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