Incidental Mutation 'H8441:Zfp609'
ID 82543
Institutional Source Beutler Lab
Gene Symbol Zfp609
Ensembl Gene ENSMUSG00000040524
Gene Name zinc finger protein 609
Synonyms
Accession Numbers
Essential gene? Possibly essential (E-score: 0.620) question?
Stock # H8441 (G3) of strain 599
Quality Score 225
Status Not validated
Chromosome 9
Chromosomal Location 65599673-65734846 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 65702169 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Glutamic Acid to Glycine at position 161 (E161G)
Ref Sequence ENSEMBL: ENSMUSP00000124089 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000159109] [ENSMUST00000160747]
AlphaFold Q8BZ47
Predicted Effect possibly damaging
Transcript: ENSMUST00000159109
AA Change: E161G

PolyPhen 2 Score 0.816 (Sensitivity: 0.84; Specificity: 0.93)
SMART Domains Protein: ENSMUSP00000124089
Gene: ENSMUSG00000040524
AA Change: E161G

DomainStartEndE-ValueType
low complexity region 83 101 N/A INTRINSIC
low complexity region 125 139 N/A INTRINSIC
low complexity region 155 176 N/A INTRINSIC
low complexity region 259 269 N/A INTRINSIC
low complexity region 365 376 N/A INTRINSIC
low complexity region 386 405 N/A INTRINSIC
ZnF_C2H2 495 520 2.14e0 SMART
low complexity region 629 638 N/A INTRINSIC
low complexity region 657 667 N/A INTRINSIC
low complexity region 724 738 N/A INTRINSIC
low complexity region 1000 1020 N/A INTRINSIC
low complexity region 1210 1219 N/A INTRINSIC
low complexity region 1257 1273 N/A INTRINSIC
low complexity region 1329 1348 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000160747
Coding Region Coverage
  • 1x: 99.4%
  • 3x: 98.8%
  • 10x: 97.4%
  • 20x: 95.0%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 19 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adamts2 A C 11: 50,675,505 (GRCm39) D677A probably damaging Het
Dido1 G T 2: 180,330,807 (GRCm39) Q214K probably benign Het
H2-T5 T A 17: 36,478,874 (GRCm39) Q125L possibly damaging Het
Itgbl1 A G 14: 124,210,699 (GRCm39) N342D probably damaging Het
Mlxipl T C 5: 135,152,815 (GRCm39) I282T probably damaging Het
Or6b13 C T 7: 139,781,871 (GRCm39) D271N possibly damaging Het
Pes1 AGAGGAGGAGGAGGAGGA AGAGGAGGAGGAGGA 11: 3,927,636 (GRCm39) probably benign Het
Phf2 C T 13: 48,957,841 (GRCm39) A1058T possibly damaging Het
Pja2 T C 17: 64,618,192 (GRCm39) D69G probably damaging Het
Pnmt G A 11: 98,278,513 (GRCm39) A160T probably benign Het
Pomgnt2 T G 9: 121,811,650 (GRCm39) Y377S probably damaging Het
Scn11a T A 9: 119,636,976 (GRCm39) I242F probably damaging Het
Slc7a1 C T 5: 148,271,355 (GRCm39) V535M probably benign Het
Stk32b T C 5: 37,614,578 (GRCm39) D310G probably damaging Het
Sult3a2 A T 10: 33,642,474 (GRCm39) H276Q probably benign Het
Susd5 A T 9: 113,925,253 (GRCm39) K379* probably null Het
Tbc1d16 C A 11: 119,039,840 (GRCm39) E656* probably null Het
Tcp10b T C 17: 13,289,748 (GRCm39) S234P probably damaging Het
Vmo1 A G 11: 70,404,572 (GRCm39) F143S probably damaging Het
Other mutations in Zfp609
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00956:Zfp609 APN 9 65,610,045 (GRCm39) missense probably benign 0.18
IGL01688:Zfp609 APN 9 65,611,307 (GRCm39) missense probably benign
IGL01718:Zfp609 APN 9 65,609,682 (GRCm39) nonsense probably null
IGL01860:Zfp609 APN 9 65,610,116 (GRCm39) missense possibly damaging 0.82
