ZMP
st6galnac4
Ensembl ID:
ZFIN ID:
Description:
alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1, 3-N-acetyl-galactosaminide alpha-2,6-sialyltransfer
Human Orthologue:
ST6GALNAC4
Human Description:
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran
Mouse Orthologue:
St6galnac4
Mouse Description:
ST6 (alpha-N-acetyl-neuraminyl-2,3-beta-galactosyl-1,3)-N-acetylgalactosaminide alpha-2,6-sialyltran
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43567 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa43567
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064461 | Nonsense | 273 | 291 | 6 | 6 |
Genomic Location (Zv9):
Chromosome 21 (position 4092587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 3689853 |
GRCz11 | 21 | 3841274 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGGCCATCGCTTCATCACAGAGAAACTGATTTACAGCCGCTGGGCGTCT[C/T]AGGGGAAACTGCGCTTCGTTTATCCTCCGTGGACATCGCAGGAACACCAG
Long Flanking Sequence:
GCCGTGGCCGTCGGCGTCGCTGACACGTACCTCTAAAAAAATTTAACTACACGTCGCAACAACGCGTAGCACAAGCTCTGTGATTGGTTGGCTTGGTATTGCTGAAAAGTGTGGGCGGGACTAAGTGTCGCGCGAGCCCGATGGAGCGATTGTTTACAAGTGTGTTAGAACTAACAATAAATAAAATATTATAATTACTTATGTATGTTTTGTCCCAAAATTCCAATCCAGCATTGACTTAAAATTGAGTCAACAGGATATCTGATCATTCATGCTTTTTTTGCTGGTCTCTTGTGTATAATGGTATTTGTCATGATGCAGTCAGCTAACATCTCTGCTTTGGCTTGTTTTGCAGTAATGCTAACCACTCATTTGTGCCATACCACTACTATGAGCCGCTGCATCTGGATGAGTGCCGCATGTACCGCGTTCACGAACACGCCAAGAGAGGCGGCCATCGCTTCATCACAGAGAAACTGATTTACAGCCGCTGGGCGTCT[C/T]AGGGGAAACTGCGCTTCGTTTATCCTCCGTGGACATCGCAGGAACACCAGCCGCCCTAATTCAACCACTTCTGCTATGTGGTCAAACGTAGGTCAGGCTTTAGTGTATGTTTACGCTAATATCACAAACCACTATGGTGCTTTTAGTGTGTAAATCCAGCCATTAGTTTGGCTTTCGAATCTTGCTGCTTTGCCTTTTTTTAATATTCGGTCCGATTTTATTGCTTTAGTATTAATGGGGTCATGAACTAACAATAGAACTCTCTAAGGTGCGTTTATGATTTTTAAAAGTTTTTTACATGAAAAAAAATCATCATTAATAAGTATCTGGCTATTTTCTGTGCTGTTTTTAATTAGAATGCTCTGTTTGGATGGGCGTGGCCAACTGTAGACTCAGAAGTAAACGCACACTGCTCTGATTGGCTGACAAACTTGCATATTAACAGAGCTTAACAAGCAGTGAAGTAGAAGTAGGTGTCAATCTTATGTGGAGGCGGAGCT
Associated Phenotype:
Not determined