ZMP
KNDC1 (2 of 2)
Ensembl ID:
Description:
kinase non-catalytic C-lobe domain (KIND) containing 1 [Source:HGNC Symbol;Acc:29374]
Human Orthologue:
KNDC1
Human Description:
kinase non-catalytic C-lobe domain (KIND) containing 1 [Source:HGNC Symbol;Acc:29374]
Mouse Orthologue:
Kndc1
Mouse Description:
kinase non-catalytic C-lobe domain (KIND) containing 1 Gene [Source:MGI Symbol;Acc:MGI:1923734]
Alleles
There are 3 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa19387 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44436 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa38228 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa19387
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 |
---|---|---|---|---|---|
ENSDART00000127770 | Nonsense | 101 | 507 | 4 | 12 |
Genomic Location (Zv9):
Chromosome Zv9_NA97 (position 31217)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50416399 |
GRCz11 | 13 | 50731308 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGAGATGTTTCCTCCACAACCGTCTGTCGAAAGCTGTCTGCTATTGGA[C/T]GAAGAGTTTTGTCCATCGAGTCTGTCGCTGCTTTCCAAGGTTTGATTTGG
Long Flanking Sequence:
GAGTGGCCCAGCCAGAGCCCAGACCTAAATCCTATTGAACATCTCTGGAGAGATCTGAAAATGGCTGTACACCGTCACTTCCCATCCAACCTGATAGAGCTTGAGAGGTTCTGCAAAGAGGAACGGGCAGAAATTCCCAAAGACAGGTGTGCAGAGCTTGTGGCATCATATTCAGAAAGACTTGAGGCTGTAATCACTGCCAAAGGAGCATCAACAAAGTACTGAGCAAAGCCTGTGAATACTGATGTACATCTGATTTATCAGCTTTTATATTTTTAATTAATTTGCAACAATCTCAAAAACTCTTTTTTAATCCACTTTGGAATAAGACTGTAACATTATAAAAGTGGAAAAAGTGAAGCGCTATCAATACTTTCCGGATGTCCTGTATGCATGACTGATTTGAGCTGATATGTCCACAGGTTCTTCACTCTGAGGCCAGGGCTTTACTCGGAGATGTTTCCTCCACAACCGTCTGTCGAAAGCTGTCTGCTATTGGA[C/T]GAAGAGTTTTGTCCATCGAGTCTGTCGCTGCTTTCCAAGGTTTGATTTGGTGGCCGTCTCATGTTTTGGATCCAAAGATTATTTATTAGGGAACTGCAGATGGCTTATGAGCTGATAATTAAATATAGAAATGTATATAAATGCTATATAAACAAGTGTAAAATGTAAACAATTGAGATGTTACCCAATTTACAGATTATTTTGCTTTGTTTAAGGACATTCTTACTTGTTATTTCTGAAAAAATAAACAGTTTTTTTTACTTGTCTATGCTGTTTTTGTCTTAATTCTAGTCCAATAGATTTTTTTTTTTTTATATTTGGACTAGAATCAAGACAAAATGAATGTTTTAAGAAGTGTTTTAATGTTTTTTTGCAGTGTGGGTGAACTGTCCCGTTTAAAAGTGTTTGCTTAATCAAAAATCTCCTGTTTATATACAGATGGACCGGATAAATGGAGTGTGCAGTTCATGGACTATAAAGCGTCTCGATCAAACTCAGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44436
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000127770 | Essential Splice Site | 412 | 507 | 9 | 12 |
Genomic Location (Zv9):
Chromosome Zv9_NA97 (position 37468)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50410148 |
GRCz11 | 13 | 50725057 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTTTCTTGGCTCCTGAATTTCAAGAACATGGAATTGTGACAGAAAAGG[T/C]TTGTCACCATGGCAGCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGT
Long Flanking Sequence:
TTTGTTGTAGGAATTCTGTAGTTGCTATGGTAACACAACAACTATAGTAATTGATCTGTTGTCCAGAGTCTACAGTCGCTACGGTAACACAACATCTTCAGTAATTGATCTGCTGTGGTGATTTTACAGTTGCTATGGCAACTGCTGTATTTGAGGAGGTACTGTAACTGTGTTGTGTGTTCCGTTAGATTACCTGTGTCTGGACTCTGTGTATGTGGGCTGTGAAGGAGAAGTGCTGTTTCTGAGGCCGAAAAACTCAGGTGTGGACATCACAGAACATCTCATCATCTTATTATTAATGTCTTTGTCTGGTGTAAAACGTATAAATAAAAATAAATAGACATCACCCTTTATATTGTAGAGTACTTCACGTGTGTGTCCAGCATTGAGCTCTAAAGTCCTGTTGTTGATCATGGCTCTCCTGTTCTCCTCCTCAGTCTCCTGCGACGCCTTTTTCTTGGCTCCTGAATTTCAAGAACATGGAATTGTGACAGAAAAGG[T/C]TTGTCACCATGGCAGCCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGTGTGCGCGTGTGTGTAGTGACTCATTGCTCAGTGTGTGACTCAGTGTTGTGTGTATATGTGTGTATTCTCTTTACAGTAGTGTGTTTGTGTGCTTCTCCTCTCCACAGGTGTGTGTGTGTGTTTGTGTGTGTGGGTGTGTGTGTGTGCTTCTCCTCTCCACAGGTATATATGTGTGTGTGTGTGTGTGTCTTCCTTTTTATTGTTTTGTATGTATGTAATGTGTGGGTGTGTCTGGGTGTGTTTGTGTGTGTGTGTGTGTAGTGACTCATTACTCAGTGTGTGCAGTGACTCAGTGTTGTGTGTGTATTTTCTTCACAGGTGTGTGTTTGTGTGTGTGTGTGTGTGTTTGTGTTTGTGTGCGTCTCTCCACAGGTGTGTGTTTGTGTTTGTGTGTGTGTGTATGTGTGTGTGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38228
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 |
---|---|---|---|---|---|
ENSDART00000127770 | Nonsense | 456 | 507 | 10 | 12 |
Genomic Location (Zv9):
Chromosome Zv9_NA97 (position 38684)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 50408952 |
GRCz11 | 13 | 50723861 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAGGAGGCTGAAGCGGCTGCTGCTGGAGATGGCCAAGCGGACCCCCATC[G/T]AGAGACCTTCCATCCAGACCGCCAAGAAGGTGCTGTGTTTTATGTTTTAT
Long Flanking Sequence:
ATGTGTGTGTGTGGGTGTGTGTTTGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGTGTGTGTGTGTGTGTGTCTTCCTATTCATAATTAAGTGTGTGTGTGTGTGTGTTTGTGTTTGTGTGCGTCTCTTCACAGGTGTGTGTGTGTGTGTTTGTGTGTGTGTCTTCCTATTCAAAATTAAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCTGTGTGTGTGTGTATGTGTTTGTGCATGTGTGTGTTTCTCTTCTTCACAGGTATGTGTGTGTGTTTCTTCTCTCCACAGGTGTGTGTGTATGGGGTCGCTGCTGTCCTCTGGGCTACTGCTAAGTTTCACTTGTCTCCCAGTCAGAAGTTGTCGATGCCCAGGAGGCTGAAGCGGCTGCTGCTGGAGATGGCCAAGCGGACCCCCATC[G/T]AGAGACCTTCCATCCAGACCGCCAAGAAGGTGCTGTGTTTTATGTTTTATGCAGCGGATGCCCCTCCAGCTGCAACCCAGCACTGGGAAAAATCCACACCACACTTATTCACACACACACACGCATACATTACAGCCAATTTACTTCATCAATTCCCCTATAGCACATGTGTTTGGACTGTGGGGGAAACCAGAGCACCCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAACACCAACTGATCCAGCCGAGACTCGAACCAGTGACCTTCTTGCTGTGAGGCCACAGTGCTAACCACTGAGACAATATTTGCAATAATGACAATTTAGTTTAAAAAAAGTGTGTAATTTGAGATTTTGATTTAATTTAAGTGTTGGGATAAATTGCAGACCGTCTGTGTGTTTCCTCAGTAAGCTGGAGCTCCAGGAAGGCAACAACAACTGAGAGATGTGAATCCAACAGTTTATTGCTCTCTTCTAAAG
Associated Phenotype:
Not determined