Incidental Mutation 'IGL01449:Zfp697'
ID 84564
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp697
Ensembl Gene ENSMUSG00000050064
Gene Name zinc finger protein 697
Synonyms
Accession Numbers
Essential gene? Probably non essential (E-score: 0.131) question?
Stock # IGL01449
Quality Score
Status
Chromosome 3
Chromosomal Location 98289278-98508893 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 98334846 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Cysteine to Arginine at position 204 (C204R)
Ref Sequence ENSEMBL: ENSMUSP00000136417 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000056096] [ENSMUST00000178372]
AlphaFold no structure available at present
Predicted Effect probably damaging
Transcript: ENSMUST00000056096
AA Change: C204R

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000056979
Gene: ENSMUSG00000050064
AA Change: C204R

DomainStartEndE-ValueType
low complexity region 83 96 N/A INTRINSIC
low complexity region 124 135 N/A INTRINSIC
low complexity region 157 168 N/A INTRINSIC
ZnF_C2H2 202 224 3.72e0 SMART
low complexity region 245 268 N/A INTRINSIC
ZnF_C2H2 280 302 3.63e-3 SMART
ZnF_C2H2 308 330 1.76e-1 SMART
ZnF_C2H2 336 358 6.78e-3 SMART
ZnF_C2H2 377 399 2.57e-3 SMART
ZnF_C2H2 405 427 2.09e-3 SMART
ZnF_C2H2 433 455 7.26e-3 SMART
ZnF_C2H2 461 483 6.42e-4 SMART
ZnF_C2H2 489 511 2.91e-2 SMART
ZnF_C2H2 517 539 9.73e-4 SMART
ZnF_C2H2 545 567 1.43e-1 SMART
Predicted Effect probably damaging
Transcript: ENSMUST00000178372
AA Change: C204R

PolyPhen 2 Score 0.985 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000136417
Gene: ENSMUSG00000050064
AA Change: C204R

DomainStartEndE-ValueType
low complexity region 83 96 N/A INTRINSIC
low complexity region 124 135 N/A INTRINSIC
low complexity region 157 168 N/A INTRINSIC
ZnF_C2H2 202 224 3.72e0 SMART
low complexity region 245 268 N/A INTRINSIC
ZnF_C2H2 280 302 3.63e-3 SMART
ZnF_C2H2 308 330 1.76e-1 SMART
ZnF_C2H2 336 358 6.78e-3 SMART
ZnF_C2H2 377 399 2.57e-3 SMART
ZnF_C2H2 405 427 2.09e-3 SMART
ZnF_C2H2 433 455 7.26e-3 SMART
ZnF_C2H2 461 483 6.42e-4 SMART
ZnF_C2H2 489 511 2.91e-2 SMART
ZnF_C2H2 517 539 9.73e-4 SMART
ZnF_C2H2 545 567 1.43e-1 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000196741
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 41 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
1700030K09Rik A T 8: 73,198,693 (GRCm39) L33F probably benign Het
Actr8 T C 14: 29,712,927 (GRCm39) probably null Het
Aldh16a1 C A 7: 44,791,391 (GRCm39) A105S probably damaging Het
Angpt2 T C 8: 18,760,641 (GRCm39) T154A probably benign Het
BC051665 A G 13: 60,930,518 (GRCm39) V278A probably damaging Het
Cap1 T C 4: 122,753,980 (GRCm39) T458A probably damaging Het
Clcn3 A T 8: 61,387,632 (GRCm39) S179T probably damaging Het
Cyp2a22 T C 7: 26,632,978 (GRCm39) D408G probably benign Het
Fam217b T A 2: 178,062,943 (GRCm39) S302R probably damaging Het
Fcho2 A T 13: 98,926,315 (GRCm39) D89E probably benign Het
Fnip1 C T 11: 54,390,334 (GRCm39) R434C probably damaging Het
Gga3 G A 11: 115,479,928 (GRCm39) T261M probably damaging Het
Gm21985 T C 2: 112,169,741 (GRCm39) F292L probably damaging Het
Gm43638 A T 5: 87,634,074 (GRCm39) S178T possibly damaging Het
Igkv10-95 G A 6: 68,657,748 (GRCm39) G68E probably damaging Het
Katnip T A 7: 125,469,857 (GRCm39) V1442D probably damaging Het
Lpcat2 G A 8: 93,597,775 (GRCm39) R180Q possibly damaging Het
Muc6 C T 7: 141,218,527 (GRCm39) A1984T possibly damaging Het
Npy4r T A 14: 33,868,322 (GRCm39) Y322F probably damaging Het
Nwd2 T A 5: 63,962,937 (GRCm39) H840Q probably damaging Het
Or7g26 G A 9: 19,230,529 (GRCm39) G233D probably damaging Het
Osbpl2 G T 2: 179,786,987 (GRCm39) probably benign Het
Pclo T A 5: 14,728,530 (GRCm39) probably benign Het
Pold4 T C 19: 4,282,921 (GRCm39) probably benign Het
Ppp1r16a A G 15: 76,578,494 (GRCm39) probably benign Het
Pprc1 C T 19: 46,053,671 (GRCm39) probably benign Het
Prkcg A G 7: 3,368,135 (GRCm39) D343G probably benign Het
Scaf11 A C 15: 96,317,007 (GRCm39) S852R probably benign Het
Slc31a2 C T 4: 62,210,933 (GRCm39) T22I probably damaging Het
Sox30 T A 11: 45,872,169 (GRCm39) D341E probably damaging Het
Tle4 A G 19: 14,442,704 (GRCm39) S339P probably benign Het
Tsg101 A T 7: 46,558,673 (GRCm39) Y78N probably damaging Het
Ttc1 T A 11: 43,629,630 (GRCm39) S179C probably damaging Het
Txnrd3 T A 6: 89,631,129 (GRCm39) S142T probably benign Het
Ubr4 C A 4: 139,140,047 (GRCm39) A1210E probably damaging Het
Uroc1 C A 6: 90,315,635 (GRCm39) P172Q probably damaging Het
Usp12 T C 5: 146,691,250 (GRCm39) D168G probably benign Het
Vmn1r32 T A 6: 66,529,916 (GRCm39) M287L probably benign Het
Vwa8 C T 14: 79,420,428 (GRCm39) Q1710* probably null Het
Wdfy4 T A 14: 32,825,994 (GRCm39) Q1219L probably damaging Het
Zbtb17 A G 4: 141,190,616 (GRCm39) T145A probably benign Het
Other mutations in Zfp697
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02313:Zfp697 APN 3 98,332,766 (GRCm39) missense probably benign 0.01
IGL03055:Zfp697 UTSW 3 98,332,810 (GRCm39) missense possibly damaging 0.51
R0724:Zfp697 UTSW 3 98,335,482 (GRCm39) missense probably damaging 1.00
R2165:Zfp697 UTSW 3 98,335,330 (GRCm39) missense unknown
R2971:Zfp697 UTSW 3 98,335,617 (GRCm39) missense probably damaging 1.00
R5749:Zfp697 UTSW 3 98,332,780 (GRCm39) missense probably benign
R5954:Zfp697 UTSW 3 98,335,909 (GRCm39) missense probably damaging 0.99
R6253:Zfp697 UTSW 3 98,334,855 (GRCm39) missense possibly damaging 0.95
R8849:Zfp697 UTSW 3 98,334,943 (GRCm39) missense probably benign 0.38
R9300:Zfp697 UTSW 3 98,334,979 (GRCm39) missense possibly damaging 0.46
R9620:Zfp697 UTSW 3 98,335,182 (GRCm39) missense probably damaging 0.99
Posted On 2013-11-11