ZMP
gpa33
Ensembl ID:
ZFIN ID:
Human Orthologues:
C1orf204, GPA33
Human Descriptions:
chromosome 1 open reading frame 204 [Source:HGNC Symbol;Acc:27647]
glycoprotein A33 (transmembrane) [Source:HGNC Symbol;Acc:4445]
glycoprotein A33 (transmembrane) [Source:HGNC Symbol;Acc:4445]
Mouse Orthologue:
Gpa33
Mouse Description:
glycoprotein A33 (transmembrane) Gene [Source:MGI Symbol;Acc:MGI:1891703]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7199 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14242 | Nonsense | Available for shipment | Available now |
sa41469 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10979 | Nonsense | Available for shipment | Available now |
sa15629 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7199
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059939 | Nonsense | 118 | 484 | 3 | 7 |
ENSDART00000137806 | Nonsense | 47 | 164 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 35279279)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34498790 |
GRCz11 | 9 | 34307975 |
KASP Assay ID:
554-4781.1 (used for ordering genotyping assays)
KASP Sequence:
CCACAAAAACATCAACGCTAACAATAAAGCAAGTCACTCAGAAGGWAAGC[A/T]GAAAAATTAGATGTTATGTTCAGATCCCTGGAGACATCGAAGGCAAACCA
Long Flanking Sequence:
GGTTCAGAAAGTTCTCAAAGTGTAATTTTATCCTACATTTTTTAAAAGAAAAATGAAGGTGTAGGTTATACAGGTGGTTGTTAAATGCAGAGCATCTCTATAAAAAAACTGCTGCAAATCTGAAAGGGATCAAACCTCAGGTAGGTAAAAAAAAGTAATGCAAAAGTAACTCAAAAGTAAAATAACGCATTAATTTCCATAAAACGCAATTAGTTACTTTTTTGGCTAAGTAACTCAATATTGTAATGCATTACTTTCAAAAGTAACTTCCCCCAACACTGTCATATGAATCATGTCAATAATAAAAAAATTAAAAAAAACAATCACAGAGCCTTTAAATGCTTTTGTTTTTGACCTTGCAGGTCCTTTTTGGTAACTACTACTCCAATACTAATAAAGTAGACATTGATCCTCAATATGTAAACAGAGTCTCAATAGAAACAGACCTTACCACAAAAACATCAACGCTAACAATAAAGCAAGTCACTCAGAAGGAAAGC[A/T]GAAAAATTAGATGTTATGTTCAGATCCCTGGAGACATCGAAGGCAAACCAGCAGACACTACTTTTCTTTTGGTTCAGGGTAAGATCTGTGGCCCTTTGTCAAACATAATTTGTGACCCTAAATCACAAAATCAGTCATACGTGTCTAGAAGATTATACACCATTCAAAAGCTGAATAAATAGGCTTTCTGTTGATGTTTGTTGAGATATAGCACAACATTTGCCCAATATACTATTTGAAACTTGGATCTGGGCATTCAAAAATTTAAGATCTGATGTATTTACGGTGGGAAATTCACTAAATGTCTTCACTGTCTTTTTTCGACTAGTATCATTTTGGCTCTTAATATAACCGTTAATATAACCCACAACTATAAACCAATAAGATTGGTTTTGTGGTCCAGGGTCACAAAATCCTAAATATACTCCTACAGAAATAGTATAATCATTTAATCTATAATGAATGTTATTTGTCCTACAGTTGCACCATCACAGCCTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14242
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059939 | Nonsense | 121 | 484 | 3 | 7 |
ENSDART00000137806 | Nonsense | 50 | 164 | 1 | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 35279270)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34498781 |
GRCz11 | 9 | 34307966 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATCAACGCTAACAATAAAGCAAGTCACTCAGAAGGWAAGCWGAAAAATT[A/T]GATGTTATGTTCAGATCCCTGGAGACATCGAAGGCAAACCAGCAGACACT
Long Flanking Sequence:
AGTTCTCAAAGTGTAATTTTATCCTACATTTTTTAAAAGAAAAATGAAGGTGTAGGTTATACAGGTGGTTGTTAAATGCAGAGCATCTCTATAAAAAAACTGCTGCAAATCTGAAAGGGATCAAACCTCAGGTAGGTAAAAAAAAGTAATGCAAAAGTAACTCAAAAGTAAAATAACGCATTAATTTCCATAAAACGCAATTAGTTACTTTTTTGGCTAAGTAACTCAATATTGTAATGCATTACTTTCAAAAGTAACTTCCCCCAACACTGTCATATGAATCATGTCAATAATAAAAAAATTAAAAAAAACAATCACAGAGCCTTTAAATGCTTTTGTTTTTGACCTTGCAGGTCCTTTTTGGTAACTACTACTCCAATACTAATAAAGTAGACATTGATCCTCAATATGTAAACAGAGTCTCAATAGAAACAGACCTTACCACAAAAACATCAACGCTAACAATAAAGCAAGTCACTCAGAAGGAAAGCAGAAAAATT[A/T]GATGTTATGTTCAGATCCCTGGAGACATCGAAGGCAAACCAGCAGACACTACTTTTCTTTTGGTTCAGGGTAAGATCTGTGGCCCTTTGTCAAACATAATTTGTGACCCTAAATCACAAAATCAGTCATACGTGTCTAGAAGATTATACACCATTCAAAAGCTGAATAAATAGGCTTTCTGTTGATGTTTGTTGAGATATAGCACAACATTTGCCCAATATACTATTTGAAACTTGGATCTGGGCATTCAAAAATTTAAGATCTGATGTATTTACGGTGGGAAATTCACTAAATGTCTTCACTGTCTTTTTTCGACTAGTATCATTTTGGCTCTTAATATAACCGTTAATATAACCCACAACTATAAACCAATAAGATTGGTTTTGTGGTCCAGGGTCACAAAATCCTAAATATACTCCTACAGAAATAGTATAATCATTTAATCTATAATGAATGTTATTTGTCCTACAGTTGCACCATCACAGCCTGTCTGTAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41469
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 |
---|---|---|---|---|---|
ENSDART00000059939 | Nonsense | 315 | 484 | 7 | 7 |
ENSDART00000137806 | None | None | 164 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 35274493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34494004 |
GRCz11 | 9 | 34303189 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGGAACACAGACACCATAGCAATCACTGACGAGAGAACTGGCAAGGCC[C/T]GAAATGATGATTTTGAAGATCGGTATGATGACAGTGGAAGTGGCCGTGAC
Long Flanking Sequence:
TGCGGTGCTTCTAATAGTCATCATCTGCTGCTGCCGCAAACGCAAACAAAAACAGAAGCTTAAAGAGTACCAAATGGAGTAGGTCACCATTTATATTCTTAAAGTAACAGTTGAATTGATTGTCGATTTTTGCAGGCTATGTTCTATATCAGGGGTGCTCAACCCTGTTTCTGGAGATCTACCTTGCTGCAGAGTTGATCTCCAACCCTTATTAAACATACCTGAACTTATTAATTAGGACCTGAACAGCACTTAATAATTACAGACAGGTGTGTTTGATATGGGTTGCAACTAAAATCTGCAGGAAGGTAAATTTCCAGGAATATTTTGGTCACCCCTGTTCAAGATTAAAAAAAATATATATGTATATATATTTTATATATTTTATTTATTACCTCAGAAAACCTGCAGTGGAATACCATGACAATTCACCTCTAGAAAATATTGACGAAAGGAACACAGACACCATAGCAATCACTGACGAGAGAACTGGCAAGGCC[C/T]GAAATGATGATTTTGAAGATCGGTATGATGACAGTGGAAGTGGCCGTGACGACTTCAGAGGCCGTGAAAATCACAAAGGAAGCCGCGATGAACTCAGAGATCACAATGATGATCGCAGAGGAAGCCGTGATGAACTGAGAGATCGATACGAGGATCGAAGAGGAAGTCGTGATGAACTTAGAGATCGCTACGAGGATCGCAAAGGAAGTCGTGATGAACTTAGAGATCGCTATGAGGATCGCAGAGGAAGTCGCGATGAACTTAGAGATCGCTACGAGGATCGGAGGGGAAGTCGTGATGAACTTAGAGATCGATATGAAGATCGCAGGGGAAGTCGTGATGAACTAAGAGAACGCTATGATGACCGCAGAGATCAATATGATGACCGTAGAGATCATTATGATGATCGTAGAGGTAGTCGTGATGATCTTAGAGATCGGTATGATGACAGAAGAGAACGGTATGATGACCGAAAAGGTAGTCGTGATGACCTTAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10979
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059939 | Nonsense | 375 | 484 | 7 | 7 |
ENSDART00000137806 | None | None | 164 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 35274313)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34493824 |
