ZMP
zgc:64105
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC393384 [Source:RefSeq peptide;Acc:NP_956706]
Human Orthologue:
C9orf68
Human Description:
chromosome 9 open reading frame 68 [Source:HGNC Symbol;Acc:25472]
Mouse Orthologue:
4430402I18Rik
Mouse Description:
RIKEN cDNA 4430402I18 gene Gene [Source:MGI Symbol;Acc:MGI:1918036]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa41082 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa16328 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa41082
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000008421 | Essential Splice Site | 162 | 338 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 72201451)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 69246470 |
| GRCz11 | 7 | 69484520 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAATCAGTGAAATCTCCAGCGACAATGGCTTCCTAACTCTTCCTGTG[G/T]TAAAAACAAACATAGATTTCGAAATGATCAGCTTTACTGCTTTATTTTGT
Long Flanking Sequence:
TGTTCGTATTGCTTCTAAGTTGGTTGATCAATACACTCAAAATACATTTTCATTTCAATTTTAAATTTAGGGAAAAAAGGTTTACACTTACAAAACTTGCTCTTGTGAATATGAAATTTGGCCTGCAGTGAGCAACGTCTCTGAAGCGGCGCTGACGGATCCACATTGCAGTTCGGCAACGCCTGGCGTCACCCATTCAAAGTGAATGGGAAGCGTTGACGCTGACGCCCCGTGTGAATGTGGCGTTATGTTGATTATCTTCTCTCAGAAAGTTAAAGTGTGATGAAATAGAGTTTTCTTTAGATTAGACTGAGGAAACACCTCTAGCATCTTTCATCTTTAGAACAAAAATAAATATCTGCATTATTAAAATTAAATTAAAATAGTTTTTTTTTTATATTGACTGATCATTTCAGGGTATCTCTCCAAGATTAGAGTTCTCCACGAAGACAACAATCAGTGAAATCTCCAGCGACAATGGCTTCCTAACTCTTCCTGTG[G/T]TAAAAACAAACATAGATTTCGAAATGATCAGCTTTACTGCTTTATTTTGTTGAAAACATTGTTTTTTTATCTGTAGAGGAGAATGAGGAGGAAAACCTCTAGAAAGTCCCGAAAACAGAGCAGCAGCTCATCCCTTAGACATCTCTCCTCTGCTCCATGCAGTCAAAGAAGAAACCACAACACAGACCAGGTATCAGAAAATAATCAGGGGGTGGCACGGTGGCTCAGTGGTTAGCAGTGTTGCCTCACAGCAAGAAGGTCGCTGGTTCGAGTCCCAGCTAGACCAATTGGCATTTCTGTGTGGAGTTTGCATGTTCTCCTCGTATTGGTGTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAAGTGAAGTGTAGTAGTGTGTGAATGTCCAATTTAGTTTATTCAATTCACCTATAGCGCATGTTTTTGGACTGTGGGAGTATGCATGTCTCTGAATAAATATCTTCAATAAATGTGTTCCACACCTTGATAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16328
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 |
|---|---|---|---|---|---|
| ENSDART00000008421 | Nonsense | 207 | 338 | 8 | 13 |
Genomic Location (Zv9):
Chromosome 7 (position 72203356)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 7 | 69248375 |
| GRCz11 | 7 | 69486425 |
KASP Assay ID:
2259-9816.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCTGTATGTTTTATTTTGTGCGCTGTAGGATCAGAGATCTTCTGGTTW[T/A]TCACCYGTCTCTGCCAGAAAGCCCAGATTTAGRAGTCTGTCACCACATCR
Long Flanking Sequence:
GATGCTAATGTTGTAATTCGATTCAATGATTTATGCAAAGCTAAGCTAAAAGTGCTCTTACCAGACCCGGATATCGGCTTCAGAAATGGTAAAACTCATCTGTTTATCTCTAGGGCAGTTGTAAAATTTGCATATTTTTAGCATTAGTATATTAAAATAAGCTTCTTCAATACTCTGATGAATGTCAATTTAATAGTGGTGCTTTTAAATAAGTGTAAACATTTGACATAACACTCAAACACACACTAATCGGTGCACCAATGAAATGTTCAACACTTTTGTGGGCGTAAGAAGTGCTTTTATAAATAAGTGTGAATTAAATGTAAGATGTAAGTTTTACCATATTAACTTGGGACAATACAGTATTGCATGCTTATATCCTGCCATGTGCACATAGTTGTCGCCAAATATGCACATATGAATATTAGGCCTTAGTTTCTTGTTTCTAAATCTCTGTATGTTTTATTTTGTGCGCTGTAGGATCAGAGATCTTCTGGTTA[T/A]TCACCCGTCTCTGCCAGAAAGCCCAGATTTAGAAGTCTGTCACCACATCGATCAAAACCATTGATAGATGCAGGTATGAACGCTGCAATACATGTATTTGCCATATTTGTTCATGCTGTTTTTTTTTAGCTTGGTGAAATTTGACATGCTTTGTTTAACCAATATGTTAATTTTTAAACCATACTTATAATATGCACCGCATGTTTTTTCTTCAGGAGACCTGAGAAGAAGCTATTCCAGATCTTGGGTTAGTTGTTTATATCATGTGTCATTCACTATATAACGGGGGCCAGCTAGTAAGTGCTGTGCAGGTAAACCTCACTCCTGTGACCTCTAAAGGTGCTCTTGTGACAAATGTTAGAGGCTGTGGTCTTTAGCCTCCTTGGTAGAGCAACTGACCCTCATGCGGAAGGTCGCCGGTTCGATACCTGGTCGGATCGGTTTGGCTGGTGTAGGACCAGCGAGGTTACATCTATACTCAAAAATACAAGCATAAATGA
Associated Phenotype:
Not determined