ZMP
galnt7
Ensembl ID:
ZFIN ID:
Description:
N-acetylgalactosaminyltransferase 7 [Source:RefSeq peptide;Acc:NP_001018477]
Human Orthologue:
GALNT7
Human Description:
UDP-N-acetyl-alpha-D-galactosamine:polypeptide N-acetylgalactosaminyltransferase 7 (GalNAc-T7) [Sour
Mouse Orthologue:
Galnt7
Mouse Description:
UDP-N-acetyl-alpha-D-galactosamine: polypeptide N-acetylgalactosaminyltransferase 7 Gene [Source:MGI
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa39648 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa30802 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa1202 | Essential Splice Site | F2 line generated | Not yet available |
| sa6596 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa39648
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 |
|---|---|---|---|---|---|
| ENSDART00000079928 | Nonsense | 19 | 652 | 1 | 12 |
| ENSDART00000114903 | Nonsense | 19 | 652 | 1 | 13 |
| ENSDART00000135666 | None | None | 211 | None | 5 |
The following transcripts of ENSDARG00000057303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 38552479)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 37423935 |
| GRCz11 | 1 | 38143113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTAAAGGTTGGATTCATCCTTCGAAGTTTGCTGGTCATCGGCACATTTT[T/A]GGGGCTGGTTTTGCTTTGGTCTTCTTTGACACCGAAGGCTGGAGACGATA
Long Flanking Sequence:
TGCATGCGTGGCACAAGGCGAGCTTCCTTGTGCAATGGTTGTGCGTGTAAACGCCCATAAACGCAAGAACTTGTGGAAGTGTCCGTTCCACGTCACCGCCCCGCACATCTCCACGGGCCTTTTATATGCTATCAATCATGCCGCACGTCCGTGTGTGTTCATTCACACATCCGTGTGTGTTTAGTCCTCATGGCTGCGTGGCGCACACACACGCAACTGCGGGCTTTTTTCATGTGACTGGCCTTTTCTGTGACTAAATCATAAAGAGGAAAGTGGGAGTTTAACTTAATAAAGGAGCAGAGGAGAGAGAGAAAGAAAACGAGAGTGAGAAGAAGGAGGGAGGGACTCGATGTGGCCATACAGGCTGCGGAGTGTTTATTTATTTGTGCAAGCTCACATTTTTCTTTCTGTTTTCTTATTTTTCAACTGATTTCCTCCCCCCAAAATGAGGTTAAAGGTTGGATTCATCCTTCGAAGTTTGCTGGTCATCGGCACATTTT[T/A]GGGGCTGGTTTTGCTTTGGTCTTCTTTGACACCGAAGGCTGGAGACGATAACCCGTTTGCTGGTGTAATGGTAAGCTAGGATGGTCGTTAGTTACCTTGACACGTTATTGTTTTCGTTCTGTGTGTTGTTATTTTTTTCACAGCCTGTGTTAGTATTCTGTAGGGTCTGCTAGCATGATGATTAGCATGCTAACTGCTGCTGTTGTCATGGAGATGAGCAGCGAGAACTGACCGATGAATTGTATCAGACCCTGAACGTTAATATTAATCTCGAAATATATGTCAATGTGTGCTTCAATAAACGGAGATATGTGTTTGCTAGCACGAACAGCTAATGTCGCTCTTTACATTCTCATAAGTAGCAAATTCAGCAAAAACCCGGAAGGTCGTTGGCTTGGGTACGTTACTGGTTGCTTGTATACACGCAGTATTAACATAACGTGCCATTATGTATCAATAATCAAAAAGCAGCTGGTTTTTTGTCAAATGAGATGATTTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30802
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079928 | Essential Splice Site | 42 | 652 | None | 12 |
