ZMP
si:dkey-162b3.1
Ensembl ID:
ZFIN ID:
Description:
polypeptide N-acetylgalactosaminyltransferase 2 [Source:RefSeq peptide;Acc:NP_001121823]
Human Orthologue:
GALNT2
Human Description:
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2 (GalNAc-T2) [Sour
Mouse Orthologue:
Galnt2
Mouse Description:
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 2 Gene [Source:MGI
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17374 | Nonsense | Available for shipment | Available now |
sa14540 | Essential Splice Site | Available for shipment | Available now |
sa12860 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17374
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021360 | Nonsense | 35 | 565 | 2 | 16 |
ENSDART00000136217 | Nonsense | 35 | 559 | 2 | 16 |
Genomic Location (Zv9):
Chromosome 13 (position 24363923)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 24009583 |
GRCz11 | 13 | 24140033 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAAATGCCTTTTMTGCTCACAATCTGTTCTCCTCTTTGGCAGGATGACTG[G/A]AGTGGCATTAATTCAAACCGAATTCAAACACACAGYAATGCAGATGACAA
Long Flanking Sequence:
ACACTTCTGTTCAATCCTGAGAAAATCTATTTAGTTCTTTTGAATTATAGCTGTCAGTTGATCTGCTACAATTTCTTCCTACTAAAATAAAATGCTTATGATATGATCAAACTCACTGAGAGGAAAAAGATACACAGCAATGCACAAACTCCTGATCTGTGGTTACTACAGCAACTAGACTTTTATAAATAACATTAGACTTAATTCAATGGAGAATAAATTACGTTTGAAGTAATTGTGCATTTTTAGGTTTGGACTTCATTGTTTTTGGCTAAAAGCTGTTATTCTTTCTGCCTTGAAATCTGCATGAAGAAAAATGTCAGATTAAGAGTACTGTTAGTGTGAATATGTGGTGTCAAAGGCAGTGCTTGCAGCCCTCAACGGCCGTAACCACTTTCTCAATACCAGTTACTGTTTAATTTGTTTTTCGATTACCATTCTAACCCTTACCAAATGCCTTTTATGCTCACAATCTGTTCTCCTCTTTGGCAGGATGACTG[G/A]AGTGGCATTAATTCAAACCGAATTCAAACACACAGCAATGCAGATGACAAAGACCACAGCCTTGAAAGTCTTCCTCTAGGTAAGAGCCAACCTGACATCTCATGTGCATAATCGTGTCAGGATTATCCCGCACTCATAATTCAACTTTTCCCTGCTTCTATCCCAAATGAATAATGGAGTGTTTCTTCTCAGGTATGGGCTTTAATGAACAGCCCGCACGAAACAAGGCATATTTTTTTATTCCCTTCATAAACAGGACTTAACCTGAGGTTATCTGTGGAAGCAGGTGTAGAAAGTCTTACTTGAGGGCTCCTGAAATGCATGAGAGTAATTTAAGAGTGGCTGTGTTACGGGCCCTAAGACAAGAGCTCTGTTTCTTCGCTCTTTATTCCCCTTTTTGTAAATGTATTCCAACTAAACTTGGCTGCTTAATACATTATGATAATAACATATGCTTTTTATAGACTTGCTGCATTTTAAAGTAGTATTATAGTAGGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14540
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 |
---|---|---|---|---|---|
ENSDART00000021360 | Essential Splice Site | 290 | 565 | 9 | 16 |
ENSDART00000136217 | Essential Splice Site | 290 | 559 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 13 (position 24310815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23956475 |
GRCz11 | 13 | 24086925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTGGAACAAAGACRAGCTCGACAAGGAAACCCCATYGCTCCTATCAAG[T/A]AAGAAAGCAATCGTGAAWCTGCTGATGTGTAATTGTCAGCYGCTTTGSGA
