ZMP
kidins220a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to rat kinase D-interacting substance of 220 kDa (RGD:619949) [Source:UniProtK
Human Orthologue:
KIDINS220
Human Description:
kinase D-interacting substrate, 220kDa [Source:HGNC Symbol;Acc:29508]
Mouse Orthologue:
Kidins220
Mouse Description:
kinase D-interacting substrate 220 Gene [Source:MGI Symbol;Acc:MGI:1924730]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23131 | Nonsense | Available for shipment | Available now |
sa8802 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19182 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa11853 | Nonsense | Available for shipment | Available now |
sa42974 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa23130 | Nonsense | Available for shipment | Available now |
sa42973 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23131
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 113 | 1694 | 4 | 29 |
ENSDART00000145664 | Nonsense | 113 | 1009 | 4 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35110950)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34995874 |
GRCz11 | 17 | 34943820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCACGTGGTAATATAATGACCTTGGTATGTTTGTGTTAAGGGGGGCTG[G/A]AGTGCGCTCATGTGGGCCGCTTATAAGGGCCGTGTGGAGGTGGCAGGTCT
Long Flanking Sequence:
ATTTATTTGTTCTGTTGTTTGTTTTTTCATCACACAGTTCTTTACTTTTTAACATTCAAAGCCTTAGAAACTGTGTGTACACTGAACCGCCCCATCTGGATTCCTTTAATTCCTACCTTACTGGAATATATGATATGTGATACTCTGTGTTTAAGATCAGCAGTTCTGTGCAGTCCTGTATATAAACTATCATGCTGTGGTCAAGTTTACTTTCTGATGGCATGAGCTGCCTATCTAGACAGCATTTTTGTTCATCATAGGCACATTTAAATGCAAAATGGAGTGTTCAAGTGCGTCTCTGTTGCCCATAAATGCTGTCTGGTTGGCAGCTAAAGCTTATAATAACAAATAAGGAAGATAAGAGACAGCCGATAGTTTGAGTCACTCCCTGACTCAGGGAAAATGTGTTTTTCCACAAAGTCCTGTGACTGAGAGATTATTATTAAGGACCATCACGTGGTAATATAATGACCTTGGTATGTTTGTGTTAAGGGGGGCTG[G/A]AGTGCGCTCATGTGGGCCGCTTATAAGGGCCGTGTGGAGGTGGCAGGTCTACTGCTGGAGAAGGGAGCAAACCCTAACATCACCGGACAGGTTTGCAGAGCCTTTACCTGATGCTTTCAAACATGTATTGTATATTAAAGCAAGACACTGCAGGAGCCGGTTGCACCAGCAGTGCGCAAGTTAAAACATAGCCTAGTTGTGACTTAAAGCGACACTACACGCTACTAAAGATTTTTGTGTTGCACCACTGAACTTAGTTTAAACGTAACGTTACGTTTTAACTTAATATTTACGGCAGCATCCCCTCACGTGTAACGGTGGAAAAGAGATGACAGAGAGATTATTTTACATCGAGGAGCTCGAGATGATAATGAATGATCTTTCCTTACTAACAGCCTTATTTTCCTCCCAGATCTCGCATTTTTTCAGTTTGTGAAAGAAGAGTTTAGTTTTTTTTCAAGAAGTGCTTTGTGTTTAATCTATCATCAATTAAAATGAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8802
