ZMP
si:ch211-95i5.2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate regulating synaptic membrane exocytosis protein family [Source:U
Human Orthologue:
RIMS2
Human Description:
regulating synaptic membrane exocytosis 2 [Source:HGNC Symbol;Acc:17283]
Mouse Orthologue:
Rims2
Mouse Description:
regulating synaptic membrane exocytosis 2 Gene [Source:MGI Symbol;Acc:MGI:2152972]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa39240 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa23489 | Nonsense | Available for shipment | Available now |
sa36810 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39240
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 |
---|---|---|---|---|---|
ENSDART00000052257 | Essential Splice Site | 109 | 493 | 2 | 14 |
ENSDART00000133016 | None | None | 277 | None | 7 |
ENSDART00000140093 | None | None | 662 | None | 15 |
ENSDART00000145619 | None | None | 150 | None | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 17480298)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 13176455 |
GRCz11 | 19 | 13094931 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATGCAGAGGCGCCTCCTACACGGAGAAAGTCCAACACGCAGGTTACAGA[G/T]TATGTATAGAAAACACACCCATACAAATTAATTAATAATAATGAATTAAA
Long Flanking Sequence:
TTTGCATTACTCAGCATTTTTAACTGTAAAAATGTTCACTTTTTTGAAACCTGATTTACACAGTAGACCAAATAACAAGAGACGTGACTGTTTAACCAGAGCAGAGGAGGTTCCCAGCTAAGAAGAATACAGAGAGACTACTGTAGATGTTTAAACAATCTGTTTCAAATGCTGTGAGAAATGAGCTGATAAATATTATGATAAAATGTAAGACGTAATAGTTGTAAACCTACTGTATTGAAGAAGTTGTTGAAAACAAAGTTAAGAGCAGTTAAAATGGTATAATGGTGCACTTTTTCGGCTCAAAACGCCATGATAAATGTCTGTAAATTATATGTGTGTGCAGATTCTGATAGAGTTGGAGACGGCGCTGTTGGATGATCAACCTCACTGGTATAAGCTACAAACACACGATGTGTCCTCTATGCCTCTGCCGAACCCCTCACCGTACATGCAGAGGCGCCTCCTACACGGAGAAAGTCCAACACGCAGGTTACAGA[G/T]TATGTATAGAAAACACACCCATACAAATTAATTAATAATAATGAATTAAATTGTTCACACTACAATTAAGTTAACTGATTTCACAATGAGAACAGCAAAAATAACATTTTAAAATTCAGTCATGTACAAATCAACTTGTCTTGTCGGAAACCATGTCTATATGTCAGTCAGTCACTATAATTGTGTGTTCAGCATGCCAGCTGTGTTAAATTTAGTTTGGGATTATGTAGTCTTTTAATGTATTTTAATGTTGAGAAGGATGTATTTTTATCAAAATACAGTACACACTGTAATGCCATAATGATAATTAAATTTAAAAATGGTTGTTTTCTATTTGAATATGTTTAAGGCATTGAAAGCTCAAAGTTTAACTTTCAGGATTTGTTGCATCACTCATCAATGTCTGATAAACATTTGATTAACATTTCCTTTTATTATTATTTTAAAGCTATTATTTTAGGATTTTTTTTATGAACAAATAATTCAAAAGAACCTTAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23489
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 |
---|---|---|---|---|---|
ENSDART00000052257 | Nonsense | 376 | 493 | 12 | 14 |
ENSDART00000133016 | Nonsense | 160 | 277 | 5 | 7 |
ENSDART00000140093 | Nonsense | 545 | 662 | 13 | 15 |
ENSDART00000145619 | Nonsense | 33 | 150 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 17389947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 13266716 |
