ZMP
mkln1
Ensembl ID:
ZFIN ID:
Description:
muskelin [Source:RefSeq peptide;Acc:NP_997859]
Human Orthologue:
MKLN1
Human Description:
muskelin 1, intracellular mediator containing kelch motifs [Source:HGNC Symbol;Acc:7109]
Mouse Orthologue:
Mkln1
Mouse Description:
muskelin 1, intracellular mediator containing kelch motifs Gene [Source:MGI Symbol;Acc:MGI:1351638]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40245 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13831 | Essential Splice Site | Available for shipment | Available now |
sa11959 | Essential Splice Site | Available for shipment | Available now |
sa31383 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa40245
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028820 | None | None | 202 | None | 6 |
ENSDART00000036354 | Essential Splice Site | 276 | 750 | 8 | 18 |
ENSDART00000137736 | Essential Splice Site | 255 | 729 | 8 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 10774218)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11710845 |
GRCz11 | 4 | 11709694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGACACGCACCACTTCTTATTGTTTTTTTTGTTTTTAACTTTCTGATTA[G/A]GCGATGGTGATGATAACAGGCCGGGCATGAGAGGAGGTCATCAAATGGTC
Long Flanking Sequence:
TGCCGTACGCTCATACGTTAAGAATACGGTCAATAGGACTTTGGAATAAGTGTCGTCAATACTGTTATAAATCTTGTTTTAATAATATGTGAGCTGAGAAAAGTTTTTACACACTTCATGTTTAAAGTTGTTCTCAGTAGATCATATTTATACACACTCTCTTGAGTGGTCACAGTGTAAATTTGCGGTAATTAGAACCTAATGTACACTCGGATTGTTTTCCGCTCAGGGAGCATGCATTAGCAAATTAACGTGCACACTTGACTCTTTATCTGCTCTCTTCCAGATGGTTTGTTTAATCAGTACATCAGCCAGCAGGATTATAAGCCACGCTGGAGTCAGATCATCCCCAAATGTAACAAAGGTACGACAGCAGTCCGCTGTGGCACTGAATCTGGACACTGGACTCCAGGAAGTCTGCTGCTGTATTAATGACTTACCGACTTCTTCCTGACACGCACCACTTCTTATTGTTTTTTTTGTTTTTAACTTTCTGATTA[G/A]GCGATGGTGATGATAACAGGCCGGGCATGAGAGGAGGTCATCAAATGGTCATTGATGTTCAGACAGGTACGTTTTACATCACGCTGCTCATTTGCAAACTTTCTGATTGGGTGGTTATCATATCACTGTTTAGCTTGTCCTGTCTTGCTCATAGTGGAATGCATGCCTTTTTGCTCTGCTGTTGCAAGTTAATGGCTGTTTTAAGCGTGCGTGTGAATTGGTGAGCTTGTTGTTTGAAGAACAGTCGATCCCGCAGCTCTGTGCATTCAGACTGACCTCGAGTAACCCACTCTACACGGCTCAGCTGACGCTCAATAGCTCAAACAACTGTCTCTGCTTATCACCATGGCTACATCAGCCTTTCAACCTCACCACACAGCTGCCTTTCAAGAAAATGACGATTTATAAGCACTTAAAGCATGTTTTTTATGCTTCGGTTTCATATTGAATCTCTTACAAAGGAGTAAGACGGCTCACCCACTCACTCTAGCTTTCTCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13831
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028820 | None | None | 202 | None | 6 |
