ZMP
LOC559305
Ensembl ID:
Human Orthologue:
B4GALNT4
Human Description:
beta-1,4-N-acetyl-galactosaminyl transferase 4 [Source:HGNC Symbol;Acc:26315]
Mouse Orthologue:
B4galnt4
Mouse Description:
beta-1,4-N-acetyl-galactosaminyl transferase 4 Gene [Source:MGI Symbol;Acc:MGI:2652891]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11710 | Essential Splice Site | Available for shipment | Available now |
sa14580 | Essential Splice Site | Available for shipment | Available now |
sa41000 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21055 | Nonsense | Available for shipment | Available now |
sa38637 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21056 | Nonsense | Available for shipment | Available now |
sa34171 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11710
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067857 | Essential Splice Site | 182 | 1167 | 5 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50637025)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48907261 |
GRCz11 | 7 | 49180037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGAATTATGGCCTTAGAGTATTTGGATTCATTCATCCTTACAAAGATGG[T/C]CAGTGTATTTCRTCAAGTTTATANTTTTTTTACAAKATTTCATCAAGTATT
Long Flanking Sequence:
CCGTCTCCCAGCTCAGGAAGAATCTTCATTTCCCTCTCTACCCACATGTAAGAGCACAATAAATGTGTCAGACAATAAAAGAACAGACAATTAAGATGAACTTGATTGTGTGACTTGTGAAATGTAGTCTGGCAAATGAAGTCAGTATGTCATTTGCAGTATTTTCATTAACAAAGCCCTAATGTTGTCCGTATATTTGCTCCAGACAGGATGTTCTGCAGACAGAGATTAACATCTGTTTTTTTATAACCTCTGCATTATTGCTAAAGCAATGTTTTGAAACTAGAGCTGTCTTTTTATTCGTCTTAGAAGTCATTTTGAGGTGTGATTCTGTGAATTGCTGTTAGTGCCTTGGGTTTTAGAGTGAATAGACCTGCAGATGCTTTTATATTTAATTCTTCCCCACAGACCAGAACCACAGTGAAGAAAATTGCAGTGGCACCAAAGTGGAAGAATTATGGCCTTAGAGTATTTGGATTCATTCATCCTTACAAAGATGG[T/C]CAGTGTATTTCGTCAAGTTTATATTTTTTTACAAGATTTCATCAAGTATTTTATCAAAAGAATTTAATAAGTGGTTATCATGGCTTAAAAGCTAATTTACTTACTGTATACAGTAGAGTGCCTAACATTAAAGAGTGCATGCTGAAAGATTTGACATAAAATCATCATTCTTCCTCAATGAGTTGTTTGTTCAGATCTGGTTCATTGATTTTAAATTTTATTAGTTGCTGTTTTTTCTTTTGTTACTATTATGAAAAATTCATCTAAGATCATTGTGTGAAAATGAGTACACCCCAACATAAGAAAACATAAAGAAACATAAAAAAAATAAAATAAAGTGGTAATCATGAGGAAAATCTGACAAAATAGCTTTGTATGGAAAATAAATGTCACATAATTAAAAAAAAATATATAAAATAATAATAATATTTTATTTGCCCAAACAGGAATTCAATGATTATAGATTTTGGTTGTACAATTATAGTCTGAGGATTAACCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14580
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 |
---|---|---|---|---|---|
ENSDART00000067857 | Essential Splice Site | 215 | 1167 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50646400)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48916636 |
GRCz11 | 7 | 49189412 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCAGAYGAGAGTCCGCTCAATGCCCGGCTYCTGGTGTWYGTGGGACAGG[T/A]GCGTTCTTWAATGCATGACCCTTYAATAAACCKRACCGCACTTCTGAGAY
Long Flanking Sequence:
TTTAAGTTGTATAATTATGCACATTGTTTACATTGACAATTATAAGGGAATGAGTTTACTCTCTTTGTTTGAGTAGAGTCAACAATCTCATTCAAACATGCACAGAGCCAGTTTAGAGAATAACGAAAGAAATAGGCAAAAAAAAAAATCAAAACAAAACACAATTTACATGTGCATGTTAAATCATGGAGGTTGCACCAAATTTGGTCCAATGTGTTATATTGAGTATTGTGGCATCCCCGATGTCTATTAGACATCCTTTAAACACGCCAAAAAATGCGTTTAAGGCTGAGATAAATCAACATTTTATCAAAGCAAACTTGCAAGTGAGAACCTGCAGGTCAGGTCAAAAGGTGATGCAGTACATCTCTGTGAATGTGATAAATTATTTATTTCAGGGGATTTCCAGTTCGCCATAGCGTCAGATGATAACTCTGAACTGTGGCTCAGCTCAGACGAGAGTCCGCTCAATGCCCGGCTCCTGGTGTACGTGGGACAGG[T/A]GCGTTCTTTAATGCATGACCCTTCAATAAACCTGACCGCACTTCTGAGACTTTCCTAGAGCTATCTGTCAGTATGTTTGTCAGTCATGTTCCCAGTCTTGTGCTCTTCTATAGACTTTTACCGGATGTTTACGTCAAAAGACTTTCTGCATTTTGGCTATTAAGTTACAGGACTGTGATTTGGGACAAAATGTGTAAAAACAGGTTTGACCAATTTTTGTCAATCTCAGTGAGTTGAATCTGATCGCAGTCTGTTTACATGTATTGTATACATTGAAATCAGGTTCACATGCATCTGTCTATAATCTGTTGAAAACACTTTAGATTACGTAACAATTCACACTATTTACTACTGGCTTATTACTTGCCTATTATTAAGATAACAGTTAGTACTTATAAATGAAGATACTTTTTTATATCCTTAACTCTGCCCTATACCTAAACCAAATACTTCCTTACTAACTAGCAGCTAATTCGTAGTTTATTGAGCTAAAAGTCTAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41000
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:
T > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067857 | Nonsense | 376 | 1167 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50711426)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48981662 |
GRCz11 | 7 | 49254438 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATGTATATCATCATATTTTGTTTTATATTTCTAGGTCTACCTTTCCTA[T/G]GTGTATCCCAATGACTTCACCAGACTTACTCATATGGAGAAAACCAACAA
Long Flanking Sequence:
TATTGCTGAGCTACAAAAAAGTAAACTAGAATTTAATGTTTCGATTAAATGTAAATGAATCTTATATATATATATTTATTATATTATATATTATTATATTATTATATTATATTTATTTATTTATTTATTTTTACTTATTTATTTATTTATTTTTTGAAGAATAGAGGACTATAGAAGACATCGGCAATCAAATCAAGGCAAAAACTAGTGTAATTGTTTTATAAATTATATAATTATAAATCGTGTTATAAATGAAATTGTTTTGTTTTTTTTATAATAAGTTTATTATTAAATGTAAACATGTATTAGTTAATACAAGGCAATGTTTTCTAGCAATTTTTAAACATTAATAAATAAACTAGGAATTTACCCAATTATATTTAACTTTGACCCACTAGCCTCAATCAAGATTCGTTTTTGGCCCTTCATAAGGAAAATTTTGGGCACCCCTGATGTATATCATCATATTTTGTTTTATATTTCTAGGTCTACCTTTCCTA[T/G]GTGTATCCCAATGACTTCACCAGACTTACTCATATGGAGAAAACCAACAAATGCTTCTACCGAGAGTCTCCGGTCTACTTGGAGAAGTATGAATCCAAACTGATCCTGACAAGAAAGTATTCAACATCTAAATACATAACTGAACACATACATATACATATGGTCACTCTTTTGAACTGTCATTTAGATTTGGCTTCTATAAATACATGAAGATGGATGAGGAGGAGGATGACCAGCCTGTTTTCTTCCCCAAACCCGATGGTCTGTGTTCAGCTGGGATCTTAATAACAGATAAGAATTCAGCAGCTGTTTGCTCTCTTTAAAACCTCATCATGAAATTTGTAATGAGCCAGGCAACATATGTGTTCCCAGGGTTCAAATCTAACACACACCAGACACCAAATGTGAGCAGAAATGGCCTTTGAGGAGTAAATAAACAGTTGGCTGTTACCTTTATTAAGACCATTACGTGGATTAGGTTGCAGTATTACAAAGATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21055
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 |
---|---|---|---|---|---|
ENSDART00000067857 | Nonsense | 378 | 1167 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50711432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48981668 |
