ZMP
adam28
Ensembl ID:
ZFIN ID:
Description:
a disintegrin and metallopeptidase domain 28 [Source:RefSeq peptide;Acc:NP_001070186]
Human Orthologues:
ADAM28, ADAM7
Human Descriptions:
ADAM metallopeptidase domain 28 [Source:HGNC Symbol;Acc:206]
ADAM metallopeptidase domain 7 [Source:HGNC Symbol;Acc:214]
ADAM metallopeptidase domain 7 [Source:HGNC Symbol;Acc:214]
Mouse Orthologues:
Adam28, Adam7
Mouse Descriptions:
a disintegrin and metallopeptidase domain 28 Gene [Source:MGI Symbol;Acc:MGI:105988]
a disintegrin and metallopeptidase domain 7 Gene [Source:MGI Symbol;Acc:MGI:107247]
a disintegrin and metallopeptidase domain 7 Gene [Source:MGI Symbol;Acc:MGI:107247]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa31442 | Nonsense | Available for shipment | Available now |
| sa11354 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31442
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000098604 | Nonsense | 36 | 762 | 2 | 21 |
| ENSDART00000130936 | Nonsense | 36 | 293 | 2 | 9 |
The following transcripts of ENSDARG00000035514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 29544252)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 27299550 |
| GRCz11 | 5 | 27899703 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACAGTTGGTCACATTCACGAACTACATGGCAAGGTTTATGAGATTGTA[C/T]GACCAATAAGATTACATGATCTGCAAAAAAGAGACTTACAGGTGAGTTCT
Long Flanking Sequence:
CTGGTAAAAAGATAACACTGGTATTTTAAAAAAACTACCATGTAAATATCTCTTTAATACTGATTGTTGTTACTGTTTAAACAGTTACACCTTAATAAACATTACCCAAACATGTTGTTAGGGGCAGACTGTAAAAATCACAGTAAAGCAAACATGCTTTAACAAAACAAGGATATCAATCTTGGCCAGAAAGTGTGTAGAACAGACATTGTCTATTGTTTTTTTCTACCTTAAAATAACAAATCTGGCATTGCTGTAGATACGTTTGTTGGCAGTTATCACTAAAATCAGCCATTCAAGTTTACACTTGTCCTTTCAATACAATATTTAGATCAGGTGAAACAGTTCTGAAATCTGAAAGCTGCATTCACAGCCTCTATATTAAAATCAAAATACTGAATGTCTGTATTTAATGAGTAATCTGTGATTCCTTGTGTGTTTGTCAATCTGCTACAGTTGGTCACATTCACGAACTACATGGCAAGGTTTATGAGATTGTA[C/T]GACCAATAAGATTACATGATCTGCAAAAAAGAGACTTACAGGTGAGTTCTTATATACTCCCTAATACTACATACAGAATTATTAAACCCCTTTGATTTTTTTTTCTTTTTTAAATATTTCCCAAATGATGTTTCACAGAGCAATTATATTTTCACAGTATGTCTGATAATATTTTTTCTTATGGAGAAAGTTTTTTGTTTTATTTCAGCTAGAATAAACACATTTTTTAAAATTTTTATTTTAAATAAAAGTTAAAATTTTTTTTTTTGATAATTCTGACTTCAACTGTATATTTGAAACCTTTTATTCAAACTAATTAATTTCTTTCCTTTGCAGTCAAGACCGGATAGAGTGAAATATGCTATGACACTGGGTGGTAGAGACATTGAAATGCATCTCCAGAAAAACACGTACGTTCGTCTTCTCAGTTTCTCCCTTGTCATCATATCTGTATATCTTGTGATATTTAATATCTGCACATGTTGCAACTCCAAAAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11354
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 |
|---|---|---|---|---|---|
| ENSDART00000098604 | Essential Splice Site | 453 | 762 | 13 | 21 |
| ENSDART00000130936 | None | None | 293 | None | 9 |
The following transcripts of ENSDARG00000035514 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 29556829)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 27312127 |
| GRCz11 | 5 | 27912280 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGACTGTGGGCTCACAATGTGCAGCAGGAGAATGTTGTGACAACTGTAAG[G/A]TAWAGTGGAGGTTTYTTGCTGTKTCATTCATCAAATCRCCAAAGGATTAA
Long Flanking Sequence:
AAAACACTATAGAAAATACTGTGAAATATTCCTTGCCTCGTTAAACATCATTTGGGGAATATATATATATATATATATATATATATATATATATATATAAATTCTGACTTCAACTGTATCTTTAATCTTTATGTGCTCTCTGTGTTTAGTATGCATGTACTGTAATATGATTGGAGATTTGTTTAAATGTACATTAGTCTTTTTTTTCCTGACATTTGAATAGCATTTACGTTATTTAACCATTGTCTGCTTTGACAAGTAAATTAATTTTCAACACATTTTTTCTCAGAACAAGTGCTTGAAAAGACATTTATTATGCGCACACAACTTGAACACACCCACTATGCTAAGAAGATGTTCTCAGTGTTGTTATTTCACAACCAAAATTAACTCTTTATGTTTTTGTATAGGAGTGTAAAAACCCATGTTGCAATGCAACCACCTGCAAACTGACTGTGGGCTCACAATGTGCAGCAGGAGAATGTTGTGACAACTGTAAG[G/A]TATAGTGGAGGTTTTTTGCTGTGTCATTCATCAAATCACCAAAGGATTAAACAACTTATTACACAACTGCTTGGGACATATACAGTGCTCAGCATAAATAAGTACACCCTATTTTGAAAATGCATATTTTCATCCATTCCTCAGTGAATATAAATATTTGCACAAAACAGATGTATTAAATTAATTAACTATTATTTAACAACTTGTTAAAATAATATGTTTGTCAGTAAACATCTTCAGAAATAGAAAGATAATACATTTAAATTTATGAAATAATTTTGAAACAAGAAAATTTCAACAATATCTTATATATTTACATATGTTTCTTAGGATTTATGCTCTTTTATTTCATTTTTACATATTATTTTTTCCCTAATGTATACATTTGGGCTACTAATTTTTGGACCATTATCATAAGTTATTTTGTCAGATTAGCTCCAGAGTTTGCTTCAATACTGAATAATGTCTATGCACATTAGTATATGTATGAGCTTTAGAAC
Associated Phenotype:
Not determined