ZMP
cdc37l1
Ensembl ID:
ZFIN ID:
Description:
Hsp90 co-chaperone Cdc37-like 1 [Source:UniProtKB/Swiss-Prot;Acc:A7YY97]
Human Orthologue:
CDC37L1
Human Description:
cell division cycle 37 homolog (S. cerevisiae)-like 1 [Source:HGNC Symbol;Acc:17179]
Mouse Orthologue:
Cdc37l1
Mouse Description:
cell division cycle 37 homolog (S. cerevisiae)-like 1 Gene [Source:MGI Symbol;Acc:MGI:1914322]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa34859 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12517 | Nonsense | Available for shipment | Available now |
sa12498 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa34859
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127331 | Essential Splice Site | 113 | 344 | 2 | 8 |
The following transcripts of ENSDARG00000044265 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10946230)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 11022096 |
GRCz11 | 10 | 10980334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGATGCTGGGCACGCTGTGTCCTGAAGCCAACCGGGATGTGTTTGACAAG[G/A]TAGCTAAACTCTAGAAAGTCATCCAGAGAGTTGATGATGTCATCATAATT
Long Flanking Sequence:
GTAAATTCATTTGAGCTTCATCTTTCTAAATTCCAGGACAAAATAACATAGACAAATTAGGTCTAAAGCACTCTAGAATTGATTCCTAAATAAGTAATCCAAATTACATTCAGTTACTTTCATCATAAAACAGATAATAGACAGTTCTAACGACTAAATTCCTTACCAAAGCAGTATTTTTCTGAGCATATATGATACTGTGATTTAGTCTCTCTCTGTGTGTGTGTGTTGTGTGACAGGCAAGTGCGGAGAGCATGGCGTCTCTGTGTCAGCGGCAGCAGCACTGTGTGAAGGCCTCCATCGCATCAGAGTGGCAGCTGGCAGAAGCGCAGGATCAGCTCTGCGGTCTGGAGCTCCACAGCTCCGAGTCTGTGGAGCAGGAGAGAGCCCGAGCACTGGCCTCCTCCACTGAACTCTCGCACACTGAACACCAGTGGAGGCTCAAAGAGAGGATGCTGGGCACGCTGTGTCCTGAAGCCAACCGGGATGTGTTTGACAAG[G/A]TAGCTAAACTCTAGAAAGTCATCCAGAGAGTTGATGATGTCATCATAATTACTGCATTGCTAGTACAGGCCACTATGGCTGCAGACAAGGAAAACATACAAAAACCTACAGTTGAAGTTAAAATTATTAGTCCTCCTGTTCAGTTTTCTTCTGTTTTGTCAGGTTTCACTGTGTTTTTTGCTCTTAAATTTAGAACTTTTTTTTTTAAAGCTACCTTTTTATTTGTTATAGGTGTAAACAGGCCTTAAGTCTTAGCGTGTTGATTTTCTGATATCCTTTTATTTTTCTTTTAGAGTATCATAAACATTACACAGTCTTGGCCAAATGAATCTGATCCAGATAAAAGCTTAAACTTCGTCCAGCGCAATGAAGAGCTCCTGAAACATTTTGGTACGCGATCTAAATTGTGGTAAATGTTTTTTAATGAGTATTGTTCATCGTAGAGCAGGTTGTCATCTCTCTCTCTCTTCTGATTGGACAGGTATGCTGGGAAGGTGGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12517
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127331 | Nonsense | 161 | 344 | 4 | 8 |
ENSDART00000127331 | Nonsense | 161 | 344 | 4 | 8 |
The following transcripts of ENSDARG00000044265 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10946758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 11022624 |
GRCz11 | 10 | 10980862 |
KASP Assay ID:
2260-2968.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGGTATGCTGGGAAGGTGGGATGACAGTCAGCGCTTTCTAGCAGAATA[T/A]CATCACCTCATCTGTGAAGAAACAGCCAATTACCTGATCCTGTGGTGCTT
