ZMP
ENSDARG00000076443
Ensembl ID:
Human Orthologue:
MGEA5
Human Description:
meningioma expressed antigen 5 (hyaluronidase) [Source:HGNC Symbol;Acc:7056]
Mouse Orthologue:
Mgea5
Mouse Description:
meningioma expressed antigen 5 (hyaluronidase) Gene [Source:MGI Symbol;Acc:MGI:1932139]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15559 | Essential Splice Site | Available for shipment | Available now |
sa14298 | Nonsense | Available for shipment | Available now |
sa38606 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18041 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15559
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 |
---|---|---|---|---|---|
ENSDART00000110279 | Essential Splice Site | 18 | 839 | 1 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 25157978)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23719730 |
GRCz11 | 7 | 23990887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTATGGGCGACCCTGGTCAATGGAACAAAGGAAGGTACTATTTCAGTGG[T/G]GAGTAYTGKATCTGAACACACTTTTGAATGGAATGWGGATTKCTTTTTGY
Long Flanking Sequence:
CATTTGAATTCATATTCAAAAATACGTTATATAATTCTTTACCATTTTAAAAATATTTAAATTCTAGTTTTACAGATGTTATTTTTGTCACATTATTTCAAATATGAGGCTAAGAAATAGCTATATTTTTTTTGTTTGGTGGGGCCAGTGAAAATGTTGACTGGGCAAGTAGAAAAAATACTTAGCGTTAAACCCTGCCATGGCCATTATTATATAACAGGCACAGAATGGTACTGTATGTATGGGCCCAAAATTCGGAGTCTGCCCAAAATGTGTCTGTTTGAGTGGGTTGTAGTGAGGAGGAGGTGGAGAAAAACAGAAATACTAAAAGCTTTGGGGCAGTTATGAAATGCTGCCTTGTGTAAAAACGCAGAAAAAATAATTTAAGTATTTGTTTTTGTCTGCATATTTTGTATATGTGATGGTTTTGTGTATTTTACTCCTCAGGTTTCTATGGGCGACCCTGGTCAATGGAACAAAGGAAGGTACTATTTCAGTGG[T/G]GAGTATTGTATCTGAACACACTTTTGAATGGAATGTGGATTGCTTTTTGTATGCACTTGAGTTATTGGAAGAACACTGGATGCATGTTATTGGTGTGGTGTTGTGTAATGTCATATAGGACGGTGATTAAGATTGTGCTGGCGATGTGAGGCTGTCCGGGGGGCAGTGCAGAGCAGCTGGTGCGTTGCAGAGGTGTAAAAGAGTGTGGGCAGAGAGACAAATGGCTTTTTCTGACTAATGACTGGACACTGGTGCCAGCATGACTCCATTGAGCCACAGTTTCACACGTCTTCATACATTAGCCGTGATGAAAGCAGTGGCAAGGAGCAAGTCTACTTTCTATCGTAGCTTTGAAGCAGAACTCTGGTAAAGTGGAAATAGAGAGGAATAAACAGAAATAAGAAGATGATATTTTAATAATAATAATTGTAATAGGAATAATAATATATAAATATGAGATCTTTAAATAGTAGTCATTATACATGGTTTAATAATAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14298
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110279 | Nonsense | 69 | 839 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 25149870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23711622 |
GRCz11 | 7 | 23982779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGAAGGCTCTAGTTTGTGAGGCCCGATCGAGGGGTCTTACGTTTGTATA[C/A]GCTCYTTCCCCGGGACAGGACATYGTCTTCTCCAGCTCTTGTGACCTCAC
Long Flanking Sequence:
TTGAAGTAGTTTAGATATAATATTTACTGTCACAAAGAATGTCTCTCTTTAAAAGAAACTTTGTAATTGAACTTTTTCAAACATAAACGGTAGTGACTTAAGGAAGCAGGAAATATTGAAAAGCAGACAAGAACCAGAAGGTATGAGAGATTGGGCTGTGTTGTGAGTATTATCTAATATTATTATTTGGCACTACTTGAATATTTGCTCTTATGCTTGATGAAAGTAGGCTTTAATATCTTTAACAAGCAATCTCTTTTTCAGCTCAATGAAAATACAACTTGACAATGCATTCATTATAATAAATAGTAAATTATGAGGTAGTGTTATTTTTATAATGGAGTTTAAAAGAGTGTGGCTTGAGAATTACATTTTTATGGCCATATCTCATCTTATATCTTGTCATTTTCTCACTCTCTTTCTATTTTTCTCTCATTGACTCCAGCTCAGTTGAAGGCTCTAGTTTGTGAGGCCCGATCGAGGGGTCTTACGTTTGTATA[C/A]GCTCTTTCCCCGGGACAGGACATCGTCTTCTCCAGCTCTTGTGACCTCACACTGCTTAAGCGCAAACTCAGACAGGTAAGAAAAAAGCTTATTGCAGTTGGATCAGTTTTCAGCCCATGCTCATATTTTACTATATTTTATTATATTTTAATATTTTATTAATATGTTTATAACTTTAGAATCTGCAAAACTCTTTTGTACAGTTTGGCCATTTTTTTAAAATGAAGGATCGCCTTGTACTTTTTCATTTCACCACTAGGTGTCAGATCTGGGCTGCCAGGCTTTTGCTCTCCTGTTCGATGACATTGATCACTCCATGTGCCAGTCAGATACAGAGGCCTTTTCTTCATTCGCTCACGCCCAGGTCACCGTGGCTAATGAGATCTTCCGTTTCCTGGGGGAACCACCTGTCTTCCTATTCTGTCCCACTGGTAGGCCAGTACATAAATATCTCAGGCTTAGTTCATTACAGAACAACAAAAAGCTTGAATCATTTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38606
