ZMP
si:ch73-85k9.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to H.sapiens teashirt family zinc finger [Source:UniProtKB/TrEMBL;Acc:A5WWF5]
Human Orthologue:
TSHZ3
Human Description:
teashirt zinc finger homeobox 3 [Source:HGNC Symbol;Acc:30700]
Mouse Orthologue:
Tshz3
Mouse Description:
teashirt zinc finger family member 3 Gene [Source:MGI Symbol;Acc:MGI:2442819]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa6506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25058 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23256 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa6506
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 |
---|---|---|---|---|---|
ENSDART00000125979 | Nonsense | 467 | 946 | 2 | 4 |
ENSDART00000142462 | Nonsense | 411 | 964 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 14319518)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14764936 |
GRCz11 | 18 | 14733448 |
KASP Assay ID:
554-4909.1 (used for ordering genotyping assays)
KASP Sequence:
CATCCATTGCAACTGGAGACCACAAGANNNNNNCACAAGAAATTACCTCT[C/T]AGAAAAGCAGTGAGTCCAAGGAGTCTGCAAATGTAAATGATGTTAGGCAG
Long Flanking Sequence:
ACCAGAAGGTTCCTCTGAGAGAGCCAAGAACGGCAATTGCTGCTAAAGTCGTGTCCTCATTCAGGAAGAGGGTTCCAGTGGAGCTGGATGTTGCAAAATCTTTGCACACTACAGAGCAGACAAGAAGTCCCAATGAAGGGCACACCAGGGATATTCTTCAGATGTACTCTGAACAAAATATCAAAGATGACTTGGATCAAAAGACAACAAGCCGTGGTGTACACTTCAAGTCTCAGAATTTGAAATGTTTGGAGTGTGGGATTTCACATGACTCTTTGCAGCAGCTGAGTGCTCACATGATGTTGACTGGTCACTTTTTAAAAGTCACCCAATCATTGCAAAAGACAGACAAAACTCCTCATCCCAAAAGTAAGTCTGAGAAGTCTCTGTCAGAGACAACATGTTCTTCCCCTCTTGCAGCCACAAGAATTTTGGAGTCATCATCCTACTCATCCATTGCAACTGGAGACCACAAGAACAAGACACAAGAAATTACCTCT[C/T]AGAAAAGCAGTGAGTCCAAGGAGTCTGCAAATGTAAATGATGTTAGGCAGAAATTGGGTCCATCAGCAAAAACGGATTACTTAACCGAAGATGATCTAAAGGAGAGTCCTAAAATGGATTTTGATATTCTTAAATCACTGGAGAATACAGTAACATCAGCCATTAACAAAGCACAGAAGGGTGCCCCGAGCTGGGGTGGTTACCAGAGCATTCATGCAGCTTATCAGTTACGAAACCATTTAAAGCCTGCTCTGCACAACCCAGGCTATATTTCTTCCTTAAAACAATCATCCAGTAGTCAGGAAGTCCAGTCCTTAGACAAGAGTAATTTGATTCCTCCAAGTACTCAACCAAGTTCTTCATCAACCACAGTTCAAGTCAGTGAGGTGGATGAACTTGAGATGAATGTAACAGAAAAAGATGCTGAAGTAGACAGAAAATTGAAAGATCTAAATGGGCAGGGATCCCCACATCCACAGCTGCTAAATTTGAAAGGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25058
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 |
---|---|---|---|---|---|
ENSDART00000125979 | Nonsense | 541 | 946 | 2 | 4 |
ENSDART00000142462 | Nonsense | 485 | 964 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 14319294)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14764712 |
GRCz11 | 18 | 14733224 |
KASP Assay ID:
554-7750.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAGGGTGCCCCGAGCTGGGGTGGTTACCAGAGCATTCATGCAGCTTA[T/A]CAGTTACGAAACCATTTAAAGCCTGCTCTGCACAACCCAGGCTATATTTC
