ZMP
anxa6
Ensembl ID:
ZFIN IDs:
Description:
annexin A6 [Source:RefSeq peptide;Acc:NP_001002038]
Human Orthologue:
ANXA6
Human Description:
annexin A6 [Source:HGNC Symbol;Acc:544]
Mouse Orthologue:
Anxa6
Mouse Description:
annexin A6 Gene [Source:MGI Symbol;Acc:MGI:88255]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17582 | Essential Splice Site | Available for shipment | Available now |
| sa32005 | Nonsense | Available for shipment | Available now |
| sa35765 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa17582
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 > C
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006073 | Essential Splice Site | 142 | 393 | 6 | 16 |
| ENSDART00000105346 | Essential Splice Site | 142 | 568 | 6 | 21 |
| ENSDART00000126260 | None | None | 202 | None | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 51572625)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 50325393 |
| GRCz11 | 14 | 49313150 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTAAAAGTGAGCTGTCCGGAGACTTTGAGAGACTCATGCTGGCTGTMGG[T/C]AAGCTTCRGCAKATCGAGATCAGTTMCTGAAACTCAYATYTGCCTTTTCT
Long Flanking Sequence:
TGGCGCAGTAGGTAGTGCTGTCGCCCCACAGCAAGAAGGTCTGGGTCGCTGGTTCGAGCCTCGGCTCAGGTTCATTCCGCTGTGGCGACCCCAGATTAATAAAGGGACTAAGCCGACAAGAAAATGAATGAATGAATAACGTTTATTTTTTACAGTGTAGCCTGACATGGCGCTAAAATAAAGAAATCATACATAAGTAATCATCTGATCCAGAGTTTGCACCAAACCAAAAACCCAACGCAGTGACCTGAATGCTGTGTGATTATTGTGCAATATTATGATTGTCAATTACATTTAGATTATTGATGTTTAAGAGTTATTGCAGTATTAGGATTATCAGAGTAGCGTGGATGAATTCAGGATGATGTAACAGAGCGAGTATATCATTGTTTGTTTTTCCCAGTGTTTGATGAATATCAGAAAATTGCAGAGAAATCCATTGAGGACAGTATTAAAAGTGAGCTGTCCGGAGACTTTGAGAGACTCATGCTGGCTGTCGG[T/C]AAGCTTCGGCAGATCGAGATCAGTTCCTGAAACTCATATTTGCCTTTTCTCTGAAATCTCACACCGTGTTTATGTATTTCACAGTTCAGTGCATCAGAAGCAGGCCCATGTTCTTCGCCAAACGCCTTTACAAATCCATGAAGGTAAAGCTGCTATAATGCATTCTGTTTTAATGTTGTTTCAGCATCGATTCTGCAATGTGTGCATCTGTGATAGTCACATCACAAAAATATGCACTGTTGAGTCAAACTGTAAAAAAAAACAACCCTTATTGTACAGAAACTATCCCTAAATTTTTTACAGTAATTTTTTGTCATTTAAAATTATATGTAGACAGGGCTTTACATTAACACCCGCCAACCCGCCAAATGCGGGTAGATTTCGGCGATGGCGGGTAAGACAGACACTCCCACTAGCCACTTTGGCTGGTTGAAAATTATTTTCCCAGATAATAATTCTTAAAAGCAGCGTTCGACAATAAGGATGGTCCAATATGCATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32005
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006073 | Nonsense | 342 | 393 | 13 | 16 |
| ENSDART00000105346 | Nonsense | 342 | 568 | 13 | 21 |
| ENSDART00000126260 | Nonsense | 167 | 202 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 51603548)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 50356316 |
| GRCz11 | 14 | 49344073 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTGGGTCTCATGATGACACCGGCCGACTTTGACGCCAAGATGATGAAG[A/T]AAGCCATGGAGGTATTTACAGGAAAATTGCAGTGATACAAATATGAACAT
Long Flanking Sequence:
CAGTATATATGATTTTGTTTCCCTATCCATCACTAGTTGAGAGGAACTGTGCGGCCATATTCAGATTTTGACCCAGCCAGTGACGCTCAAGCTCTGAGAAAAGCAATGAAGGGTTTTGGTATGTAAAAAACACAGTATGTTACGCTTGATGACATCTCTATCAACAGATTTGCAAATATAGTAAAGGATTTCCTGTGATTTAATGTTTTTCCAGGCACTGATGAGGATACGATTATTGAAATTGTGGCACGCAGGAGCAATGAACAGAGACAGGAGATCAGACAGGCTTTCAAATCTCTTTTGGGACGGGTATGTGCTAACTAAAGCAATAGTTAGCTTTGATTTTGTGTGTACTTTAATGTGAACGCGTTTGGTCTTTTGTTGATGTTTTCCATCAGGATCTCATGGCTGATCTGAAGTCAGAGCTGTCCAAAAACCTCCAGAGACTCATTCTGGGTCTCATGATGACACCGGCCGACTTTGACGCCAAGATGATGAAG[A/T]AAGCCATGGAGGTATTTACAGGAAAATTGCAGTGATACAAATATGAACATTGCAACACATCTGAAACGTTAAAGGGCAGCATGGTGGCTCAGTGGTCACCTCACAGCACAAAGGTCGCTGGTTCGATCCCTGGCCAGGCCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCTCATGTTGGCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGCTATAGGGGAATTGGATGAACTAAATTGGCCGTAGTGTATGTGTGTGTGTGTGAATGAGTGTGTATGGATGTTTCCCAGTACTGAGTTGTGACTGGAAGGACATATGCTGGAATAGTTGGCGGTTCATTCTGCTGTGGCGACATCTGATATGTATAGGACTAAGCCGAAGGAAAGTTAATGAATGTATCATTGAAAATATGGCCGCAGAGTGAACAGACTTTCCTTAAAAGGCACTTTGGTATTTTACACCTTGAGATTCCACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35765
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 > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000006073 | Essential Splice Site | 376 | 393 | 14 | 16 |
| ENSDART00000105346 | Essential Splice Site | 376 | 568 | 14 | 21 |
| ENSDART00000126260 | Essential Splice Site | 201 | 202 | 7 | 8 |
Genomic Location (Zv9):
Chromosome 14 (position 51605245)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 50358013 |
| GRCz11 | 14 | 49345770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAGAAGCAATCAGGAGATTCAGGAGATGTGCTCGGCCTATCAGAACGG[T/G]AAATATATCGCACAGAGTGCAGCAGGGGGCGCTGTTCATCTGGGAAAAAC
Long Flanking Sequence:
GACAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAACCGGAGCACCTGGAGGAAACCCACGCGAAGGCAGGGAGAACATGCAAACTCCACACAGAAACGCCAACTGAGCCGAGGTTTGGACCAGCAGCCTTCTTGCTGTGAGGCGACAGCACTACCTACAGCACTGTGCACTGTATATAGGGGTGATAGCCTTATATATATATGTGTGTGTATGTGTATATATATATGTAAGTGTGTGTATGGATATATATTTTTTATGTGTATATATGTATGTGTATGTGTATATGTATGTGTGTATATATATATATATATATATATATACTGCATTCTGCACAGAAATACCAAAAATGTCCACAGATTTTGTCCAGCTGTGAAAATAAGCAGTGTTTTATGCTTTAACAGGGTGCAGGGACTGATGAACATGCGTTGATTGAGATCTTGGTCACTAGAAGCAATCAGGAGATTCAGGAGATGTGCTCGGCCTATCAGAACGG[T/G]AAATATATCGCACAGAGTGCAGCAGGGGGCGCTGTTCATCTGGGAAAAACACACACAGCAGTTGGGCCATTTTACACTTTGCACCTTCTCTGCTGTCTACACTGCCAGACAAAAGACTTGTCACTTATCCAAGTTTTAGGAGCATGCAAATAATAACTTGACTTCTAGTTGATCATTTGGTATCAGAAGTGGCTTATATGAAAGGCAAAGGCCTCTAGATGACGCTTATTTAAAAAAAAAAAATATGATCATGCCTTGACTTTTAATGATTTCATTAGGGCAGTAAGGTCTGACTTTGTTTAGACAAAAGTCTTGTCACTGAACAGAAATAATGTCCAGTATAGAATATAAAGTCCTGCTGCAGTGGAGACAGAATGGATATTGTGTCTGACTCCATCATGAGCTTGGAGGACTGCATCCATACATCTCTGCAATGACTCTGATTAATAAAGTCATCTGGAATGGCAAAGAAAGCGTTCTTGCAGGACTCTCAGATTTCA
Associated Phenotype:
Not determined