Busch Lab

ZMP

unc45a

Ensembl ID:
ENSDARG00000003546
ZFIN IDs:
ZDB-GENE-050417-158, ZDB-GENE-050417-158, ZDB-GENE-050417-158
Description:
unc-45 homolog A [Source:RefSeq peptide;Acc:NP_001017671]
Human Orthologue:
UNC45A
Human Description:
unc-45 homolog A (C. elegans) [Source:HGNC Symbol;Acc:30594]
Mouse Orthologue:
Unc45a
Mouse Description:
unc-45 homolog A (C. elegans) Gene [Source:MGI Symbol;Acc:MGI:2142246]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa15522 Essential Splice Site Available for shipment Available now
sa18626 Nonsense Available for shipment Available now
sa44243 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa15522
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039786 Essential Splice Site 126 218 3 6
ENSDART00000103033 Essential Splice Site 126 935 3 20
ENSDART00000130466 Essential Splice Site 126 935 3 19
Genomic Location (Zv9):
Chromosome 25 (position 8885556)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 8580621
GRCz11 25 8657689
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGCTTTCCAGGATCTKCTTAGACAGCTCGGAGCTCAGATCCAGCAGAAG[G/T]TGTGGGTTAWGAGTGATGCTCGCACTGTTAATATTAATGATSTGAAAATA
Long Flanking Sequence:
TTCCACGTATATTTTTTCTGACTGTGTAGATGTCCCAGGACTCCTCTGCACTGAGGGAGGAAGGAAACAACCATTTTAAAGCCGGCGATGTCCAACAAGCTCTGACCTGCTACACAAAAGCCCTGAAGATCAGCGACTGTCCATCCGAGAGTGCAGTCCTGTACCGCAACCGCTCAGCATGTTATCTTAAACTCGAGGACTACACCAAAGCAGAAGAAGATGCCACAAAATGTAAAAAAGAAGAACACATAAGTATGTGGATTTTCATCACAAACACATCTCCTAACTAAATCGTCTGTTTCTTTGTTTTTTTTTGCTCTCAAGCTTTGGATGTTGATCCAGGTGACATCAAGGCCCGGTTTCGTCGAGCGCAGGCTCTGCAGAAGCTCGGGCGGCTGGATCAGGCGTTCATGGACGTTCAGAAATGTGCACAGCTCGAACCCAAGAATAAAGCTTTCCAGGATCTGCTTAGACAGCTCGGAGCTCAGATCCAGCAGAAG[G/T]TGTGGGTTATGAGTGATGCTCGCACTGTTAATATTAATGATGTGAAAATAACCCCATATTTGTGTTTATATATGTGTATAGGCAACACAGCTCTCCTCCACAGACTCACGGGTTCAACAGATGTTCAAACTCCTCCTGGATAGTTCAGCACCAATTGCAGACAGACAGAAGGTGGGTAAGACTTAAACGGATAGTTCACCCAAAAATGAAATCTGCTTACTATTGACTCACACGCAGGAATTTCTTTCTTCTGTTGAACACAAAACAAGATATCCTGAATAATGTTGGGGGAAAATACAGTCATTGGCGTCCATTGTATGAACACAAAATACTATAGAAGTCAATAGCTGTTTTTTCTAATAGTGTATCCTCCTTTATGTTTAGCAGAAGAAAGCAACTCAGACAGATTTAGAGCAAGTTGAGGATGAGTGAATGATGGCTGAATTTTACGCTGGGGTGATAGTAGGGTTGTAACGGTATGAATTTTTCACGGTATGATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18626
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
ENSDART00000039786 None None 218 None 6
ENSDART00000103033 Nonsense 574 935 12 20
ENSDART00000130466 Nonsense 574 935 12 19
Genomic Location (Zv9):
Chromosome 25 (position 8870163)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 8565228
GRCz11 25 8642296
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTGTTTTGATTGCAGTCCGAGGACAAAACTGTGTTGTTTGCGGTGGGAT[C/A]GACACTGGTAAACTGCACCAAYAGCTACGATGTRGAGAAGCCAGACCCGC
