Busch Lab

ZMP

si:dkey-20i20.9

Ensembl ID:
ENSDARG00000092027
ZFIN ID:
ZDB-GENE-060503-152
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:A3KPU8]

Alleles

There is 1 allele of this gene:

Allele Name Consequence Status Availability
sa32366 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa32366
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000134028 Nonsense 158 224 3 3
Genomic Location (Zv9):
Chromosome 22 (position 2024920)
Other Location(s):
Assembly Chromosome Position
GRCz10 22 2766010
GRCz11 22 2782276
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGAAACCTTACCAGTGTTCACACTGCGACAAGAGATTCAGTTTTTTA[C/T]AAAACCTGAAAGCACACGAGAGGACTCACACTGGAGAGAAACCTTACAAA
Long Flanking Sequence:
AGAACACTTATCTTAAATCTTGAAAAGATTAAAATAGGTGCCCTTTAAATACAAGTAGTCAGATACATGAAGTAAACCTAAATGTGCCCAGATGAGGCTTTTAAATTCTGTGGTGCATTTTTAATAACTTGTGCACCGATCTGTCCTCCCTCACCTATATCTTGCACTGTTAAACTCTGCTAGAGAGCCATCTGCTGTTTACAGACTTAAACTAGCCTATAGCCTATTAAAATGAACTTGTTTCCTTAATTTCAGATGTGAAGGAGGAGAGTGAAGAACTGAATGAAGATGAGGAGAAACATCAGGTCAAAAGTGAAGAAGAAACTCAATCAGAGACTGAACAAAGTATGTCAGTGAAAGGAACAGCGGTAAATAGTTTGACCTGCACTCAGTGTGGAAAGACTTTGAGCTGCAAAAGCAATCTCAAAAAACACATGAGGATCCACACTGGAGAGAAACCTTACCAGTGTTCACACTGCGACAAGAGATTCAGTTTTTTA[C/T]AAAACCTGAAAGCACACGAGAGGACTCACACTGGAGAGAAACCTTACAAATGTTCACACTGCGACAAGAGATTTGGTCATTCAGAAGTCCTAAAAACACACATGAGGATCCACACCGGAGAGAAACCGTATCACTGCACTGATTGTGGGAAGAGTTACACATGTTTATCTGCTCTACGACAACACACAAAAAAATATCACAGTAAGTAGATCATCTAAAGATCCAGGTTGCATTATTTAGGATAAAGACTGTCCCAGCAAAACCACAACTAGACAAATGAGGTGTCAAGACAAGCCCAGATGTCGGTTATAAAGTAGTTGGAGCATTTTTAATTACTCGCGCCGTCATTGAGAAGTGTAGGGTGTACTCACACTATGTACAATGTTAATAGCTTAAACTGTTGCCTGTTTACAAGCGTGGATTCCCGTGAAGGAGCTCCGGATGGAAAGTTTTGTTTTGTGTTTACCACATAGTTTACATTTAGTCATTTAGCAGACGCT
Associated Phenotype:
Not determined