ZMP
KIAA0802
Ensembl ID:
Description:
KIAA0802 [Source:HGNC Symbol;Acc:29121]
Human Orthologue:
KIAA0802
Human Description:
KIAA0802 [Source:HGNC Symbol;Acc:29121]
Mouse Orthologue:
1110012J17Rik
Mouse Description:
RIKEN cDNA 1110012J17 gene Gene [Source:MGI Symbol;Acc:MGI:1915867]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7534 | Missense, Splice Site | Mutation detected in F1 DNA | Not yet available |
sa19904 | Nonsense | Available for shipment | Available now |
sa15782 | Nonsense | Available for shipment | Available now |
sa33057 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa7534
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:
G > A
Consequence:
Missense, Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130977 | Missense, Splice Site | 315 | 888 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55037293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54720698 |
GRCz11 | 2 | 54445345 |
KASP Assay ID:
554-4009.1 (used for ordering genotyping assays)
KASP Sequence:
CTRACTWTTWAAACAAGGTAATAACATATGTTTTAACAATGTTTTAWTAG[G/A]TGGCCAAAGATGTATCGGTGCGTCTGCACAATGAACTRGAAACRGTGGAA
Long Flanking Sequence:
AAGATTTTTGCCGTTAGCGTAGATGATGTAATCAGATTCCAAAAATCAAATACTTGTAATCAGAGTTTGAAGTTGAATCTACAGTTACTTTTTTATAGATTGTGTATTTGCATAAGGGCAAGAAGTTAATATGATGTTCTATTTTAACTCCTAATGTTGATATTGTTTCCTAATAAACGTTGTTTATACAGTTGAAGTCAACATTATTAGCTCAAATATTTCCCAAAGTATGTTTAATGGAGCAAGGAATTTTTCACAGTATTTTCAATAATATTTTTTCTTCTGGAGAAAATCTGATTTGTTTTATTTCGGCTAGAATAAAAGCAGTTGGGAACTTATTTAAGACCATTTTAAGGTCAATATTATTAGCCCCCTTAATCAATATTATTTTCCGATTGTCTACAGATCAAACCATCATTTTACAATGGCTTGCCTGATTACCCTATCTATCTAACTATTAAAACAAGGTAATAACATATGTTTTAACAATGTTTTATTAG[G/A]TGGCCAAAGATGTATCGGTGCGTCTGCACAATGAACTAGAAACGGTGGAAGACAAGCGAACGCGGGCGGAAGATGAAAACGAGCTGCTCAGGCAAAAGATCATCGAAATCGAGATCTCCAAACAGGCCCTGCATAATGAGCTGGAGAGAGCCAAAGAGGTACTGTACCACAGATCACTGTATTCGAGCAAAAACTTGTTTTTGTGGTAGTAGTGTTGCTATTCTAGATGCTGTGGTGTTATATTTATAGCCATTGCAGGAGCTTTCTGGGTTATTCACAGATGTGTTGTCAACAGTTGTGTTTATAACTGTATATTCTGTTATAACTGCTGATTGCATCTTATGATACTGATATTGGTCAATTGCATTCATGACTATCCTGTTTTTTTTTAACTCGTTTGCATGTAAAGAAGAGTTTTTTAATTTACCGGTAAAGTCGTTCCGGAAATTTTTCTGGATATTTACCGCTATCACTGTGTGAAAGGGGCTATTGTCTCATTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19904
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 |
---|---|---|---|---|---|
ENSDART00000130977 | Nonsense | 460 | 888 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55074710)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54758115 |
GRCz11 | 2 | 54482762 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTGACCGGCGGAGGCCCACACACCACACGCGAAGCTGAGCTACGACTA[C/T]GACTTAAACTAGTAGAAGAAGAAGCAAACATCCTGGGGAGGAAGATTGTG
Long Flanking Sequence:
GAGCGTGCATCGGAAACATTTAACAAAATATACCCCAAGTAACGTATTTCAGATTCGCAAAAATGTAGACAGCGCCCTCTAGTGGATTTGTCATCTGAAACATACAACAAAACAGTATGTTAAGTTTTTGCCAAAAATTGTAGGCTGAAGGACATTTTTTCAAATCAGGCTGGGTTGCAAATTACACACCTTGCAGGACAACACAATATATTACATCATAGTATTTGGCTATTTTTAAAATTCTTGATATCACCTTTAGATTCAATCAAATCTTTTTTCTCCAGGAGGACAGTGCAGATCTGCGCTGTCAGCTACAGTTTGCCAAGGAGGAATCGACTCTCATGCGTAAAAAGATGGCCAAACTTGGCCGCGAGAAGGATGAACTGGAACAAGAATTGCAGAAGTATAAATCAGTGTACGGCGACGTGGACAGCCCTTTGCCTTTAGCGGAGGTGACCGGCGGAGGCCCACACACCACACGCGAAGCTGAGCTACGACTA[C/T]GACTTAAACTAGTAGAAGAAGAAGCAAACATCCTGGGGAGGAAGATTGTGGAGCTGGAAGTTGAAAACCGCGGTCTCAGAGCGGAAAATGAAGACTTGCGTAGTCAATATGAAAGGGATTGCTTTGGCCGTGAACCCTTCTCCAGCGTCCCTACCTCACCGTTTGGCGGCGATGCGCTTGAGTCTGCGAGTGAACTGCGCAGACATTTGCAGTTTGTGGAGGAAGAAGCTGAGCTCCTGCGGCGCTCCATTTCTGAAATCGAAGATCACAACAAACAGCTAACATCCGAGCTCAACCGCTTCAAATTCGGTCCCAATCAATCCGAGCGGGAATCCGAAGGAGCTGAAGGAGGACTCAAAATTGTGAATACCGCAGGTAATGGTTTTTCAAGCAGCACACTTCAGGATGAACTAAAAAACGCAAGACTCCAAGTCAACGAGTTAAGCGGGAAAGTAATGAAGCTTCAATATGAGAATCGGGTGCTAATCTCTAATATGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15782
