Busch Lab

ZMP

zgc:171928

Ensembl ID:
ENSDARG00000011809
ZFIN ID:
ZDB-GENE-081022-3
Description:
Zgc:171928 protein [Source:UniProtKB/TrEMBL;Acc:A7E2L2]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa24396 Nonsense Available for shipment Available now
sa5982 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa24396
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000037315 Nonsense 264 1214 5 23
ENSDART00000136707 Nonsense 264 1227 6 24

The following transcripts of ENSDARG00000011809 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 39635523)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 39597088
GRCz11 23 39489999
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTAAACAAGAGGCTCAGGTGCAGGAGATCAGCGGTGTGGCCCGAATTTA[C/A]AACCAGCAGTTTTTCCAGGCTCTTCAGTCTGAGATTGGTAGAGACTCATA
Long Flanking Sequence:
TGGGCGCACAAATGAGCGCTAAGGCATTTGCTATTTAAACAGCGTAGCGCAACGCCTCAAAACGACTCTTGCGCCAAGCTGAAACTACCAAAAGACTATTGCGCCGCATCTTGCGCCCCACTGTGCCGGGTGTATGATAGGGCCCTTTATCTTTATCTTTTCTACTCTTTTGCCCGCTGTACAGCACAGTTCTCAACTATTTTTGTCTTTATTTGTGCTTTTATATTTTAAAAGTAAAAATATAAACAGAAAATACTTGAATTTTATTTATTTATTTATTTTTGAGAATGTTAAATCTTTAATCTTTATTTCACTTAATTCATATTTAATATTGATTTACATCAACCCTTCCTTGTTGTCGTTTTTCCCTGTGAATATTCAGGTTTTAAGATAAAGGAGCTCCGAGGAAAGCTGGCTATTGGTATCACTGCAAACTTTGTAAACCGTCACACTAAACAAGAGGCTCAGGTGCAGGAGATCAGCGGTGTGGCCCGAATTTA[C/A]AACCAGCAGTTTTTCCAGGCTCTTCAGTCTGAGATTGGTAGAGACTCATACAAACATTTATCTTCTCTAAACGAGTGCCAGTTCTTAACTCCCATTATGCCTAATAAGCTGCATTTGGTCATGTAAAAGCTTACATTGAGGTCACCGAGCATGTAAACACATTAACCTGCTTTTCGACAGGTATTGAAGTGCACATATGGTATGTGACAAGAACTCGTTTGTAGGCTGCACGATCCATGGAAAATATGTGATATTGCTGTTGAATATTGCAATATAATATTGCAGTAATATAGCGATATTCCTTGAGATATTTTTTTTGGTTAAAAAAAATAATAATAATAATAAAAAAAAATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACATACAGACTTATTAACCCCCCTTTGATTTTTATATTTTAAATATTTCCCAATTGATGTTTAATAGAGCAAGGAAA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa5982
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
ENSDART00000037315 Nonsense 891 1214 17 23
ENSDART00000136707 Nonsense 904 1227 18 24

