ZMP
zgc:63792
Ensembl ID:
ZFIN IDs:
Description:
acidic chitinase [Source:RefSeq peptide;Acc:NP_956740]
Human Orthologue:
OVGP1
Human Description:
oviductal glycoprotein 1, 120kDa [Source:HGNC Symbol;Acc:8524]
Mouse Orthologue:
Ovgp1
Mouse Description:
oviductal glycoprotein 1 Gene [Source:MGI Symbol;Acc:MGI:106661]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37660 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43941 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa24287 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37660
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012540 | Essential Splice Site | None | 475 | 1 | 12 |
ENSDART00000104618 | None | None | 481 | None | 11 |
ENSDART00000125486 | None | None | 481 | None | 11 |
The following transcripts of ENSDARG00000008541 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 18097252)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 18000191 |
GRCz11 | 23 | 17926534 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACAGTGAGGGAAAAACAAAGGAGACTGGAGACCTGAGCGACAGAACAG[G/T]TAAATAGTAACATTGTAGTGATCGTTTTTATGCTCTTCTTACTCTACATT
Long Flanking Sequence:
TAATTATTTTATGACTACATATTAATATTCGTGACAATTGTGAGGATTTTGTGTCGCTCTTTCATGCCATGTGGTCTTGTTTTCTTCGCAATGTGTATAGCGTTCTCTCTGGTCGTGTCATGTGATTTGTTCCCCTTCCTGCCTGTTATTAGTGTTTCGCATGTTGCGGCTGTGTAAGATTCCCTTCACCTGTCTTTGTTTAATCAGTGTATGTATTTAAGTCCTGTGTCAGGCAGAGCTCTGATGTCTTCACTTGTAAGTGACTACTGTGTTCCTGTTCAATTGTTAAAATTTGATTAATAAATTGAAACCTTTTATATACGGTTATCAAAGCATTTGTTAAGAAGATTATGACAGTAATAATGACTAGGCAAATTTTATATAAAAAAAGATAAAATAAAAAAGTCTGTCAGATACTTTCCTTATATTTTCAGGTAGACAACAGGGATCTAACAGTGAGGGAAAAACAAAGGAGACTGGAGACCTGAGCGACAGAACAG[G/T]TAAATAGTAACATTGTAGTGATCGTTTTTATGCTCTTCTTACTCTACATTTGACATGTGCTCTTGTTTATTCAATCTTGATTTCGTGCTTGATTTATGCCATTAAAAAAAACCTAGTGCATTTAATGGGTTTCCATGTCAAGTAAGAACATGCAGACCACTGAGGCCAGATTGCAATGAGCATCTATTTTTCTTGTCTGTTAATTCAGGTCTTGGTTAATCATCACGTATAGGAGTGAATTTAGTGTGTGTGGGTTAAAAGCTCATACGGCTTACTCCTGACTGATATAAACATCATTCGAAGATGACCGGATTCATTTTTGTAGCTGGTGAGTGATGGAGATATAAAAATATATATAAAATATATGTAAAAATGCTTTTATATATAATTTGTTTAAAACTGAATTTGGTTTTTACTTTTGTTATTAGGCATTTCCTTGGCATTGTGCCAATGTGGTAAGTTTTCTTTGTTTTAAAACTTAATGGAAAATGCCTTTTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43941
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 |
---|---|---|---|---|---|
ENSDART00000012540 | None | None | 475 | None | 12 |
ENSDART00000104618 | Essential Splice Site | 86 | 481 | 3 | 11 |
ENSDART00000125486 | None | None | 481 | None | 11 |
The following transcripts of ENSDARG00000008541 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 18113487)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 18016426 |
GRCz11 | 23 | 17942769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATGGAATGATGAAACTCTCTACCAGTCCTTTAATGGCCTAAAACAAAG[G/A]TGCGCTTATGTTTTTTCCATGCATATATTTGTTTAATCTACTATGTAATG
