ZMP
gb:bc097249
Ensembl ID:
ZFIN ID:
Description:
LOC569692 protein [Source:UniProtKB/TrEMBL;Acc:Q4V8Q6]
Human Orthologue:
C8orf38
Human Description:
chromosome 8 open reading frame 38 [Source:HGNC Symbol;Acc:28625]
Mouse Orthologue:
2310030N02Rik
Mouse Description:
RIKEN cDNA 2310030N02 gene Gene [Source:MGI Symbol;Acc:MGI:1924197]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17886 | Essential Splice Site | Available for shipment | Available now |
| sa28721 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17886
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 |
|---|---|---|---|---|---|
| ENSDART00000075718 | Essential Splice Site | 76 | 343 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 43174911)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 40558361 |
| GRCz11 | 16 | 40508393 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAACTCGACACGACAGCACAATGAACAGTACTGTATTGACAKAGTAAGG[T/A]AAGTTTTGAGTTAAAAGGTTCATTTGCTTKATATAGTTTTACATGGAAGC
Long Flanking Sequence:
CGACTATTTCCGTTCTCCTCAATGAAGGGACTTGAATGTGTGCTGGTCATATGATGAGAACCACGTGATTTAACTGTCAATCATTTACTTGTTTAAAAAACACGTTATTATTTATATATCGCATTCTAATGAGCAATAATCACGTCTTATGTGGAAAAAAAATAATAAATCTTTCTCAGAAACGGATCTTAATTCGGTTCGGATGGAAACCGATTGTTTACATGGAAACGGAACGGACTGTCGGCGTTCCTTGAATACAGAGGAGCTGTTATTTGACGCACACGCGAGAGGAGGTACAGCTCAAGGATACTGGATGCATGAGCTGTGCTATGGCATCCAGCATCAGCATAAAGAATGGATTATTTACCACCAAAAAGTCGCTCCATGTAAATATTCCCAATCCCCGTTGTCTACAGAGGCAAACAGAGATCAAATGCACAAGAGCTGTTACAAACTCGACACGACAGCACAATGAACAGTACTGTATTGACATAGTAAGG[T/A]AAGTTTTGAGTTAAAAGGTTCATTTGCTTGATATAGTTTTACATGGAAGCAAACAGATCTGCAATTTTAGGCAAAACAGTAAGGGTTAAACCTAAAGACAATATCCCAGAAAACCAGAATAATATTAAACTGAATGTATATTTAAAAAGTATATAATATGTATATAATTTAGTTAAAATAATTTAAAAGACAACATATACACTAATTACTTTTTCCTGTGGCTAAAATTAAGATGTAACTGTACAGAACAAGAACAAACTGTAGGGCTGGGCGATATGGCAAAAATGCAATCTTGATAATTATTTTCCATATTGAACAGTATCGATATATATTTCGATATAAGTTGTTAATGCTCCCAGATTTATACGAGTATCTCAACAATGACTGAAGCCACAAAAATTAACATACTTTCAGCCGATAAATTTTCTGTGGTCGAAAAATTTGGTACATCTCTAATATCACATTTTAGTTCTTAAAGCAATATAAAGTGAGAAAGTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28721
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 |
|---|---|---|---|---|---|
| ENSDART00000075718 | Nonsense | 324 | 343 | 9 | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 43154385)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 16 | 40537835 |
| GRCz11 | 16 | 40487867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTGCAGAGAGTGAGGAAAGTCGATTTCGACGTGTTTCACCCCAGCCTA[C/T]AGAAGAGGAATCCAACACTGCCCCTTCAGCTGTATTTACGGTCATGGAGA
Long Flanking Sequence:
CCACGAAGGATTAAGGCAGTTCTGAAGGCAAAAGGGGGTCCAGCCCAGTACTAGTAAGGTGTACCTAATAAAGAGGCCGGTGAGTGTATGTATGGTATAAGTTTTCCAGGCCTTTGACATTGATGAAAATTCTGATGATAAAAAAATACATTGCTATATTGTACAAACTCAATAGACCTTACTGAAGCAATTAAACTCCACAAGATTCACATATTTGTATGTTTCTGAAGTGATATTTCAATCATTTAAATAATCTGTTATATACATATGTTAAAAAGACATGGCACCACTTTATATTATATTACCTGATTCATTTTTGCCTTTCACTTTCTTCTTAGTACTTTTAAAGCATTTCAGTAATGTATCATCCTTTAGGCTCGCTCAGACGTAATTAAACTAAGCTTGTTTGAGCTTCTTTGTGTTCTGTGCCTCAGGTTGTTTTGGAGGACTACCTGCAGAGAGTGAGGAAAGTCGATTTCGACGTGTTTCACCCCAGCCTA[C/T]AGAAGAGGAATCCAACACTGCCCCTTCAGCTGTATTTACGGTCATGGAGAAAGATCTATTGATCATCTGCTTTTTAAGATGAGCTCCTTGTCAAACGAACCAAGCTCTTGCAATAAATGATCAAGCTACTGTTGACAGTTATTGCTGTCGTTTTTCATGCTAGTACAGCTAGAAGAAGTGTTTGATTATTAAATAATTAGTATCCGTACAGAAAATAACCACAAATAACAGCAAGACACATTCTGGGAGATGATAGAATCTGGTTTGGATTTGTTCAAGTGTTTGAATAGTGTTGGTGGCATGAATTGACGCAATTATTTTAACAGTTTTTTTCTTTAATTATTTCAGGCATTTGTGAACAAATTGACAACAGTGTTACATATTTATAAGTGAGGGATGTGTCACATGCCTCTTCTGAGGGGCAAGGTCTATCAATTCTGTTTCCCATTGCATGTTCAAGTGTGGAGCAAGGTGCCATTTTTTTAGTGACACAATCAAGA
Associated Phenotype:
Not determined