ZMP
tshz1
Ensembl ID:
ZFIN ID:
Description:
Teashirt homolog 1 [Source:UniProtKB/Swiss-Prot;Acc:B3DJM5]
Human Orthologue:
TSHZ1
Human Description:
teashirt zinc finger homeobox 1 [Source:HGNC Symbol;Acc:10669]
Mouse Orthologue:
Tshz1
Mouse Description:
teashirt zinc finger family member 1 Gene [Source:MGI Symbol;Acc:MGI:1346031]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14913 | Nonsense | Available for shipment | Available now |
sa39242 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa91 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa36825 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa6555 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa14913
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 |
---|---|---|---|---|---|
ENSDART00000024639 | Nonsense | 349 | 1158 | 1 | 1 |
ENSDART00000122002 | Nonsense | 43 | 852 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 21892177)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 21825557 |
GRCz11 | 19 | 21409880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGCGATCCTTAATGGAGATGGAGGGTAAAGAAGATGCACAGAAAGTTT[T/A]GAAATGCATGTATTGTGGCCACTYGTTTGAATCYCTACAAGACTTGAGTG
Long Flanking Sequence:
CGTCGCGAACAGCCATGCAAGTACCATTGCAAGTAGCGGAGCTAGCAGCAGCAGCAACGCTAGTGCTAGCACAAAGACAAACGTGACACAGAGCAGCAATTCTACAAAAGCCACCACATTAACCAATGCCAACAATGGAACCATCAATGGTGCTAACAGTGGGGGTGTTGCATATGACTGGCACCAAGCAGCACTTGCTAAAACCTTACAGCATACGCCCTACCACTTAATGCCTGAACCAAGTCTCTTCAGCACAGTGCAGCTGTACCGGCAAAACAATAAGCTGTATGGGCCTGTGTTTACAGGTGCCAGCAAATTCAGATGCAAGGACTGTAGTGCAGCCTACGACACGCTTGTAGGTCTCACGGTACACATGAATGAAACAGGTCATTACCGTGATGATAACAAGGACAAGGAGGAGGACAGGGGCAAAAAATGGTCTAAGCCAAGGAAGCGATCCTTAATGGAGATGGAGGGTAAAGAAGATGCACAGAAAGTTT[T/A]GAAATGCATGTATTGTGGCCACTCGTTTGAATCCCTACAAGACTTGAGTGTCCACATGATCAAAACTAAACACTACCAGAAAGTGCCTCTAAAAGAACCAATGCCAGCTCTTGCCTCAAAGCTGGTGCCCTCCACCAAAAAGCGAGTGTTCCAGGACCTGATGTCTCCATGCTCACCTGACTCAATCTCTAGCACCCCTGGCATTCCATTAGCTGAGACTGCACCCACCAAAGATCCAAAAATTTCAAATCCATACGTCACGGCTAATAACCGTTATGGCTACCAAAATGGTGCAAGTTATACCTGGCAGTTTGAGGCCAGAAAAGCTCAAATTCTCAAGTGTATGGAATGTGGGAGTTCCCATGACACCTTGCAGCAGTTGACAGCCCACATGATGGTGACCGGTCATTTTCTAAAAGTCACAAACTCTGCATCAAAAAAGGGAAAGCAGTTAGTGTTTGACCCGGTGGTGGAAGAGAAAATCCAATCCATTCCTCTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39242
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024639 | Nonsense | 441 | 1158 | 1 | 1 |
ENSDART00000122002 | Nonsense | 135 | 852 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 21892454)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 21825834 |
GRCz11 | 19 | 21410157 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCAAAGATCCAAAAATTTCAAATCCATACGTCACGGCTAATAACCGTTA[T/A]GGCTACCAAAATGGTGCAAGTTATACCTGGCAGTTTGAGGCCAGAAAAGC
Long Flanking Sequence:
