ZMP
zgc:194551
Ensembl ID:
ZFIN ID:
Description:
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase 2-like [Source:RefSeq peptide;Acc:NP_001122268]
Human Orthologues:
B3GALNT1, B3GALT5
Human Descriptions:
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5 [Source:HGNC Symbol;Acc:920]
beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) [Source:HGNC Symbol;Acc:918]
beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) [Source:HGNC Symbol;Acc:918]
Mouse Orthologues:
B3galnt1, B3galt5
Mouse Descriptions:
UDP-Gal:betaGlcNAc beta 1,3-galactosyltransferase, polypeptide 5 Gene [Source:MGI Symbol;Acc:MGI:213
UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1 Gene [Source:MGI Symbol;Acc:
UDP-GalNAc:betaGlcNAc beta 1,3-galactosaminyltransferase, polypeptide 1 Gene [Source:MGI Symbol;Acc:
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18188 | Essential Splice Site | Available for shipment | Available now |
sa15397 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18188
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110293 | Essential Splice Site | 23 | 362 | 1 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 27161309)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26664254 |
GRCz11 | 22 | 26495301 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGAGCTACCGGACAAACTGGTAACAGCGGGAAAGCCRTTCTTACGGAGG[T/A]AAGTGGACAGCTGGTRAGCGCAAAAAGGAACRGCATCATACTGCCTCGTA
Long Flanking Sequence:
GCTTTAGGCTTATTCTGAAAACATATCTCTATATACATTTCTGGAGAGTGTCAAATACTTCCCAGGAGGTATGTTTTTTTTTTTTCACAGTTTTTGTTGTCATGTAAATCCACCAGAAGCTACTGTCGACTGACTGATTGCCTGACCCACCCTCCTCCTTCCCTAAACTCAACCCGTAGTGTTTTCTAAAGCATCGATTGACCTGTGCCCACCTCCTTCACTAACCCAACCGACAGTGTTTTCAAAAGCAATCCAGAAAAAGAAAAGCCCCTTGATTTTTACCACGTTTTCAGATTTTACCCCATCCTCACCCTGTTATTGACTTGTTTATTTTATTTTTTGCCTTTCTGTTTTATGTCTTACCTGTTTCCTTGATCTGTTTTTCACCAGACTTGAATCCTGTCATCGGGGTCAACTTCTCTGTGCATCTCATGTCCGCCAAAGTACATGGCGAGCTACCGGACAAACTGGTAACAGCGGGAAAGCCATTCTTACGGAGG[T/A]AAGTGGACAGCTGGTGAGCGCAAAAAGGAACAGCATCATACTGCCTCGTAGCATTTGTTTTAAAGATGAAATGCAGCCATACGTACTTCTGGCTGTATAATTCGCGATCTCCAGATATTTATATAGGGCTACATTTTCCAAATGAGCAATAGTCTTTTGGTAGTTTCAGCTTGGCGCAAGAGTTATTTTGAGGCGTTGCGCTATGCTGTTTAAATAGCAAATGCATTAGCGCTCATTTGTGCGCCCATAGGCGTTCTGGTCTAAACAGGAAGGCGTTCTGAGGCGGACCGCTGGCGCGTCGCTATTTCGAGAAACTAATAATAGATTTTTCATTAGACCAAAACTAACCCGGTCTAAACTCCGGCGCAGAATTGCGCCTCGCTTATGCACTGCTTAATACGCACAAGAGAGCAATAGGCAAATATCTTTACATATGAAAAAAAATAAATATTAAGGATATATATAGGATATAATAAGAATAGATATAGGATATAAATATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15397
Status:
Available for shipment
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:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110293 | Nonsense | 85 | 362 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 22 (position 27170866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 26654697 |
GRCz11 | 22 | 26484072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCACAAAGACCAAACGCAGACTCTCCAAACACTGAAGAAGATCCWGGGT[T/A]GTACCATGTTGCCTACCCTCGAAATTACAAATTCATCATARACCAACCGG
Long Flanking Sequence:
TCTACTTGCATTCATTTTTAGGACTGTTTAAACGCACGGTTTTACAAATAAGGCTTCTGCATGGTCCTCCAAATGTCATCAGTTTTTTTTTTTAATCCCTCTAGGCTTGGTTTAATATTAATATTCATTAACTCATTCCTTAAACCAACCTCACTCCAACCCAAGGCCTTTTTTAATCATTAAAGATTTTTAAGATTTTTAAAGACCAGTAGTGCATTCATGTGTTTTAACTGTGCGTTAAAAAGAGTTCCCTCAGATGTCTTTATCATTGAATCTTACTAGTCATTGAACTAGGCTCTTTTCGTTCCCTTCCAGCTGTGTCTCGTTTGGTCAGATGTCCTGTAAGAAGTGGCTGCTGGTTTGTTTCCTGGTTCCAGGAATTGCTTTAATGATTTACCTCGGCCACAGCCCTTTGACGAAACCCTGGCATCACGCATCAGTGCAGAGAGAAGCACAAAGACCAAACGCAGACTCTCCAAACACTGAAGAAGATCCTGGGT[T/A]GTACCATGTTGCCTACCCTCGAAATTACAAATTCATCATAAACCAACCGGGGATATGTGAAGAGCGAAAACCCTACGTGGTGATAATTGTCCCTGTGCCACCTCATGATTTTAATGCACGCAATGGAATCAGGAACACATGGGCCGGAGAAAAGGTTGTTGAGGGCAAAGAGGTGCTTGTTCTGTTTATTTTGGGCTTACATAGTGGAGATGATGAAGAAACGTTGCAGGAGCAACTGCGTAACGAGAGCCAGCAATACAAAGACCTTCTGCAGAGCAACTTCCAGGACAGCTACAGGAACCTGACCATTAAAACCATGATGATGATGGAGTGGCTCAGCAGGGATTGTCAACAGGCGTCTTACGCAGTAAAAGTGGACGCTGATGTGCTCCTCAATGTGAACAACCTAATCAATATGCTTGTGAGTCTAAACACAGTGCAGAGCAACTACATGACTGGGTTAGTGTGGGATGCTAGTCCTGTCATTCGAGATTCCTCCA
Associated Phenotype:
Not determined