ZMP
LOC100002448
Ensembl ID:
Human Orthologue:
MST1R
Human Description:
macrophage stimulating 1 receptor (c-met-related tyrosine kinase) [Source:HGNC Symbol;Acc:7381]
Mouse Orthologue:
Mst1r
Mouse Description:
macrophage stimulating 1 receptor (c-met-related tyrosine kinase) Gene [Source:MGI Symbol;Acc:MGI:99
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20791 | Nonsense | Available for shipment | Available now |
sa20792 | Nonsense | Available for shipment | Available now |
sa18851 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8795 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33939 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40770 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20793 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20791
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 |
---|---|---|---|---|---|
ENSDART00000084667 | Nonsense | 266 | 1350 | 1 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42411140)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42482194 |
GRCz11 | 6 | 42479730 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTTCTTATCTGTGCAATGGGAGAGTCTAATGAAACCAAATGCGAAGT[T/A]GCAGACTCATCTTGGGCGTCTGCCGATTAAGGACAGCGAGCTTTGGATGT
Long Flanking Sequence:
TATTGAGAACGAACCGGGAACATCATTGGACACTGATAACCAAGTTCTTGTTTTGGAGCCTCAGCAGCATCTGGACTTCCTGTACATCTGTGGGAGCACCCAGTATGGAGTCTGTAACATGCTTGAACTTGATAAAGGCAACATAGCCTCTAGCCCCGAATGTTTATTTAATAAAAAAGCCAACTCACCCTCTGATTGTCCAGACTGCGTTGCCAGTCCTCTGGGAACGAAGGTCACTGTGGTAGACGAGGGTTATTCAACATACTTCTTCACAGCAGCCACCGTCAACAGCACCATTGCTGGGTCTTTCGGCAAACACTCACTTTCTATCCGTCGCTTGCTTAACACAGAAAATGGTTTCCATGATGTGAAGAATCTGACCGTTCTTCCCAAATTCCAGGATGTATTTACAATTGACTACATCTATACATTTTCCACAACGGAATATGTTTATTTCTTATCTGTGCAATGGGAGAGTCTAATGAAACCAAATGCGAAGT[T/A]GCAGACTCATCTTGGGCGTCTGCCGATTAAGGACAGCGAGCTTTGGATGTACAGGGAAATTATTCTTGAGTGCCGCTTCGAGCCCAAACGCAGGAGAAGGAGCTTCAGGGATGTTGTTTATAATTCGGTTCAAGCTGCTCACTTCAGTACAGCTGGCAAAGAGCTTGCTGATGATCTGGGAGTGAGGATAGACAGCCCGATACTGTATGGAGTGTTCGCTGTGACGGATCAAAAGGGCAATCCAATGAGACAGTCTGCCTTGTGCGCTTTTCCATTGGACTATGTGAACAGTGCCATTGAAAAGGGGGTAGACGCCTGCTGTTCAAGTTTGACAGAGCAGATCTCAAGGGGATTGTGCCATTTCCAGCCCTGTGAAATGTGTCCAGTTGAGGTAAGTTTGCATTTTTCACTGCTTCTTTATGACAGTTTGAAAACATTTTTAAAGTTCCCATGAAACTCTTCTGTAATGAGGGAGGTTCACAACAAGGGTCAGATCCAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20792
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084667 | Nonsense | 411 | 1350 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42418002)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42489056 |
GRCz11 | 6 | 42486592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTAGAATTCAGACAGTTTGACTTGCAAAACTACTCCCACCATGGTAT[C/G]AAAGCCTTACTACAGAGTGGACTTCTTCAATGGGCAGATGAGCAATGTGC
Long Flanking Sequence:
CAACCTTACTTCATTGATATCTAATGCAATGTAGAGTAAATCTTGAAAGACTGCACACATCTCACAAATACTAATTTGGTACAAGGGTTCAAGCTTTAGCAGGAATTCATTTATCACTGCCAGATGATGTCTGGAGTCTTCTGTTTACAAGTTGTTGCTTCCTTTTCTTTGAAATTACTGCCTAGGTAGAGGTTTTATGTGTCCTTCTTTAAATTTGAATCTGCAAAAAAGTAAATAAAAATGGTGACAAGTAAAAATGTTTGTTTTTAAAATGATCAAATGCTACATTTAGTTATAGACAATGATATAAAGTGTATATTGATGTAATAGCTGATGTTGCCAGTTATATTGTGTGGAATTAATTTATTATGTTTGTACTTTCAAACAGCACAAAACAACACATAAGTGATTGATTCATTAAATACCTTCAGTTTAATGTTTTGTTTCATTTGTTTAGAATTCAGACAGTTTGACTTGCAAAACTACTCCCACCATGGTAT[C/G]AAAGCCTTACTACAGAGTGGACTTCTTCAATGGGCAGATGAGCAATGTGCTCTTCACCTCTATTCTGGTCACCACCATTGAGACCAAAACTGTGGCCCACATCGGCACAGATCACGGAAGACTTCTGCAGGTTATTATAGCATCACTCATTCATGTAGAAACAAGTTTGTTTTCTAATAGGGTAATGTTTCACCCTGATTTGAAAATTCACATTTACTCTATTTACTGACCTTTATTTTATTTTAAATCAGTAAAACTCTTTGTTCATCTTTGGATCAAAAATGAAGATGATTATTGGAATCTGATAGATTATTCTACCTGGAATCAATGTCAATTCACTTAGTAATCTAGTGCTTAAAAAAGTTTGTAAAAAGATTTAAATAAACAAACACGCAACAATAAATCCAAGCAGTTTTATCTTTGTTTTCTCAAGAGACATGATTCTTTCAGAAGCTTAAATGTGCCATGTGACACCCAATAATAAACTTAATTGGTTCCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18851
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084667 | Essential Splice Site | 787 | 1350 | 9 | 20 |
ENSDART00000084667 | Essential Splice Site | 787 | 1350 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42424942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42495996 |
GRCz11 | 6 | 42493532 |
KASP Assay ID:
2259-7997.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAAGCCGTCATTAAATACAAAGGCGGCTACAAAGACCCTGTGGAAACC[G/T]TAAGACACATTTGTATTTTGATGGGGCATTTTAAAGGGATGGTTTACCCA
Long Flanking Sequence:
GAAAGGTTATTGTGCCAGGTTATGAAATGCACTGTTTAAAAGTTACCAGCCATGGTTTAGAAATGTTATAAGTGTAGTATTTCATTATTAAGCACATGTCCCTGAGTTTTTTCCTCTTATTTCTCCATAGCGTCTCCAGTGATGGGACTTCTATTGTTTGCCGGTCTGAAGGTGTGAAGGATACTTTAGAAGTGGATGTGAAGGTTGTAATTGATGGATCGACTATTTCCTCCACAAAAACATTCAGCTACAGGGTGAATCCCGAGGTGACGGGTGTAAACCCCAACTGTGGTTTTAGAAGGTATGTCAATAATTAATATTTTTATATGTAAATATATTTATAAAAGTAGTGTGAAAGAGTGATTGAATTGTTCACTGTGTATTTTATGGTCCCGCTATAATGAAGAGGATCAAAAATTATCATCACCGGGCAGAATTTGGACTCTGTTTCCCAAGCCGTCATTAAATACAAAGGCGGCTACAAAGACCCTGTGGAAACC[G/T]TAAGACACATTTGTATTTTGATGGGGCATTTTAAAGGGATGGTTTACCCAAAAATGATAATTCTGTCATTTACTCACCCTCTACTAGTTCCAAACATTTGTGAGATTCATTTATTCAATAAATCATTCTGTTTTTGGCTTAGTCCCTTTATTAATCTAGGGGCCTGCCACAGTGGAATGAACCGCCAACTTATCCAGCATATGTTTTACGCAGCAGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACATCCATACACACTCATTCACACACATACACTGCAGCCAATTTAGCTCACCCAATTCATATGTACCGCATGTCTTTGGAATTGTGGGGGTACCCAGAGGAAACCCACGCGAACACAGGGAGAACATGCAAACTCCATACAGAAAAGCCAACTGACCCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTCTTGCGACCTACAGCTGTGCAGCCTCTATTCTGAGATTCTTTTTTTTTATTTTGGACAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8795
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084667 | Essential Splice Site | 787 | 1350 | 9 | 20 |
ENSDART00000084667 | Essential Splice Site | 787 | 1350 | 9 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42424942)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42495996 |
GRCz11 | 6 | 42493532 |
