Busch Lab

ZMP

ENSDARG00000088315

Ensembl ID:
ENSDARG00000088315
Human Orthologue:
ZPLD1
Human Description:
zona pellucida-like domain containing 1 [Source:HGNC Symbol;Acc:27022]
Mouse Orthologue:
Zpld1
Mouse Description:
zona pellucida like domain containing 1 Gene [Source:MGI Symbol;Acc:MGI:2443415]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14945 Essential Splice Site Available for shipment Available now
sa34927 Essential Splice Site Available for shipment Available now

Mutation Details

Allele Name:
sa14945
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
ENSDART00000126340 Essential Splice Site 3 371 1 9
Genomic Location (Zv9):
Chromosome 10 (position 29842615)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 29215059
GRCz11 10 29101684
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGATCTCACAGACTAAGGATWCCAAACCTGCARCAAGAATGAGACARG[G/A]TGCGTAGGATGTGTAACTACGGGACATTCKTTGAGCTGAGGATGTATTAA
Long Flanking Sequence:
TAACAATCCACCAAAAACTAAAACTCATCTGAAGCCACCTCATTGAATTTCCCAATCAAAACAGTTACATGATATGACGACTCATGTGAGTGTGCATTATTATTGTGCTTCTACGATTACTTAATATGGTACAATGATAACCTAAGGTGACATAAGTCACAGCCATATTGTTTCTTCTCCCTGGGGGATCGACACTTAGTCGTTGAGGTCTGTTATTATGATGCCAAGGATGTCTGTGCTCAAGTAAGTAAACAGGCCATTGTCACCTGCATGTCTGTGAAGAGCTGCGTAGTAGAGTTTCAGAAAGTGTCCTTGGGCGTTCCACTATATGGGACTTTTATTCACTAAAGGGCTGGGTCCACACGATAGACACACCTAAGTCTTCTGACCTTATTGCCTTTCCCTTTTTACAAAAGATAGTGTTGCACCAAAGAACTCCACAGTTTTCGGGAAGATCTCACAGACTAAGGATACCAAACCTGCAGCAAGAATGAGACAAG[G/A]TGCGTAGGATGTGTAACTACGGGACATTCGTTGAGCTGAGGATGTATTAATGATGATGACTAAATGAAATGATTGCGAATATTGTGTTATTTTTTCCACAAACAGGTTTACACTCTGCAAACCGCAGGAAATATATTCTCCTCAACATTTTCCTCTTCCTTTTAATTCCAAAATTCAACAAGAGCATTTTTTTAAGCTCCAACTGTGGATCAGATTACAGAATCCCAGGTATAGTTTTAATGTGTCTTTTTGATGGAGAACATGAAAAATAATTGCTTGTTTACATCATAAAAATGTCAGAATTATTGCTGGGTTGGTTTTGATGTACGTCCTTAAGTGTTTTCAAGCTTGAGATTCAAAATGTAATAGTTTTTTGCCTCAAGTAAGACTTTTTAGCAGATTTTGTATAACCAATCTTGTTGTATTTGTCATAATAGAGTACACAGACATCTCTGTGGATTGTGGAACAGAGTACATCAGTTTGGCCATCAGATTCTGTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa34927
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
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000126340 Essential Splice Site 321 371 9 9
Genomic Location (Zv9):
Chromosome 10 (position 29835325)
Other Location(s):
Assembly Chromosome Position
GRCz10 10 29207769
GRCz11 10 29094394
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACCCAGAGACACATATTGACTCACTGATGCTCAACGGCTCTTTCAC[A/T]GCAATGTCGCAAAAGAAAAAAGAGGGATGTTTCTCCAAGTGGAGTCACAG
Long Flanking Sequence:
CTAGGATAATTAGGCAAGTTATTGTATAATGAAGGTTTGTTCTGTATTTTGAAAAAAAAAAAAAAAAAATTCTGACCTCAACTGTATATAAATGTGTGAAATTGTTTGGGGGCCTGAGAGTGAATAATCAATTTGCTAATTTGTTTGATCAGTTGTGGAATGAATCGCCTCACTAAAATGTTGACGAACGGTGAGATGCAAGTGGCTCGTTTCTCCTTTCCAGCCTTCCGGTTTACAGAACAGTACAACCAGTCAGTGTCCACATACTATCTGCACTGCATCACGAGACTGTGTGAAATCACCACCTGCGCCGCATACAGGGTAAACGCATAAAGCACATGCTTTTGAGCTACATTAATGTAATTACACAGTGTCACTGTAAAATGCTTTTTGTAAAGTGACATTTGAAGATGATGTTCACTCTAAAATAACAATACACACATCCAATTCAACAACCCAGAGACACATATTGACTCACTGATGCTCAACGGCTCTTTCAC[A/T]GCAATGTCGCAAAAGAAAAAAGAGGGATGTTTCTCCAAGTGGAGTCACAGATGCCACCACAATCACGTCACCAGCAATCATCATAAGTGCAGATGACGGTACAACCCTTTCCTTTATAAAAATCTCAATCAATTATTTATGTAACATTGCTGTCTGAGAAAACTGACTTTATTTTTTGTATATTATATTTCAGTGGTGGCAACAAAAGAGGAAGGTGAGCTTAAATTCTTTGACCAATTGTTAATTTTCATGGCATAGCATTTATTTATATAGTGACATGAATTAACGTATCCATATATAAAAGAGAGCACACAATAAACAGCTAAAAAGCACTTTTTATATGATTATATGTACGGTTAGAATGTTTGATTTTCTTTAGTGAATCAGTTTGAATCAAATGATTAAATCATATACCTGTACTTATTGTAGGTTTTTTTGTTTGTTTGTTGTTTTAATCGTCTAATCCAATCTCTATACAAAGTCAGCGATCAAGCACTCTC
Associated Phenotype:
Not determined