ZMP
si:dkey-46g23.3
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC100136837 [Source:RefSeq peptide;Acc:NP_001108028]
Human Orthologue:
A2ML1
Human Description:
alpha-2-macroglobulin-like 1 [Source:HGNC Symbol;Acc:23336]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19930 | Nonsense | Available for shipment | Available now |
sa18745 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14917 | Essential Splice Site, Missense | Available for shipment | Available now |
sa44554 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25976 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19930
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 |
---|---|---|---|---|---|
ENSDART00000109071 | Nonsense | 211 | 1462 | 6 | 35 |
ENSDART00000110995 | Nonsense | 211 | 1456 | 6 | 34 |
ENSDART00000113517 | Nonsense | 211 | 606 | 6 | 17 |
ENSDART00000115331 | Nonsense | 211 | 1453 | 6 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 3944913)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 3629463 |
GRCz11 | 3 | 3411716 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGGACAAATGTTTCCTCCGTGAACTGGATTTTGGAGCTTTCTCATGTTT[T/A]AATCCCAGAAGCTCAGGTTGGGACGTACACACTGAGGGCTTATATTGGTG
Long Flanking Sequence:
GTACAGTTTGACATTTACCACATCCAAGTGTACTGTTAAATAACAGATTTCTCCCCAATATCAAGTTTAATTGCATCTTATCCAAACTATAAAGTTAGGGGGGATACATGATTTTAAAGTGTCTTAATATGTGAATCTGATCATGATTAACTGCCCAGTGTAAGTGCTTTTATTCTCACTTCTGCAGTGAATTTCAGAGTCGTCACCATGAGTGATAAACTTGTGCCTCTTGACCAAATGGTAAGGCTGTGTGTAGTTGCTTTCTCAACCTTTTAAAATCTGTGACTGAATGTCTAATTCTAGCTCTGTCTTGCAGTACAATCTGGTGGTGTTGGAGGTAGGAACTTGTTTGCTGCTACTCTTGACAACATTGCTTTGGATGTTTCCTTGTACTTTTTGACTGAGCTTAACCTTTTTTCACTAGGACTTTCGTAATATCCGGATAAATCAGTGGACAAATGTTTCCTCCGTGAACTGGATTTTGGAGCTTTCTCATGTTT[T/A]AATCCCAGAAGCTCAGGTTGGGACGTACACACTGAGGGCTTATATTGGTGACCGAATCATCTCCCAGAGTTTTGATGTGAAACAATACGGTACGCCTATTAATATCATCGCTAAGTGTTTAACAGCCTTTCTGGGGTCTTACAGCTCTTTCTTGTTTAGTGTTACCCAAGTTTGATGTGACCGTGAACGCACCACAGACGTATAGTGTCGCAGATGTGGGACTGAAAGTTGAGGCTTGTGGAAAGTGAGTGAAGCTTTTTTCTTTTTCTTGCTATATGTTTGTCTTGTGGATGGTCTGTTCTTGATCACCAATGTTTCTCAGGTACACATTTGGGCAGCCTGTACCTGGTCAAGTGCTAGTGCAAGTGTGCCGTCAGCCTCTTACCTATGTTCAGGATCCTAAAGTGACCAGCATTTGTCTGAATAAATCCACCAAGGTAAAACCTTTTGTACAGGGCTTGCAATTACAAATATCTGAATTTTATTAGTGTAACTTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18745
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109071 | Essential Splice Site | 922 | 1462 | 21 | 35 |
ENSDART00000110995 | Essential Splice Site | 916 | 1456 | 20 | 34 |
ENSDART00000113517 | None | None | 606 | None | 17 |
ENSDART00000115331 | Essential Splice Site | 913 | 1453 | 20 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 3939281)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 3623831 |
GRCz11 | 3 | 3406084 |
KASP Assay ID:
2261-7176.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACCATCAAGAGGACGCATTGACATAGTCACTCGAAGTCTGCGAGTTCTG[G/A]TTTGTAACTAATTCTGAAGTTTGAAAATAGAGCCCATGTGTTGGTCTTTC
Long Flanking Sequence:
CTTCCTTCCAGCCCTTCTTCCTAGAGCTCACCCTGCCTTACTCCATTATCCGTGGGGAGGCTTTTGAGCTGGTGGCCACAGTCTTCAACTATCTGTTGCAATGCATCAAGGTCTGGGTTCCCCTAATGGATCCACATATGCATGTCTCCTCTGTCCACTAATGCTGTTATTCTTTATCAGATTCAAGTGACTCCAACACCGTCCTCCAACTACACTCTAACACCCATCAATGATCAGTCTTCATCTACTCTCTCTACCAATTGGAGAAAAACCATCAAATGGGCTTTAACTGCTTCTGTTATTGGTTTGTTTATTCATTAGTGTGTGCATATATAAATGAGCATGTGAGGGTCTTCAATTGATTGCTGAAATTTGTAGGAACCGTAAACGTGACCATTAGTGCTGAGGCCAGTCCATCCCAGGAATTGTGCGGCGATCAGGATGTGACCGTACCATCAAGAGGACGCATTGACATAGTCACTCGAAGTCTGCGAGTTCTG[G/A]TTTGTAACTAATTCTGAAGTTTGAAAATAGAGCCCATGTGTTGGTCTTTCTTATGAATTTAAACATTCCTTTTTGTTCCTCTAGGCCGAAGGAGTGGAAAGAACCTTCACACGGAGTTGGTTACTCTGTCCAAAGGGTTTGTTTAGCTCAGAATTTATTCTACATTGCTTGCTCCTAGAGCTGTCTGCTGATTTTTGTTTGGTTTACAGGAAGCGTGCTTTCAGAGAGCGTGAAGATCACACTTCCTACAAATGTCATCCAGGGATCAGCCAGCTGCTCTGTATCAGTCATTGGTAAAGGGTTTCCTTAAACCGCTTAACACCATAGGGCTGCTCGACATGCTTGTAGCGATCACTACAAGCCTGCCCTTTTTGTCAAACTTTTTACTGAGTTCCAGATCTTTTTTTTATTATTATTTTTTTTTTTTAATTCTTTATATCTGGCACAATCAGTTTACCTGAGTAACCTATGCACCCATAGGTCAATTAGGTGGTTGCAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14917
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109071 | Missense | 940 | 1462 | 22 | 35 |
ENSDART00000110995 | Essential Splice Site | 933 | 1456 | 21 | 34 |
ENSDART00000113517 | None | None | 606 | None | 17 |
ENSDART00000115331 | Essential Splice Site | 930 | 1453 | 21 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 3939144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 3623694 |
GRCz11 | 3 | 3405947 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YGAAGGAGTKGAAAGRACCTTCACACGSAGTTGGTTACTCTGTCCAAAGG[G/A]TTTGTTTAKCTCAGAATTTATTYTRCATTGCTTGCTCCTAGAGCTGTCTG
Long Flanking Sequence:
ATGCATGTCTCCTCTGTCCACTAATGCTGTTATTCTTTATCAGATTCAAGTGACTCCAACACCGTCCTCCAACTACACTCTAACACCCATCAATGATCAGTCTTCATCTACTCTCTCTACCAATTGGAGAAAAACCATCAAATGGGCTTTAACTGCTTCTGTTATTGGTTTGTTTATTCATTAGTGTGTGCATATATAAATGAGCATGTGAGGGTCTTCAATTGATTGCTGAAATTTGTAGGAACCGTAAACGTGACCATTAGTGCTGAGGCCAGTCCATCCCAGGAATTGTGCGGCGATCAGGATGTGACCGTACCATCAAGAGGACGCATTGACATAGTCACTCGAAGTCTGCGAGTTCTGGTTTGTAACTAATTCTGAAGTTTGAAAATAGAGCCCATGTGTTGGTCTTTCTTATGAATTTAAACATTCCTTTTTGTTCCTCTAGGCCGAAGGAGTGGAAAGAACCTTCACACGGAGTTGGTTACTCTGTCCAAAGG[G/A]TTTGTTTAGCTCAGAATTTATTCTACATTGCTTGCTCCTAGAGCTGTCTGCTGATTTTTGTTTGGTTTACAGGAAGCGTGCTTTCAGAGAGCGTGAAGATCACACTTCCTACAAATGTCATCCAGGGATCAGCCAGCTGCTCTGTATCAGTCATTGGTAAAGGGTTTCCTTAAACCGCTTAACACCATAGGGCTGCTCGACATGCTTGTAGCGATCACTACAAGCCTGCCCTTTTTGTCAAACTTTTTACTGAGTTCCAGATCTTTTTTTTATTATTATTTTTTTTTTTTAATTCTTTATATCTGGCACAATCAGTTTACCTGAGTAACCTATGCACCCATAGGTCAATTAGGTGGTTGCAATAATTAGTGCTCAAATGGGGGAAAACAGTTGATCAAAAAATACTTAGAACCATGAGATTGAAGTGTAATTCACAGACATCCACTTTTTTTGTGAGACCAACAAACTGACTATACCTGGACCATGAACGTTCTGCACGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44554
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109071 | Essential Splice Site | 1360 | 1462 | 31 | 35 |
ENSDART00000110995 | Essential Splice Site | 1354 | 1456 | 30 | 34 |
ENSDART00000113517 | Essential Splice Site | 504 | 606 | 13 | 17 |
ENSDART00000115331 | Essential Splice Site | 1351 | 1453 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 3936550)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 3621100 |