KASP Assay ID:
2259-7997.1 (used for ordering genotyping assays)
KASP Sequence:
CCCAAGCCGTCATTAAATACAAAGGYGGCTACAAAGACCCTGTGSAAACC[G/T]TAAGACACATTTGTWTTTTGAYGGGGCATTTTAAAGGRATGGTTTACCCA
Long Flanking Sequence:
GAAAGGTTATTGTGCCAGGTTATGAAATGCACTGTTTAAAAGTTACCAGCCATGGTTTAGAAATGTTATAAGTGTAGTATTTCATTATTAAGCACATGTCCCTGAGTTTTTTCCTCTTATTTCTCCATAGCGTCTCCAGTGATGGGACTTCTATTGTTTGCCGGTCTGAAGGTGTGAAGGATACTTTAGAAGTGGATGTGAAGGTTGTAATTGATGGATCGACTATTTCCTCCACAAAAACATTCAGCTACAGGGTGAATCCCGAGGTGACGGGTGTAAACCCCAACTGTGGTTTTAGAAGGTATGTCAATAATTAATATTTTTATATGTAAATATATTTATAAAAGTAGTGTGAAAGAGTGATTGAATTGTTCACTGTGTATTTTATGGTCCCGCTATAATGAAGAGGATCAAAAATTATCATCACCGGGCAGAATTTGGACTCTGTTTCCCAAGCCGTCATTAAATACAAAGGCGGCTACAAAGACCCTGTGGAAACC[G/T]TAAGACACATTTGTATTTTGATGGGGCATTTTAAAGGGATGGTTTACCCAAAAATGATAATTCTGTCATTTACTCACCCTCTACTAGTTCCAAACATTTGTGAGATTCATTTATTCAATAAATCATTCTGTTTTTGGCTTAGTCCCTTTATTAATCTAGGGGCCTGCCACAGTGGAATGAACCGCCAACTTATCCAGCATATGTTTTACGCAGCAGATGCCCTTCCAGCTGCAACCCATCTCTGGGAAACATCCATACACACTCATTCACACACATACACTGCAGCCAATTTAGCTCACCCAATTCATATGTACCGCATGTCTTTGGAATTGTGGGGGTACCCAGAGGAAACCCACGCGAACACAGGGAGAACATGCAAACTCCATACAGAAAAGCCAACTGACCCAGCCGAGGCTCGAACCAGCGACCTTCTTGCTCTTGCGACCTACAGCTGTGCAGCCTCTATTCTGAGATTCTTTTTTTTTATTTTGGACAGAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33939
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084667 | Nonsense | 997 | 1350 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42428548)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42499602 |
GRCz11 | 6 | 42497138 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACAGAAACTGTTCGTCCTGCAGGTCTGTCAGTTTCTCCATTTCATGGCT[C/A]GGGCACCACATTCACCAGTCTGCCGTATGCCGGCTCTATGGACTCTGCAG
Long Flanking Sequence:
GCTCGAGGAGCCCTTGAGCTCGGGGCTCTCTCCCGGGACAGCATGCCAAACAAGCTTTTATAAATCATCAGCTAAGTGTGAACTCTTGAAATATTACATGAAATTGTTAGCTTTTGATCACATTGACAACTTTAGTTAAATATTTTAGAAATAAAAATCAAATATCATAATTATGTTTTTTTATTAAAATAAAACTTGGCAAAATTATGTAATTTTGAATGTTTTAAAAATACCTCATGTTTGACTGGCAGCTGCACTTGTTGAGGTTCGACTGTCCATGCATTCAAATCGCACCACAGCAGAGAATTACGACAGATCACCTGATGGCGACTACAGAAGGGGTGAGACAAGCTAACATCGATTATTTTTTGTGAAAATATTGACCCTGGCAATATATATCATTTAAAGATAATGTTGTTCAGCTTGGTACTACTCGTCCATTTTTCAACCTACAGAAACTGTTCGTCCTGCAGGTCTGTCAGTTTCTCCATTTCATGGCT[C/A]GGGCACCACATTCACCAGTCTGCCGTATGCCGGCTCTATGGACTCTGCAGCAGCTCCTCTGATGCGCCGTCAGGTCTCCATGTCTGCTCTCCGGCCAGATCTGCTGGAGGAGGTCAAGAATGTTTTAATCTCACCCGATAAGATCAAAATCCAGCATGAACAAATCATTGGCAAAGGTGACAAGTCATCTGGGTAATATGTTGAGCAGCATGTCATCTTTCTGTTCCACATTCTAATCTTAAATCTTTCTCAGGTCATTTTGGGACAGTGTATCATGGATATCTTACTGATAGTGATAACAAAGAGACCCACTGTGCAGTCAAATCACTGAATAGTAAGTAATTTAGCACTTGTTTTAATAATTGTTGTTTTTACATTACGTTATATTATGGGTGTCACGGTTGCGCAGTGGGTAGCACGATCGCCTCAGAGCAAGAAGGTCGATGGTTCAAGCAACAGCTGGGTCAGTCCCCGTGTCCACGTGGGTTTCCTCTGGTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40770
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 |
---|---|---|---|---|---|
