ZMP
ch1073-291c23.1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate vitrin (VIT) [Source:UniProtKB/TrEMBL;Acc:B8JMF2]
Human Orthologue:
VIT
Human Description:
vitrin [Source:HGNC Symbol;Acc:12697]
Mouse Orthologue:
Vit
Mouse Description:
vitrin Gene [Source:MGI Symbol;Acc:MGI:1921449]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16980 | Essential Splice Site | Available for shipment | Available now |
sa1300 | Nonsense | Available for shipment | Available now |
sa10205 | Essential Splice Site | Available for shipment | Available now |
sa16108 | Nonsense | Available for shipment | Available now |
sa22187 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16980
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 |
---|---|---|---|---|---|
ENSDART00000093160 | Essential Splice Site | 90 | 770 | 2 | 20 |
ENSDART00000137398 | Essential Splice Site | 113 | 762 | 3 | 19 |
Genomic Location (Zv9):
Chromosome 13 (position 263886)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 243905 |
GRCz11 | 13 | 374196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGCGSTCTCTGTCTTTACCCACCTGGAGAGAGTCCTTCTCYRTCTCAGG[T/C]ACTGTAGACTATTCAGGTTCACTTCWWTAGCACTTTCACAATAGCTATTG
Long Flanking Sequence:
AGAAGCCGCCGCGTTCATTATATTTGGTCTTGGTGTTCTTAAGCGCAGCTCATTTATTAGAGGAGAGCAAACACCCCAGTGGAGAATCCCCACAGTGCAGCACACTCCACTCCTCTCTGCTGTATTTCTGAGCGTGCAGCAGGGCTGAGGAGTTCATGCTCTTGTGTTTCTGGAAATGAATTATTTGCAAGTCTTTTATTTACAGCACACACATCTAATCTGCATCTTTAAATGGAAGTGTTGACTCAGTTGATTAGATTTATCATTAGTTAAATGCAAGGTTAAAAGTTGAGCTGTAGGAGTAATTCAGCTCGTAAACTAACAGATCCCTCCTGTGTGGTGTTGTTCTGTGATTGTGTGGTCAGTGGCGTGATCACCAACTCTGGAGGAAAGGTGATCGTGGCCAAAACAGCAGGACAGGCGATCTACAAGGGCAGCTTCGCCAACGGTGTGCGGTCTCTGTCTTTACCCACCTGGAGAGAGTCCTTCTCCGTCTCAGG[T/C]ACTGTAGACTATTCAGGTTCACTTCAATAGCACTTTCACAATAGCTATTGTTTCAGAGCTGCTTTACAAACGGTGCAGATTATTACATTACACTCACAATCTGAAAAGTTGAGGTTATTAGTTACCATCGACCATTTCAGTGATGTGATCTGCCCATGGACATTTCCTGCTTATTATCAAACTATTTCATAACTGTAACAAGAGGCAAGTCAGTCATAACTGTGTTAAATCAGCTCTCATGACATTATTTATGAATATATGGCTCTTTCTGGATTCTTGTAAATATTAAACATGTACAACAGGAGATACATTGGGAACATTGTTTTCGTTTACATCCCTCAACGTGGTCTATAGCTTTATTAGCAACTAACAACTTCAAATAACTAATAACTAATTACTAATACCTTCATCAGTCAAAGTTATTGTAGTTAATCTGCAGTTATATAGTATATAGGTGATGTCTGTGTACATGTTTAATGGAGTGCATTAGGTGTTCTCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1300
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 |
---|---|---|---|---|---|
ENSDART00000093160 | Nonsense | 300 | 770 | 11 | 20 |
ENSDART00000137398 | Nonsense | 292 | 762 | 10 | 19 |
Genomic Location (Zv9):
Chromosome 13 (position 256350)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 236369 |
GRCz11 | 13 | 366660 |
KASP Assay ID:
554-1215.1 (used for ordering genotyping assays)
KASP Sequence:
TCTCTGTGTTCAGACAGTAGCCAGTCTGTGCCCAACACAGGCTATAAGTG[G/A]AGCCGGACGAGCAGCGGTGACCCCGCAGGTGAGGATCACACACAAATCTG
Long Flanking Sequence:
