ZMP
si:dkey-46l15.1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC560131 [Source:RefSeq peptide;Acc:NP_001116724]
Human Orthologues:
MTSS1, MTSS1L
Human Descriptions:
metastasis suppressor 1 [Source:HGNC Symbol;Acc:20443]
metastasis suppressor 1-like [Source:HGNC Symbol;Acc:25094]
metastasis suppressor 1-like [Source:HGNC Symbol;Acc:25094]
Mouse Orthologues:
Mtss1, Mtss1l
Mouse Descriptions:
metastasis suppressor 1 Gene [Source:MGI Symbol;Acc:MGI:2384818]
metastasis suppressor 1-like Gene [Source:MGI Symbol;Acc:MGI:3039591]
metastasis suppressor 1-like Gene [Source:MGI Symbol;Acc:MGI:3039591]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11667 | Nonsense | Available for shipment | Available now |
sa40790 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31543 | Nonsense | Available for shipment | Available now |
sa20818 | Essential Splice Site | Available for shipment | Available now |
sa33966 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20817 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11667
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 |
---|---|---|---|---|---|
ENSDART00000083007 | Nonsense | 12 | 693 | 1 | 14 |
ENSDART00000134146 | Nonsense | 12 | 702 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50636437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50685915 |
GRCz11 | 6 | 50685134 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTTTTGGGCTGGTAAAATGGATGCGGGAATGGAGAAGGAGTGCAGYGCTT[T/A]GGGAGGGCTCTTCCAAATCATCATGAACGACATGAAGGTGAGTCCCTCTC
Long Flanking Sequence:
CCATGAGGAATAAAAAATACGGCGGTTGTTGCGACCTAAACTAACGTGACTATCGATCTAGCAGAGCCAAGCTTTTGAAAACGCCGAGCCAGGTACTTCGACTTTTCAACGGTCGCATTTTTCTGCGGGTTTACCTGCGCTTACGTGGCACTTTTTTGACCTGGAGACTTATTATTAAAAATCACGTTTTTAGTTATTTTTATCCTCTTTTATCGTGGCGATGCGAGGTATTTTCAGAGGTTTAGTAAGTTGCGTGGCCGGGACTAGTTTGCTTGCGCCGGGCAGCCAATCAGCGGAATAACACTCACTGTTTTTGCATTAATTTATCACATTTTGCCTTATTCACACGATAACCTTCAAAAACAGATTTCCACCGCGCCCTTCAGATATTGACAGCGGTTTTCGAGGTGAGCTTTCGCAGGCAGGAGAAGTGTCAGCGCTGCGCGTGTGCTTTTGGGCTGGTAAAATGGATGCGGGAATGGAGAAGGAGTGCAGCGCTT[T/A]GGGAGGGCTCTTCCAAATCATCATGAACGACATGAAGGTGAGTCCCTCTCAAATTAAAACAACACACCCGATGCTTTGATTTTCCCCCCATCATCATGGGTGGGTTTGGAGTGTGCCTGCACAAGGGCCCAGAATAAGTTATTTTCCAGCTGTTTTGGAGGGTTGGCAACAGTTCTGTGGTTGGTTGGCCGGCTGCTGATAGATGTGAATCCAGCCGCCTCTTCAAATCACTATTTACATCTGTGTTACAGAACATCTCAGATGTAGTAGTGTTTGTCATAGTCTATATGTTTATGAAGCATGCAATACGGTTAAAAGATGAGGTTGTCGCAGCTTTTATTTTTAATGCTAAATGGGATTACTGTCACATTACGTTAAATAAAGTACAATGGTTTAACATGTCATTGACATGCACCATGGTTATCTTGAAAGAGATAACTTGCAGAAATTTGGACTATGGTGTCATGTTTTGTTTTCGTGTACCATGCAGATCCATTGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40790
