Incidental Mutation 'IGL02694:Zfp944'
ID 303856
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 # IGL02694
Quality Score
Status
Chromosome 17
Chromosomal Location 22556970-22580381 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) A to G at 22558899 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Valine to Alanine at position 116 (V116A)
Ref Sequence ENSEMBL: ENSMUSP00000111197 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000115535]
AlphaFold E9PUS4
Predicted Effect probably benign
Transcript: ENSMUST00000115535
AA Change: V116A

PolyPhen 2 Score 0.047 (Sensitivity: 0.94; Specificity: 0.83)
SMART Domains Protein: ENSMUSP00000111197
Gene: ENSMUSG00000033972
AA Change: V116A

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: 26 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Acer3 A G 7: 97,866,084 (GRCm39) I213T probably benign Het
Alox8 T A 11: 69,077,455 (GRCm39) T432S probably damaging Het
Col4a3 T C 1: 82,688,515 (GRCm39) probably benign Het
Cyp2c54 A G 19: 40,035,987 (GRCm39) Y308H possibly damaging Het
Dscam A G 16: 96,394,476 (GRCm39) V1942A probably benign Het
F11 T C 8: 45,705,196 (GRCm39) Y115C probably damaging Het
Fam13b A G 18: 34,584,259 (GRCm39) probably null Het
Gykl1 A G 18: 52,827,257 (GRCm39) H155R probably benign Het
Lmo7 T A 14: 102,124,606 (GRCm39) V355D probably damaging Het
Lrtm2 T A 6: 119,297,846 (GRCm39) D65V possibly damaging Het
Ly6g6f C T 17: 35,300,144 (GRCm39) V235M possibly damaging Het
Mlxipl G A 5: 135,152,872 (GRCm39) probably null Het
Or11j4 A G 14: 50,630,257 (GRCm39) I15V probably benign Het
Or13a20 A G 7: 140,232,093 (GRCm39) N67S probably damaging Het
Or14a256 C T 7: 86,265,518 (GRCm39) V112I probably benign Het
Ppp2r1a A G 17: 21,171,702 (GRCm39) probably benign Het
Psmb2 A G 4: 126,603,351 (GRCm39) N193S probably benign Het
Rassf2 A T 2: 131,851,641 (GRCm39) Y34N possibly damaging Het
Ryr2 A G 13: 11,620,075 (GRCm39) F3841L probably damaging Het
Skint2 A G 4: 112,473,792 (GRCm39) probably benign Het
Spdl1 T C 11: 34,704,448 (GRCm39) I462V probably benign Het
Spopfm1 A G 3: 94,173,459 (GRCm39) M152V probably benign Het
Tlk2 A G 11: 105,112,061 (GRCm39) E138G probably benign Het
Vmn1r89 A G 7: 12,954,056 (GRCm39) E196G probably benign Het
Zfp142 A G 1: 74,609,307 (GRCm39) L1496P probably damaging Het
Zfp689 T C 7: 127,047,573 (GRCm39) D94G possibly damaging 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
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 2015-04-16