ZMP
emilin3a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate elastin microfibril interfacer family [Source:UniProtKB/TrEMBL;A
Human Orthologue:
EMILIN3
Human Description:
elastin microfibril interfacer 3 [Source:HGNC Symbol;Acc:16123]
Mouse Orthologue:
Emilin3
Mouse Description:
elastin microfibril interfacer 3 Gene [Source:MGI Symbol;Acc:MGI:2389142]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15954 | Essential Splice Site | Available for shipment | Available now |
sa34386 | Splice Site, Nonsense | Available for shipment | Available now |
sa7134 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10922 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15954
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112381 | Essential Splice Site | 110 | 687 | 3 | 6 |
ENSDART00000113858 | None | None | 711 | None | 7 |
ENSDART00000143791 | None | None | 69 | None | 2 |
ENSDART00000148178 | None | None | 308 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 23818304)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22944122 |
GRCz11 | 8 | 22965361 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTAAAGGGCCCATGCCAATGCAGAAAGGTCCTATGYCTTCATTTAAAG[G/T]TCCAATGCCTATACAGAAAGGTCCTATGCCYTCCTTTAAAGGTCCAATGC
Long Flanking Sequence:
GCAGCTCCCTTCATGAAGGCAATGAAGTGTGCTTGGGGTCAGAAATGCCCAACTACAAAGTATGATAATTAATGCATACATACAATTAATGTTTGTTAAAAAATGCATATTTGTGACATTTAGCTGATTTGCACATCCTGTCTGTTCTTGCAGGTATCGTATGTATTACAAACCAATGTATAAAGTTGCATATAAAACTGTAACTGAGCTGGAATGGAAGTGCTGTCCTGGATATACAGGTGTCGGTTGTACTGAGGGATATGGAATGAAAGCAAGGCCCCTTTTCAATGGACCAATGCCTGCACAAAAGGGTCCTATGCCTCCTTTTAAAGGACAAATGCCAATGCAAAAAGGCCCTATGCCTCCTTTTATAGGGCCTATGCATATGCAGAAAGGTCCCTCATCTCCTTTTAAAGGACCCATGCCAATGCAGAAAGGTCCTATGCCTCCTTTTAAAGGGCCCATGCCAATGCAGAAAGGTCCTATGCCTTCATTTAAAG[G/T]TCCAATGCCTATACAGAAAGGTCCTATGCCTTCCTTTAAAGGTCCAATGCCTATGCAGAAAGGTCCAATGCCTTCATTTAAAGGTCCAATGCCTATGCAGAAAGGTCCCATGCCTTCATTTAAAGGACCGATGCCAATGCAGAAGGGTCCAGTGCATTCATTTAAAAGGCCTATGTCTGCACAGAAAGGTCCAATGCCCTCTTATAAACGTCCAAATGCATCTCAAAAGGGACACATACCTTCATATAAAGGACAGTATCCCCATCCCAATGTCAATGGAAACCCCTGGATTCAGCCTCAAGCTCCAACTAATGGCATAATTGGATATCCAGTTCCTAATACTGGGCCGTCCTCCCAAGATCCTCCAATTGAATCTTACCCAGAGCACCAGGAACCGGAAGTAGATTATCCTGAACCCGTGATTGAACCTCAAGACCTTGGCCATGATATAATCCCAGAAGAGAATGAACCAGTTACTGACTACCAGGATCCTCAGCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34386
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:
C > T