GRCz11 | 7 | 49254444 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATCATCATATTTTGTTTTATATTTCTAGGTCTACCTTTCCTATGTGTA[T/A]CCCAATGACTTCACCAGACTTACTCATATGGAGAAAACCAACAAATGCTT
Long Flanking Sequence:
TGAGCTACAAAAAAGTAAACTAGAATTTAATGTTTCGATTAAATGTAAATGAATCTTATATATATATATTTATTATATTATATATTATTATATTATTATATTATATTTATTTATTTATTTATTTTTACTTATTTATTTATTTATTTTTTGAAGAATAGAGGACTATAGAAGACATCGGCAATCAAATCAAGGCAAAAACTAGTGTAATTGTTTTATAAATTATATAATTATAAATCGTGTTATAAATGAAATTGTTTTGTTTTTTTTATAATAAGTTTATTATTAAATGTAAACATGTATTAGTTAATACAAGGCAATGTTTTCTAGCAATTTTTAAACATTAATAAATAAACTAGGAATTTACCCAATTATATTTAACTTTGACCCACTAGCCTCAATCAAGATTCGTTTTTGGCCCTTCATAAGGAAAATTTTGGGCACCCCTGATGTATATCATCATATTTTGTTTTATATTTCTAGGTCTACCTTTCCTATGTGTA[T/A]CCCAATGACTTCACCAGACTTACTCATATGGAGAAAACCAACAAATGCTTCTACCGAGAGTCTCCGGTCTACTTGGAGAAGTATGAATCCAAACTGATCCTGACAAGAAAGTATTCAACATCTAAATACATAACTGAACACATACATATACATATGGTCACTCTTTTGAACTGTCATTTAGATTTGGCTTCTATAAATACATGAAGATGGATGAGGAGGAGGATGACCAGCCTGTTTTCTTCCCCAAACCCGATGGTCTGTGTTCAGCTGGGATCTTAATAACAGATAAGAATTCAGCAGCTGTTTGCTCTCTTTAAAACCTCATCATGAAATTTGTAATGAGCCAGGCAACATATGTGTTCCCAGGGTTCAAATCTAACACACACCAGACACCAAATGTGAGCAGAAATGGCCTTTGAGGAGTAAATAAACAGTTGGCTGTTACCTTTATTAAGACCATTACGTGGATTAGGTTGCAGTATTACAAAGATGCCATTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38637
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067857 | Nonsense | 453 | 1167 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50714137)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48984373 |
GRCz11 | 7 | 49257149 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGTGTCGACCCAGAGGAGGCAATCAATTCCAGCAACCGGCCAGTCAAG[A/T]GAAGCGGCCCGTCCTATCAGACATCAAGGATTACAGCAGCCACCGCCTCC
Long Flanking Sequence:
ATCAATTTTACTGTTAGAAAGGCAAATGGAGATGGATTTGAGTAAAGAAACAACAACAACAATAAAAACTCTTAACAAAAACAAACGTGAATTAATGCAAAATGATTTATTAACAGGAATTAACAAAAAAATGAACAGTTCCATAACCTGTGAACTAATACAGGTATGTGGAGAATTGTCTCAGTTTTCCAGTCTTATTGGCCTGAGTGTTTATTTTTGAGCCTTGCTGTGTCTGCCTTTTGACAGCTGCAACATGTTGAATGCTAACTGCGCGTCTGACAGCCCTAAAGATGATAATGATAAGCTGTAGATTTCTATCAACACTGCACCAGCATCACCGACTCTTTAATCAAGTCATTAAGCAATTCTCATTTCAGATTGCATGAGTTATTTAAAAGGCTTTGGTTTGATGAGGCTTGTCTCTTCTGACAGATTTCCTGGAGGAGGAAGAGGGTGTCGACCCAGAGGAGGCAATCAATTCCAGCAACCGGCCAGTCAAG[A/T]GAAGCGGCCCGTCCTATCAGACATCAAGGATTACAGCAGCCACCGCCTCCTCAAAGCCTGATAGATTAGACGGGGGTTCAAAGAGCTCCGTCTTTCAGCAAGAGAAGCAGTACGTTCAGTTTAAAGAGCAAGAGAGGAGTAAAAAAAGAACGAAAGGGGAAAGGTTTTATAGACACTCTCAGGTGGTGGATGATGAAATGACAGAAATAAGACAGGTGAAAGGGAGTACAGGTGTGCTAGAGTCTCAAAGCGGCTCTCTAAATGAACAGACGGGACCAAGTGAGGAAAATGGGGACTCCCAAACACTTTCTCTGGTTCAGAGAGGGCGTTCTTTGGCATGGGTGCTGCCTGACCCTGCACTGCAGAGCGAAAGTAAACTGATTGAAACTGCCAGCCCAACTGTGAAAGAAAGATCTCCCTTTAAGCTTCCTCATCTCTATGTCCTGGCTAATAGGATTTTAGGTAACGCAGGTAAGCCTGTGGTGGAGAAAGAATCTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21056
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 |
---|---|---|---|---|---|
