ZMP
si:dkey-72g4.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to human T-cell lymphoma breakpoint associated target 1 (TCBA1) [Source:UniPro
Human Orthologue:
NKAIN2
Human Description:
Na+/K+ transporting ATPase interacting 2 [Source:HGNC Symbol;Acc:16443]
Mouse Orthologues:
Nkain2, Nkain2
Mouse Descriptions:
Na+/K+ transporting ATPase interacting 2 Gene [Source:MGI Symbol;Acc:MGI:1923447]
Na+/K+ transporting ATPase interacting 2 Gene [Source:MGI Symbol;Acc:MGI:1923447]
Na+/K+ transporting ATPase interacting 2 Gene [Source:MGI Symbol;Acc:MGI:1923447]
Alleles
There is 1 allele of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa37124 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37124
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000090938 | None | None | 155 | None | 5 |
| ENSDART00000124633 | Essential Splice Site | 18 | 208 | 1 | 7 |
| ENSDART00000140500 | None | None | 155 | None | 4 |
| ENSDART00000145592 | Essential Splice Site | 18 | 158 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 20 (position 40145137)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 40216399 |
| GRCz11 | 20 | 40119035 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCTGCAGTGGCAGATGTACGCTGGCGTTTATATGTGGCATGCAATTGG[T/A]AAGTGATTATGCTTTAAGTGATTTATTCTTAACCTGCGATGAACTCGTGG
Long Flanking Sequence:
GCTTCCAGAGAAAGAAAGCAAAGCTTTTGCGCTTTAAAATGTGTTAATTCGGTTTCTTTCGCACGAGGGAGGAGCAATGAGAGCGTAAACAACACTGGCTGGCTTTGTTTTTCACACCCGGACCCGTGGAAGATCACATTAACATGTTTTTCAGCGCTGGATTTGGAGATAGCGTTATTTCTTCACTAACTTAAGGAAGTGTTGTCCGCGTCTCTTTGACTTTGCGTACGCGTCAATTCTACTTTTCCAAACAGCACATGCAGTTTCCTTCACATCTTTCTTCCTGCACGGTGAACCGCTTGGGATGCTTTTATCGGAAGGGCGTATTTGATTCGCGTCTCTCGCCTCCGGAGTGAAGAAAGATCCGTTTAAACCCGTTACCTGGGTATCGTTTTTGTGGAGTTACAGCGATCCACGTGGAAACACGGACTCGACGGAGAGCAAGATGGGCTGCTGCAGTGGCAGATGTACGCTGGCGTTTATATGTGGCATGCAATTGG[T/A]AAGTGATTATGCTTTAAGTGATTTATTCTTAACCTGCGATGAACTCGTGGACTCGAACCTACAACCTTTCAGCTTACACTCAAAAGATTCAGTGGCTAAGCTTTATCTCATAAAAACAAGTGAATTTGTGATTAAACTCAATGGAGTAATGCTGTGTTGAATTTCACTAGGGGGTTGATTTAATATTTTTAAATTGCATATTTTTTTTATAATTTTTAAATTATGTATTCATCTAATTTGACTTGTTAACATGTTTTTATGCAGCTGTCACTTGCACAGTCATAAAAAAATACTGGCATGTCTCCCAGAAGTGAACCTGTAAACTTAACTCAAGTGTCCATCTGACAAGTGATCAGTGATAGTGCATTAAGATGTATGTGGCTGTGAGTAATCTTAGTGGGAATGATGCAGGGCTATATGTGGAAACCCTGCCTTGTTATATTACACCGGAGGGATGATGATGCTCATGAAGGTAGGGCTTGTGTCATTAGCCTGGGGCC
Associated Phenotype:
Not determined