ZMP
adamts18
Ensembl ID:
ZFIN ID:
Human Orthologue:
ADAMTS18
Human Description:
ADAM metallopeptidase with thrombospondin type 1 motif, 18 [Source:HGNC Symbol;Acc:17110]
Mouse Orthologue:
Adamts18
Mouse Description:
a disintegrin-like and metallopeptidase (reprolysin type) with thrombospondin type 1 motif, 18 Gene
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14714 | Nonsense | Available for shipment | Available now |
sa21040 | Nonsense | Available for shipment | Available now |
sa2353 | Nonsense | F2 line generated | Not yet available |
sa12213 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14714
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 |
---|---|---|---|---|---|
ENSDART00000004120 | Nonsense | 64 | 1244 | 3 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 43059006)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 42126511 |
GRCz11 | 7 | 42461876 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGATGTTGACTCGTGTGATTTAAACTGTGTTTGTTTCACCCACAGATTA[T/A]GATTTTGCCACACCAGTGGAAGTGGACTCCTATGGAGGCTACATTTCGCA
Long Flanking Sequence:
TTGTACTGACTAAGAACAATTTTTAGTTATGTTGAAACATAAGGTCTAGTGCTTTAAAAATATACATTCATTCATTTTCTTTTTGGCCAAGTCCCTTTATTAATTAGTGTTCGCCACAGTGGAATAAACCGCTAACTTACTTAGCATATGTTTTCCGCAGTGGATGCCTTTCCAGCTGCAACCCATCACTGGGAAACACCCATGTTTTTATTAACGCCCTGTTTTTATTATACCGAGTGACAACCTCATTAGGGAGAATTTGATTGGACAAAAATGTGTGTAGTGCAGAATGAGTCATCGATGTATTTGGTGGATGTTTTTCTCAAAAAATAAATAAAGACTACACAAATAAACGAAACCAAAAATCTAACAAACATCAAGAAAAGCTACAAAACTCCTTTAAAGACTCATTACTGTTATATTAGACCACTGCAATTGACCAGTGAAAGACTGATGTTGACTCGTGTGATTTAAACTGTGTTTGTTTCACCCACAGATTA[T/A]GATTTTGCCACACCAGTGGAAGTGGACTCCTATGGAGGCTACATTTCGCATGATGTGTCAAGACATGGACGGAGTCGAAGGTCTCTGTCAGAAGCTGGCAGTTTAGTGCACTATCATGTCTCTGCTTTTGGCAAGGAACTACATTTAGACCTCCAGCCATCCCACGTGCTGGCAGAGGGGTTTACCGTACAGACACTGGGTGCAGAGGGCATCAATACAGCAACACTTGACCCCTCTATTCATAACTGTTTCTATCAAGGTTCCATACGAAACCATTCTGATTCATCTGTGGCTTTATCCACCTGTACAGGTTTGGTAAGTGTCTGCTTTTACACTAAAACATTCACTGAAATCAGATCATTAAAACCTACATACACATTTTCAATATGAATTAAATGCAGTTTGATTGAATGCTGAAGAATATTCTTCAGTGGGTTTCCTCAAGATTTTCAGATGAGGGTTAATTAGGGGTTGAGGTGTTCAGTTAGGGCTGTTATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21040
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 |
---|---|---|---|---|---|
ENSDART00000004120 | Nonsense | 295 | 1244 | 5 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 43031846)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 42153671 |
GRCz11 | 7 | 42489036 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAGTTTGAGCAGCAAATCCGAGTAAAACGCTCAGAGATCACATCGAGC[A/T]AAGAGGGTGGGCTGAACGTGGAAACTCTGGTGGTGGCAGACCGGAAGATG
Long Flanking Sequence:
ACCATGATTACCAACACGGAAAGCTTCAGAGACAACATTTCTGCGGACGCCGCAAGCAATGTATGTAAGGGAATTTCCTTTTTAGTTTTTATTTTGTATTTGGAAAGCACATTATATAATTGTAGTAGCATTCATCAGCAAACCTCTTTGAGATATTCTGACTGATTCCAAAAGCAAAACTGTTGAGTCATTATCATCTGTTGTACCGAATGAATTGAATGAAAGCTTGGAAACGGCATGTGAGGTTAATGACTGTGTATTTCCTGCTCTGTCATCGCCTCTCCACTGCTTTTATCTGGGAGCTAGCTTGGAAAGTGGACAAGCAGTTATTTGAGGCAATTTCCAGTTTCTCTCACTCTTTTTCATGAGTTTCCATGCTTTTATCTTTTCACCTGATCCTAACTACAGATACTCCCAAGCCTCCTACAGAGGATCACTTTGTCATGCCTGACGAGTTTGAGCAGCAAATCCGAGTAAAACGCTCAGAGATCACATCGAGC[A/T]AAGAGGGTGGGCTGAACGTGGAAACTCTGGTGGTGGCAGACCGGAAGATGCTGGAGAAACATGGCAGAGACAATGTCACTACCTATGTCCTTACTGTCATGAACATGGTGGGTGGAGCTACTACACTGTACTACATTAAAGACACTTTGTTTCTAAAGTGATGTGTCAAGTAATGTTATGTTAAAAAGGTCTCCAGTCTTTTCAAGGATGGGACTATTGGGAATGATATCAACATTGTTGTGGTCAGCCTCCTCCTACTTGAGAAAGATCCGGTAAGAAAGATAAGTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTCTGTTAGCCATAGCTGTTCATCTATCTGTCCATTCATCCATCCACCCACCCATCCATCTATCCATCCATCCATCCATCCATCCATCCATCCATTTTTCGGATGAGACGTTTAACGGAGGTCCTGACTCTCTGGGGTTGTTAAAATCCCAGGATGTTCTTCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2353