GRCz11 | 3 | 3403353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGACTGCCAGGCTGCACCAGTCAATCTGATGTTGACCTTCACAGTCAA[G/A]TAAATATTGCTTTTTAATATTGTTAAGGCTGCGCAGTTCTTTGTAAAGAT
Long Flanking Sequence:
GTACTGCCAGTGGTTCAGTTTACTGTTTGGTTACACGAATTTTGGAACCACTTAAAGTTTGCTTTAATTTTTTTTTAAAACTCCTAGGACACTGTGGTGGCTCTTCAGGCCTTGGCTCTGTATGCTGCTCAAGCGTTCACCCCTGGAGGCTCCAGCACAGTTACAGTTCAGTCCTCAGTGCCAGCAGGAGACGTTTTCAACTTTGCTGTGACTCCCAACAACCGCCTGCTGTACCAGAGAAATTCCCTGAACAACTTCCCTGGCACATATAGTGTTGTAGCAAGGGGATCTGCCTGTGCTTCTGTGCAGGTCTGTATGTTCACCCAATGTGTGTGTTTGTTTCTCCTGACAACTCATTGCCTTGATTTGACCTTGCAGGTTGCCTGTTTCTACAACATCCCAACTCCGGTTACAGTTGCCAGAACCTTGAGTGTTGTTGCTAAGGTGACCGGGGACTGCCAGGCTGCACCAGTCAATCTGATGTTGACCTTCACAGTCAA[G/A]TAAATATTGCTTTTTAATATTGTTAAGGCTGCGCAGTTCTTTGTAAAGATGACTCAACTTGAAGTGTCATGCAAATCAGTGTGTAAGATCAGTTTTCAGTTATTTTTTTTTCCTCTTCTCTCTCTCCTTTCTCTATACGTGCACACTACTGAAGTGCCAAGGTTTCTGTGTTAATGTTTGGCTAGTTAGTTGTCTAGTCAAGCCAACCACCACACATGCCTCCACCTATCTAGATATTACATGCTAATTTGCCTTTGCGGTTTGCTTGAATTTAAGTTAGCTGGGTTTTCCAATCATCAGATCTGAAATACTAATTTGAATTTTTTTTGTTCCCCCAGATACAATGGTCGAAAGCCAACTACTAACATGGTTCTGGTGGACATCAAAGTGTTGTCAGGATTCACTGCAGACACCTCACTGGTTTGTATGATTTAAGGGTGACTTTGGGACCTTTTTGAAACCGCTTGGTGAGTGATGGTTTTTTCCTTGCAGCTTGGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25976
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109071 | Essential Splice Site | 1360 | 1462 | 31 | 35 |
ENSDART00000110995 | Essential Splice Site | 1354 | 1456 | 30 | 34 |
ENSDART00000113517 | Essential Splice Site | 504 | 606 | 13 | 17 |
ENSDART00000115331 | Essential Splice Site | 1351 | 1453 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 3 (position 3936549)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 3621099 |
GRCz11 | 3 | 3403352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGACTGCCAGGCTGCACCAGTCAATCTGATGTTGACCTTCACAGTCAAG[T/A]AAATATTGCTTTTTAATATTGTTAAGGCTGCGCAGTTCTTTGTAAAGATG
Long Flanking Sequence:
TACTGCCAGTGGTTCAGTTTACTGTTTGGTTACACGAATTTTGGAACCACTTAAAGTTTGCTTTAATTTTTTTTTAAAACTCCTAGGACACTGTGGTGGCTCTTCAGGCCTTGGCTCTGTATGCTGCTCAAGCGTTCACCCCTGGAGGCTCCAGCACAGTTACAGTTCAGTCCTCAGTGCCAGCAGGAGACGTTTTCAACTTTGCTGTGACTCCCAACAACCGCCTGCTGTACCAGAGAAATTCCCTGAACAACTTCCCTGGCACATATAGTGTTGTAGCAAGGGGATCTGCCTGTGCTTCTGTGCAGGTCTGTATGTTCACCCAATGTGTGTGTTTGTTTCTCCTGACAACTCATTGCCTTGATTTGACCTTGCAGGTTGCCTGTTTCTACAACATCCCAACTCCGGTTACAGTTGCCAGAACCTTGAGTGTTGTTGCTAAGGTGACCGGGGACTGCCAGGCTGCACCAGTCAATCTGATGTTGACCTTCACAGTCAAG[T/A]AAATATTGCTTTTTAATATTGTTAAGGCTGCGCAGTTCTTTGTAAAGATGACTCAACTTGAAGTGTCATGCAAATCAGTGTGTAAGATCAGTTTTCAGTTATTTTTTTTTCCTCTTCTCTCTCTCCTTTCTCTATACGTGCACACTACTGAAGTGCCAAGGTTTCTGTGTTAATGTTTGGCTAGTTAGTTGTCTAGTCAAGCCAACCACCACACATGCCTCCACCTATCTAGATATTACATGCTAATTTGCCTTTGCGGTTTGCTTGAATTTAAGTTAGCTGGGTTTTCCAATCATCAGATCTGAAATACTAATTTGAATTTTTTTTGTTCCCCCAGATACAATGGTCGAAAGCCAACTACTAACATGGTTCTGGTGGACATCAAAGTGTTGTCAGGATTCACTGCAGACACCTCACTGGTTTGTATGATTTAAGGGTGACTTTGGGACCTTTTTGAAACCGCTTGGTGAGTGATGGTTTTTTCCTTGCAGCTTGGATCC
Associated Phenotype:
Not determined