ZMP
ENSDARG00000037613
Ensembl ID:
Human Orthologues:
LGALS12, LGALS8
Human Descriptions:
lectin, galactoside-binding, soluble, 12 [Source:HGNC Symbol;Acc:15788]
lectin, galactoside-binding, soluble, 8 [Source:HGNC Symbol;Acc:6569]
lectin, galactoside-binding, soluble, 8 [Source:HGNC Symbol;Acc:6569]
Mouse Orthologues:
Lgals12, Lgals8
Mouse Descriptions:
lectin, galactose binding, soluble 12 Gene [Source:MGI Symbol;Acc:MGI:1929094]
lectin, galactose binding, soluble 8 Gene [Source:MGI Symbol;Acc:MGI:1928481]
lectin, galactose binding, soluble 8 Gene [Source:MGI Symbol;Acc:MGI:1928481]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2903 | Nonsense | Available for shipment | Available now |
sa43003 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa2903
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 |
---|---|---|---|---|---|
ENSDART00000054781 | Nonsense | 67 | 358 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 17 (position 49067374)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48828880 |
GRCz11 | 17 | 48911509 |
KASP Assay ID:
554-2716.1 (used for ordering genotyping assays)
KASP Sequence:
GTGGCTGCAGKACAAAGCCACGGGCGGATGTGGCATTTCACTTTAATCCA[C/T]GATTCAGCAGTTCTCCACGTATCGTGTGYAACTTCTTGCATCATGAAAAT
Long Flanking Sequence:
CACACTCATCGAAAAAGCTGTGCCAGGCACGAAAGCTTGACAGGCGTAGCAACAACAACTAAGGAGGGCGGGGCTTAGCGAAGGGTCCATTCCAATAGTTTACCAGCCTCCCAAAATATACGCTTGCACCCATCCAAGTGTATTCTTACGTTTTCCAGAATGGCTTGGTTCCTTGGTAAATCATAAGGATTAGACAAGGGAGACCTACAGGGACAGGACTGGCCACCCCTGGCATATTATTATTTGCAGATACATATTTAAAATAACCACTGTAAGTTTTTTATTATTATCCAAATTCTTATTATTCTCCAAATTACGTATTTAGTTAATAATATTCAGGGTTTTTATTTTTCAATTAAAATGACCAAACATTTTTCTTTGCTATTGACTCTATACATCTCTTAACTGTAATATGGTATGTCTTCCGTAGGTTTCAGTTTGATTTGACATGTGGCTGCAGTACAAAGCCACGGGCGGATGTGGCATTTCACTTTAATCCA[C/T]GATTCAGCAGTTCTCCACGTATCGTGTGTAACTTCTTGCATCATGAAAATTGGGGAAAAGAAGAAAACGTGGACCTCATGCCATTTAAACAAGGAGCGTCATTTGAGACGATCATCATGGTACTTTGCGATGTTTTCAAAGTGAGTGTGAAATATAAGGCCTACTGTTGAAGTAGCTTGTTAAACTCAGGTTTAAAGTATTTTAGAACTGATATGAATTATTAGTTCTAGTAATTATTACAATTTAGATATAGAGATATGATTAGTTTTGTTATGATTTAGTTTTGTCAAGTAACCGTAATGTGACTCATTTACTCTTGTAGGTAGCAGTAAATGGTGTTCATATTTTGGAATATAAACACAGGATTCCTCTTGAGATGGTTAACACGTTTTCAGTATCTGGAAACGTAGAAGTGCATGCCATTGGCTTTATCCCTGACTCAGTAAGTGACATACATTTGTGGTGCAATATTTTTACACACCTAATTTTACTATTTCAAA
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:
sa43003
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 |
---|---|---|---|---|---|
ENSDART00000054781 | Nonsense | 79 | 358 | 3 | 10 |
Genomic Location (Zv9):
Chromosome 17 (position 49067337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 48828843 |
GRCz11 | 17 | 48911472 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCACTTTAATCCACGATTCAGCAGTTCTCCACGTATCGTGTGTAACTTCT[T/A]GCATCATGAAAATTGGGGAAAAGAAGAAAACGTGGACCTCATGCCATTTA
Long Flanking Sequence:
TGACAGGCGTAGCAACAACAACTAAGGAGGGCGGGGCTTAGCGAAGGGTCCATTCCAATAGTTTACCAGCCTCCCAAAATATACGCTTGCACCCATCCAAGTGTATTCTTACGTTTTCCAGAATGGCTTGGTTCCTTGGTAAATCATAAGGATTAGACAAGGGAGACCTACAGGGACAGGACTGGCCACCCCTGGCATATTATTATTTGCAGATACATATTTAAAATAACCACTGTAAGTTTTTTATTATTATCCAAATTCTTATTATTCTCCAAATTACGTATTTAGTTAATAATATTCAGGGTTTTTATTTTTCAATTAAAATGACCAAACATTTTTCTTTGCTATTGACTCTATACATCTCTTAACTGTAATATGGTATGTCTTCCGTAGGTTTCAGTTTGATTTGACATGTGGCTGCAGTACAAAGCCACGGGCGGATGTGGCATTTCACTTTAATCCACGATTCAGCAGTTCTCCACGTATCGTGTGTAACTTCT[T/A]GCATCATGAAAATTGGGGAAAAGAAGAAAACGTGGACCTCATGCCATTTAAACAAGGAGCGTCATTTGAGACGATCATCATGGTACTTTGCGATGTTTTCAAAGTGAGTGTGAAATATAAGGCCTACTGTTGAAGTAGCTTGTTAAACTCAGGTTTAAAGTATTTTAGAACTGATATGAATTATTAGTTCTAGTAATTATTACAATTTAGATATAGAGATATGATTAGTTTTGTTATGATTTAGTTTTGTCAAGTAACCGTAATGTGACTCATTTACTCTTGTAGGTAGCAGTAAATGGTGTTCATATTTTGGAATATAAACACAGGATTCCTCTTGAGATGGTTAACACGTTTTCAGTATCTGGAAACGTAGAAGTGCATGCCATTGGCTTTATCCCTGACTCAGTAAGTGACATACATTTGTGGTGCAATATTTTTACACACCTAATTTTACTATTTCAAATTTGACCACTTTGCACTTGTTAGTATTCACCTTATTC
Associated Phenotype:
Not determined