ENSDART00000036354 | Essential Splice Site | 480 | 750 | 11 | 18 |
ENSDART00000137736 | Essential Splice Site | 459 | 729 | 11 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 10777689)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11714316 |
GRCz11 | 4 | 11713165 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCGGAGGAYATCCAATCTCGCATCGGACACTGCATGCTCTTCCACACG[G/A]TGCGTCTCCTTAGTAATGACCCATAAAGTGATACATTGAKGCTTGTTAGG
Long Flanking Sequence:
GAGGCAGATCTACACGCTGGGCCGATATCTGGACTCCTCGGTCAGAAACAGCAAGTCTCTGAAGAGTGACTTCTACTGCTACGACATTGACGCAAACACGTGGACCCTCCTGAGTGAAGACACATCCGCTGATGGAGGACCCAAACTTGTGTTCGACCACCAGGTAAATTGCACAACCTACAGTATATGCAGGATTTATCCTCCATACCATCAGGAGTCTCTCTTTTACAGATTTATGATGAACACCTATTAAAATAATCTTCCTTTTGCGTCCTCAGATGTGCATGGACTCTGAGAAGCACATGATCTACACGTTTGGTGGTCGGATACTGACGTGTAATGGCAGCGTGGATGATGGCAGGACGTCTGAACCTCAGTTCAGTGGGCTTTACGCGTATCACTGTCAAGCTGGCAGCTGGAGCCTACTCCGAGAAGACTCGTGTAACGCAGGGCCGGAGGACATCCAATCTCGCATCGGACACTGCATGCTCTTCCACACG[G/A]TGCGTCTCCTTAGTAATGACCCATAAAGTGATACATTGATGCTTGTTAGGTCACTGCTTCTAGTGCTAATTACTCCATCAGATGCAAGAGCAACTAATAAACGATGCTAATATACACACTCATAGTCTGCTGCAGTGCTAACGTGAAATTATCATTCTTAACTTGGGATGTTGTGTGCTTGGACTGTTTTGCACATCAGAGATTAGATTAAATGGATAGCTATGTAAATAGTGGTCAAATAGAGCTGCACAATATATTGTTTTGGCATCATTGTGTGCATCTGCAATAGTCGCATCGCGAGATATGCAATGTTAAGTCTGGATTATACAGCAGTCAACATTTGAAGTGGATCAAAACCTTTAATCGAAGTTGTCTTAAATCTACTGAGCAAAACCCATTCTTGTCTTAGGACAATTTTGGAAAACTGTTTTGATCCTCTTCAAGTGTTGACTACTGTAGTTGATTAGGAGCCACAGAACACATGAGATTTGTAGAGTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11959
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000028820 | Essential Splice Site | 25 | 202 | 1 | 6 |
ENSDART00000036354 | None | None | 750 | None | 18 |
ENSDART00000137736 | None | None | 729 | None | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 10788450)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11725077 |
GRCz11 | 4 | 11723926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGATCTGCTGCTGYTTTCTGTCACTTTTTGTTTATTTGACTCGATTTGG[G/A]TGGGTGCGTGTGTKTGTACACTTTGCTTGGACGGTATGCGCTGTTTAGTG
Long Flanking Sequence:
TTTATACTATGGAAGTCAATGGTTACAGGATTTCAGCTTTCTTTAAAATACCTTCTTAAGTGTTCAAAACTTATAAAGAATTGGAACCACTGTTAAGAGAGTAAATAATGAGTAAATATTCATTTTTTAGTGAACTATCCCTCAAATATTTTACACAAAAACTCAAAAGATCAACATTTTTCATTTATTTTTTGCTGATATTTACAACGGGTGCCAATATTCGTGGAGTAATCTGTAAAATAATAAACAAAGCGTCAGTAAAAAGATTTCACAGGCATGTCTGACCTTCAGAAAGGAGTCAGTGGTTCCCCAACAGGAACAGAATGTTCTCTTCTCGCTTATGTGTGCGTGTATTAAATGTGTTTTTCACTTAAACGGGGGAGAGAAACCTTTTGTTCTGTACACTAATTGAAGCAGTTGGCTTCTAGAAAACTCAGTCAGTCTTTCTCTTGGATCTGCTGCTGCTTTCTGTCACTTTTTGTTTATTTGACTCGATTTGG[G/A]TGGGTGCGTGTGTTTGTACACTTTGCTTGGACGGTATGCGCTGTTTAGTGTGAAAGACTAACTGTGTGTTTGTTTACAGGTCCTGTGTTTATAAGAACGACCAAGCGGTGAAGGAAAACCCCACTAAGGCCCTGCAGGAAGAGGAACCTTGTCCTCGGTTTGCTCATCAGCTTGTCTACGATGAACTCCACAAGGTAATGTTGATCATGGTTTTAATCTAACCCCAAGTTTCAATCTCAGCTCTCCTCAAGCAGGGTTATTATAGTTCAGTGCTTTTTAACAACATTCCTGGAGCCCAAAAACACTGCATGATCTGCATGTCTTCTTAATCAAACACACCTGATTCAACTCATCAGCTCGTTAGCAGAGACTCCAGGACCTCAAATGATTGTGTGAGACAAAGGAGACGTGCGTGAAATTAACTATCATTTTTGTCATCTGAAGTTAACTTGGCTGGAAAAAATGGACATGAAATAATAAGTAAGGTAAAACTTTAGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31383
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 |
---|---|---|---|---|---|
ENSDART00000028820 | Nonsense | 29 | 202 | 2 | 6 |
ENSDART00000036354 | Nonsense | 577 | 750 | 14 | 18 |
ENSDART00000137736 | Nonsense | 556 | 729 | 14 | 18 |
Genomic Location (Zv9):
Chromosome 4 (position 10788542)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 4 | 11725169 |
GRCz11 | 4 | 11724018 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTAGTGTGAAAGACTAACTGTGTGTTTGTTTACAGGTCCTGTGTTTA[T/G]AAGAACGACCAAGCGGTGAAGGAAAACCCCACTAAGGCCCTGCAGGAAGA
Long Flanking Sequence:
TTAAGAGAGTAAATAATGAGTAAATATTCATTTTTTAGTGAACTATCCCTCAAATATTTTACACAAAAACTCAAAAGATCAACATTTTTCATTTATTTTTTGCTGATATTTACAACGGGTGCCAATATTCGTGGAGTAATCTGTAAAATAATAAACAAAGCGTCAGTAAAAAGATTTCACAGGCATGTCTGACCTTCAGAAAGGAGTCAGTGGTTCCCCAACAGGAACAGAATGTTCTCTTCTCGCTTATGTGTGCGTGTATTAAATGTGTTTTTCACTTAAACGGGGGAGAGAAACCTTTTGTTCTGTACACTAATTGAAGCAGTTGGCTTCTAGAAAACTCAGTCAGTCTTTCTCTTGGATCTGCTGCTGCTTTCTGTCACTTTTTGTTTATTTGACTCGATTTGGGTGGGTGCGTGTGTTTGTACACTTTGCTTGGACGGTATGCGCTGTTTAGTGTGAAAGACTAACTGTGTGTTTGTTTACAGGTCCTGTGTTTA[T/G]AAGAACGACCAAGCGGTGAAGGAAAACCCCACTAAGGCCCTGCAGGAAGAGGAACCTTGTCCTCGGTTTGCTCATCAGCTTGTCTACGATGAACTCCACAAGGTAATGTTGATCATGGTTTTAATCTAACCCCAAGTTTCAATCTCAGCTCTCCTCAAGCAGGGTTATTATAGTTCAGTGCTTTTTAACAACATTCCTGGAGCCCAAAAACACTGCATGATCTGCATGTCTTCTTAATCAAACACACCTGATTCAACTCATCAGCTCGTTAGCAGAGACTCCAGGACCTCAAATGATTGTGTGAGACAAAGGAGACGTGCGTGAAATTAACTATCATTTTTGTCATCTGAAGTTAACTTGGCTGGAAAAAATGGACATGAAATAATAAGTAAGGTAAAACTTTAGTACTTTAGTTTGAGTATCTACATTCAGTATTAACTAGTGGCTTATTATCTGCTTATTATTAAGATATTGACTGTTTATTAGCACTTTTAAAGTTC
Associated Phenotype:
Not determined