Incidental Mutation 'R1028:Zp1'
ID 95086
Institutional Source Beutler Lab
Gene Symbol Zp1
Ensembl Gene ENSMUSG00000024734
Gene Name zona pellucida glycoprotein 1
Synonyms
MMRRC Submission 039130-MU
Accession Numbers
Essential gene? Probably non essential (E-score: 0.078) question?
Stock # R1028 (G1)
Quality Score 225
Status Not validated
Chromosome 19
Chromosomal Location 10891660-10897965 bp(-) (GRCm39)
Type of Mutation missense
DNA Base Change (assembly) G to A at 10896275 bp (GRCm39)
Zygosity Heterozygous
Amino Acid Change Threonine to Isoleucine at position 150 (T150I)
Ref Sequence ENSEMBL: ENSMUSP00000025641 (fasta)
Gene Model predicted gene model for transcript(s): [ENSMUST00000025641] [ENSMUST00000168708]
AlphaFold Q62005
Predicted Effect probably benign
Transcript: ENSMUST00000025641
AA Change: T150I

PolyPhen 2 Score 0.011 (Sensitivity: 0.96; Specificity: 0.78)
SMART Domains Protein: ENSMUSP00000025641
Gene: ENSMUSG00000024734
AA Change: T150I

DomainStartEndE-ValueType
signal peptide 1 20 N/A INTRINSIC
low complexity region 184 199 N/A INTRINSIC
PD 226 269 2.33e-11 SMART
ZP 271 542 1.55e-102 SMART
low complexity region 580 589 N/A INTRINSIC
transmembrane domain 591 613 N/A INTRINSIC
Predicted Effect probably benign
Transcript: ENSMUST00000168708
SMART Domains Protein: ENSMUSP00000128543
Gene: ENSMUSG00000024734

