Incidental Mutation 'R1701:Zfp141'
ID 189719
Institutional Source Beutler Lab
Gene Symbol Zfp141
Ensembl Gene ENSMUSG00000092416
Gene Name zinc finger protein 141
Synonyms
MMRRC Submission 039734-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R1701 (G1)
Quality Score 225
Status Not validated
Chromosome 7
Chromosomal Location 42122810-42155164 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) T to A at 42125470 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Tyrosine to Phenylalanine at position 334 (Y334F)
Ref Sequence ENSEMBL: ENSMUSP00000133899 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000173489] [ENSMUST00000174407]
AlphaFold G3UY09
Predicted Effect probably benign
Transcript: ENSMUST00000173489
Predicted Effect probably benign
Transcript: ENSMUST00000174407
AA Change: Y334F

PolyPhen 2 Score 0.355 (Sensitivity: 0.90; Specificity: 0.89)
SMART Domains Protein: ENSMUSP00000133899
Gene: ENSMUSG00000092416
AA Change: Y334F

DomainStartEndE-ValueType
KRAB 18 78 4.41e-34 SMART
internal_repeat_1 146 405 8.73e-7 PROSPERO
ZnF_C2H2 410 432 4.54e-4 SMART
ZnF_C2H2 438 460 2.2e-2 SMART
ZnF_C2H2 466 488 2.95e-3 SMART
ZnF_C2H2 494 516 4.24e-4 SMART
ZnF_C2H2 522 544 9.58e-3 SMART
ZnF_C2H2 550 572 4.01e-5 SMART
ZnF_C2H2 578 600 3.21e-4 SMART
ZnF_C2H2 606 628 4.87e-4 SMART
ZnF_C2H2 634 656 5.99e-4 SMART
ZnF_C2H2 662 684 4.87e-4 SMART
Predicted Effect noncoding transcript
Transcript: ENSMUST00000174489
Coding Region Coverage
  • 1x: 99.2%
  • 3x: 98.5%
  • 10x: 96.7%
  • 20x: 93.8%
Validation Efficiency
MGI Phenotype PHENOTYPE: Homozygous mutation of this gene results in abnormal skin pigmentation. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 58 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aadacl3 A G 4: 144,190,142 (GRCm39) L53P probably damaging Het
Acadsb T A 7: 131,026,213 (GRCm39) F19I probably benign Het
Aldh3a2 C T 11: 61,147,598 (GRCm39) G303S probably damaging Het
Anks1b T C 10: 89,885,816 (GRCm39) Y171H probably damaging Het
Anxa7 A T 14: 20,510,229 (GRCm39) I385N probably damaging Het
Astn1 A T 1: 158,331,877 (GRCm39) T324S possibly damaging Het
Ccdc88a T C 11: 29,427,427 (GRCm39) V235A possibly damaging Het
Crhr2 T C 6: 55,076,255 (GRCm39) K258R probably damaging Het
Ctnnd1 T C 2: 84,439,335 (GRCm39) E786G probably damaging Het
Ctnnd2 G A 15: 30,922,127 (GRCm39) D918N probably damaging Het
Dnah9 A G 11: 65,802,750 (GRCm39) S200P probably damaging Het
Dot1l T C 10: 80,626,576 (GRCm39) S1266P possibly damaging Het
Efemp1 A G 11: 28,871,750 (GRCm39) T422A possibly damaging Het
Fam135b T C 15: 71,331,578 (GRCm39) H1137R probably damaging Het
Flot2 C T 11: 77,940,373 (GRCm39) S40L possibly damaging Het
Fras1 G A 5: 96,748,643 (GRCm39) S706N probably benign Het
Gbf1 T C 19: 46,250,114 (GRCm39) L357P probably damaging Het
Gpatch2l A G 12: 86,335,726 (GRCm39) S476G probably benign Het
Hbb-bh2 T C 7: 103,489,450 (GRCm39) T34A probably benign Het
Ints8 A G 4: 11,231,656 (GRCm39) L443P probably damaging Het
Intu T A 3: 40,618,694 (GRCm39) D233E probably damaging Het
Itprid2 A G 2: 79,466,394 (GRCm39) K75E probably damaging Het
Kctd1 T A 18: 15,102,617 (GRCm39) I259L possibly damaging Het
Lama5 A G 2: 179,863,162 (GRCm39) C108R probably damaging Het
Lgals3bp T C 11: 118,284,781 (GRCm39) Y266C probably damaging Het
Lrig2 T C 3: 104,401,993 (GRCm39) I111V probably benign Het
Mtcl2 T C 2: 156,872,539 (GRCm39) N936S probably damaging Het
Myh8 G T 11: 67,170,964 (GRCm39) C125F probably damaging Het
Or2d3c C A 7: 106,526,129 (GRCm39) C179F probably damaging Het
Or2h2 C T 17: 37,396,623 (GRCm39) V145M probably benign Het
Or51a10 T C 7: 103,699,402 (GRCm39) E53G possibly damaging Het
