ZMP
si:ch1073-380l12.1
Ensembl ID:
ZFIN ID:
Description:
LOC553524 protein [Source:UniProtKB/TrEMBL;Acc:Q58EA8]
Human Orthologue:
B4GALNT3
Human Description:
beta-1,4-N-acetyl-galactosaminyl transferase 3 [Source:HGNC Symbol;Acc:24137]
Mouse Orthologue:
B4galnt3
Mouse Description:
beta-1,4-N-acetyl-galactosaminyl transferase 3 Gene [Source:MGI Symbol;Acc:MGI:3041155]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa17326 | Nonsense | Available for shipment | Available now |
| sa43036 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa8410 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23215 | Nonsense | Available for shipment | Available now |
| sa32185 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17326
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 |
|---|---|---|---|---|---|
| ENSDART00000081904 | Nonsense | 95 | 440 | 4 | 15 |
| ENSDART00000110892 | Nonsense | 95 | 1143 | 4 | 20 |
| ENSDART00000129165 | Nonsense | 4 | 1052 | 1 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 5673816)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6447606 |
| GRCz11 | 18 | 6587971 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTTCTATTGACTAATGGAAATTTCTSTTGTGTTTGCCRCAGTATAAAGGA[C/T]AAGCTAATCTTCACRTTTTCGACGACTGGTGTGGCTCRTCTATAGCTCAA
Long Flanking Sequence:
ATAAGAAGAAGAAAATAATAATTCAATGTTTACCTGCTCTTTTGTCTATGAAGATATTTTTGTCTCATTGCACAGCTCACCTCTTTGTGTATTCAAATGTCAGTGATTCGTTCACGTTACACTGACAGTCACATATAATCTTAACAAATGTACAGTCTGAGCCTATAGAAGTCATAATTAATTCACCTTTCAATTCAAATCTTTTTCCGGCTCTAAACACATGTGATTGGCCCATGATGAACGAATGAGTCAGACCCGATAGAGGACTCGTGAGATGAACGGATCAATTCTTTTTCTGGCTCTAAACGCATATGATCGGCTTGTGCCTTTCCTTGATGAACGACTCAAAAAACTTGAAATGAACAAAAATGACCTAAATCTTATGTTGATGTTCAATTGTTCAACACTTTATCAAATTTGTTTATGCTCTTTGCAGTCTCTGTTTTTTTAGTTCTATTGACTAATGGAAATTTCTGTTGTGTTTGCCGCAGTATAAAGGA[C/T]AAGCTAATCTTCACGTTTTCGACGACTGGTGTGGCTCGTCTATAGCTCAACTACGGAAGAATCTACATTATCCACTGTATCCTCACGTATGTGGCACTGTATATTTCTGTATTGGTTATCTAGATTGGTCAGATATTCACAGCTTTATAATTAGCTTTAATTTATATTTAATTTAAAGTCTTCATTTTAAGTATTTAGCGTTTTTATTTCGGTTGCTTGCCTGAAGAACGTCTCCATCCACTTTTATAGTTTTTAAACTCACTACTTTTTAAATTTCAATTCAATAACATCCCTTTTTTTGTTTATCTTTGTAGTTTATCTTTGTAAAATATAAAAATATTTTTAATCTTCTGTGCTGTTTTTTTTTTTTCTCTAGTGCTCTTTAATAATGAAGAAAAATGTGATTTGTGATGTCATGCTAAATAATGCAATATTATATTTGTGATTCATTTAAAAAATGTTGTAACCTATTTAAGTTCATTATTAATTCAGGATAAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43036
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 |
|---|---|---|---|---|---|
| ENSDART00000081904 | None | None | 440 | None | 15 |
| ENSDART00000110892 | Nonsense | 513 | 1143 | 14 | 20 |
| ENSDART00000129165 | Nonsense | 422 | 1052 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 5686625)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6460415 |
| GRCz11 | 18 | 6600780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACACAATGAACCCCAACCGAGAAGGAAGAAGAAAAGGAGACTGCCCCAA[C/T]AACAAAACCTGGAGGATCAACAACATCCTCAAAATGCACCTTCAGAGGTA
Long Flanking Sequence:
ATTTTTGTCAGAGTAACTGAGGCACAATCTGTAAAGTCTCCACCCTCTTTTGATGCATTTTGTTTCTTTTATTGCATTAAATCAATCAGCTTGATGGTTGTGGACTGTCAGAAAGGTTCCTCATTCCCCATTTTAACACGTCTAATGTTTGTTTTTCTCAAGGAGACAGCATGTTCGGAAAAGCAGCAAACATTGGCAGAAATAAAGATAAAGATTTTCAGAAATCTAGAGAGAACGGGGAAAAGCAGCAAATTGATGGAATGGAGAAGAAGAAGAAGGTTCTCTCTGATTATGGCGACGATTATGATGATTATTCAATGAATAGACGGCGCAAACTCTTCTCCGTCCAGAAACATAGTGTGATTAGAAGAAAGAGAAACGATGGAGAGCTAAACATCAGAAATGAACAAGAGAACCAACCAAAAGAGATCCAAAAACTGCCTGAAGAAGCACACAATGAACCCCAACCGAGAAGGAAGAAGAAAAGGAGACTGCCCCAA[C/T]AACAAAACCTGGAGGATCAACAACATCCTCAAAATGCACCTTCAGAGGTAAAAAGCTACAACCAAGGAGTAAAACAAGCTTATACTGTGGACAAAATACCTGAGCAGCAGAATCCAGAACGGTTTCAGGAAAAAACCCAACGGAGGTTTAAGGAGAAACATCTACAAGCTGATGGGTCGATGGTTAAGAATGATCGAATTCACCGTCTTAAAGCCCATTACGTCAATAGTAGCAATGTGAATCCAAACCCTGCTATAGTCAGAGATGTTCCCATTGAGAAAGTTCGAGAAGCTATTGATCTAAAGGAAAAATCCATAAAAAAACCTGCCATGCTTAATGAGGTCGAGATTGAACATCCTGAATCGAATGGAATGGATAATCGGAAAGTCTTTCTTGGAGAACATGTCTACAAAGCACGCAAGAACTCATCGAATGTGGTGGAACTAAAAAAACACAGGGTGAAGAATGCTACATATGAATATTTGCATGGAGGTGAAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8410
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081904 | None | None | 440 | None | 15 |
| ENSDART00000110892 | Nonsense | 628 | 1143 | 14 | 20 |
| ENSDART00000129165 | Nonsense | 537 | 1052 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 5686970)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6460760 |
| GRCz11 | 18 | 6601125 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGATCTAAAGGAAAAATCCATAAAAAAAYCTGCCATGCTTAATGAGGTC[G/T]AGATTGAACATCCTGAATCRAATGGAATGGATAATCGGAAAGTCTTTCTT
Long Flanking Sequence:
TCCAGAAACATAGTGTGATTAGAAGAAAGAGAAACGATGGAGAGCTAAACATCAGAAATGAACAAGAGAACCAACCAAAAGAGATCCAAAAACTGCCTGAAGAAGCACACAATGAACCCCAACCGAGAAGGAAGAAGAAAAGGAGACTGCCCCAACAACAAAACCTGGAGGATCAACAACATCCTCAAAATGCACCTTCAGAGGTAAAAAGCTACAACCAAGGAGTAAAACAAGCTTATACTGTGGACAAAATACCTGAGCAGCAGAATCCAGAACGGTTTCAGGAAAAAACCCAACGGAGGTTTAAGGAGAAACATCTACAAGCTGATGGGTCGATGGTTAAGAATGATCGAATTCACCGTCTTAAAGCCCATTACGTCAATAGTAGCAATGTGAATCCAAACCCTGCTATAGTCAGAGATGTTCCCATTGAGAAAGTTCGAGAAGCTATTGATCTAAAGGAAAAATCCATAAAAAAACCTGCCATGCTTAATGAGGTC[G/T]AGATTGAACATCCTGAATCGAATGGAATGGATAATCGGAAAGTCTTTCTTGGAGAACATGTCTACAAAGCACGCAAGAACTCATCGAATGTGGTGGAACTAAAAAAACACAGGGTGAAGAATGCTACATATGAATATTTGCATGGAGGTGAAGTCAAAGCAGACGCAATGAAGAAACCCAAATACCGTGAACAAAAAGTAGATCGAGTGGTTGTAGTTGACAACCGAATAGTCGAGTATAACAATAAAGCTCATAATAATATTGCAGTTCTCCAAAAACCACACCAAAACATGCTGTATAACCAAACCAGTGAGCACAAGGATCAAGCATTTAACAACCGCTGGGGTCACGCCAATGAGGATAGAAATGGAGTTGAGAAACCGATACAGGATAATGCCATGCACGTAAAAGAGACTGAAGATAATGGAGATGAAGAAGACGCTTGGGTAAATCAGGGTTTGTCGGAGGAAGAAGACTACGAACTTGTTCACAGGCCTGCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23215
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 > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000081904 | None | None | 440 | None | 15 |
| ENSDART00000110892 | Nonsense | 633 | 1143 | 14 | 20 |
| ENSDART00000129165 | Nonsense | 542 | 1052 | 11 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 5686985)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6460775 |
