ZMP
KIAA1267 (2 of 2)
Ensembl ID:
Description:
KIAA1267 [Source:HGNC Symbol;Acc:24565]
Human Orthologue:
KIAA1267
Human Description:
KIAA1267 [Source:HGNC Symbol;Acc:24565]
Mouse Orthologue:
1700081L11Rik
Mouse Description:
RIKEN cDNA 1700081L11 gene Gene [Source:MGI Symbol;Acc:MGI:1923969]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35197 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22010 | Essential Splice Site | Available for shipment | Available now |
sa41949 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27868 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35197
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128145 | Nonsense | 99 | 998 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5288633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4655631 |
GRCz11 | 12 | 4690643 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCATCTCTGGGCAAGCTGGCACCTTACTTGTGCTCTGATGTCAAACCAT[T/A]GCCCTCATCCACCAAAGTCAAGGAGTCGCTGAAGCTGCAAGGTGTCCTCA
Long Flanking Sequence:
TGAAATGAAATGTACTTGTTCTCTGCAGAACATTATTAAAAGTTAATTAAAATCAGTATAGTGATGAAACATGTTTACAAATGTTCTGATTATCCGCGGTCTCCTAAATCTTGTTTTTTTTTTTGTGCTGTGTAGCCAGGCTGTGTAGGTGGGCTGGAGTGAAGGATTAGAGGTGCAGGCTGCCGTGCCCCTTCCCTGGCCCTGCATGGCTGCGATGGCGCCCGCTCTGACTGACGCCCCAGCCGAAGCCCGCCACATCCGCTTCAAACTCGCCTCTCCCTCGTCCACCCTGTCCCCCGGCAGCACAGAGAACAACAGCAACGCCAGCAACATCCTCATCTCAGACTCCGTCTCGGACTCCGCCGGAAGCCACAGCAACGGCAAGTGTCACATCAATTCCAACGACACCCATTACCACAGCGTCAAGGATCAGGATCCCCTGTCTAAAGCCCCATCTCTGGGCAAGCTGGCACCTTACTTGTGCTCTGATGTCAAACCAT[T/A]GCCCTCATCCACCAAAGTCAAGGAGTCGCTGAAGCTGCAAGGTGTCCTCATTAAGCAGTCAGTGCTAAAGAGCCACGGCCTGTTAAGCGGCTCCATATTTCCAAGCGCTGCTGCAGGCGGAGACTTTCTTCTGCGCAAGCGTCACCATCTTGAGCTGACTGGAGGTCAACTGAAGAGCCTGGTCAACGGTGGCGGAGCTGGGAGTACCATGGTGCCTGTGAACGGACTCTCCAAGAAAGTGGCTGTGCCTAGAGCTGCGGTGGCGGAGAAAGGTAGCGTCGCCACAGTCAATGGAGACAGCAACCAACCATCCACCAACGGGGAAGCTTTGCTATCCGTGTCCTCAAAGTCAAAGTCTGGACAGAATGGAGATGTGAAGCCACAACAGAATTCGACACCGAGCATTCAAGGTGTGTCATCACACAGGGAGCTTACTGCTTTGACTGAAAGTGCAGAGGTCAAAGCAGAACCAGGGACTCCTGTTGGTGGACTGCGCATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22010
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128145 | Essential Splice Site | 549 | 998 | 3 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5269274)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4674990 |
GRCz11 | 12 | 4710002 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTCTCGCTTGACGGACGCATCTGAGAACATTGTCTCCATTAGGTTCTGA[T/A]CAGTTTAATTATTTCAATGAATGTTGTTGTGTTTTAGTATTTAAAGAGAT
Long Flanking Sequence:
TTAACTGTCGTCACAGCCAGTTTCTGCCGGCAGATATAAACATGGCTAACCCTCTAATGACTCTCCTAGTTAACTAAACAACTGAAACGTGTCTAACTGGATTGTTCTCTTTTCTCTCTCTCAGATGGAGGAGAGCAGAAGGCCGGTTTGCCCGGGAAAGAGCCACCATCATCAGTCACTGGACGTGGCTGCAGGCGCAGATATCAGACCTGGAGTACCGCATCCGGCAGCAGGTCGACATCTACCGCCAGCTCCGCACCGGAAAGGTTAGCGCCCTTACTTTATCTGCAGTTTCGCAGAAATAACCGTTCATTTTGCTGTGTGTTAACTTTTGTTTTGCATGTTTTCCACAGGGTCCAGTGGAGCTGGGAGACTCCGCCCCTTCCTGCAAGACAGAGACTAATGAGAATATCCTGACCTCAACAACATCCCAGAATTTCTCTGAATCGCAGTCTCGCTTGACGGACGCATCTGAGAACATTGTCTCCATTAGGTTCTGA[T/A]CAGTTTAATTATTTCAATGAATGTTGTTGTGTTTTAGTATTTAAAGAGATAGTTCAGCCAACAGTGGTTCTAAACCTTTATGAGTTTCTTTATTCGGATGAACTCTAAAGAATAGATGTGTGAACCTATATTGGTCTCACGGTTCGGTTACGATTATCATGCCATCGATTCGGTGCAATTCGATTTCTTGGTGCATTACGGTGCATTGACAATGCTTTCCATACATTCCATTTAGGGGGAGGCTGAATCAAGCCGTCTGTATAACTACACAGACATACAGCACCACACTGTCTCTCATTCACACACGTACACAAACAAGGACAGCACCAAACAAACAAACAAACACACACACACACTTAAGCCCTCGCAATATGCGTTTAGCTGGGAGAGTTTGCACTGAGCGAAGCAAAAAAACAAACAAAAAGAAGCAGCACTTTTCCGACGGTCCCTTACTGAGAGAGCATCGCTCAGCGCAAGCTCTCCCAGCTAAACGCAAGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41949
