ZMP
LOC794003
Ensembl ID:
Human Orthologues:
ZP1, ZP4
Human Descriptions:
zona pellucida glycoprotein 1 (sperm receptor) [Source:HGNC Symbol;Acc:13187]
zona pellucida glycoprotein 4 [Source:HGNC Symbol;Acc:15770]
zona pellucida glycoprotein 4 [Source:HGNC Symbol;Acc:15770]
Mouse Orthologue:
Zp1
Mouse Description:
zona pellucida glycoprotein 1 Gene [Source:MGI Symbol;Acc:MGI:103073]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39675 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19555 | Nonsense | Available for shipment | Available now |
sa6601 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39674 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39673 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39675
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114006 | Essential Splice Site | 140 | 1036 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 45778402)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44621531 |
GRCz11 | 1 | 45313326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAACGAGCATCTGTTATCGAGGACGGATTTCAAGGCGATGCTCCAGG[T/C]AAGATTTCCTGTTTTATAATTATGTATGGTCGAGTGGGAATAAAGTGCCA
Long Flanking Sequence:
TCCATATTAATTTGCTGATTACACTAGCAGATTTCCCATACGAGCTCGGATGCGCTTGTGAGGAGAAGCGTTAAACTGGCGATGTCTTGCCAACTAAAAACATTAACTTCAATCCTTATATTATCAGCAATCTCACTTAATCTCAATAGTCTTCATTCTAGCGCTACGGCAAAGCGGGAAGCCGCTGATTATTCAGAAGAAAGCAGTTTCAATAGAGTGTCTAACAATTTCACCGACAAAACTTCACAACAGCTCCACATCAGCGCGTTTCAACTCAACGCAGCAAATTCGGATTTGAATCGACTTAGTGGCTCGATAAAACTTGACGACTCAAATGATCCTTCAGACAGAGCTAGCAATGAAACACAGTCGAGTAAACACACGTATGACTTGCCATACAACGACAGTGCATCTTTATTCACTATCAATGAAAACATACGAAGTAGTTTCCAGAAACGAGCATCTGTTATCGAGGACGGATTTCAAGGCGATGCTCCAGG[T/C]AAGATTTCCTGTTTTATAATTATGTATGGTCGAGTGGGAATAAAGTGCCATTTTTTCTTACATTTTTTTTCTTAGAAATTTTTCTAAATAATTCTTAAGTCTCGTTTGAAAAGTAAATGTTTAGACATGCATGGCTTTTTTTGTTGTTGTTGCTGTGTTTACCAACTCAAAAGTTTGTTAAAGATAGTGTAAAAATGTATAACAACTTCAAAATAACTAACCTTTAAACATTAATTGTACAGTATACAGAAGTGGCACAGCAATATTCTACATTTATTAGCATACCTTTGTTTATTGTCCCTGTTGATGTGACCACTGCAAACATGTCCTCTTTCTTTGCAAAAACTATATATATTTTTATTTTATATTTCAGCTCAATCAGGGGTTTCAAAAGTAGCAGAACCACACAAAATTGAATTATATAGAAGTTATTTGTTTATTGTTGGCAATAAGCATTAATTTTATACAACATCTAATTGGAACCACTGTAAACTCCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19555
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114006 | Nonsense | 404 | 1036 | 7 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 45772528)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44615657 |
GRCz11 | 1 | 45307965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATGTTTCCCCATCATCATCATCATCATCATCACCGTCATCGTCATTA[T/A]CCTGCACCTCCTGTGGATGCTCTTCCCAAATTTTCAATAAAGCCATATCT
Long Flanking Sequence:
TTCACTAATTTACAGTAGATGTACTGCACTAACAAAACAATTTACCCTAAATGGCCAAGTGTGAACACAGATTTAGCGCCACATTTGAAACCTGTTTGAGAAGATATGAGTGGTGTTCCAGTTTAACACGTTTTTACTTCTATTTTTATAGGGCAATGAGATCAATCTTGTCATCATCGTGGATGGAAAGCAGTTCACCCTTTCATGTCCCTTTCCTCACTACTGGTCTCGATTTGGTCCCTACCTTCATTCTCCATACTATCAACCACTGCAGCCCAGTCAGGTACAAGTGCCTTTTATCCCATGAGTCAACAGCACTTCTACAGAGCAATCTAAACCTACTGTAAGCCCTCACCTTGTTTATAAACATTTACCATGTAAAACCGCTTCATTTTTATTCATCAGATACCCAGTACTTATGAGTACCAGAAACCGCCTGGTCTCTTTCATCTCATGTTTCCCCATCATCATCATCATCATCATCACCGTCATCGTCATTA[T/A]CCTGCACCTCCTGTGGATGCTCTTCCCAAATTTTCAATAAAGCCATATCTGCCTCCACCTGTTGAGCAAATGCCACAAATGTTTCAGTACCCAGTTTTGCCTCCTCTGTATCTTGAGCCGTCCATTGATTTGCAACCAACTACCCCTCCAGTGACTTCATTTCTTCCTCCTACATACAATCCACCGACCCGTTCCGTCATGCAAGAGAAGGTTTTCCCTCAAATGCCCATCTTTCCCCCAGCTCCCCCTGCAAAACCTTCCAAAACATCTCCGTCACTTCATTGCACAAGAGACAGATTAATTGTAACTTTGGCCTCAGCAACAATAGACTCCATTAAGGTCAAAGGTAAGTTCAAGTGTAGTGGCCATTTCATTGCCGGAATATAAACACAATTAGACATTTAAATGCATTGCTCTTCTCATAATATTCGTAAAGATGTGGAGACAAAAGAATGGATCTCGATTTCATCGGTGTCCGCTGCCTGTAACTACAACCTTCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6601
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114006 | Nonsense | 528 | 1036 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 45772067)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44615196 |
GRCz11 | 1 | 45307504 |
KASP Assay ID:
554-4813.1 (used for ordering genotyping assays)
KASP Sequence:
TTGYTCTTCTYATAATATTYGTAAAGATGTGGAGACAAAAGAATGGATCT[C/A]GATTTCATCGGTGTCCGCTGCCTGTAACTACAACCTTCGCTCTGTAGGGR
Long Flanking Sequence:
CCATCATCATCATCATCATCATCACCGTCATCGTCATTATCCTGCACCTCCTGTGGATGCTCTTCCCAAATTTTCAATAAAGCCATATCTGCCTCCACCTGTTGAGCAAATGCCACAAATGTTTCAGTACCCAGTTTTGCCTCCTCTGTATCTTGAGCCGTCCATTGATTTGCAACCAACTACCCCTCCAGTGACTTCATTTCTTCCTCCTACATACAATCCACCGACCCGTTCCGTCATGCAAGAGAAGGTTTTCCCTCAAATGCCCATCTTTCCCCCAGCTCCCCCTGCAAAACCTTCCAAAACATCTCCGTCACTTCATTGCACAAGAGACAGATTAATTGTAACTTTGGCCTCAGCAACAATAGACTCCATTAAGGTCAAAGGTAAGTTCAAGTGTAGTGGCCATTTCATTGCCGGAATATAAACACAATTAGACATTTAAATGCATTGCTCTTCTCATAATATTCGTAAAGATGTGGAGACAAAAGAATGGATCT[C/A]GATTTCATCGGTGTCCGCTGCCTGTAACTACAACCTTCGCTCTGTAGGGGATAATGTTGTGCTCTCTTCACCACTCCCTTCCTGCCACACAACACAAAAGGTGAGTCCTCAGTGCTGAGATTTTACACATTCACTACATTCAAATCAGAAGGGCTCTTTCATATGCCCTAATCCCTTTAAAGGAACCCTTCTTTGCTCAAAGCATCATGGCTCAAAATAGCCATTGTATCCTTTAAAACCCTTTACCCCAAAGGTCAGCTTTGAGCATGTATGTTTATAATGACACTTCATTATGGCGGCATTGATAATTTTCACTCCAAAAGTGCCCTTTGGAGGGCTATGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATTATAACACCTCACTCAATATTCAAGTTTAGTGTCTTTTTTTTTTTTTAAAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39674
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114006 | Nonsense | 538 | 1036 | 8 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 45772036)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44615165 |
