Busch Lab

ZMP

sst2

Ensembl ID:
ENSDARG00000014190
ZFIN ID:
ZDB-GENE-010219-2
Description:
somatostatin 2 [Source:RefSeq peptide;Acc:NP_571802]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa30590 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa30590
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000014020 Nonsense 68 107 2 2
Genomic Location (Zv9):
Chromosome 2 (position 5369039)
Other Location(s):
Assembly Chromosome Position
GRCz10 2 5814767
GRCz11 2 5726649
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCTTTCTGAGCTGGAGTGGCTGCTCAGTAACTCGGATCCGGCAGTTTTC[C/T]AGCCTGACAGCTCATCTCTGGGATCGCTACACAGTGGACTGGAGCTTATG
Long Flanking Sequence:
ATGTTTACTGTATGATGACTGAAATGGCCTTAAACAATCACTTAATGACGACAGAATTTTACGTTTTCACACACATGCACATATTGCATGTAAACACATCAACCTTTCACAGCGCCATACTCACTACTCATGAATACTGTTAAAAGTGCTACGTTTTACTCATATTTTGACTAACATTTACAACTTTTTTTTTACTTTACCTGCTCTGCATTGTTTTGGGTAAGTAATGGTACATTTACTTGAGTGTGATTTTTCAGTACTCCGTTCACAACATAGGACATTTTTACGGTACAGTTCAGTAAAAACAACAGTGAAAGAACTGATCGCTTATGTTTTCTCAAACTTCACATTTTGACTGCCTATTTGTTCATCTACAGTCATAATTAAGTCTTTTTTTAATCTTCTAACCTGAATCTCTGCTTTATTTCCCGCAGATACCAGAGAGATACTCGCTTTCTGAGCTGGAGTGGCTGCTCAGTAACTCGGATCCGGCAGTTTTC[C/T]AGCCTGACAGCTCATCTCTGGGATCGCTACACAGTGGACTGGAGCTTATGAGAAGAGATACTAAAGAAGAGAGGAAGACCGGCTGCAAAAACTACTTCTGGAAATCCAGAACGGCATGCTAAAACTCGAAGTTACCAACATGCTGGCCATCATTTAGTCTTTCCTTTTCCTGAATCCAACACTCGTCATTTGCTGTCTTTTGAGTAATTTTAGACATTATCTGTGAAGAGTTTTCCACAGTCTCAGTATTATTTTGCTTTGAAGCATTGATTGCTTGCAATAAACTGAATACAGCATAAAAAAGTCAGCGTGTGTTATTTTATTTGCTGCTGGGCTTATTTAAACCCAAAGGTCAAATTCCCTGACTTTCACAGACTACAAAGTTAAATTTCCATGAACTATAATGAATAGTAAAACAGACAGCTCTTGCTGCTCCAGAATTTAGCGATTATGCTAATGCTAAATGTGATGCAAAGTTTCGCACATAATTTAGAGAAGCT
Associated Phenotype:
Not determined