ZMP
mep1a.1
Ensembl ID:
ZFIN ID:
Description:
meprin A, alpha.1 [Source:RefSeq peptide;Acc:NP_001025452]
Human Orthologue:
MEP1A
Human Description:
meprin A, alpha (PABA peptide hydrolase) [Source:HGNC Symbol;Acc:7015]
Mouse Orthologue:
Mep1a
Mouse Description:
meprin 1 alpha Gene [Source:MGI Symbol;Acc:MGI:96963]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17730 | Nonsense | Available for shipment | Available now |
| sa10535 | Essential Splice Site | Available for shipment | Available now |
| sa13188 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17730
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 |
|---|---|---|---|---|---|
| ENSDART00000047195 | Nonsense | 206 | 598 | 8 | 14 |
| ENSDART00000122034 | Nonsense | 206 | 598 | 8 | 13 |
| ENSDART00000130966 | Nonsense | 211 | 603 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 35501573)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 35574086 |
| GRCz11 | 20 | 35476965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTCACAGACCTAAACACACCATATGACTAYGAGTCTGTTATGCATTA[T/A]CGTCCATTTGCTTTCAACAAAGACCCCKCTATTCCTACTATTACMACCAA
Long Flanking Sequence:
CTATGTCTTGCCCTGTCTTCATGTTTCAGCTAAATTTATATCAGTCATTCAACCAGGGCCTGAGCAAGCTGAACTGCCGCTCTAGGCAAACGACAGTCATGCCACCCTTAACCCTAAAGTAAAAGTGGGGGGTGGGGTGGGGTTATAAATGAGGGCGCAGGTGGTAAGGGTAGTGTCGCGGACGCTGCCCTCTCTATTCTGGCCCCCTAGACGCGGATATAACTGAGGGTGCGGGTGGTGAGGGTAGGCTGCCGCCCTAGGTGGGTGTCTAGGTCGCCTCTATGGACGCGCCGTCCCTACATTCAACAAAGAGTTACATTTCAAAACACTTCATGTGATCTTTAAGAACACTCTGTTATAATTTTGTTTCATCATGTCTATAAAATCTCACATAATGCTTCCTTTTCTTTTCCAGGCTTGGAGCATAATTTTAACAAATATGATGACAGTTTTGTCACAGACCTAAACACACCATATGACTACGAGTCTGTTATGCATTA[T/A]CGTCCATTTGCTTTCAACAAAGACCCCTCTATTCCTACTATTACCACCAACATCCCAGAGTTCTACAAAATCATCGGACAATACCTGGACTTCAGTGAGATGGATATTGTCAGACTGAATCGAATGTACAACTGCTGTAGGTTAATAATACACAATAAGATAAATGAATTAACATGTTAGCTCGTATGTAACCTAGAAGTGGTCTGCTCTTCCACAGCCTCTTCTCTTACCCTGCTGGACCAGTGTGCTTTTGAAAAGATCAACATCTGTGGGATGGTACAGAGTTCGACTGATGATGGCGATTGGGTCCATCTTAAGAGCTCTGAGGATCATACTCTCAGCGGACAATGCAGAGGTGACAAAAAGGCCTGCAATACACATTTTCCAGAGTGGATGCAGTATGATTAAATTAAACAAACATTTTGGCTTGTGATTTCAGATTTAGGATATACTATGCACTTTGACACGTCCAGTGGACAGGCAGAGAGATCTGCTCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10535
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 |
|---|---|---|---|---|---|
| ENSDART00000047195 | Essential Splice Site | 525 | 598 | 11 | 14 |
| ENSDART00000122034 | Essential Splice Site | 525 | 598 | 11 | 13 |
| ENSDART00000130966 | Essential Splice Site | 530 | 603 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 35503746)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 35576259 |
| GRCz11 | 20 | 35479138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTGAGGATGTCTTCTGCTCGTAGCCTCACCACTGACCTGAGCAAAGG[T/C]ATTTGAGGYCATWACCATGTTTGGGGAAACAATGGGGGAAAATCAACWTG