GRCz11 | 19 | 13185182 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTTGAAGTTATTCGGGCTCGAGGTCTGGTGGGCAAACCAGGAAACAAA[C/T]AGACTCCAGGTAGGCTTTATTATTCAGTCTGATTGTGACCATGCCTTTTA
Long Flanking Sequence:
CCCTGGGGTGAAGATCTCAAAGGACAGCCAGTTTACAGAGTTTCTGGATGGCCTTGGCCCAGCCCAGCTGGCAGGAAGACAAACATTAGCCACACCTCCAATGGGTTAGTATCATCAGTCACTGTTTTAATTAGCTGCAAATAATTTCTACTTGATATTAATAGTTTTAATCATTCAGTTGTATTCTATGAGGCTTCTTATGAGTAAGCAAGAAAGAAAGCAAATGGTAGGTATAAAAATACTGGCAATATCGCCACCTTGTGGATGAAGTGCAAAAATTCTAAGCACAAAAAGATGCATGGAAAAAAAAACTGGGCTATAAACATTCTCTGCTGATGCTGAAAACACTTAACACAAATCTGAATCAATGTATTACTAATTAAATATTTAAAATGTTTTTCTTTGCAGGGGATATTCAGATTGGTATGGTGCACAGGAAAGAGAGGCTGGATGTTGAAGTTATTCGGGCTCGAGGTCTGGTGGGCAAACCAGGAAACAAA[C/T]AGACTCCAGGTAGGCTTTATTATTCAGTCTGATTGTGACCATGCCTTTTACTCTTTTTCTTTCTTAAAAAAGTATACATTCTAGGACTAATTAATGTTTATACTACAATTTCTGTGGTCCCTCATTTACAGCACCTTATGTAAAAGTATATCTACTGGATAATGGGAAGTGCGTCAACAAAAAGAAAACACGGACCGCCAGAAAAACACTGGATCCTCTTTATCAACAGCAGCTTCAGTTTGAGGAGAGTCCTGAAGGGAAGGTTTTACAGGTACTAATTAAGATCATAAACCAGGCCTGAATACTATTTTATTCAAATGTTGTTCTTTTAACATTATGAAAAAACATTGAAACATTTCATTTCAATTCAAAGTTAAAACACCAATAAAAGGTTAACATTAAAATTGAAATAAAAATCTCGAAACCATCCCGATCATTCCCCTCTCCTCTCAGATGAAATGGAGGGCCACATCAAAGGTAACCATGGGCCAACTATGTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36810
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052257 | Nonsense | 381 | 493 | 13 | 14 |
ENSDART00000133016 | Nonsense | 165 | 277 | 6 | 7 |
ENSDART00000140093 | Nonsense | 550 | 662 | 14 | 15 |
ENSDART00000145619 | Nonsense | 38 | 150 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 19 (position 17389808)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 13266855 |
GRCz11 | 19 | 13185321 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATTAATGTTTATACTACAATTTCTGTGGTCCCTCATTTACAGCACCTTA[T/A]GTAAAAGTATATCTACTGGATAATGGGAAGTGCGTCAACAAAAAGAAAAC
Long Flanking Sequence:
AATAATTTCTACTTGATATTAATAGTTTTAATCATTCAGTTGTATTCTATGAGGCTTCTTATGAGTAAGCAAGAAAGAAAGCAAATGGTAGGTATAAAAATACTGGCAATATCGCCACCTTGTGGATGAAGTGCAAAAATTCTAAGCACAAAAAGATGCATGGAAAAAAAAACTGGGCTATAAACATTCTCTGCTGATGCTGAAAACACTTAACACAAATCTGAATCAATGTATTACTAATTAAATATTTAAAATGTTTTTCTTTGCAGGGGATATTCAGATTGGTATGGTGCACAGGAAAGAGAGGCTGGATGTTGAAGTTATTCGGGCTCGAGGTCTGGTGGGCAAACCAGGAAACAAACAGACTCCAGGTAGGCTTTATTATTCAGTCTGATTGTGACCATGCCTTTTACTCTTTTTCTTTCTTAAAAAAGTATACATTCTAGGACTAATTAATGTTTATACTACAATTTCTGTGGTCCCTCATTTACAGCACCTTA[T/A]GTAAAAGTATATCTACTGGATAATGGGAAGTGCGTCAACAAAAAGAAAACACGGACCGCCAGAAAAACACTGGATCCTCTTTATCAACAGCAGCTTCAGTTTGAGGAGAGTCCTGAAGGGAAGGTTTTACAGGTACTAATTAAGATCATAAACCAGGCCTGAATACTATTTTATTCAAATGTTGTTCTTTTAACATTATGAAAAAACATTGAAACATTTCATTTCAATTCAAAGTTAAAACACCAATAAAAGGTTAACATTAAAATTGAAATAAAAATCTCGAAACCATCCCGATCATTCCCCTCTCCTCTCAGATGAAATGGAGGGCCACATCAAAGGTAACCATGGGCCAACTATGTCCCGCAGGCCCTAGTTTGGGCATCTCCTCTGTAGATAATCATTCTGTGACTGGACCATTCCCTTATTCGTCAAGCCCTCTCATATGACCATTGCACAAGAGGTAGACTGCAAGCACGGTTGCCAGAAAAACATGTGCATAA
Associated Phenotype:
Not determined