ZMP
si:ch211-284d12.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S5K8]
Mouse Orthologue:
Zan
Mouse Description:
zonadhesin Gene [Source:MGI Symbol;Acc:MGI:106656]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa19869 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa33019 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa39929 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa44549 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa6863 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19869
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 |
|---|---|---|---|---|---|
| ENSDART00000109324 | Essential Splice Site | 40 | 667 | 3 | 9 |
| ENSDART00000144438 | None | None | 56 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 47396075)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 47401351 |
| GRCz11 | 2 | 47253043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTTTGATTTTGTATTGTCCTTTAATCACCTCTCCCTCCTACGCTGTA[G/A]ATTATTTGGCAAAGTGTGACTTTGGCAGTGACTTGCCATCATCTTGTGAT
Long Flanking Sequence:
GGTCGGGAACCACTTGTGTAAATTATAAAAATTACAATAAAGCTGTCAGTTGTTCACACAATTACCGTTTTCTATATGGTAAAAGTGCACTATATAGGGGAAAAATAGTTCAGATATTTTTTAAAGGGGAAAAGCTGAACAATATGCCCCGCCCTGTCTTGTTGTTCCAGTGGAAATCACGTCAACACATCGAATAACACTCTATGTTTCAAGCCATTTCAAGGGATCTTTAAAGTAAAGTGTTAACACAAACACTTCAGCGGTAGAGGACCTGTTTGAAACCCATCAAGCTCTGATGAGTTTGAACTTTTTCAGGCCACTACAACCCCAGTGTGACCAATTTCTCGCAAGAGTAATCTCTGACACCAACATCTGTTATAACAAGACAAACTGAACCATGTTTTCAGTTTGTTTCTAGTTTTCGATTAGGCTCTTTTTCTTTCCTCACTCTGCTTTTGATTTTGTATTGTCCTTTAATCACCTCTCCCTCCTACGCTGTA[G/A]ATTATTTGGCAAAGTGTGACTTTGGCAGTGACTTGCCATCATCTTGTGATTGGACCTCAGAGGGCCCCATCAGCGCTCAGACGGCAACAGGTAATTATACTGCTGAGATCAAATTGCTGCAGAGACTGTCACGCTTTTGTGTTATTCACTGTTGTTTACCGCCAATCCATTCACCTACGACAACAACAACAGCTATTTAATAGCTTGGTAACAGCACGTAGCAGAGCTTCTTTAATACTTGTTATTCTGTTCTTCAACTTGACTTTCAAGTACACTAATCACAACATTCATCCTCTTGTATGATATACAGCATTGATTATCATGCACACAAGCTCAGAGCAGAGTGCAACCAGAGTCTACAATGTTGCATGATTGCAAGCAGAATTAGCATGTTGTGACCATGTTTCTAGCATGAATCAGCATGATTTTAGCATGAATTAACATGTTGTTAGCATGATTCTAGCGAATTAGCATGTTTCCAACATTGATTAACATGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33019
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109324 | Nonsense | 117 | 667 | 4 | 9 |
| ENSDART00000144438 | None | None | 56 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 47404299)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 47409575 |
| GRCz11 | 2 | 47261267 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAATGAAAAAAGCTCTGATCTCAATGTTCTGCTAGTGGATGGCATTCTG[A/T]AAACGCTGATTTGGACCTCAGAGGGTTCCGGCGTTGGAGACTGGAGACAA
Long Flanking Sequence:
CTAAATTCATGGTTGTTACCATTAGTTGAAACACTGAGTTAACAAGGACTAACAATGGAAAACTTTAATTTCATTATCTAACATTAGCAAATATATTTAAATAAAAGTAATAAATGTATTGTCCATTGTTGGTTCATGTTAGTAAATACAAAGTAACATTAAATGATGGGACGTTAGAGTAAAATGTTACCAAAACCATAAACACATAAAAAAATAAAACTAAACTAATAAATATTACTTAAACATTAACTATATAATATCTAATTTAATCTATCACCAAAAAAGCGCATAAGGGGTGGATGAGTTGTCTTGCAGGCCACTAAAAATCCCTCATTTTTTCCATTTCTGTCTGCATTATAGAGGAAAAGAGTCCATCTGGTGTGTTTCATCTTAAGAGTGGACCTCTTAAGATCACAGAAGACTGGTGTCTGGAGTTCTGGTACCACAAACCCAATGAAAAAAGCTCTGATCTCAATGTTCTGCTAGTGGATGGCATTCTG[A/T]AAACGCTGATTTGGACCTCAGAGGGTTCCGGCGTTGGAGACTGGAGACAAGAGTTCATCACGATCACAAAACAATCTGATGACAGCAACATCCAGGTACTGTGCAGCCATTCAAAGATTTAGATTTAGGTGTTGGGAATCTTCCAGTGGAAAATAGCTGATAATGTTAAAACATATCTTAGGGTGCATTTAAATGCCACTGATTTTATTTAAAAAAAGAAGATTCTTAAAAAGTTTTCAAAGATTGTCACAAGCCAACAAAGAGTCTCAAGAAAATTAAATGCACATAAAAAAAGTTAACAAAATCAAATGAGAAAAAAAGTAAAAACAGCTTTGTAGAAATATACAGATATAAATATAGCCAATGAAGACAGATTTGAAGAAAGGAGTTGAAATAGAAAGAGAAATTGTCACGGCCAACTGAGACTGGTTTCTCTCGAGGTTTTTTTTTTCCTTCACTTTTGTCAATTCGTGAAGTTTGTTCCTCACCACTGTTGCGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39929
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109324 | Essential Splice Site | 176 | 667 | 5 | 9 |
| ENSDART00000144438 | None | None | 56 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 47406207)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 47411483 |
| GRCz11 | 2 | 47263175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GATGGAAAAACTGCTTTTGACAGAATGGGAATACACAAGGGACGATGCGG[T/A]GAGTGGCTAATGATTATTATTATTTTCTTGATGACTTCACCAAGACTTCA
Long Flanking Sequence:
GTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATTAAAGTCAAGTCAAAGTCAGCTTTATTGTCAATTCAGCCACATGTACAGGACATATAGAGAATCAAAATTACGCTACTTTCAGACCCCAGGAGCCTAACATATAATATTAATACAAAAAGTAGAGTTCATGTGTGTTTCTAAGTGCTGGGTTGTGGCTGGAAGGACATCCGCTGCATAAAACAAATCCCAGAGTAATTGGTGGTTCTTTCCGCTCTTGCGACCCCTGATAAATCAGGGAATAAGCCTAAGGATGGAATTGTCAATATCTATATGGCATTAATTTCTCTGTTCACAAAAGAATTAGTATAACCATTGCCTGCTTCAACCAACTGCTATTGTGTTTCTGGCAGGTTCTTTTTGAAATCTCACAAGGCCTGCATGACGATGGAAAAACTGCTTTTGACAGAATGGGAATACACAAGGGACGATGCGG[T/A]GAGTGGCTAATGATTATTATTATTTTCTTGATGACTTCACCAAGACTTCAATTCACCACATTCAAATAAGTTTGTAACATGTAGAGATCTCATCCATAGGTTTACAATGTCAGCGGGGCACATTTTGGACTGATGAAAGCACTCGTTGCACCTGTAAAGACAATCAACTTGTCTGTTCTCACATGCCCTGGTCCAACGACACGTTTGGCACCTGCCACGTGGCCTCTAACCCACACTACACGACTTTCGATGGGGTCAGCTTTCAGTTTGACAGTCCCTGTACGTACATCTTGTCAAAGGTGTGCGATGATTCAGGACTGCTTCCGGAGTTTGCAGTGGAGGTGCAGAATGAGAAGAAAGAAGAATCGCACGTGACCTCCATTCAACAGGTCAATGTCAACATATACGGTCTGAGAGTGTCCATGATGAGAGCAGAGAGGAGCAAAGTCATGGTGAGGCATCAACTATGAAACCTCATGATTAAATATGAGCAGAGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44549
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109324 | Nonsense | 271 | 667 | 6 | 9 |
| ENSDART00000144438 | None | None | 56 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 47406591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 47411867 |
| GRCz11 | 2 | 47263559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGGAGGTGCAGAATGAGAAGAAAGAAGAATCGCACGTGACCTCCATT[C/T]AACAGGTCAATGTCAACATATACGGTCTGAGAGTGTCCATGATGAGAGCA
