Busch Lab

ZMP

zgc:114045

Ensembl ID:
ENSDARG00000069334
ZFIN ID:
ZDB-GENE-050913-119
Description:
hypothetical protein LOC569643 [Source:RefSeq peptide;Acc:NP_001025409]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14791 Essential Splice Site Available for shipment Available now
sa5406 Nonsense Mutation detected in F1 DNA Not yet available
sa38602 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa14791
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:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100804 Essential Splice Site 56 246 None 8
ENSDART00000113793 Essential Splice Site 56 246 None 8
ENSDART00000145832 Essential Splice Site 56 207 None 5
ENSDART00000146335 None None 253 None 9

The following transcripts of ENSDARG00000069334 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 21268100)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 19858536
GRCz11 7 20110504
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGACATCACCGTGGGGTGCTTCGTGTGCACGTCATGCTCCGGAATGTTG[T/A]GARTTATAATACCCAAGTGCATGYGATTATTAGTGATTACAAACAGATTT
Long Flanking Sequence:
TTTTTTGCGCCCACAGGAGAAAAACCGCAGCAATGAATAAATAAACGGGGCGGTTGTAAAACTCCAGGCGGATCGGCCAGTCGTGACCACGGAGGCTACGCACGCATGTGAGATTCGTTTCTTGTCAATTCAAGTGTATGGCCGGTCGATCGGACGCTTGATTTTGGCACCATACAAGAAGAAGAGCTGCAGCCGCATAGCCGTGCTCAGAATGCGGGCGTGAGAGACGGACTACGGCGGGGGAATTAAAGTGCAACGGTGGGCGAGTGAACGGCTCCCCCACAACAGTCTCGAGGGCCAGGGGGTGTGTGCGACTGCAGGGCACCAGCAGCATGTCGAACCGAAAACACCGGGACAACCAGGAGATCTGCGCCCGCAAGGTCCGCGAGCTCGCCCAGACGGGAGTGAACAAGCACTGCTTCGAGTGCAACCAACCCGGGGTGACTTACATCGACATCACCGTGGGGTGCTTCGTGTGCACGTCATGCTCCGGAATGTTG[T/A]GAGTTATAATACCCAAGTGCATGTGATTATTAGTGATTACAAACAGATTTGTATTAATGTTGTTATTCCTCAAACTCTGAACTGAACCTTCAGGAAATATGCAGATGCAGCGCAGTTACAGATCTCTGGTTGTGTTTACATTCATGAACACAGTCCGTAATTACTACTTTGTCGTTTTCAGGCGTGCCCCGGTCTCGCCTGCGTTACGTATCATTTCGTCATGATTTCAGGTTTGCCATCAATATAAACGTGTTTTCTGCATGTGGGCAAAGGAATGGTGTGATTCCACCTCAGTTTCAGTCTGCAACTGCACTTACTGTATACGAACAAACACATCTTGCTAGTTCTTCACTGTGCACTGAAGAAAAAAACAAACGCAGCCCGCTTCCTTTACGGTTTTGTCATTTGTTACTGCAAGAGGTTCTTGCAGGCTCTCATTTTCACAGCCCTGTCACATCCCACCCTATCGATGTTAAAAATGAAGGCAAGCCCTCATCTCT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5406
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100804 Nonsense 100 246 3 8
ENSDART00000113793 Nonsense 100 246 3 8
ENSDART00000145832 Nonsense 100 207 3 5
ENSDART00000146335 None None 253 None 9

