ZMP
klhl31
Ensembl ID:
ZFIN ID:
Description:
Kelch-like protein 31 [Source:UniProtKB/Swiss-Prot;Acc:Q6Q7X9]
Human Orthologue:
KLHL31
Human Description:
kelch-like 31 (Drosophila) [Source:HGNC Symbol;Acc:21353]
Mouse Orthologue:
Klhl31
Mouse Description:
kelch-like 31 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:3045305]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa38915 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa16460 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa38915
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057049 | Nonsense | 207 | 635 | 2 | 5 |
ENSDART00000102791 | Nonsense | 207 | 635 | 2 | 4 |
ENSDART00000124655 | Nonsense | 207 | 635 | 1 | 2 |
ENSDART00000129911 | Nonsense | 207 | 635 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 2123344)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2310630 |
GRCz11 | 13 | 2343395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCTGCTCAGAAGTTCATGCGAGAGAACTTCATTGAGTTCTCCGAGATG[G/T]AGCAGTTCCTCAAACTCACCTACGAGCAAATCAACGAGTTCCTCACAGAC
Long Flanking Sequence:
GCGGAAACGGCTTTAGTTGCATCTCCACCGAAGTCACCGACCCCGTCTATGCACCAAACCTCCTGGAGGGTCTGGGCCACATGAGGCAGGACAGCTTCCTCTGTGACCTCACGGTAGCAACCAAATCCAAGTCCTTCGACGTTCACAAAGTAGTGATGGCATCCTGCAGCGAGTACATCCAAAACATGCTCCGGAAGGATCCGTCTCTAAAGAAGATTGAGCTCAGTGATTTATCCCCAGTTGGTTTGGCTACAGTCATCACTTATGCCTATTCTGGAAAACTGACCCTGTCTCTATACACCATCGGCAGCACTATATCTGCAGCCTTGCTCCTCCAGATCCACACTTTGGTGAAAATGTGTAGTGATTTCTTAATGCGGGAGACTAGCGTGGAGAATTGCATGTATGTGGTCAACATTGCCGACACGTACAATCTAAAAGAGACGAAGGAAGCTGCTCAGAAGTTCATGCGAGAGAACTTCATTGAGTTCTCCGAGATG[G/T]AGCAGTTCCTCAAACTCACCTACGAGCAAATCAACGAGTTCCTCACAGACGACTCACTTCAGTTGCCTTCAGAGCTCACGGCTTTCCAGATCGCAGTCAAGTGGTTGGATTTTGATGAAAAGAGGTTGAAGTACGCTCCTGATCTGCTGTCCAACATCCGTTTTGGCACCATCACCCCCCAGGATCTTGTTAGTCACGTGCAGAACGTTCCCAGGATGATGCAGGATGCCGAGTGCCACCGTTTGCTGGTCGACGCCATGAATTACCACCTGCTGCCGTTCCAGCAGAACATCCTTCAATCCCGGAGGACCAAAGTTCGTGGAGGTCTCCGAGTTCTGCTTACTGTTGGCGGACGGCCTGCGCTGACCGAAAAGTCTCTCAGCAAGGACATTCTCTACAGGGACGAGGATAATGTCTGGAACAAGCTGACGGAGATGCCTGCTAAGAGCTTCAATCAGTGTGTGGCCGTTTTGGACGGTTTCCTTTACGTGGCTGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16460
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000057049 | Nonsense | 295 | 635 | 2 | 5 |
ENSDART00000102791 | Nonsense | 295 | 635 | 2 | 4 |
ENSDART00000124655 | Nonsense | 295 | 635 | 1 | 2 |
ENSDART00000129911 | Nonsense | 295 | 635 | 2 | 4 |
Genomic Location (Zv9):
Chromosome 13 (position 2123610)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 2310364 |
GRCz11 | 13 | 2343661 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGATGCAGGATGCCGAGTGCCACCGTTTGCTGGTCGACGCCATGAATTA[C/A]CACCTGCTGCCGTTCCAGCAGAACATCCTTCAATCCCGGAGGACCAAAGT
Long Flanking Sequence:
GCCTATTCTGGAAAACTGACCCTGTCTCTATACACCATCGGCAGCACTATATCTGCAGCCTTGCTCCTCCAGATCCACACTTTGGTGAAAATGTGTAGTGATTTCTTAATGCGGGAGACTAGCGTGGAGAATTGCATGTATGTGGTCAACATTGCCGACACGTACAATCTAAAAGAGACGAAGGAAGCTGCTCAGAAGTTCATGCGAGAGAACTTCATTGAGTTCTCCGAGATGGAGCAGTTCCTCAAACTCACCTACGAGCAAATCAACGAGTTCCTCACAGACGACTCACTTCAGTTGCCTTCAGAGCTCACGGCTTTCCAGATCGCAGTCAAGTGGTTGGATTTTGATGAAAAGAGGTTGAAGTACGCTCCTGATCTGCTGTCCAACATCCGTTTTGGCACCATCACCCCCCAGGATCTTGTTAGTCACGTGCAGAACGTTCCCAGGATGATGCAGGATGCCGAGTGCCACCGTTTGCTGGTCGACGCCATGAATTA[C/A]CACCTGCTGCCGTTCCAGCAGAACATCCTTCAATCCCGGAGGACCAAAGTTCGTGGAGGTCTCCGAGTTCTGCTTACTGTTGGCGGACGGCCTGCGCTGACCGAAAAGTCTCTCAGCAAGGACATTCTCTACAGGGACGAGGATAATGTCTGGAACAAGCTGACGGAGATGCCTGCTAAGAGCTTCAATCAGTGTGTGGCCGTTTTGGACGGTTTCCTTTACGTGGCTGGAGGAGAAGACCAGAATGATGCAAGAAACCAGGCAAAGCATGCAGTCAGCAATTTCAGCAGGTAAGATTATGCATCGTTTTGGTTATGAAACTGTTTATTGTCGGCTAGGCATGAAATATTGCATTGAATTAGTGTCCAAGTTCAACATGCAGAATTGGGCTCAGATGCAAAACAAAATTCCCACCAAGCAATGTTGTGTTTTATAGATAAATAATAGACAGTGGTGCTCAACCCTGCTCCTGGAGATCAAACTTCCTGCAAAGTTCCGCT
Associated Phenotype:
Not determined