ZMP
B8JLN9_DANRE
Ensembl ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B8JLN9]
Human Orthologue:
KIAA0664
Human Description:
KIAA0664 [Source:HGNC Symbol;Acc:29094]
Mouse Orthologue:
1300001I01Rik
Mouse Description:
RIKEN cDNA 1300001I01 gene Gene [Source:MGI Symbol;Acc:MGI:1921398]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa38662 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa21182 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38662
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 |
|---|---|---|---|---|---|
| ENSDART00000133518 | Nonsense | 142 | 641 | 3 | 11 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 4693325)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 4436356 |
| GRCz11 | 8 | 4493062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTCTTGACCCCATGATGGAGCTCCAGGACATCAAAGGCTTCAAAGCT[G/T]GAGTTACTCTTCGTCTAGTGGAAGGTAAACTGGAGGAGCTCTACTTTAGT
Long Flanking Sequence:
CACGATGGTGCAGTCATGTGGTAGAGGTGTATTGAGTATGCAAAAAAAATTGACCGTAGTGTATGAGTGTGTGTGTGTTGGGTTGCTGCTGGAAGGGCATCTCCTGCGTGAAACATATGCTGAATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAATGGACTAAGCCAAAAAAAAATGAATGAATGAATGAGTTTGGCTGGATTAACTAGTTAACTCTCTCCATTTCCTGATCTTTCAGAATGAAACGCTTACTTTACTACATCCAGTCAGCTTGCAGTATAAAAATCAAGCCACGCCCACTTTTTTCTCATATAATATTCCATTTTTATTCCATGTGCAGGTTCATGGGTTCTGGCTGGTCCAGGATGCCATTATGAGTGTTTTGGGCAGAGAAGAGGTGGCGCCACGCTCGTCTGTGGCTTTGGCCCTTTCAGGAGTAACTCTTGACCCCATGATGGAGCTCCAGGACATCAAAGGCTTCAAAGCT[G/T]GAGTTACTCTTCGTCTAGTGGAAGGTAAACTGGAGGAGCTCTACTTTAGTTCATTTCTAATGGGGGATATGCGCAAGGACTTTTCATTTTCAGTCAGCCAGCTCAAACGCTTCTTAAGGACTGTTATACTGTTACAAAATCGATATTGATTAAGATCTGATTTCTTTCAAAGCAACCTTCTTCACTGCCTGATTGATATACAATATATAGTGGGTCTTAGAACGTACAAGAAGCACTGCATTCATTTCCATTGTTTTGTGCCAGGTCTTTAAAATATGGAAATGTATTTTACTACAGTATTTTCAATGGAGTCTCTGCTCTCATCTGCTACTGCTGCTGACGACGCTTACATTTAGACAGTCTTTCATCTTTTTTTACGCTTGAACAACAAAATGAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATATATATATATATATATATATAAACACTAGGGTTTTAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21182
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000133518 | Essential Splice Site | 296 | 641 | None | 11 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 4683315)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 4426346 |
| GRCz11 | 8 | 4483052 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAAGCAGTGTGACATCACTTCCTGCCCACGTGGATTTTACCTGAACAGG[T/C]ACGAGAGTTTCATTTCAGAACTGCATTCTGCTCTATTTCTGCATTACAAA
Long Flanking Sequence:
TTTATGCCCATGGCAGTGAGACTATTTACATGTTTATATATGTGTATCAGAAGCCCCTCCCACTCTTCACTCAAAGAACAGACGGACCAATAGCAAAACAGAGCAGTCTACTGAAGCCCCGCCCCCTCCCACCTACATTCTGCCCGGAGTTTCAGAAGTTCCTCCTTTGACAACCCTTCTGCCCACAAACACACACAGTGAAGTATGTTAAACAAAACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAAACCTCTTCTGAGCTTATAATAAACTGATTCCCCTGCAGGCTCCCAGTTACCTGCTGGATCTTTCCCTCAGCTGCTGGAATCCTCCTCCTGGTTTCCGGAAACTCCAGGGCGACTTCTTTTATATCAGTGTTCACACTTTAGAGGGCAAGCAGTGTGACATCACTTCCTGCCCACGTGGATTTTACCTGAACAGG[T/C]ACGAGAGTTTCATTTCAGAACTGCATTCTGCTCTATTTCTGCATTACAAAGCCATTTTATTATGATTAGTAGTGGTATGTGGTTACAAATAAAAAAAGGACTATGTTACAACATCTTTGCCGTATGTGCATTTTGATGTACTTGTAAAAAGTCCAAATTACAAAATAAAATGTCTGGATTTATTATTTTAATGTAATTAATTGGCAAAATATGCTTAATTGTTGTGGAAATAATGTTGTGATGACAGAAATGATTACAGTGCTGCAAATAGAATTTTGCGTTTATGTATGAGCTGATAAATGATGGAGACCTGTGTGTTTGTGTGGGTGTTTCAGGTCAACTCTGGACGTGTTTGATCCTCGCCCTGCTCAGTCTACTCCAGTGTGTCACTGTCTGACCGACCTGCTGTCCCACATCAGCCCACAGTTCAAACACACACTCAGCACACTGCGGCACAGGTAACACACTCGCACACTCACAAACGCATATGGGCAATATCA
Associated Phenotype:
Not determined