Or5ac21 T C 16: 59,123,651 (GRCm39) I46T probably benign Het
Or5p76 T G 7: 108,122,731 (GRCm39) Q142P probably benign Het
Or5w16 T A 2: 87,576,894 (GRCm39) M118K probably damaging Het
Or6c202 T C 10: 128,995,974 (GRCm39) Q293R probably damaging Het
Or8g4 A T 9: 39,662,365 (GRCm39) I228F probably damaging Het
Pate8 A G 9: 36,493,114 (GRCm39) probably benign Het
Phc2 C T 4: 128,645,400 (GRCm39) P836S probably damaging Het
Pla2g7 T C 17: 43,911,415 (GRCm39) F189S probably damaging Het
Ptprk A G 10: 28,342,054 (GRCm39) D487G probably damaging Het
Ptpro T A 6: 137,420,592 (GRCm39) V1007D probably damaging Het
Rad54l2 A G 9: 106,577,692 (GRCm39) probably null Het
Robo4 G T 9: 37,314,739 (GRCm39) V198L probably benign Het
Selenbp1 C A 3: 94,844,701 (GRCm39) H119Q probably damaging Het
Slc25a13 T C 6: 6,152,525 (GRCm39) probably null Het
Slc35f5 A G 1: 125,498,330 (GRCm39) E176G possibly damaging Het
Sphkap G A 1: 83,255,236 (GRCm39) R838* probably null Het
Tenm4 G A 7: 96,552,096 (GRCm39) V2512M probably damaging Het
Tmc8 A G 11: 117,682,188 (GRCm39) probably null Het
Trim30d C T 7: 104,133,389 (GRCm39) W21* probably null Het
Ube3c G A 5: 29,806,200 (GRCm39) V281I probably benign Het
Usp17ld T C 7: 102,899,783 (GRCm39) K383R probably benign Het
Vmn1r172 A T 7: 23,359,529 (GRCm39) Y138F probably damaging Het
Vmn1r180 T C 7: 23,652,395 (GRCm39) V186A possibly damaging Het
Vmn2r25 T A 6: 123,828,754 (GRCm39) probably null Het
Vmn2r61 T C 7: 41,949,935 (GRCm39) F785S probably damaging Het
Zfp609 T C 9: 65,638,282 (GRCm39) I317V probably benign Het
Zfp879 A G 11: 50,724,060 (GRCm39) I259T possibly damaging Het
Other mutations in Zfp141
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00593:Zfp141 APN 7 42,124,731 (GRCm39) nonsense probably null
IGL00595:Zfp141 APN 7 42,126,079 (GRCm39) missense probably benign 0.08
R0577:Zfp141 UTSW 7 42,125,938 (GRCm39) missense probably benign 0.14
R0883:Zfp141 UTSW 7 42,125,480 (GRCm39) missense possibly damaging 0.85
R2290:Zfp141 UTSW 7 42,124,649 (GRCm39) missense probably damaging 1.00
R4176:Zfp141 UTSW 7 42,125,705 (GRCm39) missense probably benign 0.04
R4719:Zfp141 UTSW 7 42,126,111 (GRCm39) splice site probably null
R4897:Zfp141 UTSW 7 42,125,629 (GRCm39) missense probably benign 0.24
R5372:Zfp141 UTSW 7 42,126,620 (GRCm39) missense possibly damaging 0.91
R5438:Zfp141 UTSW 7 42,138,894 (GRCm39) missense probably damaging 1.00
R5447:Zfp141 UTSW 7 42,124,983 (GRCm39) nonsense probably null
R5743:Zfp141 UTSW 7 42,125,855 (GRCm39) missense possibly damaging 0.68
R5969:Zfp141 UTSW 7 42,138,912 (GRCm39) missense probably damaging 0.98
R6731:Zfp141 UTSW 7 42,138,924 (GRCm39) missense probably damaging 0.99
R7127:Zfp141 UTSW 7 42,124,853 (GRCm39) missense probably damaging 1.00
R7474:Zfp141 UTSW 7 42,125,678 (GRCm39) nonsense probably null
R7572:Zfp141 UTSW 7 42,124,856 (GRCm39) missense probably benign 0.03
R7830:Zfp141 UTSW 7 42,124,612 (GRCm39) missense probably benign 0.01
R7890:Zfp141 UTSW 7 42,125,903 (GRCm39) missense probably damaging 0.99
R8133:Zfp141 UTSW 7 42,124,481 (GRCm39) missense probably damaging 1.00
R8833:Zfp141 UTSW 7 42,125,687 (GRCm39) missense possibly damaging 0.82
R9238:Zfp141 UTSW 7 42,125,111 (GRCm39) nonsense probably null
R9245:Zfp141 UTSW 7 42,124,821 (GRCm39) nonsense probably null
R9339:Zfp141 UTSW 7 42,125,639 (GRCm39) missense probably damaging 0.98
R9348:Zfp141 UTSW 7 42,124,814 (GRCm39) nonsense probably null
R9498:Zfp141 UTSW 7 42,125,770 (GRCm39) missense probably benign 0.07
Predicted Primers PCR Primer
(F):5'- ATTTGCATGGCGTTCCTCCAGG -3'
(R):5'- TGCACACAATCACCTTTGTACCAGC -3'

Sequencing Primer
(F):5'- CTCCAGGTTGAAGCATCTTAAGTC -3'
(R):5'- TGTACCAGCAGGATTATAGCC -3'
Posted On 2014-05-14