ZMP
serpina1l
Ensembl ID:
ZFIN ID:
Description:
serine (or cysteine) proteinase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1,
Human Orthologue:
SERPINA10
Human Description:
serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 [Source:HGNC Sy
Mouse Orthologues:
Gm46, Serpina10
Mouse Descriptions:
predicted gene 46 Gene [Source:MGI Symbol;Acc:MGI:2684892]
serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 G
serine (or cysteine) peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 10 G
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32277 | Nonsense | Available for shipment | Available now |
sa6618 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32277
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124111 | Nonsense | 104 | 434 | 2 | 5 |
ENSDART00000129762 | Nonsense | 99 | 429 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 10726684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10552358 |
GRCz11 | 20 | 10539598 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCCCAAGGCAAGAACATTTTCTTCTCCCCAGTTGGCATCTCAATGGCTT[T/A]GAGCTTGCTGGCTGTAGGTGCCAAGGGCAGCACTCTTTCACAGATTTACA
Long Flanking Sequence:
AATAATAATAATAGCCAGGAAAAAATATGAATATTGTTTTAAAGTATTGATAGTACCTGGACATTTTTCATCACTTATAAGCAGGTCACTTCCAGGTTGGCATGCTGACATAAATTACTTAAAATGTCTAGGTTGTGAGGTTCAAAATAAAGTGTATCTGATCTGTACATTACTGTGCTCTTGTTATTAAACACAGGTGAAAAAAATGAGGGGAAATATATTCTGCTGTGCAATTGCTGCCTTGCTGGTAGCAACAGCCTGGGCGGCACCCCACGATGGCCATGAAGGCCATGACCATGGTAGCCACACTGCTGACCACCACCACCATCTCCACCATGGGAAGGACGAACCCCATCCCAGCCACAAGGGGGTCGATGCTTGCCACCTGCTCGCTCCGCACAATGCTGACTTCGCTTTTTCCCTTTACAAGAAACTTGCATCCAATCCTGATGCCCAAGGCAAGAACATTTTCTTCTCCCCAGTTGGCATCTCAATGGCTT[T/A]GAGCTTGCTGGCTGTAGGTGCCAAGGGCAGCACTCTTTCACAGATTTACAGTGGTCTAGGTTACAGTGCACTGACGCCTGAGCAGGTAAATGAGGGTTATGAGCACTTGCTCCACATGTTGGGTCACAGTCAGGATGCCATGCAGCTGGAGGCCGGCGCTGGTGTGGCCATCAGAGATGGCTTCAAGGTGGTGGATCAGTTCCTGAAGGATGCTCAGCACTACTACAACAGCGAAGCCTTCGGCGTTGACTTCTCCAAGCCTGAAATCGCTGCAGCTGAAATCAACAAGTTCATTGCCAGGAAAACCCACGACAAGATAACCAACATGGTGAAAGACCTAGATGCAGATACGGTGATGATGCTGATTAACTACATGTACTTCAGAGGTACTTAACAGACTTTTCTTTTATTATTGACATTTGTTTCTACTGATCACAGGCATCTTTCAATTTGACATTTAGCTAACATTCTTTCTATTTCATCCTGATAGGCAAGTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6618
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000124111 | Nonsense | 137 | 434 | 2 | 5 |
ENSDART00000129762 | Nonsense | 132 | 429 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 10726784)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 10552458 |
GRCz11 | 20 | 10539698 |
KASP Assay ID:
554-5218.1 (used for ordering genotyping assays)
KASP Sequence:
AGTGGTCTAGGTTACAGTGCACTGACGCCTGAGCAGGTAAATGAGGGTTA[T/A]GAGCACTTGCTCCACATGTTGGGTCACAGTCAGGATGCCATGCAGCTGGA
Long Flanking Sequence:
CATGCTGACATAAATTACTTAAAATGTCTAGGTTGTGAGGTTCAAAATAAAGTGTATCTGATCTGTACATTACTGTGCTCTTGTTATTAAACACAGGTGAAAAAAATGAGGGGAAATATATTCTGCTGTGCAATTGCTGCCTTGCTGGTAGCAACAGCCTGGGCGGCACCCCACGATGGCCATGAAGGCCATGACCATGGTAGCCACACTGCTGACCACCACCACCATCTCCACCATGGGAAGGACGAACCCCATCCCAGCCACAAGGGGGTCGATGCTTGCCACCTGCTCGCTCCGCACAATGCTGACTTCGCTTTTTCCCTTTACAAGAAACTTGCATCCAATCCTGATGCCCAAGGCAAGAACATTTTCTTCTCCCCAGTTGGCATCTCAATGGCTTTGAGCTTGCTGGCTGTAGGTGCCAAGGGCAGCACTCTTTCACAGATTTACAGTGGTCTAGGTTACAGTGCACTGACGCCTGAGCAGGTAAATGAGGGTTA[T/A]GAGCACTTGCTCCACATGTTGGGTCACAGTCAGGATGCCATGCAGCTGGAGGCCGGCGCTGGTGTGGCCATCAGAGATGGCTTCAAGGTGGTGGATCAGTTCCTGAAGGATGCTCAGCACTACTACAACAGCGAAGCCTTCGGCGTTGACTTCTCCAAGCCTGAAATCGCTGCAGCTGAAATCAACAAGTTCATTGCCAGGAAAACCCACGACAAGATAACCAACATGGTGAAAGACCTAGATGCAGATACGGTGATGATGCTGATTAACTACATGTACTTCAGAGGTACTTAACAGACTTTTCTTTTATTATTGACATTTGTTTCTACTGATCACAGGCATCTTTCAATTTGACATTTAGCTAACATTCTTTCTATTTCATCCTGATAGGCAAGTGGGAAAAGCAATTTGATGCAAAACTGACCCACAAAGCTGACTTCAAAGTGGACCAGGACACCACCGTACAAGTTGACATGATGAAAAGAACTGGCCGCTATGAC
Associated Phenotype:
Not determined