ZMP
obsl1b
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate obscurin, cytoskeletal calmodulin and titin-interacting RhoGEF (
Human Orthologue:
OBSL1
Human Description:
obscurin-like 1 [Source:HGNC Symbol;Acc:29092]
Mouse Orthologue:
Obsl1
Mouse Description:
obscurin-like 1 Gene [Source:MGI Symbol;Acc:MGI:2138628]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7206 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10142 | Nonsense | Available for shipment | Available now |
sa15355 | Nonsense | Available for shipment | Available now |
sa34721 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41505 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7206
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112542 | None | None | 888 | None | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | Nonsense | 226 | 798 | 2 | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42853730)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41978900 |
GRCz11 | 9 | 41780687 |
KASP Assay ID:
554-5082.1 (used for ordering genotyping assays)
KASP Sequence:
CAGGACATGAAGATGAAGGCAACCGTAATGGATACACKAACGGCCACTGG[A/T]AAGCACATCAGGGGAAACAAAGAAGTGGTAGACAAGTTGCKACCAGGCTG
Long Flanking Sequence:
ATGGAAATGTCTACAACCTTATAATAACTTCAGTGACAATGGAGGACAGTGGGCAATACATCTGCAAGGCAAAGAACTGCATTGGAGAGACTTATGCAGCAGCCACTTTAAAAGTAGAAGGTGAAGCACAGGAGATGGAAGTTCGGGAGGAAAACAAGCCACGCTTTCTTATCAAACCCCTCTCAACTAGGGTTGGACGAGGAGAAGATGCCATGTTCTCCTGTAAGCTGTGGGGAAACCCTAGACCAGAAGTAATGTGGGAGAAGGATGGTAAGAAGTTGAATGAGATCTTTGAGAGCACACATTTCTCCATCAGCTATCAGGATGGAGGGTGGTTCCAGCTGAAAATTTTCAAGACGAGAGCACCAGATGGAGGGGTGTATACGTGTAAGGCCAGGAATGAATTTGGAGAGAGTCTGGCAGGGGCTGTGCTGTTAGTGGATGCTGGACCAGGACATGAAGATGAAGGCAACCGTAATGGATACACTAACGGCCACTGG[A/T]AAGCACATCAGGGGAAACAAAGAAGTGGTAGACAAGTTGCGACCAGGCTGAAAGATGACCCATTACCTAATTCAGCCAAAGTAAAAATGTTTGCAGTGACAGAGGGGAAACATGCAAAGTTTCGATGCTATGTAACAGGAAAGCCAAAACCAGAAATATTATGGAGGAAAGATGGGAAACTTATCTTGTCTGGAAGACGGTACCTATTGTATGAAGACAGAGAAGGTTACTTCACACTTAAAGTTCTCTACTGCAAGCAACAGGACAATGGAGTTTATGTCTGTTCTGCTTCAAACACTGCAGGACAAACACTAAGTGCTGTACACCTCATCGTCAAAGGTAAAGTTATCTGAATTGAAATGTGAAACTTGCCGTTCAATACAAAAACAAGACTGGCATACACTTATATAGTCCAATACAATTGTGTTGCTGTCTGATGTGTCAAGCATTTGGTCCCCTAATAAGCAGTAAGTTTTATGATGATTCAGTTGTAGGAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10142
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 |
---|---|---|---|---|---|
ENSDART00000112542 | Nonsense | 139 | 888 | 3 | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
ENSDART00000112542 | Nonsense | 139 | 888 | 3 | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42838513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41963683 |
GRCz11 | 9 | 41765470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGATTGAYGGAAMTGAGCATTTCACCTGTGAAGAAGAAGGGGCWTTC[A/T]GATCTCTGATTGTCCTRAATGCTGAGTTGAGAGACTCCGGAGAGTACATT
Long Flanking Sequence:
ATGGAGTAGAGAAACTTGTTGGTGAGATTGTGGTCCTTGAGTGTGAAGTGTGTCGACCAAATGCTGAAGTTAGCTGGAAGAAGGATGGAGATGAGATTGAGGAGAATAGCAACGTAACTATCACAGAGGACGGCACAAATCGTCAGTTAACCATTCACTCCGCAGACTTTGAGGATGCAGGGCAATATGTCTGTGATGCCAGAGATGATGTCATGGATTTTTTAGTAAAAATCAAAGGTACAATTAAATGATAAGTAGATTGAAATTGTTTTGTTGAACCCATTACTACAACCAGTTAAAATTCAAGCCTCTTTCTTCCAGATCCACCACTGAAAATTCTGCGGAAAGCTGACATAGAAACAAAACGCCAGTTTATGGTATCTGATGCCATTGTGTTAAAATGTGAGATCTCAAGAGCAAATGGCGTGGTCAATTGGCTAAAAGACAATGAGAAGATTGATGGAAATGAGCATTTCACCTGTGAAGAAGAAGGGGCATTC[A/T]GATCTCTGATTGTCCTAAATGCTGAGTTGAGAGACTCCGGAGAGTACATTTGCGATGCACAAGATGACAAAGTTGTCTTCAGTGTTACTGTAGAAGGTACTACTATTTAAAAGTCAATGTACACAGTGAAAAACATGTTTGCACTTGTCTAACTAATGCTTGTCATTGGAAGTACTTTTAAAAGTACACTGTCCTAAAAACAACTACAGTATATACCCATTTATAGAACAATTAGGTATAGATAAAGTATAACTTTGCAGACATCCCAAGTTGGGTAAAGTAATTCCCGGGGGAGACAGAGTTGATTTGCGGGAGAGTGGGGGTTTGTGGGGGGTGATGGTGAGTGACGTATCTGAATGGGGGCATGTGCGTGGGACGTACCTGAAGAGCGGTGGGGGTGAGTTGCGCGCGATGTAGCTGAAGAGCTGGGAGGGACGCGATGGAGAGGGGTGTGCGACGTATTTAAGGACTGGGTGGGAGACGCACGATTTTCGGGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15355
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 |
---|---|---|---|---|---|
ENSDART00000112542 | Nonsense | 139 | 888 | 3 | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
ENSDART00000112542 | Nonsense | 139 | 888 | 3 | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42838513)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41963683 |
GRCz11 | 9 | 41765470 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGATTGAYGGAAMTGAGCATTTCACCTGTGAAGAAGAAGGGGCWTTC[A/T]GATCTCTGATTGTCCTRAATGCTGAGTTGAGAGACTCCGGAGAGTACATT
Long Flanking Sequence:
ATGGAGTAGAGAAACTTGTTGGTGAGATTGTGGTCCTTGAGTGTGAAGTGTGTCGACCAAATGCTGAAGTTAGCTGGAAGAAGGATGGAGATGAGATTGAGGAGAATAGCAACGTAACTATCACAGAGGACGGCACAAATCGTCAGTTAACCATTCACTCCGCAGACTTTGAGGATGCAGGGCAATATGTCTGTGATGCCAGAGATGATGTCATGGATTTTTTAGTAAAAATCAAAGGTACAATTAAATGATAAGTAGATTGAAATTGTTTTGTTGAACCCATTACTACAACCAGTTAAAATTCAAGCCTCTTTCTTCCAGATCCACCACTGAAAATTCTGCGGAAAGCTGACATAGAAACAAAACGCCAGTTTATGGTATCTGATGCCATTGTGTTAAAATGTGAGATCTCAAGAGCAAATGGCGTGGTCAATTGGCTAAAAGACAATGAGAAGATTGATGGAAATGAGCATTTCACCTGTGAAGAAGAAGGGGCATTC[A/T]GATCTCTGATTGTCCTAAATGCTGAGTTGAGAGACTCCGGAGAGTACATTTGCGATGCACAAGATGACAAAGTTGTCTTCAGTGTTACTGTAGAAGGTACTACTATTTAAAAGTCAATGTACACAGTGAAAAACATGTTTGCACTTGTCTAACTAATGCTTGTCATTGGAAGTACTTTTAAAAGTACACTGTCCTAAAAACAACTACAGTATATACCCATTTATAGAACAATTAGGTATAGATAAAGTATAACTTTGCAGACATCCCAAGTTGGGTAAAGTAATTCCCGGGGGAGACAGAGTTGATTTGCGGGAGAGTGGGGGTTTGTGGGGGGTGATGGTGAGTGACGTATCTGAATGGGGGCATGTGCGTGGGACGTACCTGAAGAGCGGTGGGGGTGAGTTGCGCGCGATGTAGCTGAAGAGCTGGGAGGGACGCGATGGAGAGGGGTGTGCGACGTATTTAAGGACTGGGTGGGAGACGCACGATTTTCGGGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34721
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112542 | Essential Splice Site | 353 | 888 | 6 | 13 |
ENSDART00000138938 | None | None | 232 | None | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42833636)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41958806 |
