Incidental Mutation 'IGL03172:Zfp944'
ID 411895
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 # IGL03172
Quality Score
Status
Chromosome 17
Chromosomal Location 22556970-22580381 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to T at 22559018 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Histidine to Glutamine at position 76 (H76Q)
Ref Sequence ENSEMBL: ENSMUSP00000111197 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115535]
AlphaFold E9PUS4
Predicted Effect probably damaging
Transcript: ENSMUST00000115535
AA Change: H76Q

PolyPhen 2 Score 0.984 (Sensitivity: 0.74; Specificity: 0.96)
SMART Domains Protein: ENSMUSP00000111197
Gene: ENSMUSG00000033972
AA Change: H76Q

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: 44 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
9930111J21Rik1 T C 11: 48,839,003 (GRCm39) H528R probably damaging Het
A530053G22Rik A T 6: 60,379,047 (GRCm39) noncoding transcript Het
Aagab A G 9: 63,542,676 (GRCm39) probably benign Het
Aknad1 A T 3: 108,688,519 (GRCm39) I616F possibly damaging Het
Ap2a1 A C 7: 44,553,479 (GRCm39) D629E probably benign Het
Apc2 C A 10: 80,149,220 (GRCm39) Q1425K probably damaging Het
Asf1b A C 8: 84,694,542 (GRCm39) H102P probably benign Het
Celf6 C T 9: 59,489,565 (GRCm39) A90V probably damaging Het
Chrna2 A T 14: 66,379,688 (GRCm39) Q9L probably benign Het
Csnk1g3 A G 18: 54,086,356 (GRCm39) I420M possibly damaging Het
Eml3 T C 19: 8,916,543 (GRCm39) probably benign Het
Epn3 T C 11: 94,382,456 (GRCm39) N508S possibly damaging Het
Fam120a T C 13: 49,063,812 (GRCm39) Y608C probably damaging Het
Fbn1 A C 2: 125,162,888 (GRCm39) C2133G possibly damaging Het
Fhl5 A G 4: 25,211,309 (GRCm39) F128L probably damaging Het
Fn1 T C 1: 71,680,421 (GRCm39) N428S probably damaging Het
Fxr2 T C 11: 69,540,665 (GRCm39) probably null Het
Gabrp T C 11: 33,504,388 (GRCm39) Y309C probably damaging Het
Golga2 A G 2: 32,182,168 (GRCm39) I50V probably benign Het
Ifi203 C T 1: 173,764,158 (GRCm39) G105R possibly damaging Het
Itgav A T 2: 83,596,190 (GRCm39) Q201L possibly damaging Het
Jade2 T C 11: 51,716,198 (GRCm39) T336A probably damaging Het
Kdm4b A G 17: 56,708,649 (GRCm39) D996G probably damaging Het
Me2 A G 18: 73,903,797 (GRCm39) I557T probably benign Het
Memo1 A C 17: 74,551,996 (GRCm39) L100R probably damaging Het
Mrps2 A G 2: 28,359,818 (GRCm39) N225S probably damaging Het
Ndufa2 A G 18: 36,877,278 (GRCm39) probably null Het
Or2g7 G T 17: 38,378,275 (GRCm39) C71F probably damaging Het
Or7g19 G A 9: 18,856,757 (GRCm39) S271N probably benign Het
Pak5 G T 2: 135,940,310 (GRCm39) Y501* probably null Het
Pot1b A T 17: 56,002,206 (GRCm39) F123I possibly damaging Het
Rev3l T C 10: 39,700,786 (GRCm39) V1761A probably benign Het
Samd3 T A 10: 26,106,064 (GRCm39) V14E probably damaging Het
Slc4a8 G A 15: 100,697,598 (GRCm39) A605T probably benign Het
Smgc A T 15: 91,744,642 (GRCm39) D333V probably damaging Het
Spata4 A G 8: 55,055,440 (GRCm39) I147V probably benign Het
Ttc23l G A 15: 10,537,652 (GRCm39) S206L probably benign Het
Vmn2r73 G A 7: 85,507,495 (GRCm39) H606Y probably benign Het
Vsig8 A G 1: 172,387,916 (GRCm39) N2S probably damaging Het
Wdr17 A C 8: 55,114,515 (GRCm39) I667R probably damaging Het
Yif1b A G 7: 28,937,873 (GRCm39) probably null Het
Zbtb5 A T 4: 44,994,003 (GRCm39) H460Q possibly damaging Het
Zdhhc21 G A 4: 82,724,564 (GRCm39) probably benign Het
Zkscan1 A G 5: 138,092,264 (GRCm39) Q146R probably benign Het
Other mutations in Zfp944
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00595:Zfp944 APN 17 22,558,186 (GRCm39) missense probably benign 0.10
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
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 2016-08-02