ZMP
met
Ensembl ID:
ZFIN ID:
Description:
met proto-oncogene (hepatocyte growth factor receptor) [Source:RefSeq peptide;Acc:NP_001007125]
Human Orthologue:
MET
Human Description:
met proto-oncogene (hepatocyte growth factor receptor) [Source:HGNC Symbol;Acc:7029]
Mouse Orthologue:
Met
Mouse Description:
met proto-oncogene Gene [Source:MGI Symbol;Acc:MGI:96969]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18672 | Nonsense | Available for shipment | Available now |
sa16304 | Nonsense | Available for shipment | Available now |
sa17944 | Nonsense | Available for shipment | Available now |
sa24650 | Nonsense | Available for shipment | Available now |
sa44271 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18672
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 |
---|---|---|---|---|---|
ENSDART00000104461 | Nonsense | 241 | 1382 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 19075350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18491660 |
GRCz11 | 25 | 18588060 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTCCGAKCAGTCCTACATGGATTTRGCCCCTTCACTGCGGGGGAACTA[T/A]CCACTACATTATGTCTACTCTTTCCAGAGTGGTCCTTATGTWTATTTTCT
Long Flanking Sequence:
AAAGACCTGAAGAAGAAACATGAGTATAAGACTGGACCGGTCCATGAGGGTCCAGACTGCAAGACCCCAACAGATCAATGCAGTGGTTGTGAAAACAAGCCCCGTAACATAAACAACACCAATATGGCCCTGTTAATGGAGACGTTCTATGACCTGGAACTTTTCAGCTGTGGCTCAGTCGGGAATGGCGTCTGCAGTCGTCATGTGTTAGAGGATGGGCCTCTGGGTGCGGAAGTAACTTGCATGTACACCAAAAAGAATGAAGGCAGCAGCCATGGATGCCCAGACTGCCTGGCTGGACCTGCGGGCACTCAGATCCTCAACATAATGAGCGGTCGTGTTGTGAGGTTCTTCGTTGCGAACTCTGAACCTCTTGAGTCAAACGGTCCACGTCTCCACCACACTATTTCCATTAGGAAGATGCGTGAAACTCAAGATGGCTTTGAGTTCTTTTCCGATCAGTCCTACATGGATTTGGCCCCTTCACTGCGGGGGAACTA[T/A]CCACTACATTATGTCTACTCTTTCCAGAGTGGTCCTTATGTATATTTTCTCACCGTCCAACGCGAAGGTGGCAACTCGAAAGCTTTCCACACGAGAATCGTACGCATGTGTTCTTCAGATTCTGAGATCCTGCGTTATGTAGAAATGCCCTTTGAGTGCATTTACTCTGAGCGAAGGAGAAAAAAGCGTTCGGCTCAAGTGGTTTTCAACGTTCTCCAGGCTGCTCATGTGGCCAAAGTTGGCTATGACTTTCAGCAGGAGATGGGCTTGAAAGAAGGAGAGGACGTGCTGTTTGCTGCCTTTGCCCGGAGCAAACCGGACTCACCAGAGCCCACCGCCAGCTCCGCCGTTTGCCTTATCTCCATCACGGACATCAATGAATTCTTCAAGGTTTTCATTCAGAAGGGTTACACAAGGAAACTCCATCACTTTCCAGGATCTGAAGAGAAAACCTTCAACCAGGTAAGAGCTTTCAGCTAAATCCTGAATTATCTCCGATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16304
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 |
---|---|---|---|---|---|
ENSDART00000104461 | Nonsense | 547 | 1382 | 4 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 19117842)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18534152 |
GRCz11 | 25 | 18630552 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGGGYTGTGGATGGTGCAGGACCAGCAACCKGTGCACCAGGGCCCCT[C/T]RATRCCCCCAGTCCCAATGGATCCAGGACTCCTGCCCCCTCCYCATCACC
Long Flanking Sequence:
ATAATGATAAGGTTGCACAATGATGTTTTGCTTCATCAAGGTCCACAGGGAATCATTTAGTTTTGCCTGTTTATATATATTGTTTTTGACACTCAAAGTGCTAGCAGCTGTTTCATATTTTACCAACCCCAGTTTAAGCTAAAAACATTCTTTAAATGGGTCATGAACTGTCGTTTTTTTATAAGTAGAAAATGAGGCCTGAGGATGAGTGAATTAACAGCAAATGTTCGTTTTTTGAGTGAACTCTCCATGTTACAGTAAAACAAGGTGTTACTGTCACACAAAAATGTACTCAACACGTCGCATCATATAAATCCATAAGCTAAATGAATAAATGTAATTTGGAGTGTAATATGGTTTGTGAATGGCTCCAGGTCTCAAAGCTTCCTGTGATCGGGCCTGGATGTGAGCAGTTGTGGACTTGTAGCTCGTGTCTTCTTGCTCCGGGCTTCATGGGCTGTGGATGGTGCAGGACCAGCAACCTGTGCACCAGGGCCCCT[C/T]GATGCCCCCAGTCCCAATGGATCCAGGACTCCTGCCCCCTCCTCATCACCTCGGTAAAAAAGCCTGTCTTGTCACAAACAACATTACCATGGTTTTAAAGCAGCTAATAGCACATAACTAATAGAATAAGTGCTTTCTAAGTATGGAGAGCCCCTATGAAACTCTGACCTTCATTGATTTTGCCTGATTTGCAGTATTTTCAGGGATAAGCAGGGTTTTTTTAAGCAGGGATTTCGAGGTTGTTTTTAAAAGATGTAAATTGATTGTAGATATATCAGAAGGGATTCGTTGGCCATTCTGTGCCTCTTCTAGATTGATGTAAGAGCAGGCCGAACTATATTTGTATTTGTGTCAGATCTCTTTGCTTATGATAAGTGGTGCTCTGAACACTTAATTATTAACTTGGAGCCAAAATGAGCTTTTCGTGTGCCATGTGCTCAAAGCGACGCCATCTGCTTATCAATAAAGAACTAACCGAGCAGAAATCATGCAGAAAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17944
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 |
---|---|---|---|---|---|
ENSDART00000104461 | Nonsense | 592 | 1382 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 19119964)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18536274 |
GRCz11 | 25 | 18632674 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACCAAYATCACAATCTGTGGCAAAWACTTTGGCTTTAACAAAAAAGAC[A/T]GATTTGATACCAAACTKRTAGACGTGGTGGTTGCTGGAACGAAGTGTAAA
Long Flanking Sequence:
ATTATTATTATTATTATTATTATTATTATTATTATTAAATAATTTAAAAAATATTTTAATATTTCCAATATGTCTGGGTATCTCAAGCTGCAAAGTATGTGAAGTATTTTACCACTAAACACAGAACACAATTCACCTTTAAGATCCTCACCCTCAGCTGGTGGCTCAAGCTTGAGGGCACTTTTAACACAAGAGTCTAAAGCACCGAAAAAAACAGGAAGGTTGTTTTGTTCTCTGTTTTTGTCTCCATCACCATTTACTGGAAGACCCCCTGCCATCAGAGTGCCCATACAACCAAAACAAATTATTGTCAGTGGCCATCAAACCTCATGAGCAGAGAAAGCGCTCAGCATAAAGACTCTCAGCTGGAGGATCGACACTGAAAATGAACTCACAGCTTCTTCCTTCTTTTTTCCTAGATCTCTCCTTCCTCCGCTCCACTCAGAGGTCAAACCAACATCACAATCTGTGGCAAAAACTTTGGCTTTAACAAAAAAGAC[A/T]GATTTGATACCAAACTGATAGACGTGGTGGTTGCTGGAACGAAGTGTAAATTGGAAAGGAAGGACAGTAACAATAATCGGTAAGTAGATTAATAATCCAGGATTTCTGTAAGATCTTAAAAAAGAAATATTGAAATCAAAATTATAGGTCTTAAAAAGTTGTGCATTTGCAGACTAATTTTGATGATTTAAAAAAAATGAAATAATCATTTTATTATACACATTTTTATTCTGCTATTTAAACATTATGCAATGTTTTATGCAATATAATCATTTTAGGCCTTAAAGTCTTAAATTTGCAGAAGCAATAACAAAATTTGGACATTTTAAATTGAAGGATTTTAAGCATTTTAATTTTTTTTATTATATAATATTTTTGTTTATACTCTAGTGTTACGGAATTGTTTCGCTTGTTTCGAAATTACATTTTTGGCTTTATAATTTGAAGAAGCATTGAATAATTTGAAATAATTTAAGTTGAATGAGTTGAATTAATTTTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24650
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 |
---|---|---|---|---|---|
ENSDART00000104461 | Nonsense | 645 | 1382 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 19121986)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18538296 |
GRCz11 | 25 | 18634696 |
KASP Assay ID:
2261-9591.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTCCAGCGTGGACTCTGTGGTCACAGTGCGCAGTGGCAAGGAACAGGCC[C/T]AGAAAGATGGCTTCTCATTTGTGGTAAGAGTCATCACAAATCACAGTATA
Long Flanking Sequence:
AGTGGTATTACAAAGTCTCCAATGCTTGACCCTTAATCAGAAAAAAACACTTGAATGTTTGCAAAATCCTGTAAATACAGCGTACACGTTCACATTCTCCACATATTGCAATCCTGCAGAACATTAAATTGGCTCGCTAAAGTGCTCTATTGTGCATCTCGGCCTCCCATGTCAAACCCTACTACCATTAAGACGCAGTTTTTGTGCCGCCGGACATACCACCCTACAGCCCTGCTATTGTGAGAGGCAAGGAGAAATTCCCTGGGAGAATAGCTCCTGTGTAGTTTCTGCCGAGTAGTACACTTATCATCAAATTAGCGTGGACTAATAGCCTGCTTACTCCACTGGTTCACAAGCGCGTCTTGTTCGCGGGAGATGTTTATGTCTTTATCTGTTGTATGTATGTGTGTGTGTGTGTCAGGTTGGTCTGTGGACTGGATCATGTGAACTGGTCCAGCGTGGACTCTGTGGTCACAGTGCGCAGTGGCAAGGAACAGGCC[C/T]AGAAAGATGGCTTCTCATTTGTGGTAAGAGTCATCACAAATCACAGTATAAACGCTTCAACACACTTTCCAGATATGCATTTTTGACTGCATTCCAGTACTGTGGTTTTGAAGGTGCACAAGGCACAAAGATGTTATTTCTATCTTTCTTTGTAGTCATTTGGACCTTGTGTACTTGCGCTGTGCGATTTTTAATTATCCTTAATAATTGTAGTAGGGCAGCGCAATATATAGTTTCAGCATCTACAGTATATCATAATGTTATCATTTTCAATAATCACATCACAGGATGTTCAATGTTGAGTTTGTATTATATTTATCATTCACATGTGTTTTTGAGGCCTGTGACTGTATAATGATTTTAAAAGCAGTCAGGCATAAGAATTTGTACCATTTGTAACATTAATAACGATAAATTTTATTGAATTTTTTATCTTTATTATTTTATAACTGTACTTAAATACTGTTAGACTTGATGAAAAATGATAAAACACAGTTTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44271
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 |
---|---|---|---|---|---|
ENSDART00000104461 | Essential Splice Site | 859 | 1382 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 25 (position 19136009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 18552319 |
GRCz11 | 25 | 18648719 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGCCCACTGTCACACCAAGGGGCAAAAAGAACATTCTGGAGATTAAGG[T/C]GAGCACAACACAGCCCAAAAATATTCAGTTATAACATCTGTAGTGTGGAA
Long Flanking Sequence:
TGTACCCATAGATGAGATGTGAAAGTAATGCGAATACTTAATGTTTGCGCTTATGAAACCTGAACTTAAATCTGCTTAGTCATGTAATCACCCCAACTCTTAAGAAAACATGGCTTCTGGTTAGCCTTGTATAAATCTTACACATGCTGTGCTCCTAAACAAGCAAAAGATAAAGAGAATTGGACACACAAAAGATTGCAACATGCCTCAGCACTGACTTGGCACAGTTATAATAACAGAGATGGCTAATATTCATGTTTGTCTTCTCCTCTATGCCCAGACCTGCAGTCATGATGAGGATAAGAGAAATATCCTTTGCATCACGCCCTCCCTGAAAGGCCTCAGCGTTCAGCCTCCGGTCGCCACTAAAATGACCTTCGTCCTGGATGGTTTTTCCACTGATCAGTACGACCTGCTGTACGTGGAAGATCCCAAATTTGAGGAGTTTCAGAAGCCCACTGTCACACCAAGGGGCAAAAAGAACATTCTGGAGATTAAGG[T/C]GAGCACAACACAGCCCAAAAATATTCAGTTATAACATCTGTAGTGTGGAAGCAATTCAGATGCTTTTAAAGTATGCATTGTCACGCATAGTGTCACTTAAAGTTTTTATTCAGTGTTAAATGCTACCAATGTACATTTAAATACCATTTTATGTGAAATTTATTGTCAAAATGAGGTAAGTAGCAGCAGTTTACTTTAGATCTTGAAAATAAAAAACTAGCAGATGGTTTTAAAATTAAAGTCAGAACTGCAATTTAATACAAACTCATCAGTCATCAAACTCATCAAACATAAGTCCCTCAATAGCCTATTAATAATATTAAAGAGGCTAATATGTACTAACTAGATTAAAAGCCTTTACCATTCAATTTGGAGTGCAGTTGATGACATTTAAATGTTTTTGTAATGTCGCTTCGTGTTTGGTGCAGGCCTCCAAACTGCTTGTTGCAGAAATCTTGTTTCATGTTGTTAGGATATGGTGTAAGGTTGAAATTTGCTCA
Associated Phenotype:
Not determined