ZMP
MCTP2 (1 of 2)
Ensembl ID:
Description:
multiple C2 domains, transmembrane 2 [Source:HGNC Symbol;Acc:25636]
Human Orthologue:
MCTP2
Human Description:
multiple C2 domains, transmembrane 2 [Source:HGNC Symbol;Acc:25636]
Mouse Orthologue:
Mctp2
Mouse Description:
multiple C2 domains, transmembrane 2 Gene [Source:MGI Symbol;Acc:MGI:2685335]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20880 | Splice Site, Nonsense | Available for shipment | Available now |
| sa38599 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa20880
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109942 | Splice Site, Nonsense | 286 | 665 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 16536856)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15519645 |
| GRCz11 | 7 | 15768671 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCCCGCCTCTGGAGGACCCTGAGGAGAAAGAAAACATACTGGCTAAATA[T/A]GTATGTTAAACCACAGTGCTGCTTTTAATATCTATAACCAGGCGTAGGGC
Long Flanking Sequence:
ATTACATGCAGGTATTTAATAAAGCACAAATTCAATGTAAAAGCATGTATTTACACATTAAGTACATTGTAACGAATTATTAATTGCAGTCTAAGTGCATATTAGTTAAGGCTGCTGAAAATAAAGTGGGCCGGAAATTTTTATATAAAGAAAAAAAATTCAGCAGAAGTCAACATGTCAGTCACAACTGCAGATAAAAGAGCTTCACTGGCATCCAGCCGATCTCGCAACACAAAAGCATTTCTCGCATAACTAACTTCCTGTTTGTAAAGTGTTTTTGTGGTTTAGTCTTTGTGTGTTTGTACACGTTGCAGGTCTGAAATCAACTTGTCTGAGTTGCCGCTGAATGAATCCACATTGTTTTCCTGTGACCTGGAGCCGGGCCGGGGCAAGGTGGTGTTTCTCATCACTCCCAAAGCCTGCACCGGAGCCTCCATTTCAGATCTCATCACCCCGCCTCTGGAGGACCCTGAGGAGAAAGAAAACATACTGGCTAAATA[T/A]GTATGTTAAACCACAGTGCTGCTTTTAATATCTATAACCAGGCGTAGGGCTGTGCGATTATTCAAAATCGAATCGCGAATGTTGCAATAAGTTAAGTGCAAGAGGCTGCAATATAAAATATATATGTAAACAAAAACAATGAATAACATCTTCAAAACGAGTCCGCTATGCTTCAGGAAATTAAACATGCTTCTGCAATGGTGTCGTCAGGCATCGCAGACATAGTATCGGTTGTCGTGAACTATGCCGCATTACACCAGAAGAAACGATTGAATATTGTGTCACGATGTACATTTGTTATTTATAGCTTTCCACGAAACCCTATGTCAAGGAAATCATGCCAAAATCGTGTGATCTGGCCGAGGCTTTATAGCTAGCCAATTGAGTGAGCACACTTTCGTTCTGCCCAATCAGAATTGCACAACAGAACTACGCCCACAATAAAAGCGCTGACAAGTAGGATCATGGTGTCTGCTGCTTTAGAAGCATTAATAGACAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38599
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 > G
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000109942 | Nonsense | 443 | 665 | 13 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 16550756)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 15533545 |
| GRCz11 | 7 | 15781497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTTTACACCTCGAGAACAGAAATTTCTTGAGGACAATCCCAAGTTTT[C/G]AAAGAAGGTACAGTATGACATACAGAGACAATACAATAGATGATACAATC
Long Flanking Sequence:
ACATGTATGATGTAGTAACATACTAGGGCTGCAAGTGATATACAGTTGAAGTCAAAATGATTAGCCCTCTTGTGAATTATTTTTTTTCTTTTTAAAATATTTCCTAATTGATGTTTAACAGAGCAAGGAATTTTTTCACAGTATGTCTGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTTATAAAAATTTGTCTTCAACTGTAACTAAAAATATAACAACAGTTTAGCGTGTCTTATATCATATATTTAATGTTTCGATACTGGATATTTGATAGTGTTTGTTTGTTCACTGCATTTGCCAGATCAAAGCAAGCATCATAACCTTTACACCTCGAGAACAGAAATTTCTTGAGGACAATCCCAAGTTTT[C/G]AAAGAAGGTACAGTATGACATACAGAGACAATACAATAGATGATACAATCATGATTTGAATACAATCATGATTTGAAAGAAATACTTTAAGAAATAATAATGAAAACATTTTTAACAATGTATGATTGCAACAGATTCTTTCCAGGAATATTGGTCGTGTGAGGAACCTTTTTCGTGCTGTGTCTTACTCTCACCAGTTCATCACAAGCTGCTTCACGTGGGAAAGTGTGAGGAGGAGCATTACGGCATTTCTGGTGAGCAGAGCGGCCTAATACTGACCAAAAATGTAGATGTTAATACTTATTAGTACTGGCTGACAAATGTTATCTATCTATCTATCTATCTTTCGTTCTACCATTCTTACCTATTTATTGTTTTATTTATCCTTCTATCATTCTATCGTTTTAAATTTGTTCTTACTATATATATATAGTCTATCTATCTATCGTTCTATCTACTGTTTTATCTATCTATGGTTCTATTCATCCGTCTATCCATCC
Associated Phenotype:
Not determined