ZMP
tnxb
Ensembl ID:
ZFIN ID:
Human Orthologue:
TNXB
Human Description:
tenascin XB [Source:HGNC Symbol;Acc:11976]
Mouse Orthologue:
Tnxb
Mouse Description:
tenascin XB Gene [Source:MGI Symbol;Acc:MGI:1932137]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42693 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39089 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12917 | Nonsense | Available for shipment | Available now |
sa39088 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22795 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42693
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 |
---|---|---|---|---|---|
ENSDART00000014439 | Nonsense | 623 | 2285 | 1 | 14 |
ENSDART00000132368 | None | None | 389 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 18689202)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16738950 |
GRCz11 | 16 | 16646927 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTCTTCAAAGCCTGAGGTGGACACCACACAGAAACCTGTCCAAAGTGTA[C/T]AAAACACAATTGGTGACAAGAAAAATTCTACCACTGAGTCTATAGTCAAC
Long Flanking Sequence:
AATCCTCTTCTTCAACAAGTCAATTAAATCAGACTCTCACAACCTCTCAAAAGCCTGGGGTGGACTCCATACACAAACCTGTCCAAAGTCTACAAATCACATTTGGTGGCAAGACAAATTCTACCACTAAGTCAATAGTCAACATTGTTGATGTTCAGAAACCAGCTACTAAATTAAACACCAAAATGAAAGTACAAACTCAATCTACGTCTTTAACAACAACACAGGTAAATCTGACTCTCCCATCATCTACAATGCCTGAGGTGGACTCCGTACAAAAACCTGTCCAAAGTGTACAAAACACAATTAGTGGCAAGAAAAATTCTACTACTAAGTCAACAGTTAACACTATTAATGTTCAGAAACCAGTAACTTCTTTATTGAAGACAAAACTGAAAGAACAAACTCAATCTACTCCTTCAACAAGTCAAGTAAAACAGACTCTCACAACCTCTTCAAAGCCTGAGGTGGACACCACACAGAAACCTGTCCAAAGTGTA[C/T]AAAACACAATTGGTGACAAGAAAAATTCTACCACTGAGTCTATAGTCAACACTATTAATGTTCAAAAACCAGCTACTAGATTAAACACCAAACTTAAAGACCAAACTCAATCTACTTCTTCAACAACTAGCAAAGTAAATCACACTCTTCCCTCATCTACAATGCCTGATGTGGACACTGTCAAGAAACCTATCCAAAGTCTACAAAACAAAATTGGTGACAAGAAAAATTCTACTACTAAGTCAACAGTCAACACTATTAACATTCAGAAACCAGTAACTTCTTTATTGAAGACCAAACTCAAAGAACAAACTCAATCTACTCCTTCAACAAGTCAAGTAAATCAGACACTTACAACCTCTACAAAGCCTGAGGTGAACTCCATACAGAATCCTGTTCAAAGTGTACAAAATACAGTTAGTGACACCAATAATTCCACAACTAAGTCAACTGTCAACACTATTAAAGTTCAGAAACCAGTAACTTCTTTATTGAAGACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39089
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 |
---|---|---|---|---|---|
ENSDART00000014439 | Nonsense | 698 | 2285 | 1 | 14 |
ENSDART00000132368 | None | None | 389 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 18688977)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16738725 |
GRCz11 | 16 | 16646702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTGTCAAGAAACCTATCCAAAGTCTACAAAACAAAATTGGTGACAAG[A/T]AAAATTCTACTACTAAGTCAACAGTCAACACTATTAACATTCAGAAACCA
Long Flanking Sequence:
AGGTAAATCTGACTCTCCCATCATCTACAATGCCTGAGGTGGACTCCGTACAAAAACCTGTCCAAAGTGTACAAAACACAATTAGTGGCAAGAAAAATTCTACTACTAAGTCAACAGTTAACACTATTAATGTTCAGAAACCAGTAACTTCTTTATTGAAGACAAAACTGAAAGAACAAACTCAATCTACTCCTTCAACAAGTCAAGTAAAACAGACTCTCACAACCTCTTCAAAGCCTGAGGTGGACACCACACAGAAACCTGTCCAAAGTGTACAAAACACAATTGGTGACAAGAAAAATTCTACCACTGAGTCTATAGTCAACACTATTAATGTTCAAAAACCAGCTACTAGATTAAACACCAAACTTAAAGACCAAACTCAATCTACTTCTTCAACAACTAGCAAAGTAAATCACACTCTTCCCTCATCTACAATGCCTGATGTGGACACTGTCAAGAAACCTATCCAAAGTCTACAAAACAAAATTGGTGACAAG[A/T]AAAATTCTACTACTAAGTCAACAGTCAACACTATTAACATTCAGAAACCAGTAACTTCTTTATTGAAGACCAAACTCAAAGAACAAACTCAATCTACTCCTTCAACAAGTCAAGTAAATCAGACACTTACAACCTCTACAAAGCCTGAGGTGAACTCCATACAGAATCCTGTTCAAAGTGTACAAAATACAGTTAGTGACACCAATAATTCCACAACTAAGTCAACTGTCAACACTATTAAAGTTCAGAAACCAGTAACTTCTTTATTGAAGACAAAACTTAAAGAAAAAACTCAATCTACTCCCTCAACAAGTCAAGTAAATCAGACCCATACGACTTCCACAAAGCCTGAGGTGGAATCCATACAGAATCCTGTCCAAAGTGTACAAGACACAATTAGTGGCAAGAAAAATTCTACTACTAAATCAACAGTCAACACTATTAACGTTCAAAAACCAGTAACTTCTTTATTGAAGACAAAACTCAAAGAACAAACCCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12917
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 |
---|---|---|---|---|---|
ENSDART00000014439 | Nonsense | 1467 | 2285 | 3 | 14 |
ENSDART00000132368 | None | None | 389 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 18683927)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16733671 |
GRCz11 | 16 | 16641648 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACTGTGACTATGAAGATGTCCAGTGCCATGCCAGACMCAAAAACTGWC[A/T]AGACAAGGCCAGACAAGGCAATTTTAGTGAAAGAGACAGTTACAAAGGTC
Long Flanking Sequence:
ATGTCAATGCAACAGTTTTCCATACAATGAAAAAAATGGCTAACAGAGACAGTCAAACCTACCTCCAAAACCACAGGAAATTGCTATAGTACAGGCAATGTGATCAGTTTTAATGTGAGGAATCAACATAATCTTGTATATTTTGTATGATAAACAGCTTTTTCATGGTGTTTTGTTGTTGGTGTTTTAAATTTTATAGCTAAACAGTTCATGGTTCCAAACTATTTGAATTCCAAAGGAAATTGAAAGATGTACGTAGATACAAAGATAAACATCATTGATGCTGTAATGTTTAATTTGTTACATGGAGAAAAAAAAAATCATAATTTTGTAATCATAAGAGTGTATGATACATTTTAATTATGGGTTGAACTACTTATTTAAGATTGCAAGTCTCACTTTAAATGATTTTTCCTATAGCTATAGACGAGAGGATCACAGTAACTGTTGAAACTGTGACTATGAAGATGTCCAGTGCCATGCCAGACACAAAAACTGTC[A/T]AGACAAGGCCAGACAAGGCAATTTTAGTGAAAGAGACAGTTACAAAGGTCCCAAAGAAACACACTACAGCCAAGCCAACAGTAAAGCCAAGTCCCACCGCCTCCACAGATAAAGTCCTGTCCCATACCACAGGGAAAGACAACATTAAGATTGTTGGGCAACAATCTGAAAGCATGAAACTTCAAGAACAAACAAAGGGTAAAACAACAGTCATAAAGATGGGTTCAGACAATCAAGCACAAACTGATTTAAGTGACAAGAGCCATAATGCTAAAGATGAGCCTGCCTATCAGAATGTGACTCAAAGATCTGTAAAGAAGAGTAATGGAACTTCCAAAATTCTGCATAATTTGTTTAAAGGGTCAATGAATGTAACTCGGTCCAAGACAAAGATTACTACAAGAACTGCAGGAGATCAAGGGGAAGAAAGCAAGACCAATGCTGTCTCTGCTGAAAAAGACGAGAAGTTGTTTCATGGCAATGTAACAACAGTTCAAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39088
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014439 | Nonsense | 1608 | 2285 | 3 | 14 |
ENSDART00000132368 | None | None | 389 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 18683504)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16733248 |