TTTAACCTTTTATTAAGCAAAAATCATATTTGGTAACTTCATTGACACTGATTACTATATCATTTTAACACCGATTAACACTCCAGGGTGTTCCAATACATTTTTCAGCAGGTGCCCTATAAAGATGAATCTATAATAATGCATCGTTGCATTTATTCTCAAGATCCAGCTCTACTTCAGGCCATTTGATGTCCTTTGGTAATGTATGATCAGCAGTTTCTCAATCTCCCTATCTAGTGTTTGCCAGAAGAGATTGGACGCACCCCTCGTATGCACGACCTGATTGGTTCTCTGGCAGCAGAAGGCCAACAGGTATCAGTGACGTAACTCTGCATAAACCAGCATTAAACAAGACATAAACCAAACCTAAACATGACGAGTAAATATCCATAAACAGATCATAAGTCATGCTAATCATCGTGTCTAAATCTGACATGAGGAAACCCTCACTCTCTGTGTTCAGACAGTAGCCAGTCTGTGCCCAACACAGGCTATAAGTG[G/A]AGCCGGACGAGCAGCGGTGACCCCGCAGGTGAGGATCACACACAAATCTGCTTCACATGTGCATTTCATGTGCAGGTCTGTTCTTGATGATGGAACAGCAGCATATTAATGTACACTGCAGAACATATCCAGCAGTTTCTGTATTTTGTGATTTATATTTGACTTTTCGCCTTTAGTTTATGCTGTGAGTTGCATTGTAGGATCCTTAATCTTTCTTCCTCCAACTTTTAACCTTGAAAAGTGACTTTGATGATCATTTTTAATAGTTTAAAGTGGTATGTTGTCTAAATTGTTATATGTTTTCTACTTATTTCTCTAGATATTATATTTCTTACACAATATATTATTTTAATCCACTAAAATGTCAGTAAAAGTCACTTTGTTAAACTGTAGAGTTGAGTTTTCATCATTAAATGTGGACAGAGCAGAAATCAACATCCCATAATGCAATTCACCACCGCAAATAAACAGAAAACACACAAAGTACAGGAACTGATGAA
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:
sa10205
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 |
---|---|---|---|---|---|
ENSDART00000093160 | Essential Splice Site | 540 | 770 | 18 | 20 |
ENSDART00000137398 | Essential Splice Site | 532 | 762 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 13 (position 247268)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 227287 |
GRCz11 | 13 | 357578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACGACAACGAGAAGCAGAACGTGGTGGAGAGCAACTTTGTTGACAAGG[T/C]ATTGACATGYASGACTGATCCAGCKAGATTACACGRGCTGGATTCACTGG
Long Flanking Sequence:
AGCAGGAGGTGTGTGTTTCCAGCTCTCCTCACTGACGCATTGATCGTTTGTGCAGCTCTGGAAGTGTGTAAGCAGCGACTGAAACAGTACAGTGATTGAGGCTGAACTGAGGCTGTTCTGTGTGTGTGTGTGTGTGTGCGCGTGTGTGTGCGTGTGTGTGTGTCTGTTCTGTGTGTGTGTGTGTGTGTGTGCGCGTGTGTGTGTGTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGTGTGTGTGTGTGTGTGTTTCTGGCTCTGCTCTCTCAGGGAAGGCTCTGTCCTACATCAACAAGCAGTTCTTCAGTGATGCCAATGGGAACCGCGGTGGGGCGCCCAATGTGGCCGTGGTGCTTGTGGACGGCTGGCCTACGGACCGGGTGGAGGAAGCCTCGCGCCTTGCCAGAGAGTCCGGCATCAACATCTTCTTCGTCACTATTGAGGGCCCAGACGACAACGAGAAGCAGAACGTGGTGGAGAGCAACTTTGTTGACAAGG[T/C]ATTGACATGTACGACTGATCCAGCTAGATTACACGAGCTGGATTCACTGGTCAGATACGCTACAAACACTGAGGACACCTGCTGGTTACAAGATGGAAATGCAGACGGAAATGCACAAACTAACAGTAAATAGTATGTTACTATATATATTTACAGTGATAGTTATTGTCGTTGGCATGAACGTCTCTTTAGCTTTCTCAAATAAACAAAAAAATGCCACAAAATTAATTAGGTGAAGAATAGTCAAAATTTAACACGCAAAATGCAGTGGAGTGAAAAAAGTGTTTATTGATGAGTCAAAGAGGTCTTAATCTATATTCATGTTAAATGATGAGTTGTTGTTGTTGTAATATGGTAGTCTGTATGTTTAAGTGTAGAGTTAAAGTGCAATATTATTTAATAATAGTTTTATTAATGAGGAAATTAATGATTGTGAGGAGGAATCTTGATTTGTTGTTTGTGCCCTAGGCGGTGTGCAGGACCAACGGCTTCTTCTCGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16108
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 |
---|---|---|---|---|---|
ENSDART00000093160 | Nonsense | 631 | 770 | 19 | 20 |
ENSDART00000137398 | Nonsense | 623 | 762 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 13 (position 246527)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 226546 |
