ZMP
klhl6
Ensembl ID:
ZFIN ID:
Description:
kelch-like protein 6 isoform 1 [Source:RefSeq peptide;Acc:NP_001005316]
Human Orthologue:
KLHL6
Human Description:
kelch-like 6 (Drosophila) [Source:HGNC Symbol;Acc:18653]
Mouse Orthologue:
Klhl6
Mouse Description:
kelch-like 6 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2686922]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32964 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39880 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32964
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 |
---|---|---|---|---|---|
ENSDART00000039174 | Nonsense | 385 | 614 | 5 | 7 |
The following transcripts of ENSDARG00000026990 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 36374854)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36671564 |
GRCz11 | 2 | 36654021 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTATTTTAAAACTTAAAACAGGTGGCAAGGAAACTCTGCATGATGTGTG[G/A]AAGTATAATGCATCACTGAACAAATGGATCCAGATTGAGTTCCTCAACAC
Long Flanking Sequence:
GTGTGTGAATGTGAGAGTGTATGGGAGTTTCCCAGTAATGGAAGGGAATTCGCTGCATAACACTTGCTGGAATAGTTTGTGGTTCATTCCGCTGTGGTGACCCCTTAAGAGATTAAGCCGAAGGAAAATGAATGAATGAATATTTAATATAATAAAAGGTGTTTATATATATATATATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACCTATCCAGCAAACATGTATCACTTGTAAATTTGTTGCCAACATTCTTTAATATTTTTTTATGTTCTGTACTTACACTTGAGTCTAGTTTATGATTTTTTTACTCCCCTGTCTGCATGGCTGTTTGCACTGCAGTGAAGTAGTTGTGGTTATTTTAAAACTTAAAACAGGTGGCAAGGAAACTCTGCATGATGTGTG[G/A]AAGTATAATGCATCACTGAACAAATGGATCCAGATTGAGTTCCTCAACACAGGCCGCTGGAGACACAAGATGGCAGTTGCTGGTGGAAAGGTGTATGTTTTGGGTGGCTTTGATGGAACCCAGAGATTGAATTGCGTTGAAGCCTATGATCCTTTTCACAACTGCTGGTCAGAGGTGAGTTCTGAGATTCATGACTGTTAACATCTGAATTGAGCAGTTCTCTAACTATAGGCACTTTGCAGACCTAGCAGTAAAACATAAAAAGAAATAAAAGGTTTTTAATTCAATTAAGTGAAATTAATAAGTATCTATATTTAATTCGAAGAATGTTCATTAGTTACAACCAAATTTAATTTTAATATTCATAGAAGTTTTGGGCCAAAAATGTTTATAAAGGGGAAATGTATATAATCAATGTGTATTGTCCATTAATTTATTATTGTAATGACCAAGGTTTCTGACACCTTTGATCCATTTAAAATATAAAATAAAATGAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39880
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 |
---|---|---|---|---|---|
ENSDART00000039174 | Nonsense | 480 | 614 | 6 | 7 |
The following transcripts of ENSDARG00000026990 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 36376207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 36672917 |
GRCz11 | 2 | 36655374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTACGTGATTGGTGGAGGTCCTAATGGCAAGCTGGCCACAAACAACATG[C/T]AGTGCTTCGACTCACAATCAAATAAATGGAGCCTTAAGTGTCCGATGCCA
Long Flanking Sequence:
ACATGCCATGTCATAAAGCATGAATCATCTCAGACTGGTTTCTTGAACATGACAATGAGTTCACTGTACTCAAATGGCCTCCATAGTCACCAGAGCTTAATCCTATAGAGCACCTTTGGGATATAGTGAAACGGGAGACTCGCATCATGGATGTGCAGCCGACAATCATGTCAATATGGTCCAAAATGTTTGACAAATATTTCCTGTACCTTGGTAAACCTATGCCACAAAGTATTAAGGCAGTTCTGAAGGCAAAAGGGGTCCAATCCGGTACTAGTAAGGTGTCCCAAACAGGGTGGCCGCTGAGCGTATTTTACAATAGAAAATGTATATACTGGAATCTTCGTAATGATTCTCATGAGTAAATATACTGTTTTTTGTCCTCCTTCCAGGCAGCGCCGCTTATGTTGAGTGTGAGCTCTTTCTCTGCTGCCAGCTTTGACAGATGCATCTACGTGATTGGTGGAGGTCCTAATGGCAAGCTGGCCACAAACAACATG[C/T]AGTGCTTCGACTCACAATCAAATAAATGGAGCCTTAAGTGTCCGATGCCAACTGAGGCCAAATGCACAAATGCAGTGACCTTTAAGGATGCCATTTTTGTTGTTGGTTTGTACCTTTACATTTATTAATCTGTAAGAGTGTGAATTGCATCTGCCGGTAAAACATGTGACAGTAATTGGAGATTCATTGTGCCGTTACGACCCCTAATTAAGATGGGAATAAGCCAAAGGAAAGTGAGTTTCAATATATTAAACTACTCAACTGAGATTACTATCATGCTCTGATCACTTATACAATGGAAATTAAAATTAGAGAACAAATACTAAACAACTGATTTTTTTTTAAAATGCAATCTTCATTATTAAAAATTTGAGGGAATGTTAGTCATAGAATGCTAGCAGAACAATGCTAACTCACTGAGGGACTTCAACAAAAGTCATTTTATATTTTATATCGTGCAGCTATTTGAAAATCTTATAAAAGCATTGTAAGTTCAACAA
Associated Phenotype:
Not determined