GRCz11 | 9 | 34303009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAACTGARAGATCGATACGAGGATCGAAGAGGAAGTCGTGATGAACTT[A/T]GAGATYGCTAYGAGGATCGCARAGGAAGTCGTGATGAACTTAGAGATCGC
Long Flanking Sequence:
ACCTTGCTGCAGAGTTGATCTCCAACCCTTATTAAACATACCTGAACTTATTAATTAGGACCTGAACAGCACTTAATAATTACAGACAGGTGTGTTTGATATGGGTTGCAACTAAAATCTGCAGGAAGGTAAATTTCCAGGAATATTTTGGTCACCCCTGTTCAAGATTAAAAAAAATATATATGTATATATATTTTATATATTTTATTTATTACCTCAGAAAACCTGCAGTGGAATACCATGACAATTCACCTCTAGAAAATATTGACGAAAGGAACACAGACACCATAGCAATCACTGACGAGAGAACTGGCAAGGCCCGAAATGATGATTTTGAAGATCGGTATGATGACAGTGGAAGTGGCCGTGACGACTTCAGAGGCCGTGAAAATCACAAAGGAAGCCGCGATGAACTCAGAGATCACAATGATGATCGCAGAGGAAGCCGTGATGAACTGAGAGATCGATACGAGGATCGAAGAGGAAGTCGTGATGAACTT[A/T]GAGATCGCTACGAGGATCGCAAAGGAAGTCGTGATGAACTTAGAGATCGCTATGAGGATCGCAGAGGAAGTCGCGATGAACTTAGAGATCGCTACGAGGATCGGAGGGGAAGTCGTGATGAACTTAGAGATCGATATGAAGATCGCAGGGGAAGTCGTGATGAACTAAGAGAACGCTATGATGACCGCAGAGATCAATATGATGACCGTAGAGATCATTATGATGATCGTAGAGGTAGTCGTGATGATCTTAGAGATCGGTATGATGACAGAAGAGAACGGTATGATGACCGAAAAGGTAGTCGTGATGACCTTAGAGATCGCTACAGATAAAATCATTCAGATCAATATAAAAATCAACACCTCTGATAGCACACGTACATCAAGACTTCAGTCTGATATTTGTGTTTTTATCTGAAGGACGTATTTATTAGAGAGTTTGCTCATCTGCAAAACATCTATTAGATGACTATTTTTAGATGTTAAATAAACATTTTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15629
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000059939 | Nonsense | 445 | 484 | 7 | 7 |
ENSDART00000137806 | None | None | 164 | None | 3 |
Genomic Location (Zv9):
Chromosome 9 (position 35274103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 34493614 |
GRCz11 | 9 | 34302799 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATGAACTAAGAGAACGCTATGATGACCGCAGAGATCAATATGATGACCGT[A/T]GAGATCWTTATGATGATCGTAGAGGTAGTCGTGATGATCTTAGAGATCGK
Long Flanking Sequence:
ATTACCTCAGAAAACCTGCAGTGGAATACCATGACAATTCACCTCTAGAAAATATTGACGAAAGGAACACAGACACCATAGCAATCACTGACGAGAGAACTGGCAAGGCCCGAAATGATGATTTTGAAGATCGGTATGATGACAGTGGAAGTGGCCGTGACGACTTCAGAGGCCGTGAAAATCACAAAGGAAGCCGCGATGAACTCAGAGATCACAATGATGATCGCAGAGGAAGCCGTGATGAACTGAGAGATCGATACGAGGATCGAAGAGGAAGTCGTGATGAACTTAGAGATCGCTACGAGGATCGCAAAGGAAGTCGTGATGAACTTAGAGATCGCTATGAGGATCGCAGAGGAAGTCGCGATGAACTTAGAGATCGCTACGAGGATCGGAGGGGAAGTCGTGATGAACTTAGAGATCGATATGAAGATCGCAGGGGAAGTCGTGATGAACTAAGAGAACGCTATGATGACCGCAGAGATCAATATGATGACCGT[A/T]GAGATCATTATGATGATCGTAGAGGTAGTCGTGATGATCTTAGAGATCGGTATGATGACAGAAGAGAACGGTATGATGACCGAAAAGGTAGTCGTGATGACCTTAGAGATCGCTACAGATAAAATCATTCAGATCAATATAAAAATCAACACCTCTGATAGCACACGTACATCAAGACTTCAGTCTGATATTTGTGTTTTTATCTGAAGGACGTATTTATTAGAGAGTTTGCTCATCTGCAAAACATCTATTAGATGACTATTTTTAGATGTTAAATAAACATTTTAAAAATATTTTAAATTTAGAGTCTTCTACTAGCAGGCGTTTTAAAGACATATTAGATCTTTGAACACTGCAGATTAGGGCTGCACAATGTATTGTTTGAGCATCGATATCCTAATGTGCACATCTGCAATAGTCACATCGCAGGATCTCCATTGTAGAATTAGAATTATAGTTGAATAGGAGGTCAAAACACACATGATTGTGGAGTAATTGCT
Associated Phenotype:
Not determined