ZMP
zgc:162618
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC325751 [Source:RefSeq peptide;Acc:NP_001082800]
Human Orthologue:
CHCHD3
Human Description:
coiled-coil-helix-coiled-coil-helix domain containing 3 [Source:HGNC Symbol;Acc:21906]
Mouse Orthologue:
Chchd3
Mouse Description:
coiled-coil-helix-coiled-coil-helix domain containing 3 Gene [Source:MGI Symbol;Acc:MGI:1913325]
Alleles
There are 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa13069 | Nonsense | Available for shipment | Available now |
| sa17229 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13069
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104877 | Nonsense | 399 | 449 | 8 | 9 |
The following transcripts of ENSDARG00000034933 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 3422966)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 3241161 |
| GRCz11 | 25 | 3366905 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATTCAAGCATTCAACAGAGACTTTTTTGTTCACTCTCTGTAGGCGATAT[C/T]GAATCAAGCCYGTGTGTTCAGATCTCCAGAGTCAGATCTTGAAGTGTWAC
Long Flanking Sequence:
TTTCCACCTGGCCCAGCCGGGACTCGAACCTGCGACCTTCTTGCTGTGTGGTGACAGTGCTAACCACTGAGCCTCCGTGACGCAGGTTTTTCATTGTACTTAATATTAGGAATAATTGACAATTTCCCATTGAATTATTAGACATTAATGCACACCTGAGGTGGTGATGTGGCCATGAGCAGAGTGCTTTATTTTCTAATAACACAGCAGACTAGTTTCAATAATCTGCACTTATACTATAGTTCAGTTATACACGGTAGATATTAGCATTGTTTAAAATACCGATAATTATTGAAACTGTGTGTTTTGATGTGATTATTGACTGAAATTACTGAAATCATTCAGTGTAGTGATGTAGAACTCTAATGCACTCAAAACCTGCCGGAACTACTTCAGCTGTGTGTTTATTTGAAAATAATGGCACACCTTAGAACCCTCATCAGCCAATCAAATTCAAGCATTCAACAGAGACTTTTTTGTTCACTCTCTGTAGGCGATAT[C/T]GAATCAAGCCCGTGTGTTCAGATCTCCAGAGTCAGATCTTGAAGTGTTACGCTGAGAATAAAGGACAAACTATGTGCTGCTCCAACATCGCGTCGCTGTACATCCAGTGTGTGGACCGCGCCAGACAGGTGAACCACACTTTCATTAATGTACTGGTTAAAAAACGAGTTTAGCTGTTTGGAGCATTTACTGCAGAAAAGTAATGATACTAAAAAAAGATGCTGGGTTGTTGTGACCCAACGTTAGGTAGAATATTGACGAAACAAACCATTGGGATAAAAGGTGTTATTTAAATTAATTTGAAGAAATTAATTCAGGGTTTGTTCATATTTGACCCAATGTTGGGTTCTTTGTTTTGATTAAATATACAGGTTTTTTTTTAAATTTAACTTAAATTACACTTTTTTTTTTAACCCAGTGTTTGGGTTTGTCCATAGTTGACCCAAATTGGGTTAATTTTTTTCAGTTTAACTTAAATTACACTTTTTAACCCAGTGGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17229
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000104877 | Nonsense | 444 | 449 | 9 | 9 |
The following transcripts of ENSDARG00000034933 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 25 (position 3424830)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 3243025 |
| GRCz11 | 25 | 3368769 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TYTTTGCTGAATTATTTACAGATTTGTTGTATTTATTGTTTCAGGATGAA[A/T]AGTTGAGCACTGGAGGTTGAGTTACCGSCCTGAACAKGAGANNAAAAATG
Long Flanking Sequence:
CAATGTTGGGTTAATTTTTTTTCAGTTTAACTTAAATTACACTTTTTAACCCAGTGGTTAAGTTTGTCCATAGTTGACCCAATATTGGGTTAATTTTTTCAGCTTAACTTAAATTACACTTTTTTACCCAGTGGTTGGGTTTATACATATTTGACACAATGTTGGGTTAATTTTTTATTATTTAACCTTAATTACACTTTTTTTTACCCAGTGGTTGGGTTTATACATAGTTGACCCAATGTTGGGTTAATTTTTTATTATTTAACCTTAATTACACTTTTTTTACCCAGTGGTTGGGTTTATACATATTTGACCCAATGTTGGGTTAATTTTTTTTATTTAACCTAAATTACACTTTTTATCCCAGTGGTTGGGTTTGTCCATATTTGACCCATCATTGGGTCACAACAACCTAACATTGTTTAGAGTGAATGTGCAACGTAATGGTGATTTTTGCTGAATTATTTACAGATTTGTTGTATTTATTGTTTCAGGATGAA[A/T]AGTTGAGCACTGGAGGTTGAGTTACCGGCCTGAACAGGAGAATAAAAATGGGTCATCACATTGAAAACACATCTAAATCAGTACCAAACCTTTGCTTTAACTGTTTAAAGCGCACCGTGCAGAAAATCATCTTGCAAACATCATAAGGGAATCATACCTCAGTGGAAAAAATGGATTTTTACATATTTATACATATCTTTAGGAACGAGAGCCGTGATTATTACCTCATGAATTATTACCTCAAAATATTTCAGACTCTTTCAACTGTGAAGTTTTCTTCTTTCTTTCTTGTTTGCATGACTAAAGATTCTAAGCAATGCACAATCTGAAAGCTGCAGTCTGATGTTGGTTTTGCATAGACGAACTTTAGTGCCTTTTGCTTTGAAATCTCTATTTCTTAGACAAGTTTATTTGACTTTTTAATAGCAGAGCTGGCTTTGGATTCAGATTTGTCAAAGGAAAAATGCTGTTTAAATTGCAGAATGCATATGTTTGTGCCA
Associated Phenotype:
Not determined