ZMP
ENSDARG00000044326
Ensembl ID:
Human Orthologues:
GP5, LRRC15
Human Descriptions:
glycoprotein V (platelet) [Source:HGNC Symbol;Acc:4443]
leucine rich repeat containing 15 [Source:HGNC Symbol;Acc:20818]
leucine rich repeat containing 15 [Source:HGNC Symbol;Acc:20818]
Mouse Orthologues:
Gp5, Lrrc15
Mouse Descriptions:
glycoprotein 5 (platelet) Gene [Source:MGI Symbol;Acc:MGI:1096363]
leucine rich repeat containing 15 Gene [Source:MGI Symbol;Acc:MGI:1921738]
leucine rich repeat containing 15 Gene [Source:MGI Symbol;Acc:MGI:1921738]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33899 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20747 | Nonsense | Available for shipment | Available now |
sa44639 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33899
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065101 | Nonsense | 259 | 804 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 36246647)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36490181 |
GRCz11 | 6 | 36468075 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCTGATCTGACAGAGATAGCCTTGCAAGGCAACCAAATCTCGTCCTTA[C/T]AACCAAATTTGTTTCCACACAAAAGCAAAATAGTAAAACTCTTTTTGGAC
Long Flanking Sequence:
AAGGAGCTTTTTCTAAAAATCCTCAAATAAAGAAACTGGAATTTCTCGGTACTTCGACTGAGTCTGTAGAGGTCGGAGCTTTTGAGGGTTTACCTGATATCGCCACCATTGAGATATCTAGCACAAACGTGACATCATTACCTGTTGGTGTTTTTAAGGATCTCGTCAACCTTCAAAGACTTGTTTTAAAAAGCAACAAAATCAACATCCTTGAAAAGGGGTTATTTGACGATCTAACCCAGCTCCAAGAATTATTTCTGCATATGAATGAGATCACCGCGATCGAGGAGGGGACATTTGACAATTTAGAGAATCTCAGACTTCTACATCTTGCAAAAAACAACCTCAACTCCGTATCAACATCTCTCTTTTCCAAACTCAAGAGCTTACGCATTTTCAGGCTTTATGAGAATCTGCTGACTGCAATGCCTGATGGGATTTTTGATAGTCTTTCTGATCTGACAGAGATAGCCTTGCAAGGCAACCAAATCTCGTCCTTA[C/T]AACCAAATTTGTTTCCACACAAAAGCAAAATAGTAAAACTCTTTTTGGACCATAATCTTTTGACAGAGTTGGAGCAAGAGCTATTTGTAGGTTTCATTTCATTGAAAAGTTTAACTCTGCACAACAATCAACTCACCAGCCTTCCCAATGTTCTTTTTGGAGAAATGCCCAAATTGACTGAATTGAGTTTAAACCATAACAATCTCACACACTTACCACCGGGAGTTTTCAGCCCACTTAAGAAGCTCAAAAAGTTAGACCTTTCTTCAAACCATTTCTCGATGATATCTGGAGACTTTTTTGAGGGTCTTGAGAAACTGGCTGATCTGAATCTTCAAAATAACTATATAAAGTCATTAAAACAAGAAGACTTTGACAAACTTCCGCTCCTTTCAATACTCAGACTGGAACACAATAAACTACAAAATCTTCCTGCAGATGTTTTTGACTCTCATCCAAAACTCAGTAAACTCTACCTGAACAACAACCCATGGCAGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20747
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 |
---|---|---|---|---|---|
ENSDART00000065101 | Nonsense | 282 | 804 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 36246717)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36490251 |
GRCz11 | 6 | 36468145 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAAAAGCAAAATAGTAAAACTCTTTTTGGACCATAATCTTTTGACAGAGT[T/A]GGAGCAAGAGCTATTTGTAGGTTTCATTTCATTGAAAAGTTTAACTCTGC
