ZMP
zgc:100861
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC445137 [Source:RefSeq peptide;Acc:NP_001003531]
Human Orthologue:
FAM151B
Human Description:
family with sequence similarity 151, member B [Source:HGNC Symbol;Acc:33716]
Mouse Orthologue:
Fam151b
Mouse Description:
family with sequence similarity 151, member B Gene [Source:MGI Symbol;Acc:MGI:1921192]
Alleles
There are 3 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa33602 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33602
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 |
|---|---|---|---|---|---|
| ENSDART00000017696 | Nonsense | 146 | 296 | 4 | 6 |
| ENSDART00000108621 | Nonsense | 111 | 217 | 4 | 5 |
| ENSDART00000146363 | Nonsense | 146 | 252 | 4 | 5 |
The following transcripts of ENSDARG00000020024 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 27812613)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25567911 |
| GRCz11 | 5 | 26168064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCTGGCAGCTGTATCCCAATCCATGAGTCTGCTGGAAGAGGTCCGAGAT[C/T]AGCTGAAGGGTCCTGTGTGGATTAATGCTGATATTCTTCCTGGTCCTGGT
Long Flanking Sequence:
ATCAGAATGATCCTAGTTTAGTATAAATGGATCACTTTCTCCCCATTGCACCATCTTCATTTTGGAAGAATCCCCCCTTCCACCCCATCTCCTCCTTTTTCTCCCCTTCTAAAGGGCGAGAGATCGAGACCTACCTGATCTCGGTTCTCCTGATATGCTTCTAGACCGGGCGGGAGCCCTGGGCTCAAATATCTCCGAGCTCAGGGTTCTCTCCCGGGACAGCATGCCAAACCTGCTATAAGTGCCAAGCATATCTAAGTGGGAACTCTTGAAACATAAAAGGCAGCACAGAGACCAAACCTGAAGCTTCATTTTCATTTTCAAAAATGTTTATTATTTTTAAATCGTTTAATACTGCATATTGTCCTTACCCCGAATTCCTAGCAGATTATTTGTTGCTTGTATATATTGATTTATTTTGTTGATGAATGAAAGCCATTTTGATCGACAGTCTGGCAGCTGTATCCCAATCCATGAGTCTGCTGGAAGAGGTCCGAGAT[C/T]AGCTGAAGGGTCCTGTGTGGATTAATGCTGATATTCTTCCTGGTCCTGGTGGAACAGCCACCCCTGTGGACCCTCATGTTTTCCTGCAGGAAGTGGCTCAAAGATCAGAGAATGATGTTCTGTCTTTGGGCTGGACCACTGGATGGACTGAAGATGTAGACAATCCTGGTAAGATCATTGTTATGTTACCTGAGTAACCAGCACTTTAAAAAGTATGAGTTTTATTTTATTTATAATCGGAGATGTGCGCTAGAGATTCGCGGATGGGCTATTATTTAATCTGCAACCGCATCATAAAACTCATCATCCGTCCGCCATCCATCCGCACTAACATTTTTGACCAATTTTTAAAACCGCACCCGCCCGCCATCTGCTGACTGAGCTCTTTATTTGAATGGCTTTTTCCTTTTTATTATTAAATGAATGTTTCTTTATTGATTATTAGAAAATAGAGAATGACTTTAATGACATGCAGTTAATCCAAACGTGCAAGTCAAATC
Associated Phenotype:
Not determined