ZMP
unc5b
Ensembl ID:
ZFIN ID:
Description:
unc-5 homolog B [Source:RefSeq peptide;Acc:NP_001104619]
Human Orthologue:
UNC5B
Human Description:
unc-5 homolog B (C. elegans) [Source:HGNC Symbol;Acc:12568]
Mouse Orthologue:
Unc5b
Mouse Description:
unc-5 homolog B (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:894703]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9232 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35510 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1 | Nonsense | Available for shipment | Available now |
sa13358 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9232
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 |
---|---|---|---|---|---|
ENSDART00000045951 | Nonsense | 94 | 911 | 2 | 16 |
ENSDART00000109546 | Nonsense | 123 | 940 | 3 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 29419602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29065550 |
GRCz11 | 13 | 29196000 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTAGTGAGAGAAGTAGATATCTCTRTCTCCCGGACGCAGGTAGAGGAGT[T/A]GTTTGGGCTGGARGATTATTGGTGCCAGTGTGTTGCCWGGAGCTCGGCAG
Long Flanking Sequence:
AGAACTTAAACCAACTGAGTACTGAAAACCCAATAAGTTAAGGCAACTCAAACCGTTTAAGGAAACTGATTGCTGCAAACCATTTGAGTAAAAAAAAATGGATCTATATGAGTACTGTGAACTTAATCCATTTAAGTTGAAGTAATGAGGTATTTAATTTCTCTGAGTTCAAAACTCTTTTCAAATGAGTAGAATTAACTTTTAGTAAAATATGAGTTACCTACACTTATTTCATTTGATAAAGTTGACTGTTGGGTTTTACAGTATAATTTTGTTTTAAATGTATTATTATTAAATCTCCAAAATGCATCAATATAAACACAAGTGTATTATTTTTAAACAAAACAGTGTTGCAATTTCCCTTCCTCTGTCAGGATGTATAGTGACACAAATTTGAAAGCTGAGACTGATATATTCATACTTTCCTCTTTTGTTCTCTGTCTCAGGTCTGGTAGTGAGAGAAGTAGATATCTCTGTCTCCCGGACGCAGGTAGAGGAGT[T/A]GTTTGGGCTGGAGGATTATTGGTGCCAGTGTGTTGCCTGGAGCTCGGCAGGCACCACAAAGAGCCGTCGGGCTTACGTCCGCATCGCCTGTGAGTTTGTGTTCAGCAGCTTATGTGATCTGTCGGTGTGACGTGCCTTTTAGGCATCAAACTCTGCCTGGAGATGACAGCACCTGAAGAGAACCCTAGTATTTTGAATTTAAAACACTCCCTATTTTTACTTGTGCTATTTTAATCCAGAACACATGAATACATATTTCCATATAATTAAAAAATGGAAACCCTTTTTGGTTGTTTTGGATTTCAAAAAATATGATCTGTTTGTTTTTTTCAGACTTGAGAAAGAACTTTGAGCAGGAGCCGCTTGGCAGGGAGGTGCGTCTGGAGCAGGAAGTATTACTGCAGTGTCGTCCACCAGAGGGCAGCCCGCCTGCTGAGGTGCTGTATTGTCTTCCTATGCTTTTTGCATATTTTACAGTCTATGATATAGAGGTGGATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35510
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 |
---|---|---|---|---|---|
ENSDART00000045951 | Essential Splice Site | 219 | 911 | 4 | 16 |
ENSDART00000109546 | Essential Splice Site | 248 | 940 | 5 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 29422670)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29068618 |
GRCz11 | 13 | 29199068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTGGTCGCTAAGAGACGCAGCAGCACTGCCACTCTCATCGTCTACGG[T/C]AACCACTTGACCAATTGCAGTCCCTGCATCAGTCTGAGTCACTGAGTGCA
Long Flanking Sequence:
AATTGTGCAAATGTTTTTTTTGACCCTGGATTAAATTTTCAATTATATTTTAGGATGCAAAGGTTAAAATTACATCAAATTTAAATATATTTAAAATGTGTAAAGATATTTAATTGTTCCTCACATTTATTTATATTTGAAATAAATATTGCCATAAATTATTTTATTTTATTTTATTTACCATATGGTGGAAAACATCTTTTAGAGCACGTCTGGTGCTTTTTAATGTTCTATTAAAATAATTTAAAGTGCAGTTTTGGTCCAGATGCACATCGTTGTTCTTGTAACTTTATGCATTGATTTTTTGTAATGTCACAGGTGGACTGGCTAAAGAACGAAGAGCTCATTGACCCGGCGCTGGATTCTAACTTTCTAATTACCATCGAGCACGACCTGATCATCAAACAGGCTCGACTCTCTGACACTGCCAACTACACCTGTGTGGCACGTAATGTGGTCGCTAAGAGACGCAGCAGCACTGCCACTCTCATCGTCTACGG[T/C]AACCACTTGACCAATTGCAGTCCCTGCATCAGTCTGAGTCACTGAGTGCACAAGTCAAGGGCTAATTCGGAAAACAGGAGAACTACAATCACCACTCGAGTTTATGAATATTTATAACATGGCTATCTGAAATACTCGCTACTTATTGGTCAGCTCTGGTATTCGACAGTCTGTAATGGTTGTTGTATTAATATATGACTATTTGCCTACTTGTGCTTATATAAATATACACTCACAGAGTTGAAATTGAAACTGATGTTAAATTGTAGTTCTTTTTCAGATATTTCCAAGTGATTTTTAACATATCAAGGAGATTTTTATCAGAATTTTCTTTAATATTATTATATATTTAGTGAGTATTTCCTATAAATAAATTAAGACTTTAAATTGCACTTTAAGCTGAATACTAGTATCTTGCAAATGACTTATAAAACGTTATCTACTGACTCTTAGAAAATATTTGAATATTTTATTTTATTTTATTTTTTTGTATTTAAGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045951 | Nonsense | 232 | 911 | 5 | 16 |
