ZMP
si:ch211-262h13.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC571127 [Source:RefSeq peptide;Acc:NP_001038677]
Human Orthologue:
FETUB
Human Description:
fetuin B [Source:HGNC Symbol;Acc:3658]
Mouse Orthologue:
Fetub
Mouse Description:
fetuin beta Gene [Source:MGI Symbol;Acc:MGI:1890221]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37575 | Essential Splice Site | Available for shipment | Available now |
| sa43888 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37575
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104437 | Essential Splice Site | 133 | 384 | 3 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 41863376)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38831369 |
| GRCz11 | 22 | 38818114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAGAGGGTTTCTCTTACCTTTACAGCTATGACTGCACTCTCGTACCAG[G/A]TGAACCCCTCGTCCCAGTCAGACTGCATACATCTTCAACAGTTGCAAACA
Long Flanking Sequence:
TTAATTAATAATAATAAAGATATACAGTATATGCAATTTAGTATGAACTTATCTAACTGTGATTTGGAAATCTGATAGATGCACACCTGAATCATCCTGAACTGTACATTTTTTAAAATGTGTTGATTTTATTTCATTTTTGTTTGTTTTTAAAAAAATGCTGTTTAAAAGAAAAACAAAAATCTATAAATATATAATTGTAAAACATAAAATAAGACATTTAAGAAAATGTTGGAAACAAACAACATGACAGAAATGTATAAGGGGTTTAAACAGCTTGAGGGAAAGTACAGGGTGAGTATTTTCTCATTGTCATGCTGAAATATCCCATTGCTCATCAGGCATTATTATCGTTATTATGTAGGAGAATATAAGATTGCTAATACTGTTCCATTTTTTTCTTGTGTTGTAGCAAATTTCTGGCAACTGTAACACTACAGTACTTCACACACCAGAGGGTTTCTCTTACCTTTACAGCTATGACTGCACTCTCGTACCAG[G/A]TGAACCCCTCGTCCCAGTCAGACTGCATACATCTTCAACAGTTGCAAACAAATGAACCCTGCTGTTGTCCTAGAATTCTCTATAGACCATTCAGCCTTCACCAAACCTCCAAAATAAAGCAGCTACTTTTAAATGTCAATCCTCAAATTTATTTTGCTTACACAATCTCACGGAAATCCGTAACTTTTTGATTTAGTGGCTAATTCGTATGAATTCTTACAAACTAATTCGTACAATTTAGTATGATTTGCTCATCACCCAATGACGGTTGTGGTTGGGAGCCACACCTCCTTTTTAAAATTGTAAATTTTCGTATTTCGAATTAGCCACTGAACTGACAAAACGTAAAATACTTACGTTACCTCGTGAGATCAGGCTGATTTTGCATAAAAAACAACCTCATCGTAATTACAAGTCTAGATTTAGATTTGACCTTATTAGTGTGCATCAGCATGTACGTCATTAGTGTTTAATTCTTTTTCATTTGTAAAGATATTTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43888
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104437 | Nonsense | 223 | 384 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 22 (position 41860664)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 38828657 |
| GRCz11 | 22 | 38815402 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTCAGTGTTTATACTGTATCTGCTTCCACTTTAGCCTGTTGGATTCTG[T/A]GTTGGGACGGTTTTTGGCACTGGCCACGGATTGCAAGATGTGAAGGTGTC
Long Flanking Sequence:
ACCTATACAAGCTGACTAAAGGCCCCCAAAAAGAAAACAAATGTCATTGTGTTGATGCTGCCAAACTCTTAGGACAAAAAAGAGCCCTATAAAAGCAGTTCACTGGTGTTCATTCAAATGACATCCTCGTGTTCGAGTTGAAATCCAACTAGTTATTCAATAAAAATGCTGCATGTATGTGATGATGGTATTTCTTTAACGCTCTGCACTGATCATCGCCTTCTCCTGAAGTATTAAATCTTCTCCTGTTTGGTGTCTTAGAGCACTCCTTTTCCTGCCAGTTTCGTGGAGTTCATTGTTCAGGAGTGTTCAGAGGTTCAGTGTGCGCCAGCACTCGAAGGAAAAGAGGTGGGATTCCTGCTGAACGGCAGTTCGTCACCACTGTTAACCACTTCTGTTTTGCTATTCTTTTAATTTATGAAAGTTCTCTACTTAATCAATCTGCCTGATTACTCAGTGTTTATACTGTATCTGCTTCCACTTTAGCCTGTTGGATTCTG[T/A]GTTGGGACGGTTTTTGGCACTGGCCACGGATTGCAAGATGTGAAGGTGTCCTGTGAAATGTTTCGCCCACAGGTACCACATGGTAACATGAGACATTCACAGCTTTAAAAGCCGCTGACTGATAACTCAGTGTTACGAAACAAACTGAGCCAATCCCAGTCGAGTATTCATATTGTTTATAGAAGTTTAAAGACTGAAATAGACTCTGTATTTAGTTTCTTGCCTTGTCATTGTCAATAATGTGTCACAAGACAGATGACCCAAGTGCATTGTTTTATTAAAGAGAATAAAGGTCATTTGTGTTTAGTATTACTAGTCTGTAGTAGATGTTATATTGAGACCTTTGTAAGAGAAAAAGGGTTCATATTAATTAATCTCTTCTTGTCCTTGTTAACAGATCCCACAACAGAACAACTTAAAAATTGATCAAATTAAAATTGTGATAGAATTAGGGCATTTGATGGGTAATATTTTCAATTTTGCAAAGTTCTGTTGTGTTT
Associated Phenotype:
Not determined