ZMP
zgc:153887
Ensembl ID:
ZFIN IDs:
Description:
sarcolemmal membrane-associated protein [Source:RefSeq peptide;Acc:NP_001070722]
Human Orthologue:
SLMAP
Human Description:
sarcolemma associated protein [Source:HGNC Symbol;Acc:16643]
Mouse Orthologue:
Slmap
Mouse Description:
sarcolemma associated protein Gene [Source:MGI Symbol;Acc:MGI:1933549]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa30953 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa21976 | Nonsense | Available for shipment | Available now |
| sa41914 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa30953
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 |
|---|---|---|---|---|---|
| ENSDART00000076650 | Essential Splice Site | 9 | 437 | 1 | 13 |
| ENSDART00000104444 | None | None | 823 | None | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 43448500)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 42073710 |
| GRCz11 | 11 | 42343648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGAGTGGAGGAGACTGCACTTTAATCCAACAGTACATTGAGTGTCAAT[G/A]TGAGTACACAGCATTCTTTCAAACGCCTTCCACAGCTGTACTAATGAACT
Long Flanking Sequence:
AATATTTATGGCTTCCTTTGTTTTAAAAAGATTTTATTTAAAAGAGTCCAAGCTTAATATAATTAATAACAAAAAGTAAAATAAAACAATATATTATTTTTAACTAATATTAATTTGCAGTGATCTGCTTAATGAGTTAAAAAAAGTATAAACTTAAGTGGAATACTATACAGAAACATAAATCTTGATTAGCATCAGACCTCAGTGTCCCAGTGGTGACCTGTAATTGACAGCTGTCAGTCATTGATGAGCAGCTCCGTGATTGGCTGCAGTCTACCATCTGTGTCCTTCTCCCGCCTTTTGCATCTCTGTTTGGTTTCGTCTCATATTGTGTCCTGTAGATCTGGCTTATGTTTTTAATTTCACCCGATGCCCCTCGACGTGGCATTTCTTCCATCTGCTGTTCATTTAATGGAGGGTTTTTCTTTCTTTGGTAGACCACTTTCTTTTAAAGAGTGGAGGAGACTGCACTTTAATCCAACAGTACATTGAGTGTCAAT[G/A]TGAGTACACAGCATTCTTTCAAACGCCTTCCACAGCTGTACTAATGAACTATATTATTATTATTATTATTATTATTAATCGGCATTATTAACGCAGGGAGCAGTTATTTCTGTTTTACTTTTGTAGGTTTTTTTTACACTGAGTTGCAGAGCGCAGCTAATTTTATTTCTGGTGTTGTGGCAAAAATAATGAAATTAGTTTGATCAGTAGAAATTTGTGCTGTCAAAATATAAATAGTGATTAATCCCATCCAAAAATGCTTGTATTGACATAATATATATATATTTGTACTGTGCATATTTGTTTTCTGTGTATAAATGAGCAATATCACACGAATAGCAGTGAGATATGGCTGTATATTGGCCCTGGTGCGAGGCATGCGTTGATGCCTTAGTGTCCCACCAGTGATGATATACAGCCATATCGCACTGCTACTCATGTAATACTGCGTTATATATATTTTATATATCATGTGTATAAAAAAAATCAAACACAGAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21976
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 |
|---|---|---|---|---|---|
| ENSDART00000076650 | Nonsense | 54 | 437 | 3 | 13 |
| ENSDART00000104444 | Nonsense | 440 | 823 | 13 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 43443688)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 42068898 |
| GRCz11 | 11 | 42338836 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAATAACCAGACGACAGTGGACAACAGCTTACCCAGTCCAGACAGACTT[A/T]AAGGTATTGTCACATTTCAGGCATTTTCATTTCAATTTGAATTTCTTTCT