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 |
---|---|---|---|---|---|
ENSDART00000130977 | Nonsense | 495 | 888 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55074815)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54758220 |
GRCz11 | 2 | 54482867 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGAAGTTGAAAACCGCGGWCTCAGAGCGGAAAAYGAAGACTTGCGTAGT[C/T]AAKATGAAAGGGATTGCTTTGGCCGTGAACCCTTCTCCAGCGTCCCTACC
Long Flanking Sequence:
AACAAAACAGTATGTTAAGTTTTTGCCAAAAATTGTAGGCTGAAGGACATTTTTTCAAATCAGGCTGGGTTGCAAATTACACACCTTGCAGGACAACACAATATATTACATCATAGTATTTGGCTATTTTTAAAATTCTTGATATCACCTTTAGATTCAATCAAATCTTTTTTCTCCAGGAGGACAGTGCAGATCTGCGCTGTCAGCTACAGTTTGCCAAGGAGGAATCGACTCTCATGCGTAAAAAGATGGCCAAACTTGGCCGCGAGAAGGATGAACTGGAACAAGAATTGCAGAAGTATAAATCAGTGTACGGCGACGTGGACAGCCCTTTGCCTTTAGCGGAGGTGACCGGCGGAGGCCCACACACCACACGCGAAGCTGAGCTACGACTACGACTTAAACTAGTAGAAGAAGAAGCAAACATCCTGGGGAGGAAGATTGTGGAGCTGGAAGTTGAAAACCGCGGTCTCAGAGCGGAAAATGAAGACTTGCGTAGT[C/T]AATATGAAAGGGATTGCTTTGGCCGTGAACCCTTCTCCAGCGTCCCTACCTCACCGTTTGGCGGCGATGCGCTTGAGTCTGCGAGTGAACTGCGCAGACATTTGCAGTTTGTGGAGGAAGAAGCTGAGCTCCTGCGGCGCTCCATTTCTGAAATCGAAGATCACAACAAACAGCTAACATCCGAGCTCAACCGCTTCAAATTCGGTCCCAATCAATCCGAGCGGGAATCCGAAGGAGCTGAAGGAGGACTCAAAATTGTGAATACCGCAGGTAATGGTTTTTCAAGCAGCACACTTCAGGATGAACTAAAAAACGCAAGACTCCAAGTCAACGAGTTAAGCGGGAAAGTAATGAAGCTTCAATATGAGAATCGGGTGCTAATCTCTAATATGCAGCGCTGTGATTTGGCCGCACACTTGGGAATGCGTACTGGTAGTCCACGGGATAGTGATGTAGACAGCGACGCTGGCCGAAGGGAACCAGATGAAGATGAAACAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33057
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 |
---|---|---|---|---|---|
ENSDART00000130977 | Nonsense | 796 | 888 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 2 (position 55075718)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 54759123 |
GRCz11 | 2 | 54483770 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTGGACTCCATTAATGCACGCATGAGGACTTTCCGAACCGATCTCCAG[C/T]AATTCATGGATAAAGTGGAGCATCTAGGGGATGGTTTACGGGATCGGGTT
Long Flanking Sequence:
ATTTGGCCGCACACTTGGGAATGCGTACTGGTAGTCCACGGGATAGTGATGTAGACAGCGACGCTGGCCGAAGGGAACCAGATGAAGATGAAACAGCAAGGATATTGCTGCTCCATCCCAAACGTGAAGGTCCTGTTGGCGGAGAGAGCGATTCTGATGATTTATTTGAACGTACGGCTACTTCAGGATTCGCCAGTGGTGAAAAACCTTCAGATTCTGGCGAACTGGGAGTAATCGAATTAGCTCAGCGTAGACGGGAAGACCGGGAAGCGTTTAATAATATCAGAAGGGAAGCTGAGAGGCTCGGGAAAACAGTAGAGCGGCTCATAACGGATACGGATAGTCTTATCCGGGAAGGTCGACTGGTTGTTTTGGGAGGAGATCTTCTTGCGGAGGGTGTGGAATTTAGAGGCGACGGAGACTCAGCTGAATCTAAACAAGACTCTCAGGTGCTGGACTCCATTAATGCACGCATGAGGACTTTCCGAACCGATCTCCAG[C/T]AATTCATGGATAAAGTGGAGCATCTAGGGGATGGTTTACGGGATCGGGTTGATGATCTTTCCCCGATGCCTAACCTCACAGAATCTAGCAGCTTCCTTTCTACGGTTACCTCCATGTCCAGGGATTCGCCAATCGGGACACTGGGAAGGGATCTAGTGACGGACTTCCAGGTAAGAGTTTCATGTTTTTCATCTTAATTCAGTGTTTGCATCATATGCGTTCACGTGACATGGCAACTTCCTTTCTTTTCCTTTGCCGCTTCTTCATTTAAAAGTCCCTTTTTGAGAATGCACTCAGTTATTGATTCTGCATCTTCATGTGCCATATTCTGTCAATCCCCACAAAAAAGTCATGAATGCATCACAATTGAGGCTTTCTAAATAATTTTGGCTGGCATGATACTTCGACTTGATTCATAAATATATATATATATACACAGTTGAAACTAGAAGTTTACATACACTCTAAAAAAGGAACATAACCATTTTTTTTAAATGTCT
Associated Phenotype:
Not determined