ZMP
obscn
Ensembl ID:
ZFIN ID:
Description:
Obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF [Source:UniProtKB/TrEMBL;Acc:B8JI51]
Human Orthologues:
MYOT, MYPN, PALLD
Human Descriptions:
myopalladin [Source:HGNC Symbol;Acc:23246]
myotilin [Source:HGNC Symbol;Acc:12399]
palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:17068]
myotilin [Source:HGNC Symbol;Acc:12399]
palladin, cytoskeletal associated protein [Source:HGNC Symbol;Acc:17068]
Mouse Orthologues:
Myot, Mypn, Palld
Mouse Descriptions:
myopalladin Gene [Source:MGI Symbol;Acc:MGI:1916052]
myotilin Gene [Source:MGI Symbol;Acc:MGI:1889800]
palladin, cytoskeletal associated protein Gene [Source:MGI Symbol;Acc:MGI:1919583]
myotilin Gene [Source:MGI Symbol;Acc:MGI:1889800]
palladin, cytoskeletal associated protein Gene [Source:MGI Symbol;Acc:MGI:1919583]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21250 | Nonsense | Available for shipment | Available now |
sa12899 | Nonsense | Available for shipment | Available now |
sa1115 | Nonsense | Available for shipment | Available now |
sa17011 | Nonsense | Available for shipment | Available now |
sa12781 | Nonsense | Available for shipment | Available now |
sa1045 | Nonsense | F2 line generated | Not yet available |
sa41172 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa21250
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 |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 223 | 1992 | 5 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18915602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18360490 |
GRCz11 | 8 | 18396202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGCCATGTCTTTCTCTTCAAAGACTGCATAGTCTTCTGCAAGCCAAAA[A/T]GAGAAGTTGGCACACACACCGAGGCCTACATATTCAAGAATAAAATGAAG
Long Flanking Sequence:
AAAATTAGGCAGATGGAAACAGCTATTGAGTATCATAGTATGCGGGTGATATATATCTCTATTCATAAACACAAGCTCAATGTAGATAAGTTATTATAATTGATTTAAATTAGCTATATTCCATTTGTATTTTTTAAGGAGATGATCAGGAACAAAGCAAAAAGCGGACAGAACTGTTGCCTATTAGAGGATGCCTTTGCCATGGTTTCTAGCTTGCCATGGCGTGCAGAGAACTTGCATCATCTGTCCATGATTGAAAATTACCCGGCACCTCTCAAGGGGCTCGGAGAACCCATTAGACAGGTACTGTATCATCATATTCGACTCTTTGTTTACAAGTTGACAAGATGACACATGTGAATCAGCATCCTGCTAATAAAATGTGCTTTTAGGGCCACTTTACAGCATGGGAGGAGATTCCTGAGGTCAAAAGCTCTCAGAGAGGACATCACCGCCATGTCTTTCTCTTCAAAGACTGCATAGTCTTCTGCAAGCCAAAA[A/T]GAGAAGTTGGCACACACACCGAGGCCTACATATTCAAGAATAAAATGAAGGTTTAAGCAAGCTTTCCCTTTTAATTACTTTGGCACTGTGTCCTAACTAGACATGATGCAGTGTCGTGACATGGTAAAAGTTATGTTACAAGGAGTTTTTGTCCTAACCATCTGCAGCCAACAGCTGAACAACAGTATATACTATTATGACAATGATCACCTCAGGGACAGATTATGGGCTTTATTCAGTTATAAATGCCACCAATGTGAGTTTTAATACCATTTTACATGACATTTATTCCCATATTACTGAAAGCAGCAGCAGATAGTTCACCTCAGGTCTTGAAAATAAAATTATTAGCAGACGATTCGAAAATGAAAGTCAGACGTGTGACTCAGTGCAAACCAAAATCAGTCACTCAGTAGCCTATTAATAATGTTAAAGAGGTGTAATAAGTGTTAATTAGATTAAAAGCCCTTACCATTTCATTAGAGTGTTGTTGAGACACG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12899
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 |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 259 | 1992 | 6 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18914862)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18359750 |
GRCz11 | 8 | 18395462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGATGTAAAGGACACAGCAGAAGGAGATGACAGRTCATTTGGGCTTTG[G/A]CACGAGCAWCGGGGAATGGTGAGAAAAATCATTTTGYAAGCTCGTTCCAT
Long Flanking Sequence:
TTATAAATGCCACCAATGTGAGTTTTAATACCATTTTACATGACATTTATTCCCATATTACTGAAAGCAGCAGCAGATAGTTCACCTCAGGTCTTGAAAATAAAATTATTAGCAGACGATTCGAAAATGAAAGTCAGACGTGTGACTCAGTGCAAACCAAAATCAGTCACTCAGTAGCCTATTAATAATGTTAAAGAGGTGTAATAAGTGTTAATTAGATTAAAAGCCCTTACCATTTCATTAGAGTGTTGTTGAGACACGTGTTAATAAAACAAACATTGGGCAGTCTAATCTAAATGCGGTTCGACAGACAATTTGACATTGCATTTGAAGAGATGTGTAGTACTTTACACTCCTCATATTACTGTATGTATATCATGGCACTGCTAATATCCGCAGTCTATTGCAGATTCAACACAAATACACTTGCTTTCTTCACAGTTGAGTGATATTGATGTAAAGGACACAGCAGAAGGAGATGACAGATCATTTGGGCTTTG[G/A]CACGAGCATCGGGGAATGGTGAGAAAAATCATTTTGCAAGCTCGTTCCATCCTCCTTCGTCTCTCCTGGCTCAAAGACCTGAGAGACCTGCAACAGCGCAACAAACAGCCAGCTTGGTGTAAGCCACAACTCATACTTTTGAATACATTTGTTTTGACCGCTTAAAATGACTGCATTTATGCACCTTTTTATTCATATTTATAGGTGCCCCATGCTTTGAGCAGCATCTTACTGACTATCCAGCAAAGCTTGGGCAAACTGTTAAACTGGTCTGCAAGGTCACTGGTACACCAAAGCCAGTAGTAAAGTGGTATAAAGGTAACAATAGTGTAATATGCGTGTATATAAAAATGAAGTGTTTTTATGTAATATGTGTTCTGCTGTTGTTTCACAGATGGCCACGCTGTGCAGGATGATGAGCATCACATTACATCAGAAGGACAGTTTGGTGCTTGTTATCTTGTACTGACTGGTGTCACCGTGGCACACTCCGGTCAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1115
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 |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 272 | 1992 | 6 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18914825)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18359713 |
GRCz11 | 8 | 18395425 |
KASP Assay ID:
554-1017.1 (used for ordering genotyping assays)
KASP Sequence:
CATTTGGGCTTTGGCACGAGCATCGGGGAATGGTGAGAAAAATCATTTTG[C/T]AAGCTCGTTCCATCCTCCTTCGTCTSTCCTGGCTCAAAGACCTGAGAGAC