GRCz11 | 9 | 41760593 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTATTCCATATGCACCACAAGATTTTACCTAATAACCTCTTCTAATTC[A/T]GAGGCACAGGTGCTGTTCACAAAGAGCATGGACCCAGTGGTTGCAGAGGA
Long Flanking Sequence:
ACCATTTTTAGGCAATATTCCAACATTTGCATAAAAATAGGTGAATGGAAACATGGCTATTGACTTTTGCTTTTTGGTTGTCAAATATAAATAGCTTTAAAAAGCGTTAAAACAGCTATCCGCTTGTTAAGTGTGATGTCATGTGAAGCGGTTTCCAGGTCTAAGCGCTATATCAAACTGAATAGGAAGACTCAAACAGTAATAAACATTTCCAAAGCGATGTAATACTTTCGAAAATCTTGATCGCAATATTTATATCCATGCCTAATATCCGATGACCAGAAAGTGATTTTTAGAAATTGTGAAAATAATGGTGTCTGTGACTGCAGTAGGTCCAGAGACTGTTGTGTACACCATGATTTTACATAAAATTTACTCTAATGTGTCATATGACTGAAAAGTGGTCATAAATGAATATTTTCTCAATGAGTAGTGGCTTGCACCCAGAAACAGTATTCCATATGCACCACAAGATTTTACCTAATAACCTCTTCTAATTC[A/T]GAGGCACAGGTGCTGTTCACAAAGAGCATGGACCCAGTGGTTGCAGAGGAGTTTGGAGAGGCAACACTTGAGGTGGAGGTCAGCACAGAGACTGCAGAGGTCCAGTGGATGAGACAAGGAGTGGTTATTCATCCAGGGTCCAAATTCACCTTAAGGCAGAGTGGTCGAAAACGTTCTCTCACAATTCACAAACTAACCCTTTTAGACCGAGGAACGTACAGCTGTGAAACACTTCATGATCGCACACAAGCCAAGCTCAGTGTGGAACGTGAGTCTACATTTGCCGCTATATTTCTCACTATGTGCTTTGTTAGAGTTTCTTTACAGTGACGGCCCATTAATGCAGCCCGTAGCAATGTTGTTGTCCCAAACAAACTGAATCAAGTGACCATGAGTAATGCGAGCAAGAGGCAAGCTACTTTAGTGACACTCACTCCATGGTTTGACGACAGCAAACAGGTGACTCACAGACTATTTACTGAGTCTCTGGGCACAGCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41505
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000112542 | Nonsense | 710 | 888 | 12 | 13 |
ENSDART00000138938 | Nonsense | 52 | 232 | 2 | 4 |
ENSDART00000141117 | None | None | 113 | None | 2 |
ENSDART00000144573 | None | None | 798 | None | 7 |
Genomic Location (Zv9):
Chromosome 9 (position 42823569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 41948739 |
GRCz11 | 9 | 41750526 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGTTTCAAAGCAATATCACAATGCTTAAAACTTTTAATTCCCACAGCAT[T/G]ACCAGCAAACATTGTGAAACCACTTCAGGATAAAACTGTTCTGGAGAAAA
Long Flanking Sequence:
TTGGTTTTGTCAACCCAAAACTTACTCTAGAACAGGGGTGTCCAAACTCAGTCCTGGAGGACCGGTGTCCTGCATATTTTAGTTCTGACCCCAATTAAACATGCCTGAACCAGCAAATCAATCTCTTTCTAGGTATACTAGAAACTTCCAGACAGGTGTGTTAAAGGAAGTTGGACCTAACTATGCAGGAAACCAGCTCCCCAGAAACAAGTTTGGACACCCCTACACTAAAACCTGGAGTTTGTTCAACTTGTTTTGTGCAGCAGATCTCTGGTATTTACTACACCCCAACAAATGGGAAAGCAGCTATGCCCAAAAGCCTCCCAAAAAATTCTTCAAATAAGTAATGTAATATAATGTCTACAATTTCCATCTCTATGGTTCTACAACTGTAGCCACGACTATATAATAAAATATTAAAATATAATAAACTGGATATATTATAAAAATGAGTTTCAAAGCAATATCACAATGCTTAAAACTTTTAATTCCCACAGCAT[T/G]ACCAGCAAACATTGTGAAACCACTTCAGGATAAAACTGTTCTGGAGAAAACCCGTGCCATAATGGACTGCACACTGACCAATCCCCGCTGCAGCATTCGCTGGTATAAGGGACCTAACGTCATCCTGCCCTCGGAGCACTTTGAGATATGCAGTGAAGGATGCTATCGAAAACTTGTGATCCAGCAGGTGCTGCTGGAGGATGAGGGCACCTATAGTGTTCAAGTAGGAAACTACACATCTTCAGCAAGACTAACTGTTGAAGGTGAGACTATTTCAGTTCTCTGAAACCAATTATACAAGAATAACATTATGTAACATTATGGGCTCTACTCGCCCTGCTCTTGGTGGAATTTGAGCCAACGTTTGAGAAAGAGTGCTAACACGAATGATAAAGAGAACAGTCTCAAGCTTCAGTCATTAGTGTGCTTCTCACATCTAGGTCACCAATAGAATCCCTATAGTTGTAATCACTACTTTCCCAAACACATTTTTGTCATGT
Associated Phenotype:
Not determined