Busch Lab

ZMP

NR_023326.1

Ensembl ID:
ENSDARG00000090725
Description:
wu:fj04e09 (wu:fj04e09), non-coding RNA [Source:RefSeq DNA;Acc:NR_023326]
Human Orthologue:
DYNC2H1
Human Description:
dynein, cytoplasmic 2, heavy chain 1 [Source:HGNC Symbol;Acc:2962]
Mouse Orthologue:
Dync2h1
Mouse Description:
dynein cytoplasmic 2 heavy chain 1 Gene [Source:MGI Symbol;Acc:MGI:107736]

Alleles

There are 6 alleles of this gene:

Allele Name Consequence Status Availability
sa6400 Essential Splice Site Confirmed mutation in F2 line Not yet available
sa10490 Nonsense Available for shipment Available now
sa39069 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa35999 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa6400
Status:
Confirmed mutation in F2 line
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
ENSDART00000127986 Essential Splice Site 1157 1667 29 41
Genomic Location (Zv9):
Chromosome 15 (position 43940976)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 45123431
GRCz11 15 45053124
KASP Assay ID:
554-4637.1 (used for ordering genotyping assays)
KASP Sequence:
GCCTAAAGAACCTGCACCTGGTCACAGCATGGCTCCCCCTGCKGGAGAAG[G/A]TGAGAACGCTCYGTCCGTCTGTCTGTCTCTGAAATGAAACAGATTTCTAG
Long Flanking Sequence:
GGTCCGCCTCAGAACGCTTCCTTTTTAGACCAGAACACCTTTGGGCGCACAAATGAGCGCAAATGCATTTGCTATTTAAACAGCGTAGCGCAACGCCTCAAAACCACTCTTGCGCCAAGCTGAAACTACCAAAAGACTACTGCGCCGCGTCTTGCGCCACATTGCGCCGGGTGTATGATAGAGCCCATAGGCTTAAATAGATGTCTGCGGTTAGGGGAGATATGGAGTCTTTCTCTTGTACATTTATACTACATGTACATATTGTCTTAGCATTAGACCAAATATCGTCCCATGTTTCCTCATCAATATCAGTATCCAACTCGTCCTCCCATTTGATTTGATTTCGTCTGCCTCTTTTAATGCGTGTTGTGCAGGTGGCGATGGGTCAGGGTCAGGCTGATGTGGCTCTGCAGGCTCTCAGAGAGTGTGTTCGCTCAGGTGATTGGCTGTGCCTAAAGAACCTGCACCTGGTCACAGCATGGCTCCCCCTGCTGGAGAAG[G/A]TGAGAACGCTCTGTCCGTCTGTCTGTCTCTGAAATGAAACAGATTTCTAGGTCTTATATCATTTGGGAAGTAATCAATTTGAAATATTTGCATATATTTAAGCATTCAGTGTCATTTAAACTATTGTTGGGAATTCAAAAGATCTTTAATAAAAGGGATCCTTCACCCAAAAATGGAGATTCGAGTGGTTATAAGCCCTTAATGAGTTTGTTTCTCCTGTCGAACACAAAAGAAGATATTTTGAAGAATGCTGAAAACCTGTAACCATTAACTCCCATAGTAGGAAAGCAAATACTGTGGAAGTCAATGGTTACCGGTTTCCAACATTCTTCAAATGATCTTATTTTGTGTTCAACAGAGAAAATAAAGTCAAAACGGTTTGGAACAAGTGAAGGGGCGAGTAAAGCATGACAGAGTTCTCAATTGTGGGTGAACTGTCCCTTTAAGTTCTGTCTCTCCTCTGCCTGTCTGTCTTCACTGTTATCTTGGCTGTGTAATTA
Associated Phenotype:
This allele has been associated with this phenotype by genetic linkage analysis and may not be causal.
See FAQs for more info.
Stage Entity Entity Quality Tag
Hatching:Long-pec
ZFS:0000033		 trunk
ZFA:0001115		 posterior-most
BSPO:0000037		 curved ventral
PATO:0001469		 abnormal
PATO:0000460

