ZMP
serpine2
Ensembl ID:
ZFIN ID:
Description:
glia-derived nexin [Source:RefSeq peptide;Acc:NP_956478]
Human Orthologue:
SERPINE2
Human Description:
serpin peptidase inhibitor, clade E (nexin, plasminogen activator inhibitor type 1), member 2 [Sourc
Mouse Orthologue:
Serpine2
Mouse Description:
serine (or cysteine) peptidase inhibitor, clade E, member 2 Gene [Source:MGI Symbol;Acc:MGI:101780]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6397 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa993 | Nonsense | Available for shipment | Available now |
sa42621 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa6397
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041677 | Essential Splice Site | None | 395 | 1 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 42130846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43402904 |
GRCz11 | 15 | 43283882 |
KASP Assay ID:
554-4615.1 (used for ordering genotyping assays)
KASP Sequence:
CACGAGCTCTCCATCTGCCTGAATWAAGAAGTTGAGGTGCTTGGTACAGG[T/C]TAGTGGAGAATATTATATGATTTTTGCATCKTATTTGGTTCCWTATTGGC
Long Flanking Sequence:
TTCTGATGTTGAACACAAATTGAGATGATTTGATAAGTTTCTGAGGAAAAACAAAACATTCGTTGTTGGAACAAAAAATCACTATGAAAGTCAAAAACTGCTTCCAACAGTCTTAAACCTATCTTCATTTGTGTTAAACCGAAGAAAGAAAATTGAAAAAAAATGACTGAATTTCAATTTTTGTGTGAACTATCCCTTTAAATTTTCGCCAAGGGAATACGCTGAAGGCTTGGCTCATGAATATTAATTACGTAGAGGCGTTGGGCAGTTGTTGCTCTTGCGTGGTTGGACGTCAGTCGAATGACGACATGGTTACCTAATTAATATTTAAAACATTTTGTTGTTGAAGTATTCATGAGTAGGCGGAGTCCGGCGCTCAGGACTGAGAGAAATAAATAAACGGAGGCGCGGTAGTTTTTCGTGAGGAGGAACACGAACACTCGCGGAAGACACGAGCTCTCCATCTGCCTGAATTAAGAAGTTGAGGTGCTTGGTACAGG[T/C]TAGTGGAGAATATTATATGATTTTTGCATCTTATTTGGTTCCATATTGGCTCTCCGGTTTGTTTTAAATGCAAATGAAGCATCTGTTGAGCCTGTTTTAATATCTACAGTACTTGTTTGTTTATATCGAGGACTAAGGATGACTAACACGCATGAGGATGACTTGTTTTTGGAGCTGTTTTGAGCCCCGCTGCTCTTTGCTCTCAGTCTGTGTTTTAAAGCCTATAATTAAACACTCTTGCTGAAGCTGCTAGCCTATAAAAAGTTTACTGCGGTCATCGGAAAATAACGCTTTAATGAAAACACGGTTTACTGCTGCACCGCTACATCAGATAAACTGTAACGATATTACAACTGTAACGCATGAACTGTTTTACAAGTTCATACAAGACATATTCCTTCAAGATAAAATTAATTATCTACGCTTTGTCTAACTGCAAGTTGTTCAAAACTAGTTTTAAAGACTGATATAGTGGTTAATGTTATCCAGCTGACCACAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa993
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 |
---|---|---|---|---|---|
ENSDART00000041677 | Nonsense | 122 | 395 | 3 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 42115420)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43387478 |
GRCz11 | 15 | 43268456 |
KASP Assay ID:
554-0897.1 (used for ordering genotyping assays)
KASP Sequence:
ATATTGTGACCATCGCCAACGCWCTGTTCCCTAATGAGGGATTCAGCATG[A/T]AGGAGGACTTCCTGTCTGCCAACAGAGAGAACTTCCTGTGTGAGAGTCAC