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 |
---|---|---|---|---|---|
ENSDART00000083007 | Essential Splice Site | 342 | 693 | 11 | 14 |
ENSDART00000134146 | Essential Splice Site | 342 | 702 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50541878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50591356 |
GRCz11 | 6 | 50590575 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTACAGCGGGCATGAGGAGAGAGTCAGGACACTGTCCTCCTCGGGCAAG[G/A]TACAGGATCATTTTATTGCAATAATGATGCACTGTTTTCTTACTTCTGTG
Long Flanking Sequence:
AAAAAGTATGTACAGGCAAAAGAAAACTACCACTTATGGCTCCTGATGATGCATTGGGTCATATGAAATGAAATGATCAGTCTATGCAAGAAACTCAGCAAAGGAATATTTACAACATTTAATATTTACAAGCCTAGCCTGTTGAGGAGTAAACTGACAGCAAAGTTTTTGAGTACATTAAATAAGGAGACATTAGCACTTGGTTACACTGGGATGTTTTGGAGGACTTGACAGAAACTCCACAATTGGGAAAATCCTGGTCCAATTTTGCCTTGCTTATATGTCACATTATAATAAACTGTAAATCATATTGACTTTAAAACATTGGATCATAATGTTTTGTTCTTGTTTTCTGTTGAAAAGGACTAATGAAGTGTGTTGTTGTGTAGGATCAAGGTCAGAACTCTCCTGGCACAGAAAATGGCACCTCCATGCCTCCTCTGCACAAAATTTACAGCGGGCATGAGGAGAGAGTCAGGACACTGTCCTCCTCGGGCAAG[G/A]TACAGGATCATTTTATTGCAATAATGATGCACTGTTTTCTTACTTCTGTGAATCAGTACTAAATCTGAAACAACAGGGCTTCAAAGTATGAATAATAAACTGCATGCTGCAACCTTTTTTCTTATCAATGCAACTTAATTTCATTGTACTGATGTCACTACCAATTTGCTGATAAGCACTGATATGCTTATTGCATATTAGAAATATTAAATGCCAAAAGCAGAATTAAATCTTCAAATCACCACACTGACTATTTATTAGCTTGTCTTAAACACAGCGCAGAGCTAAGGCTTTTACTACTAACACTGTCTTTAACCTGTAGCTGTAACCATGATATTTCTGTGGAAAAGTGGAATATTATAGACAATATTTGTTTTATTTTATTATTGCAGACATGATTTTAGTTAGAGATGAAAATGAATGCCCATTTCACACAAGTTGATATGATTCTTAGGATCATAAAGTATACTTTGGGTAAATTTCTCAATGGTAGTATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31543
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 |
---|---|---|---|---|---|
ENSDART00000083007 | Nonsense | 344 | 693 | 12 | 14 |
ENSDART00000134146 | Nonsense | 344 | 702 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50539073)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50588551 |
GRCz11 | 6 | 50587770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGATCGATCTTCCAAATAGTGATTGGCTTTTTTCCGCTGTGTGTAGCCA[C/T]AGTCAGCTCGAGAGCAGCTGGCTCTTACTCTAGGAGGAGGACTTAATTCT
Long Flanking Sequence:
CTGCATCGTGCTCACGAAGTTACGAGAAAATAGATAACAAGAGCAGAGCTGCGGTAAAATAATAAATAAGAAGGCTGTGGTCAAGTAAATAAATAAATTATATTCAAAAAGTGTGACTGCTGAGAGCAACAGATTCTGGAGCTAGGGACACCGGCCCTCGCGGCCAAAAAACGGACCGGCCCACCGGGAATTCTCCCGGTCCTCCCGATTAGCCAATCCGGGCCTGGCGTTAGGGCATCTGTTGTGTGTATAAACATCACATATAACTTCCCAGTGCTTGACATCGCAGGCCACCATTATCAGTGTAAAATGCATTCAAACAAACATCTGCATGTGTTAAGTAACATTGCTGTATTCAACAAATGCTCAGCATGTACAACTGATACTGGTTCCACTGCTTTCATATGTTAATCTGCAGCCCTGTGCACCTCTCGTACTGCTACAATTATTGTGATCGATCTTCCAAATAGTGATTGGCTTTTTTCCGCTGTGTGTAGCCA[C/T]AGTCAGCTCGAGAGCAGCTGGCTCTTACTCTAGGAGGAGGACTTAATTCTGAAGCTCCTCGAACCAGCAGGGATTCCCTTCACTGCTCCAGCGGATACAGCACTCAGACCACCACGCCATCCTGCTCTGAAGACACCATCCCGTCACAGCACGGTCAGTACACACATGCTGAATACACACACATGCATGATTGAGACAATTTCTTTTTCTGTCTTGTGTTTTTCCTTTTAAGCTTTTAGTGCACATATTAAAGCTTGACGTGTTCAGTAGATTTTCCTTGTGTTTCTTTGCATAACACTTTTCTCCTTTTTCAATGTTTTCACACTTTAACGTCGTTTCTCAAAACACAGTAATCCGATTTGTGGTTTGTGTGCGTATCAAATGTGAAGCAATTTCAGACTAAATCTAATGCGCTTGCACAAACCACAGGCTTGGATTGCTGTCCAAAGTGCGTGTTTTTGGCCGTTTGTATACATGTTAAATGTACTTTATTGTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20818
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083007 | Essential Splice Site | 395 | 693 | 12 | 14 |
ENSDART00000134146 | Essential Splice Site | 395 | 702 | 12 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50538918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50588396 |
GRCz11 | 6 | 50587615 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACCACCACGCCATCCTGCTCTGAAGACACCATCCCGTCACAGCACGG[T/G]CAGTACACACATGCTGAATACACACACATGCATGATTGAGACAATTTCTT
Long Flanking Sequence:
CCTCGCGGCCAAAAAACGGACCGGCCCACCGGGAATTCTCCCGGTCCTCCCGATTAGCCAATCCGGGCCTGGCGTTAGGGCATCTGTTGTGTGTATAAACATCACATATAACTTCCCAGTGCTTGACATCGCAGGCCACCATTATCAGTGTAAAATGCATTCAAACAAACATCTGCATGTGTTAAGTAACATTGCTGTATTCAACAAATGCTCAGCATGTACAACTGATACTGGTTCCACTGCTTTCATATGTTAATCTGCAGCCCTGTGCACCTCTCGTACTGCTACAATTATTGTGATCGATCTTCCAAATAGTGATTGGCTTTTTTCCGCTGTGTGTAGCCACAGTCAGCTCGAGAGCAGCTGGCTCTTACTCTAGGAGGAGGACTTAATTCTGAAGCTCCTCGAACCAGCAGGGATTCCCTTCACTGCTCCAGCGGATACAGCACTCAGACCACCACGCCATCCTGCTCTGAAGACACCATCCCGTCACAGCACGG[T/G]CAGTACACACATGCTGAATACACACACATGCATGATTGAGACAATTTCTTTTTCTGTCTTGTGTTTTTCCTTTTAAGCTTTTAGTGCACATATTAAAGCTTGACGTGTTCAGTAGATTTTCCTTGTGTTTCTTTGCATAACACTTTTCTCCTTTTTCAATGTTTTCACACTTTAACGTCGTTTCTCAAAACACAGTAATCCGATTTGTGGTTTGTGTGCGTATCAAATGTGAAGCAATTTCAGACTAAATCTAATGCGCTTGCACAAACCACAGGCTTGGATTGCTGTCCAAAGTGCGTGTTTTTGGCCGTTTGTATACATGTTAAATGTACTTTATTGTTCTTTTACAGTGATAAAGAAAGAACCTCCTCTATATGGTAGGTTTCTGAATGTCATTGCATAGACTTGATTATTATCATTGTGATCATGTACCAATAATGACCAACATTCTGTGTGTTGATTTTAGGGAATCCATGTCATATTGCAGGGGTGCATTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33966
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000083007 | Nonsense | 505 | 693 | 14 | 14 |
ENSDART00000134146 | Nonsense | 514 | 702 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50533855)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50583333 |
GRCz11 | 6 | 50582552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGCGTCCATTTCTACCGCTGGCCTGAGTGGCAGTGATGACATCACATG[T/A]CCTCCTGGAGTGACCCAAAGCAACAGAGTGCCCGGCTCCGATTTAGCTCA
Long Flanking Sequence:
ATCATAAAAATATAAATGCATAAAAAATGACAAATAATAATCAATAATAATCCAATCATTAACTAATGATCAGTAAATTATATAATGAAATGAATAATGATCATATGATTAAATAAAATAATTAAATAAAGAATAAATAAATATGGACAAATGAAAATAAAACGCAAAACAAATGAATGGTTACTTTCTTGAAGCAACACACACACACATAAGTTTGCTACAAGGATTTTCAGATCTTTAGGTAAATTCTTCAACGGTAAAAAATATTGAGGTAATCTCCAAGTGTTACATGATAAGTCCATATTGATTATTGTGACAGGCCTATTGATCACAAAAGAAATTAGTATTTTGATGCCAGTTGTAATCCTGTACTATTTTTGATCTTGCTTACAATAATAAGAATATCACAGTAACCCGAGATCTCTTTCTCTTTTATTTTAGGTGCCTCTGAAGGCGTCCATTTCTACCGCTGGCCTGAGTGGCAGTGATGACATCACATG[T/A]CCTCCTGGAGTGACCCAAAGCAACAGAGTGCCCGGCTCCGATTTAGCTCACGCCAGGCATAATCTGTGTACGTCCACTCAAAGTCTGAGCGCGATGCCGCCTCCATACTATTCCATGTTCCCCGGGCAGCCACCAGTGGGCAGCACAGAGCCGCTGTATCAAATGAGCAAGCAACAGCAGTTCACACTACACCAACAACAACAGAGGCAGTATCAGCAGCAACAACAGCAACATTACAACCAAAAGCAATACAATCAATACAATCACCAACAGCAATACAATCAAGAGCCGCAGTATCAACAGATCCATCACAAAGAGCTCCAGCAGAAACTCAAACATCAAGTTCAGCAGCAGGTTCAAAACACGCTAGCTCACAATTCCGGCATGCCAAGTGAAAGCGGGCTGAATAACTCAGCTCAGCCTGGCGTGGATCATACAGACGGCGCTCCTGAACCGAGCAGCGGTGGAGGAGATATGTTAAGTATGATACGTAGAGGAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20817
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 |
---|---|---|---|---|---|
ENSDART00000083007 | Nonsense | 691 | 693 | 14 | 14 |
ENSDART00000134146 | Nonsense | 700 | 702 | 15 | 15 |
Genomic Location (Zv9):
Chromosome 6 (position 50533297)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 50582775 |
GRCz11 | 6 | 50581994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGAAGGACACTTACCAACGATCGTTCGGCGCCTTTAATCACGCCTAACTA[T/A]CTCAATTGATTCAATTTTTTTTCGTTGAATTCGTCTGTGGCTTTTTTCCG
Long Flanking Sequence:
CATAATCTGTGTACGTCCACTCAAAGTCTGAGCGCGATGCCGCCTCCATACTATTCCATGTTCCCCGGGCAGCCACCAGTGGGCAGCACAGAGCCGCTGTATCAAATGAGCAAGCAACAGCAGTTCACACTACACCAACAACAACAGAGGCAGTATCAGCAGCAACAACAGCAACATTACAACCAAAAGCAATACAATCAATACAATCACCAACAGCAATACAATCAAGAGCCGCAGTATCAACAGATCCATCACAAAGAGCTCCAGCAGAAACTCAAACATCAAGTTCAGCAGCAGGTTCAAAACACGCTAGCTCACAATTCCGGCATGCCAAGTGAAAGCGGGCTGAATAACTCAGCTCAGCCTGGCGTGGATCATACAGACGGCGCTCCTGAACCGAGCAGCGGTGGAGGAGATATGTTAAGTATGATACGTAGAGGAGTGAAACTTCGAAGGACACTTACCAACGATCGTTCGGCGCCTTTAATCACGCCTAACTA[T/A]CTCAATTGATTCAATTTTTTTTCGTTGAATTCGTCTGTGGCTTTTTTCCGTTTAGTGAATTCGTTCGAGCTTTTTCTTGTTGCGATTTTGTGTGTTTTTGTTTTTTAAGTGGAGGCAAAACTGTTGACGATTCTTGCCACTCGAAAAGACGTTCGATTTAAGTACACTGTGCTCTAAGAACAAACGTTTTGCAGCGTCCCTGCGAATGTCGCCTCTTAATAAAGTTGATTCTGCAGGCTACGTGCTTTACATATATATGTATACTTATATATACAGATATATATGTATTTAGAGATCTAGATTGACCGTCGGAGCTTAAAGATATATTAAAGTTATTTGTTTATGTCGTATTCGTAAGCACTCAGCCTTCTGGTTAGAGATCAAAAAACTTGTGTATATATTAGCGAAACTATGGAAAGACTGTTGTATTATTCACCTCTTTGTTTCTCGTTTGTTTTGGAGATTAGATAAAGCAGCACTAGGCGTCTATTTTTGTACAG
Associated Phenotype:
Not determined