Incidental Mutation 'R6740:Zfp1006'
ID 527437
Institutional Source Beutler Lab
Gene Symbol Zfp1006
Ensembl Gene ENSMUSG00000071302
Gene Name zinc finger protein 1006
Synonyms 2610044O15Rik8
Accession Numbers
Essential gene? Probably non essential (E-score: 0.116) question?
Stock # R6740 (G1) of strain 613
Quality Score 174.009
Status Not validated
Chromosome 8
Chromosomal Location 129942835-129960527 bp(-) (GRCm39)
Type of Mutation splice site
DNA Base Change (assembly) A to C at 129960881 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change
Ref Sequence ENSEMBL: ENSMUSP00000140304 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000186619] [ENSMUST00000188757] [ENSMUST00000189965] [ENSMUST00000190157] [ENSMUST00000191043]
AlphaFold A0A087WRJ1
Predicted Effect probably benign
Transcript: ENSMUST00000186619
SMART Domains Protein: ENSMUSP00000140654
Gene: ENSMUSG00000071302

DomainStartEndE-ValueType
KRAB 4 66 1.2e-15 SMART
ZnF_C2H2 75 97 3.7e-2 SMART
ZnF_C2H2 103 125 3e-4 SMART
ZnF_C2H2 131 153 3.7e-5 SMART
ZnF_C2H2 159 181 4e-6 SMART
ZnF_C2H2 187 209 9.6e-6 SMART
ZnF_C2H2 215 237 8.7e-6 SMART
ZnF_C2H2 243 265 1.2e-5 SMART
ZnF_C2H2 271 293 9.9e-6 SMART
ZnF_C2H2 299 321 8.3e-6 SMART
ZnF_C2H2 327 349 3.8e-7 SMART
ZnF_C2H2 355 377 2.5e-5 SMART
ZnF_C2H2 383 405 3.9e-6 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000188757
SMART Domains Protein: ENSMUSP00000140555
Gene: ENSMUSG00000071302

DomainStartEndE-ValueType
KRAB 4 66 2.79e-13 SMART
Predicted Effect probably null
Transcript: ENSMUST00000189965
SMART Domains Protein: ENSMUSP00000140304
Gene: ENSMUSG00000071302

DomainStartEndE-ValueType
KRAB 4 66 1.2e-15 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000190157
SMART Domains Protein: ENSMUSP00000140736
Gene: ENSMUSG00000071302

DomainStartEndE-ValueType
KRAB 4 66 2.79e-13 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000191043
SMART Domains Protein: ENSMUSP00000139392
Gene: ENSMUSG00000071302

DomainStartEndE-ValueType
KRAB 4 66 6.1e-16 SMART
Meta Mutation Damage Score 0.9755 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.7%
  • 10x: 98.5%
  • 20x: 95.8%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 8 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Cyp2e1 C T 7: 140,343,693 (GRCm39) probably benign Het
Eea1 C G 10: 95,859,855 (GRCm39) H714D probably benign Het
Efcab8 A G 2: 153,646,814 (GRCm39) H381R probably damaging Het
Fer1l4 A G 2: 155,873,142 (GRCm39) S1313P probably damaging Het
Itih3 T C 14: 30,634,644 (GRCm39) N121S probably benign Het
Lgr6 C T 1: 134,921,748 (GRCm39) A199T probably damaging Het
Lrch1 A G 14: 75,049,063 (GRCm39) S395P probably benign Het
Rnf180 G A 13: 105,318,014 (GRCm39) A466V possibly damaging Het
Other mutations in Zfp1006
AlleleSourceChrCoordTypePredicted EffectPPH Score
R1956:Zfp1006 UTSW 8 129,948,309 (GRCm39) missense possibly damaging 0.82
R6871:Zfp1006 UTSW 8 129,960,881 (GRCm39) splice site probably null
R7060:Zfp1006 UTSW 8 129,945,613 (GRCm39) missense probably benign 0.00
R7185:Zfp1006 UTSW 8 129,946,502 (GRCm39) missense probably benign 0.38
R7696:Zfp1006 UTSW 8 129,945,794 (GRCm39) missense probably benign 0.00
R7707:Zfp1006 UTSW 8 129,945,660 (GRCm39) nonsense probably null
R8049:Zfp1006 UTSW 8 129,946,555 (GRCm39) missense probably damaging 1.00
R8765:Zfp1006 UTSW 8 129,948,070 (GRCm39) missense probably benign 0.01
R8798:Zfp1006 UTSW 8 129,945,779 (GRCm39) missense probably damaging 0.99
R8980:Zfp1006 UTSW 8 129,945,680 (GRCm39) missense probably damaging 1.00
R8996:Zfp1006 UTSW 8 129,946,016 (GRCm39) missense possibly damaging 0.78
R9336:Zfp1006 UTSW 8 129,944,149 (GRCm39) missense unknown
R9797:Zfp1006 UTSW 8 129,946,534 (GRCm39) missense probably benign 0.34
Predicted Primers PCR Primer
(F):5'- GCATTTGTGTCTGTCCACCAAG -3'
(R):5'- GCACAAAAGCTACTGGAGTG -3'

Sequencing Primer
(F):5'- CAAGTTTGGCATCTTGCTCG -3'
(R):5'- CTACTGGAGTGCAAGTCAGACCTG -3'
Posted On 2018-07-23