The following transcripts of ENSDARG00000069334 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 21275565)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 19866001
GRCz11 7 20117969
KASP Assay ID:
554-3546.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGGGGTTGTTAGGTTGGAAGGAGGACCTGGCTCTGCACATTTGACCCC[A/T]AAACCGACGGCTGTTTTGATGCACGTGACACGCAGAAGCTGAAGGAGTTC
Long Flanking Sequence:
ACAAATTCTGCACCTTTGTCAGTGAGCCGTGGGTCTTCTGAACTCTTCGAACCCCCCTGGCTACGGGCTTGTATTATATTATCCTATTATAGGTGCAAATAATTTAACTTGCATTTAGAAACACCCTTAAAAGAAAATTGCACTGACGTAGGCTGTATATTTATTTTGTGGGGTATAAAGTGAAACAATTTCACAGCATAATACTCACTACTTTCTATTCTTGAGTTCTTTTAAAATGACTACCTTTTACTTTAAGTATTAAAGAGAACAGATACTTTTATTTTACTTGCACTTCATTTTTTGGCAAGTAATGGTCCTTGAGTATGATTTCTCAGTACTATTTCCAGCACTGCTGTAGGGTCACCCTAAGCAAACATGTTTGAGGAAGTACTCTGTGTAAACTTTGTTAACGAGGCTTTAAAAGTAGCTTAACTGTGTGTATTCTTGGGCTGTGGGGTTGTTAGGTTGGAAGGAGGACCTGGCTCTGCACATTTGACCCC[A/T]AAACCGACGGCTGTTTTGATGCACGTGACACGCAGAAGCTGAAGGAGTTCTTGCAGGACAAATATGAGAGGAAGAAATGGTGAGCGAGAAGTAGTGTGGTCATAAAGGGTGTTTCAGAGCGGATCAGAATGAATTATTAATGCATGCTGAACCATGCTGCTGTTCTCACTGGATTATCTGTAGATGAAAGTCAAAGAATGCTTGACTTAAGAGGGGTCTGTTTTTTCTCCCCAGGCATTTCTCTAAAAGCAAGATGCGCCGGGATACAGACACACCGTGGGGTCCAGGGGTTCAGGCTATTCCAGCTCCACATGGGCCTGCTCAGAATCAGCCTCCGCCTGGACATCCACTGAACCCCACTAACCGGCCCACTCGCACACTGGTGAGGAAGAAACAGAGTGGTCCAGGGATTTCATATATCTTTGAATTCAAATGAAAAATGAGCGAGGCAAATAAAAGAAAATCAATAGTGCCTTTTTGAATGTGTATTCATGTCTTAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa38602
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000100804 Essential Splice Site 238 246 7 8
ENSDART00000113793 None None 246 None 8
ENSDART00000145832 None None 207 None 5
ENSDART00000146335 Essential Splice Site 41 253 2 9

The following transcripts of ENSDARG00000069334 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 7 (position 21282932)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 19873368
GRCz11 7 20125336
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCCTTATTTCACAGCCAGTAGCACTTTCAAAAACAGCTTTACTTTAGG[T/G]AAGTCCCATAATCGCACACTGCAGACACTTCAGCTGTACCTCAGACCATC
Long Flanking Sequence:
TGTGGAGAGACAGAGACCAGGAGTTATGTCTTCAGGAATTGGACCCCAGAATCATCCCTCCTCTTTCCCAGCCCTGCCACGTCCTTCAGGTACACCCAGACACAAACATTAAGTACGAGTTTGAACTCTGTTTAAAGTATGATTTTTAGTTGTTATGAATTACACAGGACACAAAGACATGTCCACATAAACCACTTCAACATTTTAACACCAAGCTCATAACCATTTCATTACACACATTTCCTCATAAACCACCAAGACACACACACACACACATCCAGTAATGTACAGACATCTTCAGCTAAAGCACAAAATACTGTCACCTCCATTATTGTCAACTCTGTTACTGTTTAAAATGTGGGATTTCACTATATATTGATATTTCTGTAATGTTTAATGCATTGTCCATTAAGCCATACCAGGTTCCTTTTAACTCATCTTCCCTCTTTTGTTCCTTATTTCACAGCCAGTAGCACTTTCAAAAACAGCTTTACTTTAGG[T/G]AAGTCCCATAATCGCACACTGCAGACACTTCAGCTGTACCTCAGACCATCTGGCTGCAATGCTGAGTGAGCCAGCCATGACAGGCAATGAGAAAACGCATTCATTACTGTGCAGATATAATGTTGCCGTATATATGTGAGTGTGTCAGGGAGAAAGAAACAGAAAAGAAAAGCTTGACGCTATGCAGAATGAAACCCCTGTGGAATGATGCTGTTAGCAATAAACCAGCGGTTTACATCAAGATCAAATTGCCAAGCAAGTTTTAATGCACAATAAACACAAACTGTTTTGGATGTCTGCAGTATTAGAGTTGAAGATCAAATTATTAGCCCTTCAGTGAAATGAATTCTTTTTAACAGAAAACAGAGATTTAAAATACACTCACTGGCCACTTTATTAGGTACACCTGTCCAACTGCTCGTTAACGCAAATTTCTAATCAGCCAATCACATGGGAGCAACTCAATGCATTTAGGCATGTAGACATGGTCAAGACAATCT
Associated Phenotype:
Not determined