ZMP
snrpb2
Ensembl ID:
ZFIN ID:
Description:
Snrpb2 protein [Source:UniProtKB/TrEMBL;Acc:Q6PBZ6]
Human Orthologue:
SNRPB2
Human Description:
small nuclear ribonucleoprotein polypeptide B [Source:HGNC Symbol;Acc:11155]
Mouse Orthologue:
Snrpb2
Mouse Description:
U2 small nuclear ribonucleoprotein B Gene [Source:MGI Symbol;Acc:MGI:104805]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38298 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39694 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15176 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38298
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057601 | Nonsense | 26 | 229 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 52203922)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 51075606 |
GRCz11 | 1 | 51709970 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCATGGACATCCGGCCGAATCACACCATCTACATCAACAATGTTAATGAT[A/T]AGATCAAGAAAGAAGGTAAAGTCTTTCGTTTGTACTGTAACTTGCGTCTA
Long Flanking Sequence:
TCAAATGGCCAATCACAAATATTGATAAACTTGATCTTAGGTGCTTTTTGAATTCAAAAATGTTGCTAGGGTAGTATATGAAAAGTTGCTAAACCTAGCAACGAAAAGTCCTAGCAATAGTGTTAGTATCACTCCGCGACAACAGGTGGCGCAACAAGCGAAACCCGATTCACAACAATAAAGGAAACGAAGAAGAAGCGAAGCGCCAGTTTCCGCTTAAATCCAGAAGTGTGGTGAGTCCGTTCATTCACTTTTATTGTGATTTTTAAATCTATCAATAAGTTGTTTCACGTTTATAATTTTATAGAGCTGCACTCAGTGTCATTTCAGGCATCTCAGAAGGCTTAAATGGGAGACACTGCGAGTGTTTTGTGTTTGTAGTTCCTCGTTGTTTATTGTACTGGATCTCTTATGTGTTTACTGCAGGGACATTTTACCTCAGTTTATTAATCATGGACATCCGGCCGAATCACACCATCTACATCAACAATGTTAATGAT[A/T]AGATCAAGAAAGAAGGTAAAGTCTTTCGTTTGTACTGTAACTTGCGTCTATATGTGGAAAAGCTTTGACATTTTTGTTTGTCTTTGCTCATTGAAGTATGTTTGAGTTAATTAGTAAAGGGCTTTTCACAGTAATAATTGCTCCACATCAGTTTTAAAGTTAAGATTGGGGTAAAGTTGCTTTTATATTATCTCCTTCATCATATAAATCCAGAAAAAAATGGTTTGCAATTTCTAAATGAGGAAATGTATTAAACTATTCAAATCAAACTAATCAAAGTACATTTCTCACGGTCAATTAAATGGTGCTAATGTTGTGTTAATCGTTTCTACAGAGCTGAAGAGGTCACTGTACGCCTTATTCTCGCAGTTCGGCCAGATTATGGACATCGTGGCTCTGAAGACCATGAGGATGAGGGGTCAGGCGTTTGTGATCTTCAAGGAGCTTTCAGCAGCCACCAATGCCCTCAGACAGCTTCAGGGATTCCCCTTCTACAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39694
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 |
---|---|---|---|---|---|
ENSDART00000057601 | Nonsense | 39 | 229 | 2 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 52203563)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 51075247 |
GRCz11 | 1 | 51709611 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATGTTGTGTTAATCGTTTCTACAGAGCTGAAGAGGTCACTGTACGCCT[T/A]ATTCTCGCAGTTCGGCCAGATTATGGACATCGTGGCTCTGAAGACCATGA
Long Flanking Sequence:
TGCGAGTGTTTTGTGTTTGTAGTTCCTCGTTGTTTATTGTACTGGATCTCTTATGTGTTTACTGCAGGGACATTTTACCTCAGTTTATTAATCATGGACATCCGGCCGAATCACACCATCTACATCAACAATGTTAATGATAAGATCAAGAAAGAAGGTAAAGTCTTTCGTTTGTACTGTAACTTGCGTCTATATGTGGAAAAGCTTTGACATTTTTGTTTGTCTTTGCTCATTGAAGTATGTTTGAGTTAATTAGTAAAGGGCTTTTCACAGTAATAATTGCTCCACATCAGTTTTAAAGTTAAGATTGGGGTAAAGTTGCTTTTATATTATCTCCTTCATCATATAAATCCAGAAAAAAATGGTTTGCAATTTCTAAATGAGGAAATGTATTAAACTATTCAAATCAAACTAATCAAAGTACATTTCTCACGGTCAATTAAATGGTGCTAATGTTGTGTTAATCGTTTCTACAGAGCTGAAGAGGTCACTGTACGCCT[T/A]ATTCTCGCAGTTCGGCCAGATTATGGACATCGTGGCTCTGAAGACCATGAGGATGAGGGGTCAGGCGTTTGTGATCTTCAAGGAGCTTTCAGCAGCCACCAATGCCCTCAGACAGCTTCAGGGATTCCCCTTCTACAATAAACCCATGGTCAGTGCCACAGCTCCTATTCCTATCAAGGAACTACACCTGAAATGATTATCACTTCAGAAAATGAAGCAGTTTGGGGCTTTTGATTGACTTTAAAGAGATAGTTCACCCAAAAATTTGAAATTGAGTAAATGGGGAGTAAATTTTCATTTTTGGGTGAACTATTCTATTGACTTTTTGTTTTATTTATTAATTTGATTAAAGATATAGTTTTTCTGCCTTTTTGCCTTATTAAGTAGATAGGACAGTACTATAGACAGGAAGTAAAGTGGAAGAGAGACAGGGTAGGGACGAGAAATGTCCTCGAGCTGGGATTCGAACTCAGGATGCCTTGAAGTGCTACTGCACCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15176
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 |
---|---|---|---|---|---|
ENSDART00000057601 | Essential Splice Site | 177 | 229 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 1 (position 52196454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 51068138 |
GRCz11 | 1 | 51702502 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWCAAACCAGACATATTTKCTGTTTAYTCATTGGCYTTATTTTATTTTTT[A/T]GGTTTCCTGGGTTTAAAGAAGTGYGTTTGGTGCCTGGAAAACATGATATT
Long Flanking Sequence:
TTTTTCTTTCTATAAATCGAGTGGGAAGCATTAAATGCAGTGTCTGCCTTTAATGGTACACATAACTTTTGTGAAAAATAAATGACATGTATAAAATAGTTTAACTTTTCTTGTATATTAAAGAATAAACGATCATTCTAAATGTCATTACCTTTAAACGATGAGACATGGATGAAACCTAGTGATTTGAAGGATAGTGGAAACTATACCAAGGTTTAAAATGATAATAAATGAGTATTTTGCACTTTTTTTAAAATTTGTAGTCAAATCATTTTTGCTCAGTGTGGCTGACAAGATTTTTTATGTATAAACTACTGTGACACTGATTGACATTTTACCTAGTGTCTTCTGTAAATCAGGGTAAAAATGATAAATAAGGAACAGAAGAAGAATAAATGAATAAATAAACTAGCTAATGGACCATTATTTTAAAGTGTTACCCAAAAAACAAACAAACCAGACATATTTTCTGTTTACTCATTGGCTTTATTTTATTTTTT[A/T]GGTTTCCTGGGTTTAAAGAAGTGCGTTTGGTGCCTGGAAAACATGATATTTCGTTTGTAGAGTTTGAAAGCGAAGCTCAAGCCGGAGTGGCGAAAGATGCACTTCAGGGGTTCAGAATCACAGCCACGTGTGCCATGAAGATCACTTATGCCAAAAAGTGATTTGGCACTGACGCCTGTTTGTCAAGAACCAAACATTTTAATGGACTTTACCTGAGGATTATTACTAATGAGTGAATCCTCGACTTTTATTTTATTTTTTGTCTTTTTCAATTAGTTTTATTACTGTTCTTCCTTTTTTTGGTATGGATCTTACTTGGTCACTAAGAACATTTTAATATTCCAGGATAGATCTTTATTTTGTACTGTGGACTGAAAAAGTTAGCCTATAAAATAAATGTCATCTCGCCCACCCATGTAACTGACGTTTTTATTTTTGTTTTTTACCTTTTTAAAAAGCACTGCATAGATGTTCTGTTTCTTTCAATCTAAACTGCATTT
Associated Phenotype:
Not determined