ZMP
jag1a
Ensembl ID:
ZFIN ID:
Description:
Protein jagged-1a [Source:UniProtKB/Swiss-Prot;Acc:Q90Y57]
Human Orthologue:
JAG1
Human Description:
jagged 1 [Source:HGNC Symbol;Acc:6188]
Mouse Orthologue:
Jag1
Mouse Description:
jagged 1 Gene [Source:MGI Symbol;Acc:MGI:1095416]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa45084 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa168 | Nonsense | Available for shipment | Available now |
sa11248 | Nonsense | Available for shipment | Available now |
sa1989 | Essential Splice Site | F2 line generated | Not yet available |
sa39691 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa45084
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 |
---|---|---|---|---|---|
ENSDART00000047851 | Nonsense | 211 | 1242 | 4 | 27 |
ENSDART00000123632 | Nonsense | 211 | 1242 | 4 | 28 |
ENSDART00000137172 | Nonsense | 211 | 1253 | 4 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51651276)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50497773 |
GRCz11 | 1 | 51141572 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGGCTGTAATAAGTTCTGTCGGCCCAGAGACGACTTTTTCGGCCACTA[T/A]ACCTGCGATCACAACGGAAACAAGACCTGTTTGGAAGGATGGGCCGGCCC
Long Flanking Sequence:
GTGAAGTTCATGTGATGCTCATGTAGTTTTTCCTGTAAGGGACATGAAGTATAAATCATAGAAGGAAACCTTTGTGATATTTCTAATCTGTTGTGTGTGTTATCCTAAAATCATCCCATTTGCAGTATAGAACAGACATTTAGCCTAAAGTCTACTTTTGTTGTTCAGAAACATCTCAACCATAAATCCAGTGCCTAAATCTGCATGTTTTGAGAGTTAGTGGTGTTCGTAATTTCATATTTAAGCTAAACAGAAGTGTCATTAAACCACAGCTGTGATCTATAATGTAATGCTCTCTTCTTTATAGGCATAAATGGACAAGTGATCGAGAAAGCGGTGCAGTCGGGCATGATCAACCCAAACCGTCAATGGCAGGTCCTGAAGCACAACGGCCCCGTGGCTCAGTTCCAGTACCAAATTCGGGTGACCTGCGACGAGCACTACTTTGGCTTTGGCTGTAATAAGTTCTGTCGGCCCAGAGACGACTTTTTCGGCCACTA[T/A]ACCTGCGATCACAACGGAAACAAGACCTGTTTGGAAGGATGGGCCGGCCCAGAATGCAACACTGGTGAGGGGACGGGGCTGTTTATCAGATTTATAATGCTGTTCCAATGCTAGAGCATGTTGTTTTCATATGTGAGGGCTCCCACTAAGTAGATATGCATTTAAAAGACATCTTATAGACATCCAAATCTAGATGTCTTGGCTTTGTTTGGGCTGACAATCTAATAATAGTCTAGTAATCTAACACAGATCAGACAGGCTGCACATGTGTCTTTGATATCTGTTTAATGACTAGTCAAATTTAGGCTTGTTTTAGCCATGACATCTATGTTCGGATGTCTGTATTTTAGATGTTTAGCTGTAAGCTGTTAGTTCAGGTCTGTAAGTCACAAAACACTGGAAAACTAATAGATAGATATTCATTGGTCTAAAGCATGGGAATGGGGTTATTCAGGCTTGTTTAGACTAAACTTATTAATGCTCTGTAGATGTAGATGACC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa168
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 |
---|---|---|---|---|---|
ENSDART00000047851 | Nonsense | 438 | 1242 | 10 | 27 |
ENSDART00000123632 | Nonsense | 438 | 1242 | 10 | 28 |
ENSDART00000137172 | Nonsense | 438 | 1253 | 10 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51640321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50486818 |
GRCz11 | 1 | 51130617 |
KASP Assay ID:
554-0096.1 (used for ordering genotyping assays)
KASP Sequence:
CGTGCGTCAATGCCCACTCCTGCCGCAATCTGATTGGTGGATACTTCTGC[G/T]AGTGCCTGCCTGGCTGGACGGGACAGAATTGCGACATCAGTAAGTATTTC
Long Flanking Sequence:
TCCAGTTTCTCCCACAGTCCAAAGACATGTGCTTGGTGAATTGAATAAACTAAATTGGCTATAGTGTATGAGTGTGTATGTGAGTTTCCCAGTACTTGGTTGTGGCTGAAAGGGCATCCGCAGTGTAAAACATGCCAGTATAGTTGGCGCTTCATTCTGTTTTGGGGACCCTAGATAAATAAGGGATTAAGCTGAAGGAAAATAAATAAATGGGGTGCCAATATTTATGCACACACATGTTCTTTCCAATAAAACAGTTGTGTTTGCAATTATTTGTTCTAAATTAGCTTTTTTGTTAATATTCTGAGCAAAAGATCAACATTTCACACACATCTTAGTGGAGGTAACTGCATATAGTTCTGTTTGGCTGCGTGTGTGTTTGGACTGCGCTCACACTAGTTTCTCTTTTTTCCATTTTTGGCCCAGATGCTAATGAGTGTGAGGAAAGCCCGTGCGTCAATGCCCACTCCTGCCGCAATCTGATTGGTGGATACTTCTGC[G/T]AGTGCCTGCCTGGCTGGACGGGACAGAATTGCGACATCAGTAAGTATTTCACAGTGTCAGATTAAAGCAACGTGAGATTGACTACATAGGCGCTCTGAGAGATCTGCAAGTGAGTTTAACTACAGGTCGGTACTGATAGCTTGCTGAAGGAAAATGCAGCAGAAAAAACAAAACAAAATTTGAATATGAGTACTTCATGAAAATGTATAAAGCTTCATATATTAGGGTTTATTTAATAATTGGTCTGATTTTATTATCATTTTATTTCAGCTTTTGTTTAAAGAGGACCTATTATGCAAAAATCACTTTTATAAGGGGTTTAAACGCAGTTGTGTGGCAACAGTCTGTGAATATAACCAGTGTCTAAGGGTAAAAATGTATTAATTGTATTAATATATTAATCTGTTTATAACAGCGGTGTTAAACGTACGGCCCGCAGGCCGGATCAGGCCCACAAACGAATTAATGCAGCCCGCGAGATGATTCTGTGAGCTGCAATT
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:
sa11248
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047851 | Nonsense | 618 | 1242 | 14 | 27 |
ENSDART00000123632 | Nonsense | 618 | 1242 | 14 | 28 |
ENSDART00000137172 | Nonsense | 618 | 1253 | 14 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51631075)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50477572 |
GRCz11 | 1 | 51121371 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCACACGGCCGCTGCCKTAGCCACAGCCAYGCCGGAGGACACTTCAGCTG[C/A]GACTGTCAAGACGGCTTCACCGGGACCTACTGCCACGAGAGTAAGTGAAT
Long Flanking Sequence:
AAGAAAATATTACTAAATATTCTAATAAATATTCATATCGACATTATAATTATTTTCATTATTGCAATAATAATTATTATGCTGTAAATTTAAAAAAATATATGAGGTATTATTGAATATTATAATAAATATTAATAATTGCTAATTAATAATTTGCAAGTAATTTAAACAAAAATAGTTTATTTTCATGAAAACTGTATAAAGAGTCAAGCTAAAATTAGTTTGGTTTCTAGATCTAGATTGATAGTCCATGTTTGTCAAACTAAATTTAAGACTACATAGATTATCAGCAACCATCTCAACTTTAAGAAGACACACACTTTGACCATCCGCTCTCATTAAACCCTGTGCTCTTTGTTGTGTCCTGCAGTGATTGACAGCTGTACGGTGGCGGTGGTGTCAAACAGCACCCCAGGCGGTCTGAGGCTAATCTCTTCCAGTGTGTGCGGTCCACACGGCCGCTGCCGTAGCCACAGCCATGCCGGAGGACACTTCAGCTG[C/A]GACTGTCAAGACGGCTTCACCGGGACCTACTGCCACGAGAGTAAGTGAATATAAGACAGCCAGAGTTCACATCCATTTACAGGTGTTTATTGAAAGAGTTCAGCAAATCCAAATCATAAATTCATTTATCAGGGGTCACCACAGTGGAATGAACCGCCAACTATTCCACCATATGTTTTACACAGCAGATGCCCTTCCAGCCGCAGCCCAGTACTTGGAAACACCCATACACTCTCACAATCACAGACACACTTATACATTACGGCCAATTTAGTTGACCAAATTCACCTATAGCGCATGCAAACTCACACACAGAACTGCCAACTGACCCGAGACTCGAACCAGCGACCTTCTTGCTGCAAGGTGACAGTGAGCCCATCTGTCGCCCCAAAACATAAATCAAAGTTGAAAGAAGGGGAATGGATAAACACTGGTCTGCTTTTCAAACACTGCTTCATGAAGCTTTACGAATCTTTTGTTTTGAATCAGCAGTTTCAGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1989
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047851 | Essential Splice Site | 823 | 1242 | 20 | 27 |
ENSDART00000123632 | Essential Splice Site | 823 | 1242 | 20 | 28 |
ENSDART00000137172 | Essential Splice Site | 823 | 1253 | 20 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51623395)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50469892 |
