ZMP
hccsa
Ensembl ID:
ZFIN ID:
Description:
holocytochrome c synthetase a [Source:RefSeq peptide;Acc:NP_001002498]
Human Orthologue:
HCCS
Human Description:
holocytochrome c synthase [Source:HGNC Symbol;Acc:4837]
Mouse Orthologue:
Hccs
Mouse Description:
holocytochrome c synthetase Gene [Source:MGI Symbol;Acc:MGI:106911]
Alleles
There is 1 allele of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19700 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa19700
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:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000034865 | Essential Splice Site | 184 | 276 | 5 | 7 |
ENSDART00000145974 | Essential Splice Site | 184 | 276 | 5 | 7 |
The following transcripts of ENSDARG00000028131 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 2 (position 14830936)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 15341763 |
GRCz11 | 2 | 15010353 |
KASP Assay ID:
2259-1737.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGAACAAGCCTGGCAAGAAATCCTGAGATGGGAGAAACTCCATTCAAA[G/A]TAAGTGAGGTGTTTAAATGGGGTGTTTGATTTGTTTCGTTTTTACTTTTT
Long Flanking Sequence:
ATGTTAGTCAAGAATATAACTAAAATTAATTAAAAACTGAATAAATATAAATTTACACACATGTACATAAGTAAATAAACAGAATCAATGATGGGCTATAAATCTGCGAAAATCTGCTCGACCATTTAAAATCTGCATTTATGAATGAAAAAATTTGCCATCATAACAATATTTTTAACTGAAAATTCCAGATCAGAATTCTGACTAAAAGATAAATAATTAATAGTCTTAAAATAAAAATCAGGTATTTCATATTCTAATCGTAACCAAACAGAAATGTCATCCCTTAACTTTTTTCAAAAATTTGCATGAATAAAATGATGTTGTAAATTAGAGTAACATTTACCAAGTTCATTGCTCATGACTGAAACTTTCACCAGATGGCGCTGGAACAAAGATGACATAAACCAGAACGATATGGGGGACATCATCAAGATTCACAATCAGAATAATGAACAAGCCTGGCAAGAAATCCTGAGATGGGAGAAACTCCATTCAAA[G/A]TAAGTGAGGTGTTTAAATGGGGTGTTTGATTTGTTTCGTTTTTACTTTTTTTAGTTGACTTCTTTACTAGGAGTTAAGGCCAAGTAGATTGTAAAAATGATCATGTAACATGAAAATGATCTATGATATAATATTATGGTTGTACTGTCATTCAGTATCCAAATAACAATTTGTTTTTATGAAACAGTTTAAAAAATTGTGGTTAATTACTGCACATTTAACTTCTCCCAGAAGTCAATAACATTCAACTAATAAAGTATATTTCTTTCTATTAAAGAGCCCTTATTATGCATTAAAAAGGGTCATATTTTGGTTTTAAGGATCTCCAACAACATACTGATATGCATGCAATGTCAAAAAAACACTTTCATTGTCTTATAATATGCATTTACTTTTACCTAATTATCCCAGCGGCCTCCATATGAATCGTTCAGCAATTCATTTGTTCCCAAACCCCTCCTTAGCACGAAGTTAATCTGCACTCATTGGACCGATGACAG
Associated Phenotype:
Not determined