ZMP
zgc:113343
Ensembl ID:
ZFIN ID:
Description:
Zgc:113343 [Source:UniProtKB/TrEMBL;Acc:Q58EF6]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23836 | Essential Splice Site | Available for shipment | Available now |
| sa16871 | Essential Splice Site | Available for shipment | Available now |
| sa9874 | Nonsense | Available for shipment | Available now |
| sa29494 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23837 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23836
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102724 | Essential Splice Site | None | 356 | 1 | 4 |
| ENSDART00000133663 | None | None | 141 | None | 4 |
| ENSDART00000134898 | Essential Splice Site | None | 229 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 2674818)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 2197917 |
| GRCz11 | 21 | 2223741 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGAAACAGTTGTTGGTTATGCCCTCCCTATGCTGTTTTTATCTCACT[G/T]TAAGTACATTCACATTATTATTATTATTTATTAGGAGATATTTAAAACGC
Long Flanking Sequence:
ATAGACATTATACTAAAAATATAAGATGTAAGATAAAAATATACTAAATGTAATAGTCACAGTATTTACATTATGGCAAATGAGTGCAAACATGAATATCCATAAAGTGTCTTTGTGCATTAGCAGCAGAACATCAGAAAGGTAGGGAGTGAGGGAGGGGGGGTGATTGTTAATGTGTACAAAGAGGAGGGGTGGCACAGGCTACAGCTCTGGGGAAGAGCTGTAGCCTAACTTGCACAAACTTGCACAAATCTTTAAAAAGTCAAGCTGCAATCGACTAACGTTTGTTTCTGAAACATTTATGGAGAGAATTTGTGTTTCAGAAAAAATATGTATATATTATAATTTACTATGTATCAGTTTCCGCCTGTGGTGGCGCTCGAGCGCTGGACACAGCGATAAGCATCCGAGTCTACCAGAAGAAGAAGAGCGCAAGAACATAAACATTAGAAGCGAAACAGTTGTTGGTTATGCCCTCCCTATGCTGTTTTTATCTCACT[G/T]TAAGTACATTCACATTATTATTATTATTTATTAGGAGATATTTAAAACGCAGTTTTTTTTCAATTAGTGTCAAACAAGTGATTATTGCTGATGAAAACATCCAGTTATTGTAGATTTTGACGTTGTAACTACTAATAATAATTTGTATATTCGCATTTACTACTTTCTTTTATTTTAAAAATATATTTATTATGTTTTTTGTCCTGTCTTTGTGATTCTGCTGCACTGTAGAAGCTCTGTCACGAAAACAAATTGCTCGTATGTGAGAACACCTGGCAATAAAGCGCTTTCTGAATCTGATTCTAAATCGGACCGTCAAAAATACACTAGACCAGTGGTTCTCAAACTGTGGTACGTGTACCACTAGTGGTACACAGGCTTCCTTCTGGTGGTACGCGGAGGAATGAAATATGTTATGTACATGCTACACACATTTAATAATTTATCAAAAATGATGTATATAATATGCCGTTATTGACATATAGCCTATATTTCTGAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16871
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102724 | Essential Splice Site | 19 | 356 | 3 | 4 |
| ENSDART00000133663 | Essential Splice Site | 19 | 141 | 3 | 4 |
| ENSDART00000134898 | Essential Splice Site | 19 | 229 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 2676638)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 2196097 |
| GRCz11 | 21 | 2221921 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGAGGAAGAACCCKKCAGAATAAAGGAGGAAGAGACAGARGAACAAATAG[G/A]TTTGTGTTTATAGTCTTTCTTAWTARTGACTGAGTAAYATTAAGGGTGCT
Long Flanking Sequence:
ATTTTTAAAGCAAATTCTCTAAATTAAACCCCAAATCAGGGAAAGAAAACTAAAGCAACACATCCCTTTATAGTCTTTCATTAATACAAAAACTATTTACTGAAGTAACCAGGCATTACATAAAATCCTTAGGATTTAGCCCTGTATAAGTCCAAAATTTCATTTATATTTGTTTTAAAAGGGTCCTAAAAAGTCTTAAATTTGATTGGAGGAAACCTGCAGAAACCCTGGTTATAATACAAAGCAGTTGCACTGATGAAATGAAACCAATTTGGAGGACCATCTATGGCACAGGTATTGTCTGCAATTGGGTTCTGTCTTTTAAACAAACAACCATTTATGCTAAACAGATAAATCAGGATATTCCCATCTTCCCACAGCTGAAGAAGTCGCAAACTGGAGGAATTACTGCAGGAGAAACAGCTGACATACTATAGTGAAGATGGAGACTGAGGAAGAACCCTGCAGAATAAAGGAGGAAGAGACAGAGGAACAAATAG[G/A]TTTGTGTTTATAGTCTTTCTTATTAATGACTGAGTAACATTAAGGGTGCTTTCACACCTACACTTTTGTTTCGGAACGTGTCTCGTTTACCCAGTTCGTTTGGCATATGTAAACAGGGCAATCGCGCTCTGTTCCGCGCCAATGTAATCGCTCCGAGATCGCTTGAATGAGGTGGTCTCGGCTCGATTGAAACAAACCCTGGAGCGGTTCGATTGCAGTGAGAAAGCGATCCAATCCGAGCGCGGTTATATCACAGTGTTTTATGGATATGTAATAGGCTTACGGCTATATGAAGAGAGAATTATGAGCATGGCGGGAAGTTTCGCGAGTCTCCGGATGCCCGCAAACAAGTGATTATCTCCCAGGAAATCTCGCGCCTAACTCCCGGTCCTCAAATAGGCATCGTCGCGCACCCTTCTCACCCCTCCCCACCGCATCTCTCCTCAGACACGTCGCTCGCTCGCGCACCCTGTCAATCACCACCAAACCACCACCTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9874
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:
C > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102724 | Nonsense | 174 | 356 | 4 | 4 |
| ENSDART00000133663 | None | None | 141 | None | 4 |
| ENSDART00000134898 | Nonsense | 174 | 229 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 2677971)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 2194764 |
| GRCz11 | 21 | 2220588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCCATTCAGCTGTGATCAGTGCAGYAAAGCATTTACATTAGAAAAATA[C/A]TTMAGACAACATCTTCATGTGCACGCTGCCGTGAAGCCCTACGTCTGCTT
Long Flanking Sequence:
CAAACACCACTGGTTTAATAACCTAATCTTTCCACAGATGCGGATGAAAATGCAGTCAGTTCACAGACTGAAGACACTTCCAGACCAAAACAAGCTGGAAGAACTGCAGTCGAAGGATCTTTCATCTGCTCCGAGTGCGGAAAGAGTTACAAAAGCAAAGACAGTCTTTACAGACACACAAGATTTCACTCTGGGCAAGGCCTGTTCACATGCACTCAGTGTGGCAAGGATTTTGTTCAGAAAGGACAGCTTGATAAACACATGAGGATTCACACCGGAGAAAGGCCGTATGCATGCTCTCAATGTGGAAAGAGTTACAATGACGCCGCTACATTGAAAATGCACACGAAGACGCACAGCGGAGAGAAACCGTTTACGTGCATTCAATGTGGAAAGAGTTTCATATATAGGAAGACTCTAAAGGATCATCAGCTCTCTCACAATGCGGTAAAGCCATTCAGCTGTGATCAGTGCAGCAAAGCATTTACATTAGAAAAATA[C/A]TTAAGACAACATCTTCATGTGCACGCTGCCGTGAAGCCCTACGTCTGCTTCTGTGGGAAAAGTTATACGACAATGAACATGTTAAATGAGCACCAGAGGATTCACACCGGAGAGAAACTGTATCAGTGCTCACACTGTGCAAAGAACTTCACTTACTCAAACTCCTTGAAAGTTCACCAGAGGATTCACACTGGAGAAAAGCCCTATCGGTGCTCTTCATGCGGGAAGAGTTTCACTCAGTTAGCAAGCTTGAAAGCTCATCAGAGGATTCACACTGGAGTCAAACCCTATGTGTGTTCAGACTGCGGGAAGAGCTTTAGTACATCGAGCAGTTTAACTGCACACCGGAGGATTCACACTGGAGAGAAACCGTATCAGTGTTCACACTGTGGAAAGAGTTTCAATCGGACAGGAGGCCTGAAAGATCATCAGAAAGTTCACACTGGGGAGAAACCACACCAGTGCTCCTCGTGTGGAAAGAGTTTCACTCAAATGTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29494
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102724 | Nonsense | 305 | 356 | 4 | 4 |
| ENSDART00000133663 | None | None | 141 | None | 4 |
| ENSDART00000134898 | None | None | 229 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 2678362)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 2194373 |
