ZMP
oca2
Ensembl ID:
ZFIN ID:
Human Orthologue:
OCA2
Human Description:
oculocutaneous albinism II [Source:HGNC Symbol;Acc:8101]
Mouse Orthologue:
Oca2
Mouse Description:
oculocutaneous albinism II Gene [Source:MGI Symbol;Acc:MGI:97454]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9009 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11052 | Nonsense | Available for shipment | Available now |
sa20754 | Essential Splice Site | Available for shipment | Available now |
sa33907 | Essential Splice Site | Available for shipment | Available now |
sa33908 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9009
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087311 | Nonsense | 159 | 807 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 37831991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37903584 |
GRCz11 | 6 | 37880731 |
GRCz11 | 6 | 37890738 |
GRCz11 | 6 | 37901127 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGGTCACCAGTCTCTCACWCATTACATCCCCGGAGAAGAGTGAAAATTA[C/A]TTCAAACTCTCTTTTCCCATCAGGTATGAAATACTGTTTAAAAGATTGTG
Long Flanking Sequence:
GATTATCATCTGCAAAGGTTTAAACTTGTCTGGATTGTGTTCTTTAGCAACACCTCTTGCAAAATGTCTACACCTTCAAACCATCCTGGTCAAATGATTATTTGATTACCTCTGAAATCCATCAAAAGTTGATAAGCTCAAAACATTTGAGAGCTAATTCAGACTTATATTTAGCTTTGTCCACTTATGGACAGATAATTGAAAATGCAGGTTATTACCAGTTTTGAATGGAGCCAATATAGTTTCAAACAGATTTCCAAGGTCAAGCTTGTTCATTTTTCCACTAAACAAATTGTGCTGCACCCAAACTCAGATCATTAGTTAGTGTCTAACTTGTGGTTTTTGTGCAGTATCACCTACATGACTCTGCATGAGCCCAGTCTGGGGTCTGGAGAGGAATCGTGGGAGGCGAGCTCTGCTGAACTGGAGAGAAGGTGCAGGCTGGGCAGTGAGGTCACCAGTCTCTCACACATTACATCCCCGGAGAAGAGTGAAAATTA[C/A]TTCAAACTCTCTTTTCCCATCAGGTATGAAATACTGTTTAAAAGATTGTGGTCAGTAAGTTATTTTTTTTTCTTAAGAAGTGAATACTTTTATTCAACATGGATGCATTACACTGGTCAAATTTGACAGTAAACTTGTTGCAATTACTTTCTATTTAAAAAAAACGATAGTCTTTGCAATTTCTGTTGATCAAAGAGACCTGAAACTTCTTTGATATTTAGTTCAATTCATGTTTATATCTATAGCACTTTTACAATGTAGATTGTGTCATAGTTCAGTTTAGTTCAGTTCAGTGTGGTTTAAATTTCCAAATACCAAATACTGAAGAGCAAATCCACCGATGCGCAGTTTCACAAGTCCCAAACCAAGCAAGCCAGTGGCGACAGTGGTGAGGAACAAAACTTCACCAATTAACAAAAGTGAAGAATATAAAACCTTGAGAGAAACCAGGCTCAGTCGTTTATACAGTTAAAGTCAAAATTATTAGCCCCCTTTTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11052
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 |
---|---|---|---|---|---|
ENSDART00000087311 | Nonsense | 185 | 807 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 37835451)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37907051 |
GRCz11 | 6 | 37904587 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGCCTAGGGATGACAAGACTCATCACCATCTTCGTTATTGTYGTTCTGTG[T/A]TCAGTAAGTTCTCCATWAATCAGACCTAATCAACAAAGTGCTTTAGCGTG
Long Flanking Sequence:
AACTTAAAGATGTTAATAAAAGTCACTTTTTTCTAACATTTTCAAGGTTAAAAGTAAAGAGAGAAATAAAGAGCAAGGTCCCATAATGCAATTCAAAAGCATAAATATATAAAACATGAACCACAAAATGTAAGACATTTCTAATTTATGTATATTATTTATCTGTCTTGTTGTGACTTAAAAACCCTTGCTGTCTACCATTTGATTATAATACAGTGTTTTTTGATTGCTTTCACTGCTTGTCCTTACTAAACCCTGACAATAGTTTTAATGCCAAAAGAGGGTTTGCCCTGGCGCAAGCTGTCATCAAATCTGGCCTCAAAAACCGAGAGCTATAGCTTCATAACTCACAATCAACTCTAAAAGCAACTGTAACTTTTTGGCACATGGCTTTCTTTCTATTGCAAAGTAGATATCACAAAAAGTGTCTGAATTTGCTTTTACAGATATTGCCTAGGGATGACAAGACTCATCACCATCTTCGTTATTGTCGTTCTGTG[T/A]TCAGTAAGTTCTCCATAAATCAGACCTAATCAACAAAGTGCTTTAGCGTGCATTCTATTGTTTTCAGTCATCTGCCTAAGTGACACTCTAAAATAACTCTATTTATCTGAATCATCAGCTGTTTTTCAGCATGTATCCCGACCGGGAGAGCCCCTGGAGGATGCTGGCGGTCTCATCCACCGAGAGCTTCTGTATCCTCCCCATTTGTGTGTCTTAGAGAGTCTGCATTGTTTCTGTTTGCATTGGCTGGATGAATAAGAGTCATTAATGCACAAGTCAAATAGTATGCTGCCACTGTCTAACGCCTCAGACCCTGCGGGGATTTTCTGTTTGGTTGGGAGATTGCACTGAAGGGCTGCACTAATTCATTTCCGTTTCTGTGACAATCTCGCCATCTGTTATTTACAGCGGCTTGTGTCATGGAAACAGTCTTGCTTATGACTCCGTGCATAACAACAGATCTGCCTGATACTTTCGGCAGACTGTGGGTCCTGTAGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20754
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087311 | Essential Splice Site | 186 | 807 | 4 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 37835456)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37907056 |
GRCz11 | 6 | 37904592 |
KASP Assay ID:
2259-7809.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGGATGACAAGACTCATCACCATCTTCGTTATTGTCGTTCTGTGTTCAG[T/G]AAGTTCTCCATAAATCAGACCTAATCAACAAAGTGCTTTAGCGTGCATTC
Long Flanking Sequence:
AAAGATGTTAATAAAAGTCACTTTTTTCTAACATTTTCAAGGTTAAAAGTAAAGAGAGAAATAAAGAGCAAGGTCCCATAATGCAATTCAAAAGCATAAATATATAAAACATGAACCACAAAATGTAAGACATTTCTAATTTATGTATATTATTTATCTGTCTTGTTGTGACTTAAAAACCCTTGCTGTCTACCATTTGATTATAATACAGTGTTTTTTGATTGCTTTCACTGCTTGTCCTTACTAAACCCTGACAATAGTTTTAATGCCAAAAGAGGGTTTGCCCTGGCGCAAGCTGTCATCAAATCTGGCCTCAAAAACCGAGAGCTATAGCTTCATAACTCACAATCAACTCTAAAAGCAACTGTAACTTTTTGGCACATGGCTTTCTTTCTATTGCAAAGTAGATATCACAAAAAGTGTCTGAATTTGCTTTTACAGATATTGCCTAGGGATGACAAGACTCATCACCATCTTCGTTATTGTCGTTCTGTGTTCAG[T/G]AAGTTCTCCATAAATCAGACCTAATCAACAAAGTGCTTTAGCGTGCATTCTATTGTTTTCAGTCATCTGCCTAAGTGACACTCTAAAATAACTCTATTTATCTGAATCATCAGCTGTTTTTCAGCATGTATCCCGACCGGGAGAGCCCCTGGAGGATGCTGGCGGTCTCATCCACCGAGAGCTTCTGTATCCTCCCCATTTGTGTGTCTTAGAGAGTCTGCATTGTTTCTGTTTGCATTGGCTGGATGAATAAGAGTCATTAATGCACAAGTCAAATAGTATGCTGCCACTGTCTAACGCCTCAGACCCTGCGGGGATTTTCTGTTTGGTTGGGAGATTGCACTGAAGGGCTGCACTAATTCATTTCCGTTTCTGTGACAATCTCGCCATCTGTTATTTACAGCGGCTTGTGTCATGGAAACAGTCTTGCTTATGACTCCGTGCATAACAACAGATCTGCCTGATACTTTCGGCAGACTGTGGGTCCTGTAGAGATGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33907
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 |
---|---|---|---|---|---|
ENSDART00000087311 | Essential Splice Site | 690 | 807 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 37924433)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 37996033 |