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 393 | 1694 | 11 | 29 |
ENSDART00000145664 | Nonsense | 393 | 1009 | 11 | 21 |
ENSDART00000021128 | Nonsense | 393 | 1694 | 11 | 29 |
ENSDART00000145664 | Nonsense | 393 | 1009 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35102458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34987382 |
GRCz11 | 17 | 34935328 |
KASP Assay ID:
2261-1324.1 (used for ordering genotyping assays)
KASP Sequence:
GTGACACACCTCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCT[G/T]AGCTGCTCTTGAGAAAYCCTAAAGATGGCCGTCTGCTCTACMGGCCCAAC
Long Flanking Sequence:
CTGCACAAGCTAAGCAAGCATGAAAAATGTGCCAAAATGTTAAAAAAGAAGTTATTTATTTGCATCAATTTAGACACATATTAACAAAGAGTGCATGGCTCCAAATGACTATTGCTGTTTTAATAGGTTTTAAGGATAATTTTGTCCTAAAGGTTCTGAGTGAACTGTTTTTCATGTAGTGTAAAATATATTTATGAATTGAATGAGCGATGTTTACATTTTCTGCTAGTTGTTTTTTCAAGGTAAATTTTGCAGTTTTTCCAAAAAATAATGAAACTCAGTAACCAAATTAAACAAGGATGTTGTTGAACACATACAAATACATTTAAGTACAATTAGGTACAAATCACTTTCACAGTTCTGTACAAATATTTCTTATTCACTAGTAAACTGCAAACAAATATATTTAGCAACTTTGTCCTGAAGCTGCATTGTTATTTTCTCAGAAAGGTGACACACCTCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCT[G/T]AGCTGCTCTTGAGAAACCCTAAAGATGGCCGTCTGCTCTACCGGCCCAACAAAGAGGGAGAAACGCCCTACAACATTGACTGCACACACCAAAAAAGCATCCTCACACAGATATTCGGAGCCAGTGAGTATTCCATCAACTTACAGATGTCAGTTTCCACAAATTCTCTAGAGCAACCGACATTAATTAATGATCAATTAATCAATTCCTCCACCAGTTAACCATAATAATGGAAGATCTGTCTGTTTTAGTGGCACATTTTCACTGGCATAACAGGATGTGGAAGGTATTGTGGGATTATAAAAAAAATGATAAGTTAGTAGAATCGTTTAATTAATAAACATAATAACTAATACAGTATACATTGTGTATTATGTTTTGCCAGATGTACACATTGGCAAAGTTATACTGTGAAAGCCACAACAAAAACAAAAAATTGTAGATTTAAAAAATCATACTTAAGTAAAAGTATCATTACTTGCCAAAAATGTAGTGTAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19182
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 393 | 1694 | 11 | 29 |
ENSDART00000145664 | Nonsense | 393 | 1009 | 11 | 21 |
ENSDART00000021128 | Nonsense | 393 | 1694 | 11 | 29 |
ENSDART00000145664 | Nonsense | 393 | 1009 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35102458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34987382 |
GRCz11 | 17 | 34935328 |
KASP Assay ID:
2261-1324.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTGACACACCTCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCT[G/T]AGCTGCTCTTGAGAAACCCTAAAGATGGCCGTCTGCTCTACCGGCCCAAC
Long Flanking Sequence:
CTGCACAAGCTAAGCAAGCATGAAAAATGTGCCAAAATGTTAAAAAAGAAGTTATTTATTTGCATCAATTTAGACACATATTAACAAAGAGTGCATGGCTCCAAATGACTATTGCTGTTTTAATAGGTTTTAAGGATAATTTTGTCCTAAAGGTTCTGAGTGAACTGTTTTTCATGTAGTGTAAAATATATTTATGAATTGAATGAGCGATGTTTACATTTTCTGCTAGTTGTTTTTTCAAGGTAAATTTTGCAGTTTTTCCAAAAAATAATGAAACTCAGTAACCAAATTAAACAAGGATGTTGTTGAACACATACAAATACATTTAAGTACAATTAGGTACAAATCACTTTCACAGTTCTGTACAAATATTTCTTATTCACTAGTAAACTGCAAACAAATATATTTAGCAACTTTGTCCTGAAGCTGCATTGTTATTTTCTCAGAAAGGTGACACACCTCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCT[G/T]AGCTGCTCTTGAGAAACCCTAAAGATGGCCGTCTGCTCTACCGGCCCAACAAAGAGGGAGAAACGCCCTACAACATTGACTGCACACACCAAAAAAGCATCCTCACACAGATATTCGGAGCCAGTGAGTATTCCATCAACTTACAGATGTCAGTTTCCACAAATTCTCTAGAGCAACCGACATTAATTAATGATCAATTAATCAATTCCTCCACCAGTTAACCATAATAATGGAAGATCTGTCTGTTTTAGTGGCACATTTTCACTGGCATAACAGGATGTGGAAGGTATTGTGGGATTATAAAAAAAATGATAAGTTAGTAGAATCGTTTAATTAATAAACATAATAACTAATACAGTATACATTGTGTATTATGTTTTGCCAGATGTACACATTGGCAAAGTTATACTGTGAAAGCCACAACAAAAACAAAAAATTGTAGATTTAAAAAATCATACTTAAGTAAAAGTATCATTACTTGCCAAAAATGTAGTGTAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11853
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 |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 396 | 1694 | 11 | 29 |
ENSDART00000145664 | Nonsense | 396 | 1009 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35102448)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34987372 |
GRCz11 | 17 | 34935318 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCTKAGCTGCTCT[T/A]GAGAAAYCCTAAAGATGGCCGTCTGCTCTACMGGCCCAACAAAGAGGGAG
Long Flanking Sequence:
TAAGCAAGCATGAAAAATGTGCCAAAATGTTAAAAAAGAAGTTATTTATTTGCATCAATTTAGACACATATTAACAAAGAGTGCATGGCTCCAAATGACTATTGCTGTTTTAATAGGTTTTAAGGATAATTTTGTCCTAAAGGTTCTGAGTGAACTGTTTTTCATGTAGTGTAAAATATATTTATGAATTGAATGAGCGATGTTTACATTTTCTGCTAGTTGTTTTTTCAAGGTAAATTTTGCAGTTTTTCCAAAAAATAATGAAACTCAGTAACCAAATTAAACAAGGATGTTGTTGAACACATACAAATACATTTAAGTACAATTAGGTACAAATCACTTTCACAGTTCTGTACAAATATTTCTTATTCACTAGTAAACTGCAAACAAATATATTTAGCAACTTTGTCCTGAAGCTGCATTGTTATTTTCTCAGAAAGGTGACACACCTCTGCATATTGCCATCCGTGGGAGAAGCCGCAAACTGGCTGAGCTGCTCT[T/A]GAGAAACCCTAAAGATGGCCGTCTGCTCTACCGGCCCAACAAAGAGGGAGAAACGCCCTACAACATTGACTGCACACACCAAAAAAGCATCCTCACACAGATATTCGGAGCCAGTGAGTATTCCATCAACTTACAGATGTCAGTTTCCACAAATTCTCTAGAGCAACCGACATTAATTAATGATCAATTAATCAATTCCTCCACCAGTTAACCATAATAATGGAAGATCTGTCTGTTTTAGTGGCACATTTTCACTGGCATAACAGGATGTGGAAGGTATTGTGGGATTATAAAAAAAATGATAAGTTAGTAGAATCGTTTAATTAATAAACATAATAACTAATACAGTATACATTGTGTATTATGTTTTGCCAGATGTACACATTGGCAAAGTTATACTGTGAAAGCCACAACAAAAACAAAAAATTGTAGATTTAAAAAATCATACTTAAGTAAAAGTATCATTACTTGCCAAAAATGTAGTGTAAGGAGAGTAAAAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42974
