Incidental Mutation 'IGL01019:Zfp607a'
ID 53688
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp607a
Ensembl Gene ENSMUSG00000020420
Gene Name zinc finger protein 607A
Synonyms Zfp607, 4732475C15Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.058) question?
Stock # IGL01019
Quality Score
Status
Chromosome 7
Chromosomal Location 27556952-27580250 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 27578042 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Serine at position 371 (C371S)
Ref Sequence ENSEMBL: ENSMUSP00000146006 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000053722] [ENSMUST00000205534] [ENSMUST00000205715]
AlphaFold Q3TQG9
Predicted Effect probably damaging
Transcript: ENSMUST00000053722
AA Change: C371S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000051496
Gene: ENSMUSG00000020420
AA Change: C371S

DomainStartEndE-ValueType
KRAB 14 75 8.48e-36 SMART
ZnF_C2H2 173 195 2.91e-2 SMART
ZnF_C2H2 201 223 3.44e-4 SMART
ZnF_C2H2 229 251 3.83e-2 SMART
ZnF_C2H2 257 279 4.87e-4 SMART
ZnF_C2H2 285 307 1.38e-3 SMART
ZnF_C2H2 313 335 4.17e-3 SMART
ZnF_C2H2 341 363 2.86e-1 SMART
ZnF_C2H2 369 391 5.14e-3 SMART
ZnF_C2H2 397 419 1.2e-3 SMART
ZnF_C2H2 425 447 4.47e-3 SMART
ZnF_C2H2 453 475 1.1e-2 SMART
ZnF_C2H2 481 503 1.45e-2 SMART
ZnF_C2H2 509 531 1.12e-3 SMART
ZnF_C2H2 537 559 1.5e-4 SMART
ZnF_C2H2 565 587 8.34e-3 SMART
ZnF_C2H2 593 615 1.12e-3 SMART
ZnF_C2H2 621 643 6.42e-4 SMART
ZnF_C2H2 649 671 6.23e-2 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000205534
AA Change: C371S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect probably damaging
Transcript: ENSMUST00000205715
AA Change: C371S

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000206136
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 50 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930022D16Rik T C 11: 109,308,737 (GRCm39) probably benign Het
Aatk T C 11: 119,903,101 (GRCm39) S375G probably benign Het
Abcg8 T C 17: 84,999,423 (GRCm39) M173T probably benign Het
B3galt2 A C 1: 143,522,495 (GRCm39) R210S probably benign Het
Bltp1 G T 3: 37,061,133 (GRCm39) probably null Het
Capn5 C T 7: 97,784,971 (GRCm39) A168T probably damaging Het
Cbx7 C T 15: 79,814,829 (GRCm39) G24D probably damaging Het
Ccdc7a A T 8: 129,788,099 (GRCm39) S77T probably benign Het
Cd200r2 T A 16: 44,729,832 (GRCm39) probably benign Het
Cdh11 T C 8: 103,406,377 (GRCm39) H32R probably benign Het
Chdh A T 14: 29,753,289 (GRCm39) N66I probably benign Het
Clca3a2 G A 3: 144,519,388 (GRCm39) Q263* probably null Het
Dcc T C 18: 71,942,161 (GRCm39) I319V probably benign Het
Depdc5 G T 5: 33,050,745 (GRCm39) M170I probably damaging Het
Dop1b T A 16: 93,607,117 (GRCm39) L2140Q probably benign Het
Frem3 G A 8: 81,341,763 (GRCm39) G1352E probably benign Het
Fsd1l T A 4: 53,694,742 (GRCm39) C389S probably damaging Het
Grin2c C T 11: 115,148,936 (GRCm39) A221T possibly damaging Het
Gstz1 C A 12: 87,210,575 (GRCm39) P153T probably damaging Het
Itgb2 T C 10: 77,378,237 (GRCm39) S22P possibly damaging Het
Krt87 G T 15: 101,336,312 (GRCm39) Q114K possibly damaging Het
Krtap5-4 A C 7: 141,857,647 (GRCm39) S106R unknown Het
Lats1 T C 10: 7,581,435 (GRCm39) V740A probably damaging Het
Mcm9 C A 10: 53,506,041 (GRCm39) G78C probably damaging Het
Mn1 G A 5: 111,569,413 (GRCm39) E1128K possibly damaging Het
Myo1f G A 17: 33,811,977 (GRCm39) R592H possibly damaging Het
Nfat5 G T 8: 108,094,146 (GRCm39) A277S probably damaging Het
Nfkbia T A 12: 55,537,327 (GRCm39) Y254F probably damaging Het
Nr3c2 A T 8: 77,635,843 (GRCm39) N315Y probably damaging Het
Otof T C 5: 30,562,560 (GRCm39) M258V probably benign Het
Panx3 C T 9: 37,572,767 (GRCm39) C261Y probably damaging Het
Pdia2 C A 17: 26,417,896 (GRCm39) G38W probably damaging Het
