ZMP
ENSDARG00000091193
Ensembl ID:
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11976 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11976
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 |
---|---|---|---|---|---|
ENSDART00000122947 | Nonsense | 46 | 646 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 16 (position 58468224)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 55236080 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCTGTTATCRTCAACTCTGTTATCGTCAACTCTGTTACCRAACTCTGT[T/A]ATTGTCAGCTCTGTTATCGTCAACTCTGTTACCGAACTCTGTTATCGTCA
Long Flanking Sequence:
TGTCGACTCTTATCGTCCATTCTATTTGTCAATTCTATTACTGTCAACTTTGTTTATCGCCAACTCAGTTAATCGTCAACTTTGCTACTGTCAACTCTGCTACATCAACTCTACCATCAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCATCAACTCTGTTACCGAACTCTGTTATCGTCAGCTCTGTTACCGAACTCTGTTTTGGTCAGCTCTGTTACCGAACTCTGTTATCGTCAGCTCTGTTACCAAACTCTGTTATCGTCAGCTCTGTTACCAAACTCTGTTATCGTCAGCTCTGTTATCGTCAGCTCTGTTACCAAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTACCGAACTCTGTTATCGTCAGCTCTGTTATCGTCAGCTCTGTTATCGTCAGCTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTACCGAACTCTGT[T/A]ATTGTCAGCTCTGTTATCGTCAACTCTGTTACCGAACTCTGTTATCGTCAGTCTTGTTATCGTTAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCATCAACTCTGTTACCGAACTCTGTTATCGTCAGCTCTGTTATCGTCAATTCTGTTATCGAACTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTGTTACCGAACTCTGTTATCGTCAGCTCTGTTATTGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATTGTCAACTCTGTTATCGTCAACTCTGTTATCGTCAGCTCTGTTATCGTCAGCTCTGTTATCGTCAACTCTG
Associated Phenotype:
Not determined