Long Flanking Sequence:
TGCTTCAACCAACTGCTATTGTGTTTCTGGCAGGTTCTTTTTGAAATCTCACAAGGCCTGCATGACGATGGAAAAACTGCTTTTGACAGAATGGGAATACACAAGGGACGATGCGGTGAGTGGCTAATGATTATTATTATTTTCTTGATGACTTCACCAAGACTTCAATTCACCACATTCAAATAAGTTTGTAACATGTAGAGATCTCATCCATAGGTTTACAATGTCAGCGGGGCACATTTTGGACTGATGAAAGCACTCGTTGCACCTGTAAAGACAATCAACTTGTCTGTTCTCACATGCCCTGGTCCAACGACACGTTTGGCACCTGCCACGTGGCCTCTAACCCACACTACACGACTTTCGATGGGGTCAGCTTTCAGTTTGACAGTCCCTGTACGTACATCTTGTCAAAGGTGTGCGATGATTCAGGACTGCTTCCGGAGTTTGCAGTGGAGGTGCAGAATGAGAAGAAAGAAGAATCGCACGTGACCTCCATT[C/T]AACAGGTCAATGTCAACATATACGGTCTGAGAGTGTCCATGATGAGAGCAGAGAGGAGCAAAGTCATGGTGAGGCATCAACTATGAAACCTCATGATTAAATATGAGCAGAGTGCATACTAATGATAGAGGGGTCAACTTTTTATTAATATTAGTTTGTGTTATACATGCTTCAGTGAATCAAAATTAGATATATAATCCAAAGACATCACTTTATTAATCAAACTTATTTAAGATTTCAGTGAGGTATATTGACCTACATTGATCTTTGATAAGCTATTTCATTAGATGTGTGATTCTCAAATACAAGATATGTTGATATAAAATATGGTGACAAGTTTGCATCCTTAAGGCCGATTCATGCTGCAGAGATGAATGCCAACACACACCAACAAAAGAAGTTGGTCATTGTATTAAGAATATTTCCCTTTCTTGTTTTGTTTTTTTACAATGCTCAGATGTTCAACGATCCAACAAGCACTGATTAAAACTGTTCAGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6863
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 |
|---|---|---|---|---|---|
| ENSDART00000109324 | Nonsense | 510 | 667 | 8 | 9 |
| ENSDART00000144438 | None | None | 56 | None | 2 |
Genomic Location (Zv9):
Chromosome 2 (position 47412215)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 2 | 47417491 |
| GRCz11 | 2 | 47269183 |
KASP Assay ID:
554-5199.1 (used for ordering genotyping assays)
KASP Sequence:
TGCTCCAGCCTAGATGCCGCAGGGCCTTGTGGGAATTGTGAAGAGCGCTG[C/A]GAGTGTGACGATGGCTTTATACTCAGCGGAGGAGAGTGTGTGCWGGAAAA
Long Flanking Sequence:
GAATTAATTAAGCAAATCACTGTATAATGATGGTTTGTTCAATAGACAATCAAAAATAAAATGTTGCTTAGGAGGGCTAATAATATTGACCTTAAAATTGTTTTTAAAAAAATTAAAACTGCTTTTATTCTAGCCGAAATAAAACAAATAAGACTTTCTCCAGAAGAAAAAATATTATAGGAAATACTGTGTAAAAATCCTTGCTCTGTTGAACTTCATTTGGGAAATATGGGAAACATTTGAGAGGGTTAATAATTCTGTCTTCAACTGTGCATAGTCATATAGTCATATACATTCTTCCACACCTTTGACTGGAACATCCTGCTTTAAAGATACTTGGAAACGTACTGTAAATCTATCAGAGAGATTGATGACAATGTTTGTGTTGTAGCGGTGGAGTGCGGTCTTCACAGTCACTATAATGCCTGCGCCAGCGGCTGCCCTCAGACCTGCTCCAGCCTAGATGCCGCAGGGCCTTGTGGGAATTGTGAAGAGCGCTG[C/A]GAGTGTGACGATGGCTTTATACTCAGCGGAGGAGAGTGTGTGCTGGAAAAAGACTGTGGATGCTGGGATAATGGACAGCATTATTCGGTAATAAAGCAGCTTAGCCATATAAAATATAAAATGATAATAAATTATTTAATACAATGAACACTATTATTCCTATTATTATTTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTGTAGTTGTTGTTGTTGTTGTTGTTATTGTTATTATTATAAAGCAATTTACAGATATTTTATAATTGCAGGTATTTGTAATAATAGTTATATTTTCATTAAATCAAGTGTATAAAATAATGTGGTACATTTAATTAACATTTAGTTATTATAATTCTAATAATTCATAATACACATATACGTTTACATATACAGTTATATAACATTTAATTATTATAATTATAACAATTAATTACAAGTAATAAATGAGTATTAGATGTACATTTTATATATATAAATGTA
Associated Phenotype:
Not determined