ZMP
B0V1S6_DANRE
Ensembl ID:
Description:
Novel protein similar to vertebrate plexin B family [Source:UniProtKB/TrEMBL;Acc:B0V1S6]
Human Orthologue:
PLXNB3
Human Description:
plexin B3 [Source:HGNC Symbol;Acc:9105]
Mouse Orthologue:
Plxnb3
Mouse Description:
plexin B3 Gene [Source:MGI Symbol;Acc:MGI:2154240]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21199 | Nonsense | Available for shipment | Available now |
sa13997 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21199
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 |
---|---|---|---|---|---|
ENSDART00000147940 | Nonsense | 308 | 660 | 2 | 9 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 8741841)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8158423 |
GRCz11 | 8 | 8197008 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGGCTTTCACCGGGAGCAACCTGCGCTGTTTGTGGCTATGGCCATGGGA[C/T]AAGCATCAACTCCTACACCCACAGACAAGTCGGCTCTTTGTGTGTACACG
Long Flanking Sequence:
AGGTGCTGTACAAGACCGACAACCCTGTGGACACACAGTATGTGGCGGCGAATGACCCAAGAGTGTCCACGGTTGGTGTTGTGGTGGAGCAAAAAGGAGTTCCTCTTATGCTCGTTGGGCGGGGCTACACCAGTAAAGGACCTGGTGGGATCCCACCAATCACAATGCGACGTTTAACCCCAGTTGAGCGACATTCTGCACCGGCGTTCTCCCATGAAGAACTTGGTAAGCTGGTGGTCGGAAGCTACTCTGAATACAACAACCACTTTGTGAATGCGTTCCACCACAACAGCTACGTCTACTTTGTGTTCTCTCGGCGCGACGTGTGGGGCAGACGAGAGTACCGAACGTATGTGTCCAGACTCTGTGCAGGAGACCCCTTTTTTTACTCTTACGTGGAGGTGCCGCTTTCTTGCAATGGAGGATATAATCTGGCTCAGGCGGCCGTGCTTGGCTTTCACCGGGAGCAACCTGCGCTGTTTGTGGCTATGGCCATGGGA[C/T]AAGCATCAACTCCTACACCCACAGACAAGTCGGCTCTTTGTGTGTACACGGTGGAGGAGCTGGACAAAGCTCTGCATGCTGCCCAGCTTCTGTGTTACACACAGGAAGGCAAAGATGTCAATAACAAAGAGAAGGCATACATCGAGTATGAAGTGTCCTCCAGATGTCTGAATCTTCCACAGGTAAGTTGTTGGCCTATGTTTACCTGTTATTCCTAAAAAGCCGATATGACAAATATCTTATATCATGATCTCACAAAAGTACCAATCCTGTACTAAAAATGTACTCTAGGGAAAGTAAAATCACACGTTTTTAAAACTTCTTAGTAAATTACAATTCAAGAGTTCACACTTAGATACTGTTTGACAACTTGTTAGTAAGTTAGCAGGTTTGGCATGCTGTCCCGGGAGAGAACCCTGAGCTCTGAGATAGTTGAGCCCAGGGCTCCCGCCAGGTCCATAAAGCATGTGAGGGGAGTACGAGGTCAGGTGTTCTCGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13997
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 |
---|---|---|---|---|---|
ENSDART00000147940 | Essential Splice Site | 471 | 660 | 4 | 9 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 8760486)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 8177068 |
GRCz11 | 8 | 8215653 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACTGCTGGAYGCCACCAAACAGAACRTCTTCGTATTGACYGAAAGAAAG[G/A]TAYTGGAGACAAACTGCTTCCTTTTATCTGSCRTCAAGTGAAACAAACAG
Long Flanking Sequence:
GACAGCAAAAGTCAATGATTCATTTCAATTATTTAACCTGACACATTTACTGTTCCGAAAAATCATAAATGTTTCTTAAAATAAAATACATAATGATGGGGAGGGGTTGTTTTTAACCCAAACATTTAAAAATAACATGTTTTAGAGCAGTAATCACAATACCATGATATTTCTATCTAAGTATCCTTCATACCATCAGAATCTCATGCCCAGTACTGATTAAATTGATTGCGATAAAGGGATAGTTCACCCAAAATCAGAATTCAGTTGTTATTACTCACCCTATGTTGTTCCAATCCCCTGAGACTTTCAGGCAGGACTTTTTGCATCTGAACATATTCTGATTTAATGTGCTTTTATTTCGAATGTAGGTATTCCTGCATGCAAATGGTACTGGGACAAAATACGACACAGTGGAGGTGGATCCAGAGAGTCCCATTAACGCTGATCTACTGCTGGACGCCACCAAACAGAACGTCTTCGTATTGACTGAAAGAAAG[G/A]TACTGGAGACAAACTGCTTCCTTTTATCTGGCGTCAAGTGAAACAAACAGCATCTGTTACATTCACACTCTCAAAGGGGAGATTACACGTTTGCTTTAACAAACATCCTTCGAATGACAGATTTCTTCAGATGAAAGTCTGGTTTCGTTTTGTTTTTTGCATTGAGCAAACGTCAACCAATAAAGCGCAGGCCTTTCAAAGTTTTTTACCAAGTCTTATCTGTCACATCCATAATAGAGAGATGTCACATCCATAACCCAGTGTTTCCCTCATAAATGCAAAAATGTATAATAATATAAAATAAATCAATTTTTTCCCAAAACCAAGCAAGCCAGTGGTGACAGTGGCGAGGAATAAACTTAACCAATTGATGAAAGTGAAGTAAAAAATATATATGGTATATTATCTATATTATCTGTATTTACAATTATTCTTCACCAATTGATAAAAGTGAAGGAGAAAAAAAACTTGAGAGAAAAACCAGGCTCAGTTGGGCACAA
Associated Phenotype:
Not determined