GRCz11 | 13 | 356837 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CGGGAGTTCGAGATCKCAGACACRGACACCCGWGTGGGCATCGTGCAGTA[C/A]ACSTAYGAGCAGCGGCTGGAGTTCGCTTTCGGACAGCACAACAACAAAGC
Long Flanking Sequence:
TAGTCAAAATTTAACACGCAAAATGCAGTGGAGTGAAAAAAGTGTTTATTGATGAGTCAAAGAGGTCTTAATCTATATTCATGTTAAATGATGAGTTGTTGTTGTTGTAATATGGTAGTCTGTATGTTTAAGTGTAGAGTTAAAGTGCAATATTATTTAATAATAGTTTTATTAATGAGGAAATTAATGATTGTGAGGAGGAATCTTGATTTGTTGTTTGTGCCCTAGGCGGTGTGCAGGACCAACGGCTTCTTCTCGCTCCCCATAGCGAGCTGGTTTGCTCTGCGTAAGGCCGTGCAGCCGCTGGTGAAGCGTGTGTGTGATACCGACCGGCTGGTGTGCAGTAAAACCTGCCTGAACGCCAACGACATCGCCTTCGTCATCGACGGCTCCAGCAGCGTCGGCACCGGAAACTTCCGCACCGTGCTGCAGTTCGTGGCTAACGTGACGCGGGAGTTCGAGATCTCAGACACGGACACCCGAGTGGGCATCGTGCAGTA[C/A]ACGTACGAGCAGCGGCTGGAGTTCGCTTTCGGACAGCACAACAACAAAGCCGACCTGCTGAACGCCATCAAGCGCATAAACTACTGGAGCGGAGGAACCAGCACCGGAGCCGCCATCACCTACGCCGCAGACCAGCTCTTCAGCAAGTCCAAACCCAACAAACGCAAGATCATGATCGTCATCACGGACGGACGCTCCTATGATGATGTGCGGGCCCCGGCGCTGGCCGTGCACCGTACAGGTTAGATTTACTGTCCTGGCCTCATACACACTGCATTACACACACCTCACACAACACTACAATAACACATCCTAGATCTGAATGGATGAAATATTCTTATAAGCTCTTTGTTTTCTGAATAGTTGAACGTGCTGACAACACAACCACACAAAACTCATCAATGGAAATCTAATGTATTAACCCATGGAGGTCTGAATTTGGAGTCACACTCAAAATCCACACTTTAGGCTGATATTGCTGTAACGTAATGTCCTGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22187
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 |
---|---|---|---|---|---|
ENSDART00000093160 | Nonsense | 633 | 770 | 19 | 20 |
ENSDART00000137398 | Nonsense | 625 | 762 | 18 | 19 |
Genomic Location (Zv9):
Chromosome 13 (position 246521)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 226540 |
GRCz11 | 13 | 356831 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCGAGATCTCAGACACGGACACCCGAGTGGGCATCGTGCAGTACACGTA[C/A]GAGCAGCGGCTGGAGTTCGCTTTCGGACAGCACAACAACAAAGCCGACCT
Long Flanking Sequence:
AAATTTAACACGCAAAATGCAGTGGAGTGAAAAAAGTGTTTATTGATGAGTCAAAGAGGTCTTAATCTATATTCATGTTAAATGATGAGTTGTTGTTGTTGTAATATGGTAGTCTGTATGTTTAAGTGTAGAGTTAAAGTGCAATATTATTTAATAATAGTTTTATTAATGAGGAAATTAATGATTGTGAGGAGGAATCTTGATTTGTTGTTTGTGCCCTAGGCGGTGTGCAGGACCAACGGCTTCTTCTCGCTCCCCATAGCGAGCTGGTTTGCTCTGCGTAAGGCCGTGCAGCCGCTGGTGAAGCGTGTGTGTGATACCGACCGGCTGGTGTGCAGTAAAACCTGCCTGAACGCCAACGACATCGCCTTCGTCATCGACGGCTCCAGCAGCGTCGGCACCGGAAACTTCCGCACCGTGCTGCAGTTCGTGGCTAACGTGACGCGGGAGTTCGAGATCTCAGACACGGACACCCGAGTGGGCATCGTGCAGTACACGTA[C/A]GAGCAGCGGCTGGAGTTCGCTTTCGGACAGCACAACAACAAAGCCGACCTGCTGAACGCCATCAAGCGCATAAACTACTGGAGCGGAGGAACCAGCACCGGAGCCGCCATCACCTACGCCGCAGACCAGCTCTTCAGCAAGTCCAAACCCAACAAACGCAAGATCATGATCGTCATCACGGACGGACGCTCCTATGATGATGTGCGGGCCCCGGCGCTGGCCGTGCACCGTACAGGTTAGATTTACTGTCCTGGCCTCATACACACTGCATTACACACACCTCACACAACACTACAATAACACATCCTAGATCTGAATGGATGAAATATTCTTATAAGCTCTTTGTTTTCTGAATAGTTGAACGTGCTGACAACACAACCACACAAAACTCATCAATGGAAATCTAATGTATTAACCCATGGAGGTCTGAATTTGGAGTCACACTCAAAATCCACACTTTAGGCTGATATTGCTGTAACGTAATGTCCTGAAAACAAGTC
Associated Phenotype:
Not determined