ZMP
si:dkeyp-33d3.1
Ensembl ID:
ZFIN ID:
Human Orthologue:
MCTP1
Human Description:
multiple C2 domains, transmembrane 1 [Source:HGNC Symbol;Acc:26183]
Mouse Orthologue:
Mctp1
Mouse Description:
multiple C2 domains, transmembrane 1 Gene [Source:MGI Symbol;Acc:MGI:1926021]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21815 | Nonsense | Available for shipment | Available now |
| sa44733 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21815
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086220 | Nonsense | 324 | 858 | 6 | 20 |
| ENSDART00000135680 | None | None | 93 | None | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 45397754)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44048817 |
| GRCz11 | 10 | 43895614 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGATGCAGCAGCAGAGTCCCCGTCTGTCAGATCTGCACAGAAAGCCT[C/T]AGATGTGGAAGGGTATTGTGAGCATCAGACTCATCGAGGGACGAAATCTC
Long Flanking Sequence:
AGCACTGTCGCCTCACAGCAAGAGCGTGGTTAGCCCAAAGAGCGTTTCACGCCTCCGAAAGCCACCATATTCACTGCATTTCGTCTTCCTCTTCTAAGAAGGAACTCATTTATTAGAGAAGAAAAAAAAACCATGATGGGATAATGAAATTTCAGCCTTGCTCTGCTTCATAATGAGTGTTGAATACTTTACTCATCATCAACTTGAGCTTCTGCTGGAGTCCCATAGGTTGTAATGAAGACCACAACTCCCATGATTCCACACTCAGTCACTGAGTCATTAAAATACACCTTTGTTTGTTGTGAATACACTCCCTCTAGTGGCCAAAATGGCATACTGTGCGTTTAACAGCAATTTTCGAGTGAACTATCTCTTGAAAGCTGCTCTAATGCATGCTAGTTGTTGAGATGTTGAATGTTTTGTGCTGTTTTGGACTGAAGCAGCAGCAGCAGCAGATGCAGCAGCAGAGTCCCCGTCTGTCAGATCTGCACAGAAAGCCT[C/T]AGATGTGGAAGGGTATTGTGAGCATCAGACTCATCGAGGGACGAAATCTCATCGCGATGGACCAGAATGGCTTCAGCGACCCTTACGTCAAGTTCAAACTGGGCCCTCAGAAGTACAAGAGCAAGGTGAGGCATTGAATATAGCAAATGTAAGTCTGCATGAACCGGAAGTTGCTGAGACTTTTATTTCAGTATGTTGATGTGCTTCAAACTGAAACAGAATATTGAGTTGGGGCGGGGCTCAAAGAGATAAAGAACCATTAAAAATATACACTATTAAAATATCTGGTCATTTTTGACCAGCTCGGGGAGATATGGAGCACCATTAGTGTCAAAAATAAATACTAATTTAAAATCAGCATGAACCAGAAGTTTTTATTTTTATTTATTTTAGACTTTTATTTCAATATGTCAATTTGCTTTGGGATATTAAGTAGGGGGCGGGGCTTTTTTGTGCATCAGTGAGCTTTAAAAACCTCAAAGAGATAAAAAAACAAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44733
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000086220 | Essential Splice Site | 571 | 858 | 11 | 20 |
| ENSDART00000135680 | None | None | 93 | None | 3 |
Genomic Location (Zv9):
Chromosome 10 (position 45387566)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 10 | 44038629 |
| GRCz11 | 10 | 43885426 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGACCGCAGTGCTGACTTTCTGGGAAAAGTGGCCATCCCTTTATTAAAC[G/T]TGAGTGTGTCTCCATCATTACACTGCAGACAGCCAGTCGAGGAGATTACT
Long Flanking Sequence:
TCAGGATCAAAGCCTGAAAGGGGCAGTTTCAGAAATTTTTTGTGTTTTGTTTTGAGCTGAAACACACACACACACACACACACACACACACACACACTATAAAGACATCTATAAAGAGGCAGAGTAGGTCACCTCTAATACACATTCATTAAATGCTCAGTAATGTTCGCAAAACATTGAAAACATGAGTGTGTGCATAAGCGTGGCTTAATATTCTGAATAATGTGCAACAGCTGGGATGTGTGAGTGATTGGTGAAAACGACTATGGGTAATGTAGTCTGGGTGACTGGCAGAGTAGTGGCTCGTGGGCGCTCCCGCAGCTGATCTTGACATGAATATTGTGTTTTATTGCTGTAACTCTCTCTCTCTCTCTCTCTCTCTCTGTGTGTGTGTCAGTAATGTAAAGGACATCCACTCAGTGCTGGAGATCTCAGTATATGATGAGGACCGAGACCGCAGTGCTGACTTTCTGGGAAAAGTGGCCATCCCTTTATTAAAC[G/T]TGAGTGTGTCTCCATCATTACACTGCAGACAGCCAGTCGAGGAGATTACTTCATTACATACTGCATGTGTGCACACACACACACACACTCACACACACGCACATATAGCATTGCTGTACTTGAGGCATTTTGTCCCCACAAAGTGATGAATGACAGAACCACACACACACACTAACAGACAAACACACACACACACACACACAAACACACACACACACACACACACACACACACACACACACACGCACATATAGCATTGCTGTACTTGAGGCATTTTGTCCCCACAAAGTGATGAATGACAGAACCACACACACACACTAACAGACAAACACACACACACACACACACACACACAAACACACAAACACACACACACACACACACACACACACAAACACACAAACACACACACACACACACACACACAGGGCTGCTGGTAATGAGCAGGTCTCTGTCAGCTCTGGATGTGCCGTATGGGGGTGTGTGTGAATGTGCGGCGG
Associated Phenotype:
Not determined