Long Flanking Sequence:
CTCAATTGGTTCCAAACCTTGCTGAACCTAAAAAAAGCGATATATTTTGTAGAAAGCTGGAAACAAGTAATCTTTGACTTCCAAAACATTTTAGTCTTCTGAATATTTAAATTGTTGTTCAACAGAAGACAGAAACCCATGTAGGTTTGTGACAAGTAAATTTTACATTTAAGTAAATGATGACAGAATTTTCAGGTTTTGATGAACTATCCCTTTAAAGTATATGCTATTGTGTGATTCTGAACAAATGTTCATTCTTTTTTCATTAATGAATTTGTAATATAACTAATCTGCCTCTTTATCCTCCCACCTGACACATGGCTGAACATGGCAATGAGCCTACTTTTACTGTAACATCACTTGAGCTTTCAGAACTTGATCCCTAAAGTAATGTGTCTAATCTTTATCCAGGTTTTGATTGGAATCTGGTTTTTAAATGGGACTACATGACCCTGGAACAAAGACGAGCTCGACAAGGAAACCCCATCGCTCCTATCAAG[T/A]AAGAAAGCAATCGTGAATCTGCTGATGTGTAATTGTCAGCTGCTTTGCGATTTTATTACTATTATTCTAGGGATTTTTTTTTCTCATTCTATATTGGCTGTTTAATGTATTGACTCTTTTGAAGTCTAACTCCAGCTGTTGGTGCTCAGTATAGTTTTGATTTACAAAGACTTTGTACTTTTGAAGACTGAGTAAAATACTTTTACCTACTGCTGCTGATGATGTCATTGCTATGTATGCATTGCATACTGAACTGTGATTGGTTTTCAGACCTAAGTGGTCATGTCTATAACACTTATATTTTATATATTTCTTTTACATATTTAGGCAACTCCATTTTTAGTGCTGGTAATAATCTGAAAATGCGAATCTAGATGCATCAAATTTTCATGTAAAAATGCTATCAGATTTTGAACAAAAGGGAAAAAAGCTCAAATAAATAAATAAATAAATAAAATGTTTTAAATATTAAAATATTTCAATATAAAAAAATTGTTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12860
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021360 | Nonsense | 440 | 565 | 14 | 16 |
ENSDART00000136217 | Nonsense | 440 | 559 | 14 | 16 |
Genomic Location (Zv9):
Chromosome 13 (position 24298155)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 23943815 |
GRCz11 | 13 | 24074265 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTWGTTTAGAGTGCCGGAWCATCAGGACATTGCATTTGGAGCTCTTCAG[C/T]AGGGTCAAAACTGTCTGGACACACTGGGCCATTTTGCAGATGGTGTGGTG
Long Flanking Sequence:
GAAAAGTACTCAAAAGCCTACTTTTTTCCTTTCTTTATATTTTTTTATTTTTTTATAAAGCTGTCAGGTGAAAAAGTAAAGCTGCTGCTCTTTATTTGCTTTTCTGTACTCTTCTTTCACATTCATTTAAACCCTGAATTAAACACCAGGCATGAGCAAGAATGTTTTGCTCATCTACTTATGATTATTATCCAATTGCATCTTAAAGCCAGCTGTAAACATGAGCTTTGATAGCCTTAAAAGAATTGAAAATTGCAAGTTTTTTTATAAACTATCCCTTAAACTGTGTAAGCTGGGCCTCTTTTTAATTGATGTTTAACTATGCAAATTAAGGAAAATTAATAGAATGAAATTCAATGTTTTTTAGTCTTAAAGCTTTCTTTTCACTACTGGAAACTACAGTCTCAAATACTTCAGCAGTGTAATCATACCTATCCTCGTGCTTGTGTCTGTTGTTTAGAGTGCCGGATCATCAGGACATTGCATTTGGAGCTCTTCAG[C/T]AGGGTCAAAACTGTCTGGACACACTGGGCCATTTTGCAGATGGTGTGGTGGGGGTTTACGAGTGCCACAACGCTGGGGGCAATCAGGTATCAAACAAAACGCAGGTACTCAACAGTCTTCTAATGTCTGGTGCAGAGCACTGGGTGATGGACTGGCAGTGAGTCTGTGTTAGCTGTAAATCATAGACACGCTTGTGGAGGGTGAGTGAGTGGTGTATAGATGAGACACGCTAGTTTCTGGATCACTTTACATGGTTCTTGCTGTAGACATGTGTGCATGTCTAAAGGATTTAAAAGGGTCTGTGTTTTTCTGTTTCAATATGATGTGATATGAAGTAAATAATATAATACATTTACATTTAGTTTAAATATATATTTCTATACATTGTATTGCATTAAATGACTTTATAATAATATATTGATGACAATATAAATAAGTAATAACGTATACATTTTATAACTAGTTGTTTTACTAGTATTGATGTGAAAAGTGCAGTATAC
Associated Phenotype:
Not determined