Long Flanking Sequence:
ATGAATGTGGTGATAAAGTGCCTTTCTTACCCAGCTGATGAAGACAAAACATGGAAGATTGCCCATGTGCCGATGCAAGTTGGGGCAAAATTCCGCTATGCATTCCAAGCAGTGAAAGGTGATTCGAGCAGCTCTGGAGGAGGTATATTCATAGATGACATCAGCCTAACAGAGACACACTGTCCAGCCGCTGTCTGGCGCATCCAAAACTTCTCCAGTATCCTTGAAAAGGCAGACTACAGCACTGTGCTGAACAGCCCTCGTTTCTACAGCCCTGAGGGTTATGGTTTTGGGATTCAAGTGATTCCACTGTCTGGCTATTCTGATTATGCTGGTAACTACACTGGTCTGTACTTCCATTTGATCAGTGGTGACAATGACATTGTGATGCAGTGGCCTGCTGTGAACCGCCAGGCCACTATAGTGGTGATGGACCAAGATCCGGATATTAGGTTGAGGATGTCTTCTGCTCGTAGCCTCACCACTGACCTGAGCAAAGG[T/C]ATTTGAGGCCATAACCATGTTTGGGGAAACAATGGGGGAAAATCAACATGTTTTAGAAACCAAAATGAAATAGAATGGTGAAGGAAATGTTAGATCTAATTTTAATTGGAAGCAATTATATTAAATTGATTGTAATAATTACAATTTAATTGAATTTATCTACATACATTTTAGGATAACTTAAACAAAATCCTCAAATTGGTTTGCATTACTGGATGTTTAACATTTGAATCATGAATTCTTGCTATATTAATTTTAACACAAGCTTGTGTGACCTTGTGTTTCTCTGACCGTCATATTTACATTATGTGAATGTGTGAGACCAAAAGGAGATCAAACATGGCCTCTATGTAAATACATTTTAAATATGGAGCAATTGTTCGTATATTAATGTTGCATCATCTTGTTTTTTTTCTTTCCCCTTTTCGCTGCATCGTCTGACAAAATTTCACATGCAGAGCTTTTGCACTGGAGTTTTTGCTTAGCATTTTTAAATTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13188
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 |
|---|---|---|---|---|---|
| ENSDART00000047195 | Essential Splice Site | 525 | 598 | 11 | 14 |
| ENSDART00000122034 | Essential Splice Site | 525 | 598 | 11 | 13 |
| ENSDART00000130966 | Essential Splice Site | 530 | 603 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 20 (position 35503746)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 35576259 |
| GRCz11 | 20 | 35479138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGTTGAGGATGTCTTCTGCTCGTAGCCTCACCACTGACCTGAGCAAAGG[T/C]ATTTGAGGYCATWACCATGTTTGGGGAAACAATGGGGGAAAATCAACWTG
Long Flanking Sequence:
ATGAATGTGGTGATAAAGTGCCTTTCTTACCCAGCTGATGAAGACAAAACATGGAAGATTGCCCATGTGCCGATGCAAGTTGGGGCAAAATTCCGCTATGCATTCCAAGCAGTGAAAGGTGATTCGAGCAGCTCTGGAGGAGGTATATTCATAGATGACATCAGCCTAACAGAGACACACTGTCCAGCCGCTGTCTGGCGCATCCAAAACTTCTCCAGTATCCTTGAAAAGGCAGACTACAGCACTGTGCTGAACAGCCCTCGTTTCTACAGCCCTGAGGGTTATGGTTTTGGGATTCAAGTGATTCCACTGTCTGGCTATTCTGATTATGCTGGTAACTACACTGGTCTGTACTTCCATTTGATCAGTGGTGACAATGACATTGTGATGCAGTGGCCTGCTGTGAACCGCCAGGCCACTATAGTGGTGATGGACCAAGATCCGGATATTAGGTTGAGGATGTCTTCTGCTCGTAGCCTCACCACTGACCTGAGCAAAGG[T/C]ATTTGAGGCCATAACCATGTTTGGGGAAACAATGGGGGAAAATCAACATGTTTTAGAAACCAAAATGAAATAGAATGGTGAAGGAAATGTTAGATCTAATTTTAATTGGAAGCAATTATATTAAATTGATTGTAATAATTACAATTTAATTGAATTTATCTACATACATTTTAGGATAACTTAAACAAAATCCTCAAATTGGTTTGCATTACTGGATGTTTAACATTTGAATCATGAATTCTTGCTATATTAATTTTAACACAAGCTTGTGTGACCTTGTGTTTCTCTGACCGTCATATTTACATTATGTGAATGTGTGAGACCAAAAGGAGATCAAACATGGCCTCTATGTAAATACATTTTAAATATGGAGCAATTGTTCGTATATTAATGTTGCATCATCTTGTTTTTTTTCTTTCCCCTTTTCGCTGCATCGTCTGACAAAATTTCACATGCAGAGCTTTTGCACTGGAGTTTTTGCTTAGCATTTTTAAATTGTT
Associated Phenotype:
Not determined