Psg19 G T 7: 18,527,971 (GRCm39) Y257* probably null Het
Ptpre A T 7: 135,280,054 (GRCm39) K586* probably null Het
Reps1 A G 10: 18,000,643 (GRCm39) R752G probably damaging Het
Rpgrip1 T A 14: 52,368,633 (GRCm39) D277E possibly damaging Het
Rpl21-ps6 A G 17: 56,222,671 (GRCm39) noncoding transcript Het
Serpinf2 T A 11: 75,327,333 (GRCm39) E198V possibly damaging Het
Sh3tc1 A G 5: 35,860,719 (GRCm39) L1046P probably damaging Het
Snw1 T C 12: 87,497,711 (GRCm39) E426G probably benign Het
Sord T A 2: 122,094,564 (GRCm39) N317K probably benign Het
Taar3 A T 10: 23,826,330 (GRCm39) D292V probably damaging Het
Tdrd3 C A 14: 87,709,618 (GRCm39) T94K probably damaging Het
Ttn C A 2: 76,687,165 (GRCm39) E736* probably null Het
Usp32 A G 11: 84,930,091 (GRCm39) V562A probably damaging Het
Vmn1r169 T G 7: 23,276,611 (GRCm39) M1R probably null Het
Vmn2r3 C T 3: 64,167,304 (GRCm39) C609Y probably damaging Het
Vmn2r69 T C 7: 85,055,739 (GRCm39) T800A probably benign Het
Vmn2r72 G A 7: 85,387,542 (GRCm39) T674I probably benign Het
Zfp160 T A 17: 21,241,088 (GRCm39) M52K possibly damaging Het
Other mutations in Zfp607a
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00164:Zfp607a APN 7 27,577,214 (GRCm39) missense possibly damaging 0.55
IGL01412:Zfp607a APN 7 27,578,109 (GRCm39) missense probably damaging 0.99
IGL03206:Zfp607a APN 7 27,577,248 (GRCm39) missense possibly damaging 0.52
R0071:Zfp607a UTSW 7 27,577,694 (GRCm39) missense probably damaging 0.96
R0304:Zfp607a UTSW 7 27,578,637 (GRCm39) missense possibly damaging 0.92
R0685:Zfp607a UTSW 7 27,577,901 (GRCm39) missense probably damaging 0.97
R0726:Zfp607a UTSW 7 27,578,574 (GRCm39) missense probably benign 0.00
R1201:Zfp607a UTSW 7 27,578,736 (GRCm39) missense probably damaging 1.00
R1304:Zfp607a UTSW 7 27,565,000 (GRCm39) missense probably benign 0.00
R1648:Zfp607a UTSW 7 27,578,493 (GRCm39) missense probably benign 0.02
R1732:Zfp607a UTSW 7 27,577,884 (GRCm39) missense probably damaging 1.00
R2194:Zfp607a UTSW 7 27,578,805 (GRCm39) missense possibly damaging 0.73
R3793:Zfp607a UTSW 7 27,578,331 (GRCm39) missense probably benign 0.01
R3808:Zfp607a UTSW 7 27,578,826 (GRCm39) missense probably benign 0.01
R4296:Zfp607a UTSW 7 27,565,073 (GRCm39) missense probably damaging 1.00
R4786:Zfp607a UTSW 7 27,578,838 (GRCm39) missense probably damaging 1.00
R4792:Zfp607a UTSW 7 27,578,078 (GRCm39) missense probably benign 0.23
R4915:Zfp607a UTSW 7 27,577,985 (GRCm39) missense probably benign 0.00
R4950:Zfp607a UTSW 7 27,578,176 (GRCm39) missense probably damaging 1.00
R5123:Zfp607a UTSW 7 27,578,523 (GRCm39) missense probably damaging 1.00
R5217:Zfp607a UTSW 7 27,577,269 (GRCm39) missense probably damaging 0.97
R5270:Zfp607a UTSW 7 27,577,730 (GRCm39) nonsense probably null
R5403:Zfp607a UTSW 7 27,578,744 (GRCm39) missense possibly damaging 0.54
R6010:Zfp607a UTSW 7 27,577,254 (GRCm39) nonsense probably null
R6224:Zfp607a UTSW 7 27,578,007 (GRCm39) missense probably damaging 1.00
R6939:Zfp607a UTSW 7 27,578,473 (GRCm39) nonsense probably null
R6953:Zfp607a UTSW 7 27,577,790 (GRCm39) missense possibly damaging 0.59
R7082:Zfp607a UTSW 7 27,578,183 (GRCm39) missense probably damaging 1.00
R7781:Zfp607a UTSW 7 27,565,000 (GRCm39) missense possibly damaging 0.90
R7909:Zfp607a UTSW 7 27,578,519 (GRCm39) missense probably damaging 1.00
R8191:Zfp607a UTSW 7 27,578,868 (GRCm39) missense possibly damaging 0.93
R8224:Zfp607a UTSW 7 27,577,536 (GRCm39) missense probably damaging 1.00
R8949:Zfp607a UTSW 7 27,577,944 (GRCm39) missense possibly damaging 0.56
R8962:Zfp607a UTSW 7 27,578,786 (GRCm39) missense possibly damaging 0.79
R9178:Zfp607a UTSW 7 27,577,382 (GRCm39) missense probably benign 0.00
R9802:Zfp607a UTSW 7 27,578,704 (GRCm39) missense probably damaging 1.00
Posted On 2013-06-28