ZMP
ilvbl
Ensembl ID:
ZFIN ID:
Description:
Acetolactate synthase-like protein [Source:UniProtKB/Swiss-Prot;Acc:Q6NV04]
Human Orthologue:
ILVBL
Human Description:
ilvB (bacterial acetolactate synthase)-like [Source:HGNC Symbol;Acc:6041]
Mouse Orthologue:
Ilvbl
Mouse Description:
ilvB (bacterial acetolactate synthase)-like Gene [Source:MGI Symbol;Acc:MGI:1351911]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10157 | Nonsense | Available for shipment | Available now |
sa19208 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa36724 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10157
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 |
---|---|---|---|---|---|
ENSDART00000016271 | Nonsense | 23 | 621 | 2 | 16 |
ENSDART00000145190 | Nonsense | 23 | 242 | 1 | 6 |
ENSDART00000016271 | Nonsense | 23 | 621 | 2 | 16 |
ENSDART00000145190 | Nonsense | 23 | 242 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 43185980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44775871 |
GRCz11 | 18 | 44769325 |
KASP Assay ID:
2261-2579.1 (used for ordering genotyping assays)
KASP Sequence:
TTAGGCTGCTCTCTGGGAGCTGCTCTTGGAGGTGTGATCTTTGCATCCTA[T/G]AAACTGGGCTTACTTTACCAGCTMTTTCATAAGGTAATGAGGATTGTAAC
Long Flanking Sequence:
GACTGCTATTCTCCAAATGAATTCACAGAACGCTGGCCGCGCGAGTACACTCAACTGCTCAAATAGCTGAGCGATTATTACGTATATAGCGTAACTCTCACATTCACCCAGTCCATTCAGAGCTTTCAGTTTGCGTGGCCCGTCAACAGGAGTGAGTTCATCGGCCTCAGCGCTGACTGCAGCAGGGGAGGAAAAGTTGGCACAGGTACAGTGTTTCCCTGACCTTAAACCAGGCTACAACAAGAACACACATGACAGCGCGTAGAAACATGACCGCCGTCTCGAGATTTGTCAAGTAACTGTACTGAAAAGTGCATTTGGAGCTTAGCGTCATTATAAGTATGTGGCTGTTTTGTTAATTTTACGCCTTTTTTATCGTCGGACAGGTCTCTAACAGGACAGGTGGGCGTCAGGTCGCAGAGCACCGTCGCGATGGACATATCCATGTATTTAGGCTGCTCTCTGGGAGCTGCTCTTGGAGGTGTGATCTTTGCATCCTA[T/G]AAACTGGGCTTACTTTACCAGCTCTTTCATAAGGTAATGAGGATTGTAACAGATATGGGTTATGAAATGTAAAGTTTTCACATCATATTGCAGCAACTTTTTGTTAACAAGTTGTCATAGAAACTGCCTTCTAAAACTAGTTAGTTTTATCTATCCATCTATCCATCTATCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATGCTTAATTACTTTAGCTATTCTGAAGTTGAAGCTGATCCATTAAGAAAGATCACTCAGTGATTTATTTTATAAATCAGACCTGATTATTTAAATTTGATCTTAATGTCTAAGTCTACAGTCTTCATTGGTTGTTGTAATTGCAAGAAAATTAACCAGTATGTTGCTGAAAATGTATATTATCTATAGCATTAATTGCTAAAATCAGTAGCCCTAAGTAGGGCTGCATAATATATTGTTTCAGCATCAATACCGCAGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19208
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000016271 | Nonsense | 23 | 621 | 2 | 16 |
ENSDART00000145190 | Nonsense | 23 | 242 | 1 | 6 |
ENSDART00000016271 | Nonsense | 23 | 621 | 2 | 16 |
ENSDART00000145190 | Nonsense | 23 | 242 | 1 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 43185980)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44775871 |
GRCz11 | 18 | 44769325 |
KASP Assay ID:
2261-2579.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGGCTGCTCTCTGGGAGCTGCTCTTGGAGGTGTGATCTTTGCATCCTA[T/G]AAACTGGGCTTACTTTACCAGCTCTTTCATAAGGTAATGAGGATTGTAAC
Long Flanking Sequence:
GACTGCTATTCTCCAAATGAATTCACAGAACGCTGGCCGCGCGAGTACACTCAACTGCTCAAATAGCTGAGCGATTATTACGTATATAGCGTAACTCTCACATTCACCCAGTCCATTCAGAGCTTTCAGTTTGCGTGGCCCGTCAACAGGAGTGAGTTCATCGGCCTCAGCGCTGACTGCAGCAGGGGAGGAAAAGTTGGCACAGGTACAGTGTTTCCCTGACCTTAAACCAGGCTACAACAAGAACACACATGACAGCGCGTAGAAACATGACCGCCGTCTCGAGATTTGTCAAGTAACTGTACTGAAAAGTGCATTTGGAGCTTAGCGTCATTATAAGTATGTGGCTGTTTTGTTAATTTTACGCCTTTTTTATCGTCGGACAGGTCTCTAACAGGACAGGTGGGCGTCAGGTCGCAGAGCACCGTCGCGATGGACATATCCATGTATTTAGGCTGCTCTCTGGGAGCTGCTCTTGGAGGTGTGATCTTTGCATCCTA[T/G]AAACTGGGCTTACTTTACCAGCTCTTTCATAAGGTAATGAGGATTGTAACAGATATGGGTTATGAAATGTAAAGTTTTCACATCATATTGCAGCAACTTTTTGTTAACAAGTTGTCATAGAAACTGCCTTCTAAAACTAGTTAGTTTTATCTATCCATCTATCCATCTATCCATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATGCTTAATTACTTTAGCTATTCTGAAGTTGAAGCTGATCCATTAAGAAAGATCACTCAGTGATTTATTTTATAAATCAGACCTGATTATTTAAATTTGATCTTAATGTCTAAGTCTACAGTCTTCATTGGTTGTTGTAATTGCAAGAAAATTAACCAGTATGTTGCTGAAAATGTATATTATCTATAGCATTAATTGCTAAAATCAGTAGCCCTAAGTAGGGCTGCATAATATATTGTTTCAGCATCAATACCGCAGTGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36724
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 |
---|---|---|---|---|---|
ENSDART00000016271 | Nonsense | 165 | 621 | 5 | 16 |
ENSDART00000145190 | Nonsense | 165 | 242 | 4 | 6 |
Genomic Location (Zv9):
Chromosome 18 (position 43192905)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 44782796 |
GRCz11 | 18 | 44776250 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAGGATATCGACCAGATGTCTCTCTTCAAGCCTCTCTGTAAGTTCTG[T/A]GCATCAGTGAGGACTGTGAGAGAAATAGTTCCCACTGTTAGAAAAGCCCT
Long Flanking Sequence:
ACCCTATTCAAACACACCTAAACAAGCTAATCAAGGTCTTACTGGGTATACTTGAAACATCCTGGGAGGTGTGTTGAGGCAAGATGGAGCTAAACCCTGCAGGGACACCGGCCCTCCAGGACCAGGATTGGTGACCCCTGGTCTAAAGTGACATTTTTGAAAAAAAAACAAAAAAAAAAACAGTCATTTTATTTGCCAATAACCTTTTCATTACATATAAAATAAACTTCTAAACCTAATCAGAGGAGCCTGAAATGCTCATTTACAAGAAAAGCGGTCAGATGGATTTAGAGGTTTTTGCATCTGAACTCTTCTTATAGTATTGCTGCAGTAAATATCACAATACTAGTATGCTGTATCGATATCCCCCTCCCTATACTGAATATGTCCTTAAAATATGTTTAATCTAAAAGACTTAGATTTTGTGTTTCTTTGCAGGGTAGAGGTGCACTCCAGGATATCGACCAGATGTCTCTCTTCAAGCCTCTCTGTAAGTTCTG[T/A]GCATCAGTGAGGACTGTGAGAGAAATAGTTCCCACTGTTAGAAAAGCCCTGGCCATCGCACAGTCTGGAACACCAGGTACAGTGGCATTGATTTGCATTATACATTTTTTTTTTACAAGTGTTTTTGTTAGATTTACATTTTTCAATATTTACCAAACAATAAACTAAAATAAATAAATAAATAAAAATTATTATTATTATTATTAAAAAAGAACAATCAGGGCATATAAACAGTTTCAATGAGGCAGTCAATAGGGTCAGTGAGCATGTTAAGGCCCAATTCTATTTTTGTACCCCTTCCCCTTCCCCTTGGCCCTTAAAACTGAGTGTGAAGGGGAAGGGCTTCAAAATTTACCCCTAAGAAATGGGACAGCACTACAACACCTGCACACATCATCAGATGTCATCGCGATCTCTTGCTTCATATGAGATCAACGATGGTGACTGTTGTAGTTATTCTAGTTTTGGTATTTATTTTCAGGAATTCACTGAAGGCATAT
Associated Phenotype:
Not determined