ZMP
rims2
Ensembl ID:
ZFIN IDs:
Description:
Regulating synaptic membrane exocytosis 2 [Source:UniProtKB/TrEMBL;Acc:Q6PC83]
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14738 | Nonsense | Available for shipment | Available now |
sa36242 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22936 | Nonsense | Available for shipment | Available now |
sa22935 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14738
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016817 | None | None | 286 | None | 6 |
ENSDART00000079296 | Nonsense | 237 | 1473 | 4 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 47344082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44525723 |
GRCz11 | 16 | 44512901 |
KASP Assay ID:
2261-0247.1 (used for ordering genotyping assays)
KASP Sequence:
CCAAACCAAAAATACRACCAAAGGGAGGAGAAGGCGGWTCGTTCGCAGTA[T/A]GCACCAGGAGAGGGCGGCATGCCACGATCGCCGTCTGACTATGGAGCCGG
Long Flanking Sequence:
TGATGGGTTGCATATTGTGTCATCAAAATGTGCTACCTACTTTTTGAATGCGAGGTATTGGACAGTCTGACGAGGTGGGACAAATTGACAGAATACTGGATCAATTAAATAAACGACTTTATCCTTAACTGACAGGGTATCAACAAGCTGCCACAAGAAAATAGTTCCAGATTGGATTTTCTTCAGCATTTGTAGTGTGAGGAGGACTTCGTTTACTGCTGTTGAGTGTTTATATGACACAATAAATCAATAGAGATCAATGGGAATCAGGCTATTATGTCCTAAATACCCAGAGTTCTTTGCACTCTTATGACACAATCCCCTTCGATGTGACTTTTGCTGATGTGCACATTGCGATATCAATGCGGAAACAATATATTGTACAGACTTACTACAATGTTATTTTTCTTTGTGCCCCACAGGAAAAGAAGCCCATCCGCAACCAGGGATCCAAACCAAAAATACAACCAAAGGGAGGAGAAGGCGGATCGTTCGCAGTA[T/A]GCACCAGGAGAGGGCGGCATGCCACGATCGCCGTCTGACTATGGAGCCGGAGATCGGCAGTGGCGGGGAGGCTGCGGGCGCTCCTATGAGGACGCGGAGGTAGCGCGAGGGGCGTACCGGGCTCGACGGGGCGGCTGGCACTCTCAGGAGGAATACCCACCCGAACCTGGCTTCCTACCCGATGGACCACCCCTCAGCGAGCACGAGCTCCAGCGCCAGCGGCAGGAGGAGTACCAGAACCGCTACCGCAGTGACCCAAACCTGGCTCGATACCCTGTCAAACCACAGCCCTACGAGGAGCAGATGCGCATGCACGCGGAGGTCTCCAGATTTATTAATTTATTTTAACAGTATTTATATTGCATCTTAACTTTTTAAGAAAAAGAAATTTGTTGTTTCTTCAATCTACTTATTTAAAATGAGCTGAAACAACCCTACAGAAAAACGGCTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGGCTGGTCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36242
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016817 | None | None | 286 | None | 6 |
ENSDART00000079296 | Nonsense | 327 | 1473 | 4 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 47343814)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44525991 |
GRCz11 | 16 | 44512633 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCGGCAGGAGGAGTACCAGAACCGCTACCGCAGTGACCCAAACCTGGCT[C/T]GATACCCTGTCAAACCACAGCCCTACGAGGAGCAGATGCGCATGCACGCG
Long Flanking Sequence:
AGGCTATTATGTCCTAAATACCCAGAGTTCTTTGCACTCTTATGACACAATCCCCTTCGATGTGACTTTTGCTGATGTGCACATTGCGATATCAATGCGGAAACAATATATTGTACAGACTTACTACAATGTTATTTTTCTTTGTGCCCCACAGGAAAAGAAGCCCATCCGCAACCAGGGATCCAAACCAAAAATACAACCAAAGGGAGGAGAAGGCGGATCGTTCGCAGTATGCACCAGGAGAGGGCGGCATGCCACGATCGCCGTCTGACTATGGAGCCGGAGATCGGCAGTGGCGGGGAGGCTGCGGGCGCTCCTATGAGGACGCGGAGGTAGCGCGAGGGGCGTACCGGGCTCGACGGGGCGGCTGGCACTCTCAGGAGGAATACCCACCCGAACCTGGCTTCCTACCCGATGGACCACCCCTCAGCGAGCACGAGCTCCAGCGCCAGCGGCAGGAGGAGTACCAGAACCGCTACCGCAGTGACCCAAACCTGGCT[C/T]GATACCCTGTCAAACCACAGCCCTACGAGGAGCAGATGCGCATGCACGCGGAGGTCTCCAGATTTATTAATTTATTTTAACAGTATTTATATTGCATCTTAACTTTTTAAGAAAAAGAAATTTGTTGTTTCTTCAATCTACTTATTTAAAATGAGCTGAAACAACCCTACAGAAAAACGGCTGGAAACCAGCCTGGAAATGGCCAAAACCCCTCTAAAACCAGGCTGGTCAACCAGCTAAAACCAGCCAACCAGCCTAGGCTGGTTTAGGCTGGATTTTTCAGCAGGGAACATAGTTGTTGAGTTTTTTGGGGGTTAACTAGATTGTTTTTAAGCTCAATCTACATAAATTTGTAAAAACTATCTAGAACCTGAAGTCCATTGACAAACTTTTATGTTGGCTTGAGAAAGCCAATGTGACTGCTTTAGGACTGGGAATGTAAGTAGGCAGAAAGCACAGCGATTGCTAGGCACTTGCTAATTTGTTTATGGCACTGCTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22936