AATAAGCTGTATGGGCCTGTGTTTACAGGTGCCAGCAAATTCAGATGCAAGGACTGTAGTGCAGCCTACGACACGCTTGTAGGTCTCACGGTACACATGAATGAAACAGGTCATTACCGTGATGATAACAAGGACAAGGAGGAGGACAGGGGCAAAAAATGGTCTAAGCCAAGGAAGCGATCCTTAATGGAGATGGAGGGTAAAGAAGATGCACAGAAAGTTTTGAAATGCATGTATTGTGGCCACTCGTTTGAATCCCTACAAGACTTGAGTGTCCACATGATCAAAACTAAACACTACCAGAAAGTGCCTCTAAAAGAACCAATGCCAGCTCTTGCCTCAAAGCTGGTGCCCTCCACCAAAAAGCGAGTGTTCCAGGACCTGATGTCTCCATGCTCACCTGACTCAATCTCTAGCACCCCTGGCATTCCATTAGCTGAGACTGCACCCACCAAAGATCCAAAAATTTCAAATCCATACGTCACGGCTAATAACCGTTA[T/A]GGCTACCAAAATGGTGCAAGTTATACCTGGCAGTTTGAGGCCAGAAAAGCTCAAATTCTCAAGTGTATGGAATGTGGGAGTTCCCATGACACCTTGCAGCAGTTGACAGCCCACATGATGGTGACCGGTCATTTTCTAAAAGTCACAAACTCTGCATCAAAAAAGGGAAAGCAGTTAGTGTTTGACCCGGTGGTGGAAGAGAAAATCCAATCCATTCCTCTTCCACCCACAACAACACGCTTACCAGCTCCTGCTATCAAGTCCCAACCAGACTCTCCAATACACCCCTCCATTATGGATGATCGGAAGGAGTTGGAAGAAGAGAAATTTGAGGAACCTGAGGAAAAGAAAATCAAGCAAGAGAAGGAAGACCCTTCTGAGAGGGTTGAAAAGTCTGAGAAACTCAGCCATTACAAATATCTTCGAGAAGAGGATCTTGAAGAGTCTCCTAAAGGTGGCCTAGATATTCTCAAGTCATTAGAAAATACAGTCTCCAGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa91
Status:
Confirmed mutation in F2 line
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 |
---|---|---|---|---|---|
ENSDART00000024639 | Nonsense | 550 | 1158 | 1 | 1 |
ENSDART00000122002 | Nonsense | 244 | 852 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 21892779)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 21826159 |
GRCz11 | 19 | 21410482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCCAATACACCCCTCCATTATGGATGATCGGAAGGAGTTGGAAGAAGAG[A/T]AATTTGAGGAACCTGAGGAAAAGAAAATCAAGCAAGAGAAGGAAGACCCT
Long Flanking Sequence:
TGCCAGCTCTTGCCTCAAAGCTGGTGCCCTCCACCAAAAAGCGAGTGTTCCAGGACCTGATGTCTCCATGCTCACCTGACTCAATCTCTAGCACCCCTGGCATTCCATTAGCTGAGACTGCACCCACCAAAGATCCAAAAATTTCAAATCCATACGTCACGGCTAATAACCGTTATGGCTACCAAAATGGTGCAAGTTATACCTGGCAGTTTGAGGCCAGAAAAGCTCAAATTCTCAAGTGTATGGAATGTGGGAGTTCCCATGACACCTTGCAGCAGTTGACAGCCCACATGATGGTGACCGGTCATTTTCTAAAAGTCACAAACTCTGCATCAAAAAAGGGAAAGCAGTTAGTGTTTGACCCGGTGGTGGAAGAGAAAATCCAATCCATTCCTCTTCCACCCACAACAACACGCTTACCAGCTCCTGCTATCAAGTCCCAACCAGACTCTCCAATACACCCCTCCATTATGGATGATCGGAAGGAGTTGGAAGAAGAG[A/T]AATTTGAGGAACCTGAGGAAAAGAAAATCAAGCAAGAGAAGGAAGACCCTTCTGAGAGGGTTGAAAAGTCTGAGAAACTCAGCCATTACAAATATCTTCGAGAAGAGGATCTTGAAGAGTCTCCTAAAGGTGGCCTAGATATTCTCAAGTCATTAGAAAATACAGTCTCCAGTGCAATCAGTAAGGCTCAGACCGGTACACCCACCTGGGGTGGATATCCCAGCATTCATGCTGCCTACCAGCTCCAAGGGTCTGTGAAATCATCTATACCTGCTATCCAGAGTGTCCAGATTCAACCAACATTCAATGCCAGCAGCTTAAAATCTTTGACCTCTGACTCCAGCACTCTGATACATTCTCCTAGCAGCCCATCACCACCACCAAACCATAAAAGCAATGTCCTAGCCATGGAGGAGTTGGTGGAGAAAGTGACAGGGAAAATTCCATCAAAGAAAGACAGGGATGAAAAATTAACTGAACGTAATTCCAAACATCTTACT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa36825
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 |
---|---|---|---|---|---|
ENSDART00000024639 | Nonsense | 713 | 1158 | 1 | 1 |
ENSDART00000122002 | Nonsense | 407 | 852 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 21893268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 21826648 |
