ZMP
becn1
Ensembl ID:
ZFIN ID:
Description:
beclin 1 [Source:RefSeq peptide;Acc:NP_957166]
Human Orthologue:
BECN1
Human Description:
beclin 1, autophagy related [Source:HGNC Symbol;Acc:1034]
Mouse Orthologue:
Becn1
Mouse Description:
beclin 1, autophagy related Gene [Source:MGI Symbol;Acc:MGI:1891828]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14704 | Nonsense | Available for shipment | Available now |
sa35233 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14704
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000115237 | Nonsense | 92 | 384 | 3 | 9 |
ENSDART00000132985 | Nonsense | 41 | 111 | 1 | 2 |
ENSDART00000143401 | None | None | 223 | None | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 15555980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14638166 |
GRCz11 | 12 | 14676469 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGACACATTATTGGACCACTTGGACACACAACTCAACATCACTGAGAAC[G/T]AGTGCCAGAATTACAAGTCAGTAACACACAATAACATCAATTACTGTAAC
Long Flanking Sequence:
CATTCAGATGTCCACTCCAAATTTATCTACTAGGAGGAGCTATAGAAATTTTTATTTTACATATGTCCCCATGAGAAATAATTGCTGTCTTAATGGGACTAAATACAACACAGGGCCAGGACTGTATAATACTAGACAAGAATCTTTAGATATTACACCATTAGATCTATATTAGTGACCAATGTCTAGTAAAGCTATTAAAATTGAAAGTGTATTTAGTTTATTGTAATTTGTATTATTAGTTATAATGAAACATATATACCATTGTAACATTTATATACAAATTTATTAATAATAAACTAGTTTCTAATTATAAGCGTTATTTATTCAGTGGATCGGTGGATCACAGCAGAGGTTTCATGTGTGCGTTTTTCCTGTAGGTGACAAGCAATCTGTTCGACATCATGTCTGGTCAGACAGATATTGATCACCCACTTTGTGAGGAGTGCACTGACACATTATTGGACCACTTGGACACACAACTCAACATCACTGAGAAC[G/T]AGTGCCAGAATTACAAGTCAGTAACACACAATAACATCAATTACTGTAACAAACTATTTTTATTTTATTTTCTGTGAGTGATGTGATGTTATTTGCCTGGTAAGATTAATTAAAGAGGTAAAGACTGGTAAACTGGTAAAGAGATAATTTATGTACACATTTTACACCATTGGGTTGTTTAATTGCCTGTGAATTGTCAGGAGCTGTTTAGAGCTGCTGTCTCAGCTTCCAGAAGAAGAGGAGGCCAGTCTACTGAATGCATTGCAGCAGTTGAAACAAGAAGAGGAATCTCTGATCCAGGAACTAGAGAGCATTGAGACAAAGCGTGAAGCCGTGGCCAAAGAGCTGGATGAGGGACGCAACCACAGCCAGCTGATGGACACTGAAGAACTTCGGTATATATGAAAAGAGTATTTACAGATGACTCATATTTTTATATGAATAGTGAATGTTTGAGAAGTGACAGTATATTAAGGGGAAAAAACATGACTGTGAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35233
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 |
---|---|---|---|---|---|
ENSDART00000115237 | Nonsense | 295 | 384 | 8 | 9 |
ENSDART00000132985 | None | None | 111 | None | 2 |
ENSDART00000143401 | Nonsense | 134 | 223 | 4 | 5 |
Genomic Location (Zv9):
Chromosome 12 (position 15581877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 14664063 |
GRCz11 | 12 | 14702366 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGTTGTAGGAATTGCCATTGTATTGTTCAGGTGGTCTGCGTTTTTTCTG[G/A]GATAATAAATTTGATCATGCAATGGTGGCTTTCCTTGACTGTGTCCAGCA
Long Flanking Sequence:
TGCACAATTGTCTCACAGCAAGAAGGTCACTGGTTCGAGCCCCGGCTTGGTCAGATGGCATTTCTGTGTGGAGTTTGCACGTTTTTCCTTGGTCGTGTGGATTTCCTCTGGGTGCTCCGTTTTCCCCCTCAAGTCCAAAGACATGCGGTATAGGTGAATTGGTTAAGCTAAATTGGCCGTAATGCATGTGTGATAATGAGAGTGTATAGGTGTTTCCCAGTGATGGGTTGCAGCTGGAAGGGCATTTGCTGCTTAAAACACATGCTGGATAAGTTGGTGGTTCATTCCGCTGTGGCGACCCCTGATGAAGGGGTCTAAGCCGAATACAAAATGAATGAATTTATTGCATTTTAAGATAGTTTACAACTGTTTTAGATTGATTGTATTGATTTCTATTATCATTTATTAATTAATTTATTTTTTTTTTTTATTGTTTTTTGTTTTGTTTTTTTGTTGTAGGAATTGCCATTGTATTGTTCAGGTGGTCTGCGTTTTTTCTG[G/A]GATAATAAATTTGATCATGCAATGGTGGCTTTCCTTGACTGTGTCCAGCAATTTAAAGAGGAGGTGGAGAAGGATGACACTGGCTTCTGTTTGCCATACAGGTGAGAATATTTTGAAAACAAATATAATAACAAAAATAGCAGATCACTTTAGTTTACCTGAAAAAAGGACAGGCCATATTAATCAAGCCATAGATGGACAAATTATTCTGCAGATATGTGGTGATTTTAAGATAATTGTCATTTACTGATATCTATGACAGAGTTAAAAAAAAAAAAAAGTCCTTTAAAAGCAGTATTTTTCTTTGTTTATTTGTGCACTTGAAATTCTCTTTGTCTTTTGTAATTAGAATGGATGTGGACAAAGGAAAGATTGAGGACACAGGAGGAAGTGGAGGGTCTTACTCTATTAAGACTCAGTTTAACTCCGAGGAACAGTGGACCAAAGCTCTCAAGTTCATGCTCACTAACCTGAAGTGGGGTTTAGCCTGGGTTTCATCT
Associated Phenotype:
Not determined