ZMP
plxna3
Ensembl ID:
ZFIN ID:
Description:
plexin-A3 [Source:RefSeq peptide;Acc:NP_001091959]
Human Orthologue:
PLXNA3
Human Description:
plexin A3 [Source:HGNC Symbol;Acc:9101]
Mouse Orthologue:
Plxna3
Mouse Description:
plexin A3 Gene [Source:MGI Symbol;Acc:MGI:107683]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10020 | Nonsense | Available for shipment | Available now |
sa34310 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34309 | Essential Splice Site | Available for shipment | Available now |
sa41125 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34308 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10020
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044000 | Nonsense | 313 | 1892 | 2 | 32 |
ENSDART00000079699 | Nonsense | 313 | 1892 | 1 | 31 |
Genomic Location (Zv9):
Chromosome 8 (position 10087560)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9504142 |
GRCz11 | 8 | 9542727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTGGRTGCACCAAGGATGGCGTGGAATACAGACTTGTTCAAGCKGCCTA[C/A]AARCATCGTCCTGGAAAGATTCTGGCACAGGCTTTGGGCCTGTCTGAGGA
Long Flanking Sequence:
AAAGAGCACTACCTCTCGGGAGCCAAAGAGTCTGATGGGATGGCTGGAGTCGTGGTGGGTGATGATGACGGAGACTTGAAGAAGAAAAAGAAAGGTGGCAGTCGACTCTTCATTGGTGCTGCAATCGATGGCAAATCAGAGTATTTTCCAACCCTCTCTAGCCGTAAACTGGTGGCGGATGAGGAAAGTGTTAACATGTTCAGTTTGGTCTACCAAGATGAGTTTGTGTCTTCTCAAATCAAGATACCTTCAGACACCCTCTCTCAGTATCCCGCATTTGATATCTACTACGTCTACGGGTTCTCCAGCCGGACTTACATCTATTTCCTCACTTTGCAACTGGATACTCAGCTCACTCAGGTGGATGTGACGGGGGAGAAGTTCTTCACCTCAAAAATAGTCCGCATGTGCTCCAATGACACTGAGTTTTACTCCTACGTAGAGTTCCCGCTTGGGTGCACCAAGGATGGCGTGGAATACAGACTTGTTCAAGCTGCCTA[C/A]AAGCATCGTCCTGGAAAGATTCTGGCACAGGCTTTGGGCCTGTCTGAGGATGAGGATGTCCTGTTCGTGATCTTCTCCCAGGGTCAGAAGAACAGGGCTAACCCACCGAGAGAAACAGTGCTGTGCCTCTTCACACTGCACCAGATTAACCTGGCCATGCGAGAGAGGATCAAGTCATGCTACCGCGGAGAGGGAAAGCTGTCTCTGCCGTGGTTGCTCAACAAGGAGCTGCCTTGCATTAATACGGTGAGTCTTTTATGTCTTTCTTTAAGTATTTTTTTTTCCAGCTAAGCATTCTTGATTTTGATTTTGCCAATGCATGGATGTGTTCACTGGCCAACCGTTCCTTTTGTTGGGGAAAGGTTTGCGTTACGCATATCAGCAATGCTAATATTCTTATCAATCTTTTTGGTTTTTGGAATTAGAGTTTAGGTAGTAGTTAATCAAGGATTTGGGCTATGTTGTCTCTCAAACCAACTGGCTTTACTTGGCAAAATCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34310
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 |
---|---|---|---|---|---|
ENSDART00000044000 | Nonsense | 531 | 1892 | 5 | 32 |
ENSDART00000079699 | Nonsense | 531 | 1892 | 4 | 31 |
Genomic Location (Zv9):
Chromosome 8 (position 9974524)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9391106 |
GRCz11 | 8 | 9429691 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGCAGCTGTAAGACGTGTCTGGGCTCTGGAGATCCTCACTGCGGCTG[G/A]TGTGTCCTGCATAACAAGTGAGTCAATGTCATGCCTTTTACAATCACTAC
Long Flanking Sequence:
TGCGCTTCGTGCTTCTGCCTTTGGATGTCTCTGGGACAAAAGCAGCTGCATGAACGCTAAAGCTTTAAATAAAAGTGAAACCATCAACAAAAGCCTGTCCCCTTCCATGTTTACAAATACAAGCGCAGCCGTTTATAGGTCATTTCTGGTTAATGATGTCAGGATTTACCGGTATTCTGGAATGGATGTGTAAACGGTCTTTTCCAAAAAAATTCCAGCACGTTCTTGCCAGTGTGAACAGAGCTTTTCTGAATTTACCAGGATGTTTACCGGTATCACTGTGAGAAAGAGGCTAAAGTCACCTGTTGTAAAACCATCTGGTAGTTAACATTCAAAGTTTCCTCTGGTATCACTAACAGTGATATGTGTGTGCAGATGTGATGTTGATGTCAGCTGGATGTTTGTGCTGTGCTTCAGGTGAGTCGTCTGCCGGTGGAGAGCTGTTCTCAGTACAGCAGCTGTAAGACGTGTCTGGGCTCTGGAGATCCTCACTGCGGCTG[G/A]TGTGTCCTGCATAACAAGTGAGTCAATGTCATGCCTTTTACAATCACTACAACTGCTGCTCTGTGCACTGCTATGCTGCCTGTGCGCTAGTTCAAGAAGGTTAAACAGCATTGCAAGACATTTACATTTGAAACTGTATGCGTGCAATATGGATTGATCTGAGAAGCTGTTTTCTGTTCTGTGCTTATGCATTTTTTGTTAATAGAAAAGTTTGTGATTGACATGGTTTTAGCCAGTTGCTTTTCTTAGTTTTGTGCCTAGACTAGTGGACTTTGAGGTGGTGCTGACTGGTCGATTGGTTGGGATTGACATCATCATCTGGTGGAGATGATTTGATTGAACAGTAATCTTTGTAGTGCGGGATGAGTCATCAGTTTTTTTGTTTTATTTTCTGAGAAGAGAGAGAATGAATTCATTAAATGCATAGACTACATTTTAAAAGTTTTGCTCACAACGGCTGCATTTATTTCATCAAAAATGTTGTAAAAACAATAAAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34309
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 |
---|---|---|---|---|---|
ENSDART00000044000 | Essential Splice Site | 1342 | 1892 | 21 | 32 |
ENSDART00000079699 | Essential Splice Site | 1342 | 1892 | 20 | 31 |
Genomic Location (Zv9):
Chromosome 8 (position 9803805)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9220387 |
GRCz11 | 8 | 9258972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTGATGTTCCCTGGCATCGAGGAGCACCCGGTTCTGAAGGAGCTGGAC[G/A]TAAGGGAACTTTTAAAACTCTCTGTGCCCAGGTGGCGTCTGTCACTCACA
Long Flanking Sequence:
ACAATTGCTTCAATATTCATTATTTAATCAGTTCTGTATAATTTAATTCAATCTTTGATTCTGTGATGGATGTTAAAACTGCCCAATTAGACAGTAAATGAGTGTCTGATCAGCATAAGCAAAGCAACCAACTACATTACAGATGAAATAAATTACATTTGAATCTTGTTAAGCTTATTGCAACTTTATAAAATAGATTAACGATTCTTAGTTATAAAGTCCATAAATCTCAGAAGAAACATAATAACCATGTGTTCTCGAAATCGGATCAAATATCCTTTAGTATTAGTCTGTCAAAGCGCGTGAGGTGTTCTCCAGTCTGACGAGCGCTTTCTTTTTGTTCTTTATTCTTCTAAGCATTCGCTGAGCTGCAGACAGACATCCAAGAGCTGACGAATGACATGGACGGTGTGAAAATCCCTTTCCTGGAGTATCGTACCTACACCATGAGAGTGATGTTCCCTGGCATCGAGGAGCACCCGGTTCTGAAGGAGCTGGAC[G/A]TAAGGGAACTTTTAAAACTCTCTGTGCCCAGGTGGCGTCTGTCACTCACAAGTGCCAATAAGTAGGTTGCCATCAACTCATAGACCGTTTTCTTTTAATCCTTCTGCCAAAAAAGGAAAGCAAAAAAAAACCCTAGATGTGCTTTAAAAAGATCCCCTAAGCTCTGAAGCTACGGTACTGCTGTCTCAGTAGTGAGCTTCAGAGCGAACGCCCCTCTTTCAGCATGCTTTTTAATTAAAACCTCAGGCAGAATGAAATCAGCAGCCCTGCAAGGCCCTGGTGGAATAGCCGTCTAGAGACGTGCCTTACCAAAAAATGTTTTGAAAATAGTCAGGAAAGAACAATTAAATCTCACCGCAGCAGAGCTTTTTTTTATTTTTTTTATTTCAAGTATGCATTCAGGCAACAATTGTTGTTGCGCGTGTTTCTCTCATCTCTTTCCTGCCTATTTTTTCCATTTATGTTTTGTTCTCCTGCTTTTTCTGACGTTCAATCAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41125
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 |
---|---|---|---|---|---|
ENSDART00000044000 | Nonsense | 1556 | 1892 | 26 | 32 |
ENSDART00000079699 | Nonsense | 1556 | 1892 | 25 | 31 |
Genomic Location (Zv9):
Chromosome 8 (position 9779689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9196271 |