IGL02441:Zfp609 APN 9 65,610,611 (GRCm39) missense possibly damaging 0.92
IGL02490:Zfp609 APN 9 65,611,250 (GRCm39) missense possibly damaging 0.92
IGL02614:Zfp609 APN 9 65,610,072 (GRCm39) missense probably damaging 0.96
IGL02794:Zfp609 APN 9 65,611,602 (GRCm39) missense possibly damaging 0.83
IGL02959:Zfp609 APN 9 65,610,675 (GRCm39) missense probably benign
IGL02967:Zfp609 APN 9 65,604,901 (GRCm39) missense possibly damaging 0.83
IGL03036:Zfp609 APN 9 65,609,927 (GRCm39) missense possibly damaging 0.89
IGL03182:Zfp609 APN 9 65,608,287 (GRCm39) missense probably benign 0.02
R0304:Zfp609 UTSW 9 65,608,470 (GRCm39) missense possibly damaging 0.89
R0487:Zfp609 UTSW 9 65,609,916 (GRCm39) missense unknown
R0505:Zfp609 UTSW 9 65,610,744 (GRCm39) missense possibly damaging 0.92
R0684:Zfp609 UTSW 9 65,638,483 (GRCm39) missense probably benign 0.01
R1480:Zfp609 UTSW 9 65,610,593 (GRCm39) missense possibly damaging 0.82
R1507:Zfp609 UTSW 9 65,702,059 (GRCm39) missense possibly damaging 0.92
R1579:Zfp609 UTSW 9 65,611,754 (GRCm39) missense possibly damaging 0.90
R1655:Zfp609 UTSW 9 65,610,836 (GRCm39) missense possibly damaging 0.46
R1692:Zfp609 UTSW 9 65,702,593 (GRCm39) missense probably damaging 0.98
R1701:Zfp609 UTSW 9 65,638,282 (GRCm39) missense probably benign 0.05
R1735:Zfp609 UTSW 9 65,610,374 (GRCm39) nonsense probably null
R1883:Zfp609 UTSW 9 65,702,040 (GRCm39) missense probably benign
R1970:Zfp609 UTSW 9 65,702,559 (GRCm39) missense probably damaging 0.96
R2059:Zfp609 UTSW 9 65,611,716 (GRCm39) missense possibly damaging 0.83
R2302:Zfp609 UTSW 9 65,702,179 (GRCm39) missense possibly damaging 0.66
R3404:Zfp609 UTSW 9 65,608,454 (GRCm39) missense possibly damaging 0.68
R3405:Zfp609 UTSW 9 65,608,454 (GRCm39) missense possibly damaging 0.68
R4514:Zfp609 UTSW 9 65,610,977 (GRCm39) missense possibly damaging 0.46
R4533:Zfp609 UTSW 9 65,610,890 (GRCm39) missense probably benign 0.00
R5043:Zfp609 UTSW 9 65,608,109 (GRCm39) missense probably damaging 0.97
R5499:Zfp609 UTSW 9 65,610,137 (GRCm39) missense probably benign 0.00
R7081:Zfp609 UTSW 9 65,609,723 (GRCm39) missense possibly damaging 0.46
R7514:Zfp609 UTSW 9 65,613,418 (GRCm39) missense probably benign 0.05
R7677:Zfp609 UTSW 9 65,604,456 (GRCm39) missense possibly damaging 0.61
R7684:Zfp609 UTSW 9 65,638,362 (GRCm39) missense possibly damaging 0.66
R8229:Zfp609 UTSW 9 65,610,782 (GRCm39) missense possibly damaging 0.66
R8266:Zfp609 UTSW 9 65,610,996 (GRCm39) missense possibly damaging 0.66
R8278:Zfp609 UTSW 9 65,604,804 (GRCm39) missense possibly damaging 0.90
R8934:Zfp609 UTSW 9 65,610,561 (GRCm39) missense possibly damaging 0.90
R8938:Zfp609 UTSW 9 65,610,561 (GRCm39) missense possibly damaging 0.90
R8940:Zfp609 UTSW 9 65,610,561 (GRCm39) missense possibly damaging 0.90
R8986:Zfp609 UTSW 9 65,610,561 (GRCm39) missense possibly damaging 0.90
R9267:Zfp609 UTSW 9 65,608,328 (GRCm39) missense possibly damaging 0.90
R9456:Zfp609 UTSW 9 65,611,125 (GRCm39) missense
R9561:Zfp609 UTSW 9 65,604,512 (GRCm39) nonsense probably null
X0028:Zfp609 UTSW 9 65,604,362 (GRCm39) small deletion probably benign
Predicted Primers PCR Primer
(F):5'- GCACACAGCATTTGGCGGTTAG -3'
(R):5'- AGCAGAAACTGGAAATGTCAGGCTC -3'

Sequencing Primer
(F):5'- TTAGTTCCCAAAGGATTGAGCG -3'
(R):5'- AAGTTTGTCACCCCAGTGC -3'
Posted On 2013-11-08