ZMP
si:ch73-92e7.2
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC100126120 [Source:RefSeq peptide;Acc:NP_001103318]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa29690 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa43746 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa29690
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 |
|---|---|---|---|---|---|
| ENSDART00000106329 | Essential Splice Site | None | 452 | None | 5 |
| ENSDART00000106406 | None | None | 452 | None | 5 |
| ENSDART00000106425 | None | None | 452 | None | 5 |
| ENSDART00000115348 | None | None | 452 | None | 5 |
| ENSDART00000145611 | None | None | 16 | None | 2 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 1611575)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 2352665 |
| GRCz11 | 22 | 2368931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACGTCAGCGCTGACGCGTTCATTCAGCGTCGAGTCTTCAGAGCTGAGG[T/G]GAGTCGTTGACGCTTTTTCTCGTGTTTACACGACAATAAAACACACTTTA
Long Flanking Sequence:
AGAAACTTTAGTTTGTCGCTTGTTTAATTGCATAGTTTAGTATATATATATATATATATATATATATATATATAATAAACTATGCATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATAAACTATGCATATATATATATATATATATATATATATATATATATATATATATATATATATACATATATATAATCCTTTATTGTGTTATAAACATTTGTTTACTGAGTTAATGACATGTTTTAGAAGTTTTATCTCTGCCATACAACATTACGTTTGACGCTATTAATTAATATAAAGAGTATTTCGCCTCACAAATGAATAAATAAACTGCCTTTTTGTCTACATTTGCAGTTGTTTTGGATTGTCAACGGTATTTTTAATTTGGTGCGTTTTTGACGATCAGTTGTTCCCGCCTCGCCGTGATGACGTCAGCGCTGACGCGTTCATTCAGCGTCGAGTCTTCAGAGCTGAGG[T/G]GAGTCGTTGACGCTTTTTCTCGTGTTTACACGACAATAAAACACACTTTACAGTTTATTAAAGCGACAATCTGCAACTAGTTTCTGCATTGAGTTCACCTCTGTCTGTATGTCTGCTGACCAAAACAATACAGCAGGCAGAGAGCAGCTCTGAGAGGACAATGTTAGCTCAGTGTTTGTGTTTTTCTGATTGTTCGTTTTTAACAAGTAATATCGTGTGTTATTACCCGTGAATATAATGGGAAGTCAGTTTGGCAGATATATGACGTTAGATACTGAAAACATTCGTTTCTGGTTATCTTTTAAAAGTTTTCTGTTTTGTCCGTTTCATCACATTTAATGGGACATTCCTATCGTGGCTGAATGTACCTAAACATCAACCAGAGAAACCCAAATGACAACTGTACTTGTAATAACCATAAATACTGTAAAAAGGACGAGTCATAATCAAATAAAGTGAAAAACAATACTATTAGGAAAAACTTAACGTGGCTTATTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43746
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000106329 | Nonsense | 232 | 452 | 5 | 5 |
| ENSDART00000106406 | Nonsense | 232 | 452 | 5 | 5 |
| ENSDART00000106425 | Nonsense | 232 | 452 | 5 | 5 |
| ENSDART00000115348 | Nonsense | 232 | 452 | 5 | 5 |
| ENSDART00000145611 | None | None | 16 | None | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 1763452)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 2504542 |
| GRCz11 | 22 | 2520808 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTATTCATGTTCTGAGTGTGGAAAGAGGTTTACACTGCTGCCATATT[T/A]AAAAAAACACGTTAAGATCCACACTGGTGTGAAAGAGTTCGTCTGCTCTG
Long Flanking Sequence:
GCCAAAAGAAAATGAATGAATGAATTGACCATCGATTGAAAGGGTCACTGACAATCATTGATTAATCATTTGCTTCCCAACTTGACATTTTTCCTACTTTTTCTTCATTTCATTTTTAGACCTGACGGTGAAGAAAGAGGAAAGTGAAGAACTGTGTGAAGATAAGAAAGTCTATCAAAGCGTTCAAACAGAAGTGAAGTCAAATACTTGCTCTTTGTGTGGAAAGACTTTTATAAAGCCATCGTATTTAAAACGACACCAGAGGACTCACACTGGAGAGATACCGTACACATGCGATCAATGTGGGAAGAGTTTCAACAAACCATCAACCCTTAATCAACACATGCTGATCCATACTGGAGAGAAAACACACAAATGTGATCACTGCGGCAAAACATTTCTAGAGCCTTCAGATCTAAACACCCATCTTACAGTTCACACAAAAGAAAAGCCTTATTCATGTTCTGAGTGTGGAAAGAGGTTTACACTGCTGCCATATT[T/A]AAAAAAACACGTTAAGATCCACACTGGTGTGAAAGAGTTCGTCTGCTCTGAGTGTGGGAAGAGTTTTAATACAGCCCGAAACTTGAAACAACACCAGATGATCCACACTGGAGAGAGACCTTACAAGTGTTCACACTGCGACAAGAGCTTCATTTACTTACAAAACCTGAAATCACATCAGAGGACTCACACTGGAGAGAAACCACACAAGTGTTCACACTGCGACAAGAGATTTGGTAATTTACATAACCTGAAACTACACCAGATGATCCACACTGGAGAGAGACCGTACAAGTGTTCACACTGCGATAAGAGATTTAGGCAGTTACAGATTCTGAAAAACCATGAGAGGACTCACACTAAAGAGAAGCCGAACACATGTACTCAGCACACATGTACTCAGTGTGGAAATAGCTTCACAAAATCACTACACCTTCAATGGCACATGATGATCCACCCTGGAGAGAGGCTGTACAAGTGTTCACACTGCGATAAGAGAT
Associated Phenotype:
Not determined