ENSDART00000084667 | Nonsense | 1065 | 1350 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42428830)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42499884 |
GRCz11 | 6 | 42497420 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTAATCTTAAATCTTTCTCAGGTCATTTTGGGACAGTGTATCATGGATA[T/A]CTTACTGATAGTGATAACAAAGAGACCCACTGTGCAGTCAAATCACTGAA
Long Flanking Sequence:
TTCAAATCGCACCACAGCAGAGAATTACGACAGATCACCTGATGGCGACTACAGAAGGGGTGAGACAAGCTAACATCGATTATTTTTTGTGAAAATATTGACCCTGGCAATATATATCATTTAAAGATAATGTTGTTCAGCTTGGTACTACTCGTCCATTTTTCAACCTACAGAAACTGTTCGTCCTGCAGGTCTGTCAGTTTCTCCATTTCATGGCTCGGGCACCACATTCACCAGTCTGCCGTATGCCGGCTCTATGGACTCTGCAGCAGCTCCTCTGATGCGCCGTCAGGTCTCCATGTCTGCTCTCCGGCCAGATCTGCTGGAGGAGGTCAAGAATGTTTTAATCTCACCCGATAAGATCAAAATCCAGCATGAACAAATCATTGGCAAAGGTGACAAGTCATCTGGGTAATATGTTGAGCAGCATGTCATCTTTCTGTTCCACATTCTAATCTTAAATCTTTCTCAGGTCATTTTGGGACAGTGTATCATGGATA[T/A]CTTACTGATAGTGATAACAAAGAGACCCACTGTGCAGTCAAATCACTGAATAGTAAGTAATTTAGCACTTGTTTTAATAATTGTTGTTTTTACATTACGTTATATTATGGGTGTCACGGTTGCGCAGTGGGTAGCACGATCGCCTCAGAGCAAGAAGGTCGATGGTTCAAGCAACAGCTGGGTCAGTCCCCGTGTCCACGTGGGTTTCCTCTGGTTTCCCCCACAAGTCCAAAGACATGCAGTATAGGTGAATTTAATAAGCTAAATTGGCCGTAGTGTGTGATTGTGTTTAGATTTTTTTCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTGAGTAAAACATATGCTGGATATGTTGGCGGTTCATTCTGCTGTGGCGACCCCATATTATTAAAGGGACTAAGATGAAAAGAAAATGAATGAATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20793
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 |
---|---|---|---|---|---|
ENSDART00000084667 | Essential Splice Site | 1082 | 1350 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 6 (position 42428883)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 42499937 |
GRCz11 | 6 | 42497473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTGATAGTGATAACAAAGAGACCCACTGTGCAGTCAAATCACTGAATA[G/A]TAAGTAATTTAGCACTTGTTTTAATAATTGTTGTTTTTACATTACGTTAT
Long Flanking Sequence:
GAAGGGGTGAGACAAGCTAACATCGATTATTTTTTGTGAAAATATTGACCCTGGCAATATATATCATTTAAAGATAATGTTGTTCAGCTTGGTACTACTCGTCCATTTTTCAACCTACAGAAACTGTTCGTCCTGCAGGTCTGTCAGTTTCTCCATTTCATGGCTCGGGCACCACATTCACCAGTCTGCCGTATGCCGGCTCTATGGACTCTGCAGCAGCTCCTCTGATGCGCCGTCAGGTCTCCATGTCTGCTCTCCGGCCAGATCTGCTGGAGGAGGTCAAGAATGTTTTAATCTCACCCGATAAGATCAAAATCCAGCATGAACAAATCATTGGCAAAGGTGACAAGTCATCTGGGTAATATGTTGAGCAGCATGTCATCTTTCTGTTCCACATTCTAATCTTAAATCTTTCTCAGGTCATTTTGGGACAGTGTATCATGGATATCTTACTGATAGTGATAACAAAGAGACCCACTGTGCAGTCAAATCACTGAATA[G/A]TAAGTAATTTAGCACTTGTTTTAATAATTGTTGTTTTTACATTACGTTATATTATGGGTGTCACGGTTGCGCAGTGGGTAGCACGATCGCCTCAGAGCAAGAAGGTCGATGGTTCAAGCAACAGCTGGGTCAGTCCCCGTGTCCACGTGGGTTTCCTCTGGTTTCCCCCACAAGTCCAAAGACATGCAGTATAGGTGAATTTAATAAGCTAAATTGGCCGTAGTGTGTGATTGTGTTTAGATTTTTTTCCAGTGATGGGTTGCAGCTGGAAGGGCATCCGCTGAGTAAAACATATGCTGGATATGTTGGCGGTTCATTCTGCTGTGGCGACCCCATATTATTAAAGGGACTAAGATGAAAAGAAAATGAATGAATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATATTATTTTATATGGTAACACTTTACAATAAGGTTCATTAGTTAAT
Associated Phenotype:
Not determined