ZMP
tjp2b
Ensembl ID:
ZFIN ID:
Description:
tight junction protein 2b [Source:RefSeq peptide;Acc:NP_001002366]
Human Orthologue:
TJP2
Human Description:
tight junction protein 2 (zona occludens 2) [Source:HGNC Symbol;Acc:11828]
Mouse Orthologue:
Tjp2
Mouse Description:
tight junction protein 2 Gene [Source:MGI Symbol;Acc:MGI:1341872]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa21212 | Essential Splice Site | Available for shipment | Available now |
| sa34328 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21212
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000018739 | None | None | 371 | None | 9 |
| ENSDART00000092355 | None | None | 389 | None | 7 |
| ENSDART00000115057 | Essential Splice Site | 489 | 1204 | 9 | 23 |
| ENSDART00000136184 | Essential Splice Site | 464 | 1179 | 8 | 22 |
The following transcripts of ENSDARG00000023443 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12021738)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11466501 |
| GRCz11 | 8 | 11504206 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGTAGAACCACAGGATGAAGAGCCACCACCACCGCCACCACCACCAC[G/A]TATGAACGTCATTTTGTAATTTCTTCATAGCTGATTGTAAAAACTGTAAT
Long Flanking Sequence:
GCCATGTAATAACATGCTATAACACTGGCATCTGATATAACGTGATGAAGTATGAATGCGAATATGTAATTTGCAACACGTTTGAAGTACACACCTGGAGAGTGCTTGAAAAGTGCTGGATTAGAAAAAAAAACTAAAACAAAAAACAGAATCTCTTTGACTGGTTGGCTACTATTAGCACTTTTTAAGGAAAAATTAATTTTATTTTTGCACATTAAGTCTGCATACTTAAAATAGAGGCAAAATATAAGGCTGTCCTGGGAAAATCTTAACTGTTAGTATGTTTTAAATATTGTGAGAACTTGAATTTTGTTATTCAGAAGCTGTCGCGTCATAACTGACATTTATCTGTTGTATTTTCAGGGAGGATCCTCAAAGCAGACTGACAAAATCCCCTGTCACTTCTTCTCCATACAAAACTGTAGAGGAGCCACATCCAGCTCAGGAGGAGAGAGTAGAACCACAGGATGAAGAGCCACCACCACCGCCACCACCACCAC[G/A]TATGAACGTCATTTTGTAATTTCTTCATAGCTGATTGTAAAAACTGTAATGACTGTGTAGTTATTAGACGCGTTATGGTTTGATATCCTTTGGCAGAGAATTGGGAATGCTATATAAACACGGCAGGGCTGACTAAATGAAACCAGAGAGTTACGAACTAAGTAGTGAAGTCTCCTTCAGCCTATTTTAAGATAGCTATAAAAAAACTATTAAACTTTAAGATGACCAAACAGTCAAACCATATACTGAAAACAAAAAAAAATTGACATTGACTTCTGAGATTTACCTCAGTGTGTTATTTACTATCAAAAGTTCATGTCGGATCCCTTAATGTGAAGCTAAATCTTTCATCAGAGAGAAATGATCCCAATGTCACAAAAATAAGAGTATTTATATATTTGCTTATATTTTATGTTTTTAAAATTAATTTTATTTATAAAAAATACACTTTTTTGCCATGATTATAACAAGTATTCACTATTGTTCAAAAGTTTGCCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34328
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 |
|---|---|---|---|---|---|
| ENSDART00000018739 | None | None | 371 | None | 9 |
| ENSDART00000092355 | None | None | 389 | None | 7 |
| ENSDART00000115057 | Nonsense | 1097 | 1204 | 21 | 23 |
| ENSDART00000136184 | Nonsense | 1072 | 1179 | 20 | 22 |
The following transcripts of ENSDARG00000023443 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 8 (position 12057079)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 8 | 11501842 |
| GRCz11 | 8 | 11539547 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGAAGACCCCTCAAAGAGGTCTTTCCTGGGCAAAGTCAAGGCCTTCGAG[C/T]AGATGGATCACTTCGCCCGCTCACAGAGGGTTCTGGAGATACAAGAAGCC
Long Flanking Sequence:
TTTGTAAACCTTAATTAAATACAAATTAAAAGTAATTTTTTTTGTTTTTTCATGTGCTAAGTTTAGTTACTATACTCTCAAAATCATCCCGCATACGTCTGCAGATTTTTTTTTAAAATATTCTGAGCAGAAAAAGCAAAAAAAAAAAAAATACGTCTGACTTTTCAATGATACAGTGCAGTCTTGGTTTTCATTCATTCAGTGCTGTTTTCTAACGCTTCACCGTGTTTCAGGTAAAAATGCTGTCTCAAGTGGAGGTGTCTCGCGGCCATTACGACCCCTCTCGAAACTACGACTCTCGTTCAAGCAGTCCCGCGAGCAGCGAACATCAGCGCAGCCTGGACTCTCCAGCAAAAGCCAAACCAGCACCTCCACCAACACCCCTGAAGCCTGCCCTCGCGTCCCGCAGCTCCAGAGGCCTCATCAACAGTGAGCCTCCGGCCGACAGTCCTGAAGACCCCTCAAAGAGGTCTTTCCTGGGCAAAGTCAAGGCCTTCGAG[C/T]AGATGGATCACTTCGCCCGCTCACAGAGGGTTCTGGAGATACAAGAAGCCCAGAACGCCAGGGTCAGTTTCAGCCTTTCATGAATATCAGAACGACAAAATAGCTTTGTTTACATTCAAAAGCAAGATGCATTTTCATCAGTCTGATCACAAATGAATGCTGCTAAATAATTAAATAATAAGATTTTATAGCGTGTTTTATTTGAAAATGAGCATTTTTACTCATTTGTACGTTTACATTGTCTGTGATACTGCTTTAGAACAAAAATATTTGTGTTTTTTAAAAAGAATAGACTTTTCAAAAAATACTGTACCAACTACTGTACACTACCTGACAAAAGTCTTGTCATCAATCCCAGTTTTAAGAGCAACAAATAATAACTTGACTTCTGATAACTGGCAGAAGGTAGATTTTTTTGATGAATCATCTGTTGAACTGCATCCCCATCAAATAATGCAGAAGACCCATTGGACCCAAGATTCTCACAGAAATCAGTCAAG
Associated Phenotype:
Not determined