ZMP
zgc:123253
Ensembl ID:
ZFIN ID:
Description:
thioredoxin-like protein 4B [Source:RefSeq peptide;Acc:NP_001032200]
Human Orthologue:
TXNL4B
Human Description:
thioredoxin-like 4B [Source:HGNC Symbol;Acc:26041]
Mouse Orthologue:
Txnl4b
Mouse Description:
thioredoxin-like 4B Gene [Source:MGI Symbol;Acc:MGI:2443724]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa2009 | Nonsense | F2 line generated | Not yet available |
sa5654 | Nonsense | F2 line generated | Not yet available |
Mutation Details
Allele Name:
sa2009
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081945 | Nonsense | 69 | 149 | 2 | 4 |
ENSDART00000109083 | Nonsense | 69 | 149 | 2 | 3 |
ENSDART00000081945 | Nonsense | 69 | 149 | 2 | 4 |
ENSDART00000109083 | Nonsense | 69 | 149 | 2 | 3 |
The following transcripts of ENSDARG00000058962 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 390270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 520394 |
GRCz11 | 1 | 515573 |
KASP Assay ID:
554-3386.1 (used for ordering genotyping assays)
KASP Sequence:
AGTAATATGGCCAGTATTTATCTGGTGGATGTCGACTCAGCTCCAGTTTA[C/A]ASCAGATACTTTGACATCAGCTTTATTCCCTCCACCGTGTTCTTCTTCAA
Long Flanking Sequence:
ACTTGCATAAATAAGTTACATGTAATAGCGGTTATTTAAACTAAATTAATTTTAAACACTTTGCTTTCATTTAGTATATATTCTATGTTTATAATCACTATGTGTATATAATGAATCTATTTGTGATTAACATTTCATGTAGTCACTTGAGTTTGACTTGATCCACGCATGTATTTCACTTAAATACCTCGATTTAGTTGGCTATTAAAGTATCTATTATATACTTGTTAGATTTGTACAGCATTTTATATTCACATTAGTGCACATTTGACAGATGTATACTTTAGTTGTGTAGTTTACAAGTCACAATTAACTCATATTAAAGTGCAATTTATGCATTATAAAGTTATAGTATGTTTTTTTTAAATGCACATTTTTTAAATAAAAGGATAAATACTGAAAGTGTTGTGTTTGTGTGATTGACAGCTGTCAAAGACGGCTCATGATCTGAGTAATATGGCCAGTATTTATCTGGTGGATGTCGACTCAGCTCCAGTTTA[C/A]AGCAGATACTTTGACATCAGCTTTATTCCCTCCACCGTGTTCTTCTTCAACGGACAGCACATGAAAGTGGATTATGGGTGAGTTCTGATCAATGTTAGATTCTGCTGGCATCAAAATGTTTATTGCGACTGAAGCTTCTATCACCATATATATGCTATAATCATCACAATGTTTATCAAAGCTGCCAAATATGTCACTTTAACAGGTGTAAGAACTAAAACAGGGTTTTGTGTGTTGCATTATTGCATGTAAATGTTCAGAGTTAACAAATGTTTAAATAAATCTAATTGCAAAATGATTATAAAGCACATTAAAAAATGTTTACTAGTAAAAGCGTTCAAATCAACAGTGATAATGAAGCACATTTATTAGTTATGTTGATGTCAGAATTTGATCAGTTGTTAACTACATTTAATAAAACAAGCTTTTATTTTAATGAATTATTAAGCATTAACAAAGACATTAACGTCAGCTAAGATGAATACATGATTTTATAGCTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa5654
Status:
F2 line generated
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000081945 | Nonsense | 69 | 149 | 2 | 4 |
ENSDART00000109083 | Nonsense | 69 | 149 | 2 | 3 |
ENSDART00000081945 | Nonsense | 69 | 149 | 2 | 4 |
ENSDART00000109083 | Nonsense | 69 | 149 | 2 | 3 |
The following transcripts of ENSDARG00000058962 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 390270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 520394 |
GRCz11 | 1 | 515573 |
KASP Assay ID:
554-3386.1 (used for ordering genotyping assays)
KASP Sequence:
AGTAATATGGCCAGTATTTATCTGGTRGATGTCGACTCAGCTCCAGTTTA[C/A]ASCAGATACTTTGACATCAGCTTTATTCCCTCCACCGTGTTCTTCTTCAA
Long Flanking Sequence:
ACTTGCATAAATAAGTTACATGTAATAGCGGTTATTTAAACTAAATTAATTTTAAACACTTTGCTTTCATTTAGTATATATTCTATGTTTATAATCACTATGTGTATATAATGAATCTATTTGTGATTAACATTTCATGTAGTCACTTGAGTTTGACTTGATCCACGCATGTATTTCACTTAAATACCTCGATTTAGTTGGCTATTAAAGTATCTATTATATACTTGTTAGATTTGTACAGCATTTTATATTCACATTAGTGCACATTTGACAGATGTATACTTTAGTTGTGTAGTTTACAAGTCACAATTAACTCATATTAAAGTGCAATTTATGCATTATAAAGTTATAGTATGTTTTTTTTAAATGCACATTTTTTAAATAAAAGGATAAATACTGAAAGTGTTGTGTTTGTGTGATTGACAGCTGTCAAAGACGGCTCATGATCTGAGTAATATGGCCAGTATTTATCTGGTGGATGTCGACTCAGCTCCAGTTTA[C/A]AGCAGATACTTTGACATCAGCTTTATTCCCTCCACCGTGTTCTTCTTCAACGGACAGCACATGAAAGTGGATTATGGGTGAGTTCTGATCAATGTTAGATTCTGCTGGCATCAAAATGTTTATTGCGACTGAAGCTTCTATCACCATATATATGCTATAATCATCACAATGTTTATCAAAGCTGCCAAATATGTCACTTTAACAGGTGTAAGAACTAAAACAGGGTTTTGTGTGTTGCATTATTGCATGTAAATGTTCAGAGTTAACAAATGTTTAAATAAATCTAATTGCAAAATGATTATAAAGCACATTAAAAAATGTTTACTAGTAAAAGCGTTCAAATCAACAGTGATAATGAAGCACATTTATTAGTTATGTTGATGTCAGAATTTGATCAGTTGTTAACTACATTTAATAAAACAAGCTTTTATTTTAATGAATTATTAAGCATTAACAAAGACATTAACGTCAGCTAAGATGAATACATGATTTTATAGCTT
Associated Phenotype:
Not determined