ZMP
si:ch211-214d15.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q7SZV6]
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 |
---|---|---|---|
sa16716 | Nonsense | Available for shipment | Available now |
sa19203 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13733 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16716
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001102 | Nonsense | 224 | 927 | 2 | 22 |
ENSDART00000136489 | None | None | 422 | None | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 23157584)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 23387807 |
GRCz11 | 18 | 23376873 |
KASP Assay ID:
2261-2225.1 (used for ordering genotyping assays)
KASP Sequence:
CTCAGGACACTCCTAATGAAACCAGTGACTTTGATGATCTSTCAGAACAT[G/T]AACGAAAYGTGAGTATTTTTRAAAGAAAATGTACTTTTAGACATTATCRT
Long Flanking Sequence:
CAAACACAGTTTTTAAAAAATTTAAAACTGTTTTTATTCTAGTCGAAATAAAACAAATAAGACTTTTTTCAGACGAAAAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTTTTAAATACTATTTGGGAAATATTTAAAAAAGAATAAAAAATCAAAAGGGGGCTAATAATTCTGAATTCAACTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATACAGTATTCTACTATTTAACCTCAAAAAAGAAATGTGTATGTTGCCAAATCCTCAATTTGCCATCTGTTGTATTCAATGTACAATAGATAAATGACAAACATTACTCAGTTCTTAGCAGAGGCAAACTAATGCAGAACTGTCTCATCTGATACAGCTTAATCTCTCCCTCAGGACACTCCTAATGAAACCAGTGACTTTGATGATCTGTCAGAACAT[G/T]AACGAAATGTGAGTATTTTTAAAAGAAAATGTACTTTTAGACATTATCATTCTACACAGTCAGTGTAGCTTTTTCTATTTGGAATAGTGCCAATGTTACTAATATTAATAAAAAATCATCCAGGCTTGAGCAAAGTGTCCTGCACGCTACTTTTCAGATCTCAGGAGGGTTAACAGAGAGTCAAAGTGCTGCAGGTCTACAGAAGCTCCAGTATCTTCTCACCATCAATCTAAAGGAAGGCAGAAACCTGGTTGTCAGAGACCGTTCAGGTACTGAACTCTTAAACACTGACTAATACAGATGACTAATGTTGGATGACACTGGCTGGTGTGGTTTAATTCATACAGTAGATGTTGCATTGCTGTATGCTTGCATCACTATGCTTACTTTAATAGTTATTATATCTATATTTAGGTCATTTTGACCTTGTAGTTTGGCCTAGAATTCATAAGCCACACCTTTATGTTGTGACTATTTTACAGAGAATTTAGTGGAATGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19203
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001102 | Essential Splice Site | 375 | 927 | 7 | 22 |
ENSDART00000136489 | None | None | 422 | None | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 23177913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 23408136 |
GRCz11 | 18 | 23397202 |
KASP Assay ID:
2261-2226.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAAATCAAAGTCAAACGATCTAACATCTTTTTTTTTTAATCATTTTTT[A/G]GAAGTGGCTCCTAAGAAGAAAGGGATCCTTCAATAAGGTTTGTCTTGAGA
Long Flanking Sequence:
GCTGTTGTGACCCCTGATAAATAAAGGGACTAAGCCAAAGGAAAATGCATGAATGATGAATTATTTTAGATTAAAAAATAGTGTAATACTACTAGTAATTCTTCCACCAATGATGAATGCAGGTGTATGATCGTGACCTAAGATCCAATGACTTCATGGGATCAAGCAGCTTTCCTCTCAGTAAACTGGAGCTGGACAGGTGATGAACTTTATCATTTGATTATTACTTCATTATTACTTTCATTATCACCCCAAATAATGTCTTGTCAGAATGAAACAGATAAAGATTTGTGCTTTCCTCCTGCAGGATGGTTCTGATGACGCTGTCTCTGGAAGACCCCAACAGTGAGGAAAGCGATATGGGAGTGATCATTATAGAGGCCTGTCTGTCCATCCGAGAGGAACCGGCCAAACGAAATGTAGGACACCAAACAGTCCAAATTGTCTTATTTCAAATCAAAGTCAAACGATCTAACATCTTTTTTTTTTAATCATTTTTT[A/G]GAAGTGGCTCCTAAGAAGAAAGGGATCCTTCAATAAGGTTTGTCTTGAGAAACGTTTATCATAATACTTCTATTCAGTTGTAGATTTTTTTAAAGTGACTCAGTAAAAGTAAAGTTAGTACATTGATATCTTTTATATCACATTTGCCCACTGGAGGGCAGTAGATCTTCACCATCTTCCTCATACATTCTTCACTAAAGTTACACTAATTTCTGCAAGTTTTTGACTTGCAAGCTTTTGACTTTACCTTTACTTTACTTTCTCCTGTTAAGTTAGCAAATCTGTCATGCATTTTTGTGCAGATTCGTTTATAAATGAGGATATATTTACCTCACAGTGACAGGGAAAGCTTTTTTCTGTTCAAGGCTCTAAAGGTTTGCAATATATAATTTCTCTGAATAAAATCTGTGCCAAATACTACTGTAGAGAAAGGTTTGGTGCAGTGGATATTTTAGTATATTGTATTTATGTCAATCAATTTCATATCAATACATTGTATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13733
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001102 | Essential Splice Site | 799 | 927 | 18 | 22 |
ENSDART00000136489 | Essential Splice Site | 316 | 422 | 9 | 12 |
Genomic Location (Zv9):
Chromosome 18 (position 23220187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 23450410 |
GRCz11 | 18 | 23439476 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTGCAGGAGCACATGTCGGTGGCTGAGGACGAGGACGAGGATGAAAAG[G/A]TATTCCGCCGGTGTCATGCCTGCTTTTTTGATTAACCGCTGACTTTTATA
Long Flanking Sequence:
CTCTTTGTGCACCACCAGCCTGTCTCGGTGGCGTATGTGAGGCATCGGAGCCGGGCTGCGCTCTCTGCCAATGTTAAAGCCTCCATCACCTCGCGCTCACCCCTCGGCCTAGCAGAAACAGAGCGGCGTGCTTGCATTCAATCGGCAGAAAGGGTCAGGGATGTCTTGATAGAGAGTGATCAAGGCACCTGAACAGCCCAGATTAAATGCCTTCCTTGCATGCGCGAGTGTGTTTATGTTGTGAAGAAATGAGATTGCTTGGTTGTGACACGGAAGGCCCCTCTCATTCACCTCCTCCTTTTGTGCGAGGTCACCCGAGAGGCAGTTGCTACGGCAACAGGGCCTCTCCCAATGGGGGTGTATACACAAGCGAAGGTTTCATTACGAGGTGTTTGTTAAGAAAATGCTCCATTGCCCACGTGCGTCTCAATCTCATCTCTTTTCTCCTTCTTTTGCAGGAGCACATGTCGGTGGCTGAGGACGAGGACGAGGATGAAAAG[G/A]TATTCCGCCGGTGTCATGCCTGCTTTTTTGATTAACCGCTGACTTTTATAGAGCCTCTCCAGGCTGTCCTTGGGGTGCTGCATAGACGGACTGTGCGCTGTACCTTTAATACTGCATTTAACTCGGGACTGCAACTTAAATGTGTTCAAAACGAGGACAGACGATTCAGCAAGCACATTTTCCCTCCAGTACTTTCACACACGTCCTCTGGGAGTTCTCGCTCATACGACAAATGGATTTGGTTGCTTTGCTGTGGTCCTTTGAAACGCAGAAATAAGCACAGAACGGCATCATTAATTGAAGTTTGTCATCCGCTAGGGAATAGAGAAGCATTGTGAGGATTTCGAGGCATGCACGGCTAAATAGGGAGGCTGGACTGCAGTTGAACTTCCTCTTTTAGCATTTTTATTTATTTTTTTATGCTTAAGATGAATCATTAGACTAATTACAAATTCACCCAAATCTGCTTAGATCCAATTATTCATAAAATAAGAAAAGAT
Associated Phenotype:
Not determined