Long Flanking Sequence:
GCACCTTTGGGATGTGGTGGAACAAGAGATTCACATCATGATGTGCAGCCGACAAATCTGCTGCAACTGTGTGATGCTGTCATGTCAATATGGAGCAAAATCTCTGAGGAATATTTCCAGTACCTTGTTGAATCTATGCCACGAAGGATTAAAGCAGTTCTGAAGGGAAAAGGGGGTCCAAACTGGTTCTAGTAGTTTCACATCACATTATAGAAAGAGTTATTTATAAACTTTTATAAATTCTTTGTGTTTTTGCTATGACGTAGCCATTAAAGCTGATATGGAAACTTTCTATTGGATATATACTCTGAATGATAACTCGAGAATAAGTCAAAGACCAACATTTATTTTCACATGTTAAACATCAAATTAATATTGTTTTTCTTCTGTCAGGTCCATATAAGATGTTGCGGAAGCTTCATAAGTCTTTGACGACAAAATCTAATGCTGATATTGTGACCATCGCCAACGCACTGTTCCCTAATGAGGGATTCAGCATG[A/T]AGGAGGACTTCCTGTCTGCCAACAGAGAGAACTTCCTGTGTGAGAGTCACAGTGTGGACTACAGTGACCCGGAGGCAGCCGCACAGTCCATCAATGACTGGGTGAAGAACAGCACTAAAGGTTCATACACTCACTCATTCACTCACTTGTTCAATAACTCATTCACTCACTTATTTATTCAATAACTTATTTCCTTTTAGTCACTCATTCCCTTACTCAATCATTCGCTCACTTATTCATTCATTCATTATTTCAATAACTCATTTATTCACTCACTCATTCAATAACTCATTCACTCACTTATTTATTCAATAACTTATTATTTCCTTTTAGTCATCCATACACTCACTCAATCATTCGCTCACTCATTCATTCATTCATTCATTCATTATTTCAATAACTCACTCACTCACTCACTCACTCCTTAATTAATTGATTTACTTACTCCCTTAGTCCTTCACTTATTTGTTAATTTATTTCGCTCATTTATTCACTCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42621
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041677 | Nonsense | 335 | 395 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 15 (position 42095721)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 15 | 43367779 |
GRCz11 | 15 | 43248757 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCTTTGGCATTTGTGTGTGAAACAGGTTCAGAGTCCATCTACGTGTCC[A/T]AAGCCCTTCAGAAAGCCAAGATAGAGGTCAATGAGGACGGAACCAAAGCC
Long Flanking Sequence:
AGACGCAGATTCAGAGTTACAAATGAGGTTTTTTATTATTAGCAAAAAATATCAATACTACAAACGTGAACACATTAGGTGAGCAGGGTAACCCTGTGTCCTAACAACATGATATGTGAGGAGATTTGCAGTAATAGGCAATTTGGCTGTTTGCACCAGACGAAACGCGACAGAAATTTAAATAAAGCCATTCAGAAGCACAGAATAGTGCACTCACTGCACTTCAATAAAATGGTAAGGTTTATAATCTAATTATTAGATATTAAACCTCTTTAACAGTATCAAATGTACATGCTAAATCACTGATATGTTGGTGTCATCAATCTGGCAACCTGCACTTGCATGTGTTTTGAACCAGGCGTGCAATACCTAGTTCAACCACTAGGTGACAAACTTGCATACTGCACCTTTAAATGAAATTCGCTTGGCGTATTGAAGTTTTGTGCTCTTAACCTTTGGCATTTGTGTGTGAAACAGGTTCAGAGTCCATCTACGTGTCC[A/T]AAGCCCTTCAGAAAGCCAAGATAGAGGTCAATGAGGACGGAACCAAAGCCTCCGCCACCACATGTGAGTTCCTGTGTCACATAGTAAAATAATGACATTTTTTTAATGTGGTTAACAAGACAGTGCATTACATGGGAGAATTGTAATCTAGACAGTTTAAAAGTTCTGTGAAGTGCTTTGAAATGTGCAGATGTTTTATTCGATGTAAGTCATGACGTATCGTTGAGGTATTTAAAACTATTTACAGGTCTATTTCCGTACTCATTTGAATTGAGAAACTTTTTAGTCCTATCACACGTATTAGGCATGGATATATGTATTGCGATCGTGATTTTCTAAAATATTACATCCCTTTATAAACGTTTATTATTGCCAGTAATTGAGCCGCTTCAGGTGACGTCACACTTAACAAGCAGATAATCTCAACTGAAACATGAAGACAGGGTGGGACTTATAGTAGCTCCTCCCCCATTTAAAAAAAAAAACAATAGCGTTTTTTT
Associated Phenotype:
Not determined