Incidental Mutation 'R5585:Zfp995'
ID 438680
Institutional Source Beutler Lab
Gene Symbol Zfp995
Ensembl Gene ENSMUSG00000078546
Gene Name zinc finger protein 995
Synonyms 2210404O09Rik
MMRRC Submission 043139-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.065) question?
Stock # R5585 (G1)
Quality Score 225
Status Not validated
Chromosome 17
Chromosomal Location 22098551-22128907 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) C to T at 22106339 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000139581 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000106026] [ENSMUST00000190066]
AlphaFold E9Q6M3
Predicted Effect probably benign
Transcript: ENSMUST00000106026
SMART Domains Protein: ENSMUSP00000101647
Gene: ENSMUSG00000078546

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 noncoding transcript
Transcript: ENSMUST00000189719
Predicted Effect probably benign
Transcript: ENSMUST00000190066
SMART Domains Protein: ENSMUSP00000139581
Gene: ENSMUSG00000078546

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
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.6%
  • 20x: 96.3%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 39 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1600014C23Rik A T 17: 46,044,670 (GRCm39) I17N unknown Het
4932414N04Rik A G 2: 68,571,770 (GRCm39) T549A probably benign Het
9330159F19Rik C A 10: 29,101,271 (GRCm39) S548Y possibly damaging Het
Aanat A G 11: 116,487,799 (GRCm39) Y166C probably damaging Het
Adra2a G T 19: 54,034,670 (GRCm39) A9S probably benign Het
Ap4m1 A G 5: 138,170,502 (GRCm39) Y17C probably damaging Het
Arhgap33 T G 7: 30,223,260 (GRCm39) M891L probably benign Het
Calm5 A G 13: 3,904,372 (GRCm39) D22G possibly damaging Het
Ccdc15 C T 9: 37,188,699 (GRCm39) R795H probably benign Het
Cngb1 T A 8: 95,989,767 (GRCm39) I323F probably damaging Het
Cyp26b1 A G 6: 84,554,171 (GRCm39) F74L probably damaging Het
Dpagt1 G A 9: 44,240,439 (GRCm39) probably null Het
Ercc8 C T 13: 108,312,123 (GRCm39) P196S probably damaging Het
Gm10985 A C 3: 53,752,674 (GRCm39) Y19S probably damaging Het
Hfm1 G A 5: 107,059,305 (GRCm39) S239L probably benign Het
Hgf A G 5: 16,769,799 (GRCm39) D91G possibly damaging Het
Lefty2 T A 1: 180,720,828 (GRCm39) V27D possibly damaging Het
Lrp2 G A 2: 69,294,968 (GRCm39) T3450I possibly damaging Het
Lrrc38 A G 4: 143,076,961 (GRCm39) I75V probably damaging Het
Ncor2 C A 5: 125,144,975 (GRCm39) E556* probably null Het
Nedd9 A G 13: 41,469,950 (GRCm39) L401P probably damaging Het
Nfatc4 T C 14: 56,064,212 (GRCm39) L163P probably damaging Het
Nln T C 13: 104,161,569 (GRCm39) N667S possibly damaging Het
Or5w20 A G 2: 87,727,019 (GRCm39) T159A possibly damaging Het
Pnpla8 T C 12: 44,329,847 (GRCm39) I133T probably benign Het
Psma1 C T 7: 113,873,302 (GRCm39) G12S probably damaging Het
Psmd3 G A 11: 98,573,707 (GRCm39) G51D possibly damaging Het
Ptprb A G 10: 116,216,759 (GRCm39) Q1959R probably damaging Het
Rhbdf1 A G 11: 32,160,222 (GRCm39) probably null Het
Rnf167 T C 11: 70,540,308 (GRCm39) V110A probably damaging Het
Rrp9 C T 9: 106,362,525 (GRCm39) S470F probably benign Het
Rtn3 G A 19: 7,435,560 (GRCm39) P125L probably benign Het
Scube1 C T 15: 83,561,124 (GRCm39) C156Y probably damaging Het
Tgm2 A T 2: 157,973,375 (GRCm39) Y245* probably null Het
Timeless T C 10: 128,076,112 (GRCm39) I68T probably damaging Het
Ttn A G 2: 76,645,054 (GRCm39) S12934P probably damaging Het
Vwa5b2 T A 16: 20,413,428 (GRCm39) Y214* probably null Het
Yars2 T A 16: 16,122,484 (GRCm39) N7K probably damaging Het
Zfp142 G A 1: 74,617,404 (GRCm39) Q150* probably null Het
Other mutations in Zfp995
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01800:Zfp995 APN 17 22,099,972 (GRCm39) missense possibly damaging 0.64
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
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
Predicted Primers
Posted On 2016-10-26