a
Ensembl Gene ENSMUSG00000094441
Gene Namezinc finger protein 955A
SynonymsAI842447
Accession Numbers
Is this an essential gene? Probably non essential (E-score: 0.107) question?
Stock #IGL02894
Quality Score
Status
Chromosome17
Chromosomal Location33241519-33255040 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) A to T at 33242452 bp
ZygosityHeterozygous
Amino Acid Change Cysteine to Stop codon at position 235 (C235*)
Ref Sequence ENSEMBL: ENSMUSP00000008830 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008830]
Predicted Effect probably null
Transcript: ENSMUST00000008830
AA Change: C235*
SMART Domains Protein: ENSMUSP00000008830
Gene: ENSMUSG00000094441
AA Change: C235*

DomainStartEndE-ValueType
KRAB 10 71 7.08e-15 SMART
ZnF_C2H2 230 252 7.29e0 SMART
ZnF_C2H2 258 280 5.72e-1 SMART
ZnF_C2H2 290 312 6.57e-1 SMART
ZnF_C2HC 291 307 9.75e0 SMART
ZnF_C2H2 318 340 7.67e-2 SMART
ZnF_C2H2 346 368 3.16e-3 SMART
ZnF_C2H2 374 396 1.18e-2 SMART
ZnF_C2H2 402 424 2.99e-4 SMART
ZnF_C2H2 430 452 2.09e-3 SMART
ZnF_C2H2 458 480 6.57e-1 SMART
ZnF_C2HC 459 475 4.03e1 SMART
ZnF_C2H2 486 508 1.28e-3 SMART
ZnF_C2H2 514 536 2.36e-2 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 54 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9130204L05Rik A T 3: 91,088,393 F67L probably benign Het
A630023A22Rik T A 14: 34,054,860 probably benign Het
AF529169 T G 9: 89,603,102 I81L probably damaging Het
Aurka T A 2: 172,366,948 probably null Het
Cacna2d3 C T 14: 29,064,319 probably null Het
Cdh12 A G 15: 21,586,294 Y733C probably damaging Het
Cdon A T 9: 35,455,426 E199D probably benign Het
Celsr2 A T 3: 108,395,210 L558Q probably damaging Het
Clcnkb C A 4: 141,407,819 R536L probably benign Het
Cyp3a11 G A 5: 145,869,026 Q151* probably null Het
Dnah7a A T 1: 53,577,328 V1158E probably benign Het
Dnah8 G T 17: 30,721,110 E1677* probably null Het
Dock3 T C 9: 106,930,099 N1343S probably benign Het
Dock6 T A 9: 21,811,815 E1603D probably damaging Het
Fam91a1 C T 15: 58,443,231 T589M probably benign Het
Fat2 T A 11: 55,256,653 N3921I probably damaging Het
Gm10188 A G 1: 132,229,299 probably benign Het
Grid2ip A G 5: 143,391,108 E976G probably benign Het
Hapln3 G T 7: 79,121,773 Q123K probably benign Het
Hnrnpul1 G A 7: 25,750,904 P128S possibly damaging Het
Hsd3b1 T A 3: 98,852,929 I249F possibly damaging Het
Kbtbd3 A T 9: 4,331,444 H606L probably benign Het
Krt82 T C 15: 101,542,720 Y418C probably damaging Het
Mcm3ap C A 10: 76,477,767 A565E probably benign Het
Naip2 C T 13: 100,183,789 V240I probably benign Het
Naip2 A G 13: 100,160,997 S844P probably damaging Het
Notch2 T A 3: 98,102,432 C558* probably null Het
Npdc1 T A 2: 25,407,995 H185Q probably benign Het
Olfr1164 T C 2: 88,093,763 I58V possibly damaging Het
Olfr1183 T G 2: 88,461,726 Y148D probably damaging Het
Olfr447 A T 6: 42,911,517 probably benign Het
Osbpl3 A T 6: 50,346,332 I257N possibly damaging Het
Pkd1l2 T A 8: 117,013,891 T2156S probably damaging Het
Ppp1r13b A G 12: 111,831,454 probably benign Het
Ppp3ca C A 3: 136,797,812 H49N probably damaging Het
Prrc2c A T 1: 162,678,057 L1100I probably damaging Het
Ptpn21 A C 12: 98,689,632 probably benign Het
Ptpn7 A T 1: 135,143,168 M332L probably damaging Het
Ptprq T A 10: 107,667,424 Q791L probably benign Het
Ptprz1 G A 6: 23,035,149 R1966H probably damaging Het
Ralgapa1 T A 12: 55,717,069 Q1404L possibly damaging Het
Reln C A 5: 21,885,548 M3437I possibly damaging Het
Slc13a1 T C 6: 24,137,042 probably benign Het
Slc4a11 T C 2: 130,687,155 probably null Het
Slc9a2 A G 1: 40,763,602 E604G probably benign Het
Sod3 T G 5: 52,368,006 S16A possibly damaging Het
Taok3 A G 5: 117,263,613 I650V probably benign Het
Uggt2 T C 14: 119,081,799 I270M probably damaging Het
Ugt3a2 T A 15: 9,367,401 I410N probably damaging Het
Ush2a G A 1: 188,451,846 S1449N probably damaging Het
Usp29 A T 7: 6,961,634 M159L probably benign Het
Vmn1r122 A T 7: 21,133,724 F135L probably benign Het
Wdr11 T C 7: 129,631,166 probably benign Het
Zc3h14 T A 12: 98,758,943 probably null Het
Other mutations in Zfp955a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01115:Zfp955a APN 17 33242580 nonsense probably null
IGL01859:Zfp955a APN 17 33243719 missense probably benign 0.45
IGL02612:Zfp955a APN 17 33244065 missense probably damaging 0.99
IGL02933:Zfp955a APN 17 33243709 splice site probably null
R0145:Zfp955a UTSW 17 33242456 missense probably damaging 0.98
R0577:Zfp955a UTSW 17 33242094 missense probably damaging 0.99
R0963:Zfp955a UTSW 17 33243752 missense probably benign 0.00
R1588:Zfp955a UTSW 17 33241817 missense probably benign 0.00
R1614:Zfp955a UTSW 17 33242332 missense possibly damaging 0.72
R1704:Zfp955a UTSW 17 33241725 nonsense probably null
R1994:Zfp955a UTSW 17 33241646 missense probably damaging 0.99
R2043:Zfp955a UTSW 17 33242553 missense possibly damaging 0.94
R2091:Zfp955a UTSW 17 33242757 nonsense probably null
R2091:Zfp955a UTSW 17 33242757 nonsense probably null
R4077:Zfp955a UTSW 17 33241701 missense probably benign 0.15
R4078:Zfp955a UTSW 17 33241701 missense probably benign 0.15
R4689:Zfp955a UTSW 17 33242066 missense probably damaging 1.00
R4735:Zfp955a UTSW 17 33241722 missense probably benign 0.09
R4870:Zfp955a UTSW 17 33241725 nonsense probably null
R4904:Zfp955a UTSW 17 33242188 nonsense probably null
R5180:Zfp955a UTSW 17 33242618 missense probably benign 0.15
R6006:Zfp955a UTSW 17 33241686 missense probably damaging 1.00
R7132:Zfp955a UTSW 17 33241615 nonsense probably null
R7403:Zfp955a UTSW 17 33243746 missense probably benign 0.01
R7457:Zfp955a UTSW 17 33244051 nonsense probably null
R7547:Zfp955a UTSW 17 33242823 missense probably benign 0.05
X0062:Zfp955a UTSW 17 33242002 missense probably benign 0.37
Posted On2015-12-18