Long Flanking Sequence:
CTTGCGTGCGTGCGTGCCAGAAGTTGCCTGCTCTTGTATCGTAAGTTTTATTTCTGTGTGGTGATGTACTTCCAACTAAAATGGAAATATTAAGTAGGGCATATATAAGGGTATAAACCTTTTATATATACAGTATATTTATATAAATATATATGTATTTGAAGCTGAAACTACACAGACACATACTAAGAACACCAAAGATGTATTTAACATCTTGTAAAAAAGGGGCAAAATGGGTGTAAAATATGTATATACATGTATGTGTGTATATATGCTTTTTATTTGTTTGTTCCAGGATTGGCCTCCCAACTTATATGTTACTTCACCAACTGGTCTCAGTACAGACCTGATGTTGGCAAGTACATGCCATCCAATGTGGATCCACATCTGTGCACTCATTTAATTTATGCCTTTTCCATTATTAATAATGAAAATAAACTGACAACCTACGAATGGAATGATGAAACTCTCTACCAGTCCTTTAATGGCCTAAAACAAAG[G/A]TGCGCTTATGTTTTTTCCATGCATATATTTGTTTAATCTACTATGTAATGTAATCCTAAAAGTCACTATTTGCTCTAGAGTATTATAGTGAAGAATAATGCTAAATGTTTAACTTAACAGTAACTCCAACCTGAAAACTCTGTTGGCTGTTGGTGGATGGGAATTCGGCTCAGCTCAGTAAGTTCTGCTGTATTTTGATAGATCAGAATGTGTTACAGATATAACCCTCGTTCCACAAAGAAGGAAATGGAAATGTTATGTTGGTACAACAATACTCAACAACAATTGGGTTATTGGCAGATAACTATTCACTCTAAGAAAGAGGTCTGACTCAAAAGCTGCGGTCACACTGGGCTTTTCCTCCCATAGACTTTCATTCATACGCAAGCGAATGCGTCAGACCGGAAACACAGGGTCATGGTCTAGTTTTGCAGGTTGCTGTGGTGCAAAGTTCAAGCTTGGTGAACTCTGACCTGCGAAATCGCATCACTTGACTGCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24287
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000012540 | None | None | 475 | None | 12 |
ENSDART00000104618 | Essential Splice Site | 343 | 481 | 9 | 11 |
ENSDART00000125486 | None | None | 481 | None | 11 |
The following transcripts of ENSDARG00000008541 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 23 (position 18117819)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 18020758 |
GRCz11 | 23 | 17947101 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGACAGGAGTGGGTGGGATTTGATGACCAGGAAAGCTATGAGACTAAGG[T/A]GAGTATGCTAAAGTATAAAACATAAATGTATTTCTCATGCTCTCGGTAAC
Long Flanking Sequence:
GATGTTTAAATAAAATTTTGGTAGCTATTCAGATATCTTCAATGCAACACTTGAGTCACTGCAGGTTAGAATAGTCTAGAAACACAACAGCAAATAATTAAATGCTCATGACAATGCAGGACTTTGCAATGAACTACTGGCGAGATCAGGGCGCTCCTGTGGAGAAGCTCAGGATGGGCTTTGCTGCGTATGGAAGAACGTTTCGCCTGTCGTCTGCGGACAATGGAGTTGGAGCTCCAGCTAGTGGTGCTGCTTTAGCTGGAACATACACCAGAGAAGCTGGATTCTGGTCCTATTATGAGGTCTAATCTTCAGCCTTAAAGCATAATTTTTATTGTGGAAATACAATCAGAAGATTTCCTGACAGATCGTCTCCCAACAGATCTGTACTTTTCTACAAGGAGCCATTGTGCAACAGATTGTTGATCAGAAAGTTCCTTATGCAACAAAAGGACAGGAGTGGGTGGGATTTGATGACCAGGAAAGCTATGAGACTAAGG[T/A]GAGTATGCTAAAGTATAAAACATAAATGTATTTCTCATGCTCTCGGTAACTAGGTCTGGTCTGTTTTAGGTGGACTACCTGAAGGAGAAAGGCTTTGGAGGAGCTTTTGTCTGGTCTCTGGATCTTGATGACTTCAGTGGTCAGTTCTGTGGGCAGGGCAAATACCCTCTTATTGGACACCTCCACACGCTGCTTAATATCAGCAACACTGGTAAAAACATCTCTGTGAAGCCCATTATGATGATATTAGTGCCATTAAATCATTGTGATTGACCAGAACCAATTATTTCTGCAAACCATCCAAGCTGATTAATACTTTTAAGAGAAAATATAAAATTCTAATTTTTTCCTGCAGATTTCCCATCTCTCCCCCCAAGCACAACAGATAAGGCCAGTGGGACCTCTACAACAGCATCTGCTGCTGTACCTCATACCACAATACCTCCTGTTGTACCGACAGCTCCCTCAGGATCAGACTTCTGTGCAAGCAGATCAGAGGG
Associated Phenotype:
Not determined