Incidental Mutation 'R5746:Zfp146'
ID 445784
Institutional Source Beutler Lab
Gene Symbol Zfp146
Ensembl Gene ENSMUSG00000037029
Gene Name zinc finger protein 146
Synonyms OZF
MMRRC Submission 043199-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.190) question?
Stock # R5746 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 29860694-29869175 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to C at 29861818 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Serine to Glycine at position 75 (S75G)
Ref Sequence ENSEMBL: ENSMUSP00000058588 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000062181]
AlphaFold Q8BQN6
Predicted Effect probably benign
Transcript: ENSMUST00000062181
AA Change: S75G

PolyPhen 2 Score 0.004 (Sensitivity: 0.98; Specificity: 0.59)
SMART Domains Protein: ENSMUSP00000058588
Gene: ENSMUSG00000037029
AA Change: S75G

DomainStartEndE-ValueType
ZnF_C2H2 16 38 1.01e-1 SMART
ZnF_C2H2 44 66 5.5e-3 SMART
ZnF_C2H2 72 94 3.44e-4 SMART
ZnF_C2H2 100 122 2.27e-4 SMART
ZnF_C2H2 128 150 1.98e-4 SMART
ZnF_C2H2 156 178 3.89e-3 SMART
ZnF_C2H2 184 206 6.99e-5 SMART
ZnF_C2H2 212 234 1.6e-4 SMART
ZnF_C2H2 240 262 5.5e-3 SMART
ZnF_C2H2 268 290 1.82e-3 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000136508
Coding Region Coverage
  • 1x: 99.3%
  • 3x: 98.7%
  • 10x: 97.4%
  • 20x: 95.6%
Validation Efficiency
Allele List at MGI
Other mutations in this stock
Total: 28 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Adora3 A G 3: 105,815,126 (GRCm39) E292G possibly damaging Het
Ank1 C T 8: 23,606,612 (GRCm39) T1187I probably damaging Het
Ankrd16 T A 2: 11,789,178 (GRCm39) I255K probably damaging Het
Atp6ap1l T C 13: 91,031,698 (GRCm39) N328S probably benign Het
Cbln3 A G 14: 56,120,601 (GRCm39) S144P probably damaging Het
Cdh12 T A 15: 21,358,810 (GRCm39) L78Q probably null Het
Cpsf1 C T 15: 76,484,037 (GRCm39) R761H probably benign Het
Cyp2d10 T G 15: 82,289,472 (GRCm39) E213D probably benign Het
Gba2 T C 4: 43,568,465 (GRCm39) probably null Het
Glb1l2 G A 9: 26,708,086 (GRCm39) A29V probably benign Het
Gm11149 C T 9: 49,457,494 (GRCm39) G393S probably damaging Het
Igkv6-29 C A 6: 70,115,584 (GRCm39) G70V possibly damaging Het
Kcnma1 T C 14: 23,544,635 (GRCm39) N574S probably damaging Het
Kdm2b A G 5: 123,017,427 (GRCm39) V1099A probably damaging Het
Kel C T 6: 41,675,961 (GRCm39) G243E probably damaging Het
Ly6g A T 15: 75,028,596 (GRCm39) N19Y possibly damaging Het
Nexn TCTTCCTTC TCTTC 3: 151,948,513 (GRCm39) probably benign Het
Nod2 T C 8: 89,390,970 (GRCm39) S411P probably damaging Het
Plekha6 G C 1: 133,200,045 (GRCm39) R208P possibly damaging Het
Ptpn14 G A 1: 189,578,610 (GRCm39) probably null Het
Smg6 G A 11: 75,030,113 (GRCm39) G211E probably damaging Het
Stx16 G A 2: 173,935,292 (GRCm39) G156R probably damaging Het
Tbc1d15 T C 10: 115,046,184 (GRCm39) S440G probably damaging Het
Tpm2 A G 4: 43,519,731 (GRCm39) V85A possibly damaging Het
Ttf1 G T 2: 28,955,754 (GRCm39) A373S probably damaging Het
Vmn2r11 T A 5: 109,201,560 (GRCm39) T315S probably benign Het
Zcchc14 T C 8: 122,331,378 (GRCm39) probably benign Het
Zfp994 A G 17: 22,420,254 (GRCm39) Y232H probably damaging Het
Other mutations in Zfp146
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL02170:Zfp146 APN 7 29,861,905 (GRCm39) missense possibly damaging 0.51
IGL02485:Zfp146 APN 7 29,862,015 (GRCm39) missense probably benign
IGL02796:Zfp146 UTSW 7 29,861,983 (GRCm39) missense probably benign 0.01
R2043:Zfp146 UTSW 7 29,861,664 (GRCm39) missense possibly damaging 0.92
R4166:Zfp146 UTSW 7 29,861,865 (GRCm39) missense possibly damaging 0.50
R4385:Zfp146 UTSW 7 29,861,847 (GRCm39) missense probably benign
R5270:Zfp146 UTSW 7 29,861,900 (GRCm39) missense probably benign 0.03
R5271:Zfp146 UTSW 7 29,861,900 (GRCm39) missense probably benign 0.03
Predicted Primers PCR Primer
(F):5'- CATGCACAATCAGCGACGTG -3'
(R):5'- AAGCCCCTTTGCCTGTAAGG -3'

Sequencing Primer
(F):5'- CAGGTACTTTTTCTGGCCAAAAGC -3'
(R):5'- GTATGTGGGAAACTCTTCAGCCAC -3'
Posted On 2016-11-21