ZMP
rimbp2
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to chicken and human RIM binding protein 2 (KIAA0318) [Source:UniProtKB/TrEMBL
Human Orthologue:
RIMBP2
Human Description:
RIMS binding protein 2 [Source:HGNC Symbol;Acc:30339]
Mouse Orthologue:
Rimbp2
Mouse Description:
RIMS binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2443235]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13674 | Splice Site, Nonsense | Available for shipment | Available now |
sa34470 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41282 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34471 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12091 | Essential Splice Site | Available for shipment | Available now |
sa2429 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13674
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 |
---|---|---|---|---|---|
ENSDART00000001313 | Splice Site, Nonsense | 123 | 1085 | 5 | 22 |
ENSDART00000136269 | Splice Site | None | 1165 | None | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46135178)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44008311 |
GRCz11 | 8 | 44001730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCAGTCACCTTTGTGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTTA[T/A]GAAGGTAATGAGGATTCGATGAGTAAGATCTCGGAGCTCATCCGGCCTCT
Long Flanking Sequence:
ATTATGAAAAAAAAGATGCCTGACCCCAAATTTTTGAAATTGAATATAGTATGTTGTTTGTGTTTTAATCAAGATATCAGTTGATTATTGTGCACTTCACAATTGTTCATCTTCAGGTTATTATTTTCATCCTCTCCCTTTCTCACATTATACAGCAGGCATGTGCTTGATCCTGGAGGGCCGGTGTCTCTGCAGAGTTTTGCTTCAACACTAATCAAACACACCTGAACACCCTAATCAGTGTCTTCAAGATCACTAGAAAGCTACAGGCAGGTGTGTTTGATTAGCAAAACCATGCGGGACATCGGCCCTCCAGGATGGAGTTTGCCCATCCCTGTTATCAAGTATCTTGCTATCAAGGTGCAAGGAAACTCTTTTGAAGTTTGCTCTGATAAACCAGCGGTGATGATGACGGAAGGAGGAGGATGTGGTTATACGCAGTAATGAAGTAATCAGTCACCTTTGTGTATATGTGTGTGTGTGTGTGTGTGTGTGTGTTA[T/A]GAAGGTAATGAGGATTCGATGAGTAAGATCTCGGAGCTCATCCGGCCTCTGCAGATGACTGAGGGGGAAAAGGTAGAGCTCCTGTCTGTCAAACCTAGTTTCCTGTCACGCAGCACACCCTCCAGCCCACGGCGGGCCTTCCTCTCTGAGGTGCGGCCCGTCATCGCCACTGCTGTGAGTATCACACAACCACTGCTACTTCTGTTTACCCAGAATTTGATCCATGCTTTATTTTTTAGTGTGAGAAAAAAGAGTGAAATACATCATAGGAACTAAAGCACTGTAGAATGAAATAGATGAGATTAGCTTTTTTTTTTTGGAGAAGACAATTTGATTCTGTGTGTAAACAAAATGATGAATAAAGAAATATTCATTCATTCATTTTCTTTTCGGCTTAGTCCCTTTATTAATACGGGGTCGCCACAGCGGAATGAATCGCCAACTTATCCAGCACATGTTTTGCGCAGCGGATGCTCTTCCAGCTGCAACCCATCGAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34470
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 |
---|---|---|---|---|---|
ENSDART00000001313 | Nonsense | 201 | 1085 | 7 | 22 |
