Incidental Mutation 'IGL01800:Zfp995'
ID 155497
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp995
Ensembl Gene ENSMUSG00000078546
Gene Name zinc finger protein 995
Synonyms 2210404O09Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # IGL01800
Quality Score
Status
Chromosome 17
Chromosomal Location 22098551-22128907 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 22099972 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 87 (H87Q)
Ref Sequence ENSEMBL: ENSMUSP00000139581 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106026] [ENSMUST00000190066]
AlphaFold E9Q6M3
Predicted Effect possibly damaging
Transcript: ENSMUST00000106026
AA Change: H87Q

PolyPhen 2 Score 0.642 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000101647
Gene: ENSMUSG00000078546
AA Change: H87Q

DomainStartEndE-ValueType
KRAB 13 76 8.19e-20 SMART
ZnF_C2H2 183 205 8.81e-2 SMART
ZnF_C2H2 211 233 3.21e-4 SMART
ZnF_C2H2 239 261 4.72e-2 SMART
ZnF_C2H2 267 289 1.98e-4 SMART
ZnF_C2H2 295 317 5.59e-4 SMART
ZnF_C2H2 323 345 4.24e-4 SMART
ZnF_C2H2 351 373 9.73e-4 SMART
ZnF_C2H2 379 401 5.29e-5 SMART
ZnF_C2H2 407 429 8.02e-5 SMART
Predicted Effect possibly damaging
Transcript: ENSMUST00000190066
AA Change: H87Q

PolyPhen 2 Score 0.642 (Sensitivity: 0.87; Specificity: 0.91)
SMART Domains Protein: ENSMUSP00000139581
Gene: ENSMUSG00000078546
AA Change: H87Q