GRCz11 | 1 | 45307473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACAAAAGAATGGATCTCGATTTCATCGGTGTCCGCTGCCTGTAACTA[C/A]AACCTTCGCTCTGTAGGGGATAATGTTGTGCTCTCTTCACCACTCCCTTC
Long Flanking Sequence:
CGTCATTATCCTGCACCTCCTGTGGATGCTCTTCCCAAATTTTCAATAAAGCCATATCTGCCTCCACCTGTTGAGCAAATGCCACAAATGTTTCAGTACCCAGTTTTGCCTCCTCTGTATCTTGAGCCGTCCATTGATTTGCAACCAACTACCCCTCCAGTGACTTCATTTCTTCCTCCTACATACAATCCACCGACCCGTTCCGTCATGCAAGAGAAGGTTTTCCCTCAAATGCCCATCTTTCCCCCAGCTCCCCCTGCAAAACCTTCCAAAACATCTCCGTCACTTCATTGCACAAGAGACAGATTAATTGTAACTTTGGCCTCAGCAACAATAGACTCCATTAAGGTCAAAGGTAAGTTCAAGTGTAGTGGCCATTTCATTGCCGGAATATAAACACAATTAGACATTTAAATGCATTGCTCTTCTCATAATATTCGTAAAGATGTGGAGACAAAAGAATGGATCTCGATTTCATCGGTGTCCGCTGCCTGTAACTA[C/A]AACCTTCGCTCTGTAGGGGATAATGTTGTGCTCTCTTCACCACTCCCTTCCTGCCACACAACACAAAAGGTGAGTCCTCAGTGCTGAGATTTTACACATTCACTACATTCAAATCAGAAGGGCTCTTTCATATGCCCTAATCCCTTTAAAGGAACCCTTCTTTGCTCAAAGCATCATGGCTCAAAATAGCCATTGTATCCTTTAAAACCCTTTACCCCAAAGGTCAGCTTTGAGCATGTATGTTTATAATGACACTTCATTATGGCGGCATTGATAATTTTCACTCCAAAAGTGCCCTTTGGAGGGCTATGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNAATTATAACACCTCACTCAATATTCAAGTTTAGTGTCTTTTTTTTTTTTTAAAGAAATTTCATATTACTAATTTATAGTTTGCTACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39673
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000114006 | Essential Splice Site | 857 | 1036 | 14 | 19 |
Genomic Location (Zv9):
Chromosome 1 (position 45766196)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 44609325 |
GRCz11 | KZ115980.1 | 5428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTCCCTCAGTCTAAATTACGGCACAATCACCAGAGATTCGCCTGTAAG[G/A]TACATGTAGTAATTCAGTTACACTGGTTCTCAAACAACCGAGCAGCATTC
Long Flanking Sequence:
ATGCATAGTGTATATACAGTAAGTGACCCACAAAACATGTTTCATGGGTGTATTTTTTTTAAACAGCCAAAAATACATTGTATAGGTCAAAATGATTGATTTTTAGTTACTTTAGCAAGTAAATATCAAGTCCCATGGAGATATTTTATACATTTCCCATTGTAAGTGTATCAATTTTTGATTAGTTATGTGCAAGTCATTCTTGTAGATTGTTTTAATGTTTATTTTTGGAAAACCTTACATTCCATATTTAAGTTGTATCTCAACCAAATATCATCCTTTCCTAACCATACATCAATGGAAAGCTTATTGATTCTCCAAACAAAGACGACTGGTCATTTATGACTGATTTTGTTGTCCATGGTCACAATGTGCATGTAAATCTAACTGAGCTGTCTCTAGGAGGTGGGTAAAATCGTCATCTACATGGTAGAGATCCTGAACAGAGTGCAGTCCCTCAGTCTAAATTACGGCACAATCACCAGAGATTCGCCTGTAAG[G/A]TACATGTAGTAATTCAGTTACACTGGTTCTCAAACAACCGAGCAGCATTCTGACACATAATATTCCTGTTTTCTCCAGGCTCGTAGTTGAGTGTCGGTATTTACCTGGATCAGTGGTAAGTGTGGGTTACCTGGTTAAAAGCCCCTCTCTTGGACCCTCCATCAAAGCTCAGGGAGTGTTTGGAGTTCAGCTCAGAATTGCTAAAGGTTTGTTTTTAATAGTTTTTGTTTTATTTTTTATTTTAAATATAAACCATCTGCAAGTATATGCTATACATGTGTTTAGGGAAAAGATACATGCGGGTTTTGTGCACTAAATGCCTCTTCTTTTTTCATTCAGATGAGCACTATAAAAACTTTTACCCACAATACCACCAGCCTCTGCAAATGCTGCTGGGGAAACCCCTTTATCTGGAAGTGCGTCTGCTGAACCCTCCGGATCCAACTGCTGTGCTGCTGGTGCATTACTGTGTTGCTTATCCACGCTCTGCAAAATCTGCA
Associated Phenotype:
Not determined