GRCz11 | 19 | 21410971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAATTCCATCAAAGAAAGACAGGGATGAAAAATTAACTGAACGTAATTCC[A/T]AACATCTTACTGCTGAATTACCCTCTCCGGTTCTCAAAGAGAGAAAAGAC
Long Flanking Sequence:
TGGAAGAAGAGAAATTTGAGGAACCTGAGGAAAAGAAAATCAAGCAAGAGAAGGAAGACCCTTCTGAGAGGGTTGAAAAGTCTGAGAAACTCAGCCATTACAAATATCTTCGAGAAGAGGATCTTGAAGAGTCTCCTAAAGGTGGCCTAGATATTCTCAAGTCATTAGAAAATACAGTCTCCAGTGCAATCAGTAAGGCTCAGACCGGTACACCCACCTGGGGTGGATATCCCAGCATTCATGCTGCCTACCAGCTCCAAGGGTCTGTGAAATCATCTATACCTGCTATCCAGAGTGTCCAGATTCAACCAACATTCAATGCCAGCAGCTTAAAATCTTTGACCTCTGACTCCAGCACTCTGATACATTCTCCTAGCAGCCCATCACCACCACCAAACCATAAAAGCAATGTCCTAGCCATGGAGGAGTTGGTGGAGAAAGTGACAGGGAAAATTCCATCAAAGAAAGACAGGGATGAAAAATTAACTGAACGTAATTCC[A/T]AACATCTTACTGCTGAATTACCCTCTCCGGTTCTCAAAGAGAGAAAAGACCTGCCAAAACCAGATGATCTTACTAAGCCAACAAAGAATGGCACTGTAGATAAAGACCTAGAGCACACTCCAGTTCGAGAAGGAGAATACAAGGAAAGCCATGCAGATAATCCCATAAAAAATGGAACGGATGCCCTCAAAACGCAAGTCAGCAATGGTTGCGGTAATTTAGGAATCATCACTGACCACTCACCAGAGCAGCCTTTAGTTAACCCCCTCAGTGCATTGCAGTCTATCATGAACACTCATTTGGGTAAGGCTTCCAAAACAGTCAGTCCACTCCTGGACCCCTTAGCAATGTTGTACAAGATTAGCAACAACATGATGGAAAAACCCATGTACAATCCAGCTCAGGTCAAACAAGTGGAGCCCATCAACAGATATTATGAAAATGACGACGATCAGCCCATGGACTTGACAAAGTCCAAAAGTGGCATTGGCCCCACAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6555
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000024639 | Nonsense | 1075 | 1158 | 1 | 1 |
ENSDART00000122002 | Nonsense | 769 | 852 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 19 (position 21894355)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 21827735 |
GRCz11 | 19 | 21412058 |
KASP Assay ID:
554-4558.1 (used for ordering genotyping assays)
KASP Sequence:
AACTCCCTCCACATACATTAACCACTTAGAGTCYCATTTGGGCTTTAGTT[T/A]GAAGGACCTCTCAAAGTTATCAATAGACCTCATAAGAGACCAGCAAGCAG
Long Flanking Sequence:
TCCTCTTCGGGAGAATGCCCTAATGGACATCTCTGACATGGTAAAGAACCTGACTGGTCGCTTGACACCAAAGTCGTCAACACCTTCCTCTATATCAGAAAAGTCAGATGCAGATGGATGTGCTTTTGAGGATGGTCTGGAGGATCTTTCACCTATTCAAAAGAGGAAAGGCAGGCAGTCAAACTGGAACCCTCAGCATCTGCTGATTCTTCAAGCTCAGTTTGCATCCAGCCTTCGAGAAACCCCTGACGGAAAGTACATAATTACAGACTTAGGTCCTCAGGAGCGTGTACATATTTGTAAGTTTACAGGTCTCTCTATGACCACCATCTCCCACTGGTTGGCGAACGTCAAGTACCAACTCAGACGGACAGGTGGAACCAAGTTCCTGAAGAACATAGACTCGGGCCATCCACTGTTCCTGTGTAGTGATTGTGCCTCCCAGTTTAGAACTCCCTCCACATACATTAACCACTTAGAGTCCCATTTGGGCTTTAGTT[T/A]GAAGGACCTCTCAAAGTTATCAATAGACCTCATAAGAGACCAGCAAGCAGTCACAAAAATGATCACAGACAAGACATTCCGTGCCCTTGACTTGAATGAGGAAGACTCTAATTCCATATTTCAGTGCAAACTGTGCAATAGGACTTTTGTCAGCAAGCACGCAGTGAAACTGCACCTCAGCAAAACACACGGGAAGTCACCGGAGGACCACCTGATCTTTGTTACTGAGCTGGAAAAGTTAGAAAAAGCCTAAGGAAAGCAGGCTGGTGGCAGTGAAGTGACTGAATTGAGAATCATTGCACTACATCACTGTACTGCACTGCGCCTGAACTGAGCCTTCAAAATCAGTCCAACTTGTCGTGAAACTGCCTGATTGGACCATGATCTGTTTCAGTTTTTTTTTCTTCCTCGTTGTTTTCAGTCTCTTTGTTTCTATCTCTTGCTTTGTACTGTATTTATCTAATACGTGTTGGTTATGTGCATGTTCTGTTTTTTTAAAC
Associated Phenotype:
Not determined