ZMP
B0S6Y4_DANRE
Ensembl ID:
Description:
Novel protein similar to human and mouse stereocilin (STRC) [Source:UniProtKB/TrEMBL;Acc:B0S6Y4]
Human Orthologue:
STRC
Human Description:
stereocilin [Source:HGNC Symbol;Acc:16035]
Mouse Orthologue:
Strc
Mouse Description:
stereocilin Gene [Source:MGI Symbol;Acc:MGI:2153816]
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12839 | Nonsense | Available for shipment | Available now |
sa14630 | Essential Splice Site | Available for shipment | Available now |
sa20874 | Nonsense | Available for shipment | Available now |
sa12801 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12839
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110410 | Nonsense | 19 | 1679 | 1 | 31 |
ENSDART00000111423 | None | None | 1622 | None | 34 |
Genomic Location (Zv9):
Chromosome 7 (position 14800199)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13681212 |
GRCz11 | 7 | 13925074 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAYTGACAGGAACAGACTCTCAGGATTTCTGTACAACATCTCCATGTACT[T/A]ACAGGAGATGAGCGCCGAGTTAGATGATGGCCAGGGTTTTAGTGACRACC
Long Flanking Sequence:
GCCTCTTTAGCATTTCCAAAACGCTCCATTTTCGGGGCTCGAAAACTCTGGGGTAGTGTGGATGGAAGCTGTTCCTGTAACAAATCTTTAAATCTAAAATGTATTAGTGTAAATGGGGCCTAAGTTTACCCAACTATGACGATGTCTGAGAAACTCAGAAATGTAAAAAAGGGTGCATACAGGCTGTTTGTGTGCCATTCCCTGCTATGACAACTAAATTAGTTTGTTTGTCTGTACAGGAAGCAAAAAAGAAGACCAAAGGGAGGCTATATTAAAAGAGCTTGTCGAGATTTGGAGGAAAGGTGGAGGATGGAACCCATACCGAGTACAGCCGCCAGCAGAAAGACGAAAAGATCAACAAATCCAATCCATCGTGAAGGGCATCATGGGAGGCCTCAAATCCCTCGGAGTCCTGCCGAAGAAAAAAAGCATCCCATCTATAAACAAATCCATTGACAGGAACAGACTCTCAGGATTTCTGTACAACATCTCCATGTACT[T/A]ACAGGAGATGAGCGCCGAGTTAGATGATGGCCAGGGTTTTAGTGACGACCAGTTTTGGGAGAACCTTCTCTATTCTCTCCTCCAGACCGGAAGGGAAGCCTCGCTTGGCATGTGGGATGGGAAAAGTCCCCCGCGACCCACTTTTAGGCTTCAGGATCTGTTCCTGTCTCTTAGGGGAAGCCCACATTGGGATGGACTTCTAGGTTTGGTGCAAAGCCTTTTAACCCTCTCCGAAAAGCAGCCCCAGAAGCCCATTTTAACTTTTATTTCGCAGAATTGGAAAACCATCAGTGCTTTGCTGGAAACGGTCCTCCAGGCGGTGGTCAGCGGGACGTACGGACAAGCTGTCGCAGGTCTCCAGGGTTTCATATGCGTCTTGAAAGGACGGAATGATTGCTCTTTTAACCTGAGCTGGCTTGAGCAGCTTATAAGCTTCATGGAGACCAGAAACTGGAAACCTGTGGTCAGTCTTCATCCTGTGAATGTGGAGAGCCATCAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14630
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110410 | Essential Splice Site | 1203 | 1679 | 20 | 31 |