| ENSDART00000114903 | Essential Splice Site | 42 | 652 | None | 13 |
| ENSDART00000135666 | None | None | 211 | None | 5 |
The following transcripts of ENSDARG00000057303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 38552551)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 37424007 |
| GRCz11 | 1 | 38143185 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTTGACACCGAAGGCTGGAGACGATAACCCGTTTGCTGGTGTAATGG[T/A]AAGCTAGGATGGTCGTTAGTTACCTTGACACGTTATTGTTTTCGTTCTGT
Long Flanking Sequence:
GTGGAAGTGTCCGTTCCACGTCACCGCCCCGCACATCTCCACGGGCCTTTTATATGCTATCAATCATGCCGCACGTCCGTGTGTGTTCATTCACACATCCGTGTGTGTTTAGTCCTCATGGCTGCGTGGCGCACACACACGCAACTGCGGGCTTTTTTCATGTGACTGGCCTTTTCTGTGACTAAATCATAAAGAGGAAAGTGGGAGTTTAACTTAATAAAGGAGCAGAGGAGAGAGAGAAAGAAAACGAGAGTGAGAAGAAGGAGGGAGGGACTCGATGTGGCCATACAGGCTGCGGAGTGTTTATTTATTTGTGCAAGCTCACATTTTTCTTTCTGTTTTCTTATTTTTCAACTGATTTCCTCCCCCCAAAATGAGGTTAAAGGTTGGATTCATCCTTCGAAGTTTGCTGGTCATCGGCACATTTTTGGGGCTGGTTTTGCTTTGGTCTTCTTTGACACCGAAGGCTGGAGACGATAACCCGTTTGCTGGTGTAATGG[T/A]AAGCTAGGATGGTCGTTAGTTACCTTGACACGTTATTGTTTTCGTTCTGTGTGTTGTTATTTTTTTCACAGCCTGTGTTAGTATTCTGTAGGGTCTGCTAGCATGATGATTAGCATGCTAACTGCTGCTGTTGTCATGGAGATGAGCAGCGAGAACTGACCGATGAATTGTATCAGACCCTGAACGTTAATATTAATCTCGAAATATATGTCAATGTGTGCTTCAATAAACGGAGATATGTGTTTGCTAGCACGAACAGCTAATGTCGCTCTTTACATTCTCATAAGTAGCAAATTCAGCAAAAACCCGGAAGGTCGTTGGCTTGGGTACGTTACTGGTTGCTTGTATACACGCAGTATTAACATAACGTGCCATTATGTATCAATAATCAAAAAGCAGCTGGTTTTTTGTCAAATGAGATGATTTCTGGATATCTTACAGGATAGTTCCATGCTCTAGTACTTATTGTAGACTAAAGGGGTCTTCGAAATAATTTGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1202
Status:
F2 line generated
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000079928 | None | None | 652 | None | 12 |
| ENSDART00000114903 | Essential Splice Site | 378 | 652 | 6 | 13 |
| ENSDART00000135666 | Essential Splice Site | 132 | 211 | 3 | 5 |
The following transcripts of ENSDARG00000057303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 38565964)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 37437420 |
| GRCz11 | 1 | 38156598 |
KASP Assay ID:
554-1111.1 (used for ordering genotyping assays)
KASP Sequence:
TGGGTAGCAAGGAGAAGCAGAAGAGACTAACTAGAACTGAGCCCTATCGG[T/A]AATTTAAAGCCATAATCCTGAGCTGATTAGGGCTGACCACAACACGCATA
Long Flanking Sequence:
ATAAGACCGAGCCCTATCGGTAAACTTCCCTCCCTCCATAAGCATGAACATTAAATCCATTTTGTCTCTCTCTTGTTTTGTCTCCCCCACCCCGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGCGTCCATGTTTGCTTGCATGGACGTCTCCCTTGCCTCCCCTCTGTCCTCTGTGGCCATGTTCAGAACGGTGTGCACAGTGCCTCTCATAGACTCTATTAACGGCAAGACTTACACCATCGAGGCCCAGGGGGGCGGGGACGAGGATGGCTTTGCCAGAGGAGCATGGGACTGGAGCATGCTTTGGAAACGCGTGCCTCTGGGTAGCAAGGAGAAGCAGAAGAGACTAACTAGAACTGAGCCCTATCGG[T/A]AATTTAAAGCCATAATCCTGAGCTGATTAGGGCTGACCACAACACGCATAAGCGGAGGGACCCGGTCTCTCTCTTATAAAGTTTGGTGGTGGTCTGCTTGTCTTTGTTGCTTTAACAGTTCAGCTCCTTTAATGCTCATTAGAGACTTCCTGCAAGCGTACTAACTGCTTTGAAATGGTCATAAAGCAATGAAGTCATTTAAATAAATGACTTCATATATTATGACTCATTGAGCTGTTCTGATTAAGTCAACACCTGAACTACTTGAATTTAAAAAGCGTCAATCCTCGTTTCTGCTTCTCTTTGCATGCAGTCTTGCCTTCTAACTAATCTAGTGACTTGGCACATGCTTACCAAGAGTGCGTGTTCTTAGTCTTTGCCTAATCTTCACATTATGCTGATTTCTGTCCACTTCCTTGCAGTCTTTTCAAGCTGAGGTTTACTAAAAAAAAAGACACAAAAATGTTAGCAAAAAATATGAATGTCTTTATGGTATCTCT
Associated Phenotype:
Normal
| Stage | Entity | Quality | Tag |
|---|---|---|---|
| Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa6596
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 |
|---|---|---|---|---|---|
| ENSDART00000079928 | Nonsense | 392 | 652 | 7 | 12 |
| ENSDART00000114903 | Nonsense | 392 | 652 | 7 | 13 |
| ENSDART00000135666 | Nonsense | 146 | 211 | 4 | 5 |
The following transcripts of ENSDARG00000057303 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 1 (position 38569156)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 1 | 37440612 |
| GRCz11 | 1 | 38159790 |
KASP Assay ID:
554-4885.1 (used for ordering genotyping assays)
KASP Sequence:
TGTGTGTCAGGTCTCCTGCCATGGCTGGAKGGCTGTTTGCAATTGAGAGA[G/T]AATTCTTCTTTGAGYTGGGTCTTTATGATCCAGGCCTTCARATCTGGGGA
Long Flanking Sequence:
TGTAATTGTTTTTGTATTTAAAAAAAAAAATACAATTCCACAAGATCTGCTGCCAAAGCCACTGCAAAATCAGTCACTTTAGGCTCCAAAAAAATGTGAATGTCCTACAAAATCTTAAAAGGACTGATATTTGCAAGATTACAAAATTATTCCTCCTTGAACATAAATGTTGTTTTAGCATTTAGCAAGGAAATGATATCAAACTGTTGAGGAAACATACGATTTGATTAACTGGGATTTAAAAATGGCTCCGAGTTAACTATTTTGAGTACACTTGTGTGTGAACAGGTCTACTGAGTTTTGATAAAACACACAAAATACATTTTGATTGACAAAACTGAATGTATTTCAGATTTGTACCACCTGTCTGAACAAGGCCTTGTCTCTTAATGTTATGAAATAGTGTATCATGGAAGAAAAAAAAGGTGAAACATTCTTGACAGGTGAATTTGTGTGTCAGGTCTCCTGCCATGGCTGGAGGGCTGTTTGCAATTGAGAGA[G/T]AATTCTTCTTTGAGCTGGGTCTTTATGATCCAGGCCTTCAGATCTGGGGAGGTGAAAACTTTGAGATCTCATACAAGGTAAACTTTTTTGTATAAGTGTGTTTATTTTCCAGGTTAATCCTGTAAAAATTCTTTACAGTTTTATTTTTCAAGATTCAATTTGATTGGTCACACCTATGTAATTGGCAGTTACTTGTAAATAATGACTATTTTGTTTGCAGCACTTTAGAACTGTATGTGTATATCCTGCTCGAATGTGTAGTCGTGTGTGTTCTGCCTTGTCAGCTGATCATAGTGATATGGATAGGTTTGCATAAGCTAAATTTGCCGACATGTTTACATAATCAAAAATATGCAGTTATGATATTTGGATTTTTCAACAAAGTACAATTGAGATTATATTTGAAAAGAAAACACTCACATCACAATATAGACTAGCTCTTTCTGCACATCATGAAGATTGTATCTGTCCATCACATAGTAATAAATTTACCAGCAGCT
Associated Phenotype:
Not determined