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 |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 459 | 1694 | 12 | 29 |
ENSDART00000145664 | Nonsense | 459 | 1009 | 12 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35098069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34982993 |
GRCz11 | 17 | 34930939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGATATGCTGGGTTATGACCTGTACAGCAGTGCTCTGGCTGATATCT[T/A]GAGTGAACCCACAATGCAGCCTCCCATCTGTGTGGGCCTTTATGCCCAGT
Long Flanking Sequence:
AAACCTTGTAATTTGTTTACAATTTTTTTAATCATTTTTAATATAACAGTCAATCTGATTTAATGAACAATTTTCAGCATTATTCAAGGCATCTGATGTACCTGTATTCATATTGCACAATTTATCATAGAAAAGAAAAATATCCTAAAGTCACATTTTTCCAATATTGTGCAGCCCTAAAGCAAACTATTGCGACTAAATATTATGTTGGAGGTTTTCTTTTTTAATGGACTAAAAAATGGCATAAACTTAATGGAAAGCCAAAAATTTAACACCTATTGAAAAACCAAATCTCAAAATGAACCAGTGCATAAAAACACTGTTTTTGCCAGTAGTGTCTCTCGACCATCAATGATGTGCTCACTAGATTATTCATTGATATCCCTACCTCAGTCAACCCTGTATCTCAAACTTTTCCTCTGCAGAGCACCTGTCTCCCTCTGAGTGTGATGGAGATATGCTGGGTTATGACCTGTACAGCAGTGCTCTGGCTGATATCT[T/A]GAGTGAACCCACAATGCAGCCTCCCATCTGTGTGGGCCTTTATGCCCAGTGGGGCAGCGGCAAGTCCTTCCTACTGAAGAAACTGGAGGGTATGAGCCTGACCACATGTTAAATGCTATGTCATGCAGTTTATTGAATCACATATATAGGTTCCTTGTTGGATCTTTATCATCTAGGTGAGGTGTGATTTGTGTGTGTGTTTTTTTCTGTATACCAGATGAGATGAAGACATTTGCCGGGCAGCAGGTGGAGCCGTTGTTTCAATTTTCATGGCTGGTGGTGGTTTTGACTCTGCTGCTGTGTGGATCTGTGGCTTTGGTCCTCGGCTTTGCTGTCGACACAAAACTGGCCATCGCTGTAGCCCTCACTCTGCTCGCTCTCATGTACATCTTCTTTGGTGAGAAATGGACAAATTTATTGTCCAGAGTATTTATATTGGCCAATTGTACTTTTTTTATTTGCAACATACAACAGTGAAGGAAAACTTAAAATTAGGGATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23130
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 |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 842 | 1694 | 18 | 29 |
ENSDART00000145664 | Nonsense | 842 | 1009 | 18 | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 35080216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34965140 |
GRCz11 | 17 | 34913086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCTCAACAGTGTGCTGCGCGACTCCAACATCAACGGCCATGACTACATG[C/T]GAAACATCATCCACCTGCCCGTGTTCCTCAACAGCCGTGGCCTCAGCACT
Long Flanking Sequence:
TATAGCAGATAACAGAAGTATTTATTACCTAACTTCAAGATAAAGTAATAAATACGGTCATACATTTCATAATCATTATAAATGTTAATTAATCCATTAGTGTACAAATAAATAATGTAAAATAAAAAGACTGAATTATATTAAAATACCAGTATACAGCAAATACTAAATAAGGATTTTTTATGTTAAGTTTATGTAACACATTGAAATACACTTTTTTTTATCATTATTATTATTTTTTGTTTTAGAAAAAAATGCTTCACAAGTAATAAAGGAAAAATGAAAAGTTCAAACAAGATATAACAAGTTCGACCATGTTTTCCACTTTTTATAAGGAGGAACCATCCACTTGTTTATTCTGTTTGCAGGTTCGGGTGCTCTTTTCCAAAGGTCCCTTCATCTCCATCTTTGCCAGCGACCCTCATATCATCATTAAAGCCATAAACCAGAACCTCAACAGTGTGCTGCGCGACTCCAACATCAACGGCCATGACTACATG[C/T]GAAACATCATCCACCTGCCCGTGTTCCTCAACAGCCGTGGCCTCAGCACTGCTAAAAGACTCTGCATTTCCACAGCAGCCAATGGAGCCGATCAACTGAACAATGATGGTCAGTATAAAGAGACTGCTGAAGGCCAAACTTCAGAATTATTAGTCTCCCTGAATTATTAGGTCCCCAGTTTTTTTCCCCCAATTTCTGTTTAATGGTGGTACGCTTGCAGTGTGAGTGCAAAGCGCATCTGAACCCAATACTGAAGATGTGACGTCACTTTTAAGGGACTGTTTCATACGGATTTATTAATCATTCTTACTTTTCATTGTTCACCTCCTAATACATGCAGCACAAGGACTTTTATAATAATTTATTAGCTTCAAAGGTGGTGGATTTGTTCAGCAAAATATTTGACTGCGTGATATAACTAAACAATGCAAAGCGCATCTCTTCCTGTTATACTGAATAGTTGTATCATCAATGATGTAAGAGTGCTCAAGTTCGGAAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42973
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000021128 | Nonsense | 1486 | 1694 | 29 | 29 |
ENSDART00000145664 | None | None | 1009 | None | 21 |
Genomic Location (Zv9):
Chromosome 17 (position 34982054)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 34866978 |
GRCz11 | 17 | 34814924 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCACTAAAAACCCACCCAGACGCAAAACCAAAGGACAGGGCCCTTATTA[T/G]CACAGTTTACCGAGTGACGAAGACGACTCTGGAGATGAGGAAACTGATGC
Long Flanking Sequence:
TGTGTTTTCTACCCGATTGCTAGTCTGACTTGGCATGTTCTCTCACATTTAGCAGTCTAAAGTCATTGACCTGATCTTTTCCTTCAGGCCAATACTCACCGGACCCCCAGCTTATCCAGTCTAAACTCTCAGGAATCATCTAATGACATCTGTAAGCTGACCGACAAGCAGCAGGCCGAGTATCACAGTGCATACCAAGAGTACATCTCCCACATGTCCCATTTGGAAGCATCTGCTGCAGGACGAGAAAGTCAAACTCAAGCCCTGTCCAGCCAGCTCCTCTCAACCAGCTCTGAGGACAAGATTAAAGAAGGAGACCAAGATGGACGCAAACCCTTTGGCAAAAAAGGCCCCAAACCTACAGACACCATGGCAGACTTCTCCTCCCCCCCAGATAGTGGTCTTCTAGACCCCATTACAGAGGAGGATGAGAAGTCCGATCATGGGTCTGCCACTAAAAACCCACCCAGACGCAAAACCAAAGGACAGGGCCCTTATTA[T/G]CACAGTTTACCGAGTGACGAAGACGACTCTGGAGATGAGGAAACTGATGCAACCCCGCTTCTAAAAGACGAGCCCTGGGGCGCAGAACCAGATCTAGACCACTTGTCGAAAGGAAAAGGCTTCGTCTCAGATATCATGCTGGACAAGAAGTCGTCCGACTCTGGAGTAAGGTCCAGCAGAAGCTCATCTGACCACTCCCTGCAGGACGAGGAGAAGGAGGAGAAGTCAGAAGAACAGGAGGCCCAACTGATTGAGCTGGTTGTTGAGAGTCCGGTTAAAAAGCGGGTGTTACCAAACAGGTTGAGCAACCTTCAGGATGAAGCCTTGGCCCGCATGTCAATCTGCTCTGACGCTCCATCTGAAGGCAGCACCCCTGAAGAAAGCTGGCCCGCTCCAGCCGTGAGCAACCTCAACTGCTCGGCCAATAATACAGCAATCAACAACAACATCAACAACAGTGGCCAGCAGGAGACCCTCGACTCAACCGACTGCCCCTCACT
Associated Phenotype:
Not determined