Busch Lab

ZMP

klhl36

Ensembl ID:
ENSDARG00000030251
ZFIN ID:
ZDB-GENE-050522-324
Description:
Kelch-like protein 36 [Source:UniProtKB/Swiss-Prot;Acc:Q503R4]
Human Orthologue:
KLHL36
Human Description:
kelch-like 36 (Drosophila) [Source:HGNC Symbol;Acc:17844]
Mouse Orthologue:
Klhl36
Mouse Description:
kelch-like 36 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2385305]

Alleles

There are 5 alleles of this gene:

Allele Name Consequence Status Availability
sa11523 Nonsense Available for shipment Available now
sa36593 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa25056 Nonsense Mutation detected in F1 DNA Not yet available
sa14457 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa11523
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039585 Nonsense 33 605 3 6
ENSDART00000134920 Nonsense 38 76 3 3
ENSDART00000142942 Nonsense 69 107 3 3
Genomic Location (Zv9):
Chromosome 18 (position 12678429)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 13233273
GRCz11 18 13201785
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
YTCATAATCACCAGGTGTATCGATGKKYAGACCAAGCTAACAACCTCCTG[C/T]AAGGCTTAAATGAGCAACGACAGCATGGTCAAATGTGTGATGTGGTWCTG
Long Flanking Sequence:
CAGATTAATAAAGAAGAAAATGAATGAATGGAATCATATTAAAAATATATAATGAATGCTTTAATAGAATAAAAGTAATTAAATTGATGGACAATACTATATATAATTTTTTATATAAATAATAATAATGTTTAAATAGTTATCATAATTCATTAACTTTTATTGTTACATACCCAATAATTGCATTATTATCAATAAACATTTTAAAATGCTTTAAGTTAAATTTACAGGTTTTTTGCACAATAAAAATAATATAAATAGTACTGTCACATGATAAAAACTCTTGTTATGCTGGTCTGAAAAATTTATTTGGCATATCAACATCACATGATGACCAGAACAAATCTTATGCATCCAGACTGAACAGTGCCCATAAAGAGTAAATGAACTAGTGCTGTTAGAATGATGGGGGGAAAATCATATTATCTTTTAAAGTTTCTTTCAATTGTCCTCATAATCACCAGGTGTATCGATGGGCAGACCAAGCTAACAACCTCCTG[C/T]AAGGCTTAAATGAGCAACGACAGCATGGTCAAATGTGTGATGTGGTACTGGTAGCTGATGACCAGCGGATTCCTGCACATCGGGCTCTACTCGCTGTATCCAGTCCTTACTTCCAGGTAGGCTTAAATTTTGTTTGCTGCAATAAATAGCTGAAGCTTTTATCATGGAATGTGTCATTATTACAATATTTACCTAAGCTGCTAAAAAGGCTACTTTAACAGGTATAATAACTAAAAAATACTTTGTGTATTGCTTTACTGTATATACATATCAGGAGTAAATACATTTAAAAAAACAAATTAAATAGCAAAATGACGATAAAGTAGTGTAACACTTTGTAATAAAGTCTCATTGGTAAATGATAGTTAATGCATTAAAATCAAAGTTAATATAAAAAGTATGGCGCCACTTTATAACTGCTATGTACTTGCATCAGAAAATAAATACAATGTACTTACTGTGTTCATAAAGTATTGCAGAAGACTTCTAGTGTTCTTATG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa36593
