ZMP
mlc1
Ensembl ID:
ZFIN ID:
Description:
membrane protein MLC1 [Source:RefSeq peptide;Acc:NP_001098409]
Human Orthologue:
MLC1
Human Description:
megalencephalic leukoencephalopathy with subcortical cysts 1 [Source:HGNC Symbol;Acc:17082]
Mouse Orthologue:
Mlc1
Mouse Description:
megalencephalic leukoencephalopathy with subcortical cysts 1 homolog (human) Gene [Source:MGI Symbol
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10246 | Nonsense | Available for shipment | Available now |
sa32194 | Nonsense | Available for shipment | Available now |
sa13089 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10246
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091729 | Nonsense | 69 | 391 | 2 | 12 |
ENSDART00000130141 | Nonsense | 73 | 395 | 1 | 11 |
ENSDART00000141893 | Nonsense | 70 | 392 | 1 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 14523075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14968493 |
GRCz11 | 18 | 14937005 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCAGCTGGATCAGCCTGGCCCGCTACATCCCTGCTTCAGCTACAGAGTCT[G/A]GCTTTACAGYGTGGTTGTAGGGGTAAGCAGATTTGCACCACCTTGACTGA
Long Flanking Sequence:
CAGCTCATATTGAATAAGTATTTTGAACAAACACCAGATGTCTTTTTTTGAGATATAGGTCTGTGATTGGATGACTTTGAAATGTTGACCTTGTAAAGTCAAATGTGTTGAATGTTAATTTAAGGCTTGGATGCTGAGGTAATTTCATTAAAAGGATCACATCAGTCTGTCAATACTCTGTAAGCCATATACTTTACCTCCTTCATAAATGTTTGCCTTCAGTGAGTTTTTCTCACCAAGTCGATACATGCGATTTAAACAGATTGTGTCTCTAGGGTGCCTCATGGATTTGAGGATGCAGCGAGAGGAGGCATCGGCTCAGGAAGTGTTCAGCTATGCCCAGATGTCCACCCTGGAGAGAAACAGCGGTGTAGGAACGCTGAGTCGGCATCTAGAGCGCGAGCGATTGGAGAGAGACGGCTACACGGTGGATGTCAGAGCCAGTGACCTGCAGCTGGATCAGCCTGGCCCGCTACATCCCTGCTTCAGCTACAGAGTCT[G/A]GCTTTACAGTGTGGTTGTAGGGGTAAGCAGATTTGCACCACCTTGACTGACAGACTTAGCACACTGATTTTCTCAGTCGTCTAAATGTGTCTATCTGTATCTGACCCTCAGAGCAGCTTGCTGATAGCGTCGGCTTTCTCGCTCTACATGGGTAATGTGTTTCCTGCTGCAATGGATTACCTGCGCTGTACTGCTGGATCTGTGAGTGTTTCACCTTGGGTTTGTTCGGGAAGGATTCATAGGGCCATTTGTCAGACTGACATTCGTGTATGTGTTTGCTTTTGGCTTGCAGAGTATACCAGCAGCAGTGGTGAGCTTCGCCATTGCCAAGAACAGACAAGTCGCAGTAAGTGAACCATTGTTTTTTTTCAGTAAGTACAGAGAAATGAACTCTGTCTACCTCAAGGAGCCATTGAATGAAAATCTGGATATATCTATGCATAGATGAATAATAAGACATAAGCATACCGTGATCCACAAACACCACTGTTTCCTCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32194
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091729 | Nonsense | 212 | 391 | 7 | 12 |
ENSDART00000130141 | Nonsense | 216 | 395 | 6 | 11 |
ENSDART00000141893 | Nonsense | 213 | 392 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 14518242)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14963660 |
GRCz11 | 18 | 14932172 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGGCCCAATGATTGTGACCCAAACATCGTTCCCCACTCGTCTTTTC[A/T]AGGCCTTCGCCGTGAGTCGCCTACAAATGAGATTACGTGTGTGTGTGTGT
Long Flanking Sequence:
ATGTTAGTTTCTTATTTTCTTCTTTTTTGTGTGTGTTATTATTTAGATCACTGATTCTGCATGAAACATACACTCATTTGTGATTTTGGGGGGAAAAAATCATTATGCTAAATGTTTTTTGTCATTTTTATATTTCTCTAGTTTTAGTTTATTTGGTTTAGTGTTTTTAATAAATTAACTTTAGCCTTTAATATTTCAAAGATTCCTCAGAATTATATATTAATTTTATTAATGTTTATGTTACAAGTTATGTCAGCTTCAATGTACAATTTGCATAATAATTGCATAATATTTTGATGCTGCTTCCTAGATTCCAACTAAAGCAAGATATCATCGCCATGCGAAATGTCTATGATTTACAATAATTGTCTGCAGCTTATGCAGTTTACATTTTACATGCTCTCCCTCTTTTCCTCATTGCTCTCATCCATCTTTTTCTCCAGCCGGTGTCTGAAGGCCCAATGATTGTGACCCAAACATCGTTCCCCACTCGTCTTTTC[A/T]AGGCCTTCGCCGTGAGTCGCCTACAAATGAGATTACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCGTCACTGTATATTCACACTGTTTCTCCAACATAGGTAATTGAGCTCATAGTGGGCATCGCTGCAGTTTTTGGAGGAATTATTGCCCTCAATTTGGGCGCTCTTCTCCCAGAGCCTTACCTTTCTGTTACCTTCTTCTGGATTCTGGCAGCGGTGAGATTGGTTCATTTTATTAAATACTAGAACTGATTATTGTAACCAGCGTGGTTCATTTTTTCTTTCTTATGTGATACAGTGTTTCCCCAGTGCCATCGCCAGCCATGTGGTGGCAGAAAATCCCAGCAAAAGTCTGGTGAGTCTCCATCAGGATCTCTCTCCAGCAATTATGAGCAGTGCAATCGAACGTCCCTGGAGCATGTTCACCTTTCTCATTCATTCACAGTTGAAGTCAAAATGATTAGCCCTCTAATTTTTTCCTTTTTCAAATATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13089
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000091729 | Essential Splice Site | 273 | 391 | 9 | 12 |
ENSDART00000130141 | Essential Splice Site | 277 | 395 | 8 | 11 |
ENSDART00000141893 | Essential Splice Site | 274 | 392 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 18 (position 14517879)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14963297 |
GRCz11 | 18 | 14931809 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGTGCCATCGCCAGCCATGTGGTGGCAGAAAATCCCAGCAAAAGTCTGG[T/A]GAGTCTCCATCAGGATCTCTCTCYAGCAATWATGAGCAGTGCAATCGAAC
Long Flanking Sequence:
AATTGTCTGCAGCTTATGCAGTTTACATTTTACATGCTCTCCCTCTTTTCCTCATTGCTCTCATCCATCTTTTTCTCCAGCCGGTGTCTGAAGGCCCAATGATTGTGACCCAAACATCGTTCCCCACTCGTCTTTTCAAGGCCTTCGCCGTGAGTCGCCTACAAATGAGATTACGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTCGTCACTGTATATTCACACTGTTTCTCCAACATAGGTAATTGAGCTCATAGTGGGCATCGCTGCAGTTTTTGGAGGAATTATTGCCCTCAATTTGGGCGCTCTTCTCCCAGAGCCTTACCTTTCTGTTACCTTCTTCTGGATTCTGGCAGCGGTGAGATTGGTTCATTTTATTAAATACTAGAACTGATTATTGTAACCAGCGTGGTTCATTTTTTCTTTCTTATGTGATACAGTGTTTCCCCAGTGCCATCGCCAGCCATGTGGTGGCAGAAAATCCCAGCAAAAGTCTGG[T/A]GAGTCTCCATCAGGATCTCTCTCCAGCAATTATGAGCAGTGCAATCGAACGTCCCTGGAGCATGTTCACCTTTCTCATTCATTCACAGTTGAAGTCAAAATGATTAGCCCTCTAATTTTTTCCTTTTTCAAATATTTGCTAATTTTGGTTCTACCCAGGTTTTGGAAAATATTTTTTTAACAGTTTAGTTATGTTTGATTTTCTTATTAAACCTGAACCCCTGTTGGCATTTTTTGGAACCAGCCCCGGAAATATTGTGCTTGAAGAAGAAATATGTAGAGTTATTGGTTTTACCACAATATTGGTTAGGCCAGGGGTCACCAATCCTGGTCCTGGAGGGCCGGTGTCCCTGCAGGGTTTAGCTCCATCTTGCCTCAACACACCTGCTTGGATGTTTCAAGTATACCTAGTCATACCTTGATTAGCTTGTTCAGGTGTGTTTGATTAGGGTTGGAGCTAAAATCTGCAGGGCACCGGCCCTCCAGGAACAAGTTTGGTGA
Associated Phenotype:
Not determined