Long Flanking Sequence:
ACATGACATTTATTCCCATATTACTGAAAGCAGCAGCAGATAGTTCACCTCAGGTCTTGAAAATAAAATTATTAGCAGACGATTCGAAAATGAAAGTCAGACGTGTGACTCAGTGCAAACCAAAATCAGTCACTCAGTAGCCTATTAATAATGTTAAAGAGGTGTAATAAGTGTTAATTAGATTAAAAGCCCTTACCATTTCATTAGAGTGTTGTTGAGACACGTGTTAATAAAACAAACATTGGGCAGTCTAATCTAAATGCGGTTCGACAGACAATTTGACATTGCATTTGAAGAGATGTGTAGTACTTTACACTCCTCATATTACTGTATGTATATCATGGCACTGCTAATATCCGCAGTCTATTGCAGATTCAACACAAATACACTTGCTTTCTTCACAGTTGAGTGATATTGATGTAAAGGACACAGCAGAAGGAGATGACAGATCATTTGGGCTTTGGCACGAGCATCGGGGAATGGTGAGAAAAATCATTTTG[C/T]AAGCTCGTTCCATCCTCCTTCGTCTCTCCTGGCTCAAAGACCTGAGAGACCTGCAACAGCGCAACAAACAGCCAGCTTGGTGTAAGCCACAACTCATACTTTTGAATACATTTGTTTTGACCGCTTAAAATGACTGCATTTATGCACCTTTTTATTCATATTTATAGGTGCCCCATGCTTTGAGCAGCATCTTACTGACTATCCAGCAAAGCTTGGGCAAACTGTTAAACTGGTCTGCAAGGTCACTGGTACACCAAAGCCAGTAGTAAAGTGGTATAAAGGTAACAATAGTGTAATATGCGTGTATATAAAAATGAAGTGTTTTTATGTAATATGTGTTCTGCTGTTGTTTCACAGATGGCCACGCTGTGCAGGATGATGAGCATCACATTACATCAGAAGGACAGTTTGGTGCTTGTTATCTTGTACTGACTGGTGTCACCGTGGCACACTCCGGTCAATACATGTGTTATGCAACCAATCCCGCAGGGAATGCAAGC
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:
sa17011
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 |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 410 | 1992 | 9 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18912107)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18356995 |
GRCz11 | 8 | 18392707 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCTCCRAGTTTCAMAACCAGACTGCAGAACGCAGTGCTTGTAAAAGGA[C/T]AAGATGTGCAGTTCAWGTGTTCCACACAATCTGTTCCTTTCCCATCAAYA
Long Flanking Sequence:
ATCAAGTAACAATGAACCGACGAAGACATGAGGGAAGAGAGCACATTATAAAGGGAGGAAACAGCATAAGGACCAGGCGTAAACACAGACTAACGAGGACTAGATGAGGGCTAAACAAGGGGGTGTGACACCTGGAAACAAGGTGGGAGGAACAGAGGAAGCACATGGTGAATACAAACACAGGCTAAGCCATGTGATCAGACATAACATAAACATAGACACATGGAACGTAGACAACACAGAAAAGACAGACAAGGAAGGGCTATGACAGAGTCGTGATAAATAATGATCTCTTCCTTTGCTCAAACCATTTTTATGCTGAAATGAAATGCCTTCCTTTTAAACTAAAAATGCATTTATGATAACATGTTTTTGCATATGTGAAATTGATGTGATTTTGCTGTATATGTAACTATAAATTGAAAAAAGTATGTATATTGGTTCGTTAAGTGCCTCCAAGTTTCACAACCAGACTGCAGAACGCAGTGCTTGTAAAAGGA[C/T]AAGATGTGCAGTTCAAGTGTTCCACACAATCTGTTCCTTTCCCATCAATAAGGTAAATCTGTTTTTATTCAATCATAATTATGTAATGTCATTGTTATACAAAACATCACACAGTCTACATGCACAGGTGGTTTAAGGATGACATTCAGCTTGAGGACAGTAGGAAACACCTGATCCAGTCTGATGTTCAGACAGGAATTCTTACTCTTACTATAAAGAAAGCTGACGAGGCCGACGTGGGTCAATACCAGTGTGAGGTACCAGAGGATTCCATTGTTCATTAAGTTCATATTATCTATGGATCTCATTATATACACTTTCTTTGTGTTCATGATACAGCTACTGAACGAAGTGGGCAGTGCCATGTGTAAAGCTGAACTCTGTGCTCCAGCAGCAGAAGCTGTGACAGTCAGCTCTCAGAAACAATCACAAACTGTCCCAGGTAGGATGAAGAGGAATATGAACAGCAGTTACTTTTTAAAAGGGTGATTCACCCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12781
