ZMP
lman1
Ensembl ID:
ZFIN ID:
Description:
Lman1 protein [Source:UniProtKB/TrEMBL;Acc:Q58EK8]
Human Orthologue:
LMAN1
Human Description:
lectin, mannose-binding, 1 [Source:HGNC Symbol;Acc:6631]
Mouse Orthologue:
Lman1
Mouse Description:
lectin, mannose-binding, 1 Gene [Source:MGI Symbol;Acc:MGI:1917611]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37243 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa43588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13208 | Nonsense | Available for shipment | Available now |
sa16718 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37243
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102304 | Essential Splice Site | 126 | 513 | 2 | 13 |
ENSDART00000123476 | None | None | 100 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 9238722)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 10610775 |
GRCz11 | 21 | 10703403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTGGCATTTCGTGTTTCCGGACGAGGACGAATGGGAGCAGATGGATTGG[T/A]AAGTAAGAGGAGTATAGCTATTAAATATTTATTTAATAATTGATTTGTAT
Long Flanking Sequence:
GATTTATGTCAACAGAGAAGTAAGCGCTCAGCTGCTACTCATATTTATTGGTATTGTGCCAAACAGCCTATTACATATGAGCATGTGATAAGGATCAAATTACGCAACACAAATATTGTTCTTTCTCAGATTAATAATGCGTGATATTATTTTTTTAATGTAAGATTAAATGATATATTTGAATGATATATCGTCTGCCAGTATATGCACACATATACTGTATGCATCTTATTTTAGAGTAAACTTTAATCCAAGGAAGTAAATTCATATCAGAGTGGTAAAAACCTGTTTGAGGAACATTCAGTGTTAAAATAATTTTCCGTTCCCTTTTTTTCCCCCTCCAGATGCTATTCCCAGTTCAGATCAGGTCCGAATCACACCTTCTCTCCGGAGCCAGAAGGGTTCAGTATGGACAAAGTCCCCTGTGAGTTTTGAACATTGGGAAGCTGAAGTGGCATTTCGTGTTTCCGGACGAGGACGAATGGGAGCAGATGGATTGG[T/A]AAGTAAGAGGAGTATAGCTATTAAATATTTATTTAATAATTGATTTGTATATATAATCAATAATTGAATATAGATTGTACACGTAAGCCTTAATACATTTTTGGCTTTGAGTATAGGCACATGTTGTTATCGTTATGACAGTGAAGGGTCAAGTTGACTTATTTTTAGGGATATGATAACCTGATTGCTCGTGTCACAGGTTAAATCCTAGATCTGGGTGATCTGTGAGCTGTTGAGTCACTGATGCTGTAAAAATGATCTAACAAAGTCACTAAAATGACTTATTTTAATAAGTTAATTAGGTTTCAACTAAGTTATATAAAGTTTAACTTAATATTTGTTGTCAGTTTGACTGTTGTACTTTGAAATGACTAGAAAAGTTAATTTGATTCAACTAAAAAATTGAAGTCAGCAAGATTTCTTTTTACAGTTTAGCACACTTCTGAGTCAAGTCAATTCAAGTTTATTTGTTTAATAATAATTTACAAAATAATAAGAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43588
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000102304 | Nonsense | 198 | 513 | 5 | 13 |
ENSDART00000123476 | None | None | 100 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 9246907)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 10618960 |
GRCz11 | 21 | 10711588 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCCAGTGATGGCACGACCCAGGCACTAGGCACATGTCTTAGAGACTTC[A/T]GAAACAAACCTTACCCTATACGCACCAAAATCACTTATTACAAGCAGACG
Long Flanking Sequence:
GTGGCTCATTTGTAAATGCAAGACTTTAGAAAAAAAAAAAAAAAGAAATTATGTACTCTGGTGACACGGTGGCTCAGTGGCACTGTCGCCTCACAGCAAGAGGTTGCTAGTTTACATCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTCTCTGTGTTCACATGGGTTTCCTTCGGGGGCTCTGGTTTCCCCCACAGTCCAAAGAGATGCGCTATAGGTGAATTGAATAAACTAAATTGGCCATAGTGTATGTATGTAAATGAATGTGTATGGATGTTTCCCAATACTGGGTTGCTGCTGTAAGGGCATCCGCTGTGTAAAACCTATGCTGGATAAGGCTCAACTCTGGAAGTATGGCTATTAATTTAAGTTCACTTTAGTAGTTGATCGATACCCTATTCACCTGCACCTACAATATTCCATATGTTTTTGATAAATTATATTTTCTTTCCTCCAGTGATGGCACGACCCAGGCACTAGGCACATGTCTTAGAGACTTC[A/T]GAAACAAACCTTACCCTATACGCACCAAAATCACTTATTACAAGCAGACGTTATCGGTAAGTTGAGAGTAATAAAGTTAAGACTGAATAACTTGCTATCATTTGTCCATTTGACCCTAATAACAGCATTTGTGTGTTGTTGAATTTTCCATTGTAAATATATAAACTAATAGTCAAATGTTTGAGCAAAGTCTGGTGTGTTTTTGCCAGCTTTAATAAAGTCTAAATATTCTCAATGGTTTCAGGTTTTCATTAATAACGGCTTCACTCCTGACAAAGATGATTATGAGTTCTGTACCAAAGTTGAGAACATGATCATTCCTGGAACTGGTTATTTTGGCATCTCTGCAGCCACTGGAGGACTTGCAGGTATTTATTAAAATCCAAATCTATCTGCCAATATAATATAATCTTATTTTGTCTTAATTTCCAACCAGTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTATTTTTTGTTTTATTTTAGAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13208
