Busch Lab

ZMP

gemin5

Ensembl ID:
ENSDARG00000079257
ZFIN ID:
ZDB-GENE-031112-9
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.
Availability:
Order Allele From ZIRC
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.
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