ZMP
lmnl3
Ensembl ID:
ZFIN ID:
Description:
lamin L3 [Source:RefSeq peptide;Acc:NP_694505]
Human Orthologue:
LMNA
Human Description:
lamin A/C [Source:HGNC Symbol;Acc:6636]
Mouse Orthologue:
Lmna
Mouse Description:
lamin A Gene [Source:MGI Symbol;Acc:MGI:96794]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44066 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa8565 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44066
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000023944 | Essential Splice Site | 279 | 584 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 46176387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 46005500 |
GRCz11 | 23 | 45850291 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGATCCGCCAGTATAAAGACGAGCTGGAGAAAACCTTCAACGCCAAGG[T/G]CAACAACACCACACACAACTGCAGAACAGATCCTGTTTATATCCGTGTGT
Long Flanking Sequence:
GGAGGAGCTACTCTATGCCCTGCAATCTCAACTGAAAGATGAAGAGGCATCAAATATCGAATAAAAAATGCACATTTCAAAGCACTTCAGTAGACCTTTAAGGGTGCTATTAATGATTAAAAATTAAAAACTGCTTTCATTTCAACCGAAACAAAACAAGACTTTTTATATTGTGAAAATAAACAGTCTGTTAAACAGTCTTGTAACATGGGAAGTATTTGAAATGGAGTTAAAATGTCTGCTGTAATGCGTGTGCATGTGTGTGCATGTGTGTGTGTGTGCGTGTGTGTGTGCGTGCGTGCGTGCGTGTGTGCGTGCGTGTGTGCAGGAGGTGCGAGAGATGCGCAGTCGTCACGAGTCTCGTTTGCTGGAGCTGGACTGCGGTCGACAGAAAGAGTTTGAGGGTAAACTAGCAGAAGCCATGAAGCAGCTGCGAGACGAGCACGAGACGCAGATCCGCCAGTATAAAGACGAGCTGGAGAAAACCTTCAACGCCAAGG[T/G]CAACAACACCACACACAACTGCAGAACAGATCCTGTTTATATCCGTGTGTTTACTGTGCTTTAAGATGAGTTTATTGGTATTGTTTTCTTGAAAATTTTAATAGTTAAACATATTTAAAACTTATTTCTTGCCTCTAGCATTTTAGTGTGTTTCAGTTTATAGATATATTATTTTAATTATTGCACTTTGGATCAAGTATGGTGGTGTAAAATTGTGCCCTGTGTATAATGTTTGCCTAGCCTTATTATTATTATTATTTATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTTATTATTATTATTATTATTATTATTATTGTTGTTGTTGTTGTTATTATTATTATTATTATTTATTGTTTTATTATTATTATTATTAGTAGTAGTAGTAGTATTATTGGTATTTTTATTGTGTATTATTATTATTATATAATCTACTTTTGTATAATCTACTTATAATTACTTTTTGTAATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8565
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 |
---|---|---|---|---|---|
ENSDART00000023944 | Essential Splice Site | 321 | 584 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 23 (position 46175169)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 46006718 |
GRCz11 | 23 | 45851509 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACTCCGACTGGAGTCTCAGACGCAGCAGATCAACAACCTGCAGAAACAGG[T/A]GACGCTTCCACCACACAGCTCTGGAGTTCTTCAGARAGGCTTTCAGTGCA
Long Flanking Sequence:
TTCATTTTTATTTAAATGATTTCTATATTTTCAATTTTTAAATTAGCAAATACTGCATGTAATATTTATTTTATTGTAATTTTAAATTAATTGTCTTTAAAAAATAGACTTTAGTATTTTTCATATATTTTATACATTTATTTTTTGTGAGTTTTTTGTTGCATTAGTAAGTGTATATTATATTGCTATATTTATTTTTTTGTGTTTTTTTCTTTTTGTTGTTTAATACATTTCTGTATTTGTTTGTTTGTTTGTTTGTTCTATTCACATTCTTTTCTCTATTTTTTTCTATACTATCAGAATAAATGGTGCCCTAAGCAGTTGTTTTTTTATCATGTTATGCATTTTCACAGTGTTTATTTGTCTCTCTCAGCTGGAAAACGCCAAGCAGACGGCGGTGAAGAACAGTGATTTCGCCTTCTCCACTAAAGAGGAGCTGGCAGGAACTAAACTCCGACTGGAGTCTCAGACGCAGCAGATCAACAACCTGCAGAAACAGG[T/A]GACGCTTCCACCACACAGCTCTGGAGTTCTTCAGAGAGGCTTTCAGTGCAGCACGGTGACCGTTTAGAATCTCACAGGAGTTTCAACTTAAATGTGTTCCTTTGATCTTTCTGTTCTTCAAAGCATCCGCAAACATACAATGTATCATTTCTGCTGAATGTATATACAGCCAAAGTCAAATTTATCTGCGCTCTTTTGAATATTTTTGTTAAGTATTTCCTAAATTATGTTTAACAGATTCAGGAATTTTTCACAGTATTTCCTCTAATATATTTTCCGTTTGAGAAAGTCTTATTTGTTTTATTTTTAGCTAGAATAAACACAGTTTTTACTTATTTTATTTTATTTTTTTATTTTAAGGTCAATATTTTTAGTCCCCTTAAGCCTTTATTTATTCGCCCCTTGATGCACTTATTTAAATTTTCAGTCAAATACAGTATTGTATGGGAAATTGTAATTAAAATGTAGATTTTGCACTACTGATTGACCTTCAGTTGTCC
Associated Phenotype:
Not determined