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 |
---|---|---|---|---|---|
ENSDART00000102304 | Nonsense | 417 | 513 | 11 | 13 |
ENSDART00000123476 | None | None | 100 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 9264341)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 10636394 |
GRCz11 | 21 | 10729022 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTATGTGTTGTGCTGTGGTTTGCAGGAACTCTCTGTCAGGCTCTCTRAAG[C/T]AGCTGGCAATGGGGCAGCATCAGGGAAACGCAGGAGGATTGGGCTCATAT
Long Flanking Sequence:
CACGCTAAATTGTGTTACGTTTATATATGCAAATGAGGCATTGTTTCCAGAAAGAAAAAAGCTATTTTTGTAAAATAAAAATGTATGTAATCATAGATTTTTATGACTCCTTTTTAGAAACTGTATCATATAATTGTATTATAAATAATTACGTAAGTTATTTTATATATATATATATATATATATATATATATATATTTTTTTTTTTTTTATATTTAAATATTTTATTATTATCACAAAATCATTATATAATTATTGTAAAAAATATTTAATATTGAAATTAAAATTAGAGATAGAAATGGATAACACATGACTGTTGTATTATGACTGGAAAAATCGCAAACTTGCACCCTGGAGTTGAAATCCCTTCGTTCGTCATTCTTAAATTCTTTTATATCGGATGGATTGTGACCATCATGTGTTTGTAAACCCGAGCGCTCCAGTAACATTGTATGTGTTGTGCTGTGGTTTGCAGGAACTCTCTGTCAGGCTCTCTGAAG[C/T]AGCTGGCAATGGGGCAGCATCAGGGAAACGCAGGAGGATTGGGCTCATATGAAACTGTCCAGCACTTCAATGACATCAAGGAGCATCTGCACGTTGTCAAGAGGAACATCGAGCACATTATTCAGAAAAATGCTGTGAGTTGATCTTTTAAGAATGAATCTGTAGTTTTTAGTTTTGTTGACAGATTTGTCTGTTTTTTATTTGCCAGCTTAATATTATTATTATTATTTATTTTTTATTATTTTTATTATTTAGCTTAATTTGATTAAAATGTCTAAAATTAAAATAACTAAAAAATAAAGTAAAAATTCAAACTGAAGTAAATTAAGATTTTTTTTTATTTTTAAAAAATAAATACATTAAATTAATGTATATTAATTTCTAATAACTAATTTTCTTTTGTCTTTGCAATGATGACCGTAAATAATATATTACTGGTTGTAGTACTAGTTAATTATTTTATTACACACACACACACACACACACACACACACACACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16718
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 |
---|---|---|---|---|---|
ENSDART00000102304 | Nonsense | 480 | 513 | 12 | 13 |
ENSDART00000123476 | None | None | 100 | None | 3 |
Genomic Location (Zv9):
Chromosome 21 (position 9265637)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 10637690 |
GRCz11 | 21 | 10730318 |
KASP Assay ID:
2261-5274.1 (used for ordering genotyping assays)
KASP Sequence:
TGCAGAGAAGCTGAAGTGCCCTGAACTTCCTCCATTACCAACSTGTCTCT[C/A]GACCACACACTTCCTCATCTTYATTGTCATCCAGTCCCTCCTCTTCTTCG
Long Flanking Sequence:
ATTTTAAAGTGACATTAAAAGGCTTAACTAGGTTAATAAGATGAACTAGTCAGGTTAGGGTAATAAGGCAAGTAATTCTATACAATGGTTTGCTCTGTACACTATCGAAAAAAAATATAGCTTAAAGGGGCTAATAATTCTAGCCGAAATTTAAATTCTAGCCGAAATAAAACAAATAAGACTTCCTCCAGAAGAACAAATATTATCAGACATACTGTGAAAATTTCCTTGCTCTGTTAAACATTATTTGGGGGGGGGGGGGGGGGTGTAATCAAAAGGGGGCTAATAATTCTGACTTCGTGTGTGTGTGTGCGTGTGTGTGTTTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTTTCTATTAAATGGTCTTGTTATCACACTCTTTAGAATCCTGCAGAGAAGCTGAAGTGCCCTGAACTTCCTCCATTACCAACCTGTCTCT[C/A]GACCACACACTTCCTCATCTTTATTGTCATCCAGTCCCTCCTCTTCTTCGGCTACATCATGTACAAGTCAGTTTGTTTGTTTGTTTTTTTAAATCACAAGTGCTAAAATCACTTTCAGTGTCTTTTAAATTAAGCATTCTTTAATAATGAAAGCAAAATGGAAAACCATTGCAGCATACATTGTTTGGTATGCAAAGGCAAAAACTGTGACCACTTTTTAAAAGAATGTTTTAGTTGTAATCGATCAAGATTTCCCAAAATAACAAGTACATTTGAAGGCGCTGAATATTAACTTGCATTTTAATGCCCTTTTCTCTATATTTGTCATTTCCAGGAGTCAGCAAGAAGCAGCGGCGAAGAAGTTTTTTTGATGATTCGTAGTTCTTGGTAAACGCAGCACAACATGTAAATTGTCCACTTTTGTTAATTTCCCGTTTGTTTTCTGTTGGCAAACTGTAAATTTATTCTACTTGAAGTATTTAGTTAGTTTAGCAGTTTTT
Associated Phenotype:
Not determined