Consequence:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112381 | None | None | 687 | None | 6 |
ENSDART00000113858 | Splice Site | None | 711 | None | 7 |
ENSDART00000143791 | None | None | 69 | None | 2 |
ENSDART00000148178 | Nonsense | 37 | 308 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 23818050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22943868 |
GRCz11 | 8 | 22965107 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATAAACGTCCAAATGCATCTCAAAAGGGACACATACCTTCATATAAAGGA[C/T]AGTATCCCCATCCCAATGTCAATGGAAACCCCTGGATTCAGCCTCAAGCT
Long Flanking Sequence:
AGGGATATGGAATGAAAGCAAGGCCCCTTTTCAATGGACCAATGCCTGCACAAAAGGGTCCTATGCCTCCTTTTAAAGGACAAATGCCAATGCAAAAAGGCCCTATGCCTCCTTTTATAGGGCCTATGCATATGCAGAAAGGTCCCTCATCTCCTTTTAAAGGACCCATGCCAATGCAGAAAGGTCCTATGCCTCCTTTTAAAGGGCCCATGCCAATGCAGAAAGGTCCTATGCCTTCATTTAAAGGTCCAATGCCTATACAGAAAGGTCCTATGCCTTCCTTTAAAGGTCCAATGCCTATGCAGAAAGGTCCAATGCCTTCATTTAAAGGTCCAATGCCTATGCAGAAAGGTCCCATGCCTTCATTTAAAGGACCGATGCCAATGCAGAAGGGTCCAGTGCATTCATTTAAAAGGCCTATGTCTGCACAGAAAGGTCCAATGCCCTCTTATAAACGTCCAAATGCATCTCAAAAGGGACACATACCTTCATATAAAGGA[C/T]AGTATCCCCATCCCAATGTCAATGGAAACCCCTGGATTCAGCCTCAAGCTCCAACTAATGGCATAATTGGATATCCAGTTCCTAATACTGGGCCGTCCTCCCAAGATCCTCCAATTGAATCTTACCCAGAGCACCAGGAACCGGAAGTAGATTATCCTGAACCCGTGATTGAACCTCAAGACCTTGGCCATGATATAATCCCAGAAGAGAATGAACCAGTTACTGACTACCAGGATCCTCAGCCAGATCATCAAACTTCCACAACAGTAGAGAGTGAGACAGAGCCTATTCGCAATGCACAAGTGCCCTCTGGTGGGAGTGAAACAAACCAAGGTAAATGAACCATTTATTATACTGTAGTTACACTCTCTCTCTCTAATATAAACAGTTGTAGTAGAATCTGTATTTGTTTGTACAAAATAAAGCCTTCAATGTGCCATAAGTAATTAAATAAATGTAATTCATTTATAGAACATGATGACAACAATATTGAAGATGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7134
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112381 | Nonsense | 234 | 687 | 5 | 6 |
ENSDART00000113858 | Nonsense | 274 | 711 | 5 | 7 |
ENSDART00000143791 | None | None | 69 | None | 2 |
ENSDART00000148178 | Nonsense | 292 | 308 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 23817147)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22942965 |
GRCz11 | 8 | 22964204 |
KASP Assay ID:
554-4607.1 (used for ordering genotyping assays)
KASP Sequence:
GTCAAAACACCACCCTTCAAAGACTATCWGGTGGGTCAGTGAACCTTAAT[C/T]AAACTGAAATCCAAAAGGCCCTGGAAACAATGGTGGAGTCCAAAATGAGT
Long Flanking Sequence:
GTATTTGTTTGTACAAAATAAAGCCTTCAATGTGCCATAAGTAATTAAATAAATGTAATTCATTTATAGAACATGATGACAACAATATTGAAGATGAGCGGTTGGACAGGATAGAAGAGGATGTGCAACGACTTTCTCTTGGTCTTGAGACTCTCCGAGGTACAGTGACAGGTTTGGAGGACAGCTTGCGTGCTTCCCTTCGTGAAGATGCCAATAGGATGTTAACTGCCCTGATTTCTGCAGCACCCAGCCCTATCTCTGCTCCTTCCTTGTCTAGAGACTCTACTGTGGGCTTTGGAGATCTACCTGGAGGTGCACCGGATATTGAGGGATCAGATGTGGTGGGACACTTTCCAAACTTGGTCGATTTAACTGAAAAGGTTACAGAGCTGCGAGCAGAACTTGTGGCAAAGTCATCTGAGCTGGAAAAATTGAGAGGAGCAGTTGTGAGTCAAAACACCACCCTTCAAAGACTATCAGGTGGGTCAGTGAACCTTAAT[C/T]AAACTGAAATCCAAAAGGCCCTGGAAACAATGGTGGAGTCCAAAATGAGTGAAGCTCGGGTCACCATATTAGATGGCTTTGAAAAACGAGTGGAAAGTGCAGAGGAGCGATGCGAGAGTCGAATGGCAGAGGTGCGACTCCAATGCAAAGAGGAAAGTTTAGATGGACAAGATCAGATTGAGCAAGTCCTAGACATAAGGGCTGAAAGATTGAGGGCAGAACTACAAAAGCTGCAGGCTCAGCTTCAAGACCTGGAGCCTGAAGAGGGTTGCTGCATTGCCATATCAGGTCTAACTGAAAGGGTCATTTATATGGAGCAGTCAGTGGAAGGTTTGAATGAATCCCAAACACACCTACGTGCTGAAATTGGTGGACACAAGGACCATATAGATGGCATGTTGGAAGGCCGACTGGCTTATGTGGAATCCAAATTGAATATTGCATTCAATCAAGAGGAAACAAACATTAACAAAAGTGAGCCTGATAACCTGGAGGTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10922
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112381 | Nonsense | 329 | 687 | 5 | 6 |
ENSDART00000113858 | Nonsense | 369 | 711 | 5 | 7 |
ENSDART00000143791 | None | None | 69 | None | 2 |
ENSDART00000148178 | None | None | 308 | None | 2 |
Genomic Location (Zv9):
Chromosome 8 (position 23816861)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 22942679 |
GRCz11 | 8 | 22963918 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTCAGCTTCAAGACCTGGAGCCTGAAGAGGGTTGCTGCATTGCCATAT[C/A]AGGTCTAACTGAAAGGGTCATTYATRTGGAGCAGTCAGTGGAAGGTTTGA
Long Flanking Sequence:
TGTGGGCTTTGGAGATCTACCTGGAGGTGCACCGGATATTGAGGGATCAGATGTGGTGGGACACTTTCCAAACTTGGTCGATTTAACTGAAAAGGTTACAGAGCTGCGAGCAGAACTTGTGGCAAAGTCATCTGAGCTGGAAAAATTGAGAGGAGCAGTTGTGAGTCAAAACACCACCCTTCAAAGACTATCAGGTGGGTCAGTGAACCTTAATCAAACTGAAATCCAAAAGGCCCTGGAAACAATGGTGGAGTCCAAAATGAGTGAAGCTCGGGTCACCATATTAGATGGCTTTGAAAAACGAGTGGAAAGTGCAGAGGAGCGATGCGAGAGTCGAATGGCAGAGGTGCGACTCCAATGCAAAGAGGAAAGTTTAGATGGACAAGATCAGATTGAGCAAGTCCTAGACATAAGGGCTGAAAGATTGAGGGCAGAACTACAAAAGCTGCAGGCTCAGCTTCAAGACCTGGAGCCTGAAGAGGGTTGCTGCATTGCCATAT[C/A]AGGTCTAACTGAAAGGGTCATTTATATGGAGCAGTCAGTGGAAGGTTTGAATGAATCCCAAACACACCTACGTGCTGAAATTGGTGGACACAAGGACCATATAGATGGCATGTTGGAAGGCCGACTGGCTTATGTGGAATCCAAATTGAATATTGCATTCAATCAAGAGGAAACAAACATTAACAAAAGTGAGCCTGATAACCTGGAGGTGCAATTGGAAGGGAAGATTAAAGCTCTTGAAACCCGTCTCTTGGCAGCAGTAGAAGAGCTCGGTAATGTCACAGCACCAACTTTACTCGAAGGTCAAGCTGTTCCTTCACTGGAAACAGAGGTAGAATTGTTAAGAAGAAGAGTTGAGGATGATTTGGACCATCTACAGAAACAGCTCAAATCCATGGAGGTTCTTTGTACTTCAGCTTGTGTTCCACAGCCTGTTCTAACAGGATATGCAGCTCCATTGGCTACCGATGAGGACAAACACGAAGACAACCTTAAAGAAA
Associated Phenotype:
Not determined