DomainStartEndE-ValueType
Pfam:Zona_pellucida 3 61 5.6e-8 PFAM
Coding Region Coverage
  • 1x: 98.5%
  • 3x: 97.1%
  • 10x: 91.8%
  • 20x: 78.7%
Validation Efficiency
MGI Phenotype FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The zona pellucida is an extracellular matrix that surrounds the oocyte and early embryo. It is composed primarily of three or four glycoproteins with various functions during fertilization and preimplantation development. The protein encoded by this gene ensures the structural integrity of the zona pellucida. Mutations in this gene are a cause of oocyte maturation defect and infertility. [provided by RefSeq, May 2014]
PHENOTYPE: Female homozygous mutants produce oocytes with abnormal zona pellucida. Fecunditiy is significantly reduced, probably due to precocious hatching. [provided by MGI curators]
Allele List at MGI
Other mutations in this stock
Total: 30 list
GeneRefVarChr/LocMutationPredicted EffectZygosity
Ak7 AGAGGAGGAGGAGGAGGAGGA AGAGGAGGAGGAGGAGGA 12: 105,676,448 (GRCm39) probably benign Het
Ano8 GCCTCCTCCTCCTCCTC GCCTCCTCCTCCTC 8: 71,933,615 (GRCm39) probably benign Het
B3galt4 G A 17: 34,169,813 (GRCm39) R142C probably damaging Het
Bpifb9a G C 2: 154,104,327 (GRCm39) E257Q possibly damaging Het
Cdh19 T C 1: 110,882,314 (GRCm39) I59M probably benign Het
Cmah A G 13: 24,619,645 (GRCm39) D171G probably damaging Het
Colec12 T C 18: 9,866,837 (GRCm39) S683P unknown Het
Dixdc1 C T 9: 50,614,546 (GRCm39) A168T probably benign Het
Dpp6 A G 5: 27,871,425 (GRCm39) D461G probably benign Het
Entpd3 A G 9: 120,387,427 (GRCm39) H208R probably benign Het
Fuz T C 7: 44,546,350 (GRCm39) I39T probably damaging Het
Gprin3 T C 6: 59,331,594 (GRCm39) N238D possibly damaging Het
Itpr3 G T 17: 27,310,343 (GRCm39) A403S probably benign Het
Mroh2a G A 1: 88,163,098 (GRCm39) R376H probably benign Het
Mtor G C 4: 148,623,287 (GRCm39) G2046R possibly damaging Het
Myh13 T C 11: 67,247,007 (GRCm39) S1243P possibly damaging Het
Net1 A T 13: 3,934,375 (GRCm39) C441S probably damaging Het
Nlrp4e T C 7: 23,021,169 (GRCm39) F552S probably damaging Het
Or2y15 G A 11: 49,351,047 (GRCm39) M180I probably benign Het
Or4k47 A T 2: 111,451,870 (GRCm39) L183Q probably damaging Het
Or9i16 C A 19: 13,865,159 (GRCm39) Q138H probably damaging Het
Ovch2 T C 7: 107,395,755 (GRCm39) I88V probably benign Het
Phf1 A G 17: 27,153,307 (GRCm39) T42A possibly damaging Het
Pkhd1 A G 1: 20,187,950 (GRCm39) Y3453H probably damaging Het
Rabgef1 T G 5: 130,241,703 (GRCm39) L369* probably null Het
Rufy1 A T 11: 50,305,425 (GRCm39) probably null Het
Sec16b T C 1: 157,388,487 (GRCm39) V618A probably benign Het
Sh3rf1 A G 8: 61,846,821 (GRCm39) R876G possibly damaging Het
Slc26a8 A G 17: 28,891,772 (GRCm39) Y126H probably damaging Het
Vwa8 C T 14: 79,145,670 (GRCm39) R116C probably damaging Het
Other mutations in Zp1
AlleleSourceChrCoordTypePredicted EffectPPH Score
IGL00481:Zp1 APN 19 10,896,141 (GRCm39) missense probably damaging 1.00
IGL01504:Zp1 APN 19 10,896,375 (GRCm39) missense probably damaging 0.99
IGL02260:Zp1 APN 19 10,894,078 (GRCm39) unclassified probably benign
IGL02465:Zp1 APN 19 10,897,851 (GRCm39) missense probably benign 0.09
IGL02634:Zp1 APN 19 10,896,871 (GRCm39) unclassified probably benign
IGL02714:Zp1 APN 19 10,895,976 (GRCm39) missense probably damaging 1.00
IGL03234:Zp1 APN 19 10,892,187 (GRCm39) splice site probably benign
IGL03404:Zp1 APN 19 10,891,825 (GRCm39) unclassified probably benign
R0504:Zp1 UTSW 19 10,893,571 (GRCm39) missense probably damaging 0.98
R0554:Zp1 UTSW 19 10,897,926 (GRCm39) missense probably benign 0.29
R1279:Zp1 UTSW 19 10,895,941 (GRCm39) missense probably damaging 1.00
R1460:Zp1 UTSW 19 10,896,242 (GRCm39) missense probably benign
R3425:Zp1 UTSW 19 10,895,956 (GRCm39) missense probably benign 0.00
R3832:Zp1 UTSW 19 10,893,888 (GRCm39) missense probably damaging 1.00
R4420:Zp1 UTSW 19 10,892,124 (GRCm39) splice site probably null
R4669:Zp1 UTSW 19 10,896,269 (GRCm39) missense probably benign 0.31
R4849:Zp1 UTSW 19 10,896,198 (GRCm39) missense possibly damaging 0.90
R5134:Zp1 UTSW 19 10,897,926 (GRCm39) missense probably benign 0.29
R5170:Zp1 UTSW 19 10,897,918 (GRCm39) missense possibly damaging 0.56
R5510:Zp1 UTSW 19 10,896,769 (GRCm39) missense probably damaging 1.00
R6284:Zp1 UTSW 19 10,893,867 (GRCm39) missense probably damaging 1.00
R6307:Zp1 UTSW 19 10,894,084 (GRCm39) missense probably null 0.45
R6378:Zp1 UTSW 19 10,892,217 (GRCm39) missense probably benign 0.15
R6608:Zp1 UTSW 19 10,896,344 (GRCm39) missense possibly damaging 0.93
R6697:Zp1 UTSW 19 10,892,199 (GRCm39) missense probably benign 0.05
R6862:Zp1 UTSW 19 10,893,877 (GRCm39) missense possibly damaging 0.84
R7054:Zp1 UTSW 19 10,896,104 (GRCm39) missense probably damaging 0.98
R7253:Zp1 UTSW 19 10,893,933 (GRCm39) missense probably damaging 0.99
R7483:Zp1 UTSW 19 10,895,280 (GRCm39) missense possibly damaging 0.72
R7591:Zp1 UTSW 19 10,896,835 (GRCm39) missense probably damaging 1.00
R8857:Zp1 UTSW 19 10,893,888 (GRCm39) missense probably damaging 1.00
Z1176:Zp1 UTSW 19 10,895,278 (GRCm39) missense probably damaging 1.00
Z1177:Zp1 UTSW 19 10,895,968 (GRCm39) missense probably damaging 1.00
Predicted Primers PCR Primer
(F):5'- GAATCCAGCTCAGTCAATTCCCAGG -3'
(R):5'- AGTTTCCATTAACAGCAGCCAGCC -3'

Sequencing Primer
(F):5'- TCAATTCCCAGGGCTCCAG -3'
(R):5'- ACTGGGTGTAGTCAACAGCC -3'
Posted On 2014-01-05