Incidental Mutation 'IGL01150:Zfp648'
ID 50355
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp648
Ensembl Gene ENSMUSG00000066797
Gene Name zinc finger protein 648
Synonyms Gm10178, LOC207678
Accession Numbers
Essential gene? Probably non essential (E-score: 0.091) question?
Stock # IGL01150
Quality Score
Status
Chromosome 1
Chromosomal Location 154076933-154081435 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 154081110 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Leucine at position 423 (H423L)
Ref Sequence ENSEMBL: ENSMUSP00000083370 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000086195]
AlphaFold D3Z0W3
Predicted Effect probably damaging
Transcript: ENSMUST00000086195
AA Change: H423L

PolyPhen 2 Score 1.000 (Sensitivity: 0.00; Specificity: 1.00)
SMART Domains Protein: ENSMUSP00000083370
Gene: ENSMUSG00000066797
AA Change: H423L

DomainStartEndE-ValueType
ZnF_C2H2 236 258 1.82e-3 SMART
ZnF_C2H2 264 286 1.28e-3 SMART
ZnF_C2H2 292 315 1.2e-3 SMART
ZnF_C2H2 321 343 1.95e-3 SMART
ZnF_C2H2 349 371 8.94e-3 SMART
ZnF_C2H2 377 399 8.34e-3 SMART
ZnF_C2H2 405 427 4.54e-4 SMART
ZnF_C2H2 433 455 4.47e-3 SMART
ZnF_C2H2 461 483 5.81e-2 SMART
ZnF_C2H2 489 511 1.2e-3 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 40 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Abcb1a A G 5: 8,752,550 (GRCm39) D507G possibly damaging Het
Actl6a A G 3: 32,766,313 (GRCm39) I60V probably benign Het
Adra2c T C 5: 35,438,485 (GRCm39) F419S probably damaging Het
Afap1l2 T C 19: 56,918,618 (GRCm39) Y105C probably damaging Het
Arid4b C T 13: 14,369,959 (GRCm39) Q1152* probably null Het
Arsj A G 3: 126,232,433 (GRCm39) D393G probably benign Het
Avp T C 2: 130,422,593 (GRCm39) probably benign Het
Cacna2d3 C T 14: 28,905,598 (GRCm39) V390I possibly damaging Het
Ccdc25 T A 14: 66,097,651 (GRCm39) M195K possibly damaging Het
Cdhr2 T A 13: 54,878,931 (GRCm39) S979T probably benign Het
Cog2 T C 8: 125,269,630 (GRCm39) F390S possibly damaging Het
Dennd5b A G 6: 148,969,583 (GRCm39) V290A probably benign Het
Ebf1 T C 11: 44,759,927 (GRCm39) L188P probably damaging Het
Galt T C 4: 41,757,786 (GRCm39) probably benign Het
Gm12830 C T 4: 114,702,261 (GRCm39) T141I unknown Het
Herc2 T A 7: 55,830,881 (GRCm39) W2965R probably damaging Het
Hrg A G 16: 22,777,909 (GRCm39) probably null Het
Ighv8-5 T C 12: 115,031,194 (GRCm39) Y115C probably damaging Het
Igkv12-89 A G 6: 68,812,127 (GRCm39) V14A probably benign Het
Nav2 A C 7: 49,102,269 (GRCm39) T295P probably benign Het
Niban1 T C 1: 151,593,472 (GRCm39) V719A probably benign Het
Nrg1 G A 8: 32,407,903 (GRCm39) T110I probably damaging Het
Or4c31 T C 2: 88,292,419 (GRCm39) V264A possibly damaging Het
Or51h1 A C 7: 102,308,699 (GRCm39) K224Q probably benign Het
Or7g29 A T 9: 19,286,535 (GRCm39) I214N probably damaging Het
Pclo T C 5: 14,726,926 (GRCm39) probably benign Het
Polg2 T C 11: 106,668,258 (GRCm39) probably null Het
Ptges G T 2: 30,782,720 (GRCm39) R111S probably damaging Het
