ZMP
si:dkeyp-86b9.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate dynein, cytoplasmic, heavy polypeptide 1 (DNCH1) [Source:UniProt
Human Orthologue:
DNAH10
Human Description:
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:2941]
Mouse Orthologue:
Dnahc10
Mouse Description:
dynein, axonemal, heavy chain 10 Gene [Source:MGI Symbol;Acc:MGI:1860299]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa20435 | Nonsense | Available for shipment | Available now |
sa6980 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20436 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20435
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087708 | Nonsense | 571 | 3330 | 10 | 58 |
ENSDART00000135878 | Nonsense | 1597 | 4262 | 24 | 70 |
Genomic Location (Zv9):
Chromosome 5 (position 29978050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27733348 |
GRCz11 | 5 | 28333501 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATGAAGGAGAGAAGCAGGCACTGAAGCAGTATGCAAAGAAAATGCAC[C/T]AGCAGATCAATGACCTGGTGAAACGCATCACAGAACCCTTAAAGAAGAAT
Long Flanking Sequence:
ATTGACAGATGTATGACAACATAGCAGCTTTGCGTTTCGATACGGGAATGAATGGAGAGATGGTGGCAAATGCACTTGTGTCTGCTGAGGGGGAGGTGATGGAGCTCAAACAGCCTGTACCTGCAGAGGGCCGCGTGGAGGACTGGATGACTGCGGTGCTGTTGGAGATGAGAAGAACCAACAGACTCATCACCAAAGAGGCTATTTACTTCTACAGCCACCAAAAGTCAAGGTAAGTCCAATATTAAATGCCATGCTACACAATCATGACCCAGCACTATCAATCTAAGCTGATCGCTTGCCTTTCTGATTATAATTTGCAAGAAGTTTATAAAATGGTCTTCTGCTGTTCTGTCAGAGTGGACTGGATGCTTGACTACCAGGGTATGGTGGTACTAGCAACAAACCAGGTATGGTGGACCTATGAGGTGGAAGATGTCTTCAGGAGGATGAATGAAGGAGAGAAGCAGGCACTGAAGCAGTATGCAAAGAAAATGCAC[C/T]AGCAGATCAATGACCTGGTGAAACGCATCACAGAACCCTTAAAGAAGAATGACAGACGAAAAATCAACACTGTCCTCATCATTGATGTCCATGCTAGAGATATTGTGGACTCTTTTGTCAGAGACAGGTACGATACAAACAACGTGCAGTCATTTACTGTGTTACACAGTAAATCAAAAATGGAGGAAAACTATACTCTAAAGTGAAAATTCTATTTTTTTTTACCTTGTGTGATCCAAAATGTACATGACTTTGTTCAGATGAACATAAGTCTCTTCAAGGCAAGTCATTTTACTCGGCAGCCATCTTTGAAACGCCTCTCGGCCAGTATGCTTGGGCATTCTGTTTGAATGGAAAACATCAAATTCTCCAAAAGTACTTGCCAAGCTTGTGATTACATTTCGTATTACGAATAGCCAGCAAAATTAAACAACAACTGTCTATTTAGTTTCATTTCTAAATGTTCATATCACACAAAATCTGCAGAGACTCACGTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6980
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
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 |
---|---|---|---|---|---|
ENSDART00000087708 | Nonsense | 1437 | 3330 | 26 | 58 |
ENSDART00000135878 | Nonsense | 2376 | 4262 | 38 | 70 |
Genomic Location (Zv9):
Chromosome 5 (position 29993908)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27749206 |
GRCz11 | 5 | 28349359 |
KASP Assay ID:
554-5010.1 (used for ordering genotyping assays)
KASP Sequence:
TCATTGCAGCCATGGGGAAGGCAGGYGGTGGTAGGAATGAAGTGGACCCA[C/T]GATTCATMTCTCTTTTCAGTGTGTTCAACATCCCCTTCCCTGAGGAGGAA
Long Flanking Sequence:
TGCCTTAATTAACAGCATCATTATAAGTAAAATATAATAAACTACAATAATGAATATAATATAACAAATTAGTATAATAAGTCTCACCTTTTCCCAGATAATGATGACCATCAATTTCTCATCAAGAACAACCTCTATGGACCTGCAGAGGACTCTGGAGGCAAATGTTGAAAAGAGAACCAAGGACACGTTTGGTCCTCCTATGGGCAAAAGGCTCCTTGTCTTTATGGATGACCTCAACATGCCAAGGGTAACACTGTGTTTATACTGTACATCATCTCTCAAATCAGTTTTACAACACTGCTCATAATGGATTCACATTTGTTTGTTCTCAGGTGGATGAATATGGAACTCAACAACCTATAGCTCTCCTCAAGCTTCTGTTGGACAGGGGTGGCATGTATGACCGAGGAAAAGAACTCAACTATAAACTCATAAAGGACCTGGGCTTCATTGCAGCCATGGGGAAGGCAGGCGGTGGTAGGAATGAAGTGGACCCA[C/T]GATTCATCTCTCTTTTCAGTGTGTTCAACATCCCCTTCCCTGAGGAGGAATCCCTACATCTCATCTACTCTTCTATTCTAAGAGGACACACCAAGGTGCAAGAGATATTTCAGCTTCTTGATTAAAAAATGATGGGATGTGCTGACATGAAGTCAAATATTAAATATAGGTGTCTATTGTAGGGCTGCACTGATGGAATGAGATATTTCTTCATTGCAATTATTTTCTCATGTTGTGTTTATAATTTAGATTTTCGTATAAATATTTATCTTGATTCTATTTTATGATTTTTAAATCAGAATTATGTCTATTTTATTTTATAGCCCTTTGAGGAGTGCATCCGAAACATCTGTGACAAGCTGACGTTTTGCACTCTGGAGCTGTACAAAACCATAATTAAGGATTTACCGCCAACACCTTCCAAGTTCCACTACATCTTTAACCTGAGAGATCTCTCCAGAGTCTACCATGGCCTGACGCTGACCAACCCTGAGAGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20436
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087708 | Nonsense | 3187 | 3330 | 56 | 58 |
ENSDART00000135878 | Nonsense | 4119 | 4262 | 68 | 70 |
Genomic Location (Zv9):
Chromosome 5 (position 30021643)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 27776941 |
GRCz11 | 5 | 28377094 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGGTGCAGGTGAATGAAGGAGAGCCGTACGTGATGTGGCTCTCAGGTT[T/A]GCATATCCCTGAATCGTACCTGACTGCGTTGGTCCAGGCCACGTGCAGGA
Long Flanking Sequence:
GCTGTTACAAGGTATTAAATTTTGCATCATTTTTGATTATACAGTTATATAACGTTATTATAGTTGTTAACTAAAGTTAGAAATTTTGGGATGCTATGTAGTTTATGAAATTGATAGAATCCTGCCATACTTGATGTCGCACTGCTCTGTTTACTACAGTAACGAAGGCAGCACCATTATTTTTGCTGTTCTATAGGCGACACCTTATGGATTAACATTTTTATAAAGTATATGAGTATTGTTTCAGTTTAGGATTAGTTTCTTACAATCCATATTTAGGGAATATATTTAAAATGTCACTAATGTTACTGGTTCAGTAGTGATAATGTCTTAAAATGTATGAAAAGAGTGTAAAAAATGTCTTAAAAGGTTTTAAATTTTACTCTCTGATTCCTGTATATACCCTGTTTTAAATGTAATGAATGGCCTACTAAATAAATGCCTTTTTTCATTGGTGCAGGTGAATGAAGGAGAGCCGTACGTGATGTGGCTCTCAGGTT[T/A]GCATATCCCTGAATCGTACCTGACTGCGTTGGTCCAGGCCACGTGCAGGAAGAACGGCTGGCCTCTGGATCACTCTACTCTCTACACACAGGTCACACAATACAGCAGCGAGGACCAGGTCAAAGAGAGACCAGGACAAGGTGAGGGCATGTGCACTAAATGAACACAAAGATACTGTGAGTCAAGAACAGACTGAAAACACGCTCTTTCCGTTTTTGTCTCTCAGGATGTTTTGTATCAGGACTGTATCTGGAGGGTGCAGACTGGGACATTGACAACGGGTGTTTGGTGCGCAGCAAACCAAGAGTCCTGGTGTCTCAGCTACCCATCCTCAAAATCATCCCTATTGAAGCACGTCGCCTCAAACTACAGGCAAGACTTTCCTTATTAAAAACAAGAAACTACTGGCACCTCTGAGTTTAAATTGATATTTTGACCTTTACGGATTTTCTATTTTTTCCATTTATTTTTTTCATTCTAATGGAAAGAAAACATCCAAA
Associated Phenotype:
Not determined