ZMP
tjp1
Ensembl ID:
ZFIN ID:
Human Orthologue:
TJP1
Human Description:
tight junction protein 1 (zona occludens 1) [Source:HGNC Symbol;Acc:11827]
Mouse Orthologue:
Tjp1
Mouse Description:
tight junction protein 1 Gene [Source:MGI Symbol;Acc:MGI:98759]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa40924 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa7069 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20982 | Essential Splice Site | Available for shipment | Available now |
sa13285 | Nonsense | Available for shipment | Available now |
sa34097 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40924
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 |
---|---|---|---|---|---|
ENSDART00000108721 | Nonsense | 436 | 1699 | 10 | 29 |
ENSDART00000148347 | Nonsense | 361 | 1637 | 9 | 28 |
Genomic Location (Zv9):
Chromosome 7 (position 32439466)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30833806 |
GRCz11 | 7 | 31104956 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGAGATGAGGAGCGCATCTCTAAACCAGCGGCTCTATCCACTCCAGTT[A/T]AGATGGCTGAGGATGCTCTTCTGGCTCCGCCCAGCGAACAGCCCGGGGAC
Long Flanking Sequence:
AAGCCTTTAAATTGCACTTTAAGCTGAACACTAGTATCTTGAATAAATATATAGTAAAATATTATTTACTGTCACCATGGCAAAGATAAAAGAAGTCAGTTATTAGAAATGAGTTATTAAAACTATTAAATTTGGAATATTTACACAGAAATTGGCGAAGAATATAAAATAATTAATATTTAACTGAAGGGCCAATAATTCTGACTTCAACTGTAGACTTTCAGTCAAAAGTACCTGCATAATGTTCTGTTATTAGTTGTCCGTGCCTGTAGCCCGATGAATACATTTAGACGTTGGTCAAGTAATATACACATGAAACTAAAATCTGCCTTGTACAGTGCAACCTAAAATATTATTATTATTTTTGTTTAAATAAAGTACATGTTCATGTTTGTCTACTACAAAGCTTATTTCTGACTGTGATCTGCGCATTTGCCTGCAGCCATAGAAGTCGAGATGAGGAGCGCATCTCTAAACCAGCGGCTCTATCCACTCCAGTT[A/T]AGATGGCTGAGGATGCTCTTCTGGCTCCGCCCAGCGAACAGCCCGGGGACAAACAGATCCCTCCACTGCCAGGTCTGGACTTTCAGCTGTCTTCTGTCTTTCCCGTTGCTCTCTCATTGGCATGCGAAGGACCTCTTAAAATATATGATGAGGCAATTCACATCTCTCTGTTTTCTTATTTACTCTATTTTCCTTTTTTTTTAAGGTGCAATTTCATGTGAGGTCATCTTAATTTACAAGTAAAGGCATATTATGATCATGCAGCCAATACAGTGTTAGTTTTAATGTTTAAATATTATATTAACTCAATAATAATGAAAAAATTCATAGAACGTTAGAATGAAATCCAAACAGGCATTTTTCTCATAAGTAGAATATTGTAATGCTCTTTATAAGGGATATAAAACTCAACCAACGTTCTATCAATGATATCTCTTCTCTAATTACACGTTCACTAGCTTAAGGGTAGGAAAAACCTTTACCTCACAAATGATTGCAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7069
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108721 | Nonsense | 449 | 1699 | 10 | 29 |
ENSDART00000148347 | Nonsense | 374 | 1637 | 9 | 28 |
Genomic Location (Zv9):
Chromosome 7 (position 32439505)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30833845 |
GRCz11 | 7 | 31104995 |
KASP Assay ID:
554-5211.1 (used for ordering genotyping assays)
KASP Sequence:
CCACTCCAGTTAAGATGGCTGAGGATGCTCTTCTGGCYCCGCCCAGCGAA[C/T]AGCCCGGGGACAAACAGATCCCWCCACTGCCAGGTCWGGACTTTCAGCTG
Long Flanking Sequence:
TGAATAAATATATAGTAAAATATTATTTACTGTCACCATGGCAAAGATAAAAGAAGTCAGTTATTAGAAATGAGTTATTAAAACTATTAAATTTGGAATATTTACACAGAAATTGGCGAAGAATATAAAATAATTAATATTTAACTGAAGGGCCAATAATTCTGACTTCAACTGTAGACTTTCAGTCAAAAGTACCTGCATAATGTTCTGTTATTAGTTGTCCGTGCCTGTAGCCCGATGAATACATTTAGACGTTGGTCAAGTAATATACACATGAAACTAAAATCTGCCTTGTACAGTGCAACCTAAAATATTATTATTATTTTTGTTTAAATAAAGTACATGTTCATGTTTGTCTACTACAAAGCTTATTTCTGACTGTGATCTGCGCATTTGCCTGCAGCCATAGAAGTCGAGATGAGGAGCGCATCTCTAAACCAGCGGCTCTATCCACTCCAGTTAAGATGGCTGAGGATGCTCTTCTGGCTCCGCCCAGCGAA[C/T]AGCCCGGGGACAAACAGATCCCTCCACTGCCAGGTCTGGACTTTCAGCTGTCTTCTGTCTTTCCCGTTGCTCTCTCATTGGCATGCGAAGGACCTCTTAAAATATATGATGAGGCAATTCACATCTCTCTGTTTTCTTATTTACTCTATTTTCCTTTTTTTTTAAGGTGCAATTTCATGTGAGGTCATCTTAATTTACAAGTAAAGGCATATTATGATCATGCAGCCAATACAGTGTTAGTTTTAATGTTTAAATATTATATTAACTCAATAATAATGAAAAAATTCATAGAACGTTAGAATGAAATCCAAACAGGCATTTTTCTCATAAGTAGAATATTGTAATGCTCTTTATAAGGGATATAAAACTCAACCAACGTTCTATCAATGATATCTCTTCTCTAATTACACGTTCACTAGCTTAAGGGTAGGAAAAACCTTTACCTCACAAATGATTGCAACAACAGCAAATGACAACAATCCAGCATTTCAGTTAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20982
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108721 | Essential Splice Site | 655 | 1699 | 14 | 29 |
ENSDART00000148347 | Essential Splice Site | 580 | 1637 | 13 | 28 |
Genomic Location (Zv9):
Chromosome 7 (position 32446437)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30840777 |
GRCz11 | 7 | 31111927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGAAGAACCACCAGGAGGTGGAAAGAGGCATCATTCCCAACAAGAACAG[G/C]TGATCCTACTATAATGCATCAACAGTAAATAGACAACCTTCAGCTATTGT
Long Flanking Sequence:
CAAAAAACCCTCTTGAGAAATGTTTTTATTTAATGTCCCCCTCTGAGCAGCTTCAGCTCTCACCAGGGAAATTAATAATTTTACTCTCGGTGGGGCTTGGGCAAGGGGGTGCTCAATGGAAACCTCCTAGTTTGCCTGTGCCTAGAAACGGATATCTTTCAGTAGTAATTACTAAAATAATTGTTTTTTTTCCCACCCCACTATGTAGACCGTTTTGGCCTTTATAAGATCAAAAATGATTACTTCTTCATTACCGTCTTGTTTATCCCCTGTCCTCCAGTGTACCGGCGAATAGTGGAGTCTGATGTGGGCGACTCCTTCTACATCAGGACACACTTTGAGTACGAGAAAGAGTCTCCTTATGGGCTGAGCTTTAATAAAGGAGAGGTGTTCAGAGTGGTGGACACTCTCTACAATGGCAAACTGGGCTCCTGGCTGGCTATCCGCATCGGGAAGAACCACCAGGAGGTGGAAAGAGGCATCATTCCCAACAAGAACAG[G/C]TGATCCTACTATAATGCATCAACAGTAAATAGACAACCTTCAGCTATTGTATATGATATCATTATTTTGTGTAGATCCTATATTGATCATTGTTTTAGTTCCTAAAAAGAGCGGAGAATCAAAAATGAGTATACATCTGACCTGGTGTTGCCATCTTCTCTTCAGGGCGGAACAGTTATCAAGCGTACAGTACACACTCCCCAAGACTGCAGGTGGTGATCGTGCTGATTTCTGGAGGTTCAGAGGCCTGCGCAGTTCAAAGAGGAACTTGCGCAAGAGTAGAGAAGATCTGTCAGCTCAGCCCGTTCAGACCAAGTTCCCTGCTTATGAAAGGGTGGTTCTTAGAGAGGGTATGTGTGTAGATAAGAGTGCACAATATATGTTTTATGTTAGCTTTTTTTAGGACCAGTATTGAATATATACAGTAGGCAACTTTTGAAATGAATCAAAACCTCTCATCAGGTTGTCTGTCCTTAAACTATTAAAAAGCACCCATTTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13285
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 |
---|---|---|---|---|---|
ENSDART00000108721 | Nonsense | 1172 | 1699 | 22 | 29 |
ENSDART00000148347 | Nonsense | 1097 | 1637 | 21 | 28 |
Genomic Location (Zv9):
Chromosome 7 (position 32460365)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30854705 |
