ZMP
agrn
Ensembl ID:
ZFIN ID:
Description:
agrin [Source:RefSeq peptide;Acc:NP_001170923]
Human Orthologue:
AGRN
Human Description:
agrin [Source:HGNC Symbol;Acc:329]
Mouse Orthologue:
Agrn
Mouse Description:
agrin Gene [Source:MGI Symbol;Acc:MGI:87961]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15437 | Essential Splice Site | Available for shipment | Available now |
sa381 | Splice Site | Available for shipment | Available now |
sa11435 | Essential Splice Site | Available for shipment | Available now |
sa12413 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15437
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111465 | None | None | 156 | None | 3 |
ENSDART00000114067 | Essential Splice Site | 294 | 1787 | 4 | 32 |
ENSDART00000134993 | Essential Splice Site | 219 | 1712 | 3 | 31 |
ENSDART00000147313 | None | None | 156 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 24063467)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23850033 |
GRCz11 | 23 | 23776584 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGCGCTCTTCAGAAACAGATACAGATGCAACACAAAGGACCATGTGG[T/G]AAGTCCAAACACAANNNNNNACACACACACACATGCATTGATGCCACTCW
Long Flanking Sequence:
CATTTTTGCACCATATGTGAACCCGGCAATGTTTGACATAGATACATGTTTGTGTGAATAGTAAAGGGGAGTCACTCCAGATCCTACAATGTTTACTTAGATAGCTTGGCTGTATAGGATTCAGTTATCATCATCATAAATAGCCAAAACCAGTGTGTACAGAATCCAGATTAAGCACTACGCTTACTACAAATTGAACTACACTTCCTCCCCCTCACTTTCTTTTCCTTCTTCCTATAAGTCAAACGATAACTTGTTTCTCTGCTTTTTGGGGCAGATCTTAACCTGGAGAGCCCCTGCCTGAAGAAGACCTGCGAGTTTGGAGCCGTGTGCGTGGTGAAGAACAGCGAAGCAGTGTGTGAATGCTCAGACGCCTGTCCGCAGGACCAAGACCCTGTTTGCGGCAGCGATGGGCACACGTACAGCAGCTCATGTCAAATGAAGGCCATGGGATGCGCTCTTCAGAAACAGATACAGATGCAACACAAAGGACCATGTGG[T/G]AAGTCCAAACACAAACACACACACACACACACATGCATTGATGCCACTCACTCCCTCACTGCCTTTCATCCTCGTCCACCCCCTGCACTTAAGCACTCCACCGATATTTCAAGAGAGGACTGTAATTTTCCTCCTCCGCAACCTTTTTTTTTTGTTGAAACGATGCACTTAAGTTAGAATTAAAGAGGGCAGCATCCTTCACAGTAATTGTTTGCGTGAGTCATGGGTTTTTTTGTCGGGCTTTTGTAAGCTCGCTCTAGATAAGTCTACAGAGAGGCCTGCTCGCCCCCCAAACAAACGCGTGTTTATGTGCGTTCTTTACAAAAGACTTGTAAATCATTTTCGATGGCTGTCTTTGTGCTTTCGCTTGGGAGGGGAATATTAAGTGGATTTTTTTTTTACTGGGAAACTTTGAAAAGCCTGTCTCGTTCGCTGTCAGCTTACGTTCAGGAAGAATGAGGTAGAACCATTGTGTCATGCGGTTTATACATGCGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa381
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 > C
Consequence:
Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111465 | None | None | 156 | None | 3 |
