Incidental Mutation 'IGL02971:Zfp955b'
ID 365793
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp955b
Ensembl Gene ENSMUSG00000096910
Gene Name zinc finger protein 955B
Synonyms C430039G02Rik, A430003O12Rik, Gm4455
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # IGL02971
Quality Score
Status
Chromosome 17
Chromosomal Location 33508518-33526215 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 33519940 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Methionine to Lysine at position 57 (M57K)
Ref Sequence ENSEMBL: ENSMUSP00000097011 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000099414]
AlphaFold L7N232
Predicted Effect probably benign
Transcript: ENSMUST00000099414
AA Change: M57K

PolyPhen 2 Score 0.109 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000097011
Gene: ENSMUSG00000096910
AA Change: M57K

DomainStartEndE-ValueType
KRAB 10 70 3.04e-14 SMART
ZnF_C2H2 230 252 7.68e0 SMART
ZnF_C2H2 258 280 5.72e-1 SMART
ZnF_C2H2 290 312 6.75e0 SMART
ZnF_C2H2 318 340 5.81e-2 SMART
ZnF_C2H2 346 368 3.16e-3 SMART
ZnF_C2H2 374 396 1.18e-2 SMART
ZnF_C2H2 402 424 7.78e-3 SMART
ZnF_C2H2 430 452 3.16e-3 SMART
ZnF_C2H2 458 480 1.1e-2 SMART
ZnF_C2H2 486 508 2.09e-3 SMART
ZnF_C2H2 514 536 6.67e-2 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000182230
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 45 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
A930018P22Rik C T 2: 103,953,564 (GRCm39) T130I probably benign Het
Ahi1 T C 10: 20,876,450 (GRCm39) L787P possibly damaging Het
Atf3 A G 1: 190,909,640 (GRCm39) S10P probably benign Het
Cdr2l A G 11: 115,281,726 (GRCm39) N77S probably damaging Het
Cnp A G 11: 100,467,525 (GRCm39) D156G probably benign Het
Cntn3 A T 6: 102,145,894 (GRCm39) D982E probably damaging Het
Col22a1 A G 15: 71,878,587 (GRCm39) L190S probably damaging Het
Csmd3 C T 15: 47,777,325 (GRCm39) probably benign Het
Dnah5 A G 15: 28,384,607 (GRCm39) D3117G probably damaging Het
Dock5 T C 14: 67,994,558 (GRCm39) E1834G probably null Het
Eea1 A G 10: 95,877,389 (GRCm39) T1368A probably benign Het
Fam83f T C 15: 80,556,350 (GRCm39) V78A probably benign Het
Fcgbp G A 7: 27,800,898 (GRCm39) V1315I probably damaging Het
Fsd2 A T 7: 81,198,671 (GRCm39) Y364* probably null Het
Gm21976 G A 13: 98,439,057 (GRCm39) G16R probably null Het
Guca2b A G 4: 119,514,885 (GRCm39) S59P probably damaging Het
Hars2 A G 18: 36,919,231 (GRCm39) E123G probably damaging Het
Hdac2 A T 10: 36,876,370 (GRCm39) K462* probably null Het
Huwe1 T A X: 150,710,622 (GRCm39) probably benign Het
Iqgap3 T A 3: 87,997,611 (GRCm39) N262K probably benign Het
Kat6b A G 14: 21,719,826 (GRCm39) S1502G probably damaging Het
Mapkapk3 A T 9: 107,134,279 (GRCm39) D328E probably benign Het
Naca C T 10: 127,877,437 (GRCm39) probably benign Het
Npffr1 T C 10: 61,449,918 (GRCm39) V64A probably damaging Het
Oga A G 19: 45,750,682 (GRCm39) F671S probably damaging Het
Or2t49 A G 11: 58,393,211 (GRCm39) L57P probably damaging Het
Or8b3b T A 9: 38,584,564 (GRCm39) M72L probably damaging Het
Pcca A G 14: 123,126,945 (GRCm39) D718G probably damaging Het
