Busch Lab

ZMP

si:ch211-184m19.1

Ensembl ID:
ENSDARG00000016532
ZFIN ID:
ZDB-GENE-030131-2941
Description:
Novel protein [Source:UniProtKB/TrEMBL;Acc:Q5TYS6]
Human Orthologue:
C1orf9
Human Description:
chromosome 1 open reading frame 9 [Source:HGNC Symbol;Acc:1240]
Mouse Orthologue:
AI848100
Mouse Description:
expressed sequence AI848100 Gene [Source:MGI Symbol;Acc:MGI:2138346]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa23655 Nonsense Available for shipment Available now
sa31041 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa44935 Nonsense Mutation detected in F1 DNA Not yet available
sa36995 Nonsense Mutation detected in F1 DNA Not yet available
sa36994 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa23655
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026969 Nonsense 7 1314 1 23
ENSDART00000137605 None None 300 None 10
ENSDART00000143590 None None 1029 None 17
Genomic Location (Zv9):
Chromosome 20 (position 14696326)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 14885572
GRCz11 20 14781552
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCGAGGATGTTGGTCCCCGCGGGAAGATAATGAAGAAGCTGCGCGTGT[T/A]GTTCCTGTGCTCCGTTTTAGCTCTCCTGTGCTGGTAAGTCAAATCATTAT
Long Flanking Sequence:
TTCAGATATCAGTCACATTTTTAAACCCCAAAGTCATTAAACATTTTAACGCTAAAATATAGCAAAGTTGCTAAGTTATTTCCCCAAGCGAATGATCTGGAAGTCTTTCAAACCTCTTATCATTCGAGCTGACGCGTCTGATGACAAAACTTCCAACTCATCTAGACCCCAAAGAGTAGGCGGGGTCAACGTAAAACTCGATTTCTATTGGTCGAGGGCGAGGCAGCAGGAGCTGTGAGCGCTGGATCAACAGCAGCACGGAGCAAACGCAGACGGGAAGCAGTCAGGCGGGCAGCGCTTCTCAACGGGGGGTTTAAACGTAGAAAACTGACCCAAGTGTCTGCTCTGTACCGTGAAACACACCCCCTTTACCTTGATACAGTTGCGAACAATTAGCATTATTAGCTAGTCTTTGTCTCTGTCGTCAGTATAGGGTGAGAATAGATAAAAAAGCGAGGATGTTGGTCCCCGCGGGAAGATAATGAAGAAGCTGCGCGTGT[T/A]GTTCCTGTGCTCCGTTTTAGCTCTCCTGTGCTGGTAAGTCAAATCATTATTTTAATACAACACAGTTACAATGTATCTAAGCTGTAAAACATTAATACTTTGACAACGACGTCATTCAAAACTCTATATTTTTTCTTGATAGCATCGATGCTAGATGCTAACGTTAGTTCAATCGCTTTAGAGGTGGGATGTGTGTTTATAAGCTTTATGGCTGAAGACATCAAATTAAATAAGCCTAGTGCTGTTTTTATTCATTTATTGTTGTGGGGTTGATGCTTACGCCTTTTGAAATTTGCTGTCAGCCTGTTGAAACAGTACTGGACCACCAGCTGTCCACTATATGTGTGGATGTAGGGAACGCAATGTTCAGAAAACAGAAAGCCCACCATGCATTGTTAAGCTGTAATCAATAATTTAACATTATTCCGTGATTGATGTATGCATTTATTATATTTTTTTGAAGATTAAATCTGACCATAATGGTAATGAGCTGATATGGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa31041
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
ENSDART00000026969 Essential Splice Site 353 1314 7 23
ENSDART00000137605 Essential Splice Site 76 300 2 10
ENSDART00000143590 Essential Splice Site 76 1029 2 17
Genomic Location (Zv9):
Chromosome 20 (position 14635996)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 14825242
GRCz11 20 14721222
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCGTCGAATGCGGGGCCAAAATTCTTTCGGCCAACAACGAGGCTAAGG[T/G]AAATATGGTGCAGATGGTGGTAAAACAGCATTTGGAGCAGAAAAAAAAGA
Long Flanking Sequence:
GCTGTCTTTGCTTTTGCCTTATAGCAATTTAATGTTAAGATTTATAATGTGTATATATTACTTTTATTTTATGTCAAGCCTCTCTTGGACAGGTGTTGAGAATTAGCAAGTCTGCCAAAAACACTTCAGTGTTCAGTATAATTGGGATGTCATATAAACGATAAACATCAATTTATTTATTTATTTTAATTTCACAGGACCTTTAAAGCTCAATAACTTAGCTTTGTGTAGTTAAAATTCTTTATTAAAAACTTTACCATTCTTATTCCGTTACAGATGCTATTTGCATACATTAAGATCTGGATAATGTCCAGAGGGCAAAATTTGCTTTTGACAGATGACCTAAATGTTGCCTGTTTGCTTGGTTTCAGGTCAGTCTCTGCACACTTCATCAAATGGCAGCCCTCATCCAGTCAAAAAGGTCCAAAAGAATTTCAAGAATAACTACGCTTCCGTCGAATGCGGGGCCAAAATTCTTTCGGCCAACAACGAGGCTAAGG[T/G]AAATATGGTGCAGATGGTGGTAAAACAGCATTTGGAGCAGAAAAAAAAGATGGAGTAGTGTTCAGCAGGGGCATAAATGAGACAGTTGTTTGATTACTATTTTTGTTTCTGCATCTTCAGTGTTATTTATCCACTCTAGATCTAACATTGCCTGTGTGTTGCTGTGTTTTCAGAGCACATCTGCCATCCTGATGGAGAACATGGATCTGTACATGCTGAACCCCTGCAGTACCAAGATCTGGTGAGTCACTGCAGAGAAACAGACTGCAGCAGCTGCTCTCAGACTATGAGAAAACAATTTTACAGTGGGTCCTGCTGCAGAAAATTATAGTTGACGTAAATGTTTTAAATATGATGGCATTCGATCTAAATTTATACTTTTTAAAATTATTAAGCCAATTTGAATAACCTGGTAATTAAGCAATCACTGCTTAATTTGAATTTGAAAATGTATTTTACAAGACCAAACCCATGTATATATTGATTTTTACTGTCATACA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44935
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026969 Nonsense 483 1314 13 23
ENSDART00000137605 Nonsense 206 299 8 10
ENSDART00000143590 Nonsense 199 1029 7 17
Genomic Location (Zv9):
Chromosome 20 (position 14625358)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 14814604
GRCz11 20 14710584
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATTCTGTGAATATCAGGGTGTTTGGCACCAGTATGGTGGAGGAGTA[T/A]GATGAGATTGCAGACTCTCAGTACACGTCAGAGAGAGCTGAATATCTGGA
Long Flanking Sequence:
AGAAGCTACCGTCTAATCGCTGTTATTTTACAATCCGCATGATGCAAATTGTTTTATAAGGGATCATGTGCAACCCTTGTGGGTGCATAACGTTTCTTCCAGATTCCCTTTTGTATGTCTTCCTGAGACTGGTCATTTAAGTGGAAATCTGCTTTTATTTTCTTCTGTGCGAGTCCCCTGTAAAACCTGTTTTTAAAGACCCCCACTAAGCTGGGCAAAGGTCAGAGTGATTCTAGATGTTTTATAGAATGCATAGATAAGCTGTACTGAAGATCACAGAAGGTTTTTACAGTAGTATTTCTCTCCCTGACGCCTGATGTCTTATCTGTACACTGACCGTTTGCTCTTTAAGATAATACAGCAAACATTTTTTTACAAATGAGCCGTTTGCATTTTTTGTATTGATTTTCATATTTGCTCTGTTAATAATCTTTGTGATGCTCATGTTTGTTTAATTCTGTGAATATCAGGGTGTTTGGCACCAGTATGGTGGAGGAGTA[T/A]GATGAGATTGCAGACTCTCAGTACACGTCAGAGAGAGCTGAATATCTGGATGAAGATTATGGTGAGATCAAATCTGCAAATGCTTCCACACAGGAAGTCAACACTATGACAAAAATATACAATTTATGATTCATGTTGTGCAACTATGTGCTGTTTTTAGAATAAGTACAAACAGTGTAATTTTAAGCTTAAGAATTTGTATATTTTTAACACTAAAAAAAAAAGTCACATGGCACTTTTCGCCCCATTTATATGCATGTGAATGCACTAGACTGGAAATCTAAGCTTGTGCTAAAATTTTTGCATTTCACTGCATTCAAAAGCTGACGCTGGGTGAATTCCGACGTGTGAATTTGTTATGTTAATGCATGAGGCCAGCAGAAGATCAAAACATGACTTCTCTGCACAGAAATGTAAAATATGGAGGAAATCGCTCATTTAATTAGCGTCACATCATCTTGTTTCATTCTGTCTCTTTTTGCAGCACCATTTGAACAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36995
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
ENSDART00000026969 Nonsense 490 1314 13 23
ENSDART00000137605 Nonsense 213 300 8 10
ENSDART00000143590 Nonsense 206 1029 7 17
Genomic Location (Zv9):
Chromosome 20 (position 14625339)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 14814585