GRCz11 | 7 | 31125855 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGGTCACCCTCAGWCACGAAACGACACCGGCTACGACACAGGTCGACCT[C/T]GATAYGGCAAACCAACCTCTGGACCAAWCCGACACGATGAACCACCACCA
Long Flanking Sequence:
TGAGTCTTCCTCTATTGCAGGTCTCTCTTCTGACTCTCTGCTTCATTCTTCAACTTTTAATCCGAATATTAATCACTTCTGGTTTCTGCCGTTTCATTCAATTCAATTGATTGCTGTGGTTTATGCATGTTATTTATGCAGTTTCACTTACAACTCTCCTCATTTGGCTTGATCGACAGATGTACAAGAAGGATATCTACCGACCCAACGAACCGGTGCAGATAAGCCAAAACCCTATGCAGCCCAACTACTACCAGGAAGACAAGCCATACAGAGATTATGACCACCAGCCCTACCGCTATGATGGAGGCTACATGGAACCAAAGGCTCGTAACTTTGACCCACATTTTGAGGACAGCGTGCCTCCATATAATGATCAATGGGGTCAGTATGACCACACCTCTGGGTATGAACCTCAAACGCTCTACGAGGATGGTCTGAACCGCTTGTATGGTCACCCTCAGTCACGAAACGACACCGGCTACGACACAGGTCGACCT[C/T]GATATGGCAAACCAACCTCTGGACCAATCCGACACGATGAACCACCACCATCACGCCCACAATATGACACTCAACAAACCTCTCGTTCCCCAGAACCGCCCAAACAACAATACTACGACCCTTCCCAAAGGCCTTCCTACACTCAAGCTCCACAAAAAGGCTATATGAACTCTGAAGCACCGGTAACGCCACCCAAACCTGAGTCGCTCTCACCGCCTTTGGAGCCTGCTCTTCCTCCTCCACCTCCTCCAGCCGAAGCAGAGGATGATCCCGCCATGAAGCCCCAGTCGGTGCTCACCAGGGTGAAGATGTTCGAGAACAAGCGATCGGTGTCTGTAGACAGAGCCAGAGAGTCTGCAGACTCTGGTATTCGGGTGAGTTGATGGTCTGCATGTCTACTCACTAAATATACACTTGGGCTAAATAATTCATATGTTCATCTTTCTGCTTCCTGTAGCCTGTGGACATGGTGCCTAAACCTGGCGCTGCCTCCGTGCCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34097
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000108721 | Nonsense | 1223 | 1699 | 22 | 29 |
ENSDART00000148347 | Nonsense | 1148 | 1637 | 21 | 28 |
Genomic Location (Zv9):
Chromosome 7 (position 32460518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 30854858 |
GRCz11 | 7 | 31126008 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACAACAATACTACGACCCTTCCCAAAGGCCTTCCTACACTCAAGCTCCA[C/T]AAAAAGGCTATATGAACTCTGAAGCACCGGTAACGCCACCCAAACCTGAG
Long Flanking Sequence:
CTCTCCTCATTTGGCTTGATCGACAGATGTACAAGAAGGATATCTACCGACCCAACGAACCGGTGCAGATAAGCCAAAACCCTATGCAGCCCAACTACTACCAGGAAGACAAGCCATACAGAGATTATGACCACCAGCCCTACCGCTATGATGGAGGCTACATGGAACCAAAGGCTCGTAACTTTGACCCACATTTTGAGGACAGCGTGCCTCCATATAATGATCAATGGGGTCAGTATGACCACACCTCTGGGTATGAACCTCAAACGCTCTACGAGGATGGTCTGAACCGCTTGTATGGTCACCCTCAGTCACGAAACGACACCGGCTACGACACAGGTCGACCTCGATATGGCAAACCAACCTCTGGACCAATCCGACACGATGAACCACCACCATCACGCCCACAATATGACACTCAACAAACCTCTCGTTCCCCAGAACCGCCCAAACAACAATACTACGACCCTTCCCAAAGGCCTTCCTACACTCAAGCTCCA[C/T]AAAAAGGCTATATGAACTCTGAAGCACCGGTAACGCCACCCAAACCTGAGTCGCTCTCACCGCCTTTGGAGCCTGCTCTTCCTCCTCCACCTCCTCCAGCCGAAGCAGAGGATGATCCCGCCATGAAGCCCCAGTCGGTGCTCACCAGGGTGAAGATGTTCGAGAACAAGCGATCGGTGTCTGTAGACAGAGCCAGAGAGTCTGCAGACTCTGGTATTCGGGTGAGTTGATGGTCTGCATGTCTACTCACTAAATATACACTTGGGCTAAATAATTCATATGTTCATCTTTCTGCTTCCTGTAGCCTGTGGACATGGTGCCTAAACCTGGCGCTGCCTCCGTGCCCAAAGCCAATTCTTTAAGTAACCTGGATCAAGAGAAGACCTTTAGGTAATGAGCTTGAGTATGAAGTATAAATCAGTGTGTTAGAATAAATGAGCATTGGTGTCTATTTAAAGGACACACATTTAAGCACACACGCATATCATTTTATAACATGC
Associated Phenotype:
Not determined