Busch Lab

ZMP

obsl1b

Ensembl ID:
ENSDARG00000077388
ZFIN ID:
ZDB-GENE-050809-29
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.
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
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