Pde6a A C 18: 61,397,326 (GRCm39) D670A probably damaging Het
Pramel7 T A 2: 87,320,417 (GRCm39) E292V probably benign Het
Prmt9 A C 8: 78,291,698 (GRCm39) M357L probably benign Het
Ptgfr A T 3: 151,540,963 (GRCm39) S182T probably benign Het
Rtraf A T 14: 19,866,260 (GRCm39) M152K possibly damaging Het
Satb1 T C 17: 52,049,717 (GRCm39) D579G possibly damaging Het
Serpinb6a A G 13: 34,115,453 (GRCm39) probably null Het
Slc5a9 T C 4: 111,747,497 (GRCm39) I297V possibly damaging Het
Slf1 T A 13: 77,195,223 (GRCm39) probably benign Het
St8sia2 C T 7: 73,616,559 (GRCm39) V139M probably damaging Het
Tas2r114 T C 6: 131,666,243 (GRCm39) M262V probably benign Het
Tmem147 A G 7: 30,428,847 (GRCm39) probably benign Het
Tmem220 A G 11: 66,924,933 (GRCm39) probably null Het
Uspl1 A G 5: 149,125,156 (GRCm39) N35S possibly damaging Het
Vmn1r170 A T 7: 23,305,759 (GRCm39) I54F possibly damaging Het
Vmn2r121 T G X: 123,037,591 (GRCm39) I810L probably damaging Het
Wbp2nl A T 15: 82,189,945 (GRCm39) T46S possibly damaging Het
Other mutations in Zfp955b
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00537:Zfp955b APN 17 33,521,847 (GRCm39) missense probably damaging 1.00
IGL02073:Zfp955b APN 17 33,519,564 (GRCm39) missense possibly damaging 0.69
IGL02126:Zfp955b APN 17 33,521,238 (GRCm39) nonsense probably null
IGL02237:Zfp955b APN 17 33,520,893 (GRCm39) missense probably damaging 1.00
IGL02587:Zfp955b APN 17 33,519,624 (GRCm39) missense probably damaging 1.00
IGL03034:Zfp955b APN 17 33,521,142 (GRCm39) missense probably benign 0.22
IGL03493:Zfp955b APN 17 33,521,519 (GRCm39) missense probably benign 0.35
R0269:Zfp955b UTSW 17 33,524,437 (GRCm39) missense probably damaging 1.00
R0373:Zfp955b UTSW 17 33,521,496 (GRCm39) missense probably benign
R0617:Zfp955b UTSW 17 33,524,437 (GRCm39) missense probably damaging 1.00
R0684:Zfp955b UTSW 17 33,521,947 (GRCm39) missense probably benign 0.00
R1778:Zfp955b UTSW 17 33,521,788 (GRCm39) missense probably benign 0.07
R1874:Zfp955b UTSW 17 33,524,427 (GRCm39) missense probably benign 0.10
R3893:Zfp955b UTSW 17 33,521,968 (GRCm39) missense probably benign 0.01
R3938:Zfp955b UTSW 17 33,524,390 (GRCm39) missense probably damaging 1.00
R4082:Zfp955b UTSW 17 33,521,129 (GRCm39) missense probably benign 0.08
R4672:Zfp955b UTSW 17 33,524,233 (GRCm39) unclassified probably benign
R4956:Zfp955b UTSW 17 33,524,209 (GRCm39) unclassified probably benign
R4998:Zfp955b UTSW 17 33,524,125 (GRCm39) unclassified probably benign
R5276:Zfp955b UTSW 17 33,522,031 (GRCm39) missense probably damaging 1.00
R5341:Zfp955b UTSW 17 33,524,095 (GRCm39) unclassified probably benign
R5558:Zfp955b UTSW 17 33,521,161 (GRCm39) missense possibly damaging 0.88
R6086:Zfp955b UTSW 17 33,521,478 (GRCm39) missense probably benign
R6170:Zfp955b UTSW 17 33,521,084 (GRCm39) missense probably benign 0.00
R6306:Zfp955b UTSW 17 33,522,160 (GRCm39) missense probably benign 0.07
R6519:Zfp955b UTSW 17 33,521,051 (GRCm39) missense possibly damaging 0.55
R9286:Zfp955b UTSW 17 33,521,683 (GRCm39) missense probably benign 0.04
Posted On 2015-12-18