Long Flanking Sequence:
GGTCGGAGCTTTTGAGGGTTTACCTGATATCGCCACCATTGAGATATCTAGCACAAACGTGACATCATTACCTGTTGGTGTTTTTAAGGATCTCGTCAACCTTCAAAGACTTGTTTTAAAAAGCAACAAAATCAACATCCTTGAAAAGGGGTTATTTGACGATCTAACCCAGCTCCAAGAATTATTTCTGCATATGAATGAGATCACCGCGATCGAGGAGGGGACATTTGACAATTTAGAGAATCTCAGACTTCTACATCTTGCAAAAAACAACCTCAACTCCGTATCAACATCTCTCTTTTCCAAACTCAAGAGCTTACGCATTTTCAGGCTTTATGAGAATCTGCTGACTGCAATGCCTGATGGGATTTTTGATAGTCTTTCTGATCTGACAGAGATAGCCTTGCAAGGCAACCAAATCTCGTCCTTACAACCAAATTTGTTTCCACACAAAAGCAAAATAGTAAAACTCTTTTTGGACCATAATCTTTTGACAGAGT[T/A]GGAGCAAGAGCTATTTGTAGGTTTCATTTCATTGAAAAGTTTAACTCTGCACAACAATCAACTCACCAGCCTTCCCAATGTTCTTTTTGGAGAAATGCCCAAATTGACTGAATTGAGTTTAAACCATAACAATCTCACACACTTACCACCGGGAGTTTTCAGCCCACTTAAGAAGCTCAAAAAGTTAGACCTTTCTTCAAACCATTTCTCGATGATATCTGGAGACTTTTTTGAGGGTCTTGAGAAACTGGCTGATCTGAATCTTCAAAATAACTATATAAAGTCATTAAAACAAGAAGACTTTGACAAACTTCCGCTCCTTTCAATACTCAGACTGGAACACAATAAACTACAAAATCTTCCTGCAGATGTTTTTGACTCTCATCCAAAACTCAGTAAACTCTACCTGAACAACAACCCATGGCAGTGTGATTGTAACCTGTTGCCATTCTTTGAATGGCTGAAGGACAATGAAGACAAGGTTAAATCAAAACCTCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44639
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000065101 | Nonsense | 673 | 804 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 6 (position 36247889)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 36491423 |
GRCz11 | 6 | 36469317 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAACAACACTACAACCAACAACTACAATTCCTACCACATCAGCACTT[C/T]AAACAACAGTTGCAACAACTTCAGTTTCTACAACCATGTTAATCCCTACC
Long Flanking Sequence:
CGACAACAACTACTCAACCCACAACTGTGCCAACCACCACCGCTACAACTACAGCTTTAACAACAACATCAGTGCCAACCACCGCATCAACAACTACTCCACAACCAACAACTGCACCAATAACAACATCAGTGCCAACCACCGCATCAACAACTACTCCACAACCAACAACTGCACCAATAACAACATCAGTGCCAACCACCGCATCAACAACTACTCCTCAACCAACAACTACAACCCTTAAGACTACATCAATGCCAACCACGATATCAACAACTACGCTACAACCAACAACTACAACATTGACAACCACATCAGAGCCAACCACAATATCAGCAACTACATTACAACCAACAACTACAACCCAGAAGACTACATCCATCCCAACAACTATATTTCAACCAACAAATACAACCCTGAAGACTACATCCATGCCAACAACCATTCCAACAACAACAACACTACAACCAACAACTACAATTCCTACCACATCAGCACTT[C/T]AAACAACAGTTGCAACAACTTCAGTTTCTACAACCATGTTAATCCCTACCACTATTACAAGTCGCATAACAACCTTACCACCCAGCACGACAACAAGGAGAACCACACCATTTCTGACCACAGCGAACAGTTTCACATGTGGCTCTCTTCAGACACCTCCATCAAGCCACACTTCTGTCCACGAGTACTCATCATGCAAGGAACTGGCGATATTTTACACTACTTTGCTGCTGGTGGAAATATGCTGTACTCTGGTGCTGGCCAAATACACTTATTCATTATACTGCTCACTGGAGCAAAGGGAGAGACTGCACAACCAAGTCAAGCTGACTCACTTCTCTTATACTAAGTCTATTTCTCTTAGGCCAGTGGACGAGACAGAAACTATAACACTATGATTTATATTTGCATTTATTTATTTGTTTTCTTTTTGGCTTAGTCCCTTTATTAATCAGGGATTGGCACAGTGGAATGAACCACCAACTTATACAGCATATGTT
Associated Phenotype:
Not determined