Busch Lab

ZMP

zgc:113208

Ensembl ID:
ENSDARG00000035610
ZFIN ID:
ZDB-GENE-050417-450
Description:
hypothetical protein LOC550591 [Source:RefSeq peptide;Acc:NP_001017892]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa40409 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8818 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa40409
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000051623 None None 285 None 6
ENSDART00000138716 Essential Splice Site None 207 1 6
ENSDART00000146035 None None 148 None 5
Genomic Location (Zv9):
Chromosome 5 (position 24404711)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 22117583
GRCz11 5 22621383
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAATTGGCGGCGGTAGTCAAGGCAAAACTGTTTATGTAGTTTGATTGTGT[G/A]TTACGTGTAGGCTTGGGCGGTATCCAAATTTTGAGACCGTCAAACCGCCT
Long Flanking Sequence:
AAACATATTATTTTAACCTACTGTTCTTAATCTTTTTTATTATTTTAAATTTGAAATAAATGTTATTAAATCAATAAAAACGTAGAATACATATAGAATACTTTATAACATACTCAGAAACGTAGCTACATTTAGTAAATCCAGATAAACTGAGAAATTACAGTATGTAGCTCACTTTGTGGCTTAAAGAAATAGATTTCAGCATCTTCCCCTGAAAGATACAAAGAATTAAGAACGCTTTCATTATGAAACAGGCGTTTTCACAAATAATTTAGGGGGTTTCTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTATGTTACGTTTTGTTAGTCATGCAGGCAAGCCCTCATTGGGCAAGCCTCTCACTCACCACGTGAGCATGCGCAGTTTAGCGTGTTGCGTAAACCAGGAATTGGCGGCGGTAGTCAAGGCAAAACTGTTTATGTAGTTTGATTGTGT[G/A]TTACGTGTAGGCTTGGGCGGTATCCAAATTTTGAGACCGTCAAACCGCCTCCATATTTTACCCCGGTATCCGGTATTACCGGCGTATAATAAAAAAAATTATGACGTAAGGCTCAGACAGCGTCACCAAACTGTTGGCTTGAGCCTAAACCATTCAGAAACTGAATACCTTCTATGCAATCTTAGGCTCGCAGTCAGAGAGGAGAGGGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGAGACGGCCTCTCTCTCTCTCTATCTCTCTCTTACACACACACACACACACATCTCTCCCGCGATTTATTCAGAAATTTACTCCCACACCGTAAGAAATCTGGCCGGCTCCCGCGGAACAGCAGCGATTGACAGCTTTATTAAGTCGAACCCGTTTACAGCCCGACATTATTCAAGTGTGCTCATGCACACAGCTCTAATGCATTTTTTTCAAGAATGAGTCATTTATATGTTTTAACATCATTTATTCGTAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8818
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
ENSDART00000051623 Nonsense 261 285 6 6
ENSDART00000138716 None None 207 None 6
ENSDART00000146035 None None 148 None 5
Genomic Location (Zv9):
Chromosome 5 (position 24389772)
Other Location(s):
Assembly Chromosome Position
GRCz10 5 22102644
GRCz11 5 22606444
KASP Assay ID:
2259-5698.1 (used for ordering genotyping assays)
KASP Sequence:
TCCGGTCCGGTTGTGCTTACGACAACGTTACTGTTTCCCCAGTGGTCAGA[C/T]AGACTCTACAGCACTGGGGGTACAAACTCACSCCGGAGGACTACAAGCAA
Long Flanking Sequence:
CCTTTATTTCTGATAGGCAAAGTAAGGCAAGTTTATTCATATAACACATTTCATACGCAAAGGTAATTCTAAGTGCTTCCCTTAAATAAGATAAGCAACTAAACAAAGATAAGAAAGGCATAGCACAGACAGATGCATACACTTACTGTATATCGCATACTGTTTTTCATCTACGATAGATTAATGTAGTAAATAGTAGACAAGTATGCAGTTTTGAATGCTTTCAGCCTCTTTACTTGAGCAGTTCCCCTTATACCTGATCAGAATGACATATCAAAATATTCAATCTCAGGTCAAACTTTTATGTTTACCTTCATTCATTCATGTTTTGGCTTCGGTGCAGGTTTTACCAGGGCAGGCGGACAGAGGACGATGCTCGTCAAATCAGTCGCTGGTCCAAATGTGCAGGAGTCAAAGGCCGGTGGCGGAACAACCTCATCACGAAAGTGGTCCGGTCCGGTTGTGCTTACGACAACGTTACTGTTTCCCCAGTGGTCAGA[C/T]AGACTCTACAGCACTGGGGGTACAAACTCACCCCGGAGGACTACAAGCAAGGAGCAAAGAGAGTCAAGCTCAAATAAACAGGTCTTATTTGTTTGAGTACAATGCGGAATTGGGGGATTTTAGCTGTTATTAGTGCATGACGTGTCTATTTTAATAATTGATGTTTTGTCTGACTGGGGGACTTGACTAGCTGTGGTAATACTACTGCTGTGTTTGGTTCCCATTGGACATGTTTTGGGAAACTGAAAGGTGACTTCAATAATTCATAAATATCTTATTTTTAAATTGGGATCTCAGGCAGAAGCAGATGCAGACACTCCTTATTTTGTTCCTATTACTGATTTGCATAGCTGAACACCACATGTGCCTTGGAGCAATATAGCGAACTGATTTGTGATCGGATGTGGTCATCGTCACACTGATTTTATGACAGTAATTTGTTCTGCTGTGTTTATTTTTAATACATGGTGAAGATGCTTACATATTTGCATAATAAGATG
Associated Phenotype:
Not determined