ZMP
zgc:66109
Ensembl ID:
ZFIN ID:
Description:
S-arrestin [Source:RefSeq peptide;Acc:NP_956853]
Human Orthologue:
SAG
Human Description:
S-antigen; retina and pineal gland (arrestin) [Source:HGNC Symbol;Acc:10521]
Mouse Orthologue:
Sag
Mouse Description:
retinal S-antigen Gene [Source:MGI Symbol;Acc:MGI:98227]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11585 | Nonsense | Available for shipment | Available now |
sa7528 | Missense | Mutation detected in F1 DNA | Not yet available |
sa15523 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa11585
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 |
---|---|---|---|---|---|
ENSDART00000025788 | Nonsense | 155 | 392 | 6 | 15 |
ENSDART00000145035 | Nonsense | 155 | 392 | 7 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 5138217)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5583945 |
GRCz11 | 2 | 5495827 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACAGCACTGTGCTGTTGAGTTTGAGGTGAAAGCCTTCTGTGCTGAGAGC[C/T]AGGATGCCAAAGTTCGCAAAYGGTTAGTCTTCATCTTTTTCTAYAACATA
Long Flanking Sequence:
GTCATTTAAGGCTAGTTTATATGGTATTTCTGCATCTAGTGATCAGCGTGACCTCAATAGTATCTAGATACAGCCTTTATGATGAAAGCTGAGATTGCATCGCTCAGAGATGCAATGTCAGACACAATGCACTCAATGGAGCTAGTGATGTCACTGTGAGGGGTGGGGTTAGGTGAGCACATTAAAAAGCATTAGATGCATCTCAGATTGCATCTGCACCAAGTCTGCAGCCAGACCTCTCTCCGTGACCCACGGCCAGGGCCGTGCAGAGACCCTTTGAGGGTAGACTCTGAGTCCTAGGCTATCCAGGTCAGCTGTTTTAGCATTAGCTTTTAGCATAATGATTCCAGGGTAGCCTTAAATAGGCTTTGGTCCTACTCTGACATAATTGTTTCTCTAGTATGCTTGTGATGTACTGTATGACCTCTGTTTTAGTATCTCATCTGTTTTCACAGCACTGTGCTGTTGAGTTTGAGGTGAAAGCCTTCTGTGCTGAGAGC[C/T]AGGATGCCAAAGTTCGCAAACGGTTAGTCTTCATCTTTTTCTATAACATATGAAGGAAACACTGGATAGTGCTATTCTGGGGTCCATTCTTCGTAACTTGCTTAAATGATCTAAGATGATTAGGCAGATCCTGGATCTTTTAATCTTGATAACAGATCTCTGGCTAATTTGGTTCTTCAAACAGGTTCGCGAATCAGATTAAAATGTCTGGATGAACTGATCTGAGATCATTACGTGTATTGTGAAGGACAGATCTATCGATCCCCGAAATCAAGATCAGCAATGGAACGATTGGCTGACGGCATAGCAGCGTAATGACATCATCTGATTAATATTCAATTATCCATGTGAGCTAAATTACATCAAATTAGCAGTAAACGGTTTGTTAAATAGGATAAGCAATAACTTTACACCTTGTTGTGGGCTGTATGGCCCTTTCATGTGTGAAGAGCGATCTCTTTAGTTTTACAGTTAGCTGATTTTCCTTATTATAGTAGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7528
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:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025788 | Missense | 215 | 392 | 8 | 15 |
ENSDART00000145035 | Missense | 215 | 392 | 9 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 5134639)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5580367 |
GRCz11 | 2 | 5492249 |
KASP Assay ID:
554-4299.1 (used for ordering genotyping assays)
KASP Sequence:
ATTATCTTATTTTATTTTTTCCTTGTAGACGTACTATCAYGGAGAACCCA[T/G]CAACRTAAGGGTCAAAATCAATAACCAATCCAACAAAAATGTGAGGAACA
