ZMP
fam160b1
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC100038786 [Source:RefSeq peptide;Acc:NP_001083035]
Human Orthologue:
FAM160B1
Human Description:
family with sequence similarity 160, member B1 [Source:HGNC Symbol;Acc:29320]
Mouse Orthologue:
Fam160b1
Mouse Description:
family with sequence similarity 160, member B1 Gene [Source:MGI Symbol;Acc:MGI:2147545]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1584 | Nonsense | Available for shipment | Available now |
sa28195 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15432 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1584
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084474 | Nonsense | 342 | 503 | 8 | 11 |
ENSDART00000127930 | Nonsense | 342 | 747 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 44252509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 43489624 |
GRCz11 | 13 | 43623449 |
KASP Assay ID:
554-1526.1 (used for ordering genotyping assays)
KASP Sequence:
GACGCTGCTGCTTTTGCTGGCAAACGTGCACTTATTTCCTTTTTATCGTG[G/A]CTGGACTATTGTGATCAGCTCATCAAAGAGGCTCATAAGGTAAAATCAAT
Long Flanking Sequence:
TATCCATCTATCCATCTATCCATCTATCTATCTCTCTCTCTCTATCTAACTCTATATCTTACTCTATCTCTTTCTATGTCTATCTTTATATCTCTCGCTGTCTTTAATACAAGTTAAACTAAATATTAAATTTAATTTTTAATGTAAATATAGTTTTCTACATATCCTTTTTTCACTAAATGACAAATAGTAAATTAAATTAGTTTAATTTATATCCAGCTATATAATATTTACCTGTTTTTTTTTTTGCTAATAAGTTATAATATTAACACGTCCAACTGTTTTAAAAATGTTTTTAATCATCTGATATTCATTTTATTTTTTGCCAATAAAATAATTTAAAAGATATTGCTATATGTTCTATATTGCCTAGAGATGTGTTGAACTGTTTTGGATGTTTGTTAAAAGTGTATGTGTGTTTGTAGGCTGGATGTGTACAATCTAAAAGAAGACGCTGCTGCTTTTGCTGGCAAACGTGCACTTATTTCCTTTTTATCGTG[G/A]CTGGACTATTGTGATCAGCTCATCAAAGAGGCTCATAAGGTAAAATCAATACAAACAAAAAACACAAATTTAACCAAAACAATTATTTATTTTCATATCAAATAAATGGTTTCATAATTATTTTTTATTTATATTTTTCTATTTATTTTTTTGTGTTTTTTTTTTATTTCCCTACTTTATTCATTTGTTAATAAATTTCTTATTATTTTTTATTTAATGTTCTATCACTTTATGCATATATGATTTGTGTATATTTGATACTTTATATTATTATTATTATAATGTATTTATTTTTATTGTTTTATTTTTTAATGTTATATCATTTCATGCATATATGCTTTTGTGTATGTGTAATACTTTATATACTTTAATACTTTAATACTTTACTTTATACTTTAATATATATATACATTTTAAAGTCAAAATTATCAGCCCCTTTAAGCTCTATATATATTATACTCATGGTTTTTTTGTAACTTATTTTGTGTTTGATTCCTCTG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa28195
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084474 | Essential Splice Site | 355 | 503 | 8 | 11 |
ENSDART00000127930 | Essential Splice Site | 355 | 747 | 8 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 44252468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 43489583 |
GRCz11 | 13 | 43623408 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATCGTGGCTGGACTATTGTGATCAGCTCATCAAAGAGGCTCATAAGG[T/C]AAAATCAATACAAACAAAAAACACAAATTTAACCAAAACAATTATTTATT
