Busch Lab

ZMP

LOC797302

Ensembl ID:
ENSDARG00000044755
Human Orthologue:
GCNT4
Human Description:
glucosaminyl (N-acetyl) transferase 4, core 2 [Source:HGNC Symbol;Acc:17973]
Mouse Orthologue:
AC174082.1
Mouse Description:
glucosaminyl transferase 4, core 2 [Source:RefSeq peptide;Acc:NP_001159537]

Alleles

There are 3 alleles of this gene:

Allele Name Consequence Status Availability
sa14310 Nonsense Available for shipment Available now
sa32341 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa14310
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065781 Nonsense 255 426 5 5
ENSDART00000114285 Nonsense 247 413 1 2
Genomic Location (Zv9):
Chromosome 21 (position 14043712)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 15744667
GRCz11 21 15840644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGCAGAAACATGGTGGAAAGCAAGTGGCCTGGAGGAAAGAAAATCCGCW[G/A]GAGTRTTCATCATCTGCTGAAAAATAATGATTCAGAGTACTACGATTTTC
Long Flanking Sequence:
ATTAACTGATGCAGCGATCGCAAATGCCACCATTGACTGCGAATGGTTTGTATCATCACAGGGCTACAATGACATTCAGGTCACTGAGTCCGAGCGTGAATTTCCTCTTGCTTACTCTTTAGTTGTTCATCAAGATGCCGCTCTTGTGGAAAGACTCCTGAGGGCCGTTTATGTGCCGCATAACATCTACTGCATACATTATGATCGAAAGTCTTCCACTGACTTTATGTTAGCAATGAACGGTCTGGCCCGCTGCATCCCAAACGTCTTCATTGCCTCAAAACTGGAGAGAGTTCAGTATGCAGGAATCTCACGACTCAGAGCGGATCTGAATTGTCTGTCAGACCTCCTCGATTCTGAGGTCAAGTGGAAGTACGTCATCAACCTGTGCGGTCAAGATTTCCCACTGCGGACAAACGCTGAGCTGGTGTCAGATCTGAAGGGTCTTAAAGGCAGAAACATGGTGGAAAGCAAGTGGCCTGGAGGAAAGAAAATCCGCT[G/A]GAGTGTTCATCATCTGCTGAAAAATAATGATTCAGAGTACTACGATTTTCCAGTCAGTACTCCAGAGGAGAAACCTCCACCACCTCACAACATAGAGATGTTTGTAGGCAGCGCTTACTTCACTCTCTCAAGGGAATTTGTGTATTTTGTTCACTGGAGTTCCCTTGCCAAAGATTTCCTGGCTTGGTCTGAGGATACATTCTCACCTGATGAACATTTCTGGGCAACTTTGGTTCGTGTGCCTGGAGTGCCTGGTGAGGTGCCGAGATCAGATCCGGAAATCTCCGAACTGATCAGTAAAACTCATCTGGTGAAGTGGTCATATTTAGAAAATGATCTTTACCCAGAATGCACTGGAGTCAGTGTGCGTTCTGTCTGTATTTATGGTGCTGCTGAGCTCAGATGGCTCTTAAACTACGGTCACTGGTTTGCTAATAAGGTGGATCCAACTGTGGACCCTGTTCTTATTGAATGTTTAGAAGAAAAACTTGAAGAAAAAC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32341
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000065781 Nonsense 401 426 5 5
ENSDART00000114285 Nonsense 387 413 2 2
Genomic Location (Zv9):
Chromosome 21 (position 14044149)
Other Location(s):
Assembly Chromosome Position
GRCz10 21 15745104
GRCz11 21 15841081
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGCTGCTGAGCTCAGATGGCTCTTAAACTACGGTCACTGGTTTGCTAAT[A/T]AGGTGGATCCAACTGTGGACCCTGTTCTTATTGAATGTTTAGAAGAAAAA
Long Flanking Sequence:
TGAAGGGTCTTAAAGGCAGAAACATGGTGGAAAGCAAGTGGCCTGGAGGAAAGAAAATCCGCTGGAGTGTTCATCATCTGCTGAAAAATAATGATTCAGAGTACTACGATTTTCCAGTCAGTACTCCAGAGGAGAAACCTCCACCACCTCACAACATAGAGATGTTTGTAGGCAGCGCTTACTTCACTCTCTCAAGGGAATTTGTGTATTTTGTTCACTGGAGTTCCCTTGCCAAAGATTTCCTGGCTTGGTCTGAGGATACATTCTCACCTGATGAACATTTCTGGGCAACTTTGGTTCGTGTGCCTGGAGTGCCTGGTGAGGTGCCGAGATCAGATCCGGAAATCTCCGAACTGATCAGTAAAACTCATCTGGTGAAGTGGTCATATTTAGAAAATGATCTTTACCCAGAATGCACTGGAGTCAGTGTGCGTTCTGTCTGTATTTATGGTGCTGCTGAGCTCAGATGGCTCTTAAACTACGGTCACTGGTTTGCTAAT[A/T]AGGTGGATCCAACTGTGGACCCTGTTCTTATTGAATGTTTAGAAGAAAAACTTGAAGAAAAACGGCGGAGACTCGCAGTGAATTGACCTCGTTTTCATCATTGAGGAATTGTTTTGGAATTTAAAACAAAGTTGAGCCATTTATTGCGGAAAGTAGTTTAAAAATGCACTTTATGTTGTTATACAGTAAAAGTGTTCCTGAAGATGTGATTTAGCCAACATGATGTGCAATTCTCTTGTTATGATTTGATGAGACAAAATGTGAATTTTATTATGTGGGTTTGCATTTACACACTGTTTTCAACAACAACAACAAAAAGAAAAACTATATATTTATTTTCATTTACTTTAGGGACATGAGAATGCACACTTTTTTAAAAAGCAGAAGGTTAAAAACATGATGCATAAACATCCATGCACACAAAAGCAAGTTTATAAATGAGTGTGTTCAGTCTTCAAGCATGTGTGTGTGAGAACTTGACAAAACAACAATGCTGGACT
Associated Phenotype:
Not determined