Long Flanking Sequence:
GCTAACCACTGAGCCACTGTTGCCCTGTTTTAGTTTTTAGTCTTGGTAATTAATCTTTTAATTTAAAATTGAGGAGTGTTTACTAATCAAAGAGTCAGATCTATCAATTGAAATCATTGTCGTTTAGTTTTTGTAGCTCCAGCAAACGCATCTATTTGTGCATGTGTTTACATGTAATACATATTAAGTCCATTTAGCATGTGCATGTGGCTGTCTTTTTCTCTTTCCCAGATGGCTCTGCAATGAATCTCTTCCTCCAGCATCGCGGCGCTGGGCCATCGAGGGTCTGGCTTACCTCACGCTGGACGCCGATGTCAAAGAGGACCTGGTTGAGGACAAGAAAGCTCTTCAGGCCATGTTTGAGCTGGCCAAGGTTTCGCTTTTTCTGCAGTTTTGGAGATAAACGTCCGCTTATTATGCTAATCCTCCTCGGCTCCTTAAACTCGTGTTTTTGTTTTGATTGCAGTCCGAGGACAAAACTGTGTTGTTTGCGGTGGGAT[C/A]GACACTGGTAAACTGCACCAACAGCTACGATGTGGAGAAGCCAGACCCGCAGATGGTGGAGCTAGCTAAATATGCTAAACAACATGTACCAGAGGAGCATCCAAAGGTGATTTATGCGGATAGGATTGTTATGTTGGTCAAAAATGAACTTATTGTTATTAATAATTTATGCTTGTTAAGTTTTAAAATCCATATATTGTCTTTTTTAGGATACAGCAAAATTATTCAGTGGCTGTTAAGCTCCAAAAAGCAGCATAAATGTAACACTTTAAATTAATTAACAAAAGTCGATCGTTATTTTGAACTACTTGTTTCCTTTATTTTTTGTTATTTTTATATATTTCATGTAATTTATTTGGTCTTAGTAATTGATTTATTATTTGTTATGTCATAGATTATTTAATATTTAGTTTGCTTTGGCAATGCTTTAATACATATGTATATATACAGTTGAAGTCAGAATTATTAGCCCCCTTTTGAATTTTTTTACTTTTTAAAAT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44243
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000039786 None None 218 None 6
ENSDART00000103033 Nonsense 601 935 12 20
ENSDART00000130466 Nonsense 601 935 12 19
Genomic Location (Zv9):
Chromosome 25 (position 8870083)
Other Location(s):
Assembly Chromosome Position
GRCz10 25 8565148
GRCz11 25 8642216
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGGAGAAGCCAGACCCGCAGATGGTGGAGCTAGCTAAATATGCTAAA[C/T]AACATGTACCAGAGGAGCATCCAAAGGTGATTTATGCGGATAGGATTGTT
Long Flanking Sequence:
TACTAATCAAAGAGTCAGATCTATCAATTGAAATCATTGTCGTTTAGTTTTTGTAGCTCCAGCAAACGCATCTATTTGTGCATGTGTTTACATGTAATACATATTAAGTCCATTTAGCATGTGCATGTGGCTGTCTTTTTCTCTTTCCCAGATGGCTCTGCAATGAATCTCTTCCTCCAGCATCGCGGCGCTGGGCCATCGAGGGTCTGGCTTACCTCACGCTGGACGCCGATGTCAAAGAGGACCTGGTTGAGGACAAGAAAGCTCTTCAGGCCATGTTTGAGCTGGCCAAGGTTTCGCTTTTTCTGCAGTTTTGGAGATAAACGTCCGCTTATTATGCTAATCCTCCTCGGCTCCTTAAACTCGTGTTTTTGTTTTGATTGCAGTCCGAGGACAAAACTGTGTTGTTTGCGGTGGGATCGACACTGGTAAACTGCACCAACAGCTACGATGTGGAGAAGCCAGACCCGCAGATGGTGGAGCTAGCTAAATATGCTAAA[C/T]AACATGTACCAGAGGAGCATCCAAAGGTGATTTATGCGGATAGGATTGTTATGTTGGTCAAAAATGAACTTATTGTTATTAATAATTTATGCTTGTTAAGTTTTAAAATCCATATATTGTCTTTTTTAGGATACAGCAAAATTATTCAGTGGCTGTTAAGCTCCAAAAAGCAGCATAAATGTAACACTTTAAATTAATTAACAAAAGTCGATCGTTATTTTGAACTACTTGTTTCCTTTATTTTTTGTTATTTTTATATATTTCATGTAATTTATTTGGTCTTAGTAATTGATTTATTATTTGTTATGTCATAGATTATTTAATATTTAGTTTGCTTTGGCAATGCTTTAATACATATGTATATATACAGTTGAAGTCAGAATTATTAGCCCCCTTTTGAATTTTTTTACTTTTTAAAATATTTTCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATGTCTGATAATATTTTTTCTTCTGGAGAAAGTCTTA
Associated Phenotype:
Not determined