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Ensembl ID:
ENSDARG00000061576
ZFIN ID:
ZDB-GENE-050119-4
Description:
gliomedin [Source:RefSeq peptide;Acc:NP_001073634]
Human Orthologue:
GLDN
Human Description:
gliomedin [Source:HGNC Symbol;Acc:29514]
Mouse Orthologue:
Gldn
Mouse Description:
gliomedin Gene [Source:MGI Symbol;Acc:MGI:2388361]

Alleles

There are 4 alleles of this gene:

Allele name Consequence Status Availability Estimate
sa39210 Nonsense Mutation detected in F1 DNA During 2018
sa10951 Nonsense Available for shipment Available now
sa18587 Nonsense Available for shipment Available now
sa9035 Essential Splice Site Mutation detected in F1 DNA During 2018

Mutation Details

Allele Name:
sa39210
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087960 Nonsense 24 542 1 9
Genomic Location (Zv9):
Chromosome 18 (position 38087183)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 39668886
GRCz11 18 39649894
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
None
Flanking Sequence:
AGTTGAGAAGAACCGGAGGCTTCAGGCAGTGCGGTGGCCGGATGTCCTGG[C/T]AGTTCCGCTGGATGCTGTATAGCGTTTGTATATTGACGGTGATCAACTGT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa10951
Current 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
Order Allele From EZRC
Mutation:
T > A
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087960 Nonsense 86 542 1 9
ENSDART00000087960 Nonsense 86 542 1 9
Genomic Location (Zv9):
Chromosome 18 (position 38087371)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 39669074
GRCz11 18 39650082
KASP Assay ID:
2261-2481.1 (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
AGCTCCGTGGTAGAGTTTATGACGCARGTGAWTGAAGATGAAGCAGAGTA[T/A]CAATAMTCAAGRAACAAGCGACGCCGGCAGCACCGAGGGACGCGGCCCTT
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18587
Current 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
Order Allele From EZRC
Mutation:
C > T
Consequence:
Nonsense
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087960 Nonsense 119 542 1 9
Genomic Location (Zv9):
Chromosome 18 (position 38087468)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 39669171
GRCz11 18 39650179
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
CCTTTGAGGAGCAYGAGGGRAGCGTWGGAGAGGAAGTCCTRAGTGATTTC[C/T]AGTACKCGTTTCAGCAGCCGCCTGGACCRGTTTACCAGCACAAAACSRAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa9035
Current Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
We currently estimate that this allele will be available during 2018.
Mutation:
A > T
Consequence:
Essential Splice Site
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000087960 Essential Splice Site 168 542 3 9
Genomic Location (Zv9):
Chromosome 18 (position 38089555)
Other Location(s):
Assembly Chromosome Position
GRCz10 18 39671258
GRCz11 18 39652266
KASP Assay ID:
None (used for ordering genotyping assays from LGC Genomics)
KASP Sequence:
ATAYACTTATAAAATCAAGTTTACTGTTTGGTTTATTTTTTGGCTTCCAC[A/T]GGACCACCAGGACCACCAGGAATTGCAGGTAGGAAATCAATTATYCAAAT
Associated Phenotype:
Not determined

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