The following transcripts of ENSDARG00000011809 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 39662113)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 39623678
GRCz11 23 39516589
KASP Assay ID:
554-3763.1 (used for ordering genotyping assays)
KASP Sequence:
MWGAGCAGATTCCTGAGGAGCCCAAACCCAAACCGTCCCTGCGCAAACTC[C/T]AGCAGAGCGAAGAGGAGAAGGTGGATCTGTTGAGCCAGGATTCAGACTCT
Long Flanking Sequence:
AAAAATCCAATCCAAAAACTTTTTGGAGGGGCAGTTAAAAAGCTGAAATATCTCTATGATGCTTACAAAAAATGTAAAATTGTGTTTTATTCATTTTCTAGAATCATACTGAGAACGGAAGTAAGGAGGACAAAAATGGAGAAACAACAGCGGCTTCATCCCCACCTGCGCATCTCTCAATAAAGCGTAAGGGCTCGTACAAGATCTCTGTTGACCCTGACTTTGATGAATCAACTGAGTTTCCTGCTCCAGACCAAGATGAACCACCTGATCTTGAGGAGTCCCATCAACCTCCCAAACCTTCAGAGCTCAGTGCGGAAAACACAAACATGGAAAACCAACAACACAACATCAATCCAGTTCCTGCCCCGCGTGGCTCCAGAGCTCCGCTCCCGAAACCTCGCACTGTCCATAATGTGGTGCACGAACCCTGTAATATTCCAGAGGAAGCAGAGCAGATTCCTGAGGAGCCCAAACCCAAACCGTCCCTGCGCAAACTC[C/T]AGCAGAGCGAAGAGGAGAAGGTGGATCTGTTGAGCCAGGATTCAGACTCTGAGACACGGGGCTCGTCTTCTGCCGCCTCCACCTCCTCCTCATCCAAACAGCATGAAGAGGAGGGCTACTGGAGCGGAGGCACGACGTGGGGGAAGAGCCATCGTGAGCAACGAAACCGCCCCTGCATAAGGAGGAAGAGTGAACCTCCGCTGCCGCTGACTGGCCATTCTCAGCACGGAAAGATGCGCTCCAAGTTTTCCCCGTGGAATCTGTCTTCACCGCGGCTCCAGCAGCGATTCAGCGTTCACAGAGTTCCTGCAGGTTGGAAAATATTTTGAAACCTTTTTTTTTTTATTATTCATTCATTTCACTTTAGCTTAGTCTCTTATTAATCAGTGGTCGCCACAACGGAATGAACCGCCAATTAATCCATCACGTGTTTTATGCAGCCAATGCCTCTCCAGCCGCAACCCAGTACTGGGAAACTCACATTCACACAGATACACTAT
Associated Phenotype:
Not determined

Mutation Details

This allele has been removed from public view.

Allele Name:
sa29991
Status:
Less stringent filtering
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
n/a
Mutation:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000037315 Essential Splice Site 994 1214 17 23
ENSDART00000136707 Essential Splice Site 1007 1227 18 24

The following transcripts of ENSDARG00000011809 do not overlap with this mutation:

Genomic Location (Zv9):
Chromosome 23 (position 39662426)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 39623991
GRCz11 23 39516902
KASP Assay ID:
2261-8159.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTTCACCGCGGCTCCAGCAGCGATTCAGCGTTCACAGAGTTCCTGCAG[G/T]TTGGAAAATATTTTGAAACCTTTTTTTTTTTATTATTCATTCATTTCACT
Long Flanking Sequence:
TGCGGAAAACACAAACATGGAAAACCAACAACACAACATCAATCCAGTTCCTGCCCCGCGTGGCTCCAGAGCTCCGCTCCCGAAACCTCGCACTGTCCATAATGTGGTGCACGAACCCTGTAATATTCCAGAGGAAGCAGAGCAGATTCCTGAGGAGCCCAAACCCAAACCGTCCCTGCGCAAACTCCAGCAGAGCGAAGAGGAGAAGGTGGATCTGTTGAGCCAGGATTCAGACTCTGAGACACGGGGCTCGTCTTCTGCCGCCTCCACCTCCTCCTCATCCAAACAGCATGAAGAGGAGGGCTACTGGAGCGGAGGCACGACGTGGGGGAAGAGCCATCGTGAGCAACGAAACCGCCCCTGCATAAGGAGGAAGAGTGAACCTCCGCTGCCGCTGACTGGCCATTCTCAGCACGGAAAGATGCGCTCCAAGTTTTCCCCGTGGAATCTGTCTTCACCGCGGCTCCAGCAGCGATTCAGCGTTCACAGAGTTCCTGCAG[G/T]TTGGAAAATATTTTGAAACCTTTTTTTTTTTATTATTCATTCATTTCACTTTAGCTTAGTCTCTTATTAATCAGTGGTCGCCACAACGGAATGAACCGCCAATTAATCCATCACGTGTTTTATGCAGCCAATGCCTCTCCAGCCGCAACCCAGTACTGGGAAACTCACATTCACACAGATACACTATGGCCAATTTCATTCATTCATTTTCTTTTCGGCTTAGTCCCTTTATTAAGTTGGGGTCGCCACAGCAGAATGAACTGCCAACTTATCCAGCATATGTTTTACACAGCAGATGTTCTTCCAGCTGCTACTCATCACTGGGAAACAGCCACACACACTCATTCACACACATACACTACAGACAATGTAGCCTACCCAATTCACCTATGTGACTCTTTGGACTTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCAACGAATTTGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGGCCCAGCTGGGATT
Associated Phenotype:
Not determined