Rbbp4 T C 4: 129,216,668 (GRCm39) probably benign Het
Rundc3a T C 11: 102,284,602 (GRCm39) V34A probably benign Het
Scn3a C A 2: 65,327,709 (GRCm39) probably null Het
Sec14l3 T C 11: 4,026,238 (GRCm39) probably benign Het
Strip1 C T 3: 107,534,047 (GRCm39) probably null Het
Svep1 T A 4: 58,070,302 (GRCm39) I2495F probably benign Het
Syne1 A G 10: 5,393,154 (GRCm39) S71P probably damaging Het
Tedc1 C T 12: 113,126,808 (GRCm39) R357* probably null Het
Tmem161b C T 13: 84,440,526 (GRCm39) R133* probably null Het
Tnnc2 A T 2: 164,619,753 (GRCm39) I71N probably damaging Het
Vps13d T C 4: 144,875,845 (GRCm39) N1554S probably benign Het
Wfdc3 A T 2: 164,574,123 (GRCm39) probably benign Het
Other mutations in Zfp648
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00585:Zfp648 APN 1 154,079,935 (GRCm39) missense possibly damaging 0.88
IGL01557:Zfp648 APN 1 154,080,426 (GRCm39) missense probably benign
IGL01757:Zfp648 APN 1 154,080,671 (GRCm39) missense probably damaging 0.98
IGL02247:Zfp648 APN 1 154,079,923 (GRCm39) missense probably benign 0.01
PIT4519001:Zfp648 UTSW 1 154,080,687 (GRCm39) missense probably damaging 0.98
R0001:Zfp648 UTSW 1 154,081,032 (GRCm39) missense probably damaging 1.00
R0256:Zfp648 UTSW 1 154,081,414 (GRCm39) missense probably benign 0.08
R0266:Zfp648 UTSW 1 154,080,632 (GRCm39) missense probably damaging 1.00
R0371:Zfp648 UTSW 1 154,080,413 (GRCm39) missense possibly damaging 0.66
R1498:Zfp648 UTSW 1 154,081,119 (GRCm39) missense probably damaging 1.00
R1562:Zfp648 UTSW 1 154,080,138 (GRCm39) missense probably benign
R1687:Zfp648 UTSW 1 154,079,988 (GRCm39) missense probably benign 0.15
R2128:Zfp648 UTSW 1 154,080,353 (GRCm39) missense probably benign
R2427:Zfp648 UTSW 1 154,080,819 (GRCm39) missense probably damaging 1.00
R2567:Zfp648 UTSW 1 154,080,695 (GRCm39) missense probably damaging 0.98
R2844:Zfp648 UTSW 1 154,080,881 (GRCm39) nonsense probably null
R3711:Zfp648 UTSW 1 154,080,304 (GRCm39) missense probably benign 0.30
R4491:Zfp648 UTSW 1 154,080,873 (GRCm39) missense probably damaging 1.00
R4693:Zfp648 UTSW 1 154,080,152 (GRCm39) missense probably benign 0.01
R5666:Zfp648 UTSW 1 154,079,963 (GRCm39) missense probably benign 0.00
R5670:Zfp648 UTSW 1 154,079,963 (GRCm39) missense probably benign 0.00
R7432:Zfp648 UTSW 1 154,080,783 (GRCm39) missense possibly damaging 0.84
R8069:Zfp648 UTSW 1 154,079,862 (GRCm39) missense probably benign 0.34
R8137:Zfp648 UTSW 1 154,081,110 (GRCm39) missense probably damaging 1.00
R8282:Zfp648 UTSW 1 154,080,535 (GRCm39) missense probably benign 0.25
R9023:Zfp648 UTSW 1 154,080,914 (GRCm39) missense probably damaging 0.98
R9489:Zfp648 UTSW 1 154,080,110 (GRCm39) missense probably benign 0.17
R9520:Zfp648 UTSW 1 154,081,221 (GRCm39) missense probably benign
R9605:Zfp648 UTSW 1 154,080,110 (GRCm39) missense probably benign 0.17
Z1088:Zfp648 UTSW 1 154,080,266 (GRCm39) missense probably benign 0.00
Posted On 2013-06-21