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128145 | Nonsense | 658 | 998 | 7 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5266317)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4677947 |
GRCz11 | 12 | 4712959 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGTGATGTGTGGCAGCGCTCGATCCCTCCTGAAAGCAGACTCGCCGTA[T/A]GATCGCCCTCTGCTGGAGAGAGTCGCACATCACGACCGCAGTGTCCACCC
Long Flanking Sequence:
TTTTTTTTACAATCCTATTTGCTGAAATACTAAAAGAAAAACTCCACAATTGTGTTATCAAGACTTTCAGAAAAGGGAAAAATAGTGTGAGACTGATAATGGCAGCAAGAACAGAGAATAATGTCAGGTTTACTGTCCTGCCCCCATAGACACTGCATAACAAACACATTGCACAAGCCGTAATTAGTTTTGTTTTTGTAATTTGATGCAAAGATAATATGATGCATACATAAATACATATAAATGTTCATGTGTTTTTTTTAAGATAAAAATATTAAAAACTTTCAAGCATTTAAGATTATTGATGATTGCTAAACACTAAAACAGTGTTGTGAAAAGGCTCCATATCACAGGAGCATGTTTTAGTTGTTGGTTCTAATGTGTGACCTACGTTTTCAGGTTCAGAGAGTGTGTTTCTCTCCTCTGCGAGTGTGTGAGGTCAACAGCTCGTGCGTGATGTGTGGCAGCGCTCGATCCCTCCTGAAAGCAGACTCGCCGTA[T/A]GATCGCCCTCTGCTGGAGAGAGTCGCACATCACGACCGCAGTGTCCACCCCGTTCTGTCCATGCAGTCAGGTGAGAGGAGAGATAACAGCGGTTTTAGAATCAATTCAATTGCAGGTAGTTTTGTACATAATTATTTACATGATTAAAAATAATAGCTTTATAAAGTACAATGTAGTGATGCATTTAAGGAAAGCAAATTAGTTTAAATAACAGCTTAAACTAAAACTTTTGTTAATTGTCATTGAATAAAATGTATCTATATCGTTTATTAATTTCTGTTTAACGGAGAGATGTTTTTTTTCAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATCTGACTAGATATTTTTCAAGACACTTCTATACAAGTTAGTGACATTTAAAAGCTTAACTAGGCTAATTAGGTGAACTAGGCAGGTTAGGGTAATTAGGCAAGTTATTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27868
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000128145 | Essential Splice Site | 749 | 998 | 9 | 15 |
Genomic Location (Zv9):
Chromosome 12 (position 5260365)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 4683899 |
GRCz11 | 12 | 4718911 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATATATATATGTGTGTGAATTGTATTTGTGTTTTTTCCTTTTTTTAAGTA[G/A]CACCGAAAGTGGTGATGGATGCAGGCAGTCCATGTCCGTCTCTGTCCGGT
Long Flanking Sequence:
TCTAAAACTAAAAAATTATTCGCTTCACCAACTGAAATCATGTCACGCTCACCCAAACCGAACCTCTGCAAACACTGCGATAACGTCACATTCACATTATAGTATAAACCAGGCTTAAGATGGCTTTGTAAGTAAAATAAGACAATACAGTTACATGTAATGCTGTCAAAAAATTAGTCACATCCATCAAAGTTTGTAATTACATATTTTATCTTTGTGTGCATTATATTCAAAGATTTTGCATATAAATATAAATAAACAGATTGTCAATATTTATGCATTACAAATGCATACATTAATAATTATTAATGCACATAATAAATAAACAGGTCGCACTACAACCATTATCTGCAGTCGCACTAATGCACCTAAATATATTATAAGGTCGCATAGATTAATTTTCGGGCGCATATGCGACCAAAATGGTCGCAATTTCGAGCCCTGATATATATATATATATGTGTGTGAATTGTATTTGTGTTTTTTCCTTTTTTTAAGTA[G/A]CACCGAAAGTGGTGATGGATGCAGGCAGTCCATGTCCGTCTCTGTCCGGTCTTCACTCTACCAACACCAGTCCTCTGACCAGACAGCTCTCCCTCCCGATCGAGAGCAGCACTCCTCTGGGAAGCAATGTGGTACGTTCATAAGTTCAAAATTTTACTTACTAAACTAATTAGATTGCTGTGTGTTTTATGATATGCTATAATACATTTAAACGTGCATTGTTTTTTATTATTATTTACCATGTATACATAGACATTACGGTAAACATTAGGTCATAAAAATTTACTTGAATGTCCCGGAAAAGTTATGAAAAAATCATGGAATTTTAGTTGTAAAAATGTGCATGAACCCTGTCACAGGCAAATCAATGCTTGTTCATGTGAGTAACAAGAACACATTGTAAACTATCAGAGACGTGATCTCAGAGAATTGCCGAGTAGTTGCTGAGACGTGAGATATTTGGCATGCTAAATATCTGGAGCTGTCAGCGATTCAAATCA
Associated Phenotype:
Not determined