ZMP
unc119.1
Ensembl ID:
ZFIN ID:
Description:
Protein unc-119 homolog B [Source:UniProtKB/Swiss-Prot;Acc:Q90Z08]
Human Orthologue:
UNC119B
Human Description:
unc-119 homolog B (C. elegans) [Source:HGNC Symbol;Acc:16488]
Mouse Orthologue:
Unc119b
Mouse Description:
unc-119 homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2147162]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa34459 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa34458 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa34459
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 |
|---|---|---|---|---|---|
| ENSDART00000019907 | Nonsense | 91 | 243 | 2 | 5 |
The following transcripts of ENSDARG00000009629 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 41810866)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 39824446 |
| GRCz11 | 8 | 39858220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGACTATTTGTGTAAACTAGAGGACAACATCTACAATATTGACTTTACA[C/T]GATTTAAGATCCGAGACCTGGAGACTGGGACAGTGCTTTTTGAGATTGCC
Long Flanking Sequence:
AGAGTTTAAATGGTAATGGAAACCCTGGATGAGTCCAGGAATTTTGACATGGCTTTTTCAAGGCCTGGAACAGTTTTGGAAAAACGGAAATGGATTTTTTTTTATAAGTATACAGATTGTAAAATCTGTATACTTGAATGTATGCTAGTTGTCTTCTTTTCTGTGCTTGGCCAAGCACATACTTTTTACACTATTAGTGCTGTGGATTGTGGAAGTGTTATTTAAATACAATTAACATTTAAAATTAAATAGATTGCTGCATATTTTGCAATATAATGTAATAAATTTGATAGTGCATTGTTTTTCTAATTAATTGCCACAGATATGTAGACATTAAAATTTACTTAAAAGTCTTGAAAAAAATCATGGAATTATAGTAGGAAAATGTGTATGAACCCTGACTGTGTTCATCTCTTGTAATAATAAAGTACATGATGCATTTCCCCTCCACAGACTATTTGTGTAAACTAGAGGACAACATCTACAATATTGACTTTACA[C/T]GATTTAAGATCCGAGACCTGGAGACTGGGACAGTGCTTTTTGAGATTGCCAAACCACCACACTGTGGTATGTTATCTTTCTTTGTTTTCCAAGTTTCAGTTAAACCAATTGATGTAATCACACAGAGATTCTATCATCAACTTGACTTAATTTACACAAGATAAATTCAGGAGCCTTGAACAAATGTAAACCAAAATCTAAATGATTTGAAATTTTGTTACTTAACGCATGATGAATTATTGTGAATTTTCCATCTATGTATGTTTAAAAAATAACTTTAGTCAAAATGGCTTAACTGTTTTGTCTTAATTGTCTAGTAAAATGTCAGTCTAATGATGTGTCATCAGTGTTTCCTTTGCATTTCTGAAAATATTGTCATCCCATTCACATACAGTACATCTGAAAAAAAACAGCCCAGTGTACACAGTCACATAAAATAACATTTCTTAACATAGCATTGGAGGCCACCATTGTTGGTTTGTAAAAAATAATACAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34458
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000019907 | Essential Splice Site | 113 | 243 | None | 5 |
The following transcripts of ENSDARG00000009629 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 41808815)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 39822395 |
| GRCz11 | 8 | 39856169 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAATGTTGCTTTGACAACTAGCTAAAGTAATTGTTTGTTTGTTCTTTC[A/T]GACCTTGATGAAGAGGACGATGAAAACCGAGACGCTGACACCAGTGCGGG
Long Flanking Sequence:
TTGCAAAATAAGTGTACATTTAAGCTAAAGGTCTTTTTTGGTGCACTTTGTTAAGTTAACATGTAAGATCAAAGGATAATTTAGTCAAATTCCGTTTTTAAATATGATCGTTTTAAGTTGATATTATAAAAAAATAATGCGAACGTTAGACATTGTAAATGTATGTTTTAAAACAAATGGTTCATTTAACTTTCAACACATCTGTATTTAAAAAGGTTTATGATTTCATGTTAAAAACTATTTCCTTAAGAATAAACTGCATGGAACTTCTGTTTAGAACTTTAGGTCTTTAGTTTTGTCAATAATTTGAGTTATACTTTTTCATTTGTATTTTTTCCTTTATAACCTAAAGTTTATTTATTTTTTTTGTCAGTGTAGTTTTTTTGTTTTTGCTTTAGCATATAAAGTTTTCAGCTATTTAAGTACATCAACTTAAACTAAAAAAAGTTGAGAAATGTTGCTTTGACAACTAGCTAAAGTAATTGTTTGTTTGTTCTTTC[A/T]GACCTTGATGAAGAGGACGATGAAAACCGAGACGCTGACACCAGTGCGGGACGATTCGTTCGCTATCAGTTCACACCAGCATTCCTTAAGTTACGCACAGTCGGAGCCACGTAAGTCTCTCTAATAAACACAGCCATGTGGATTCTGCAGTGTAAACAAACCTCCGCGAGTCTGAAATTCACTTGACCAGCTTTCATGTTTAGAAACAAAGGCCCTTGTGTGTCATATCCTGCAACACTTGAGCAACGTCTCTAGCCCAATCCCACAGAAACCATGAATAAATCATGTTTTGACCTCAGTGATTTCTTCAGTTCTGTTGTAAACATAAGCAGACTTGTGTTAGTGTAGATGATTGTCAGATTGTCTGGTTTACTTTGGTGTTATTAAACCATTAAAGGCCTAATTAGTTACAGAAAACAAAACTGAATGGTCTTTTGGGATTGAATGGGTGATCATGAGCTGTTTTTTCCTTTACCTCACACTTCCTCAGGGTGGAGTTC
Associated Phenotype:
Not determined