GRCz11 | 6 | 37993569 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTTTGTTTTTTGGTCTATGGCTTGATTTTTCTCTGTGGTGTGTTTTTAA[G/A]GCTCTCGCTCAGCTGCAGCTCATCGACTACATTGGGGAGCAGACTGCAGT
Long Flanking Sequence:
TTGAATATTTAAAGTGCATTGTCATGAAAGATAAAAAGTTTAACTTCTTATTATAAAATATTCTAATGTTATGTTTATTTTTTTATCTATCCTATTTATAAGTGAAGAAAGAGAAAGGGAGCGACTTAGAGATTAGATTGGAAGTCTAAGTAAGAGGAAAGTGAGCTCGTCAGCAGCAGAAATGCTGGGTTTGCTGTTTGTGTAGGTTTAATCCTTTGTTTTGTTCGCTGGACAGTATTCACACAGGGAAGCCCACCCTTTGGGCCCAGTGGGGAGCTTAACGCTGCTCCAAGATAAACTGTTTGCCCTCTATAGCAGAGCCAGCATTCACAATCACTCAAAGCAGGGTTCAGCGCAAGCACCCAGATATAAAAAATATATATACTTCATGAATTTTGATATTTAAAAGTTTAAAGGATTGAAAATCAGAGCTGTCAGGGTAAATGTCTGTTTTTGTTTTTTGGTCTATGGCTTGATTTTTCTCTGTGGTGTGTTTTTAA[G/A]GCTCTCGCTCAGCTGCAGCTCATCGACTACATTGGGGAGCAGACTGCAGTGTTGATAAAAGTGAGTATTGACTTTGTACCGACTTTAAGGGGAAGTTCACTATTCATTTACTGTTGTTTTGAGTCACTGCAGAAGGTAAACAAATCAGCACAAAACATCTAAATCATGCCATTGATTATAATGCAAACACACAATGGTAATGTGAAGTGCAATGTTACGATGTAGCATTAGCTGTGTTTCTGTTTATATAATAATCACATGGTTGGTTGCATGTTTGCAGTATTAAAAATATTTGGTTACACTGTTTTTGTGATTTTCAATAAACATTTTATTAATAAAAAAAAATCAAAAAGCTCAATTAAGCTACTCACTTGCTGCTAATTAACAGTTAGTAAGATAAGCTGCGGTGCAAAGTTCAAGCATGGTGAACTCTGATCAGCGAAATTGCATCGCATGATTGCGTGAGACCAATAGAGGATCAAAACATATCCTCTCTGTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33908
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087311 | Essential Splice Site | 745 | 807 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 6 (position 37940963)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 38012563 |
GRCz11 | 6 | 38010099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGAGTTCTGAGTTCCTGTGCCTAATGGAATTATATATTTTTCCTCCAC[A/T]GATTCCAGTACTCATAAATCTCAGTCAAGATGCCGATGTCAACTTGCCAA
Long Flanking Sequence:
CCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCAACTATCCATCCATCCATTCATCCTTACATTCCTTACATCCATCTATCCATCTGTCCATCCATCCATCCCTCGTCCGTCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCATCCAATTTAATTTAACTATTTTTCTATCATTTTATCTACAATCGTCTACAATGCAGTCTATCATTCAGCTGGTCAATCTATAGCTCTACCGTTATATTGTTTGATCATTCTATTCCTTTCTATATCATTATATATGTCTTTTTATTGTTCTATCCATCTATCTATTCTTTCATTGTTCTTATGTTCTATAATGCTATCTGTTGACAATAACATTCTGCTATTATTTGAGTTCTGAGTTCCTGTGCCTAATGGAATTATATATTTTTCCTCCAC[A/T]GATTCCAGTACTCATAAATCTCAGTCAAGATGCCGATGTCAACTTGCCAATCAAACCTCTCATATTTGCATTGGCTATGGGAGCATGCCTTGGAGGTCAGTCACATATTTTCTGTATTATAAACGTGTGTAAACATACAAACAAACCTGCCATTATCCAAATCTTGGCTTAAGTGGTTTGATGAACTGGATACTTTAGTACCATTGTAAACTTTCATGCAAATCACAACAAGCCACCACCTAACACTGTTTTATGCTAGTAACTCAGACCTTTGAATTATAAAACAGGTCTCTTTTAATAACATCATGTCACCATTAATAATCTGTAGTTTTTTTCAATGCCACTCACTTCTTCCTCACCCACACTGAAAGCATCACTGAGCACAAATAGATCACGCTACATTTAGGAATGTAGTGTGCTTACAAGGCCATCTGAAAATGCCTCATTGCTTGTTTGGCTCTGAGGACACGGTGAGAAAGATGTGGCAGTGCTGCTGCCTA
Associated Phenotype:
Not determined