ZMP
fam98b
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC780841 [Source:RefSeq peptide;Acc:NP_001073130]
Human Orthologue:
FAM98B
Human Description:
family with sequence similarity 98, member B [Source:HGNC Symbol;Acc:26773]
Mouse Orthologue:
Fam98b
Mouse Description:
family with sequence similarity 98, member B Gene [Source:MGI Symbol;Acc:MGI:1915465]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32177 | Nonsense | Available for shipment | Available now |
sa13030 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32177
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084268 | Nonsense | 204 | 358 | 6 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 53162486)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 52548053 |
GRCz11 | 17 | 52634353 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGTTCAGGAGGAGCTGGAGAAGATCAACAGCACTCTGTCGGCGGAGTA[C/A]GAGTGCCGGCGGCGGATGCTCATCAAACGCCTCGACGTCACTGTGCAGTC
Long Flanking Sequence:
TACTTCCATTCATTTTGAGATGTTAAATACGGCCGGTTCTGCTGCATGATGCTGCTAACGGATCTGTTCTTATGATATTACTCTAGTTTGTCTGTGTAGTCGTGAACACACGTGTTTGTAGAGCGAGCAGTTTATTATTCCTGGTCATTTCTCTCATAGGCAGCTGAATCGGAAGTTCTGAACCAATCGCAAAATCGAGCGCACACTGAAGAATAAGGCCACTAGATCAGCTCGATGATGTGTGTGAATATGAACACCCATAACCTGACTGTCCATGGTGTTTTCTGTGGTGGTTCAGGTCAATGTTCTGCTGGAGAAGCTTCCAGAAACACACATCGGAGCTCCAGCGCTGCAGAGGAGCATCAGTGCAGAGCAATGGGTGAGAGTGCGTCTGAGCTCCATCAGCTGTGTGTGTGTGTGTGTAAAGTGTGTGTGTAAAGTGTGTGTGTGTGTGTTCAGGAGGAGCTGGAGAAGATCAACAGCACTCTGTCGGCGGAGTA[C/A]GAGTGCCGGCGGCGGATGCTCATCAAACGCCTCGACGTCACTGTGCAGTCCTTCAGCTGGTCGGACAGAGCCAAGGTGACCACACACACACACACACACACACACACACACACACACACACACACACACTATATTTAAATCTTATGCTGTTTGTAACATTCCTGTATTGTGTTATTGACTATTGCAGTGTGAGTTTTGGCTATTTTTGACCGCTCATCAGAACGCTCTGATTTAATGTAGAAGTTACCACCCACTGCTCTGATTGGCTCACTGTTTGTCATATCAACATTGCTAAACAGACTGTGCACCAGCAGCAGGCATCAGTCTTCTGTGGAGGCGTCCGGCGGGAGAACTTTAGGCTTAGTTGAGCTTATGCTCACTGGCCGCTTTATTAGGTACACCTGTCCAACTGCTGGTTAACGCAAATGTCTAATCAGCCAATCACATGGCAGCAGCTCACTGCATTTAGGCATGTAGACATGATCTGCTGCGGTTCGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13030
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084268 | Nonsense | 325 | 358 | 8 | 8 |
Genomic Location (Zv9):
Chromosome 17 (position 53160459)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 52546026 |
GRCz11 | 17 | 52632326 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCACCTGGAGGAAGAGATCTGATGGAGGAGRAGGACRAGGGGCGGGATA[T/G]AGAGGAGGAGGAGGNNNNANNNTGGCAGACKGGTGGAGGAGAYGGCTGGAGGAC
Long Flanking Sequence:
TTGTTTTGAATGGGGGAAAGTGTAACGGGCAATATGGTGAATAAAGCCCCACCTACTAGTACAGGAGCCAATCAGTGATCACTATAGACTGAGATGTTAATTAATTGCCTCCAGATCCTGTCATCTTCAAACACCGCGTGTTCATTACGCGTCTGCATTGTCTTCTGAAGCTCAAGTCATTTAGTAAATAAAGATCCTACCACAGCAAACACAGTGTTTACTGTTGATATTTGGCGCCAGATAAACAGGAAGTGATGATTTTGTTCTTGTTGATAGAAACGCTGCTTTATTCGCACGTCTCATATATTTTATTGATGTGCACTCATTTTATTCGCATTATTGGATGGAGACATAGCTGCTGTCTCTGCTGTTGGTGTTCAGATCTTGATGGGTCGAGTTCCTGACCGCGGCGGGCGTCCGTCCGAGATCCAGGCTCCTGCACCGGAGATGCCCACCTGGAGGAAGAGATCTGATGGAGGAGGAGGACAAGGGGCGGGATA[T/G]AGAGGAGGAGGAGGGGGATGGCAGACTGGTGGAGGAGATGGCTGGAGGACAGGAAGATGGAGTCGAGGAGGAGGACGAGGAGGTGGACACTACTATCACTGACTGATGAACAGCAGAGACACTGGAGGACACTCTTTTTAAACGAGCGTGTGATTGATTCCTTTAGCTATTGAACTTGTACATGATTAGACTAGATCATGGAGACGATGAAGAATAAAGACAGGAAACACCACTAGTGAATACATATTTGAGCTGAGTTCACACAAATCACGACAAATGCATGAAATCAGAGGCAATAGCTGATTCAAGCGAGCGACAGTAGCATGGTGTGAATTGTTAAAGAGAGAATGGCCTGTGAGATATTTGGCTCGCTGAATATGTGGAGCTGTGGGAGATTCACAGTCCTGCTGTGTGAAAACAGGGTAAATGCAGGAATCAGTGAAATTCAATACCTGTTAAGACCTTTTAAGACACTTTCCATTTATTTTAAGACCTCATCG
Associated Phenotype:
Not determined