Incidental Mutation 'IGL01115:Zfp955a'
ID53076
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: 0.080) question?
Stock #IGL01115
Quality Score
Status
Chromosome17
Chromosomal Location33241519-33255040 bp(-) (GRCm38)
Type of Mutationnonsense
DNA Base Change (assembly) T to A at 33242580 bp
ZygosityHeterozygous
Amino Acid Change Lysine to Stop codon at position 193 (K193*)
Ref Sequence ENSEMBL: ENSMUSP00000008830 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000008830]
Predicted Effect probably null
Transcript: ENSMUST00000008830
AA Change: K193*
SMART Domains Protein: ENSMUSP00000008830
Gene: ENSMUSG00000094441
AA Change: K193*

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: 34 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4430402I18Rik T C 19: 28,944,442 probably null Het
Abcc10 T C 17: 46,310,426 T934A probably benign Het
Ankzf1 T C 1: 75,192,615 L55P probably damaging Het
Aoc1 T C 6: 48,906,197 S336P probably damaging Het
Bmper T C 9: 23,399,689 probably benign Het
Capza2 A G 6: 17,654,123 N58S probably damaging Het
Cdca2 A G 14: 67,714,697 V75A probably damaging Het
Chmp7 A G 14: 69,721,323 S181P probably damaging Het
Colq A G 14: 31,545,128 probably benign Het
Dennd5b A G 6: 149,009,748 probably benign Het
Has3 A G 8: 106,878,688 T509A probably benign Het
Hsh2d T C 8: 72,200,619 S282P probably damaging Het
Impg2 C T 16: 56,259,440 P536S possibly damaging Het
Naip1 T A 13: 100,443,720 probably null Het
Napb T C 2: 148,707,169 Y111C probably damaging Het
Olfr1132 T C 2: 87,635,384 D121G probably damaging Het
Osmr A G 15: 6,847,201 probably benign Het
Pcdh10 A G 3: 45,392,775 T1002A probably damaging Het
Plcg2 T C 8: 117,557,329 W122R probably damaging Het
Prpf19 C T 19: 10,900,203 T204M probably damaging Het
Ptbp1 T A 10: 79,859,962 probably benign Het
Ptpre T A 7: 135,670,764 D402E probably damaging Het
Siglec1 T C 2: 131,074,502 N1176S probably benign Het
Son A G 16: 91,659,458 T1698A probably benign Het
Speer2 C T 16: 69,861,651 W42* probably null Het
Taf5 T C 19: 47,075,082 V357A probably benign Het
Tctn1 A G 5: 122,264,207 S55P probably benign Het
Tmem115 T A 9: 107,534,582 L35Q probably damaging Het
Tmem30c T A 16: 57,276,117 probably benign Het
Tmprss7 T C 16: 45,660,789 D678G probably damaging Het
Ugt1a7c A T 1: 88,095,245 Q42L probably damaging Het
Unc13b T A 4: 43,258,492 V4099E probably damaging Het
Usp36 G A 11: 118,285,960 L11F probably damaging Het
Zranb2 T C 3: 157,546,691 probably benign Het
Other mutations in Zfp955a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01859:Zfp955a APN 17 33243719 missense probably benign 0.45
IGL02612:Zfp955a APN 17 33244065 missense probably damaging 0.99
IGL02894:Zfp955a APN 17 33242452 nonsense probably null
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 On2013-06-21