ZMP

zp3.2

Ensembl ID:

ENSDARG00000089352

ZFIN IDs:

ZDB-GENE-050626-121, ZDB-GENE-991129-7

Description:

zona pellucida glycoprotein 3.2 [Source:RefSeq peptide;Acc:NP_001020357]

Human Orthologues:

POMZP3, ZP3

Human Descriptions:

POM121 and ZP3 fusion [Source:HGNC Symbol;Acc:9203]
zona pellucida glycoprotein 3 (sperm receptor) [Source:HGNC Symbol;Acc:13189]

Mouse Orthologue:

Zp3

Mouse Description:

zona pellucida glycoprotein 3 Gene [Source:MGI Symbol;Acc:MGI:99215]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa42845	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42844	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa42845

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074173	Essential Splice Site	213	427	2	8

Genomic Location (Zv9):

Chromosome 17 (position 2367256)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	2412901
GRCz11	17	2589287

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTATCCGCACTGATGGTGCAGTTGTTGGTGTTCAGTGCCACTATCCAAGG[T/C]ACATTAACGTCTTCGGTGCTTAATACAACAGGGTAAACCACTTCGGTTCC

Long Flanking Sequence:

GGACGCCCTGTTGTTGGTCAGGACCCAAACTCTATGGTGCTTATCTTTGACTATCCAATTCAGGAGCCTGACAGTGTGGTGATGGTAAGAAATCCCAATTCTTTTCCAACCTCCATGTAGTATCTTAATGGTTGAGCTTTGAAAAGTAGATTCATGTAGTTTTAAAGACTTGTCCAGGTCAAGTTAACCTTTAAATTCTAAGATGTACTGAATGTTGTCTGGTTGTACTGTATGTTTGATCTCCCACCATTGGCATGTCCACTGGAACCCAAATCAAGAAATTTATGCTTTAATTCTTAGCAGTGCAGCAGCAGTGTCTAAAGCATCTCAAACCTGTCTAATCTTTAGTGGAACTTGTTAACTTGAGATTCTTTCATCAGATGACTGAGGATGAGCTTGTCTACACCTATACTGTTACCTACACCCCTGAAGCGTTTCCTGGGACTCCTATTATCCGCACTGATGGTGCAGTTGTTGGTGTTCAGTGCCACTATCCAAGG[T/C]ACATTAACGTCTTCGGTGCTTAATACAACAGGGTAAACCACTTCGGTTCCAGCCATGTAGGTCATTGTTGAAACCAGTCCATTTTTAATTCTTTACCTCCAGGCTTCACAATGTGAGCAGTAATGCCTTGATGCCAGCATGGACCCCTTATGCCTCAGCAGAGCTTGGCGAGGATATCTTGGTCTTCTCCCTGGATCTCATGACTGGTTGGTGCAGTTTCTTAAACCTCATTCTTTTAAGATTTACTGTATCTAAACCCTTTCTTACTCTTGCAGATGACTGGTCTTATCAGAGGCCCTCAAATGTGTATTTCCTGGGCAGCGTGATTAATATTGAGGCATCTGTGATGCAGTACAATCATGTGCCTCTGCGTGTGTATGTGGACCGCTGTGTGGCAACTCCAGTACCTGATCCTGAAGCTCTGCCAAGATATTCCTTCATTGAGAATCATGGGTAAGATACTGCACTAGCGGTGTTGAATCATGTCCAGGGCGATCAGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42844

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000074173	Nonsense	360	427	6	8

Genomic Location (Zv9):

Chromosome 17 (position 2365790)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	2411435
GRCz11	17	2587821

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTCTCCTGCAGATCTACATTACATGCATTGTGAGGGCCACTGTTGCTGCC[A/T]GACATAGTGACCATCTGCACAAGTCCTGCTCCTTTGCCAATGGGTATGTT

Long Flanking Sequence:

AACTATTATAGCAACTTCAAAATGGGTATTTTGGGCCTTGCTGTTGTCAGCATTTGGAAGGGATCAGACCTTTCCAGAATAGTCTCAAGACTGTCAAGTTCTGGGATTGTTTTGTAAAAGCATGTCCACTAGCTTTCAGAGTTGCATTTGGGCTTAAGTTGCTAACCTTTCTAAAGGAGTTACCTTGAATCATTGGTAGTATCAGTTTATGCTTTTCCTCTTTGTGCCCTTACAAACATGGTTAAATAGCTTTACCCATAACTTCTGCCATCAGGTGCTTTGTAGATGCCAAGACTACAGGTTCCAGCTCCCACTTTTTGCCTATAGTCCAAGAAGACAAGCTCCGTTTCCAGTTGGAGGCCTTCATGTTCCAGGATGCACCCAGTCCTTTTGTATGTACTATTCAGTATTGAGTAAATCCAGCATCTTGTCTTTGTTATTTAATAACTTGTCTCCTGCAGATCTACATTACATGCATTGTGAGGGCCACTGTTGCTGCC[A/T]GACATAGTGACCATCTGCACAAGTCCTGCTCCTTTGCCAATGGGTATGTTGATAACGTTGAACAGTCTTTTTGCTCCTGTTGAAGGTGTTTGGTCTGACTTTTTTGTTTGTTGCAGATGGTTTGCCAATGATGGACACCATGGAGCCTGTAACTGCTGCGACTCTACATGTGGTGTTGAAGGCCAACTTACTGGGGATGGCTTTAGAGGTGTGTTCCTCTACTCTTACTGCGTTTTGCTTTTCACTTCAGTTCTCTCGTTTAACTTTGGTTTCCTCTCTTCTAGGCATTCAGTGGGAAGGCAAGACCTTGGTTGGTCCTGTAGTGGTCAAAGACACGCAGAGGAATCTTGTTTGATAAAGTGAATGCCTGATGAATTGTGCTTGAACTCAGTTTTTAATAAATGTCTGAAACCTTATCTTTGGCTTGGTATCAAGTTTTGTGAAGCCGGTTACCTATAACTGTAGGATGAAAAACAATGGTTCAGTAGTCAAGTGGTTCA

Associated Phenotype:

Not determined