ENSDART00000067857 | Nonsense | 566 | 1167 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50714478)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48984714 |
GRCz11 | 7 | 49257490 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGGGACTCCCAAACACTTTCTCTGGTTCAGAGAGGGCGTTCTTTGGCATG[G/A]GTGCTGCCTGACCCTGCACTGCAGAGCGAAAGTAAACTGATTGAAACTGC
Long Flanking Sequence:
CTCTTTAATCAAGTCATTAAGCAATTCTCATTTCAGATTGCATGAGTTATTTAAAAGGCTTTGGTTTGATGAGGCTTGTCTCTTCTGACAGATTTCCTGGAGGAGGAAGAGGGTGTCGACCCAGAGGAGGCAATCAATTCCAGCAACCGGCCAGTCAAGAGAAGCGGCCCGTCCTATCAGACATCAAGGATTACAGCAGCCACCGCCTCCTCAAAGCCTGATAGATTAGACGGGGGTTCAAAGAGCTCCGTCTTTCAGCAAGAGAAGCAGTACGTTCAGTTTAAAGAGCAAGAGAGGAGTAAAAAAAGAACGAAAGGGGAAAGGTTTTATAGACACTCTCAGGTGGTGGATGATGAAATGACAGAAATAAGACAGGTGAAAGGGAGTACAGGTGTGCTAGAGTCTCAAAGCGGCTCTCTAAATGAACAGACGGGACCAAGTGAGGAAAATGGGGACTCCCAAACACTTTCTCTGGTTCAGAGAGGGCGTTCTTTGGCATG[G/A]GTGCTGCCTGACCCTGCACTGCAGAGCGAAAGTAAACTGATTGAAACTGCCAGCCCAACTGTGAAAGAAAGATCTCCCTTTAAGCTTCCTCATCTCTATGTCCTGGCTAATAGGATTTTAGGTAACGCAGGTAAGCCTGTGGTGGAGAAAGAATCTAATAGCAATAAAATTTACATTACAAGACCTCGTCCGCCAGTAAGCAGACCCAAACCTCCTGTGGAAGTGTTTCCCGGGGTCTTTCTTTACCAATCTAGGAAGTCCAAGAGGCTTGTGGATTTGAGTTCAAAATGGAGGTCCTTAAAAACACAAGCTGCTGCTTCTGCCCCCTGGGCGAACTTCCCCTTAATGGACCACAAGACTTCCACCCAATCTGCCCTGTTAAAGCAAAGCCATCTCTCCTCGCCCACAGAGCCTGGGCCTCATAATAAGGGTGACCCTACAGCCTCCATATCAGATCCAGACAGCGTGCCCCCATCAAGCTCAGAAAAAAGAGACCACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34171
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000067857 | Nonsense | 1063 | 1167 | 18 | 20 |
Genomic Location (Zv9):
Chromosome 7 (position 50726250)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 48996486 |
GRCz11 | 7 | 49269262 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCACATTCACTTCCCTCACAACATCCTGGAGAGCATCAGGAAGCACTG[T/A]GTTGAGGGCAGACTGGCCTTTGCACCCATCGTCATGAGACTGGACTGTGG
Long Flanking Sequence:
ACGAAATTGTTGACATTTTTGCAGATTTATAAAAAAAAAAAAAGAAAAACTGAAATATCACATGGTCAGACCCTTTGCTGTATGACACTAATGTAATTCAGGTGCTGTCCGTTACTTCTGATCATCCATGGGATGGTTCTACACCTTCATTTGAATTGACTGATTGGACTTGACAGCTTACAATGACCTTATAGCTCATAATGCTATTTATTTATTTAAACACACTAACAAGAACTCGCAATGTTATAAAATGTTTTTTTTTATGTTGTCAGGAAGTAAGTTTTTTCTTTACATTGTTTGTACTATTTGAAACATGCTGATGCTGTAACTGTGAACTGTAAAGTGATTTGTGGTCTACAATATGTATTTCTTTGTTCATTACTAAAATACTAGTATAAAACATCTTCCATGGGATTTCAGGACAGTCACAGCATAGTGTTCCTGTGTGACCTGCACATTCACTTCCCTCACAACATCCTGGAGAGCATCAGGAAGCACTG[T/A]GTTGAGGGCAGACTGGCCTTTGCACCCATCGTCATGAGACTGGACTGTGGGAGCTCGCCTCTGGAGCCTGATGGTAAAACATACATTATCTATTGATGATAAGCAATAAACACTTACTTACTTACTTACTTACTTACTTACTTACTTACTCCCAGGGTTGTTTATTTCGAAGTTGATATACATCTAATTTTTATGAGGTGGATTGTTAGCCCAACGCTCAACCCCCAACCTGGAGGACCAGGACACACACACATACACTACGGACAATTTAGCTTACCCATTTCACCTATAGCGCATGTCTTTGGACTTGTAGGGGAAACCAGAGCACACAAAGAAAACCCATGCCAACACCGGAGAACATGCAAACACAGAAATGCCAACTGACCTTTTTACTGTGAGGCGAAAACTCTACCCACTGCAAACACCATACTCCTCCAAACACTTACAGCATACAGCAGCATATATACAAATACAAATTTAGTTTGAATGTTTCTTTCACA
Associated Phenotype:
Not determined