Incidental Mutation 'R1365:Zfp979'
ID 155997
Institutional Source Beutler Lab
Gene Symbol Zfp979
Ensembl Gene ENSMUSG00000066000
Gene Name zinc finger protein 979
Synonyms Ssm1, 2610305D13Rik
MMRRC Submission 039430-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.190) question?
Stock # R1365 (G1)
Quality Score 206
Status Not validated
Chromosome 4
Chromosomal Location 147696394-147726970 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 147697681 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Asparagine at position 343 (Y343N)
Ref Sequence ENSEMBL: ENSMUSP00000101345 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000037565] [ENSMUST00000105720] [ENSMUST00000133006]
AlphaFold A2A799
Predicted Effect probably benign
Transcript: ENSMUST00000037565
AA Change: Y343N

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000038153
Gene: ENSMUSG00000066000
AA Change: Y343N

DomainStartEndE-ValueType
KRAB 28 88 2.06e-16 SMART
ZnF_C2H2 257 279 2.06e1 SMART
ZnF_C2H2 285 307 2.53e-2 SMART
ZnF_C2H2 313 335 1.95e-3 SMART
ZnF_C2H2 341 363 1.4e1 SMART
ZnF_C2H2 369 391 9.08e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000105720
AA Change: Y343N

PolyPhen 2 Score 0.001 (Sensitivity: 0.99; Specificity: 0.15)
SMART Domains Protein: ENSMUSP00000101345
Gene: ENSMUSG00000066000
AA Change: Y343N

DomainStartEndE-ValueType
KRAB 28 88 2.06e-16 SMART
ZnF_C2H2 257 279 2.06e1 SMART
ZnF_C2H2 285 307 2.53e-2 SMART
ZnF_C2H2 313 335 1.95e-3 SMART
ZnF_C2H2 341 363 1.4e1 SMART
ZnF_C2H2 369 391 9.08e-4 SMART
Predicted Effect probably benign
Transcript: ENSMUST00000133006
SMART Domains Protein: ENSMUSP00000114677
Gene: ENSMUSG00000066000