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 |
---|---|---|---|---|---|
ENSDART00000110279 | Nonsense | 634 | 839 | 15 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 25141565)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23703317 |
GRCz11 | 7 | 23974474 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCAGCAGTGAGTTGTTCAGTCACCCTCCTCCTCTATTCCCCACCTCT[C/T]GACTCTACAACATACGACCATTCTTGCAAAAAGACAAGGTGACTCAGGCA
Long Flanking Sequence:
TTTTGTTTTGGATCACAAGAAACCCGGGACTCGCAAAATCTCAGAGAGACTGAATATTTATTGTTTTACTGCATTTTTATATAAAACACAGCCTTGAGCAGAACAGACTTTGAAATGCATAAAAAATGTACCAACCCCAACATTTTGAACAATAATTTATGTTTAAAAATGCACTGTGGATGCATTAAAACATGCCACATCAGTTCTGGACACTCGTTCTGATGAGTCTTGAATGAACTGTTCACAGGGTGTGGAGCTTCCTCGGGGGCGGAGTTACATGGTGTAGAGGCAGAGCCATGGGTGTTTAAAGGGGGTCTATCTGGAGAGGTGCAGGTGGGAATGGCACAAATAATTCAGGCTCACTAATGAACTTGTTTGTTTATTGCCAGTCTTTTCCTGACTCGTTTTTTTTCTGTTTCTGGGATGTGAATCAGATGCTTCTGCCTGTGGGAACCAGCAGTGAGTTGTTCAGTCACCCTCCTCCTCTATTCCCCACCTCT[C/T]GACTCTACAACATACGACCATTCTTGCAAAAAGACAAGGTGACTCAGGCATATAAGTTAACCCAAGGACTAACCCTAACCGATTCTACATATATGACATAAATGACTTTTGTTGTTTTTTCCCCAACTCTAGGTGGAGCTGTATCGAATGGTGCATCAGCTGCATCAGAGGGGTAAAGGAGGTCAGGATGCTGCCTTCTGCCATCCAGACCTAATTGGAGACAGGTAAGACTTAGAGTGCTCTCAAGCATATTTCAGCCCCTGTGTAACAATTTATACATTTTAATTGTCTTTAAATGCCTCCATTTGAAATTGAATCTTCTGATTGCAGTCACTGATTTCTGATTTTATTTATTTAAATGTAAAAATTGTGTCTGTATAAACAAAAACATCTCGATTTGGAAATGAATCAGCAACCTAATAAACAATTAATACATTTCATTTGATACATATTTATTTTTAGCAAAACAATGACTCAAACATTGATTAAAATTAAAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18041
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110279 | Essential Splice Site | 677 | 839 | 16 | 19 |
Genomic Location (Zv9):
Chromosome 7 (position 25141339)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 23703091 |
GRCz11 | 7 | 23974248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAGGTCAGGATGCTGCCTTCTGCCRTCCAGACCTAATTGGAGACAGG[T/A]AAGACTTAGAGTGCTCTCAAGCMTATTYCAGCCCCTKTRTAACAATTTAT
Long Flanking Sequence:
TCTTGAATGAACTGTTCACAGGGTGTGGAGCTTCCTCGGGGGCGGAGTTACATGGTGTAGAGGCAGAGCCATGGGTGTTTAAAGGGGGTCTATCTGGAGAGGTGCAGGTGGGAATGGCACAAATAATTCAGGCTCACTAATGAACTTGTTTGTTTATTGCCAGTCTTTTCCTGACTCGTTTTTTTTCTGTTTCTGGGATGTGAATCAGATGCTTCTGCCTGTGGGAACCAGCAGTGAGTTGTTCAGTCACCCTCCTCCTCTATTCCCCACCTCTCGACTCTACAACATACGACCATTCTTGCAAAAAGACAAGGTGACTCAGGCATATAAGTTAACCCAAGGACTAACCCTAACCGATTCTACATATATGACATAAATGACTTTTGTTGTTTTTTCCCCAACTCTAGGTGGAGCTGTATCGAATGGTGCATCAGCTGCATCAGAGGGGTAAAGGAGGTCAGGATGCTGCCTTCTGCCATCCAGACCTAATTGGAGACAGG[T/A]AAGACTTAGAGTGCTCTCAAGCATATTTCAGCCCCTGTGTAACAATTTATACATTTTAATTGTCTTTAAATGCCTCCATTTGAAATTGAATCTTCTGATTGCAGTCACTGATTTCTGATTTTATTTATTTAAATGTAAAAATTGTGTCTGTATAAACAAAAACATCTCGATTTGGAAATGAATCAGCAACCTAATAAACAATTAATACATTTCATTTGATACATATTTATTTTTAGCAAAACAATGACTCAAACATTGATTAAAATTAAAATTAAAAATGTAAACATACTAAGCATGATTGTTTTGTGGAAGAAAACATTAAACATTTAACTAATTAACATATTAATATTTCACAATTTTACTGTTTATACTGTATGATCAAATAAATGTAGCACATGTAAACTTGGCCACAATTTATAACAAGGATTAATTAATGAATGTGTTTACTTACATAAACAAAGAATCAACAATACTTAAACAGCATTTATAAATCATAGTTA
Associated Phenotype:
Not determined