GRCz11 | 1 | 51113691 |
KASP Assay ID:
554-2934.1 (used for ordering genotyping assays)
KASP Sequence:
TACCGCTGTGAGTGCGCCAGTGGCTTYGCAGGACCAGACTGCCGCATCAG[T/C]GAGTGAATGCTTTATTCAGCATTTAGYAGTACGATTTTATTATAAAGAGT
Long Flanking Sequence:
TTAATTTAATTTATAAACACCAGAAACAATGTTTAATCTTCACTTTCATCTTCACTAAACCACTTACATGTATTAAATATTATTAATGTACGGTAAGCGATTAATTGTATTTTATTAATGACATTTAATTTGATTTTATAGCCATACACTGTGATAAACTGCAGTATTTATCTTCATGATGAATTATGATACATTTTAGCTGAAAAAATTACAAGTTTTGCCTGAAAATACCACAAATGTAGCTTTTTAATGGAGGAGCTTTGGCTGCATACAGCATCAATTGAATGTATTAAATATTTTTTATTGAAACCTGTTAAATTAACATTTTTTGTAACAATGAACACATTTGTGAACATTTTGAAAATCTCCCATCATTTTCCAAGTCATCTTATCAATATGTGTTCTCTGTGCAGTTATAACAGTGGGACATGTGTGGATGGGGATAACTGGTACCGCTGTGAGTGCGCCAGTGGCTTTGCAGGACCAGACTGCCGCATCAG[T/C]GAGTGAATGCTTTATTCAGCATTTAGTAGTACGATTTTATTATAAAGAGTGATTGCACGTTAAAACGGTTCTCTTTCCCTCTACAGACATCAATGAGTGCCAGTCGTCACCCTGTGCGTTCGGCTCTACCTGTGTGGATGAAATTAATGGCTACCGCTGCTTGTGTCCACCAGGCAGAACCGGACCCAGATGTCAGGAAGGTACAGTTCCCATTATTTATACTTGCACTTTAATCCAAATTAAAGGGAGACTTAAAAATTGTATTTAGTCACTATGTAATCTGTTTTATGGCTTTGCTTTTTCTGTTGGACACAAAAGAAATAATGTTGAAGCTCAAAACCATTGACTTCCATAGTAGGGAAAACAAACACTATAAAAGTCAATGGTTACAGGTTACAGCATTCTTCAAAATAACTTTTTTTGTATTCATCAGAAAAAATAACCAAGTAAAGTGTGAGTGAATGAATTTAATAGTATTTATCAAGCTTTTTATTGCTCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39691
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 |
---|---|---|---|---|---|
ENSDART00000047851 | Nonsense | 1057 | 1242 | 26 | 27 |
ENSDART00000123632 | Nonsense | 1057 | 1242 | 26 | 28 |
ENSDART00000137172 | Nonsense | 1068 | 1253 | 25 | 26 |
Genomic Location (Zv9):
Chromosome 1 (position 51619715)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 1 | 50466212 |
GRCz11 | 1 | 51110011 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAGCAAACACAGTGCTAACAGCTCCGTCATCGGCTCCATCGCTGAGGTT[C/T]GAGTGCAGCGCAAACAACCGCAAAACCCCAACGGTGAGACATCACAGCAA
Long Flanking Sequence:
CGCCAGTAACGAGATCCATGTGGCCATTGTGAGTGATTTAGCGCAAAATAACTCTAATAAACTTTTATTTGCAATTTTTTATGAAATGTCTTATTATCCATATGGTATTAAAGAATGACAAGAAATATCGAATTCATAATGGTGTATAATAATGTATTATATTATTATTGTTCTATTTTGTCATTTTTATGGAATTTATATAATTCAAATAAAATGAATACTATATAACACTATTATTCTTGATTATTTTATTTTTATTTGTTGTATTTGTGTTGTTAAATATTTACCGTAATGCATTTCATTTTGCTTTATTTAAATTAGAACATTTAAGTCATAAAAAAATGACTTGAATAAAAAAAAAAAAATGTTGTGTTTTCTAGCATGTGACTGAGAACGGCATTCATGGCCGGGTTCCTGTTAAGGAAATTACAGACAACATCATTGATCTGGTGAGCAAACACAGTGCTAACAGCTCCGTCATCGGCTCCATCGCTGAGGTT[C/T]GAGTGCAGCGCAAACAACCGCAAAACCCCAACGGTGAGACATCACAGCAAGCTCTTAAACTTTACAGGAAACAGTCTTGAAAGAACGTTTTACTGGGCAAGGATTGCATTAAATTTATCAAAAGTGACAGTAAATTCATGTTACAGAAATTGTATTTTAAATAAATGTTGTTCTTTTGAACAAAAAACATCATAATGACTGCTTAAGGACCATCTAGCTTTTCTCACAGGAATACACAGCATTTTTAAATATTATGCATGTTTTCAATATTATTTACGTAATAATAACACTTTTTGTCAACAATAAAAGAACATTAATAAATACAACCATTTAAATGAATTTAAAAATGTAAAAATAAATTAAATTTCACAGTATTACTGTTTTTAGTGTTAATGTATCGGCCAATAATCGGTATCAGCTTATTGCTAAAAATCAGCCAACTATAAGGTTAAATTATATTCTCAATCAAAATAAGGCAGGAAAAATGCTAATTTGTATAA
Associated Phenotype:
Not determined