Incidental Mutation 'IGL02677:Zc2hc1c'
ID 303178
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zc2hc1c
Ensembl Gene ENSMUSG00000045064
Gene Name zinc finger, C2HC-type containing 1C
Synonyms 2810002I04Rik, Fam164c
Accession Numbers
Essential gene? Probably non essential (E-score: 0.116) question?
Stock # IGL02677
Quality Score
Status
Chromosome 12
Chromosomal Location 85321060-85346132 bp(+) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to C at 85336850 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Aspartic acid to Alanine at position 169 (D169A)
Ref Sequence ENSEMBL: ENSMUSP00000051664 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000059341] [ENSMUST00000121930]
AlphaFold Q8CCG1
Predicted Effect probably benign
Transcript: ENSMUST00000059341
AA Change: D169A

PolyPhen 2 Score 0.312 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000051664
Gene: ENSMUSG00000045064
AA Change: D169A

DomainStartEndE-ValueType
low complexity region 93 106 N/A INTRINSIC
coiled coil region 207 254 N/A INTRINSIC
Pfam:zf-C2HC_2 378 402 3.6e-10 PFAM
low complexity region 433 444 N/A INTRINSIC
Pfam:zf-C2HC_2 489 513 3.1e-11 PFAM
Predicted Effect probably benign
Transcript: ENSMUST00000121930
SMART Domains Protein: ENSMUSP00000112609
Gene: ENSMUSG00000008822