Long Flanking Sequence:
TTCAAGTCTCAGAATTTGAAATGTTTGGAGTGTGGGATTTCACATGACTCTTTGCAGCAGCTGAGTGCTCACATGATGTTGACTGGTCACTTTTTAAAAGTCACCCAATCATTGCAAAAGACAGACAAAACTCCTCATCCCAAAAGTAAGTCTGAGAAGTCTCTGTCAGAGACAACATGTTCTTCCCCTCTTGCAGCCACAAGAATTTTGGAGTCATCATCCTACTCATCCATTGCAACTGGAGACCACAAGAACAAGACACAAGAAATTACCTCTCAGAAAAGCAGTGAGTCCAAGGAGTCTGCAAATGTAAATGATGTTAGGCAGAAATTGGGTCCATCAGCAAAAACGGATTACTTAACCGAAGATGATCTAAAGGAGAGTCCTAAAATGGATTTTGATATTCTTAAATCACTGGAGAATACAGTAACATCAGCCATTAACAAAGCACAGAAGGGTGCCCCGAGCTGGGGTGGTTACCAGAGCATTCATGCAGCTTA[T/A]CAGTTACGAAACCATTTAAAGCCTGCTCTGCACAACCCAGGCTATATTTCTTCCTTAAAACAATCATCCAGTAGTCAGGAAGTCCAGTCCTTAGACAAGAGTAATTTGATTCCTCCAAGTACTCAACCAAGTTCTTCATCAACCACAGTTCAAGTCAGTGAGGTGGATGAACTTGAGATGAATGTAACAGAAAAAGATGCTGAAGTAGACAGAAAATTGAAAGATCTAAATGGGCAGGGATCCCCACATCCACAGCTGCTAAATTTGAAAGGGAAATCACTGATGCTAAAATCTCCAAGTCCTGAGAGCACTGTTACATCAATGAGCAAGATCACTGAAGGTAAAACAGAGGAAAAAGAAACTCGGAAGCACAAACAAGACCCAACCTCCACTTCAAATCTGTATGATGATTCTAGTTTACTCTCTGCCCAGCCTGAGCCAAAACAACCCTCTGTCAGCCCTCTAAGTGCCCTTCAGTCTGTTATGAACCTTCATCTCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23256
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 |
---|---|---|---|---|---|
ENSDART00000125979 | Nonsense | 756 | 946 | 3 | 4 |
ENSDART00000142462 | Nonsense | 711 | 964 | 1 | 1 |
Genomic Location (Zv9):
Chromosome 18 (position 14318618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 14764036 |
GRCz11 | 18 | 14732548 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACATTCCAACTGCCATGAAATTTGCAGAGACCAGCCGATAGACTTGTCC[A/T]AAGGTAAAAATGAACAGTACCTTACAACTGCCTCTGTCCCAGGCAAAGCT
Long Flanking Sequence:
AGATGAATGTAACAGAAAAAGATGCTGAAGTAGACAGAAAATTGAAAGATCTAAATGGGCAGGGATCCCCACATCCACAGCTGCTAAATTTGAAAGGGAAATCACTGATGCTAAAATCTCCAAGTCCTGAGAGCACTGTTACATCAATGAGCAAGATCACTGAAGGTAAAACAGAGGAAAAAGAAACTCGGAAGCACAAACAAGACCCAACCTCCACTTCAAATCTGTATGATGATTCTAGTTTACTCTCTGCCCAGCCTGAGCCAAAACAACCCTCTGTCAGCCCTCTAAGTGCCCTTCAGTCTGTTATGAACCTTCATCTCGGTAAAGCTGCCAAACCGGTAAGGCCTGTCCAGGACCCTATGAGTATGCTTCTCAGGATGAGCAACAGCATGGCGGAAAGGGCCGCTCTTGCCGGTCCATCTGGACACTCAACGAAACTTAGCCAGTTACATTCCAACTGCCATGAAATTTGCAGAGACCAGCCGATAGACTTGTCC[A/T]AAGGTAAAAATGAACAGTACCTTACAACTGCCTCTGTCCCAGGCAAAGCTTTGAGCTCCTCTATATCTGGTGCATCTGTGAGTGAATCAAATAGTCCCAAAATCTTCACACCAGTAAGTCCTTTGCATGAAAATGCTCTCTCTGACATCTCCGACATGTTACGCAATCTCTCAGACTCTAGAGTTTCGAAGCCACCAACACTTCTATGTAGGCCAGAGCAGTCAGAAATTGAGGGTTCTCGTACTTCAGAAGAGGCAGAGGATACGTCCATAGTGCACAAACGTAAAGGTAGGCAGTCGCACTGGAAACCCCAGCACTTGCTGATTTTGCAGGCTCAGTTCACGTCCTGCCTCAGGCAGACAGCTGATGGAAAGTATGTGATATCAGACTTGAGCTCCCAGGAAAGGATGGTCATATCACACATAACTGGTCTGTCTATGACAACCATCAGCCACTGGCTTGCCAATGTGAAATATCAGCTGAGACGAACAGGCAGAACA
Associated Phenotype:
Not determined