ZMP
wu:fc09a11
Ensembl ID:
Description:
annexin 11a isoform 2 [Source:RefSeq peptide;Acc:NP_899670]
Human Orthologue:
ANXA11
Human Description:
annexin A11 [Source:HGNC Symbol;Acc:535]
Mouse Orthologue:
Anxa11
Mouse Description:
annexin A11 Gene [Source:MGI Symbol;Acc:MGI:108481]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35446 | Nonsense | Available for shipment | Available now |
| sa28085 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35446
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 |
|---|---|---|---|---|---|
| ENSDART00000057948 | Nonsense | 293 | 483 | 8 | 15 |
| ENSDART00000101775 | Nonsense | 336 | 526 | 8 | 15 |
The following transcripts of ENSDARG00000077383 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 16360259)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 16180294 |
| GRCz11 | 13 | 16311286 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTGGCCTCGCGCTCTAATGCTGAGATCCGAGAAATCAATCAAGTTTTC[A/T]AAGCTGGTGCGTACTTGACTCATATTGCTTAATTCCTTCCTTCTGCAATT
Long Flanking Sequence:
TATAAAGTAACTTTCAAAACTTTGACAATTGTCAGATTTACTTATTAACAACAAGTGGCATCATAAAATATTTTTAAATATGACTTTATAGTGTGACGATTTGGTTTGTACAAATAGACCCAAAATAAAACAAGACAAATTTCGAATGCATTATGGAGGTTAAATGGTGTAAATTCATAAAAAAATGTAAATAGGTTGAATGCATATTAAAGCAAATAGTATTAGTTGTATAACATAAAAAACATGCTTTACCAAAACACAAGCACAAAATGAGAATGTTTGAAGAATGTCCCTGCAGCTATTTGCCATGCAACAATTAACATTTAGAGTGAACCGTTTCTTTAAGGTGCACAGATAATAGAATCTCTGATTAGATGTTTTGATATCCCATTAATAATGTGCTGATTATTTGACAGGGAGCAGGGACAGATGAGGCCTGTCTGATTGAAATCTTGGCCTCGCGCTCTAATGCTGAGATCCGAGAAATCAATCAAGTTTTC[A/T]AAGCTGGTGCGTACTTGACTCATATTGCTTAATTCCTTCCTTCTGCAATTACAGATTTGATTACTTCCCAATCAAGCGTCTGCTACATGTCAAACCTGCTTTAATACGAAGCTCTACAGTAAAATGTGGTGATTGATAACACTCAGTGTTTTGTTTTAGAGAATAAGAAGTCACTGGAAGATGCCATCAGTGGAGACACCTCTGGACATTTCCGCAGACTTTTGGTCTCTCTTGCTCAGGTACAGTTGCTGTATTTCTTAATTTATGGATTTAATAAAAATCAAAACAAACTCATAGACACGACCGGCTTTTATATGCAAGATCTGAAGTAGTCATTTATTTGATGAAGGGGGATGAAAAAAATCTCTTGAGTATTTGATTAGATTGTTTTTATTATTATTTATTAAAATTTATTTTACAGTTTCTGACATAGCTTTATTATTATAATTATTATTATCAGTAGTAGTAGTATTAGTATTATTTTTAGTCGCCGTTGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28085
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 |
|---|---|---|---|---|---|
| ENSDART00000057948 | Essential Splice Site | 321 | 483 | 9 | 15 |
| ENSDART00000101775 | Essential Splice Site | 364 | 526 | 9 | 15 |
The following transcripts of ENSDARG00000077383 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 13 (position 16360499)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 13 | 16180534 |
| GRCz11 | 13 | 16311526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGAGACACCTCTGGACATTTCCGCAGACTTTTGGTCTCTCTTGCTCAG[G/A]TACAGTTGCTGTATTTCTTAATTTATGGATTTAATAAAAATCAAAACAAA
Long Flanking Sequence:
AACATGCTTTACCAAAACACAAGCACAAAATGAGAATGTTTGAAGAATGTCCCTGCAGCTATTTGCCATGCAACAATTAACATTTAGAGTGAACCGTTTCTTTAAGGTGCACAGATAATAGAATCTCTGATTAGATGTTTTGATATCCCATTAATAATGTGCTGATTATTTGACAGGGAGCAGGGACAGATGAGGCCTGTCTGATTGAAATCTTGGCCTCGCGCTCTAATGCTGAGATCCGAGAAATCAATCAAGTTTTCAAAGCTGGTGCGTACTTGACTCATATTGCTTAATTCCTTCCTTCTGCAATTACAGATTTGATTACTTCCCAATCAAGCGTCTGCTACATGTCAAACCTGCTTTAATACGAAGCTCTACAGTAAAATGTGGTGATTGATAACACTCAGTGTTTTGTTTTAGAGAATAAGAAGTCACTGGAAGATGCCATCAGTGGAGACACCTCTGGACATTTCCGCAGACTTTTGGTCTCTCTTGCTCAG[G/A]TACAGTTGCTGTATTTCTTAATTTATGGATTTAATAAAAATCAAAACAAACTCATAGACACGACCGGCTTTTATATGCAAGATCTGAAGTAGTCATTTATTTGATGAAGGGGGATGAAAAAAATCTCTTGAGTATTTGATTAGATTGTTTTTATTATTATTTATTAAAATTTATTTTACAGTTTCTGACATAGCTTTATTATTATAATTATTATTATCAGTAGTAGTAGTATTAGTATTATTTTTAGTCGCCGTTGTTGTCGTAGTAGTCGTCGTCACAGCCGTTGTAGTAGTAGTCTTAGTCATAGTAGTACTAAAAGCAGTCGTTGTCATGGTCGTAGTCATAGTAGTAATCGTATTAGTATTGGTCGTTGTAGTAGTAGTCGTCGTTGTCATAGATGTAGTAGTCGTCATCATAGCAGTAGTCATAGTGGTAGAGGTTATAAAAGTAGTATTAGTAATAGCATTAGTCGTCGTAGTTGTCGTATTAGTAGTAGTTGT
Associated Phenotype:
Not determined