GRCz11 | 8 | 9234856 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAATTTTAATCCCAGACTGATTCATTGATTGTCCTCCAACAGAATGGCGG[C/T]AGGGTCGACTGACCAGAATCATCCTCCAAGATGAAGACGTCACCACAAAG
Long Flanking Sequence:
ACGGTTTTAGTTATTCCCTTAAAGTGGGAATAAGAAGTGACCCGCATAGTAGGATAACAAATACTAATGAGGTCAATGGTCACCAACCATTCAAAATAAAAATACAGAATAGAAAATCACACACACACACTGAATTTGGAGGCAGGACTTTTGTATAATTGACTAATGACAAGTGTTTAGAATAAAGTTCCACAATAAAATTAAGAACTTAAACAATAAAATGAAAAAAGAAAAATTAAATATTGATCAAGATATCTTCTTTTGGGTTAAAAAAAAAAAAAAGAAACTCATAAAAGTTTAGATCAACTAAAGGGTGAGAAAAATGACAGATTTGACATTTTTTGGTGAACTATCCTGTTAAAAATGGACAAAATCTTGACTGTTATATAGAAGCGATTGGCATCATGGCAAATGTTTTATTTCAGACATGTTGAAACCTCCTCCTCCTCCTAATTTTAATCCCAGACTGATTCATTGATTGTCCTCCAACAGAATGGCGG[C/T]AGGGTCGACTGACCAGAATCATCCTCCAAGATGAAGACGTCACCACAAAGATCGAGAGCGACTGGAAGAGACTGAACACACTGGCACATTACCAGGTTCGACAACATTTCCTGGCAGCTGCTCCATAACGATATGCAAATTTACAAGTGCTGGTCATGTACTGCGCAAAAATGGAGATGTTTTTTTATAGTTCTCCTCTTTTCTCCATCTCAGGTGACAGATGGGTCTTTGGTGGCTTTGGTTCAGAAGCAAGTATCCGCTTACAACATCGCCAACTCTTTCACGTTCACTCGCTCTCTCAGTCGATACGGTAAGCCGCAATCTCTTGGATCGCTTTACGCCACACAATCCTCGGCTTTAGCCATGTTTGTTTAATATATCGTGGATTCCTGCAGCGTTTTGTGTTGTGCCTCGTGCAGCATGTCTGAATCAAATGGGAATTTAAGATCTTTTCACCAGCCGTTCTGGGCTGGAGTCTTGAAGCTTTTCTGTAAAACACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34308
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000044000 | Essential Splice Site | 1861 | 1892 | 31 | 32 |
ENSDART00000079699 | Essential Splice Site | 1861 | 1892 | 30 | 31 |
Genomic Location (Zv9):
Chromosome 8 (position 9770932)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 9187514 |
GRCz11 | 8 | 9226099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCGCGCTCAGTGAACTGTATTTCTACATCAACAAGTACAAAGAAGAGG[T/C]GAGACCTGCGGCTGCGTTTCACATCCAATCCTGAACACCACACTTTTACA
Long Flanking Sequence:
TTGAGGGTGGGATTAGCCTGTCATTCACATGAGGACCAACAATAGGAAACCTCAACCATCCTTTCAATTCCTTAAGTCTTTTCTTAACCATTTTAGTCTGATAACACAACTTCTGATTCATGTCGATTTACAAAGTGCATTTCTTTAATTCCTGTAAGCAATAGAAATAGACTGTTTGCCTTAGCAGGCACCACAAATTAGTCATTTACAGATCCAGGCAGCCTAAAATGAAATGAATCAATCTGGTTTTCATTTTCTCCTGCATATTAACAGCAAATGCTCTTTTACATTTCAGAGTAGATGATTTGCTTTAACCGGAGTTATTTACATGTGTTTGTGTTTTTCAAGATATTACCGTGACATCAGCAAGATGCCAAGTATCAGTGATCAGGATATGGATGCCTATCTGGTCGAGCAGTCTCGTCTCCATGGCAACGAGTTCAACACACTGAGCGCGCTCAGTGAACTGTATTTCTACATCAACAAGTACAAAGAAGAGG[T/C]GAGACCTGCGGCTGCGTTTCACATCCAATCCTGAACACCACACTTTTACACTGAGTACTAGCATTCAGGGGTCAAGTGGCTTGGTTGGCATAAAGTGGGTGATGTGGCTTTTTCTGGATGTGAATCAAGCCTCTGCTAAACTAAGCTTTCAGTCAGATCAAAGCAACAACACCCAACATAATATAATATAGTAAAATACACTATATATGAGCATTGTCACACAAGTAGCAGTGAGATATGGCTGTATATCGGCATTGGTGGGAGGCGTGCGTTGTGCGTTGCCTTAGTGCCCCCAACAGTGCCGATATACAGCCATATCACACTGCTACGAGTGTGATATTGCGTTTATGCAACCGCTTGACGGCATAATTGTGTATATAAAAACAAAATCAAACATGGAGAGTCTCAAAAACCCTTTTGTATGAGGAACTACTTTCTTCCGGATTCAAATCATAAGCTGACAGTTAAACAGCTGAGCAAGCATCTTTTAAACTTTAGAT
Associated Phenotype:
Not determined