Mutation Details

Allele Name:
sa10490
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:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127986 Nonsense 1252 1667 32 41
Genomic Location (Zv9):
Chromosome 15 (position 43932433)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 45131974
GRCz11 15 45044581
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GATGATGNNNNNNTGTTTATGTATTTTTCACAGGGTTGGACAAAGTTCTA[T/A]GAGTTTTCTCTGTCAGATCTGAGAGCYGGCTTCGAGATCATTGACCGTCT
Long Flanking Sequence:
TTTTGACTACAAATGATTTTGATATGATTACATGAGGATTGTGGTCTGTGGCTGATTTGACGAAGCAAAACATATGCTGGAATAGTTAGTGGATCTATCCACTGTGGCCACCTCTGAAATCGAGACTAAGCCAAAGAAAAAATGAATGAATTGGTGATGGGGATTATTGCGTAAAATTGCTGCTGAAGCAGCAGAGCAGTGCTTTTACATCAGCAGCTTTTCCTCCTATGAAAAGGTTTTCTGTCAAACATTTGCCTAGCTGAAATAATGTCTGCTTGTGAAAAAAAACGGGAACAAAGAAAAGATGAATGAGTTCACTGTGTCCATGGAAATTCACGTCTGGCTTTTGAAAAATCACTTCATATTTAATCATGATTCAGACATTTCGAGAGTGAGCTGCTGTTGCGCAAGCTGAATATATGAACCGATTGTGATGATGATGATGATGATGATGATGATGATGTGTTTATGTATTTTTCACAGGGTTGGACAAAGTTCTA[T/A]GAGTTTTCTCTGTCAGATCTGAGAGCCGGCTTCGAGATCATTGACCGTCTGTTTGAAGGTGTGTATTATCTATTCGTGTTGTACATTGATGTGTGTGTGCACTCCAGAGGTTGTGCTAACCGAATATTTTCCGTCATTGACGTCTCAGTGACGGACAAATCACAAAGGTGATCCGTCATTTTGAGTGTGATTAGTTGTAATTTGTAGCTAACTGTAATTCCCACTCCTGTCCAGCTGATGGCGATGTCGTTGTTTTGTCTCCTCTTTGTCACCGCTGCGTACAGTTGCAAAATTGTCACAGCAGCTGAGTGTGAGAAGTTTATTTAAACTGCCAAATTGATGTGATATTAATAATAAAGGTAAAAAAAAAAGAGGAAGTGATGCAGTGGACGATGAAGAACGAACAAAAATCCTCAGTCTCCGACAGCTGTTACGGCCGGGTCAACCAAGCGGCAGCATGTGAGGTGCGTTGGAGTGCGTTGTGAGCACTACCGGACTCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39069
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000127986 Essential Splice Site 1374 1667 35 41
Genomic Location (Zv9):
Chromosome 15 (position 43922694)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 45141713
GRCz11 15 45034842
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCGTTGCACAGTGAGAATATCTGTGTGTGTGTGTGTGTGTGTGTGCA[G/T]GTGATCTCTCAGCTGAGGATTCTGAGCAGGCCTGTCGCAGCAGGATCTAA
Long Flanking Sequence:
TATGTGGCTGCTAAGGATTTTAGCATGTCTGCCTGAACATCCTGTTTTACTGAATGAAATATGCAAATCACCCTCATTCAGCTCAATGTCGCTCACACACACACACACACACACACACACACACACACACACACACACATTCTCTTTGAGTTCAGATGTTACATCGCACTCCTATTTGTCACTGTCAGGTTTAGACTGATGTTAGCCACACACACACACACTGCTGTAGAGACTGTGTTTGTGTGTGTGTCTGTGTGTGTGTCTGTGTCTGTGTCTGTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTGTTTGTTGTAAGCTTTTGTAATGAGACCAATTTATCATGAGTAAGAATCGCCCACTGCAGCGTTTCCACAATCACAGAGAGATGGAGCATCGTTGCACAGTGAGAATATCTGTGTGTGTGTGTGTGTGTGTGTGCA[G/T]GTGATCTCTCAGCTGAGGATTCTGAGCAGGCCTGTCGCAGCAGGATCTAAGTTCGACAGAGAGATCTGGTCTAGTGCGCTCTCACCTGTGCTCAACCTGTGGAAACGGCTCAACCAGGTACCAAAACGTCACACGCAAGGTTTTAATTGAATTTGATGTATATATTGGATCTATATATATATATATATATATTGATATATTTGTGCAGTGATTTTTTTATTTATCCAANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTGCAACTAAAATAGAAGTATTACATGCAAAACATGCAATCAAATATAATATAAAAACTATTAAATATTCCTAATTAAATATAAATTAAAACATTTTCAAAATTATTTTTTACTCTTTGTCTTAATCCACTATTTTAACATGCAAACTCCACTCAGAAATGCCAACTGACCCA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa35999
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
ENSDART00000127986 Nonsense 1666 1667 41 41
Genomic Location (Zv9):
Chromosome 15 (position 43896445)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 45167962
GRCz11 15 45008593
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGAGATCATGACACGTGGATCCAGAGCGGAGCGGCTCTCTTCCTCAAA[C/T]AGCAGTAACACAAACACACACACTTTATACTGACATTAGCATCACTTTAG
Long Flanking Sequence:
GTGTCCTCCGTTCCTCCATGTCACATGGCTTGGATCCCGCAGGTAACACATACAGTTTGTCTCTAAATATCCTGTGAAGTGCTCTGAAATGTGCAGTTTTGCTTGATATGTGATGCAATTTAAACTGAAACATAAAGTGAGAGGGCGGGACAGAGTAGCTCCTCCTCTTTTTTTGATTACAGCCAATAGGGTAAAGCCATAGACAGCATTATTAACCTGAGAGAAAAACAATTGAAGTCTATGTAACATCCTCACTAAAACAGGAAAACAAACATGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGTGTGTGTGTGTTTCAGAGTGAGTGCTATGGGCTGTTATTCTCCAGACGAGTGTATCTCTCTGCCGGTGTACAGCAGTGCTGAACGTGTGTGTGTGGTGACAAACGTACAGCTGCCGTGTGCTGGAGATCATGACACGTGGATCCAGAGCGGAGCGGCTCTCTTCCTCAAA[C/T]AGCAGTAACACAAACACACACACTTTATACTGACATTAGCATCACTTTAGATTGTTTTGAGTGTCTTGGTCTTCATATGACGGTGTTTTTGCTGCATTCCAGCGGCTGTGAGACTGTAGTTTTATTCAGTCTTATATTCTGCAGATATTTATATGATCAAATAAACGAGTTTTCCTGGAGATCCCTCTCTTTCTCTGCTTTCAACACCACTGCATGTTTTGCATGAGTAAAACTGTACGTGCGTATGTCAGCCGAAACGTAGCATAGCTGTGAACAATGAGAAATTATGCAGCGTGAATGTGTGTGTTTATTTATTTATACTTTCTCTTGTTCACAGTGGTGTTCCGGCTGTTATTTGACATTACTTTGACAAAACAGTTCTTTCAAAAGTCTTTATTAATAATAAACTATAACTAATGTTTTGGGGTGGCATGGTGGCTCAGTGGTTAGCACTGTGGCTTTGCATGTTCTCCCCGTGTGGGTTTCCTCCGAGTGCTTCA
Associated Phenotype:
Not determined