Long Flanking Sequence:
TGGTGGTTCATTCCACTGTGGTTGACCTCTGAAATAGAGACTAAGCCGAAGGAAAATAAATAAATAAAATTTATAAATAACAGTTTTGGTCATTTATTTATTTTCGGTTTAGTCCCTTTATTAATCTGGGGTCGCCACTGCAGAATGAACCGCCAACTTATCAAGCATATTTTTTTTACGCAGCGGATGCCCTTCCAGCTGCAACCCATCACTTGGAATCACACACTCATGCACACACAGTATGGTCAATTTTATCATGCCCAATTCACATAGCGCATGTCTTTGGACTTGTGGGAGCACCAGAGAACACCCACAGCAACATGGGGAGAGCATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGAGGCTCGAACCAGCAACATTTTTGCTGTGAGGCGAACGTGCTACCCACTGCGCCACCACGTCACCCTACAGTTTTTCTTACATTATCTTATTTTATTTTTTCCTTGTAGACGTACTATCACGGAGAACCCA[T/G]CAACGTAAGGGTCAAAATCAATAACCAATCCAACAAAAATGTGAGGAACATCATCCTTTCCGGTGAGTGCATTAACAAATCAGCAGACTAAGGCTATTTTGACTCGTTTAACCAAGTCTTATGTACACCCGGACTGTATATATAACATAAAACACTTGTGATTGTCTGTTATTTAGTGGAACAAAACGCCAACGTGGTGCTGTACTGCAATGACAATTATATGAAGGTGGTGGCCACAGAGGATTCTGGGTAATCAGTTTAGTTCAGTTCATTCATTCATTCAATTTCTTGTCGGCTTAGTCCCTTTATCAATCCAAGGTCGTCACAGCAGAATGAACCGCCAACTTATCCAGCACATTTTTTACACAGCGAATGCCCTTCCAGCCGCAACCCATCTCTGGGAAACATCCACACACATATTCACACACACACTCATACACTACAGACAATTTAGCCTATCCAATTCACCTGTACCGCATGTCTTTGGACTGTGGGGGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15523
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 |
---|---|---|---|---|---|
ENSDART00000025788 | Essential Splice Site | 332 | 392 | 11 | 15 |
ENSDART00000145035 | Essential Splice Site | 332 | 392 | 12 | 16 |
Genomic Location (Zv9):
Chromosome 2 (position 5131778)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 5577506 |
GRCz11 | 2 | 5489388 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGGAATCATGGTGTCTTACAGAGTTGTTGTRAAGCTTATTGTTGGAGGG[T/C]TAGTATTCCCACAACACAATRTAGTCTTCTTATGTATATTCCCACCAAAA
Long Flanking Sequence:
TAGTAAAATAGTATGTACTGTCATCATGGCAAAGATAAAATAAATCAGTTATTACAGATGAGTTATTAAAACTATTATGTTTAGAAATGTGTTGAAAAAAACTGGCTCTCCAATAAACAGAAATTGGGGGGAATATATACAGGAGGGCTAATAATTCTGACTCCAACTGTATAATAATAAGCAGCTATTTTGCCTGCAGGCACTCTGTTGATTCTGGTGCCAAACTGGAGAAAGTCTACACTTTGCTACCCCTGCTGGCCAATAACAGAGAACGCCGAGGAATTGCGCTGGATGGAAAATTAAAGCATGAAGATACTAATCTAGCCTCTTCCAGCATGTGAGTCTTTGTGACCATAAAATGTGAACATTTTAAATAAATCATTGAACAATGGATATTAATTGTGTTATTGCTCCATCGCAGCATTAAAGAAGGCGTTCAGAAGGAAGTTCTGGGAATCATGGTGTCTTACAGAGTTGTTGTGAAGCTTATTGTTGGAGGG[T/C]TAGTATTCCCACAACACAATGTAGTCTTCTTATGTATATTCCCACCAAAAGTCACACATTCATTGTTTGTTTGTTTTTTAATCTAAAGATATCCACACATTTGCAGTTTTCTGTATTTTGTGATTCATGATTTTGTTTTCCCCCATTTATTTATGCTTGTAAATTGCATTATGAGACCTGGATCTATCTTGCAACAACTTTTAAGCTTGAAAAGTAAAAAAAAAAAAAAGACTTTTATTGACATTTTTAATAGTTTAAAGTGATATATTGTTCAATTCAATTCAATTCAGCTTTATTTGTATAGCGCTTTTACAATATAGATTGTGTCAAAGCAGCTTCACATAAATGGTCATAGTAACTGGATCAGTGTAGTTCAGTTTTTAGTGTTTAAGTTCAGTTCAGTTCAGTTTAGCTCAGTTCAGTGTGATTTAATCATTACTGAGAGTCCAAACACTGAAGAGCAAATTCATCGATGCGTAGCTCTACCAATCCTGAACCAT
Associated Phenotype:
Not determined