ZMP
zgc:154079
Ensembl ID:
ZFIN ID:
Description:
endothelin-converting enzyme 1 [Source:RefSeq peptide;Acc:NP_001071260]
Human Orthologue:
ECE1
Human Description:
endothelin converting enzyme 1 [Source:HGNC Symbol;Acc:3146]
Mouse Orthologue:
Ece1
Mouse Description:
endothelin converting enzyme 1 Gene [Source:MGI Symbol;Acc:MGI:1101357]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35104 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11416 | Nonsense | Available for shipment | Available now |
sa21930 | Essential Splice Site | Available for shipment | Available now |
sa9969 | Nonsense | Available for shipment | Available now |
sa35103 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa5844 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa11183 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa35104
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088329 | Essential Splice Site | 147 | 752 | 4 | 19 |
ENSDART00000136859 | Essential Splice Site | 192 | 797 | 4 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28816705)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27692691 |
GRCz11 | 11 | 27939865 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCAACCTGTGGGAACATAACATGGCTGTCATGAAGAACTTGCTAGG[T/G]AAGAAAAACACAACGAAGAAATAGTTGTATTATTTTAATACTGCTTGATG
Long Flanking Sequence:
TAGGATATTTATGATGTGCAGAGTGAATGCAGTTTGAGATACAGCACTGAAAGTGTAGCTCACTCAAACCCAGAACCATAATCAAAGCTGTGTTGATTTATTTCTCAATCTTATAAAGATAAGTAAGTGATGTGGGGATGTGTGCCAGAACTGCACTTAATTTATGAACGTCCTGGTGGAAATGACATCAGGAAGGCTTTCTTGTCTGTTTTGACATGTATGTGATGTATATGCATACGCAGCAGCTTATTTATGTACATGTACTGTTTTTTTGGTTTTTTTGTAGCTCATCCAGGTCTGTGCCTGTCGGAGCCATGTGTGAGTGTAGCCAGTGCAGTTCTGGGGTCTCTCGACCGGTCGGTGGACCCCTGCCAGGACTTTTATAACTTCGCATGTGGAGGCTGGATGAGGAAAAACCCCCTGCCTGAGGGCAAGTCCCGCTGGGGGCCTTTCAGCAACCTGTGGGAACATAACATGGCTGTCATGAAGAACTTGCTAGG[T/G]AAGAAAAACACAACGAAGAAATAGTTGTATTATTTTAATACTGCTTGATGATTAAATATATACAGTGTCGATCATAAATGAGTAAATTCTCTCTATAGGATGCTATTGACCTTATTCTTAAATGCGGAAGTGCGCCTGTTTTCGCGATTGTCTTAGAACTTCCGATTTAGTCGCCTATGGGAGAAATGACAAGGAATAATAAACGGCAGAAAATGGCCAAACTACTTGCTCAACAAACAAATATTTGCATGACTACACAGACCAAGTAGCATAATATAATAAGAAAATATTAAATTGCAACATCAAGCAGCGTAACGAGCAGTTGTTAACGTCAAAAAATGAATGGAAGTGAATGTGACCGGAAGTCGCGAGACAAAAAGATTCAAATGGCAGCGCCCACTCGTCAGCTGAGAATAAGGTGAATACAATAAGATATTTGTTCATATAGATTAGATTAATTAGTAAGTAAAGCCAAAACTAGAACTAGTTTAACAAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11416