GRCz11 20 14710565
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGTGTTTGGCACCAGTATGGTGGAGGAGTATGATGAGATTGCAGACTCT[C/T]AGTACACGTCAGAGAGAGCTGAATATCTGGATGAAGATTATGGTGAGATC
Long Flanking Sequence:
CTGTTATTTTACAATCCGCATGATGCAAATTGTTTTATAAGGGATCATGTGCAACCCTTGTGGGTGCATAACGTTTCTTCCAGATTCCCTTTTGTATGTCTTCCTGAGACTGGTCATTTAAGTGGAAATCTGCTTTTATTTTCTTCTGTGCGAGTCCCCTGTAAAACCTGTTTTTAAAGACCCCCACTAAGCTGGGCAAAGGTCAGAGTGATTCTAGATGTTTTATAGAATGCATAGATAAGCTGTACTGAAGATCACAGAAGGTTTTTACAGTAGTATTTCTCTCCCTGACGCCTGATGTCTTATCTGTACACTGACCGTTTGCTCTTTAAGATAATACAGCAAACATTTTTTTACAAATGAGCCGTTTGCATTTTTTGTATTGATTTTCATATTTGCTCTGTTAATAATCTTTGTGATGCTCATGTTTGTTTAATTCTGTGAATATCAGGGTGTTTGGCACCAGTATGGTGGAGGAGTATGATGAGATTGCAGACTCT[C/T]AGTACACGTCAGAGAGAGCTGAATATCTGGATGAAGATTATGGTGAGATCAAATCTGCAAATGCTTCCACACAGGAAGTCAACACTATGACAAAAATATACAATTTATGATTCATGTTGTGCAACTATGTGCTGTTTTTAGAATAAGTACAAACAGTGTAATTTTAAGCTTAAGAATTTGTATATTTTTAACACTAAAAAAAAAAGTCACATGGCACTTTTCGCCCCATTTATATGCATGTGAATGCACTAGACTGGAAATCTAAGCTTGTGCTAAAATTTTTGCATTTCACTGCATTCAAAAGCTGACGCTGGGTGAATTCCGACGTGTGAATTTGTTATGTTAATGCATGAGGCCAGCAGAAGATCAAAACATGACTTCTCTGCACAGAAATGTAAAATATGGAGGAAATCGCTCATTTAATTAGCGTCACATCATCTTGTTTCATTCTGTCTCTTTTTGCAGCACCATTTGAACAAATTTGGCATTCTTGAACTCTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36994
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000026969 Nonsense 491 1314 13 23
ENSDART00000137605 Nonsense 214 300 8 10
ENSDART00000143590 Nonsense 207 1029 7 17
Genomic Location (Zv9):
Chromosome 20 (position 14625334)
Other Location(s):
Assembly Chromosome Position
GRCz10 20 14814580
GRCz11 20 14710560
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGCACCAGTATGGTGGAGGAGTATGATGAGATTGCAGACTCTCAGTA[C/A]ACGTCAGAGAGAGCTGAATATCTGGATGAAGATTATGGTGAGATCAAATC
Long Flanking Sequence:
ATTTTACAATCCGCATGATGCAAATTGTTTTATAAGGGATCATGTGCAACCCTTGTGGGTGCATAACGTTTCTTCCAGATTCCCTTTTGTATGTCTTCCTGAGACTGGTCATTTAAGTGGAAATCTGCTTTTATTTTCTTCTGTGCGAGTCCCCTGTAAAACCTGTTTTTAAAGACCCCCACTAAGCTGGGCAAAGGTCAGAGTGATTCTAGATGTTTTATAGAATGCATAGATAAGCTGTACTGAAGATCACAGAAGGTTTTTACAGTAGTATTTCTCTCCCTGACGCCTGATGTCTTATCTGTACACTGACCGTTTGCTCTTTAAGATAATACAGCAAACATTTTTTTACAAATGAGCCGTTTGCATTTTTTGTATTGATTTTCATATTTGCTCTGTTAATAATCTTTGTGATGCTCATGTTTGTTTAATTCTGTGAATATCAGGGTGTTTGGCACCAGTATGGTGGAGGAGTATGATGAGATTGCAGACTCTCAGTA[C/A]ACGTCAGAGAGAGCTGAATATCTGGATGAAGATTATGGTGAGATCAAATCTGCAAATGCTTCCACACAGGAAGTCAACACTATGACAAAAATATACAATTTATGATTCATGTTGTGCAACTATGTGCTGTTTTTAGAATAAGTACAAACAGTGTAATTTTAAGCTTAAGAATTTGTATATTTTTAACACTAAAAAAAAAAGTCACATGGCACTTTTCGCCCCATTTATATGCATGTGAATGCACTAGACTGGAAATCTAAGCTTGTGCTAAAATTTTTGCATTTCACTGCATTCAAAAGCTGACGCTGGGTGAATTCCGACGTGTGAATTTGTTATGTTAATGCATGAGGCCAGCAGAAGATCAAAACATGACTTCTCTGCACAGAAATGTAAAATATGGAGGAAATCGCTCATTTAATTAGCGTCACATCATCTTGTTTCATTCTGTCTCTTTTTGCAGCACCATTTGAACAAATTTGGCATTCTTGAACTCTAGCTTG
Associated Phenotype:
Not determined