ZMP

KNDC1 (1 of 2)

Ensembl ID:

ENSDARG00000059910

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38217	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38218	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38217

Status:

Mutation detected in F1 DNA
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
ENSDART00000083839	Nonsense	101	474	4	17
ENSDART00000129195	Nonsense	210	579	6	18

Genomic Location (Zv9):

Chromosome Zv9_NA856 (position 29075)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	50368058
GRCz11	13	50682967

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGTATGTCTGACCTATGTGTGAATGTGTTCAGGTTGCACCAGTGGACAGT[C/T]GAGCAGAGACTTTGCTGCTGATGCTGCAGGACTCGCCCAGAAAGAGGCGT

Long Flanking Sequence:

GATAGATAGATAGATAGATAGATAGATGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGATATATGGATAGATAGATATTTTTGTAGCCCCCATTAAATATTCCCAGAAAGAGTAATTTCTGCACTCGTTAAGTAATGATCTGCGAGAAATTAATTGAGATGAGGTGTAATTATTCTGTCCATTAATTGTGTCCAGCAGAGCGAGTGCAGATCCCTCATCAGACAGCACTAAAGTCTACCAGCGCACTCTGGATCTACTACAGTTCTGGATCACAGACGCACAGCTAGTGGACTTCAGCTCTCACTCCTGCCTTCAACACACACTGGACGCCTTCCTGACCTCTGAGGTGTGTGTTTGTTTGTTTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGCGTGCGTGCGTGCGTGCGTGTGTGTGTGTGCGTGTATGTCTGACCTATGTGTGAATGTGTTCAGGTTGCACCAGTGGACAGT[C/T]GAGCAGAGACTTTGCTGCTGATGCTGCAGGACTCGCCCAGAAAGAGGCGTGTCTGTGGTCAGTCATGTGACCTGTCAATCAGCAGCCCAGAAGACGAGGAGTCGCTGCTTTCAGTGCAGCCCTTATGCAGGAGATCATCCACACAGGAGCCTGCCAGAAACGTAAAATCAACATAATCAACACTACAAACCACCTGTAGGACACACTCCACCTCTCCGTATGCTCGGAGATCAAGATTTAGACTTGTAGAATTAATAATTAGACGTATCGTAGCATTTACAGTGGTGTGAAAAAGTGTTTGACCCTTTACTGGTTTCTTTTGTTGTTGCATGTTTGTTTCACTTTAATGTTTCAGATCATTAAATTATTAGTCAAGCATAACAGCAGTAAACACGTCATGCAGTTTTGAAATGAAGGTTTTATTATAAAGGGAAAACAAAATATAAAACTACACAGCCCTGTGTGGAAACGTGTTTGACTCCTAAATGTAATAACTGGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38218

Status:

Mutation detected in F1 DNA
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
ENSDART00000083839	Nonsense	468	474	17	17
ENSDART00000129195	Nonsense	573	579	18	18

Genomic Location (Zv9):

Chromosome Zv9_NA856 (position 41592)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	50355858
GRCz11	13	50670767

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCTCCAGACGAGCGACCGGCACGCGCGCAGGATCCAGGACACACTCCGA[C/T]GAGTCAAGGCCTCATTTCAGTGAAGCAGAGCTGGACGTGTTTCCATTACG

Long Flanking Sequence:

TTAATAATTGTCTGCAAGGTTGTGTGTGTGGGTGTATGAGAGAGATGTGTGTGAGTGTGTTTATTGATTGTGTGCACGTTTGTGTGTATGTGTAGAAGTGTGAGGTGTGTGTGTGCATGTGTATGTGTGTGTTTAATGGTTGTTTGCAAGTTTGTGTGTGTACTTGTGTGTATGAGAGAAGAGTGTGCGTGAGTGTGCAAGTTCTGTGTGCAAGCAGGGTTATTATCTATAATACAATATAATGTGTGTGTGTATGTGTCTGTGCATGTGTGTGTGTGTGCTGTCCTCTCTTCAGGAATATAGCGCGTGTGGTCAGTCAGGTCCAGGCGTTTCAGGAGCGTGTGTATCCGTATCCTCCAGACTCTGAGCTGCAGTCGTATCTGCGAGCGCGAATCCTCCACTTCGGCCGCTGTGACGTCACTCTCCTCGCCTCCGAAAACCACACACACTCCCTCCAGACGAGCGACCGGCACGCGCGCAGGATCCAGGACACACTCCGA[C/T]GAGTCAAGGCCTCATTTCAGTGAAGCAGAGCTGGACGTGTTTCCATTACGCCTCAGAGCGGACAGTAGGGCTGCACCACACTGGATAAATATGACATCTGCTTGCTTTCCTGTGATATCGAGATATGAATATAATTTCAGCAGAGGATTTGAACAGCTTTATTTGGAAACGTTTCATTTATTTAGATAGACTGGGATCTATTTCTACACTACCTGACAAAAGTCTTGTTGTAGGAGCAGCAGATAATAACTCGACATCTAGTTGATCATGTGTAAAAGTGTCAGAAGGTGGATTTCTCTGCTGAATCGTCTGTTGATCTGCATCTCAATCATCACCAATACTGCAGAAGACCTACTGGAACCAGCATGGACCAAGATTCACACAGAAATCAGTCAAGTTTGGTGAAGGAGACATCATGGTTTGGGGTCATTCAGTATGGAGAGATCTGCAGAGTGGATGATCAACATCAACAGCCTGAGGTATCAAGACATCTGTGCTGC

Associated Phenotype:

Not determined