DomainStartEndE-ValueType
KRAB 13 76 8.19e-20 SMART
ZnF_C2H2 183 205 8.81e-2 SMART
ZnF_C2H2 211 233 3.21e-4 SMART
ZnF_C2H2 239 261 4.72e-2 SMART
ZnF_C2H2 267 289 1.98e-4 SMART
ZnF_C2H2 295 317 5.59e-4 SMART
ZnF_C2H2 323 345 4.24e-4 SMART
ZnF_C2H2 351 373 9.73e-4 SMART
ZnF_C2H2 379 401 5.29e-5 SMART
ZnF_C2H2 407 429 8.02e-5 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 38 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcc2 A G 19: 43,772,734 (GRCm39) Y48C possibly damaging Het
Acsm3 T C 7: 119,373,866 (GRCm39) S251P possibly damaging Het
Ano5 G A 7: 51,222,823 (GRCm39) probably null Het
Ccdc65 C T 15: 98,606,946 (GRCm39) A51V probably benign Het
Cspg5 A G 9: 110,080,218 (GRCm39) probably benign Het
Dhx30 A G 9: 109,914,581 (GRCm39) V935A possibly damaging Het
Disp3 T A 4: 148,334,258 (GRCm39) K1012* probably null Het
Dock2 T C 11: 34,647,100 (GRCm39) N18S probably damaging Het
Dst A T 1: 34,301,173 (GRCm39) I1180F probably damaging Het
Elp2 A G 18: 24,750,548 (GRCm39) Y295C probably benign Het
Eml2 A G 7: 18,935,122 (GRCm39) probably benign Het
Fat4 A G 3: 39,035,878 (GRCm39) T3177A probably damaging Het
Flrt2 A T 12: 95,746,462 (GRCm39) I267F probably damaging Het
Gm5611 T G 9: 16,941,767 (GRCm39) noncoding transcript Het
Gstcd A G 3: 132,790,335 (GRCm39) probably null Het
Gucy1b2 T C 14: 62,649,104 (GRCm39) M476V probably benign Het
Jak2 A G 19: 29,263,693 (GRCm39) probably benign Het
Kcnt1 T C 2: 25,778,137 (GRCm39) F85S probably damaging Het
Kcnu1 G A 8: 26,427,528 (GRCm39) V282M probably damaging Het
Lancl1 T G 1: 67,060,029 (GRCm39) E132A probably benign Het
Or4g7 T C 2: 111,309,209 (GRCm39) F27L probably benign Het
Or5b106 A G 19: 13,123,993 (GRCm39) F10S probably damaging Het
Pigm G A 1: 172,204,770 (GRCm39) A169T probably damaging Het
Ppargc1a A G 5: 51,652,063 (GRCm39) Y212H probably damaging Het
Ppp1r13l A T 7: 19,111,936 (GRCm39) probably benign Het
Pramel12 T C 4: 143,145,650 (GRCm39) L373P probably damaging Het
Rictor T C 15: 6,804,182 (GRCm39) I554T probably damaging Het
Sbno1 G A 5: 124,519,568 (GRCm39) probably benign Het
Sesn2 G T 4: 132,226,418 (GRCm39) L194I probably damaging Het
Slc26a2 A T 18: 61,334,801 (GRCm39) Y217* probably null Het
Sptbn5 G T 2: 119,886,908 (GRCm39) probably benign Het
Tmem184a A T 5: 139,798,899 (GRCm39) S17T possibly damaging Het
Trhr T C 15: 44,092,603 (GRCm39) M280T possibly damaging Het
Ube2j1 A T 4: 33,045,115 (GRCm39) E129D probably benign Het
Ube4b A T 4: 149,415,951 (GRCm39) S3T probably damaging Het
Vmn2r49 A T 7: 9,710,601 (GRCm39) C710* probably null Het
Vmn2r82 C T 10: 79,192,581 (GRCm39) R53C probably benign Het
Zdhhc2 T C 8: 40,917,284 (GRCm39) L227P probably damaging Het
Other mutations in Zfp995
AlleleSourceChrCoordTypePredicted EffectPPH Score
experienced UTSW 17 22,106,321 (GRCm39) start codon destroyed probably damaging 0.98
R2906_Zfp995_673 UTSW 17 22,099,247 (GRCm39) missense probably benign 0.00
wise UTSW 17 22,099,493 (GRCm39) missense probably benign 0.06
R1164:Zfp995 UTSW 17 22,098,960 (GRCm39) missense probably damaging 1.00
R1167:Zfp995 UTSW 17 22,098,960 (GRCm39) missense probably damaging 1.00
R1592:Zfp995 UTSW 17 22,106,321 (GRCm39) start codon destroyed probably damaging 0.98
R1669:Zfp995 UTSW 17 22,098,945 (GRCm39) missense probably benign 0.12
R1883:Zfp995 UTSW 17 22,099,622 (GRCm39) missense probably benign 0.00
R2044:Zfp995 UTSW 17 22,099,575 (GRCm39) missense probably damaging 1.00
R2906:Zfp995 UTSW 17 22,099,247 (GRCm39) missense probably benign 0.00
R4454:Zfp995 UTSW 17 22,098,932 (GRCm39) missense probably benign 0.17
R4670:Zfp995 UTSW 17 22,106,320 (GRCm39) start codon destroyed probably null 1.00
R5265:Zfp995 UTSW 17 22,099,604 (GRCm39) missense possibly damaging 0.55
R5393:Zfp995 UTSW 17 22,099,473 (GRCm39) missense probably benign 0.01
R5585:Zfp995 UTSW 17 22,106,339 (GRCm39) splice site probably benign
R5735:Zfp995 UTSW 17 22,101,010 (GRCm39) missense probably benign 0.05
R6243:Zfp995 UTSW 17 22,099,269 (GRCm39) missense probably damaging 1.00
R6318:Zfp995 UTSW 17 22,099,493 (GRCm39) missense probably benign 0.06
R7311:Zfp995 UTSW 17 22,099,641 (GRCm39) missense probably benign 0.01
R7472:Zfp995 UTSW 17 22,099,181 (GRCm39) missense probably damaging 1.00
R7529:Zfp995 UTSW 17 22,099,333 (GRCm39) nonsense probably null
R7765:Zfp995 UTSW 17 22,100,984 (GRCm39) missense probably damaging 1.00
R8156:Zfp995 UTSW 17 22,099,115 (GRCm39) missense probably damaging 1.00
R8995:Zfp995 UTSW 17 22,099,172 (GRCm39) missense probably benign 0.00
Z1176:Zfp995 UTSW 17 22,101,035 (GRCm39) missense possibly damaging 0.57
Posted On 2014-02-04