Busch Lab

ZMP

LOC571584

Ensembl ID:
ENSDARG00000059294
Human Orthologue:
MARCO
Human Description:
macrophage receptor with collagenous structure [Source:HGNC Symbol;Acc:6895]
Mouse Orthologue:
Marco
Mouse Description:
macrophage receptor with collagenous structure Gene [Source:MGI Symbol;Acc:MGI:1309998]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa27312 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa16897 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa27312
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082368 Essential Splice Site 256 388 12 17
Genomic Location (Zv9):
Chromosome 9 (position 786190)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 800532
GRCz11 9 800165
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATACTGGAGACGGCTATTGGATCATTGCTATTCTTCCCTCTTTCTTGTT[T/A]GGCTTATATTCCAGATATGTCGAAATCCTAGATCAAGAAGCATTTTTGAT
Long Flanking Sequence:
TACCTGGAGGAAAAGGCTCACCTGGACCAAAGGGAGACACTGGAGTTGGCCTTCGAGGTAAAGGATGAGTGTTGAAAAATACATGACCACAAAAGTGACCTGTGTTGTTAATAACCTTGGACATATAATTGTTTTCAGGACTCACAGGACAACAGGGGCAAAAGGGAAGTCAAGGCTTGCCAGGTAAAGAGAAAGCAGTAGGCAGATGGTAAACACTGGGTTTGTACACAACACAACCATAATTCAATGCTGTATGCAGGTGTCCCAGGAGCTCGAGGTGCGAATGGAGAAAAGGGTGATCGAGGTCTATCAGGTGAGTTTATTCATAACGTTTATTAATGACAAGAGACTACAAATGACACTATCTTGATTTTAATAAAAAAATTATTAATTTTTAAAACCGTTATTAATATGTCCTTTAAAATAGCTCTCATTTATATCATTCTACCCCATACTGGAGACGGCTATTGGATCATTGCTATTCTTCCCTCTTTCTTGTT[T/A]GGCTTATATTCCAGATATGTCGAAATCCTAGATCAAGAAGCATTTTTGATTTCAGAAAAAATAATCTGCCAATGGGCTAGTACAATAATCATATGTCAAACCTAAAACAAGGTTATTTTACTTACCGCACTACCCTTTCTTGTCTTACGGAAAAGCTCAGAACTTCAGAAAACAAGACAGCTTTTACTTGTCTAGGAAATGCTTCTCAATTTAAGAATTTTATTCTAGATATTTAGTCTATAAAGAAAAAAAAACACTCTAAGTAAAGCGATTTACAGTGTAATCACCACATTCTGCCTGAAAAACAATTGAAAAGATATACACAATACTGTTATAAACCACCTGGAAGTGACAATGCATGTATTGTGGACTGCTAGTGAAACCCTACTAAGAAAGAGTTGACCATCTCTGTCTGTTCCTTAACTTTCTTTCTTTCATTTTATTTGAAATCTCTTAGGGCAAAAGGGAGATCAAGGTATGTCTCAGCACATCTTTAGCAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16897
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000082368 Essential Splice Site 345 388 16 17
Genomic Location (Zv9):
Chromosome 9 (position 784021)
Other Location(s):
Assembly Chromosome Position
GRCz10 9 798363
GRCz11 9 797996
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAGAATGCTGGGCTTCCAGAGATCCACRCAGGTCTACACTGACGGTTCAG[G/A]TGACGTCTTTGTCTATGGRTTWAGTTCATGGTWTGGGGGTTAGTAAAGGC
Long Flanking Sequence:
CAATTGGAAACTTTTTGATTTAGTGGCTAATTTGTATGAATTCGTACAATCTAATTCGTACAATTTAGTACGATTTGCTTATTCCCCAATGACGGTTGGGGTTAGGGGTGGGGTTGGGTGCCACGCCTCCTTTTTTAAAATCGTACATTTTCATACAACTGAACTTGTACGAATTAGCCACAAAACTGACAAAACGTAAAATACGTTTCCTCGTGAGATCAGGCTGCATGTTCCAGTTTTGCACATCAGTCTAATTCGCACCTTTGTACTGAAACACAGCTGCTGACCTGCACTTTAGCATCAGTTTACCCTCATGTGCGTTTGTTTTTCTTCATCAGTGGTCCGTCTCGTGGGAAGCTCCACCCGTGGAAGAGTGGAGGTGTTTTATCAGAACGTCTGGGGGACGGTGTGTGACGACAGCTTCGATAATTTGGATGCGCTGGTGGTGTGTAGAATGCTGGGCTTCCAGAGATCCACACAGGTCTACACTGACGGTTCAG[G/A]TGACGTCTTTGTCTATGGATTAAGTTCATGGTATGGGGGTTAGTAAAGGCTATGGTTTTTAGCACGCTATGAAGGGACAGTTCATCCAAAAATGTTAATGTTAATTCACATCGGATGATGTGAAGAGGGAAATGTTAGTTCTGTCATCATTTCCTCATCTCCACTGTATGATTTTCTTTCTTCTGTTGAACAAAAGAATATATTTTAAAGAATTCTGGTGAAAAAAGCAGCCATTAGCCCCTTTCCGGCACTTTTCCGGAGGTCTGTATGTGTGAACAGGTCCTTATTGAAAAAAAAAAAAACGGTAAATTCGTTCTGTCTATTTTCCGGAAAGAGGGGTTGTAACATTACAGGTAATTAGTCGGAATGATGTGCTGTGACATTACCCAGCTAGCAAAATTCATGTGGCTCAAACTCGGCCCACACCAGACACTTACATCCGGCCCACATACCGCATGGAATGATGGCACTTGGGCGGTCCGTTCCTGTTTGCCAGAACT
Associated Phenotype:
Not determined