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039585 Essential Splice Site 72 605 4 6
ENSDART00000134920 None None 76 None 3
ENSDART00000142942 None None 107 None 3
Genomic Location (Zv9):
Chromosome 18 (position 12676353)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 13231298
GRCz11 18 13199810
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATTGTTATGATATATTGAATTATTGAATATCGGCATATGTCTTCTTTC[A/T]GGCCATGTTCACCCTGGGCATGCGGGAGGAACACGAGTCTGAAATAGAGC
Long Flanking Sequence:
CTCTGCATGATACGTTCAAGCTAGTCAGGGCAGGTGAAAACTCAAAAGATTTATTCAAGACCCTGAAACAAGATTTTCAACTAAACTTGTCATGCCCGTTTTCTATACACTGTCCCTTCTAAAACACATAATAGACAGGACGACTCTGTCTCAGATCAGACTTGTTTTAGACTTGCAGACTCATTTAGACCTGTAAGACTTTTTGAAGATGCTGTTTGACTGCAGAACAACATGTCTTAATAAAGAATTCTGTTTGTAACGAGTCTCCTGGCTTGAGTTCTTCAGTAGCCAACACTACTGAACCTTACTTGGCAGAGTTATCAAACTAAAAGGTTTTAAATGTGATGAACAACCATGTCCAATCCATCAATCTGAACATTCTTAATACACACTATAACAATAATTATTTACAGCATTTTTAAGCGCCCATTATATAAAAATTGTCTTTGTTTATTGTTATGATATATTGAATTATTGAATATCGGCATATGTCTTCTTTC[A/T]GGCCATGTTCACCCTGGGCATGCGGGAGGAACACGAGTCTGAAATAGAGCTAGTAGGAGCCTCCTATGTTGGCGTTAAAGCCGTAATAGACTTCCTATACAGCGGCAATTTACCTCTCGACGGAGGAAACATCGATTACGTCCTGGAAACAGCTCACCTTCTGCAAGTGTGGCAAGCTGTGGATTTCTGTTGTCAGTATTTAGAAAAAGAGGTACGTGAAGACAACTACCTGTACCTTCAAGAACTCGCCTTGCTATACAGTCTAGATCGGCTGGATGCCTTCATAGACAGATTTATTTTGAAACATTTCAGCACACTTTCCATCACTTCCGAGTTCCTCCAGGATGTGCGGATGTTCAAGCTTTGTGCTTACCTTTCCAGCGAACAAGTGCAATGCCTAAACGAGGAAACTCTTTTTGAGGTTGCCTTTAAGTGGTTGAAACAAAAACCTGAACGTCTTGAATTCGCCCTTCAGCTCCTTTCCAACATTCGTTTCGCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa25056
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039585 Nonsense 193 605 4 6
ENSDART00000134920 None None 76 None 3
ENSDART00000142942 None None 107 None 3
Genomic Location (Zv9):
Chromosome 18 (position 12675986)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 13230931
GRCz11 18 13199443
KASP Assay ID:
554-7362.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTCCATCACTTCCGAGTTCCTCCAGGATGTGCGGATGTTCAAGCTTTG[T/A]GCTTACCTTTCCAGCGAACAAGTGCAATGCCTAAACGAGGAAACTCTTTT
Long Flanking Sequence:
CAATCTGAACATTCTTAATACACACTATAACAATAATTATTTACAGCATTTTTAAGCGCCCATTATATAAAAATTGTCTTTGTTTATTGTTATGATATATTGAATTATTGAATATCGGCATATGTCTTCTTTCAGGCCATGTTCACCCTGGGCATGCGGGAGGAACACGAGTCTGAAATAGAGCTAGTAGGAGCCTCCTATGTTGGCGTTAAAGCCGTAATAGACTTCCTATACAGCGGCAATTTACCTCTCGACGGAGGAAACATCGATTACGTCCTGGAAACAGCTCACCTTCTGCAAGTGTGGCAAGCTGTGGATTTCTGTTGTCAGTATTTAGAAAAAGAGGTACGTGAAGACAACTACCTGTACCTTCAAGAACTCGCCTTGCTATACAGTCTAGATCGGCTGGATGCCTTCATAGACAGATTTATTTTGAAACATTTCAGCACACTTTCCATCACTTCCGAGTTCCTCCAGGATGTGCGGATGTTCAAGCTTTG[T/A]GCTTACCTTTCCAGCGAACAAGTGCAATGCCTAAACGAGGAAACTCTTTTTGAGGTTGCCTTTAAGTGGTTGAAACAAAAACCTGAACGTCTTGAATTCGCCCTTCAGCTCCTTTCCAACATTCGTTTCGCTCTCATCCCGTTTTATTTACTAAAATATTATGTTTTGCCTAACGTACATTCCCTGCTGCCTCTGGACACAAGCTGCAAGGTGTTAGTTGAGGAAGCAATAGACTACCACAGGAAGCTCAGCGCTCAGCCTGTAATGCAGACACAGCGAACAGGCCTTCGTGGAGGTGTGGAGTGTCTGCTGCTGCTGGGAGGAGAAGTGTCCGAGCGTGGAGAAGGTTTGAGTGCTGAGGTTTGCTGGCTGGATGAAGAAGCAGGGAAGTGGGTTGAGGAGACTAAGATGCCAGCGCCAAGGAGTCAGCATTGTGTGGCGGTTTTGGGTGGATTCATTTTCACAGCCGGTGGGAGCTGCTCACCGGACAACGGGGGAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa14457
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039585 Nonsense 272 605 4 6
ENSDART00000134920 None None 76 None 3
ENSDART00000142942 None None 107 None 3
Genomic Location (Zv9):
Chromosome 18 (position 12675749)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 13230694
GRCz11 18 13199206
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGCCTCTGGACACAAGCTGCAAGGTGTTAGTTGAGGAAGCAATAGACTA[C/A]CACAGGAAGCTCAGCGCTCARCCTGTAATGCAGACACAGCGAACAGGCCT
Long Flanking Sequence:
GGCAATTTACCTCTCGACGGAGGAAACATCGATTACGTCCTGGAAACAGCTCACCTTCTGCAAGTGTGGCAAGCTGTGGATTTCTGTTGTCAGTATTTAGAAAAAGAGGTACGTGAAGACAACTACCTGTACCTTCAAGAACTCGCCTTGCTATACAGTCTAGATCGGCTGGATGCCTTCATAGACAGATTTATTTTGAAACATTTCAGCACACTTTCCATCACTTCCGAGTTCCTCCAGGATGTGCGGATGTTCAAGCTTTGTGCTTACCTTTCCAGCGAACAAGTGCAATGCCTAAACGAGGAAACTCTTTTTGAGGTTGCCTTTAAGTGGTTGAAACAAAAACCTGAACGTCTTGAATTCGCCCTTCAGCTCCTTTCCAACATTCGTTTCGCTCTCATCCCGTTTTATTTACTAAAATATTATGTTTTGCCTAACGTACATTCCCTGCTGCCTCTGGACACAAGCTGCAAGGTGTTAGTTGAGGAAGCAATAGACTA[C/A]CACAGGAAGCTCAGCGCTCAGCCTGTAATGCAGACACAGCGAACAGGCCTTCGTGGAGGTGTGGAGTGTCTGCTGCTGCTGGGAGGAGAAGTGTCCGAGCGTGGAGAAGGTTTGAGTGCTGAGGTTTGCTGGCTGGATGAAGAAGCAGGGAAGTGGGTTGAGGAGACTAAGATGCCAGCGCCAAGGAGTCAGCATTGTGTGGCGGTTTTGGGTGGATTCATTTTCACAGCCGGTGGGAGCTGCTCACCGGACAACGGGGGAGATTCTGCAAGTGACATGCTGTATCGGTACGATCCCCGGAGATGCCATTGGATCAAGGTGATTTGTTTGTCTGCTGACTGTTTGGATAGTTTGTGACATTTAAGTTTTAGCTGTAATGTTCCAGGGCGGATTTTGGCAGTAGCTGGTCTAGCTTCAAAGGCTACTCCTCACTGTTGCATACAAAAGACGAAGTAAAAGAGCGGGTGATCAAGTCAAAGAGGTGGGGTCGGGGTGGGGTT
Associated Phenotype:
Not determined