ENSDART00000136269 | Nonsense | 147 | 1165 | 4 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46142025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 44001464 |
GRCz11 | 8 | 43994883 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGGATTTAATTCACATGGATCGATTTAACTGGTTCTGTTTGCAGTTA[T/A]AACCCTTACGATGGCCCCAATGAGCATCCTGAAGCAGAGCTCCCCCTGGT
Long Flanking Sequence:
AAAATGCATGTAGTTGTGTTTACAAAGCATTTATTAACATACAAAGTTACCATTACTATACGCCTGAATAATAAGATACATAAATGTTGATTTCAATAGTTTGTTAATCATTTACTTATGCATTCTGAATTCTCTAAAAAACCATCGACTACTCTTAAATACAAATGCAATGCTTAATTTAGTAATGAAAAATTTATTACTCATATGTTATGAAAATACAGTTTTTTTATAAATTAAGAATAGAGCATTTCTAACTGCAGTTATAAACTGCTTAATAACGTTTATTAATGTAGAGTTCATGTTTAACAGATAATGAATTCACTATACTAATGCCTAATAAATGAATCGTAGTTTATAGTTATTATAAAGTGTTACCCAAATTTATTTGTCACATCATAGTTAAAAGACAATAGGCAAATAGAAAGTTTAATTGGATAGATTTAAAATTTTAGGAGGATTTAATTCACATGGATCGATTTAACTGGTTCTGTTTGCAGTTA[T/A]AACCCTTACGATGGCCCCAATGAGCATCCTGAAGCAGAGCTCCCCCTGGTGGCTGGGAAGTACCTGTATGTCTATGGAACCATGGATGAGGACGGCTTCTATGAGGGTACGTTATACTTTGGCAAGTGGAAATTGAGGATGAAGCTTATCGAAATTGTGTCATGAAGCTTATTGCTGCATGAATCGCCACAATTTCAAGAGTGAATTGCTGAGTGGATGTATTGAAATTAAGAATGGATTATAGCCTAAAAAGGGTCCAGAGAGCACTACTGTTATTTCATTGAAAATATGTCATTTATCTTGATTCATTGCCATCTTAAAGATCCATTGTAGAGACGTTTTTTTAGGGCGCACAGTAAAATGTATTACATTTTGTCCACACTTCATTCGTTATAATGAGAAGATTTATGAGCATACTTTATACTGAGCAAAACTTTAACATTTAAAATTAACATTTTTAAAAATATTTTGAAACATACTGTAAATGAATGCTATTGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41282
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 |
---|---|---|---|---|---|
ENSDART00000001313 | Nonsense | 455 | 1085 | 10 | 22 |
ENSDART00000136269 | Nonsense | 429 | 1165 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46146112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43997377 |
GRCz11 | 8 | 43990796 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTA[T/A]GATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCC
Long Flanking Sequence:
AGCTTGGGCATGAGCACGGGGCTGGGCATCGATTATCTGGGACCCTGCAGCAACGGGACAGGCACGCTGGACGTGAACATCGACGAGATCGGAGAAGACATCGTGCCTTACCCTCGCCGCATTACCTTGATCAAACAGCTGGCCAAGAGTGTCATTATAAGTTGGGACCCTCCAGTGGTGCTGCCCGGATGGACGCCTATCAGCGGCTACAATGTGCTGGTTGACCAGGAGGTGCGCATGAGCATTCCCTTCGGTGGACGCACCAAATCTCTGATCGAGAAGTTGAACTTGACTGTCTGTACGCACCGCATCTCCATCCAGAGCATGACGGAACGGGGCCTTTCCGATCCGCTGCGCTGCACACTTCTGGTGGGGAAAGACGTGGTGGTGGCGCCCTATTACCTTCGTGTGGAGAACATCACTCAAGCGTCTGCCGAGCTCACCTGGATGCCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTA[T/A]GATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCCCATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTGGCAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTGCACACAGCCAGCCGGTGGGTCACTTAGCGCATGCTTCATTTTTGCATGTTCACTTCTTATTACTAAGTGATTTGAGATCTGGTTATCACTAGGGCTGTTAATCGATTCTAATATTCATGTGGATTAATTGCATAATATTTCATTGCGTCACAGCTCGCCATGCGTTCTTGCAAAAACCTGAAGTTGGTACTTCAAGACTGAATTGCTCCAGTGGTAGGAAAATTTCTTATTACAGAATTTACATGCAAGTCGGGGGTTAATATATGTTGCATTTTTACTTTTTCTAATGAAAATATTATATGGGGAGAGGCCTAAAATTTAAAGGTAATAACACCCTAGTGGATGCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34471
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001313 | Nonsense | 489 | 1085 | 10 | 22 |
ENSDART00000136269 | Nonsense | 463 | 1165 | 5 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46146214)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43997275 |
GRCz11 | 8 | 43990694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTG[G/A]CAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTG
Long Flanking Sequence:
GTGCCTTACCCTCGCCGCATTACCTTGATCAAACAGCTGGCCAAGAGTGTCATTATAAGTTGGGACCCTCCAGTGGTGCTGCCCGGATGGACGCCTATCAGCGGCTACAATGTGCTGGTTGACCAGGAGGTGCGCATGAGCATTCCCTTCGGTGGACGCACCAAATCTCTGATCGAGAAGTTGAACTTGACTGTCTGTACGCACCGCATCTCCATCCAGAGCATGACGGAACGGGGCCTTTCCGATCCGCTGCGCTGCACACTTCTGGTGGGGAAAGACGTGGTGGTGGCGCCCTATTACCTTCGTGTGGAGAACATCACTCAAGCGTCTGCCGAGCTCACCTGGATGCCGAGCAACAGCAACTACAGTCACATGATCTACTTGAATGATGTGGAGTATGATGTAGTAAAGCCTGGAGGCTACAAATACCACTTCTACAACCTGAAGCCCATGACGGTGTATAAGATACGGGTGGTGGCGCGACCCCATCAGATGCCCTG[G/A]CAGCTTCCTCTTGAGCAGAGGGAAAAGAAGGAGGTCTCGGTGGAGTTCTGCACACAGCCAGCCGGTGGGTCACTTAGCGCATGCTTCATTTTTGCATGTTCACTTCTTATTACTAAGTGATTTGAGATCTGGTTATCACTAGGGCTGTTAATCGATTCTAATATTCATGTGGATTAATTGCATAATATTTCATTGCGTCACAGCTCGCCATGCGTTCTTGCAAAAACCTGAAGTTGGTACTTCAAGACTGAATTGCTCCAGTGGTAGGAAAATTTCTTATTACAGAATTTACATGCAAGTCGGGGGTTAATATATGTTGCATTTTTACTTTTTCTAATGAAAATATTATATGGGGAGAGGCCTAAAATTTAAAGGTAATAACACCCTAGTGGATGCCTACACATGCTTTTTTGATCAGGTGGTACACTAACGTTTGACTTACACTAATTAGCCTTCTGTACATACTGCACATCACATCACAAAGTCATAAGTAAGGTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12091
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000001313 | Essential Splice Site | 974 | 1085 | 19 | 22 |
ENSDART00000136269 | Essential Splice Site | 1056 | 1165 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46187911)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43955578 |
GRCz11 | 8 | 43948997 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGCTCYAGCACTTGTATATATTTGNTTTTTTGTCCTTYTTTTGTCTCTC[A/T]GAAAGGAAMAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGAT
Long Flanking Sequence:
GCAAATCCACAGAATGATGATGATGATCTTTTTCCATGTACATGGAGATACAAGGTTTCTGTCTGACAGTAACATGTTACATTTTTTCCAGATTTATTTCCATTTTTTATTGGTTAAATATTCAATATAGATTAGTTTGGACTCCACAGTGCATGATTTGGGAACTTATTTAAAGTCATTCAAGACAAGGTGCTGCACGTGTCAGGGAAAAACACAGTATTTTGTTGTATAATTATTGTCCTAAAAAGCATTTAATTAATTAAAAATCATGCCATTGGCTGAATCCAGTAGTTTGGACAATAGATTTTTTTGATCAATAACATCAAATTCTTGTCATCCTGCAAAACTGTCTTTCTTGTTGTTCATTAATTATGCATTTGTTGTGTATTTATTTTGATATTCATTTATTTGTAGTTAACAAAAGCTATTAAAGATAATTTCGCTTTACTATCGCTCCAGCACTTGTATATATTTGTTTTTTTGTCCTTTTTTTGTCTCTC[A/T]GAAAGGAACAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTATGACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCTGGGCTTTCTTGTACTTATGGTCTCATCCCATAAGTTTTTGATTTTTATGCTGGCTTGCCTGGATGTCTGCCTCTGTGATAGCCACGAAATTCATTTTCAGCTTATTGTCTGCTTCTGCGGCTAAAGTGTGATTTGTATTTTTATGTTACTGTTCATTCAGGTGGCACATGTTTAGAGACAAAAGTTTTATATCAAATACTTATAATGTCATTCCAAACCTAAATTAACTTCTTGGAAGTTTTTTTAATGCTGAATGTGTATTTTTTCATTATCTTTAAATAGATTTACCATATACATCTCTTTTCTGCCTAATTATTTTTAGCACCATTTATACATATATATATAGGCCCCCTTTGAATTTTTTTTTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2429
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 |
---|---|---|---|---|---|
ENSDART00000001313 | Nonsense | 996 | 1085 | 19 | 22 |
ENSDART00000136269 | Nonsense | 1078 | 1165 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 8 (position 46187980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 43955509 |
GRCz11 | 8 | 43948928 |
KASP Assay ID:
554-2878.1 (used for ordering genotyping assays)
KASP Sequence:
GGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTA[T/A]GACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTC
Long Flanking Sequence:
TAACATGTTACATTTTTTCCAGATTTATTTCCATTTTTTATTGGTTAAATATTCAATATAGATTAGTTTGGACTCCACAGTGCATGATTTGGGAACTTATTTAAAGTCATTCAAGACAAGGTGCTGCACGTGTCAGGGAAAAACACAGTATTTTGTTGTATAATTATTGTCCTAAAAAGCATTTAATTAATTAAAAATCATGCCATTGGCTGAATCCAGTAGTTTGGACAATAGATTTTTTTGATCAATAACATCAAATTCTTGTCATCCTGCAAAACTGTCTTTCTTGTTGTTCATTAATTATGCATTTGTTGTGTATTTATTTTGATATTCATTTATTTGTAGTTAACAAAAGCTATTAAAGATAATTTCGCTTTACTATCGCTCCAGCACTTGTATATATTTGTTTTTTTGTCCTTTTTTTGTCTCTCAGAAAGGAACAAAAGGAGTGGAAGACAGCATGCAGTGTCGACGCGGAGGATGGTGGCACTGTATGATTA[T/A]GACCCCAGAGAAAGCTCGCCTAATGTAGATGTGGAGGTACTAATGGAGTCCATTTTTTCTGGGCTTTCTTGTACTTATGGTCTCATCCCATAAGTTTTTGATTTTTATGCTGGCTTGCCTGGATGTCTGCCTCTGTGATAGCCACGAAATTCATTTTCAGCTTATTGTCTGCTTCTGCGGCTAAAGTGTGATTTGTATTTTTATGTTACTGTTCATTCAGGTGGCACATGTTTAGAGACAAAAGTTTTATATCAAATACTTATAATGTCATTCCAAACCTAAATTAACTTCTTGGAAGTTTTTTTAATGCTGAATGTGTATTTTTTCATTATCTTTAAATAGATTTACCATATACATCTCTTTTCTGCCTAATTATTTTTAGCACCATTTATACATATATATATAGGCCCCCTTTGAATTTTTTTTTTAAATTTCATTAATAATTAATGTTCTACAGAAAAATTTTCACAGCATGATATTTTTTCTTCTGGATAAAGTCT
Associated Phenotype:
Not determined