Incidental Mutation 'R5969:Zfp141'
ID 470739
Institutional Source Beutler Lab
Gene Symbol Zfp141
Ensembl Gene ENSMUSG00000092416
Gene Name zinc finger protein 141
Synonyms
MMRRC Submission 044152-MU
Accession Numbers
Essential gene? Non essential (E-score: 0.000) question?
Stock # R5969 (G1)
Quality Score 225
Status Validated
Chromosome 7
Chromosomal Location 42122810-42155164 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) C to A at 42138912 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Arginine to Leucine at position 40 (R40L)
Ref Sequence ENSEMBL: ENSMUSP00000145574 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000173489] [ENSMUST00000174407]
AlphaFold G3UY09
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173439
Predicted Effect probably damaging
Transcript: ENSMUST00000173489
AA Change: R40L

PolyPhen 2 Score 0.981 (Sensitivity: 0.75; Specificity: 0.96)
Predicted Effect noncoding transcript
Transcript: ENSMUST00000173599
Predicted Effect probably damaging
Transcript: ENSMUST00000174407
AA Change: R40L

PolyPhen 2 Score 0.966 (Sensitivity: 0.77; Specificity: 0.95)
SMART Domains Protein: ENSMUSP00000133899
Gene: ENSMUSG00000092416
AA Change: R40L

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
Meta Mutation Damage Score 0.6467 question?
Coding Region Coverage
  • 1x: 99.9%
  • 3x: 99.6%
  • 10x: 98.1%
  • 20x: 94.2%
Validation Efficiency 99% (67/68)
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: 59 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Aaas A C 15: 102,258,999 (GRCm39) Y19D probably damaging Het
Abca13 T A 11: 9,242,214 (GRCm39) L1359* probably null Het
Ahi1 A T 10: 20,860,292 (GRCm39) D671V probably damaging Het
Ahnak T C 19: 8,993,949 (GRCm39) S5078P probably damaging Het
Ankhd1 A T 18: 36,733,887 (GRCm39) T584S probably damaging Het
Apba2 T A 7: 64,394,195 (GRCm39) L568* probably null Het
Cenpn C A 8: 117,667,276 (GRCm39) L300I probably damaging Het
Cmya5 A T 13: 93,226,052 (GRCm39) L3012Q possibly damaging Het
Cnnm1 T C 19: 43,479,911 (GRCm39) S819P probably damaging Het
Cpa6 A T 1: 10,559,108 (GRCm39) S87T probably benign Het
Crybg2 T A 4: 133,803,003 (GRCm39) probably null Het
Csmd1 T A 8: 16,121,367 (GRCm39) T1777S probably benign Het
Csmd3 G T 15: 47,811,386 (GRCm39) P1235Q probably damaging Het
Cxcr4 T A 1: 128,517,584 (GRCm39) N24Y probably benign Het
D630003M21Rik G T 2: 158,059,628 (GRCm39) H91N probably damaging Het
Ece1 T C 4: 137,689,051 (GRCm39) probably null Het
Edc3 T C 9: 57,620,711 (GRCm39) S11P probably damaging Het
Eif1ad14 T C 12: 87,886,248 (GRCm39) D127G unknown Het
Exoc3 G A 13: 74,320,305 (GRCm39) Q719* probably null Het
Fam13a A G 6: 58,942,183 (GRCm39) M203T probably damaging Het
Fchsd1 C T 18: 38,092,926 (GRCm39) probably benign Het
Fhip2a C T 19: 57,372,555 (GRCm39) R602* probably null Het
Fxyd2 T A 9: 45,319,628 (GRCm39) I30N probably damaging Het
Gapt A G 13: 110,490,480 (GRCm39) V61A probably benign Het
Glb1l2 C T 9: 26,692,038 (GRCm39) A74T probably damaging Het
Gpr35 T C 1: 92,910,942 (GRCm39) V2A probably damaging Het
Gtf3c1 A G 7: 125,244,848 (GRCm39) S1729P possibly damaging Het
Heatr5a T C 12: 52,005,823 (GRCm39) T51A probably benign Het
Kat6b G A 14: 21,720,860 (GRCm39) M1737I probably damaging Het
Kif20a G A 18: 34,765,468 (GRCm39) A822T probably benign Het
Klk10 A G 7: 43,434,409 (GRCm39) Y267C probably damaging Het
Lgmn T C 12: 102,372,086 (GRCm39) Y98C probably damaging Het
Lyst A C 13: 13,862,398 (GRCm39) probably null Het
Man2a1 A G 17: 64,932,375 (GRCm39) K154R probably benign Het
Mfng A T 15: 78,648,582 (GRCm39) V165D possibly damaging Het
Mto1 A G 9: 78,360,187 (GRCm39) E225G probably damaging Het
Notch3 C A 17: 32,372,858 (GRCm39) C571F probably damaging Het
Nup205 C T 6: 35,154,513 (GRCm39) probably benign Het
Or51b6 T A 7: 103,556,117 (GRCm39) I157N probably damaging Het
P2ry14 T A 3: 59,022,579 (GRCm39) I303F probably damaging Het
Pcnx3 T C 19: 5,735,563 (GRCm39) D421G probably damaging Het
Pdlim4 T C 11: 53,954,482 (GRCm39) H75R possibly damaging Het
Phf21a A T 2: 92,051,956 (GRCm39) H17L probably damaging Het
Ppid T A 3: 79,505,024 (GRCm39) N122K probably damaging Het
Ppp4r3a T C 12: 101,009,838 (GRCm39) I613V probably benign Het
Prcp C T 7: 92,566,974 (GRCm39) P229S probably benign Het
Ralgds T C 2: 28,432,426 (GRCm39) V85A probably damaging Het
Rgs22 G A 15: 36,015,782 (GRCm39) T1034I probably benign Het
Slc4a3 T C 1: 75,526,623 (GRCm39) V48A probably damaging Het
Snx16 A T 3: 10,503,217 (GRCm39) M10K possibly damaging Het
Svep1 G A 4: 58,070,977 (GRCm39) Q2270* probably null Het
Tmem185b T G 1: 119,455,193 (GRCm39) I318S probably benign Het
Tnik C T 3: 28,675,097 (GRCm39) R657C probably damaging Het
Top3b T C 16: 16,701,429 (GRCm39) probably null Het
Trim40 C T 17: 37,193,319 (GRCm39) R203H probably benign Het
Triobp T A 15: 78,851,740 (GRCm39) N631K probably benign Het
Ubr3 T G 2: 69,809,730 (GRCm39) Y1233* probably null Het
Vgll3 A G 16: 65,636,449 (GRCm39) D200G probably damaging Het
Vmn2r24 G A 6: 123,755,981 (GRCm39) E18K probably benign 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
R1701:Zfp141 UTSW 7 42,125,470 (GRCm39) missense probably benign 0.35
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
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'- GACAATCAGCACTGTCTAGGAC -3'
(R):5'- AGTCAAAATGTCCTCCGTCCC -3'

Sequencing Primer
(F):5'- ACAGACTGAGAGCTGAGACTC -3'
(R):5'- AATGTCCTCCGTCCCACATCATAG -3'
Posted On 2017-03-31