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 |
---|---|---|---|---|---|
ENSDART00000088329 | Nonsense | 207 | 752 | 6 | 19 |
ENSDART00000136859 | Nonsense | 252 | 797 | 6 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28814824)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27690810 |
GRCz11 | 11 | 27937984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCTGGGGCTTGAAAGGCCCGTGGGAGAAGGATAACTTCCAGGAGGTTT[T/A]ACGGATTGTGTCAGCCAACTTCCGAACCTCTCCCTTKTTCACTGTTTTTG
Long Flanking Sequence:
GAAACTAAAATTAAAGTATGTAAGACACAACAGAACACGTCTTTTAATTTATGAATAAAGCAGGAATGATGTTAGCATGAAGGCTCCTACTAACTTATTGGCTTCATTTCACTTTGCTATAAAGGATTTGTCATATACATTTTTTTTTTTAAAATTTGTATATTCAGAGAACACCAGCATGAAAAGCTTGAGCAGAGCAGAGCAGAAAGCCCAGTGGTATTACCAAGCCTGCATGAACGAGAGCAAAATTGAAGAGCTTGGAGCAAAACCACTCCAGGACCTCATCAATCAGGTGACCTCAGATACACACACACAATCCCAGTCACCTTATTTTAACAAAACGAAGCTCCAAAGATCTGCTGTAAACATATCAGCCTTAATGAAAACCAGCTCTTAGTCTTATTCTGGGATAATAATTCTTAATAACGGAACATTGTTTTTCCAGACGGGAGGCTGGGGCTTGAAAGGCCCGTGGGAGAAGGATAACTTCCAGGAGGTTT[T/A]ACGGATTGTGTCAGCCAACTTCCGAACCTCTCCCTTTTTCACTGTTTTTGTCAGCACAGACTCAAAAAGCTCCAACAGCAACATCATACAGGTGGAAACACTTATGATTTTGTTCATTTCAATCATCGTGACATGTCGACGGGAAACTCTGCACTGTTTTAGATATGGTGCTTTCTTTTATGAGTGCTGTCAGAATTTATTATGTCTAGGGCTGTTTATTTAACATGTTAATTAGATATGTAAAACAATATATGGTTTTAATGCATCCAAGCCCAGACCTGAGTAAATGATAGTATATTTCATATAATAGTTTGACTCCTTGCCAATGAAGCCTATGGAATGTTGTTATATGACTTTTTAAATTCAAAACATTAAGGCAAGAATGCCCATTTTTCATATTGTTTTGTATCATATTCGTGTTGTATTATAAAGTTCAGTAAATAATACATTAATATTGTGTTACATTTTAGACTCAACTGTGTCTGTTTTTGCTCCAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21930
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 |
---|---|---|---|---|---|
ENSDART00000088329 | Essential Splice Site | 260 | 752 | 8 | 19 |
ENSDART00000136859 | Essential Splice Site | 305 | 797 | 8 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28812766)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27688752 |
GRCz11 | 11 | 27935926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGGAAACGTTGTGCTGTGGTCTAAAGCTGGTGTTGTCATTCCTCCTTTA[G/A]TATTTAAATGCTTACTTGAACTTTTTGGTGGAACTTGGAGTCCTCTTGGG
Long Flanking Sequence:
TGGAGCATACAAAACATTCAAGAATGTTGGCAACCAAGCTGTTTTGCAACTGCAATAAAGAGGATTTAAATATATCCAAATAGCGATTGAGAAGCAACTTCTGAAAATAAGCATGACCATTATAGCCAAAAAAAGTAATAGCTTCTATTATTAAAAAAATATTTCTTTCTTTTGTCTTTTTAGTGCTTTTCACATTTACCATAATGACTTTTCTGAAATAAATTGTTATTTTGGGTCAGTTTCCTAATTAAATTGTTTATAGATTGACATTCCATATTGTTATACAGTAATGATACATGTCACTGTAGCTTTTCTTTGTTGATACTAAAACACACTGTCATTTTTGTGCAGGTGGATCAGTCAGGATTGGGACTCCCCTCTAGGGAATACTATCTCAATAAGACCGCCAATGAAAAGGTAAACAAAGTGACCATATGTTGTTCATGAACGTGGGAAACGTTGTGCTGTGGTCTAAAGCTGGTGTTGTCATTCCTCCTTTA[G/A]TATTTAAATGCTTACTTGAACTTTTTGGTGGAACTTGGAGTCCTCTTGGGCGGCTCACAGGACACCTCGCAGAAAATGATGGAGGAGATCATCGAGTTTGAAACCACCCTGGCAAACATTACTGTGCCTCAGGTGGAGCGACGGGATGAGGAGAAAATATATTATAAAATCCAAGCCAAAGAGTTGGCGGTGAGTGTTCCTTACTAGTTACTATAGCACTGATTTAAATGCATGGTTCTTCTCTGCTGGATCATGACTAGACCAGCAGATTTGTAAGTCCATCATGCAATCTATTTATTTACTTGCATATATATTCAGTTTTGATTTTAATTTCAGTTATATTATTAAATAATATGCAAATGTTAATATGATTTATATACAATACAGTTTATAAAGTAATATTTTCAGTTTTTATTAGATATACATTATATGATAGACTTGCATTGTTTACCAAACAAGTGGTCTTAATGGGGTTTGCATTGAAAATTAAAAGTTAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9969
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 |
---|---|---|---|---|---|
ENSDART00000088329 | Nonsense | 324 | 752 | 9 | 19 |
ENSDART00000136859 | Nonsense | 369 | 797 | 9 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28810937)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27686923 |
GRCz11 | 11 | 27934097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGGCTGGAAATCCTCATCAGTGATGTGTTTRTATGTTGTGCTGCAGACAT[T/A]GGCTCCTGCCATAGACTGGATGCCTTTCCTSTCTTCTGTTTTTGCCCCGG
Long Flanking Sequence:
TTTGTTTTGACATAAGATCATTTTGATTACCCCACTGCCAGATTAATTTACTTGTTTTAGGGAAAAACTTAATTTTGACATGTTATTTCTTAAAACAAGACAATATTATCTAGAAAATGCTTCTTAATTTAAGAATTTGTACATATTGGACTAGATACAAGACAAAAAATCTAAGTAAGAAAAGGTTTTTTTGGCAGTGTAAGCTCATTTTGCAAGTCACCTAAGGTTAAACAGTTGAGTTTTATCATTTTTTTATGAATTCAGCCAATCTTCTGGTATGGCAGAAGAAAACATTCTCCAGCTAGATCATTTTTTTAACTATTTTTAATAAAGTGCAGTTAAATGTCTGATATTTTGTCAACTTGTGATTTTTTTCAATCAGAGTCAAGATGTCGAAACCTAAAGTTCTATTACCTTTACAGCATAGGATTTACTTTATAGGTTGAGTGTGGGCTGGAAATCCTCATCAGTGATGTGTTTATATGTTGTGCTGCAGACAT[T/A]GGCTCCTGCCATAGACTGGATGCCTTTCCTGTCTTCTGTTTTTGCCCCGGTTGAACTAAATGATTCTGAACCTGTGGTCGTATACGCTAAAGAATACCTCCAGAAAGTCTCCGAGCTCATCAGCAACACAAACAAAAGGTAACCCAACGTTAGCCAGATCACTTCTGCACATTTATGACTATGTAACACCTGTGGAAACGCACATTCTCTATTGTTTCAAATTGTCAGATAGCTGAGATCAAAGCTAATGTGTTTCCTGCAGTGTCTTAAACAACTACATGATCATGAAAGTGGTGCGGAAAATGGTGTCCATCTTAGACCAGAAGTTCCAGGATGCAGAGCAGCGTTTCCTTGAAGTCATGTACGGCACCAAGAAGGTAAGAAATGAAGATCAAAGCTGTCATCTGTCAGCCTGAAGCAAAACTGCTCCGGAAAGAGCCATCAAATATCACATAACAACTCATGTTTTTTCACATTTATTTCAGTCCTGTTTCCTGTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35103
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 |