Long Flanking Sequence:
TATATATGACAAACACAAATAAAAATATATAATAATAATAAATAATAATATTAATAAAATGATACATAAAATGACATTATAGATGAATGTAACACACATTAGGCTGTACAACAATACAGAAAATATACTCCTTAGTTGTGCTTTCTTACAATCAGTGTTTAGTTAATATACTTTAAGTTAAAATGACGCCAGTGTTACCGGTTGAAACCTAAAGTGGGTAAAGGTATTGAATGTCATTCTCTGATTCCTGTATTTATATATTAATTAGGCATAAAAGTCCATAATAAGCTCTTAAGTGTGTTTTTATGTAGATGGGGATTTAAAACAAAAACAAAAAAAACTCCGGTCATAAAAGTACCGGTGTAGTGTGGACATTGCTTCAGTCGAACAATACAGCTCAAGTCATTTTTTTGTGATTTTATTCTGCAGAAGTCATCGATGCACATCTTCAGAATAACCAGACGACAGTGGACAACAGCTTACCCAGTCCAGACAGACTT[A/T]AAGGTATTGTCACATTTCAGGCATTTTCATTTCAATTTGAATTTCTTTCTTGACCAAACCTTTACGTCACATTACGCTATGATGAAATCTGATGGCAATGAGGAGACCGTTTACACCAGCGGCCTCCATTTAAAATTGAATTAAACAACTCCACTCTCTGGGAGGCAGGAATGAACTTTAGTTATTTTTATCATCCTCAAAGATCATGACCTGGTCAGGGTCATTGCTGTAATGAGCACTAATGAGATCAGCATTATTAGCTGTCTATTATTGCTCATGATAATACTCTAGTTCTATTGTGCCCAATAATACAAATGTAATGCATTTTTAGTGTTACCACTAATATGATAAGCAAAAAACATTTTAAATCAGTTCCACCTTAAAGTAATAATGATAATAATAAAAATAATATTCAGAATAGTAATTATTGGAATAATAATCAGATTAAAAATAAATAAAAAAACAAATAAACCATTTGTTAACTTTCTTTTACAAAACTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41914
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000076650 | Nonsense | 238 | 437 | 8 | 13 |
| ENSDART00000104444 | Nonsense | 624 | 823 | 18 | 23 |
Genomic Location (Zv9):
Chromosome 11 (position 43430461)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 11 | 42055671 |
| GRCz11 | 11 | 42325609 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTGCAGGGAGACCTGAGCATCGTCACTGCCGAGCTGGACAAATGGAGA[C/T]AGACGGCAGCCAAATATGAAGTGGAGATCAGCAATCTGCAGGCCAGCTTT
Long Flanking Sequence:
CTGCCCCGATAAACACCCTGGCTTGCGATGGCTCAACAGTGGAAATGCAGCTGTTATCATCATTATGGGTTGAAAGCTAGTTTTCAGTTGCCAAAAATCATTTGCAGATAGAGTAAACTAGTGAATTTACAGAGAGTTAATTTTATCAAATATAGTGTTGCATTGGATTGGTGCTAAACTCATGCACTACACAGTTGGGTGCATTGTAAAACAATGGCAAAAACGCACTTCCTCACTGAAGAATAAGTGTCATTTGGGATGCAACTAATAACTCTTCTTTACCTTCAGCTCAACTAGCGAAGCTGCAGACTGATATGGAGGCTTTGCGAGAACAGCGAGAGAACACTATCACCACCACTCGAGAGGAGCTGTACAGCGCTCAGGAGGAGATCCTGGTGCTCCGGCACGCCATGGAGGCCGCCACCGCCGAGCGGGAGCGAGAGATCACCGCCCTGCAGGGAGACCTGAGCATCGTCACTGCCGAGCTGGACAAATGGAGA[C/T]AGACGGCAGCCAAATATGAAGTGGAGATCAGCAATCTGCAGGCCAGCTTTCAGCTCCAGAGCCAGCACCAGGAGAGAGCTAGCCAGCTCCAAGGTACTCCATACAATTTTTAGGTCACAGCTGTAGTCCGTGATGTTTTTGTGTGTGCATGCGTGAAACAATCACCTGAAATTATTTTACATTTATGAAGCAGAGGCTTTTATCCACAATTACTTGTGAATTTTTGAGCTAGTACAAAGCCAGCCAGAGTTTCAAAAATGTTCTCTTTGACATTTTATTTGAAATCTTTTTGTTAGTTTCTTTTGTATTAAACATTCATCAAAGGCGGCGACACTAAAGCTCCAAAGTGCTAATTTGCCATAAGCAAAAAAGAAAAACGTACATTGGCCATATCTGATCTGTGCTATATGGGAGAAAAAAAATCAGGATTGAGTCACTTGAACAGTGCAGCGTAAATTCAACCTTAATGTCATTTTAACACATTAAAAGTTGCAGATGCA
Associated Phenotype:
Not determined