DomainStartEndE-ValueType
KRAB 28 88 2.06e-16 SMART
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.4%
  • 10x: 96.5%
  • 20x: 93.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Arhgef28 G A 13: 98,211,632 (GRCm39) T117M probably damaging Het
Asb15 T C 6: 24,567,269 (GRCm39) I530T possibly damaging Het
Brca1 T C 11: 101,392,822 (GRCm39) N1673S probably benign Het
Cd48 A T 1: 171,527,129 (GRCm39) Q185L probably damaging Het
Cog2 A T 8: 125,267,713 (GRCm39) K343I probably damaging Het
Dars2 G A 1: 160,872,564 (GRCm39) Q546* probably null Het
Dst A G 1: 34,227,275 (GRCm39) K1623E probably benign Het
Epn1 G A 7: 5,096,369 (GRCm39) R221Q probably benign Het
Gtf2b T C 3: 142,477,227 (GRCm39) I33T probably damaging Het
Hsf4 G T 8: 105,997,726 (GRCm39) R156L probably damaging Het
Itch A G 2: 155,054,951 (GRCm39) N752D probably benign Het
Kif28 G A 1: 179,567,552 (GRCm39) Q73* probably null Het
Mamdc4 T C 2: 25,456,036 (GRCm39) Y790C probably damaging Het
Med1 T C 11: 98,046,821 (GRCm39) probably benign Het
Mfsd13a C T 19: 46,354,943 (GRCm39) T40I probably benign Het
Nf1 A G 11: 79,438,711 (GRCm39) probably null Het
Oxct2b G A 4: 123,011,162 (GRCm39) V361I probably benign Het
Pid1 T C 1: 84,015,862 (GRCm39) M168V probably damaging Het
Plk1 A G 7: 121,767,852 (GRCm39) D419G probably damaging Het
Rasl10b G A 11: 83,308,665 (GRCm39) probably null Het
Rps24 A G 14: 24,541,830 (GRCm39) T6A probably damaging Het
Sem1 T C 6: 6,560,501 (GRCm39) D26G possibly damaging Het
Sin3a C T 9: 57,032,487 (GRCm39) R1141* probably null Het
Slf1 C T 13: 77,274,490 (GRCm39) A68T probably damaging Het
Trmo A G 4: 46,380,278 (GRCm39) S364P probably damaging Het
Uchl3 A G 14: 101,891,528 (GRCm39) E10G probably damaging Het
Usp14 C T 18: 10,000,490 (GRCm39) probably null Het
Vmn1r203 T A 13: 22,708,756 (GRCm39) M179K probably benign Het
Vps13a A G 19: 16,596,810 (GRCm39) Y3103H probably damaging Het
Zfp804a T C 2: 82,087,590 (GRCm39) L473P probably benign Het
Other mutations in Zfp979
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL01285:Zfp979 APN 4 147,699,853 (GRCm39) missense probably damaging 0.98
IGL01865:Zfp979 APN 4 147,699,774 (GRCm39) missense probably benign 0.03
IGL02336:Zfp979 APN 4 147,699,808 (GRCm39) missense probably damaging 1.00
R0336:Zfp979 UTSW 4 147,697,592 (GRCm39) missense possibly damaging 0.86
R1440:Zfp979 UTSW 4 147,698,493 (GRCm39) missense possibly damaging 0.96
R1714:Zfp979 UTSW 4 147,698,442 (GRCm39) missense probably damaging 1.00
R1796:Zfp979 UTSW 4 147,697,740 (GRCm39) missense probably damaging 0.99
R2155:Zfp979 UTSW 4 147,697,915 (GRCm39) missense possibly damaging 0.86
R3735:Zfp979 UTSW 4 147,697,939 (GRCm39) missense possibly damaging 0.93
R3963:Zfp979 UTSW 4 147,697,588 (GRCm39) missense probably benign 0.34
R3972:Zfp979 UTSW 4 147,702,876 (GRCm39) nonsense probably null
R4471:Zfp979 UTSW 4 147,697,913 (GRCm39) nonsense probably null
R4983:Zfp979 UTSW 4 147,698,371 (GRCm39) missense possibly damaging 0.94
R5310:Zfp979 UTSW 4 147,698,375 (GRCm39) missense possibly damaging 0.95
R5805:Zfp979 UTSW 4 147,698,067 (GRCm39) missense probably damaging 0.99
R5861:Zfp979 UTSW 4 147,697,966 (GRCm39) nonsense probably null
R6598:Zfp979 UTSW 4 147,698,223 (GRCm39) missense probably damaging 0.99
R6599:Zfp979 UTSW 4 147,698,083 (GRCm39) missense probably benign 0.40
R6925:Zfp979 UTSW 4 147,697,999 (GRCm39) missense possibly damaging 0.86
R7684:Zfp979 UTSW 4 147,697,799 (GRCm39) missense probably damaging 0.99
R7801:Zfp979 UTSW 4 147,698,435 (GRCm39) missense probably damaging 0.96
R8035:Zfp979 UTSW 4 147,697,763 (GRCm39) missense probably damaging 1.00
R8086:Zfp979 UTSW 4 147,698,004 (GRCm39) missense probably damaging 0.99
R8244:Zfp979 UTSW 4 147,697,933 (GRCm39) missense possibly damaging 0.92
R8369:Zfp979 UTSW 4 147,697,548 (GRCm39) missense possibly damaging 0.73
R8880:Zfp979 UTSW 4 147,697,836 (GRCm39) missense probably benign 0.00
R8887:Zfp979 UTSW 4 147,698,219 (GRCm39) missense probably damaging 0.96
R8988:Zfp979 UTSW 4 147,697,984 (GRCm39) missense probably benign
R9016:Zfp979 UTSW 4 147,697,504 (GRCm39) missense possibly damaging 0.68
R9356:Zfp979 UTSW 4 147,698,358 (GRCm39) missense probably damaging 0.96
Predicted Primers
Posted On 2014-02-11