ENSDART00000111423 | Essential Splice Site | 1146 | 1622 | 23 | 34 |
Genomic Location (Zv9):
Chromosome 7 (position 14832881)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13713894 |
GRCz11 | 7 | 13958685 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGATATTGATCTRAACGACTTGGACCCCTCATTTGCTGCAAGCTTACC[G/A]TGAGATCAATTCTGTGCTACCCACAATCCTTTTGTTTGTTTTGCTCTTCT
Long Flanking Sequence:
TTACTTAAGTATGATTTTTCAGTACTCTTTCCACCACTGCTGTTGAACAATAAAAAAGTTGAATTATAAAAATTAAAAAAATCAAGGCATGATCATATTTTATTTTGGTAAAATAAGCGTAATCTAGAGGCCTTTGCCTTTCATTTAAGCCACTTCTGATGCCAAATGATCAACTAGAAGTCAAGTTATTATTTGTTGCTCCTAAAACTTAAATAGGCGACAAGACTTTTGTCAGGTAGTATAGGTGTGAAGTCTGTCTAATCTATTAGACATCTATTAAACACAAAATTGTTTGGTGGAGAAATAATGTTTCATTATTAAAATGCATGTCTCACCTACTAAAAAATCCCTTTTGGTGTCTCTGCATCAAACATGCAACGACATTTTATGATTCCATCAAATTTTATGTTTCCACAGAGGAAATGCATTGTGTTGGAGTTACAGCAACAGCCTGATATTGATCTGAACGACTTGGACCCCTCATTTGCTGCAAGCTTACC[G/A]TGAGATCAATTCTGTGCTACCCACAATCCTTTTGTTTGTTTTGCTCTTCTTCTTACTTGCAGGGACTTATTGTTGTATTTGGTCTCAAAGGTTGACCATGATGGAGCACCTGTCTAACTCCTCACTCATAGGCGTACTGGAGCATGTTCGACAACACTTCATTGACTTCCTGCAGCTTCCACGACACAAACAAACGGCTCTGGCAGAGAAAGCTATTGACGTACTCGTAAGACTGGAATTATTGCAGATCTTCAACATTTCATCACTGAATCCTTTATGAGCACATTGGATATAAATACAGTGGAAACAGTAGCTTTGTGAAATGTTACTACAATATAAAACTTTTAACAGGGTATAATAGTTGAAACATTTTGGAGTACCATGGTATTTTTAAGCTTGTACCAGACATAGACATATTATTTCTTTTCTGTTTAATATGTTATACATTAAAATGTTTCTATAAAAGCAGCCATTACGTTGCTTTTTAGTGTCACATTCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20874
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 |
---|---|---|---|---|---|
ENSDART00000110410 | Nonsense | 1234 | 1679 | 21 | 31 |
ENSDART00000111423 | Nonsense | 1177 | 1622 | 24 | 34 |
Genomic Location (Zv9):
Chromosome 7 (position 14833063)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13714076 |
GRCz11 | 7 | 13958867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTACTGGAGCATGTTCGACAACACTTCATTGACTTCCTGCAGCTTCCA[C/T]GACACAAACAAACGGCTCTGGCAGAGAAAGCTATTGACGTACTCGTAAGA
Long Flanking Sequence:
AAGTTATTATTTGTTGCTCCTAAAACTTAAATAGGCGACAAGACTTTTGTCAGGTAGTATAGGTGTGAAGTCTGTCTAATCTATTAGACATCTATTAAACACAAAATTGTTTGGTGGAGAAATAATGTTTCATTATTAAAATGCATGTCTCACCTACTAAAAAATCCCTTTTGGTGTCTCTGCATCAAACATGCAACGACATTTTATGATTCCATCAAATTTTATGTTTCCACAGAGGAAATGCATTGTGTTGGAGTTACAGCAACAGCCTGATATTGATCTGAACGACTTGGACCCCTCATTTGCTGCAAGCTTACCGTGAGATCAATTCTGTGCTACCCACAATCCTTTTGTTTGTTTTGCTCTTCTTCTTACTTGCAGGGACTTATTGTTGTATTTGGTCTCAAAGGTTGACCATGATGGAGCACCTGTCTAACTCCTCACTCATAGGCGTACTGGAGCATGTTCGACAACACTTCATTGACTTCCTGCAGCTTCCA[C/T]GACACAAACAAACGGCTCTGGCAGAGAAAGCTATTGACGTACTCGTAAGACTGGAATTATTGCAGATCTTCAACATTTCATCACTGAATCCTTTATGAGCACATTGGATATAAATACAGTGGAAACAGTAGCTTTGTGAAATGTTACTACAATATAAAACTTTTAACAGGGTATAATAGTTGAAACATTTTGGAGTACCATGGTATTTTTAAGCTTGTACCAGACATAGACATATTATTTCTTTTCTGTTTAATATGTTATACATTAAAATGTTTCTATAAAAGCAGCCATTACGTTGCTTTTTAGTGTCACATTCACAAAACTTACTGATTTTATGTTAAGGTAAACATTTCACAACATACTAAAAATATTAGGTTGAGTTGCTTAATATTGTTTTTGTGGAAACTGCTTTAAAAAATGTTGAAATAACAGCAAATATTTTGTAAAAAACACATGTTTGCTCTCAGTTCAACTTGATGATCAAAAGCATGTCACAAATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12801
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000110410 | Essential Splice Site | 1390 | 1679 | 24 | 31 |
ENSDART00000111423 | Essential Splice Site | 1333 | 1622 | 27 | 34 |
Genomic Location (Zv9):
Chromosome 7 (position 14838540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 13719553 |
GRCz11 | 7 | 13964344 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAGGGATTACGAGAAAAGAKGAACGTCCTCATCCACAGGATCATTAAAG[G/T]TCGATGGTGGATGAGACRSGGTGAGTCGTGTTCTGTGTTCATTCACAGAA
Long Flanking Sequence:
ATTGTTTGTTTAACACTCATACTGCCATTTCTGACAGTCCAAACTCACAGATTTAAAAATGCTTTGTGCTAAGCATGACCCATCTTGTGCTATCCTGTTTTTTGGATTGTTTAAATGTCGTTACACTATATGTTGCATTCATATCTCAGTTAAGTTCATTTAGACATCTTTTTAGTTGTTTTGGACCGCTCATTTGGTACACTCCAGGTTTTGGATGGCAGCGTTTATACGTATTCATACAACCTACACTAATAAAGCCATCGCACAAAAGTTTGTTTTAGTCAAACCTGCCAAGTGTGAACACAACCTAACACCAAAGGCTCAGTATATCATCACGTTAAACCTACATTTTCCCTTCAAGGGTGATTTAGGTAAAGACACGGTTGAGCAGGTTCTGATGAGCCAGTGGATTTGGAAAAACAGCGAACTGGGAGAAGCTTGCTGGGACTTAAAGGGATTACGAGAAAAGATGAACGTCCTCATCCACAGGATCATTAAAG[G/T]TCGATGGTGGATGAGACGCGGTGAGTCGTGTTCTGTGTTCATTCACAGAATCCCTCAGATGTTCCCTTTAGAGAGGTACTGTAAACCAGTGGTTCTCATTTCTGGTCATTGCGACCCCTCGCTCTGCTCCCTTTAAGGCAAGTCATTTCACTCGATAGCCATCTTTGAAACATCTCTCGGTCTCAAACACAACATTGTGTTTGAATGGGGAAACATCAAATTCTCCAAAATTTCTTGCTAAGCTAATGATTAAATATCATATTAGAATCACCAATACAATTAAAAACAACTTTAGTTTAATTTTTAAACATTCGAATCACACAAAATCTGCAGAAACTCACGTCTGGTCTGATCCTCTCCTGCAGAGAATCGTCAGACTATAACAATCGATGATTGGCTGCTGTTGTTCATTCGCCATATTGACCGTTACTATTTTTCCTATTCAAAAGTATACAAGTGACATGTCTTGTGTATTCTATAGTCTTTGACATTATGCATGT
Associated Phenotype:
Not determined