ZMP
si:ch211-166a6.5
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:B0S504]
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 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21182 | Essential Splice Site | Available for shipment | Available now |
| sa13449 | Essential Splice Site | Available for shipment | Available now |
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 |
|---|---|---|---|---|---|
| ENSDART00000114890 | Essential Splice Site | 254 | 1315 | None | 27 |
| ENSDART00000141915 | None | None | 717 | None | 16 |
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
Mutation Details
Allele Name:
sa13449
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 |
|---|---|---|---|---|---|
| ENSDART00000114890 | Essential Splice Site | 970 | 1315 | 20 | 27 |
| ENSDART00000141915 | Essential Splice Site | 372 | 717 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 4656038)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 4399069 |
| GRCz11 | 8 | 4455775 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTYAGTCTKCTGGCAAAAGTTGCYYATGTTCAGGGTCATCCTGCTGAGG[T/C]GTGTTNNNNNNNNNNNNNNGGGTGTGTCTTCCTWCCCAGTGTGTCCAAAA
Long Flanking Sequence:
AGAGTGCTGAGACATGCCATTATACCACCTGACTTTGAAAATGATTTTTTCAGTCAATGTCCGCAGGAAACTCTTTCTCATTGCTGTGTTTTGTGAACGTCCCGCAGCTTCGTCTCAGAGAATATGCCTTTGACAGTCGTAACAAAGCTCCCATCTCTCCTGATGATGTGCTCAATGTTCTTCCTGTCGTCAAACACATCACGATGACAACCAGCGACGCCACGCGGATGTTCATGGCGGCCCAAAACAGCCTTCAGAAAGGTATTCATCGACCAATATGATAGTATTAAATGCTTTTTCTATGATAGTTGCTTGAAGCTTTTATTGTGAAATACAATATTATAATGATCTTCCCGTAGGTTTGCTGGAGAAGGCGTACGAGCAGCTGAAAGAAGCGTCGTATCTCTTCAGTCGTGTGTGTGATGATCTTCATCCTGAAGCCTGTCACTGTCTCAGTCTGCTGGCAAAAGTTGCTTATGTTCAGGGTCATCCTGCTGAGG[T/C]GTGTTATGTGCACTATGTAGGGTGTGTCTTCCTTCCCAGTGTGTCCAAAAGCACAAATAGCCCAAGGGTTAGAGTACTAAAGGGTTACTAAACCTTACTAAGGGGTTTAAATACAGTTGTGTGTGAATACAACCAGCTTCTAATGATTAAAATGTACAAATAAATTTCTTTTTCAATCACACTTGATAAAAACAGTCTGCAGAAACACTGTGATTGACAATCTCCCTTCGTACAAGTCATCAGAGGGGAAAAGCTCCGCCCATCTCTCCCTCATTAGCATAGCACATTAGTCTTGCTTCTGAATCTGCCAATATGCTGACACACAGGCATTCGTAGATCGGCCCTCTTTAAAAAAAGAGCACACTCTCATTTGAATTTAAAGCGACAGTCACCAAATTGCCACAATTAGGATCAAAAGGGTGAAAACCAGAGAGTTATATAACATTATCTGTGTGGTATTTTGAGCTGAAACCTCACACACACACACACTCTAGAGACAT
Associated Phenotype:
Not determined