ZMP
dnajc5g
Ensembl ID:
ZFIN ID:
Description:
DnaJ (Hsp40) homolog, subfamily C, member 5 gamma [Source:RefSeq peptide;Acc:NP_955917]
Human Orthologue:
DNAJC5G
Human Description:
DnaJ (Hsp40) homolog, subfamily C, member 5 gamma [Source:HGNC Symbol;Acc:24844]
Mouse Orthologue:
Dnajc5g
Mouse Description:
DnaJ (Hsp40) homolog, subfamily C, member 5 gamma Gene [Source:MGI Symbol;Acc:MGI:3045263]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37120 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39300 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37120
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 |
---|---|---|---|---|---|
ENSDART00000061393 | Nonsense | 111 | 199 | 3 | 6 |
ENSDART00000136771 | Nonsense | 111 | 199 | 3 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 38801108)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38873520 |
GRCz11 | 20 | 38776399 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTTGGAGAAGAAAGTGTCAAATACTACTTCCTCATGTCAAAGTGGTG[G/A]TTCAAGGTGAGAGCTAGTTTTCATATAAGCAGAGCTGTTATTTACTGTTT
Long Flanking Sequence:
CATTCCTTGCAAACGTTTAAACGCATTCTTAAACACCACTGATTGGCCATTGTGGTCATGCCCTTAACAGAAATTACTGTTATTTGGTCATTTTTACATTTTTTTTTTTGTACCGATTGGTACCAAAGTTGATTCGTTTGACAACACTACTTTGCTGTATGAACTTAAATGATTTCAATGAACAGCCATTTATGTGTGTTGCATTGTCCATGATTGAAGCAATATCAAAACTGTGCATGCAGTATTTACTTCAATCATTGTTTTAACACATGCATGATTCTTTGCATTTACAGAAAACTAGCTCTGAAATACCATCCAGACAAGAATCCAGACAATCCTGAAGCTGCAGAAAAGTTCAAAGAAATTAATAATGCCAACTCTATCCTCACCGATGAGACTAAGCGCAAGATCTACGATGAGTACGGTTCCATGGGACTCTACGTGTCGGAGCAGTTTGGAGAAGAAAGTGTCAAATACTACTTCCTCATGTCAAAGTGGTG[G/A]TTCAAGGTGAGAGCTAGTTTTCATATAAGCAGAGCTGTTATTTACTGTTTACTCCTTGTGTTGACCTACACAGACATTCTGTAGTGGAATATTTGCCAGATCTAGACTACACAATTTCAGCCTGATTTGGCACAATCAGTTGGATGTAGTGTGTTGTAGTGGTGGTTTATGAGTTATAATTGGGATCAGAATTGCAAGAATTCATCACTTGGTTTTATATAGTGTTTTATAGTGGTTAAAGGGAGAGCTCATCCAAAAATTCACATTTACTGTTACTGTAAACTTTTATTAGCTTTTTTTTATTTTGCCTTTACTTGTTCCAAACCTGTTTGACTTATTTTCTTCTGTTAAACGCATAAAAAGATATTATGAAGAAAGCTGAAATCTTGTAATTATTGACTTCCATAGTAGTGAAAAAAACTACGGAAGTTAATGGTTAAAAGTTTCCAACATTTTTCAAAATATCTTGTTTTGTGTTTAACAGAAGACAGACAGAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39300
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:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061393 | Essential Splice Site | None | 199 | None | 6 |
ENSDART00000136771 | None | None | 199 | 5 | 5 |
Genomic Location (Zv9):
Chromosome 20 (position 38790405)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 38862817 |
GRCz11 | 20 | 38765696 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCCTAATGTAGTGTGCTTATCGCTGGACATCACGGCACCAGGACTAAAC[T/G]GTGCCACTTGCGCCACACCCTGACTCTGACCCACTGGAAACGAGTGGCAC
Long Flanking Sequence:
ACTATAACATACACGGTATAAAATGCAGGGTTCCACACAATGAATTTTTGTTGGAAAAACATGAAGGAATGAAGTTAAATTGTTAGTTAACTTAGTTAAGTGAATTGAACATAAAACGAAAATGTTCCCCTCCAAAAACTCAAATGTTTTTCAGCTAATCTTGAATGGGTAGTTTGAACAAGCAGCAAATGCAGTTTTTGAGTGTGTATCAATTATCCCCTTTTACTTCAGAGTAACAAGACATGATCAGTCTCTAATTTTGTCCTTAATGTTTTTATGTTTTTGTAGGCGCAGATGTCCCTATTTTGATCCAGCCCAGTTCCACGGCCAACACCTCAGAGTCTAAGCATTTCGCAGCCAGCCAGCCCGTGTACAACACCCAGAAATGAGCCACCTGCCTGGCCCTGGTCCCGGTCATCACCGAGGGGTCCTGCTGACGGACTGTAAAGGCCCCTAATGTAGTGTGCTTATCGCTGGACATCACGGCACCAGGACTAAAC[T/G]GTGCCACTTGCGCCACACCCTGACTCTGACCCACTGGAAACGAGTGGCACTTTGCCAAAAGACAAGGAAGCCTCTGCCAATCTCACTTTATCTGTGTCTCCATTTGTGTGTACGTCTGTCTGTTCGCTCGTCTATAACCACACGCTCATTTCAAAGTCATATAAGACTGGTGCCATTGGGCAGTGCTCCAGAAGGGAAGTGGGTTTTAAATTTGGGGGTGTTTTTTTTTTTTTCTTCTTTTTTTTGTTTTTCTGGTCCTGGCTATTTATTTATTTCATTCGATTTTTTTTTTCTACTGTGTTCGAAGCATGGTTGTGAGTGGAATGATCATATGAGTGCATGCAAAGCAATAACAGCATGCCTCTACTATACAGCATAGGAACATGTGCGCAAAAAAAAAAACTTCCCACTTCTCTTCCTCCACATGCCATTATGTGGCTTTTTTTATTATAAGTTTAAGTTTGCTGTCATCTGTTACATTTTGCTTTGTTACATTTCAT
Associated Phenotype:
Not determined