DomainStartEndE-ValueType
Pfam:Acylphosphatase 64 156 4.5e-25 PFAM
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 48 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
4931406B18Rik G T 7: 43,150,519 (GRCm39) Y84* probably null Het
Adam5 A G 8: 25,302,395 (GRCm39) probably benign Het
Aipl1 T C 11: 71,920,222 (GRCm39) E282G possibly damaging Het
Akp3 A G 1: 87,052,994 (GRCm39) D61G probably damaging Het
Anpep A G 7: 79,488,478 (GRCm39) S451P probably damaging Het
Csnka2ip A G 16: 64,298,675 (GRCm39) L119P probably damaging Het
Ddx19a T C 8: 111,716,241 (GRCm39) E53G probably benign Het
Ddx50 C T 10: 62,452,072 (GRCm39) R116Q unknown Het
Ddx60 A T 8: 62,441,166 (GRCm39) E1078D probably damaging Het
Dpy19l1 T C 9: 24,396,368 (GRCm39) D116G probably damaging Het
Dsg4 A G 18: 20,597,933 (GRCm39) T668A possibly damaging Het
Dspp A G 5: 104,323,843 (GRCm39) T329A possibly damaging Het
Eftud2 T C 11: 102,737,440 (GRCm39) T554A probably damaging Het
Enpp1 T C 10: 24,555,083 (GRCm39) probably benign Het
Ext2 A T 2: 93,537,590 (GRCm39) F599I probably damaging Het
Fahd1 A T 17: 25,068,504 (GRCm39) I191N probably damaging Het
Fcrl2 A T 3: 87,166,694 (GRCm39) S100T probably benign Het
Fras1 T A 5: 96,692,883 (GRCm39) C181S probably damaging Het
Garre1 T A 7: 33,941,834 (GRCm39) probably benign Het
Gcnt4 A G 13: 97,083,741 (GRCm39) I346V probably benign Het
Gfra1 G A 19: 58,441,787 (GRCm39) T48I probably damaging Het
Kcnma1 A G 14: 23,513,224 (GRCm39) Y392H probably damaging Het
Klc2 T C 19: 5,161,696 (GRCm39) Y298C probably damaging Het
Lamb3 G A 1: 193,021,830 (GRCm39) V1011I probably benign Het
Ldb1 T C 19: 46,024,594 (GRCm39) probably benign Het
Mcph1 A G 8: 18,675,609 (GRCm39) K11E probably damaging Het
Myc A G 15: 61,861,513 (GRCm39) H374R probably damaging Het
Myom1 A G 17: 71,391,344 (GRCm39) Y853C probably damaging Het
Or4k38 A T 2: 111,166,147 (GRCm39) I92N probably damaging Het
Pakap C T 4: 57,856,263 (GRCm39) P572S probably benign Het
Pclo A G 5: 14,726,943 (GRCm39) probably benign Het
Pde3a G A 6: 141,350,898 (GRCm39) probably benign Het
Per1 T C 11: 68,997,486 (GRCm39) V887A probably benign Het
Prokr1 G A 6: 87,565,350 (GRCm39) probably benign Het
Rb1cc1 A G 1: 6,319,643 (GRCm39) I1021V probably benign Het
Ryr1 T C 7: 28,810,033 (GRCm39) E344G probably benign Het
Sec24c A T 14: 20,739,710 (GRCm39) D529V probably damaging Het
Slc1a6 T C 10: 78,624,898 (GRCm39) V101A probably damaging Het
Srrm1 G A 4: 135,052,415 (GRCm39) P658L unknown Het
Tap2 G A 17: 34,431,021 (GRCm39) V374M probably benign Het
Tex15 T A 8: 34,061,108 (GRCm39) D179E probably benign Het
Tmem8b T C 4: 43,686,092 (GRCm39) L241P probably damaging Het
Tmprss11g T C 5: 86,640,149 (GRCm39) D160G probably benign Het
Trim30a C T 7: 104,085,120 (GRCm39) C30Y probably damaging Het
Ttn A G 2: 76,601,840 (GRCm39) probably benign Het
Ush2a A G 1: 188,466,882 (GRCm39) R2849G probably damaging Het
Usp5 A G 6: 124,796,389 (GRCm39) V570A probably damaging Het
Vipr1 T C 9: 121,489,349 (GRCm39) probably benign Het
Other mutations in Zc2hc1c
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01763:Zc2hc1c APN 12 85,336,450 (GRCm39) missense probably benign 0.03
R1053:Zc2hc1c UTSW 12 85,343,330 (GRCm39) missense probably damaging 1.00
R1696:Zc2hc1c UTSW 12 85,337,555 (GRCm39) missense possibly damaging 0.86
R1724:Zc2hc1c UTSW 12 85,336,586 (GRCm39) missense probably benign 0.00
R1905:Zc2hc1c UTSW 12 85,337,288 (GRCm39) missense probably benign 0.03
R1996:Zc2hc1c UTSW 12 85,343,434 (GRCm39) missense probably benign 0.31
R4463:Zc2hc1c UTSW 12 85,337,071 (GRCm39) missense probably damaging 0.97
R4834:Zc2hc1c UTSW 12 85,336,982 (GRCm39) missense probably damaging 1.00
R5070:Zc2hc1c UTSW 12 85,337,288 (GRCm39) missense probably benign 0.03
R5943:Zc2hc1c UTSW 12 85,336,483 (GRCm39) missense probably damaging 1.00
R6184:Zc2hc1c UTSW 12 85,343,218 (GRCm39) missense probably damaging 0.96
R6701:Zc2hc1c UTSW 12 85,336,446 (GRCm39) splice site probably null
R6704:Zc2hc1c UTSW 12 85,337,258 (GRCm39) missense possibly damaging 0.84
R6719:Zc2hc1c UTSW 12 85,337,446 (GRCm39) missense probably damaging 1.00
R7665:Zc2hc1c UTSW 12 85,343,336 (GRCm39) missense possibly damaging 0.69
R8125:Zc2hc1c UTSW 12 85,343,386 (GRCm39) missense probably damaging 1.00
R8154:Zc2hc1c UTSW 12 85,336,946 (GRCm39) missense probably benign 0.00
R8268:Zc2hc1c UTSW 12 85,336,595 (GRCm39) missense probably benign 0.02
R8356:Zc2hc1c UTSW 12 85,337,471 (GRCm39) missense probably damaging 0.97
R8678:Zc2hc1c UTSW 12 85,337,084 (GRCm39) missense probably benign 0.07
R8875:Zc2hc1c UTSW 12 85,336,549 (GRCm39) missense possibly damaging 0.87
R9056:Zc2hc1c UTSW 12 85,343,230 (GRCm39) small deletion probably benign
Posted On 2015-04-16