| GRCz11 | 21 | 2220197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACCGGAGGATTCACACTGGAGAGAAACCGTATCAGTGTTCACACTGT[G/T]GAAAGAGTTTCAATCGGACAGGAGGCCTGAAAGATCATCAGAAAGTTCAC
Long Flanking Sequence:
GAAAGAGTTTCATATATAGGAAGACTCTAAAGGATCATCAGCTCTCTCACAATGCGGTAAAGCCATTCAGCTGTGATCAGTGCAGCAAAGCATTTACATTAGAAAAATACTTAAGACAACATCTTCATGTGCACGCTGCCGTGAAGCCCTACGTCTGCTTCTGTGGGAAAAGTTATACGACAATGAACATGTTAAATGAGCACCAGAGGATTCACACCGGAGAGAAACTGTATCAGTGCTCACACTGTGCAAAGAACTTCACTTACTCAAACTCCTTGAAAGTTCACCAGAGGATTCACACTGGAGAAAAGCCCTATCGGTGCTCTTCATGCGGGAAGAGTTTCACTCAGTTAGCAAGCTTGAAAGCTCATCAGAGGATTCACACTGGAGTCAAACCCTATGTGTGTTCAGACTGCGGGAAGAGCTTTAGTACATCGAGCAGTTTAACTGCACACCGGAGGATTCACACTGGAGAGAAACCGTATCAGTGTTCACACTGT[G/T]GAAAGAGTTTCAATCGGACAGGAGGCCTGAAAGATCATCAGAAAGTTCACACTGGGGAGAAACCACACCAGTGCTCCTCGTGTGGAAAGAGTTTCACTCAAATGTCTAATCTGCGGGTTCATATTGAAAAAATTCACAGCCCAAAGTTGCTTGAATAAGAAATATTTAATCATGTAAAAAATGTAATCTGGATCACATTGATTCAGATTTGAAAATCCCATGTTTTGTTATCCAGGATTAACTGATCTATCTTACTTTTATGACAGTTTTTAAAAGGAACTTTGGGTTGGATCACTGTGATCCAAATACCAAATTTCAGGATTATCAAATCCCGTTTACCACAGCCTTAAATGGAACCAACAGCATAGCCGACTGGTTTAGCAAAGAACAACAAGTAGGCGAAAAACCAGCGGCCACAAACAACCATTGTTTGTTTTAATGGTAAGAACCTGGGGTCCGTTCTTCGTACGTGGATTACTCGGTTAGCTGGATTTGGATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23837
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000102724 | Nonsense | 333 | 356 | 4 | 4 |
| ENSDART00000133663 | None | None | 141 | None | 4 |
| ENSDART00000134898 | None | None | 229 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 2678446)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 21 | 2194289 |
| GRCz11 | 21 | 2220113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCATCAGAAAGTTCACACTGGGGAGAAACCACACCAGTGCTCCTCGTGT[G/T]GAAAGAGTTTCACTCAAATGTCTAATCTGCGGGTTCATATTGAAAAAATT
Long Flanking Sequence:
GCAAAGCATTTACATTAGAAAAATACTTAAGACAACATCTTCATGTGCACGCTGCCGTGAAGCCCTACGTCTGCTTCTGTGGGAAAAGTTATACGACAATGAACATGTTAAATGAGCACCAGAGGATTCACACCGGAGAGAAACTGTATCAGTGCTCACACTGTGCAAAGAACTTCACTTACTCAAACTCCTTGAAAGTTCACCAGAGGATTCACACTGGAGAAAAGCCCTATCGGTGCTCTTCATGCGGGAAGAGTTTCACTCAGTTAGCAAGCTTGAAAGCTCATCAGAGGATTCACACTGGAGTCAAACCCTATGTGTGTTCAGACTGCGGGAAGAGCTTTAGTACATCGAGCAGTTTAACTGCACACCGGAGGATTCACACTGGAGAGAAACCGTATCAGTGTTCACACTGTGGAAAGAGTTTCAATCGGACAGGAGGCCTGAAAGATCATCAGAAAGTTCACACTGGGGAGAAACCACACCAGTGCTCCTCGTGT[G/T]GAAAGAGTTTCACTCAAATGTCTAATCTGCGGGTTCATATTGAAAAAATTCACAGCCCAAAGTTGCTTGAATAAGAAATATTTAATCATGTAAAAAATGTAATCTGGATCACATTGATTCAGATTTGAAAATCCCATGTTTTGTTATCCAGGATTAACTGATCTATCTTACTTTTATGACAGTTTTTAAAAGGAACTTTGGGTTGGATCACTGTGATCCAAATACCAAATTTCAGGATTATCAAATCCCGTTTACCACAGCCTTAAATGGAACCAACAGCATAGCCGACTGGTTTAGCAAAGAACAACAAGTAGGCGAAAAACCAGCGGCCACAAACAACCATTGTTTGTTTTAATGGTAAGAACCTGGGGTCCGTTCTTCGTACGTGGATTACTCGGTTAGCTGGATTTGGATATTGACGATTTGACATGATCCAGGATCGTTTCGTTTTTCAAAGCTGATCCAAGAGTTGTTGTCATAGCAACAGTTCTGCTAGGTCA
Associated Phenotype:
Not determined