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 |
---|---|---|---|---|---|
ENSDART00000016817 | None | None | 286 | None | 6 |
ENSDART00000079296 | Nonsense | 986 | 1473 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 47268276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44466976 |
GRCz11 | 16 | 44431331 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGTTCAGACCAGCCCCACAGGGACCCCCATAAACAGCCGGAGAGGAAGA[C/T]AGCTGCCACAACTGCCTCCAAAGGGGACGCTGGAGAGAAGTATGTTTGCC
Long Flanking Sequence:
ATATATATATATATATATATATATATATATATATATTTATAAAAATGACATACAAAAAACCTACAAATATCACCCTTATTTTTACCTTTCCCATATATTGAGTATTACCTTTGCAGTGCAGTTATTGCTAATCATTTAGTTTCATTCACACAAAATGTCAATGGACAACCACAATGTTTACTTGTTGTTGTTTTTTTTTTTACTCCCCAGCTTCATTCTGATGGATATGCATGATATTATTTAACATGCTTTTTAATAACCCTCTTTTTTTAATGTGTCATTTTATAACAGTTTGCTTTTTATTTGCTGAAATCTCTTCTTTGTCAGCATTTCCTCACTAACAGTACCCTGTCAACGTTTAGGGTATTTATTGCCTTTCATTACGATAATAAAGAACAGTAATAATGGTGTTTGGTGTGTTTTTCTGCAGGGCTCATCCTCGCGGTGGATCGGTTCAGACCAGCCCCACAGGGACCCCCATAAACAGCCGGAGAGGAAGA[C/T]AGCTGCCACAACTGCCTCCAAAGGGGACGCTGGAGAGAAGTATGTTTGCCTTTCTGTGTCGCTTCTTGTTGGCTTTTGCTCTTGCTGAGGTGTTTGTTTGAGAGGTGCGACTGGAAAACACTGACTGCGGCAAAAGGGTTTGCTGTATCTGCTCAGTAATTCATTAAATTCCACAGTTACAGTGGTCACCTATTCATTCACCGGGGGGAGAAAAAAATATGTAGCTGTTCTTAGAAAGAAACATTCGCCTATTGATTTACCTGCAGTGTTGCCAGATATAGCTGACTTTTTCCAGCCCAAAAGTTATCCGAAACCCACCCAAACGTTCAAAAGATTAATATTTTATTTTATTTTATTTTATTTAAATCAAAATTAACCTAGTTACTTTAACTGTCATCATTTTTAACCATACAGCATCCAACACCAGCAGTCACAGAGCCACAATAGTAAAATTACAACATAACCGGACCACATCAAATCACCCTCTCACCCACACACTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22935
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 |
---|---|---|---|---|---|
ENSDART00000016817 | None | None | 286 | None | 6 |
ENSDART00000079296 | Nonsense | 1214 | 1473 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 16 (position 47215411)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 44414201 |
GRCz11 | 16 | 44379125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGCCGTAAGCCTGGTGGGAACGGACGACAAGAAACGGCGCTCCAGCATC[G/T]GAGCTAAGATGGCGGCAGTGGTGGGATTGAGCCGAAAGAGTCGCAGCGCT
Long Flanking Sequence:
CTATTAAGCAGGTGTGAGTTGGAGTTCGTTGAAGCAAAACTATGCAGAGCTGCGGCACTCCAGGAATTGAGTTTGAAACCATTGCATTAGAACATCACAACCTATACTGAAGCACAACTATGAAGCACCCTGAACTGATTGGAGGCCTAAACCATTTACCCTATGACCTGAATCTCCATTCCACATCTCCCTCCAATTACCTAACTCTTTCCTTTCTCTCCTCCATTATCCATCCGTCCGTCCATCCATCCATCCCTTCATCCATCTGTCCCTCACTGCTCTCCTCCTCTCCTCACATCTGTCCACCACGGGCCGCCACTGACAGTGAATTTACATCCAAAATGAAAAACAGGCAAATGGGAACGGCGGCTGGAGGCAACATGACCAAGAGCACCAGCATCGGCGGAGACATGTGCAGCCTGGAGAAGACCGACGGCAGCCAGTCGGACACGGCCGTAAGCCTGGTGGGAACGGACGACAAGAAACGGCGCTCCAGCATC[G/T]GAGCTAAGATGGCGGCAGTGGTGGGATTGAGCCGAAAGAGTCGCAGCGCTTCACAGCTCGGTCAGACAGGTAGGACACCCGTCATGTCTCTGTGCTTGTCTCTAACCCCACAGTACTTTATTTTCCTTTAGTTAGCTGCTGTCTTCTTCCCGATGGCTTTAATGAGTCTGCTTTTCTTGCATCAGCTCTAACGACTTCACTTCTGTTTAAACAGCTTGTTTCTAGGGAAAAAAAGTGTAAATTGGGTCAAAACAGACAGAAGACCGCAGAATAATTCAGTCTCTGTGTTTTACATCTCTTTCTTGTCGTGACAAAAGTTCACTGATTGTTTCAGGCTTCTTCTTTTTCAGTCAAGTGTGCGACTAATGAACATCCAACTGCTTAAGTTTTGGGTTTCTCAGTGCTATTGCATGATTAGAAGCAAAAGTAACATGGTATTATGTTGTTTTAGACAGAGCTGCTTGTACTGTGGTGATGTTTTTGGACATTTATCGTTGGTA
Associated Phenotype:
Not determined