Busch Lab

ZMP

colm

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 6 alleles of this gene:

Allele Name Consequence Status Availability
sa10951 Nonsense Available for shipment Available now
sa18587 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa10951
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
Transcripts:
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)
KASP Sequence:
AGCTCCGTGGTAGAGTTTATGACGCARGTGAWTGAAGATGAAGCAGAGTA[T/A]CAATAMTCAAGRAACAAGCGACGCCGGCAGCACCGAGGGACGCGGCCCTT
Long Flanking Sequence:
GTGGATTATGCTGGTCAGCCCACGGTCATGCTGAAGAATGGACTCTACTGCATATAAATCAGGTGACTGCACAAGCGGGGGGTTTCTTCTCCAGCAGCCCTCAGTTGCGCACAGACAGACTCTGATTGTCCTCTTTCATCTTTATTTTGGGGAAATACTCTAGACGCTTCTTTTTTCAGCCTTTATTTTTGAAAAGTATTGTTATTCTGGTGGTTTTCAGGACACACTTTTGAATTTCTGAGAATGCTGGATCCACTGGCTGAGTTGAGAAGAACCGGAGGCTTCAGGCAGTGCGGTGGCCGGATGTCCTGGCAGTTCCGCTGGATGCTGTATAGCGTTTGTATATTGACGGTGATCAACTGTGCCGGCCTGGTTCTACTCCTGGTACAGCAGAGGGATTTGTGGGCGCAGCTGATTGAGGTGGAGAGGCAGATGGTGGAGATCTCTCAGAGCTCCGTGGTAGAGTTTATGACGCAGGTGAATGAAGATGAAGCAGAGTA[T/A]CAATACTCAAGGAACAAGCGACGCCGGCAGCACCGAGGGACGCGGCCCTTTGAGGAGCACGAGGGAAGCGTTGGAGAGGAAGTCCTGAGTGATTTCCAGTACTCGTTTCAGCAGCCGCCTGGACCAGTTTACCAGCACAAAACCGAGGAAAAAGATGGAATGATGATGATGATGACATACTCCATGGTGCCAGTAAGAAACTCACTCTATGATATCAATGATCTATTGATGCGTGTTCTTTTCCTAAAGGAAATTGTAAATAAAATGTTGACAACAGTAACTCCTGTCCAGTAACTTTAGTTATAAACAGTATAGTAAGTTTATAGATTAATGTGCCATTTTTCCCTCCAATTTTTATAGTTCACAACTGTTTTATGCCTGAATTTCTTTAACAAAAATATTATTATTGGTTATTAGTTAAAAAATGTGCCATGTTATTGTAATTATACAAATGTAAAAAAAATTATTGTAATTTTATTTTTCCTCCCTGATTAAAACAG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa18587
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
Transcripts:
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)
KASP Sequence:
CCTTTGAGGAGCAYGAGGGRAGCGTWGGAGAGGAAGTCCTRAGTGATTTC[C/T]AGTACKCGTTTCAGCAGCCGCCTGGACCRGTTTACCAGCACAAAACSRAG
Long Flanking Sequence:
CCCTCAGTTGCGCACAGACAGACTCTGATTGTCCTCTTTCATCTTTATTTTGGGGAAATACTCTAGACGCTTCTTTTTTCAGCCTTTATTTTTGAAAAGTATTGTTATTCTGGTGGTTTTCAGGACACACTTTTGAATTTCTGAGAATGCTGGATCCACTGGCTGAGTTGAGAAGAACCGGAGGCTTCAGGCAGTGCGGTGGCCGGATGTCCTGGCAGTTCCGCTGGATGCTGTATAGCGTTTGTATATTGACGGTGATCAACTGTGCCGGCCTGGTTCTACTCCTGGTACAGCAGAGGGATTTGTGGGCGCAGCTGATTGAGGTGGAGAGGCAGATGGTGGAGATCTCTCAGAGCTCCGTGGTAGAGTTTATGACGCAGGTGAATGAAGATGAAGCAGAGTATCAATACTCAAGGAACAAGCGACGCCGGCAGCACCGAGGGACGCGGCCCTTTGAGGAGCACGAGGGAAGCGTTGGAGAGGAAGTCCTGAGTGATTTC[C/T]AGTACTCGTTTCAGCAGCCGCCTGGACCAGTTTACCAGCACAAAACCGAGGAAAAAGATGGAATGATGATGATGATGACATACTCCATGGTGCCAGTAAGAAACTCACTCTATGATATCAATGATCTATTGATGCGTGTTCTTTTCCTAAAGGAAATTGTAAATAAAATGTTGACAACAGTAACTCCTGTCCAGTAACTTTAGTTATAAACAGTATAGTAAGTTTATAGATTAATGTGCCATTTTTCCCTCCAATTTTTATAGTTCACAACTGTTTTATGCCTGAATTTCTTTAACAAAAATATTATTATTGGTTATTAGTTAAAAAATGTGCCATGTTATTGTAATTATACAAATGTAAAAAAAATTATTGTAATTTTATTTTTCCTCCCTGATTAAAACAGTATTTTTATATTTGTATATTTAATTGTTTTAATATATATATTTTAATAAAAATGTTTTATAATAATTTGAATAAATTGTAGATGACACCCTCTAAAG
Associated Phenotype:
Not determined