ZMP
gemin5
Ensembl ID:
ZFIN ID:
Human Orthologue:
GEMIN5
Human Description:
gem (nuclear organelle) associated protein 5 [Source:HGNC Symbol;Acc:20043]
Mouse Orthologue:
Gemin5
Mouse Description:
gem (nuclear organelle) associated protein 5 Gene [Source:MGI Symbol;Acc:MGI:2449311]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24000 | Essential Splice Site | Available for shipment | Available now |
sa45744 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24000
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109211 | None | 868 | 1446 | 22 | 32 |
ENSDART00000137309 | Essential Splice Site | 859 | 1440 | None | 28 |
Genomic Location (Zv9):
Chromosome 21 (position 35742947)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36736195 |
GRCz11 | 21 | 36421375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCTCCAGCAGGACTGCCTGACTCTTGCTGCTGTAAGACACTCACACGG[T/C]AAGAACAATCAGCTGGAAAACATAAACATAATATAATAGTTAGTAGTAAA
Long Flanking Sequence:
TTTAAATATTTTCCCAATTTTATTTAACTATTTACATGATAAATAAATGAAAATAGTAATAAATCAAATATGTAATGAAGTACTAAATAAAGGGACAATTAAGTAAATAGTCTACTAAATAAGCAAATCCATCAGATAAGTAAATAATCATTGAGTAAATGTTAAGTAATATGTACATTTAGTAAGTAAATTAATACTTAGACAAGTAAAAAAATTAGTAAGTAAATAGTAAGCAAGTATATAAATAGCAGTTTGTTATTACTAGTATCGCAGCTCTTTAGAGAACCTTCAAAATGTTTTCGATTTTTCAAAGCATGCTTGATGTCCTGCATATTGCTTTCACTCTTCTGATCTCCCCTCTACTGTTGATTTGTAGATTTGTCTTTAAAAAAGAGAAAGCCGCGCTCTATTCTTCCTCTCAGCACTTCGATGGATCACCGACCCAAAGACGAGCTCCAGCAGGACTGCCTGACTCTTGCTGCTGTAAGACACTCACACGG[T/C]AAGAACAATCAGCTGGAAAACATAAACATAATATAATAGTTAGTAGTAAATCATTAAATAAAGAGCAAGAAAATAAACAAAAATTAAATAAATAAATAATTGACTTTCAATTATGTATATAATACATCTTGGATCATTTATATTTAAAAAAAATAAATAAATAAATAGAGAGTAAGTAAATAATAAATAAATAGTAAGTAAATAAATAACCTGTTCATCCATTCATTTTCTTTTCGGCTTAGTGCCTTTATTAATCTGGGGTCGCCACAGCAGAATGAACCGCCAAATTATCCAGCTTATGTTTTACGCAGCGGATGCCCATACACGGACAATGTAGTTTACCCAATTCACCCATTTAGCATGTCTTTGGACTTGTGAGGAAAACCGGTGCACCTGGCAGAAACCCATGCAAACACAGGGAGAACATGCAAACTCCACACAGAAACGTCAACTGACCCAGTCAGGGCTCGAACCAAGAACCTTCTTGCTGTGAGGTTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45744
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000109211 | Nonsense | 1290 | 1446 | 30 | 32 |
ENSDART00000137309 | Nonsense | 1279 | 1440 | 26 | 28 |
Genomic Location (Zv9):
Chromosome 21 (position 35757034)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 36750282 |
GRCz11 | 21 | 36435462 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTTTCATCTGTTATCCACTCATGTATGAGAAATGGTGGACGTCAACGT[C/A]GACCAATAACAGCATCAGCAACGGTCATCGTTTAACTCTGACTGACGGAG
Long Flanking Sequence:
GCATTAACACTTCCAAAATGCTAGCAGGCAGTGGGGTGTTAATGTTCCTCTGTGTCGAGTTTCTTCACTGGTGTTTTTTCTGAACGCTTCCTAATGTACAAGTGGTTTAAACTCGCTCATTTTGAGGCAGGAACCGGCGGACTTTAACTGTAAGTTAAACACAAAACAAAACTTTCCATCCGGAGCTCCTACACAGGACTTGACGCTTGTAATCAGTCGCTCCAACGGATTCGCGCGGTTCATAAATCAGTCTAATCCACATCTTTGGGTGGAAACAGCTTATTATAATTTTGGTAGAGAAGAGTCGTATATCATGTCAAGTTTGTCAAACGTTTTACCATTAATCGATTAAAATCATTGTTTTCTACCAGGTTTGGAGTCGGTGGCGCTTTACAAACAGAAACTAGACCCGTCTGACGAGAGAAGCTTGGCGATTTCTCAAAGCATCGAGGCTTTCATCTGTTATCCACTCATGTATGAGAAATGGTGGACGTCAACGT[C/A]GACCAATAACAGCATCAGCAACGGTCATCGTTTAACTCTGACTGACGGAGATGAAGAGAAGTGTAACGGAGAAGCTCAATCTGATGGCTTCTGGAAGATTCTTCTGTCAGAAGCTCACGCTGATCTGCAGGCCAACCAGAGAGCCATAGCGGAGATTCAGAAAAGAGTCAGCAGCCTGATTCAGCAGCACAGCAGGTGTAAAGACCCAGAGACGGCTCTGGAGGGATCTGCTGGAGGAACGGGGTATTTCTGATGCTCTGCTTTATTCCTGTGCTTTTGATTCAAGTGCTTCAAAGACATGTCTAACAGCTGCTGTGTGTCTTTCTCCAGCAGCGAGTCTCTATCTGCGCTCACCGCACAAGTTGCTGAACACCATAAAGCTCTCGCCGCCGTCCCGGAACACATCAGGGTAAGCTGCTCTGTTTGCGTATCAAGTTGTGTTTCCAGATCCAAGCCCCGCTACATGTTTAAAGAAATATCAATAGCCGTTCACGACCACC
Associated Phenotype:
Not determined