---|---|---|---|---|---|
ENSDART00000088329 | Essential Splice Site | 408 | 752 | 10 | 19 |
ENSDART00000136859 | Essential Splice Site | 453 | 797 | 10 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28810558)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27686544 |
GRCz11 | 11 | 27933718 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGATGCAGAGCAGCGTTTCCTTGAAGTCATGTACGGCACCAAGAAGG[T/C]AAGAAATGAAGATCAAAGCTGTCATCTGTCAGCCTGAAGCAAAACTGCTC
Long Flanking Sequence:
CAGAGTCAAGATGTCGAAACCTAAAGTTCTATTACCTTTACAGCATAGGATTTACTTTATAGGTTGAGTGTGGGCTGGAAATCCTCATCAGTGATGTGTTTATATGTTGTGCTGCAGACATTGGCTCCTGCCATAGACTGGATGCCTTTCCTGTCTTCTGTTTTTGCCCCGGTTGAACTAAATGATTCTGAACCTGTGGTCGTATACGCTAAAGAATACCTCCAGAAAGTCTCCGAGCTCATCAGCAACACAAACAAAAGGTAACCCAACGTTAGCCAGATCACTTCTGCACATTTATGACTATGTAACACCTGTGGAAACGCACATTCTCTATTGTTTCAAATTGTCAGATAGCTGAGATCAAAGCTAATGTGTTTCCTGCAGTGTCTTAAACAACTACATGATCATGAAAGTGGTGCGGAAAATGGTGTCCATCTTAGACCAGAAGTTCCAGGATGCAGAGCAGCGTTTCCTTGAAGTCATGTACGGCACCAAGAAGG[T/C]AAGAAATGAAGATCAAAGCTGTCATCTGTCAGCCTGAAGCAAAACTGCTCCGGAAAGAGCCATCAAATATCACATAACAACTCATGTTTTTTCACATTTATTTCAGTCCTGTTTCCTGTCATTCATAATTTAACGTTGCCATAGTTGGCATTTTAAGGAACTTACTGTTAAGGACAAAATTATTAGCCCCTTTAAGCTATATATTTTTCTTGATAGACACAGAACAAACCATTGTTATACAATAACTTGCCTAATTACCATAACCTGCCTACTTAGCCGACTTAACCTAGTTAAGCCTTTACATGTAACTTTAAGCTGTATAGAAGTGTCTTGAAAAGATCTAGTAAAATATTATTTACTGTCATCATGATAAAGATAAAATAAATCAGTTATTAGAAACGAGTTATTAAAACTATTATGTTTAGAAATGTGTTAAAAAAATATTCTCTCTGTTAAACAGAAATTGGGGAAAAAAACAAGAGGGCTAATATATATATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5844
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 |
---|---|---|---|---|---|
ENSDART00000088329 | Essential Splice Site | 576 | 752 | 15 | 19 |
ENSDART00000136859 | Essential Splice Site | 621 | 797 | 15 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28802064)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27678050 |
GRCz11 | 11 | 27925224 |
KASP Assay ID:
554-3800.1 (used for ordering genotyping assays)
KASP Sequence:
TTCCTGCAGGCATTTTCCAGGCTCCCTTTTACAACCACGCTTGGCCAAAG[T/C]AAGATTGTTTTCCATTAACAAAACCCTCACCTGCTTATTAAGCCTYGTCA
Long Flanking Sequence:
TGTATAAGCAATAATGCCCTTCGTCCTTTTTGTCTTTGACCAATAGAAAATAAAAAATATATGTAACCCTTGATCACAAAATCTGTCAGAAATAAAATTGGACTTTATTATTTAAATTAAAAGCTGATATAAGCAAATAAATAAGGAACTATTGTATAGTTTGTTAAATTTGGACGAAATTTGACTATAATACAACTACATATATATTTGAAAATCTAAAAATGGTATTTTTATATATATACTTTAGATAATGTACAAAATGTCTTGATGGAACATGATATTTAATTATTATTCGAATGATTTTTGGCAAGACACATGTCAGTTTTTGTGTACTGCAGTGATCATTGAAGTCAGATTTTTTTTTTACTTCTCTTCTCTGCGTGTACAGATGGAGTATGACTCCACCTACTGTCAATGCCTACTACAACCCGACAAAGAATGAGATGGTTCTTCCTGCAGGCATTTTCCAGGCTCCCTTTTACAACCACGCTTGGCCAAAG[T/C]AAGATTGTTTTCCATTAACAAAACCCTCACCTGCTTATTAAGCCTCGTCAATTTCAGCAAATATGTCATCATAAACACATCATTCTCTTGTTTTTTAGAGCCATGAATTTCGGTGGGATAGGTGTGGTTATGGGGCACGAACTCACCCATGCTTTTGATGATCAAGGTCATTTATTATTCCTTATTTCAGATCTGCTGTGTGAGACTCAGTCAGTTGTTGTGATAGAAGAAATATAGTCTTGCTCTCTTTCATTATCATACATATAGGTGCTAATTTTATTTAAATAATACTGCATATTTAAAGTTTAAGCAACAACATTCTTACCTAGAGAATCGTCTAATGCCTTTGCTGTGACTTTTGCGGTGAGAAATGCAGCAAACAGAGTTATACAAAGGAGGTTTCTCTGAAATACAGCTTATGGTTAAACATAATTTTAGTTTTTTCTCTAAACTACCATACCTTAAGTTTAAAATGAAATGTTCTCATTTCATATGTGGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11183
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088329 | Nonsense | 599 | 752 | 16 | 19 |
ENSDART00000136859 | Nonsense | 644 | 797 | 16 | 19 |
ENSDART00000147386 | None | None | 142 | None | 4 |
Genomic Location (Zv9):
Chromosome 11 (position 28801898)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 27677884 |
GRCz11 | 11 | 27925058 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATAGGTGTGGTTATGGGGCACGAACTCACCCATGCTTTTGATGATCAA[G/T]GTCATTTATTATTCCTTATTTCAGATCTGCTKTGTGAGACTCAGTCAGTT
Long Flanking Sequence:
AATTTGGACGAAATTTGACTATAATACAACTACATATATATTTGAAAATCTAAAAATGGTATTTTTATATATATACTTTAGATAATGTACAAAATGTCTTGATGGAACATGATATTTAATTATTATTCGAATGATTTTTGGCAAGACACATGTCAGTTTTTGTGTACTGCAGTGATCATTGAAGTCAGATTTTTTTTTTACTTCTCTTCTCTGCGTGTACAGATGGAGTATGACTCCACCTACTGTCAATGCCTACTACAACCCGACAAAGAATGAGATGGTTCTTCCTGCAGGCATTTTCCAGGCTCCCTTTTACAACCACGCTTGGCCAAAGTAAGATTGTTTTCCATTAACAAAACCCTCACCTGCTTATTAAGCCTCGTCAATTTCAGCAAATATGTCATCATAAACACATCATTCTCTTGTTTTTTAGAGCCATGAATTTCGGTGGGATAGGTGTGGTTATGGGGCACGAACTCACCCATGCTTTTGATGATCAA[G/T]GTCATTTATTATTCCTTATTTCAGATCTGCTGTGTGAGACTCAGTCAGTTGTTGTGATAGAAGAAATATAGTCTTGCTCTCTTTCATTATCATACATATAGGTGCTAATTTTATTTAAATAATACTGCATATTTAAAGTTTAAGCAACAACATTCTTACCTAGAGAATCGTCTAATGCCTTTGCTGTGACTTTTGCGGTGAGAAATGCAGCAAACAGAGTTATACAAAGGAGGTTTCTCTGAAATACAGCTTATGGTTAAACATAATTTTAGTTTTTTCTCTAAACTACCATACCTTAAGTTTAAAATGAAATGTTCTCATTTCATATGTGGTAGAATAACTCTGATTTTTACCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAATTAAGGCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTCAAATATTATTTACTGTCATCATGGATGGCCAGGATAAAAAAAAACAGTT
Associated Phenotype:
Not determined