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004120 | Nonsense | 975 | 1244 | 19 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 42985459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 42200058 |
GRCz11 | 7 | 42535423 |
KASP Assay ID:
554-2668.1 (used for ordering genotyping assays)
KASP Sequence:
CTGAGGAAGGTGACGTACCAGCGGGAGGAGGTGGCSGCTCAGTCCTTGTG[C/A]CCAGTAATGGCTCCGGCTCAACTACAGCCCTGCAACACACAGTCATGTCC
Long Flanking Sequence:
CAATCAGCAATCAGTAAGGCTCAATTGATCATGTGACATAAAAGACAGGGGGGGAAAAAATCAAATACAAACCAGTTATTTTAAGTCATAAATGATGTTGATGCAGTATGGATGTCCAGTGTCCTCCTCCATGTTAAAATGTGATAAAATAATAAAAACACAAGCTTTGTGTCTAAAGGTTTTTATATTTTTGATCACCAATCAGCAAGACTCAGTGGACCATGTGACATAAAAAAATAATGGTGTTGTCTTTATATATTTATTGTTGTAAATAACTGTGTTTAATAGTAGACTATAGTAAAGTACTATGCTCACTTCTGAGGTAATGTGAAATAGCTCGGGTTCATGCCTCAAGATCAGATGTTTTGTCTTGACAGCTGGACCACAGGTAAATGGGGAGTGTGTAGCAGAACATGTGGAGGTGGCCAGCAGACGAGAAACATCCGCTGCCTGAGGAAGGTGACGTACCAGCGGGAGGAGGTGGCCGCTCAGTCCTTGTG[C/A]CCAGTAATGGCTCCGGCTCAACTACAGCCCTGCAACACACAGTCATGTCCTCCAGAGTGGAGTACCAGCTCCTGGACCCAGGTACTGTTGGATTACACACAATATTCTGTCAATTCTTTGCACTTTATGTTTTTTTTCAGCATTTTAGTTTTTGTGGTTTGAAAAGAGTGGATTCACAATGTCACTTGTACAGTCTGACTAGTGTGTAATTGTATTGTGTTAAGTTTTAAGATGTTTTGTAGAGTATACTGTATATGCAGTCAGGTATATATGTTTAGGATAAATAGGATAGGTTATTTTGTTTTGCTTAAGTTTCAATGATGACCAAATATATTACAAAACCTACAGAGAAACAAAACAAGAAAAAAAGTATATCTTATTACTTTATTTTAGGGTACAATTCTTGCTATTGCCAAACCATTACCTATGACATTTCACTCAACAAACTAATTTGCTTATTAAGGTAATGAGATCATACAGAATATGTACTTTACACAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12213
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000004120 | Essential Splice Site | 1146 | 1244 | 21 | 23 |
Genomic Location (Zv9):
Chromosome 7 (position 42981082)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 42204435 |
GRCz11 | 7 | 42539800 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCGGACCTTCTGTGACACTGGGCTGGTACTCTTCTCCTTGGCTGCAGG[T/C]TTGTGTAACTAGCTCTTCATAACTAATCAGTCCTTTGTTSTGTCTCTATT
Long Flanking Sequence:
TAATACAAAAGTTATAAAAAAAAAAAAAACTAAGTAAGTTTTAAGTGACTCATGATTGTAATATATTACTTCTAAAAGTAACTTAACCCAACCCTGCCCATTAGGAAGTGTTATGGCCAATTAAACACTGCGTGTGCGTGGATATTAATGATCCTTTGTGGATCGTCAGAGTCTTTGTCGATTTTCTCATTGGCATTTTGTTTTACCCTCATAGGATTTGCATGGAAACAATGTGTTATCTAATTGTTGGGTTATTTGACAGTGTTCGGCCTCCTGTGGAGCAGGAGTAAGGAGAAGAGAGCTGCACTGTGGGGAGAAAGACTCTCAAGGAGGCTACACCGAGTTCCCTGCGAGGAGGTGCAGGAACTTACAAAAGCCTGAAGCAGATCTCGAGCAATCCTGTAATAACGGCCCTTGCCCAGAGCCCTTGGCACCCCAGCTCCTCCAGCCTGGCGGACCTTCTGTGACACTGGGCTGGTACTCTTCTCCTTGGCTGCAGG[T/C]TTGTGTAACTAGCTCTTCATAACTAATCAGTCCTTTGTTCTGTCTCTATTCTGCCAAGGCTCTAATATTTCGGTCCTGTCTCTGTGTATTTCAGTGCACAGTGTCCTGTGGTGGTGGGGTGCAGACACGCAGTGTTCAGTGTCTGAGACAGGGGCGTCCGTCAGTGGGCTGTTTCCCTCACCAGAGACCGATAAGCTCACGGGCCTGCAATACACACTTCTGTCCTGCTCCAATCCCAGTGCCAGTCCCACCTCCTTCACCCACTCTTAAAGGTAAAAGCTGCTTTAGTTTAACATTTGACATTCGAATCAAACAAAACATCATTTTCAGTCTGTACTGCTATTTAAACACTTTTGGTCAGTAAAATTATAAAATAAAAAGTGCTATAAAGCAAGTATAACTAAATACTGTTTTAAACTTTCTACTAACTCTTTTTCCCACCATTGACTAGAAATCTTGTCTCAAATTATAAGATAATCAGAGAACATTAAAGTCAGATT
Associated Phenotype:
Not determined