ZMP
zgc:66432
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC327616 [Source:RefSeq peptide;Acc:NP_956132]
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]
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 |
|---|---|---|---|
| sa42796 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42795 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa42796
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058620 | Essential Splice Site | 179 | 599 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 44835445)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 42115953 |
| GRCz11 | 16 | 42065985 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTTTTATTTCCATTATGACCTCAATGACTGTGATAGCTCGTTAATGG[T/G]AAGTACTGAACGTTAACCTCATAAAGTCAAGGACACTGTAAAAAAAAAAA
Long Flanking Sequence:
CTTTCTTGGACTGCTGCAATTCGCCAAAACTCACGCTCAGGCTCCCGGGGGTCACCGAGCATATAGAGATGTCGCGTCCACGGAGCAGCTGCTCGGCGCGGTCAGGCCGTGGACTGGAGCAGGCAGCGAGTTTATAAGGAATCCTCCGATTATGCCCCCCTATCATATTTTCCCAATGTTCCAGGATTATCCGGTTCCTTTAGTTGACATGGAGCTGTTCAGACCTGTGTCCGAGAATAGACACTTTCCGCGGCTGTTGACAAGTATTTTAACACCTCCAGTGAGCGCTCCGCGCGTCCAGGTGTCTCCCGCGCGCAACGCCCGGGGAGTGGAGGTCTGGTGCGGCTACAGGAAAGTCTCTGTGCGCCTGAACAAGAGTCTGCTCGGATTCAGGAGTTCACCGTCTGCCTTTCAACTGGGAACCTGTCCCGTCTCTCGTTTCGACGACTACTTCTTTTATTTCCATTATGACCTCAATGACTGTGATAGCTCGTTAATGG[T/G]AAGTACTGAACGTTAACCTCATAAAGTCAAGGACACTGTAAAAAAAAAAAAAGCTGCAAAAAGTTAAGGTAACTCAAACCAATTAAGGAAACCAATTTCAACAAACTATTTAATGAGGTAAAGTTAGTTTTATATTCGGATATTCAGACAATCTCCTTAATAACATTGTTTCATAATTCAAGTATTCTTTGCAAATTCTAAAAAGGGCAAATCATGTAAGCAGCCAATGACTATCAAAGTACAACATTGTTCACAGTCAATTAGATAGTGTTAATTTAGTCATACTTTTCTGCTAATTCCGATCGAATATTCAAAGCAGCATGGTACACAATATAGAGACTTGTGAATGAAGGGATAAACGAATGTGCAAATATATAACCAACTTTACCTCTATAAACTATTTAAGTTCAAACACTACCCAGGTGAAAAAGAAGTGCTCTTAAATATTTTACCAATGTACCTAAAATGTAGATAGTATGTTTAAAGCACAATTACAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42795
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058620 | Essential Splice Site | 400 | 599 | 8 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 44828407)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 42108915 |
| GRCz11 | 16 | 42058947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGACTGTCTGTGTGTAAACTGAAAACATTACATCTTTTGCTTCTACAAC[A/T]GCTTATTTTCCCAGTATGACACAATCTCTGATATCAAGCAAACCCTGGAT
Long Flanking Sequence:
TTTTTTTTTTTTTTTTTTTATTCAGTTGAATAAAAATCTATTCATCCATTTATATATTAGCAAAATAATTAGCAGTGTTTGCATGTCCTTTACTGCATAGAATTCATTAAAATAGAAGTATATAGAAATAACATTCATTACAAGTTGATTTCTAAGTAAAAAAAAATAGTAAAATATTTTCCAGTCATGTATTTCATCATTGAAGATTTCTTAACAAAAACAACGTAAAAATCTCATCACAATCCTTAATAGACCATCAACTGCACTGACACTGTTTCAATTCACTACAATCTTCTATGTAAAGCTGCTTTGACACAATCTACATTGTAAAAGCGCTATTAAAAAACAACGTTTTTTTTTTTAACTCAATAAAATCTAGAAAAAAAATGGTCAAATGTGGTCAAAAGAGATTTTTAACAGCAGGTGTAAACTGGAACAAGTCTCGTTGTGTCGACTGTCTGTGTGTAAACTGAAAACATTACATCTTTTGCTTCTACAAC[A/T]GCTTATTTTCCCAGTATGACACAATCTCTGATATCAAGCAAACCCTGGATTTTGGACCGTAGTCAACAAAACTTATTAAACATTAAAGGAGGATGGGTCAATATTAAAGGGGGCCCAGAGAAGAAGTTCAAGAGCGCTACAGGAATCGATGAAGAGAAAGATGATGATGGTGACACTTTGGAGATTGTGAGTGATATTGAAGAACAAACAGAAGTAACAAAGGAAAACAAGAAGATGAGTGTTATGCATTTGGATGAGGATGTTGAGGTAATTGTTGGGAGTAAGGAAATTACTGCTACAGAGTCCGTTCATTCTGGACATGTGGAGTCTGATGGGAAAGAGATGGGTAGAGTTTTAAAGATTGGGAAAGTTGCTGGAAGACCCAGGAGCAGAAGTGGAGCTGGTGTGATGGGAGAGCTTTTGGAAGATGTTAAAATGTCCAGCAAAAGTGGAATAAATAAAATGGTTAACATTACCAAAGATGAGATGGACTTTAAAGA
Associated Phenotype:
Not determined