ZMP
ENSDARG00000079756
Ensembl ID:
Human Orthologue:
AC087465.1
Human Description:
Tyrosine-protein kinase SgK269 [Source:UniProtKB/Swiss-Prot;Acc:Q9H792]
Mouse Orthologue:
C230081A13Rik
Mouse Description:
RIKEN cDNA C230081A13 gene Gene [Source:MGI Symbol;Acc:MGI:2442366]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32513 | Nonsense | Available for shipment | Available now |
sa44230 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8851 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa24602 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa32513
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 |
---|---|---|---|---|---|
ENSDART00000111151 | Nonsense | 222 | 1725 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 7704860)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7225312 |
GRCz11 | 25 | 7399352 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACGAGTTTCCCTCAGTGACAGCACAGAGGTCATTAGCACTGAGGGTGGA[C/T]GATTCTGCTATCCAGAATTCTCCAGCGATGGTGATGATGAGGAGGAAGAT
Long Flanking Sequence:
GTGCAGGGCAGGTCCGCCCACCTGTCGCCAAGAAACCTACTATTGCCGTAAAGCCTACAATGATGCTGCCATGCTCCCCACCAGGATTGGACTCTGAGGGAAATGTGCCAAGGCTTGCAGAGGGACCACAGGTCACTAAGAGCTCACCTTTTACCGTGTGGAACCACAACAGCCTGAATAGCCTCAGACCTGCAGGGACAAACAACAATCAAGGGGAGGATTTGGTCGGGCAAACAGAGGCATACAGTGCAATCTCCCTGCAGCCAACTAGCAGCAACAACAATGGACTGACAGATGTGCTAAAAGAGATTGCTGGATTGGGATCTTCTCCAAGCACAAGTAGAAATGACTTTTTTGGCAGGATCTGCAGTTCATATCGACGCTCGTTAGAGAGGGGCCTTCCAGCGGCAAGCTGTCTTCATGCTGGAAGTAGCGGAAGAGGAGCGATGAAACGAGTTTCCCTCAGTGACAGCACAGAGGTCATTAGCACTGAGGGTGGA[C/T]GATTCTGCTATCCAGAATTCTCCAGCGATGGTGATGATGAGGAGGAAGATAGTGATGAGGATGATGATGGAGAACATGACAGTTGGGATGAAAGCGACGAAGAGTTGCTAGCAATGGGGATAAGAATGCGGGGTCAACCTCGTTTTGCTAATTTTCGTGCCGCCACTCTGTCCCCAGTTCCTTTTGCTTTAGTGAAAAAGTGGAATACAGTGCCTCTACGTAACCGTTCACTACAGCGTTTCTGTGCAGTCGATTATGATGACAGTTATGATGAGATTCTCAATGGATACCCATCTGTTGACTCAAATGGAGCTCCTGCTCTTCTCTCATACACTTCTGACCACCAGGGAAGTGGCTTTTTGTCCACTTCTGAGTCCACCACCTCACCTGAGTCCTTGGCATCTCTTCCTGAAGAAACTTGCACTGAGAGCAGTCGGGACACTGATGACCATAGAAATGGTCTTCCTTTCCCACCTAACAAAGAAACATCAAGTAGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44230
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 |
---|---|---|---|---|---|
ENSDART00000111151 | Nonsense | 746 | 1725 | 1 | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 7706432)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7226884 |
GRCz11 | 25 | 7400924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTTTTAGCCCATAGCAGTTTGGATCGTATTCGTAACCCCAGCAGTGAG[C/T]AACCCCCAGAGGGCAGTAAAGATTGCCAACTTGCATCAAGTGGAAGTTCA
Long Flanking Sequence:
CCTTCGGCTCAGCTCGCACAGTGCCAACTAAATCCCCCAATTTGTCTGAGATTAAATTCAACAGCTACAACAATGCTGGCATGCCCCCATTTCCCATCATCATCCGCGATGAGCCTGCATATGCACGCAGCTCTAAAAAAGCAGTGAAGGTTCCCATAGTGATTAATCCCAGTGCTTATGATAACCTGGCTGTTTACAAGAGTTTCCTGGGACTCAACGGTGAACTGCCACATTCCAAACCTGGCGCTGGGGAGCGAGTGGCCAGCCACACATATGAGGAGATTGGATCTTCTGAAAGTTCTCAGCCCTCTCCATCTGAGCAAAAACCTCCTCCAATCAGCGCAGATTTAACTGCTACCGGGGAATTGAGGACAACCACAGTAAATGATGGCAAATACAGGACTACAACAGGTGTTGCATTCCATGCTGGTATCCAGAGCACTAACCCTGCCTTTTTAGCCCATAGCAGTTTGGATCGTATTCGTAACCCCAGCAGTGAG[C/T]AACCCCCAGAGGGCAGTAAAGATTGCCAACTTGCATCAAGTGGAAGTTCAGGTCAGAGAGAGAAAGCAAGTGCTGTCTTGTCTCAGATTGTGTCTTCAATTCAGCCGCCGGTTTCTCCACCAGAGTCTCCTGCCGGCCAGAGTAAAACCTGCAGTGCTGAGGAGCTTTACTCACTGCCACCAGATGCTTCCAGAGACACTACTGTGAACAGACCTAAGTCACTCCATTGTTCTGCAGAACCTCACAAAGAAACACCACACAAACTCCTTCCCAAATCTCAGAGTGCCTCTGCTGCTGTACCACCCACAAGCCCCAAATCTGAAACATCTGCCCCATTCCCCCCGGTCCGGTCTAGCTCTTCTCCTTACCATTCAAGCAACCTGCTCCAAAGGCACTTCAACTGGACCAGACCAGCTGGGGCCAAATCTACTGATGGAGAGACCAGTCCTGGTGCAGAGGGCAGGCGTTCCAGTGATGGCAACAAGCCAAAACGCTGGATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8851