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 1602 | 1992 | 27 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18894918)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18339806 |
GRCz11 | 8 | 18375518 |
KASP Assay ID:
2260-0393.1 (used for ordering genotyping assays)
KASP Sequence:
TTYTGGAAACCTGTGCCATCCAAAGAGCTTGTCACATATTGTATTCAGTA[T/A]AGTGTAAATGGTAAGAATAYATACTAAAGSAATACACTCAGTYCCAWCTR
Long Flanking Sequence:
GTGTGCATGTACGTGACATGGGCATATACAGTATAATAGCTCATATAACATGTGCTAGCCACATCTTTACAAATATGTTTGAGCATATTAGTGAGTTAGCTGATCAGCATCCGCAACTGTCATCGAGTTAGTATGGTCACTAATGTTTGAGTGAAGCATTTATTTTGAGCTGTGATCAAAACAAACTGGAATTACAAATGCATTTCGATTTTATTTGACAACTTTCAGCCAATCAGAATTAAGAATTTCAGCAGATAAATTACTATTTAAGATAAATGACTATTCAAAGGCTTGTGTTAGGGTTGATACTTTTTTTTGGTTTTAAATGAAGAGCTTACTAGCTATTTGTAAGAGATTTTTAAAAGTATTTTGTTGTATGTTCTACAAGAATGTCCAGTCAAACCATCCAGGCCAGATGTAATTCAGCTTGCAGGAGGAGGAGCTCTTGTCTTCTGGAAACCTGTGCCATCCAAAGAGCTTGTCACATATTGTATTCAGTA[T/A]AGTGTAAATGGTAAGAATACATACTAAAGCAATACACTCAGTTCCATCTATTTATATTATTTTTCCAGTGTGTTTTTGCTTTCTGTTGTACTTAATAAATAATGTATTTTCCTTTATGTTAGGTGGCGAGTGGAGAGTGTTGTCAGAAAATGTCACAGATAGCTGTTTCACTGCTAAAACCCTACCAAGAGGACCAGGATATATGTTCAGAGTTTCCTATCACACTAAGACAGGGCTGGCACCTTTCAGTGATCCATCACCACCTGCCTTCATGGCAATACCTTATGAAGGTATGCTAATTAAAATAAAAATAACACTGAAGTTAAATAGTTTATTTACACCCTATAACAGATCTCTGTAACTGCTCTGTTTCTGTCTTGTACTGTTTTTTCCATCAAAAATATGACTTTCTAATAATAGGTTCATATTAGACTGCTTATTTAAAAGGCAAAGTGTTCGTAAAAATTAAAAATTGCTGATAAATTACTCACCCTAAGGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1045
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000063577 | Nonsense | 1750 | 1992 | 30 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18892538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18337426 |
GRCz11 | 8 | 18373138 |
KASP Assay ID:
554-0948.1 (used for ordering genotyping assays)
KASP Sequence:
ATATCAAGTGCTCCGTCGACTCRGCCACCCTCGAATCGTCCAGCTGCATT[C/A]GGCCATCCTCACCTCCACCTGCCTGCTGCTTATAGAGGAGCTGTGCTCAG
Long Flanking Sequence:
GAGGATAAATAACAAAATATATAGTCCAGGTAAACAACGGAGAACGGAGACAGCTGTGGTTGTAAATCAGTGTAGATGACAGACCGGGTGTGGGCGCGAAAGAATGTATGGAAATGTAGTTCTAAAGCCACTGTAGTTAGCTGGGGGTTGCTGACGAACTACAGTGGCATCTGGTGGACAACACAGTCATGACATTAACTGCTCAGAAAATAATTCATTACCATTATTGTCGATATTTTCTTATATCATTTTAATTACAATCATTATAATCCCTTAATTTAGGTGATAAGTTATAATGAGATAGTGTGGGCTAACAAGTGTATGTGGTTTTTTTTTTTTCAGAGGCCGTTTCAGTGTGGTGATGCAGTGCGAGGACAGCCGCAGCTCTCAGATGCTGGCAGCTAAAATGACTCCCTACAAACCAGAGCAGAGGCAGCTGGTTTTGAGGGAATATCAAGTGCTCCGTCGACTCAGCCACCCTCGAATCGTCCAGCTGCATT[C/A]GGCCATCCTCACCTCCACCTGCCTGCTGCTTATAGAGGAGCTGTGCTCAGGGCGAGAGCTGCTTTATAACCTCGCAGAAAGGTAGAGAATGCATTTTCATAGATGCTGCTTGAAATCATGGTTTGTAACAGTGTGTGTTGTAAAAAAAGTTGTTTTGCTGGTTTGTAGGAATCTTTATTCAGAAGCACACGTGACTGACCTGCTGGAGCAGATTCTGAGCGCTGTGGATTACCTGCACAGTCGACGCATTGTACACCTGGACCTGAAGTCAGATAACATGCTTGTGACGGGCAAAAATTTAGTGAAGATTGTGGATTTAGGCTCCGCTCAGCCGTTTAATCCAGGACAGGCGCTGAACATTGAACATATCAGGGAAATGACAGATAATAAAGGTAAATCAAAGATACTGTAGTATGATCTAAAAACTATTGCTTTTGATTTTACTAATATTTATTATTCTTTATTGGAAATTTGGGAAAAGATTGAAAAAATTATAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41172
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 |
---|---|---|---|---|---|
ENSDART00000063577 | Essential Splice Site | 1852 | 1992 | 31 | 34 |
Genomic Location (Zv9):
Chromosome 8 (position 18892144)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 18337032 |
GRCz11 | 8 | 18372744 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACAGGCGCTGAACATTGAACATATCAGGGAAATGACAGATAATAAAGG[T/A]AAATCAAAGATACTGTAGTATGATCTAAAAACTATTGCTTTTGATTTTAC
Long Flanking Sequence:
CTGGCAGCTAAAATGACTCCCTACAAACCAGAGCAGAGGCAGCTGGTTTTGAGGGAATATCAAGTGCTCCGTCGACTCAGCCACCCTCGAATCGTCCAGCTGCATTCGGCCATCCTCACCTCCACCTGCCTGCTGCTTATAGAGGAGCTGTGCTCAGGGCGAGAGCTGCTTTATAACCTCGCAGAAAGGTAGAGAATGCATTTTCATAGATGCTGCTTGAAATCATGGTTTGTAACAGTGTGTGTTGTAAAAAAAGTTGTTTTGCTGGTTTGTAGGAATCTTTATTCAGAAGCACACGTGACTGACCTGCTGGAGCAGATTCTGAGCGCTGTGGATTACCTGCACAGTCGACGCATTGTACACCTGGACCTGAAGTCAGATAACATGCTTGTGACGGGCAAAAATTTAGTGAAGATTGTGGATTTAGGCTCCGCTCAGCCGTTTAATCCAGGACAGGCGCTGAACATTGAACATATCAGGGAAATGACAGATAATAAAGG[T/A]AAATCAAAGATACTGTAGTATGATCTAAAAACTATTGCTTTTGATTTTACTAATATTTATTATTCTTTATTGGAAATTTGGGAAAAGATTGAAAAAATTATAATCCATGTGCTCATCAAACCCTAATTTAATTAATCATAATTACAGTGACTGAATTCAGTATTTACTCAATAAAAAAAAAAAAACAGTTTTTAGTTTTAATATACACTGGCCACTTTATTAGGTACATTTTACTAGTACCGGGTTGGATTTCCTTTTGCCTTCAGAACTGCCTTGAACCATCGTGGCATAGATTCAACAAGGTACTGGAAATATTCCTCAGAGATTTTGCTCCATATTGACATGATAGCATCACGCAGTTGCTACAGATTTGTCCGCTGCACATCCATTATGCAAATCTCCCATTCCACCACATCCCAAAGGTGCTCTATTGGATTGAGATCTGCTGACTGTGGAGGTCATTTGAGTACAGTAAACTCATTGTCATGTTCAAGAAATCA
Associated Phenotype:
Not determined