Long Flanking Sequence:
GAGTTGATGATGTCATCATAATTACTGCATTGCTAGTACAGGCCACTATGGCTGCAGACAAGGAAAACATACAAAAACCTACAGTTGAAGTTAAAATTATTAGTCCTCCTGTTCAGTTTTCTTCTGTTTTGTCAGGTTTCACTGTGTTTTTTGCTCTTAAATTTAGAACTTTTTTTTTTAAAGCTACCTTTTTATTTGTTATAGGTGTAAACAGGCCTTAAGTCTTAGCGTGTTGATTTTCTGATATCCTTTTATTTTTCTTTTAGAGTATCATAAACATTACACAGTCTTGGCCAAATGAATCTGATCCAGATAAAAGCTTAAACTTCGTCCAGCGCAATGAAGAGCTCCTGAAACATTTTGGTACGCGATCTAAATTGTGGTAAATGTTTTTTAATGAGTATTGTTCATCGTAGAGCAGGTTGTCATCTCTCTCTCTCTTCTGATTGGACAGGTATGCTGGGAAGGTGGGATGACAGTCAGCGCTTTCTAGCAGAATA[T/A]CATCACCTCATCTGTGAAGAAACAGCCAATTACCTGATCCTGTGGTGCTTCCGGCTACAGGCAGAGAAGGTGACTGCTTTCTCTTCAAAATACATACACACACTTCTGATTATTTCAGCTTTTTTGAAGTTTGTATTATCTAGGTCTTGGAGATTTAGGCAGTTATTACATTTAAAATGTTCAAAGCAGTCAGTATCTATAATCATCACAATAAATGTACTTTGCTCCTTACCAATGAAAACAAATGGTTTACTGTTCATTTAAATTACTCTTTCGCTGTCGAACATGACAAACACACACTAGATTAACATTTTACAAGTCTGAGGTACATTTTATTAACTTTGTATTGCGTTTTTCTGCCCTTTTCATTTAAAGGGCCGGTTCATTCAAAATGGAAACTTCTGTCATCCTTTACTTACCCTTCACTTCTTCCAAACCTGTTTGAGTTTCTTTCTTCTTTCTTCACAAATGAAGATATATTGAAGTAGGTTGGTAAAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12498
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127331 | Nonsense | 161 | 344 | 4 | 8 |
ENSDART00000127331 | Nonsense | 161 | 344 | 4 | 8 |
The following transcripts of ENSDARG00000044265 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 10 (position 10946758)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 11022624 |
GRCz11 | 10 | 10980862 |
KASP Assay ID:
2260-2968.1 (used for ordering genotyping assays)
KASP Sequence:
ACAGGTATGCTGGGAAGGTGGGATGACAGTCAGCGCTTTCTAGCAGAATA[T/A]CATCACCTCATCTGTGAAGAAACAGCCAATTACCTGATCCTGTGGTGCTT
Long Flanking Sequence:
GAGTTGATGATGTCATCATAATTACTGCATTGCTAGTACAGGCCACTATGGCTGCAGACAAGGAAAACATACAAAAACCTACAGTTGAAGTTAAAATTATTAGTCCTCCTGTTCAGTTTTCTTCTGTTTTGTCAGGTTTCACTGTGTTTTTTGCTCTTAAATTTAGAACTTTTTTTTTTAAAGCTACCTTTTTATTTGTTATAGGTGTAAACAGGCCTTAAGTCTTAGCGTGTTGATTTTCTGATATCCTTTTATTTTTCTTTTAGAGTATCATAAACATTACACAGTCTTGGCCAAATGAATCTGATCCAGATAAAAGCTTAAACTTCGTCCAGCGCAATGAAGAGCTCCTGAAACATTTTGGTACGCGATCTAAATTGTGGTAAATGTTTTTTAATGAGTATTGTTCATCGTAGAGCAGGTTGTCATCTCTCTCTCTCTTCTGATTGGACAGGTATGCTGGGAAGGTGGGATGACAGTCAGCGCTTTCTAGCAGAATA[T/A]CATCACCTCATCTGTGAAGAAACAGCCAATTACCTGATCCTGTGGTGCTTCCGGCTACAGGCAGAGAAGGTGACTGCTTTCTCTTCAAAATACATACACACACTTCTGATTATTTCAGCTTTTTTGAAGTTTGTATTATCTAGGTCTTGGAGATTTAGGCAGTTATTACATTTAAAATGTTCAAAGCAGTCAGTATCTATAATCATCACAATAAATGTACTTTGCTCCTTACCAATGAAAACAAATGGTTTACTGTTCATTTAAATTACTCTTTCGCTGTCGAACATGACAAACACACACTAGATTAACATTTTACAAGTCTGAGGTACATTTTATTAACTTTGTATTGCGTTTTTCTGCCCTTTTCATTTAAAGGGCCGGTTCATTCAAAATGGAAACTTCTGTCATCCTTTACTTACCCTTCACTTCTTCCAAACCTGTTTGAGTTTCTTTCTTCTTTCTTCACAAATGAAGATATATTGAAGTAGGTTGGTAAAAAT
Associated Phenotype:
Not determined