Long Flanking Sequence:
CTATCTAACTCTATATCTTACTCTATCTCTTTCTATGTCTATCTTTATATCTCTCGCTGTCTTTAATACAAGTTAAACTAAATATTAAATTTAATTTTTAATGTAAATATAGTTTTCTACATATCCTTTTTTCACTAAATGACAAATAGTAAATTAAATTAGTTTAATTTATATCCAGCTATATAATATTTACCTGTTTTTTTTTTTGCTAATAAGTTATAATATTAACACGTCCAACTGTTTTAAAAATGTTTTTAATCATCTGATATTCATTTTATTTTTTGCCAATAAAATAATTTAAAAGATATTGCTATATGTTCTATATTGCCTAGAGATGTGTTGAACTGTTTTGGATGTTTGTTAAAAGTGTATGTGTGTTTGTAGGCTGGATGTGTACAATCTAAAAGAAGACGCTGCTGCTTTTGCTGGCAAACGTGCACTTATTTCCTTTTTATCGTGGCTGGACTATTGTGATCAGCTCATCAAAGAGGCTCATAAGG[T/C]AAAATCAATACAAACAAAAAACACAAATTTAACCAAAACAATTATTTATTTTCATATCAAATAAATGGTTTCATAATTATTTTTTATTTATATTTTTCTATTTATTTTTTTGTGTTTTTTTTTTATTTCCCTACTTTATTCATTTGTTAATAAATTTCTTATTATTTTTTATTTAATGTTCTATCACTTTATGCATATATGATTTGTGTATATTTGATACTTTATATTATTATTATTATAATGTATTTATTTTTATTGTTTTATTTTTTAATGTTATATCATTTCATGCATATATGCTTTTGTGTATGTGTAATACTTTATATACTTTAATACTTTAATACTTTACTTTATACTTTAATATATATATACATTTTAAAGTCAAAATTATCAGCCCCTTTAAGCTCTATATATATTATACTCATGGTTTTTTTGTAACTTATTTTGTGTTTGATTCCTCTGTTATGTTAGTCAGCTGCTGCAGTTCTGGCTCGAGCTGTAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15432
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084474 | Nonsense | 484 | 503 | 11 | 11 |
ENSDART00000127930 | Nonsense | 484 | 747 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 44249368)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 43486483 |
GRCz11 | 13 | 43620308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAACCYGGTGCKRCGCTGCTTGGAAGAAAGAAAYTACAGCGAGAACAAA[C/T]AGCAGGAGGAGCGAGAGGAGCGCGAGCACATGGAGAACGGCCAACCGCAT
Long Flanking Sequence:
CCAATCAGATTTGAGAACCAGACAGAACTGTTGTATGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATCAGAGTATAATATTTGTTTTCTTATTTATACCTTTTCCTATAAATAATTTTTTTAAAATATATGAACTGTACTTTCATGTACATTTAGAATGAATAAATAACAACTGTATATATTATATCATGCCTATAAAAGAATATTATTGGATAGTTATCTCGCCATACATCTCCAACTCCAGCAGTTTTCAATGTTTGACCTTCCTGAAGTCCTGATTCTGTCTCGTTTTTAGATAAGTATCATGACCCTACGACTCTTTGAGCATCTGCTCCAGAAGCCATGTCAGCACATTCTTCAAAACCTGGTGCTGCGCTGCTTGGAAGAAAGAAATTACAGCGAGAACAAA[C/T]AGCAGGAGGAGCGAGAGGAGCGCGAGCACATGGAGAACGGCCAACCGCATGACGCCGTGTAAGAGCTGCTGTGCTTCAGATTGATGCTTCTAGTAAATGCTCAATGCTCAATCATTAATGAACTGCAATTTCTCAATGAATAAACCTCAATGCATGTCAAATGTTTTGCATTTTGTACAGTGATGCTTCGAGGACAACACACACACACTTAATACACAATTACACTTCATTAAACATGTACACATAGACGTCACCTATATACTGTATAACTGCAGGTGAACTTTTTATACATAATAACTTTATTTTCTTTTCGGTTTAGTCACTTTATTTATCAGGGGTCGCCACAGAGGAATGAACTGCCAACTTATCCAGCACATATTTTACTCAGCGGATGCTATTCCAGCTGCAACCCATCACTGGGAAACACCCATACACTCTCATTCACTACGAACAATTTAGCCTACCCAATTCACCTGTACTGCATGTCTTCGGACTGGGGG
Associated Phenotype:
Not determined