| GRCz11 | 18 | 6601140 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATCCATAAAAAAACCTGCCATGCTTAATGAGGTCGAGATTGAACATCCT[G/T]AATCGAATGGAATGGATAATCGGAAAGTCTTTCTTGGAGAACATGTCTAC
Long Flanking Sequence:
TGATTAGAAGAAAGAGAAACGATGGAGAGCTAAACATCAGAAATGAACAAGAGAACCAACCAAAAGAGATCCAAAAACTGCCTGAAGAAGCACACAATGAACCCCAACCGAGAAGGAAGAAGAAAAGGAGACTGCCCCAACAACAAAACCTGGAGGATCAACAACATCCTCAAAATGCACCTTCAGAGGTAAAAAGCTACAACCAAGGAGTAAAACAAGCTTATACTGTGGACAAAATACCTGAGCAGCAGAATCCAGAACGGTTTCAGGAAAAAACCCAACGGAGGTTTAAGGAGAAACATCTACAAGCTGATGGGTCGATGGTTAAGAATGATCGAATTCACCGTCTTAAAGCCCATTACGTCAATAGTAGCAATGTGAATCCAAACCCTGCTATAGTCAGAGATGTTCCCATTGAGAAAGTTCGAGAAGCTATTGATCTAAAGGAAAAATCCATAAAAAAACCTGCCATGCTTAATGAGGTCGAGATTGAACATCCT[G/T]AATCGAATGGAATGGATAATCGGAAAGTCTTTCTTGGAGAACATGTCTACAAAGCACGCAAGAACTCATCGAATGTGGTGGAACTAAAAAAACACAGGGTGAAGAATGCTACATATGAATATTTGCATGGAGGTGAAGTCAAAGCAGACGCAATGAAGAAACCCAAATACCGTGAACAAAAAGTAGATCGAGTGGTTGTAGTTGACAACCGAATAGTCGAGTATAACAATAAAGCTCATAATAATATTGCAGTTCTCCAAAAACCACACCAAAACATGCTGTATAACCAAACCAGTGAGCACAAGGATCAAGCATTTAACAACCGCTGGGGTCACGCCAATGAGGATAGAAATGGAGTTGAGAAACCGATACAGGATAATGCCATGCACGTAAAAGAGACTGAAGATAATGGAGATGAAGAAGACGCTTGGGTAAATCAGGGTTTGTCGGAGGAAGAAGACTACGAACTTGTTCACAGGCCTGCGTTTGACGTGGAAGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32185
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 |
|---|---|---|---|---|---|
| ENSDART00000081904 | None | None | 440 | None | 15 |
| ENSDART00000110892 | Nonsense | 992 | 1143 | 17 | 20 |
| ENSDART00000129165 | Nonsense | 901 | 1052 | 14 | 17 |
Genomic Location (Zv9):
Chromosome 18 (position 5692629)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 18 | 6466419 |
| GRCz11 | 18 | 6606784 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGAGCTCACTTTGACTTCCTTTCTATTGTGTGTCCTTTGATTCAGGTAT[C/T]AGTACCTCAGGTTGAGCGGAAACTTTGAGAGATCGGCCGGACTGCAGGCA
Long Flanking Sequence:
AGGGACTGTGATTCAAAGCCACACCCCCTGAAATCGCGTTTATTCCTCGTCAACACAGGCTTGCTTGGTTTGAGACTTGTGGAGCTGCGCATCGATGAATTTGCTCTTCAGTGTTTGGACTTTCAGCGGTTAAAATTAAACCACACCGATCTGAACAAAACTAAACAACTCTGGAAACTGGACTGACACGTTTCAGTTTACTAGAACTTCTATGTTAAGCTGCTTTGACACAATCTACATTGTAAAGGCACTATAGAGATAAGCATGAATTGAATTTAATTGAATTAATATCAGCTGCACATATTGTGATTTCAAGCATGTTTTTTTTTAGTAGACCACAACCTTTGTGCGGAAGTGGTGTACATGTTTTCACCCTGGTTTTGTGCATACGGCATGTTTATAAATGAGACCCACTGTTCTAATGCTCCATGTGCTTGGAAAATGTAAAATGAGAGCTCACTTTGACTTCCTTTCTATTGTGTGTCCTTTGATTCAGGTAT[C/T]AGTACCTCAGGTTGAGCGGAAACTTTGAGAGATCGGCCGGACTGCAGGCAGGAATTGACCTCATTACTGTAAGTTTAAGATTCACAATCATTCACACAGCAGACAAATGCTTGAAATTCTGCAATCTGTGTTAAAACATGACACTAATGCCTAGTTCAGACTGCATGATTTTAGCCCCGATTTTGGCTCGCCGACAGGTTTTGAGAAATCGCCGACAAATGCCTGAAATCACAGGCAAATCACTGCTCGTGCACGTGAGTGACAATCACACAGTATGAACGATCAAAGACGCAATCTGAGAGAATCGCCGATGAGTCGCCGATGCCTGCGAGATATTTGGCATGCTAAATATCTGGAGCTGTCGGCGATTCAAATCATGCCGTGTGAATTGAGTTTTGACTGAAAATAACATCAGCCATCGCCTACAATGCGAGAGCGGCTTTCACTTGTGTGTGCGTGTGTGTTAGAGATGCGCGGTTGGCGGTTATAGCCGCGGACTC
Associated Phenotype:
Not determined