ZMP
oclnb
Ensembl ID:
ZFIN ID:
Description:
occludin b [Source:RefSeq peptide;Acc:NP_001008618]
Human Orthologue:
OCLN
Human Description:
occludin [Source:HGNC Symbol;Acc:8104]
Mouse Orthologue:
Ocln
Mouse Description:
occludin Gene [Source:MGI Symbol;Acc:MGI:106183]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa20421 | Nonsense | Available for shipment | Available now |
| sa20422 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa20421
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 |
|---|---|---|---|---|---|
| ENSDART00000007247 | Nonsense | 170 | 468 | 3 | 9 |
| ENSDART00000098514 | Nonsense | 163 | 461 | 4 | 10 |
| ENSDART00000134432 | Nonsense | 170 | 471 | 3 | 9 |
The following transcripts of ENSDARG00000003091 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 27859105)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25614403 |
| GRCz11 | 5 | 26214556 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCATCCTGGTGGTGTCGAGACAGAGCAGTTCCCAGTCTCCCAAATTCTA[T/A]CTGGCCACCATCATTATTTGTGCCATTCTGGCTGCACTCATGCTCATCGC
Long Flanking Sequence:
AGTTTTTATTTTTACTCATCCTATCTCCCTTTCAGTCAGCACAGATCCTCCCATCGCACAGTTTCTTACCACCCCGATGAAATGCTTCACTTCTACAGCTGGAAGTCCCCCCCGGGTGTCATGAAGATTTTATGCATCATCATCATCATTATGTGTGTGGCTATGTTTGCCTGCGTAGCTGCCACATTGGCATGGGACTATGACGCCAACAACATGGGCCTTGGTGGTCTTGCCAGTCTTGGTATGGGCAGTAGTGGTGGAGGGTATAACGGTGGAAGCTATAATGGTGGTTCAGCTGGTGGATATGGAGGATACGGTGGAGGTATGGGAGGCTACGGTGGAGGTATGGGAGGCTACGGATACGGAGGAGGAACGTACATGGACCCAAAATCAGGCAAAGGCTTCATCATCTCTATTGCTGCAATTACCTTCATCGCTATTCTCATCATCTTCATCCTGGTGGTGTCGAGACAGAGCAGTTCCCAGTCTCCCAAATTCTA[T/A]CTGGCCACCATCATTATTTGTGCCATTCTGGCTGCACTCATGCTCATCGCCACTATTGTTTACCTGGTCACGGTTAACCCCACTTCTCAGACATCTGGATCCATGATGTATAATCAGATCCTGCAGCTTTGTGCACAGTATCAGAACCAAGACCAGGCCTCTGGCATCTTCATCAACCAATACTTATACCACTACTGTGTTGTGGATCCTGAAGAGGTGAGCAGGAAGCAGGCCATCTACAGTGTGTGTGTAAAAAAACAACCAGGCAGTATTTAGTGGCTGTAGAAATTGCATCGCTGTAAAAAATTGATTTCTTTCCAGTTTTTAATGCCCAGTTACATTTCACCTACCTTTTAGAGTTTGTTATTATCAGAACAAGCGTAATAATTTTATATTGTGTAGAAGTGCTAGTTGAGATTCAACTCTACAAATGCAAATCTGCCGCATTGTCCAGTATTTTGGTTTCTCATTTACGTTGATGTTAATGTTATGTGTTTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20422
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 |
|---|---|---|---|---|---|
| ENSDART00000007247 | Nonsense | 420 | 468 | 7 | 9 |
| ENSDART00000098514 | Nonsense | 413 | 461 | 8 | 10 |
| ENSDART00000134432 | Nonsense | 423 | 471 | 7 | 9 |
The following transcripts of ENSDARG00000003091 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 5 (position 27862839)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 25618137 |
| GRCz11 | 5 | 26218290 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTGGCAGATGCAGATCGAGAGCTCGACAGGCTAGAGGAAGGCAGCCCA[C/T]AGTTCATGGTATGTAATTTAGGAGACAACAGTTGCCTTAAAGTTTAGATC
Long Flanking Sequence:
ACCACAAGGCTGTTTTCTTTCTGTTGTTTACAGTTAAATAGTGCTGAGATTACACCCAACTCATTTAATGTGCTTATTTTATTAAACGTGTTTTCCACAGTAGTGCTTCAGACTTGACAAGCTCTGTGAGTGGATTGAAGGGCAAACTAAGAGCATATGACGCTGGAGAGTCTGGAGATGAGCTTGACACAGAGTATGAAACGTAAGAACAGTCCTTGTATTACAGTCAATAGTATTTACACATTAAAAAATACTCCGATTTGGTGACTTTTTACGTAATAAACATCACATTTGTCTTACTCCCCCCTCCCTTAATACTTTGCTGTCTTCCTCTCAGTGAATATCCTCCCATCATTAATGAGCAGGAGAGACTCGAGTACAAGAGAGACTTTGACAGAGACCACATGGTGTACAAGCGTCTTCAGGCTGAACTAGATGATATTAATCAGGGTTTGGCAGATGCAGATCGAGAGCTCGACAGGCTAGAGGAAGGCAGCCCA[C/T]AGTTCATGGTATGTAATTTAGGAGACAACAGTTGCCTTAAAGTTTAGATCTCCATCTTAATGAGTGTTATCATGCTGATTCAGCTAAATCTAAAACCTGCTTGTCTGTCACAATATTTTGCACTCTTCTGGTTATGCTTGGAAATGTCAACAATTTTTTCTACAGTACATTTATCATTCAGATATGTTGCATTAATGTATCTCTTTTTCCCTAAATAGGATGTCATGGATGAATACAACAGGCTCAAAAGTTTGAAGAAGGTAAACTTTTTATTTTACTTTTTTTTTTTGTATATTTACCCCCCGTAGGCTACATTTTGTTTGGAACAGTAATGAATTTTATATGTACCATCTGTTGAACAGCTCTTCGTAGTAAAGGCTTGTAATTTACAGTTAAAGTCAGGATTATTAGCCCTACTTTGATTTTTTTTTTTTTAATTAGTTTCCAAATTATGTTTAACAAAGCAAGCACATTTTCACAGTATGTCTGATAATATCTTT
Associated Phenotype:
Not determined