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 |
---|---|---|---|---|---|
ENSDART00000111151 | Nonsense | 1492 | 1725 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 7718517)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7238969 |
GRCz11 | 25 | 7413009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CACRTCACGCATTGCGATCTGCGCCTYGAGAACCTCCTCCTGGTACACTG[T/A]CAGCCTGGAAACCCTTGGAACCTGGAGSTCCTGGAACCGAACAACAACGC
Long Flanking Sequence:
GCAGCCTTGGCAGATATTTCTGATGAATATTAATGTTCCCGTTTTGTCTGATCTCAGATCTGTCGAGGTGTGGTGAAGGAGACCCAGCAGCAGTTTTTCCACAGCCTAGCCGTTCGGCAGAGCATTGCTGTTCACTTCAACATCCAGCAGGACTGCGGGCACTTTCTGGCAGACGTTCCAGCACGCCTGCTTCCTTGGGAGCAAAAGGAGGATAAAGATGAGCGAGGCGGTACAGAAGGAGGAGAAGATGAAAAAGAGGATGCAGCAGGTCCAGGTGGGAAACTCTGCAGTTGTGTTGTAGTGATCACTCGTGAGGTGCCCTTCCAGACAGTGGCGGATTTCGTACGTGAAGGTGTGGAGCGGCACGCAAGAAACCCTGAGCTCTATGAACGGCAGGTGTGCCTGCTGCTCCTGCAGTTGTGTGCGGGATTGGAGCACATGAAACCCTACCACGTCACGCATTGCGATCTGCGCCTCGAGAACCTCCTCCTGGTACACTG[T/A]CAGCCTGGAAACCCTTGGAACCTGGAGCTCCTGGAACCGAACAACAACGCCGCATCCGGATCTTCCACTGCAGCAGCTTCTGCATGTCCTGCTCGCCTCATTATCAGCAACTTTTCTCAGGCCAAACTCAAGAACGTGGTACTGGAGCCTGCTTCGTTCCGAGACCATTCCCGTCTGGCACCCGAACTTCTCACTGCCACACAGTACCGCAAGTGCGATGAATTCCAGACCGGCATACTAATCTATGAGATGCTACATCGTCCGAACCCATTTGAGGATAGTCCGGAGCTAAAGGAGAGGGAATACTGCAGCTCTGATTTGCCCCAGTTGCCACTACGATCCCTCTACTCCAACGGCCTTCAACAACTCGCCACATTGCTTCTCAACCCTAACCCTTCCGAACGCATCCAGATGGCGGATGCAAGGGCATGTTTGCAGTGTCTTTTATGGGGTCCACGAGAGGATCTGTTTAATTCGCTGAACCCTGGAGCCGGGACAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24602
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 |
---|---|---|---|---|---|
ENSDART00000111151 | Nonsense | 1661 | 1725 | 4 | 4 |
Genomic Location (Zv9):
Chromosome 25 (position 7719022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 7239474 |
GRCz11 | 25 | 7413514 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGAGAGGATCTGTTTAATTCGCTGAACCCTGGAGCCGGGACAGTCCAA[C/T]GACACACTGTCCTGCAGAACTGGCTGGACCTGAAGCGAACACTTATGATG
Long Flanking Sequence:
CTGGAAACCCTTGGAACCTGGAGCTCCTGGAACCGAACAACAACGCCGCATCCGGATCTTCCACTGCAGCAGCTTCTGCATGTCCTGCTCGCCTCATTATCAGCAACTTTTCTCAGGCCAAACTCAAGAACGTGGTACTGGAGCCTGCTTCGTTCCGAGACCATTCCCGTCTGGCACCCGAACTTCTCACTGCCACACAGTACCGCAAGTGCGATGAATTCCAGACCGGCATACTAATCTATGAGATGCTACATCGTCCGAACCCATTTGAGGATAGTCCGGAGCTAAAGGAGAGGGAATACTGCAGCTCTGATTTGCCCCAGTTGCCACTACGATCCCTCTACTCCAACGGCCTTCAACAACTCGCCACATTGCTTCTCAACCCTAACCCTTCCGAACGCATCCAGATGGCGGATGCAAGGGCATGTTTGCAGTGTCTTTTATGGGGTCCACGAGAGGATCTGTTTAATTCGCTGAACCCTGGAGCCGGGACAGTCCAA[C/T]GACACACTGTCCTGCAGAACTGGCTGGACCTGAAGCGAACACTTATGATGATCAAGTTTGCGGAGCGTTCTTTGGAATCGGGCTGCGGTGTGAGTTTGGAGGACTGGTTGTGCTGTCAGTATCTGGCTTTCTCTACCACTGAATCTCTCAGTAGAGTGATAAAGATCCTGCAGCAGCCGCAGGGTGTGCTTATATGATTTTATGTGCTTATATCACACTAAGGACACTTGTGCGCTGTACAGAAGTGTGATTTTTATTCGAGGAACCTAATCTTTTGACTTTGTTGGTGAATGTGTTTGCGTTTGGTTTACTTGTGATTTGGACTGTGGTGATAGATTGATGCATTGCGAATTGAGAAATGATTCTGCATCGATTTCTACGAATTCATTGTGATTTCTCTCTTGAATTGACTCAGAGCTTAGTTTTAACAAAACACTTGCAGCCATACTTGCATCCAATTTCTTAGACACACTACTTACTAAAATAATCATTCATAAAGT
Associated Phenotype:
Not determined