GRCz11 | 16 | 16641225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAACTCGGTCCAAGACAAAGATTACTACAAGAACTGCAGGAGATCAAGGG[G/T]AAGAAAGCAAGACCAATGCTGTCTCTGCTGAAAAAGACGAGAAGTTGTTT
Long Flanking Sequence:
TAGACGAGAGGATCACAGTAACTGTTGAAACTGTGACTATGAAGATGTCCAGTGCCATGCCAGACACAAAAACTGTCAAGACAAGGCCAGACAAGGCAATTTTAGTGAAAGAGACAGTTACAAAGGTCCCAAAGAAACACACTACAGCCAAGCCAACAGTAAAGCCAAGTCCCACCGCCTCCACAGATAAAGTCCTGTCCCATACCACAGGGAAAGACAACATTAAGATTGTTGGGCAACAATCTGAAAGCATGAAACTTCAAGAACAAACAAAGGGTAAAACAACAGTCATAAAGATGGGTTCAGACAATCAAGCACAAACTGATTTAAGTGACAAGAGCCATAATGCTAAAGATGAGCCTGCCTATCAGAATGTGACTCAAAGATCTGTAAAGAAGAGTAATGGAACTTCCAAAATTCTGCATAATTTGTTTAAAGGGTCAATGAATGTAACTCGGTCCAAGACAAAGATTACTACAAGAACTGCAGGAGATCAAGGG[G/T]AAGAAAGCAAGACCAATGCTGTCTCTGCTGAAAAAGACGAGAAGTTGTTTCATGGCAATGTAACAACAGTTCAAGCTGAGAAGAAGTCTGATAAGCCTGAAATTGATGCAAGTGTTGAATCCAAAGCTCATATGAAGCATTTCAGTAAAACTAGCAGCAGATTATCTGTCATTGGGTCAGTTGAGGTTCATAACATCACTTCTACTGGCTTCATTATGTCTTGGGAAGCACATCGAGACAAGTTCAAAAACTTCACTGTCACAAGAAGGGAAATCAAAGCAGGAAATGAAGATTCTGAGAAAATTCATGAAGCAATAGAAAATGTAACAGATGCTGAAAGGCTGGGATCAAACAGAACCTTGACTAAAATACTCAGTAGCAAATCTGAAGGAAACGCTATGAAAAAGTTTTCACAAATTCTAGCTGGTACAACTCGATCATATCATTTTAAAGGCCTTCAACCTCAAACTCAATATGCGATTTCCTTGTTTGGCTCTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22795
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 |
---|---|---|---|---|---|
ENSDART00000014439 | Nonsense | 1941 | 2285 | 7 | 14 |
ENSDART00000132368 | None | None | 389 | None | 9 |
Genomic Location (Zv9):
Chromosome 16 (position 18671716)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 16721515 |
GRCz11 | 16 | 16629492 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTGACTTTATCTGGCAGTTCTGTGGAGCACCAGCTTAGAGCACTTCAT[A/T]GATCTTCTTTATACATGGTGAAAATGACAAGTCAAGTCAACAGGCTCCAG
Long Flanking Sequence:
ACAGCTCAAAAAATGTGTTTTGGTGTTTCGTGACCCTTTAAGGAAGTGGGTGGTTGGGTCAATCAATACAATTGATTGTGTTTATAGAAGGAGGAGGGTGGGTCAATTGATCGGTCAGTCAGTTAGTCAGTCAGTCAGTCATATAATCAGTCAAACAGTCAGTCAACAATAGCCTCTGGTGGGTTTATGCAAGAACAGCAGGCACGAATGGCACTCGTAAAAGAAATTTGAGATCTCAAAAAGCCTGCACAGCAACCTCTCGTGGATTCTCAAAAAATGCAAAAGAAAGTGCCCCCTGGGATGTATTTTGTGGTCTTCAGAAATGTATATAGAAGTAGCTTTTCAGAATGAGCCTGGGTTGGAACTGTCATGACTTTATTCAATATTTTTTTCTTTTCTGCTTTTTTTTTTTTTTTTTTTTTTGCTTTCTAGCTCCTAATGTGACTATTACAGTGACTTTATCTGGCAGTTCTGTGGAGCACCAGCTTAGAGCACTTCAT[A/T]GATCTTCTTTATACATGGTGAAAATGACAAGTCAAGTCAACAGGCTCCAGAGTAGCTCAGTCTCCACATCTTTCACAACAGGAAGTGGTGAGTAAACACAGTCATGGTGCTATATAAAAGCATTTTATTGGTTACACTTTAAAAATAAGTTCACTAACATGAACTATGAACAATTCTTGTACACCATTGAAGAATTAAAATTAACATTACTTGTTAACTAGTGTTAGCAAGTGTTATCTAGTACTAACAATGAGTCATTTTATTTTCATTAGCTAACATTAACAAGGATGAATAAATACTGTAATAATGGTATTGTTCATTATGTTTATGTTAGTAAATACATTGACTAATATCATTACACGGCTGTCAGGAATATTTGATTCTGATTGGTTATTTTCAAGGTTGGACATTCCAAAGTATGTTATTCTACTGTATATAAAAACCTCTGAAACACAGGATCCTTCAGGTACTTTAAAAAATCTGGACCATCAGTAAATACA
Associated Phenotype:
Not determined