ZMP
zgc:162160
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC561782 [Source:RefSeq peptide;Acc:NP_001082862]
Human Orthologues:
KCNJ6, KCNJ9
Human Descriptions:
potassium inwardly-rectifying channel, subfamily J, member 6 [Source:HGNC Symbol;Acc:6267]
potassium inwardly-rectifying channel, subfamily J, member 9 [Source:HGNC Symbol;Acc:6270]
potassium inwardly-rectifying channel, subfamily J, member 9 [Source:HGNC Symbol;Acc:6270]
Mouse Orthologues:
Kcnj6, Kcnj9
Mouse Descriptions:
potassium inwardly-rectifying channel, subfamily J, member 6 Gene [Source:MGI Symbol;Acc:MGI:104781]
potassium inwardly-rectifying channel, subfamily J, member 9 Gene [Source:MGI Symbol;Acc:MGI:108007]
potassium inwardly-rectifying channel, subfamily J, member 9 Gene [Source:MGI Symbol;Acc:MGI:108007]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36231 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36231
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084730 | Nonsense | 132 | 432 | 3 | 4 |
Genomic Location (Zv9):
Chromosome 16 (position 44977456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 42257964 |
GRCz11 | 16 | 42207996 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATCGCCTACGCCCGAGGAGATCTGGAGCACACTGATGATAATGACTG[G/A]ACACCTTGTGTGAATAACCTCAATGGCTTCGTCTCAGCGTTTCTTTTTTC
Long Flanking Sequence:
TGGGTCTGTGAGAGTTTAGGCAGAACTTTGCTGCACTTCAATATAAGAAAGAAATAGACATGATAATGAAATGCAGTTCAACTTTGAAAACGACATCTAACACATTAAATGATATTGTCACTATTTTAGTCTCTTCACACTTTTTAAAACTTCTACTTTTTCCATTCCTCAAACAAACTGCAGGTCCCCACAGACCGTACAATGGTGGTTGGGGGAGTCGTGGGTGGAGGAGATTGTTCTGAACCCGTAGGAGCTCCTCTGAAAAAACGCCGCCAGCGATACGTGGAGAAAGACGGCAAGTGCAACGTCCACCACGGAAATGTGCGTGAAACCTACCGCTACCTGACAGACATCTTCACCACGCTAGTGGATTTAAAGTGGCGCTTCAATCTGCTGGTCTTCACACTGGTCTACACCACCACATGGGTGTTTTTTGGCTTCATCTGGTGGCTCATCGCCTACGCCCGAGGAGATCTGGAGCACACTGATGATAATGACTG[G/A]ACACCTTGTGTGAATAACCTCAATGGCTTCGTCTCAGCGTTTCTTTTTTCCATAGAGACTGAGACCACCATTGGTTACGGGTATCGTGTGATAACAGACAAATGTCCAGAGGGGATCATCCTGCTTCTGATTCAGGCCATTTTGGGCTCCATCGTCAACGCCTTTATGGTGGGCTGCATGTTTGTGAAAATCTCCCAACCAAAGAAACGAGCCGAAACACTCATGTTTTCCAACACCGCTGTGATATCCGTGCGGGACAGCAAGTTGTGTTTGATGTTCCGTGTCGGTGACTTGCGTAACTCGCACATTGTGGAGGCCTCCATTAGGGCGAAGCTTATCCGCTCGAAACAGACGAAGGAAGGAGAGTTTATTCCTCTCAACCAGACGGACATCAATGTGGGCTTTGACACGGGGGACGATCGGCTGTTCCTCGTGTCGCCGTTGATTATTTGCCACGAGATCAACAAGAACAGCCCATTCTGGGACGTCTCTCAGGAGCA
Associated Phenotype:
Not determined