ZMP
zgc:195212
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100189619 [Source:RefSeq peptide;Acc:NP_001128617]
Human Orthologue:
C11orf80
Human Description:
chromosome 11 open reading frame 80 [Source:HGNC Symbol;Acc:26197]
Mouse Orthologue:
Gm960
Mouse Description:
predicted gene 960 Gene [Source:MGI Symbol;Acc:MGI:2685806]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa35749 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa42440 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35749
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000128881 | Essential Splice Site | 45 | 562 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 14 (position 47012795)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 44329922 |
| GRCz11 | 14 | 44791234 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTGGTTGTCGTGAGAGCTCTGCGTGAATCACCTGCGACTTTAACCGG[T/G]AAAACACGAAGACACTACAGTCAAACTTTACTTAACGTTACTAGACATTA
Long Flanking Sequence:
GATAGACTTCCCTATTTACAATGTGGGAACTGGGAAGCACTAAAAAAAGTGCATGACAGTGGGCTGTAAAGAGTCCCGTTCAGCAGGCTTTAGCGCCATCTAGTGGATCGGGTGGGCAGCACAAGTACAAGTTTGCTTTCTGAAGGATGATATTTTGATTAAAAATACAAATGTATTGTGGTTTACGACAGGTATTATTGACGTGGGATTCTTTATAAGTTCCTTATGTGTTTTATTTATTTTTTGTTTGTTTGATTATTTGATTGGTTTTCTGAAAATGTTTTATTCGGCCTTTGTGTCGCTTTACGTTACTGTGACTGTATATTATACGCAAACACTTCTGTGAATATACTGAACATATTACTTTTTTAACTGATTTTTTTGTAGGTTTTGAGGTGTTTGTTTGCTTTAGTGCAGCGGGAATGTGGACAGTGCAAACGGTCAGGTGGACTGCTGGTTGTCGTGAGAGCTCTGCGTGAATCACCTGCGACTTTAACCGG[T/G]AAAACACGAAGACACTACAGTCAAACTTTACTTAACGTTACTAGACATTAGTACGTTCTGTAAGCTTTTTGAGTGACTTAAATTGTTTGTATTTATATTACATGTATCATGACACGTGCTGTCAGGTAAAGTTTGTTTTATATTCACAAATTCGTTCAGTGACAACTTGTCCCTACTGAAAAAAACATCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTCGACCAGGCTGGTTTTAGAGGGGTTTTGGCCATTTCCAGCCTGGTTTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCGTGACCAGCCTAGCCAGGCTGGGAGCCCAGCCAAAACCAGCTATGTCCAGCTTAAACCAGGCTGGTCAAGCTGGTTTTACCTGGATTTAGCTGGTCATTTTCCAGTCTGACCAGCTAAGACCAGGCTGGAAATGGCTGGAAACCAGCCTGGAAATGGCCAAAACCCAGACACTGCCTATATTGTTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42440
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000128881 | Essential Splice Site | 546 | 562 | 15 | 16 |
Genomic Location (Zv9):
Chromosome 14 (position 47024465)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 14 | 44341592 |
| GRCz11 | 14 | 44802904 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCCAGAATGACTGAAGACAAACCCTCAGTTAAACTGATAAATGAACAG[G/A]TTGATACATCTATAGCTACAGTTTAAGTCAGAATTATTAGCACCCTGTAT
Long Flanking Sequence:
AAACTAAATTGGCAATGGTGTGAATGAGTCTATATGTGTGTCCCAGTACTGGGTTGCAGCTGAAAGGGTATCCGCTGCGTAAAACGTTTGCTGGAATAGTTCATTCCGCTGTGGCGACCTCTGAGAAATTAGAGACTAAGCCGAGGGAAAATGAATGAATGAATGAAAATTTGTCTTCCTAATTCAAGTCTTTCGGCAGCTATTGACATTAAAGCAGCACACACATCATTTATAGTTGTCTGAGATTATTGTGTTTTGATTTATGTTTTCCAGCATTTGAAAATCCCCCATTACTGTCTTCTAAGAGGATTCACTGCGATCTTGAATCTTCAAGTTTCATCTCTGAGAAGAGGCAATGCACAGAGCCGTTCTCTGAAGATTCAGACACAAATGAGACATCAGACTTCCAGAAAAGTCCCTTTTCTCTTGTCCATCTTCCTCAGATTCAACAAGCCAGAATGACTGAAGACAAACCCTCAGTTAAACTGATAAATGAACAG[G/A]TTGATACATCTATAGCTACAGTTTAAGTCAGAATTATTAGCACCCTGTATATTTTTCCCCAATTTTTGTTTAATGGAACAGAATTGAAGGATTTAGAGTATGAAATCAGCATAAAACCAGAGAAGTTTTTTTTCAACACATTTCTAATCATAATAGTTTAATAACTCTGTCGTCTGACTTGTTTTTTGGTCCTCAATCTGGCAACCTGCACTTGCGTTTGTTTTGATCCAGGAATGCAATATCTAGTTAAACCACTGGTTGTCAAACTTACATACTGCATCTTTAACCATCTTTTAGGAAATATAGTGATCAAAAATAAAGTGAACACTATAACTCCAAGTCCTGGGGCTAATATTTGTGAATTCAACTGTATATTAAATGCTGTAAAACGCACATTTAATCTGTAGCCCAGCTCTGTCAAAAAATATGTGTGTTGTGTGCATGTCTGAACTGTTTTTTTTTTATGTTTTTGAAGGTGGAGGAGCAGTGGCTTCAAGAGC
Associated Phenotype:
Not determined