Incidental Mutation 'IGL00595:Zfp944'
ID 5772
Institutional Source Australian Phenomics Network (link to record)
Gene Symbol Zfp944
Ensembl Gene ENSMUSG00000033972
Gene Name zinc finger protein 944
Synonyms 6330416L07Rik
Accession Numbers
Essential gene? Probably non essential (E-score: 0.223) question?
Stock # IGL00595
Quality Score
Status
Chromosome 17
Chromosomal Location 22556970-22580381 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 22558186 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 354 (S354G)
Ref Sequence ENSEMBL: ENSMUSP00000111197 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115535]
AlphaFold E9PUS4
Predicted Effect probably benign
Transcript: ENSMUST00000115535
AA Change: S354G

PolyPhen 2 Score 0.101 (Sensitivity: 0.93; Specificity: 0.86)
SMART Domains Protein: ENSMUSP00000111197
Gene: ENSMUSG00000033972
AA Change: S354G

DomainStartEndE-ValueType
KRAB 13 76 2.08e-21 SMART
ZnF_C2H2 183 205 1.01e-1 SMART
ZnF_C2H2 211 233 1.07e0 SMART
ZnF_C2H2 239 261 1.95e-3 SMART
ZnF_C2H2 267 289 1.22e-4 SMART
ZnF_C2H2 295 317 2.24e-3 SMART
ZnF_C2H2 323 345 1.82e-3 SMART
ZnF_C2H2 351 373 5.99e-4 SMART
ZnF_C2H2 379 401 4.79e-3 SMART
ZnF_C2H2 407 429 2.99e-4 SMART
ZnF_C2H2 435 457 4.17e-3 SMART
ZnF_C2H2 463 485 1.36e-2 SMART
Coding Region Coverage
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
2310057J18Rik G A 10: 28,849,954 (GRCm39) R161* probably null Het
Adam20 T A 8: 41,249,084 (GRCm39) F398Y probably benign Het
Ano1 T A 7: 144,192,250 (GRCm39) I374F probably damaging Het
Apol10a A T 15: 77,369,135 (GRCm39) N45Y probably null Het
Asnsd1 A G 1: 53,386,647 (GRCm39) S327P probably damaging Het
Ccdc83 T A 7: 89,893,252 (GRCm39) K168N probably damaging Het
Chmp1b2 A G X: 106,831,450 (GRCm39) S189P probably damaging Het
Dpysl4 G T 7: 138,676,092 (GRCm39) V274F probably damaging Het
Fxr2 T G 11: 69,540,018 (GRCm39) S292A probably benign Het
Gm15130 T A 2: 110,969,322 (GRCm39) D132V unknown Het
Gpr161 A G 1: 165,146,372 (GRCm39) H436R probably benign Het
Jaml C T 9: 45,012,287 (GRCm39) probably benign Het
Kcnc2 A T 10: 112,297,893 (GRCm39) S606C probably damaging Het
Kcnc2 G T 10: 112,297,892 (GRCm39) E605D probably benign Het
Kcnrg T C 14: 61,845,359 (GRCm39) I133T probably damaging Het
Kdm7a A G 6: 39,121,444 (GRCm39) I837T probably benign Het
Lactb2 A G 1: 13,700,350 (GRCm39) L227S probably benign Het
Lats1 T G 10: 7,578,069 (GRCm39) S398A probably benign Het
Llgl2 T A 11: 115,725,710 (GRCm39) D19E probably benign Het
Nup107 A T 10: 117,609,257 (GRCm39) C365* probably null Het
Nup107 T C 10: 117,609,273 (GRCm39) probably null Het
Plekhf2 T C 4: 10,991,022 (GRCm39) K107E probably damaging Het
Rnf139 A T 15: 58,770,391 (GRCm39) I139F possibly damaging Het
Rsbn1 A G 3: 103,836,006 (GRCm39) N348S probably benign Het
Rttn A T 18: 88,992,464 (GRCm39) Q136H probably benign Het
Syne2 C T 12: 75,972,420 (GRCm39) T1052I possibly damaging Het
Tom1l1 A T 11: 90,565,566 (GRCm39) L101Q probably damaging Het
Tubal3 A G 13: 3,983,015 (GRCm39) N265S probably damaging Het
Zfp141 T C 7: 42,126,079 (GRCm39) N131S probably benign Het
Zfp961 G A 8: 72,722,272 (GRCm39) A262T probably damaging Het
Other mutations in Zfp944
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00917:Zfp944 APN 17 22,558,765 (GRCm39) missense probably benign 0.00
IGL01093:Zfp944 APN 17 22,562,615 (GRCm39) splice site probably benign
IGL02113:Zfp944 APN 17 22,558,047 (GRCm39) missense possibly damaging 0.88
IGL02694:Zfp944 APN 17 22,558,899 (GRCm39) missense probably benign 0.05
IGL03135:Zfp944 APN 17 22,558,737 (GRCm39) missense probably benign 0.00
IGL03172:Zfp944 APN 17 22,559,018 (GRCm39) missense probably damaging 0.98
R0121:Zfp944 UTSW 17 22,558,249 (GRCm39) missense possibly damaging 0.69
R0336:Zfp944 UTSW 17 22,558,009 (GRCm39) missense probably damaging 1.00
R0755:Zfp944 UTSW 17 22,558,889 (GRCm39) missense possibly damaging 0.63
R1536:Zfp944 UTSW 17 22,558,697 (GRCm39) nonsense probably null
R1708:Zfp944 UTSW 17 22,558,026 (GRCm39) missense probably damaging 0.98
R1886:Zfp944 UTSW 17 22,558,960 (GRCm39) missense probably benign 0.04
R1928:Zfp944 UTSW 17 22,560,065 (GRCm39) missense probably damaging 0.96
R1950:Zfp944 UTSW 17 22,558,681 (GRCm39) missense probably benign 0.16
R2075:Zfp944 UTSW 17 22,558,178 (GRCm39) nonsense probably null
R2101:Zfp944 UTSW 17 22,558,809 (GRCm39) missense probably benign 0.41
R2433:Zfp944 UTSW 17 22,558,193 (GRCm39) nonsense probably null
R4698:Zfp944 UTSW 17 22,558,180 (GRCm39) missense probably damaging 1.00
R4986:Zfp944 UTSW 17 22,558,211 (GRCm39) missense probably damaging 1.00
R6451:Zfp944 UTSW 17 22,557,846 (GRCm39) missense probably benign 0.40
R6566:Zfp944 UTSW 17 22,558,726 (GRCm39) missense possibly damaging 0.96
R6752:Zfp944 UTSW 17 22,558,500 (GRCm39) missense probably benign 0.01
R7064:Zfp944 UTSW 17 22,558,560 (GRCm39) missense probably damaging 1.00
R8193:Zfp944 UTSW 17 22,558,861 (GRCm39) nonsense probably null
R8323:Zfp944 UTSW 17 22,558,235 (GRCm39) missense probably benign
R8328:Zfp944 UTSW 17 22,558,705 (GRCm39) nonsense probably null
R8902:Zfp944 UTSW 17 22,558,761 (GRCm39) missense probably benign 0.41
R8915:Zfp944 UTSW 17 22,558,507 (GRCm39) missense probably benign 0.05
R9130:Zfp944 UTSW 17 22,560,031 (GRCm39) missense probably damaging 1.00
R9248:Zfp944 UTSW 17 22,562,619 (GRCm39) critical splice donor site probably null
Posted On 2012-04-20