ENSDART00000109546 | Nonsense | 261 | 940 | 6 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 29424359)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29070307 |
GRCz11 | 13 | 29200757 |
KASP Assay ID:
554-0142.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTTATTAGTAAGTGGAGGCTGGTCATCCTGGACAGAGTGGTCAGAATG[T/A]AATGCTCAGTGTGGGCGGGGCTGGCAGAGACGGACACGCAGCTGCACCAA
Long Flanking Sequence:
GACCAACAGTATGATATCCCTCAATTAATGCACAACGTGTTTACTTTTGTATTCAGACTTGTGTTAAATTTTTATTCTTTCATTTTTCATTGACTGTTTCAAACATGCTCCATTCTATTCTAATTAAACTGCATGCCAATGTAAACATATCTGATTAATATCTGATCCTGTATTAATAATATGTGTCTCTGGCTGTCTGGTATTAGTAAAAATCCTTCAAATATGACACAAAGGGGTTACTTTTGCATGCTTGCTTGTATTTGTTTTTTATTTTTCTCATTTTCCAAACACTATTTCAAACATTCTCCCTTCTCGTCAGATCTCATCGATTGCCTAAATTCACTGAGAAATGGATAAAAATATTCATTTTCAAAATGGGGTGTACTCAATTATACTGAGCACTGTACACATTCTTGATAAGCTGTATTAATAGTATTTGTCTCTGGCTCTCTGTTATTAGTAAGTGGAGGCTGGTCATCCTGGACAGAGTGGTCAGAATG[T/A]AATGCTCAGTGTGGGCGGGGCTGGCAGAGACGGACACGCAGCTGCACCAATCCAGCACCACTCAATGGAGGAGCCTTCTGTGATGGACCGCCCTTCCAGAGAGTCACCTGTACCACCCTCTGTCCAGGTAAACGCTCAACACAAATTCACCCCTGTAACCTTTGACCTGAGCCACTGTGTAATCACTGATGTGTTTTCCTAGTGGATGGAGGCTGGACCGAGTGGGCCAAGTGGTCTGCGTGTGGGACGGAGTGCACACATTGGCGCAGTCGTGAATGTCAGGCTCCACCGCCACGTAATGGAGGACGACACTGCAGCGGCAGCATGATGGAGAGCAAGAACTGCACTGAGGGATTATGTGCACGCAGTAAGTCATGTGATTCAGCATCATCAGTGGGAAAATGTCTTGGAATGTTGGTCTGGATATCATATTAACAAGTGGCAGATATGGAACTGGTCCACACTGGGGTTATTGCTGACTGTCAGCAAAATGTCAATAT
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:
sa13358
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000045951 | Nonsense | 627 | 911 | 12 | 16 |
ENSDART00000109546 | Nonsense | 656 | 940 | 13 | 17 |
Genomic Location (Zv9):
Chromosome 13 (position 29440311)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29086259 |
GRCz11 | 13 | 29216709 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACTAGGAGGTGCTGACTGTGGGAGAGGAGAGTCTRTCGTCACCCTGTTA[T/A]CTGCAGGTGGAGGAGCAGAGTTGTCATATCCTSATGGAGCAGCTGGGCAC
Long Flanking Sequence:
AGTCTGTTTCACTAGTAAATATCTCTTTATTCTTTAGATTTGCTCCTTTTTTTTTTTAAATTGTTTGGTATAATCTAATTACACAAGTTAGCAAAATAAATAACCCAGTTCTAGTGCCTAGTGTAGAACCAGTTAATTGTTTATTTTAACAATATTTTTATTGTAAGTACATGTCAAATGCTTTAACAAGACATTTACATTTGTGTTTTTTGCTGTGCTTTGTTACTCTTTGGAGCTGTTCATATGAATGATTATAGCATGTGAACATTGCCAATCGAGCAGCGTTTAGTTACCTTTTAAGGCACAAACAATATATTGAATATTTATCAAACACATGTCAAGGATTTATTGTAAGATTATATTGCAATGATTATCATTATTGTTTTACTGCCTAGCTTCACATAATTAACATTTGAACAGTATTGCTTTAACTCCTGTTTTCCTCCCATCCACTAGGAGGTGCTGACTGTGGGAGAGGAGAGTCTATCGTCACCCTGTTA[T/A]CTGCAGGTGGAGGAGCAGAGTTGTCATATCCTGATGGAGCAGCTGGGCACTTATGGGCTGGTGGGACAGTCGGCTCCTCCTCGGCCGGCCTGTAAGAGACTGCAGTTGGCCCTGTTTGCCCCTCGGGCCCCGTGCCTCTCTCTGGACTACAGTCTGAGGGTTTACTGCATACAGGACACCCCACATGCCCTCAAGGTTAGTCTGTCTTCCCTTCTTAACTAGCCATCTCATGTGTATTTGACCTGTGAATAAGCTATAATTCTGTGTTGTTGTTTTCTGCAGGAAGTATTAGAGGTTGAGAGAAGTCTGGGTGGGGTTTTACTGGAGGATCCCAAACCTTTGCTTTTTAAGGACAGTTACCACAATATGCGGCTGTCGATCCATGACATCCCTCATTCACACTGGAGGAGCAAACTCCTGGCTAAGTATCAGGTGAGAGACTTTATGCTGTTGTTGGTCATATGGTTATCCTTTTTTTAGTTAATTAACTTTTTATAATA
Associated Phenotype:
Not determined