ENSDART00000114067 | Splice Site | None | 1787 | None | 32 |
ENSDART00000134993 | Splice Site | None | 1712 | None | 31 |
ENSDART00000147313 | None | None | 156 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 24103335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23889901 |
GRCz11 | 23 | 23816452 |
KASP Assay ID:
554-0361.1 (used for ordering genotyping assays)
KASP Sequence:
CATTAAAATCTGTATGAAACCCAACAGCTGTATATGTGTGTGTGTTTTTC[A/C]TCAGACTGTGGTTCAGGAGGCTCCGGCTCGGGATCTGAGACTTGTGAACA
Long Flanking Sequence:
AACAACAACCATTAAATTACAGAAACTTATCGTAAAATAACTGACGTTAAATTTAAAAAATGACTGTAAATTTAAGGAAATTTCTGTGATTTAACGTCCGTTATTTTACGGTAAACTTCTGTAATTTAACGGACAATGTTTTATGTTGTTGTTTTTTTTCCAGCACTCCAGCTGCCGGGAAAAAAAGTGAAGTAACAGATCTTTCTTTTACAGTGTTGGGTTACTCTGTTTTTTTTTTCTGTTTCTGTTTTTTATTCGCCTTTGAGAGTGATTTTGTATAACAGACTTTTTTTTTTTTTAAGAATTAGTAAAAAACAGAAGTTTTATTAGGATGGTGACAAATATGTAACATTTTACTGACAAGAACCGTAAAACATTTTAATTCCACCTTTAAAAACTCTAGCCAGCTAGACAGGTGCAGCTATAGTGCAGTTATAATCACTTCAATACCATTAAAATCTGTATGAAACCCAACAGCTGTATATGTGTGTGTGTTTTTC[A/C]TCAGACTGTGGTTCAGGAGGCTCCGGCTCGGGATCTGAGACTTGTGAACAGGACCGATGTCGCCGATATGGAGGAACGTGGGACGATGACATGGAGGACGAGCGATGTGTTTGTGAACTAAACTGTCAGATTGTGCTGCACAGCCCGGTGCGTCCCACACCACCATAACCAATCGCCCGAGCATTTGACTTTTCCAAATGTGTGCTAAATCTTGTTGAATCCATTAATCGTGCTGTGTTAACCTCTATGTGTGCTTACGCAGGTGTGCGGCTCTGATGGAAACACGTACTCCAGCGACTGTGAGCTCAAGAAGACCAGGTGCGAAAAGCAAATAGACCTGAGTGTCCAAAGCCAAGGGCCCTGTCCAAGTAAGAGACTAAATTCAGATCCATTATTCATCCTGTACTGTGTAATGTTGTGATGGCCAGTGTTGTTTTTTTTAAGATGGATAAACTTCTGATGTTCTTATTTAGAGGTTTCTGTATATATACAGTTAAAGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa11435
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111465 | None | None | 156 | None | 3 |
ENSDART00000114067 | Essential Splice Site | 1597 | 1787 | 28 | 32 |
ENSDART00000134993 | Essential Splice Site | 1522 | 1712 | 27 | 31 |
ENSDART00000147313 | None | None | 156 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 24177898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23964464 |
GRCz11 | 23 | 23891015 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TATGAGTGCGCCTGCCGCCAYGGATTCTCCGGACACCACTGCCAGGACAG[T/A]AAGTTCCTTATTTAATCACTTTTTAAAAATCATATTACCCAATATAGCTT
Long Flanking Sequence:
TTTAATTTGTGTTTATGATGATTATGACTTCAGCATATCTAAAAAGCTATTCCATCGCAGGGTAAATTTGTGTGGCTGCAGTTGTAGCAGCCTTTGCTTTTGGACCAATCTTCAGTGCTGAATTCACCCTCATGCTCTATCATAACATCACAACTCACAAGGCAACTTTTCACCTTGACGAGAAATCTTGTCGTGATTTAGTCTTGTGAGATATTGTAGCCCGAGGTCTCATCACACCCCTAGTATTAGCTGAAAAATATTTATCTGTGACAACACAGAAATTGTATATATAATATTGTATATCGGTCTCCACAGATTACTTTGATGGGAATTCCAATCCTGAAAGCTGATAATGCCCTTTCGTCCACTGACGTGTCCATGTATCCTAATCATCCCTGCTCCAAAGACGTTTGTGAGAATGGAGGCCGCTGCAACCCCCAGCTGAACAGCTATGAGTGCGCCTGCCGCCACGGATTCTCCGGACACCACTGCCAGGACAG[T/A]AAGTTCCTTATTTAATCACTTTTTAAAAATCATATTACCCAATATAGCTTCTCCGCCAACTCCCTCACACTCCTTAAAGGCAAGATTTGCATGCGTCTTTAGCATACATCAACATACTGTACAGCTTACTTAAAAGAAATAGCTCTTGGCAGCTCTAGCCAGTCATATGCTCCATATGTAGATTTAGCTAAATCCACGCCTCCAAACTTTCACAAATAACACCATCCTCGATTCGTATGCTTATCGCAAACACACATTGGCACAGTCGCAAAAACCTAAGAACTTTTGCTCACCTCATTAACCTTGCAGGGTCCTTGTGTTGCATCTTTAACCTTAATTAAGCCACACAAGCATGAAGCCTGCGATACATCACACTCTTTTTCTAGCTTTGCTTTAATTAACAATGCCCTGTCTCACATCGATTGGTGTAATTTCACTCCGTCTTCTCTCCCCCTTTCCAGCAATATTTGAGAAGTCCGCTGGGGACACGGAGGCCATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12413
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111465 | None | None | 156 | None | 3 |
ENSDART00000114067 | Nonsense | 1694 | 1787 | 30 | 32 |
ENSDART00000134993 | Nonsense | 1619 | 1712 | 29 | 31 |
ENSDART00000147313 | None | None | 156 | None | 2 |
Genomic Location (Zv9):
Chromosome 23 (position 24190320)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 23976886 |
GRCz11 | 23 | 23903437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCCAAGCCTGTGGTGCTGCGCTCCACTGTACGGGTCAACACCAACCACTG[G/A]ATACGAATTAAGGCCAGCAGGTAAAATGCTAAAAAKCWTTTCCAGYATCT
Long Flanking Sequence:
GCCTCTGGTGGATTGATGCGAGAAGAGCAGAAATTTAAGATCTTAAAAAGTGTACAAAGGAGCCTGGTGGATTTGCGAAAGCAAAACCTGCAAAAAATTATAGCTCCTGGGACATATTTTACACTCTCCAGAAATGTAAACAGGGGTACATATTCACAATGCGCCCGGGTTGCTCTATCAACTGTTAAATTTTCACCCATGGTTGTTAAACTTGCAGGTAAGTCTCAGTGGTTAACTCAGCACCTCTAAAAGAGCAATAGAATTTTGATAGCATTTCCTGTTTCTCTTTGATCTAGCGAGAAAGCCCTGCTGGTGAATAAATTCGAGCTGAGCATCAGGACGGAGGCTACGCATGGTCTGATTTTGTGGAGCGGAAAGGGAGTTGAGCGCTCTGACTACATCGCCCTCGCCATTGTGGATGGAAGAGTACAGATGACCTATGACCTCGGCTCCAAGCCTGTGGTGCTGCGCTCCACTGTACGGGTCAACACCAACCACTG[G/A]ATACGAATTAAGGCCAGCAGGTAAAATGCTAAAAATCTTTTCCAGCATCTCCACACATTTACAGTAAGGTTGTTTTTTCTGCTAGATGGGTCAAGCTAGTAGTTCAGACTTCTGCTTGCAATACCAAAATATTCAGTGTTGAGTCATTCTCAACATTTTCAGTGTTCAGGAGAAATAGAAATGTATTTATATTTGATTAGTTTATCTATAATTTCACACTTTTTTTAAATATGTTTTTTGTTTGTTTAATATGTACACTACTGTTTCATCATTTGAGGGAAGTATTTTTTTAAGGATTCTTATGTTCATGAAGGCTGATTTTATACAAAAAACAGTAATATTGTGGAATATTATTACAATTTAAAATCCTTTTTATTTTAAGATATTTTAATTACACATTATAAAGCTTCATTCAATTACAAAGCTATACAAGTCATTCTGGACTTCAATGCCACATGGTCATTTAGAAATCAACCTAATACAGATGTGTTGGCTTTAAA
Associated Phenotype:
Not determined