ZMP

kctd7

Ensembl ID:

ENSDARG00000061580

ZFIN ID:

ZDB-GENE-060804-2

Description:

BTB/POZ domain-containing protein KCTD7 [Source:UniProtKB/Swiss-Prot;Acc:Q0VFV7]

Mouse Orthologue:

Kctd7

Mouse Description:

potassium channel tetramerisation domain containing 7 Gene [Source:MGI Symbol;Acc:MGI:2442265]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6178	Nonsense	Mutation detected in F1 DNA	Not yet available
sa16727	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa6178

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
ENSDART00000087977	Nonsense	94	313	2	4
ENSDART00000134922	Nonsense	120	339	2	4

Genomic Location (Zv9):

Chromosome 10 (position 33841851)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	32943200
GRCz11	10	32887060

KASP Assay ID:

554-5248.1 (used for ordering genotyping assays)

KASP Sequence:

TCCCCTTGAATGTAGGAGGAACATATTTCACCACTCGCCTGTCCACCCTG[C/T]GACGTTATGAGGACACTATGTTGGCCGCCATGTTTAGTGGCCGCCACCAC

Long Flanking Sequence:

GGTTCAATTCAATGGATGTGTTCATCTCCAACATAACAAAAGGGTTGTCAATTTGAACAGTGCACAAGGGTTAAATAATAGTCATATTTTTCACTATTACTATCCATTCATTTTGCAAGGGCTAGTGATTCATCGTTTTTATCACCAGTTGACCCTGTTGTTTATTAGATCTATATTGTGCACTGCATTGAATTAACTCATATACTTATAGTAGTTACATGTTTTTGTTACATTGATTATTCTATTGGCCTTATTTTGTAAGTCGCTTTGGGTAAGAGGATATCCCAAATTATTAAATGTTAAATGACAGTATGTTGCAATCCTTGTTATGACTTTAAAAACATAAAAAAATTCTTACCAACCCTAACCTCTCGATCGCTAGTGAACATTGAGACTGATGTAAAAATGCTATTTCCGTCGCTCCTCTTTCTCCACAGTTTCCTGAGGTCATCCCCTTGAATGTAGGAGGAACATATTTCACCACTCGCCTGTCCACCCTG[C/T]GACGTTATGAGGACACTATGTTGGCCGCCATGTTTAGTGGCCGCCACCACATTCCCCGAGATGCAGAGGGACGATATTTCATCGACCGGGACGGAACATATTTTGGGTAAGTGTTTAGATTAGTGAATATCTGATTATGGTCGCTGCCTAGAATCCAGAAATACAAAGTAAACATTTTGATTAGCTGAATATAGCGTTTGGTGGATTACTTAAATAACTGCTTGATATCCAGTTAAAAATGACATGCTTATATGAAGCTTTGTATATACTTCTCTGGCTTTAGGGATATTTTGAATTTCTTGCGCGAGGGTGAGCTGCCTCAGAGGGACCGTGTTCGTGCCGTGCACAGGGAAGCTCAATATTATGCTATTGGACCTCTTTTGGAAAACCTGGAAGACACACAGCCTCTCACTGGAGAGAAAGTGCGACAAGCTTTTCTTGATCTCTTGCCCTATTATAAAGGTAATATGAATAATTAGAGGCTTAACTACATAATAATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16727

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

T > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000087977	Essential Splice Site	129	313	2	4
ENSDART00000134922	Essential Splice Site	155	339	2	4

Genomic Location (Zv9):

Chromosome 10 (position 33841743)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	32943092
GRCz11	10	32886952

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GAGATGCAGAGGGACGATATTTCATCRACCGGGACGGAACATATTTTGGG[T/A]AAGTGTTTAGATTAGTGAATATCTGATNNNNNNCGCTGCCTAGAATCCAG

Long Flanking Sequence:

CATTTTGCAAGGGCTAGTGATTCATCGTTTTTATCACCAGTTGACCCTGTTGTTTATTAGATCTATATTGTGCACTGCATTGAATTAACTCATATACTTATAGTAGTTACATGTTTTTGTTACATTGATTATTCTATTGGCCTTATTTTGTAAGTCGCTTTGGGTAAGAGGATATCCCAAATTATTAAATGTTAAATGACAGTATGTTGCAATCCTTGTTATGACTTTAAAAACATAAAAAAATTCTTACCAACCCTAACCTCTCGATCGCTAGTGAACATTGAGACTGATGTAAAAATGCTATTTCCGTCGCTCCTCTTTCTCCACAGTTTCCTGAGGTCATCCCCTTGAATGTAGGAGGAACATATTTCACCACTCGCCTGTCCACCCTGCGACGTTATGAGGACACTATGTTGGCCGCCATGTTTAGTGGCCGCCACCACATTCCCCGAGATGCAGAGGGACGATATTTCATCGACCGGGACGGAACATATTTTGGG[T/A]AAGTGTTTAGATTAGTGAATATCTGATTATGGTCGCTGCCTAGAATCCAGAAATACAAAGTAAACATTTTGATTAGCTGAATATAGCGTTTGGTGGATTACTTAAATAACTGCTTGATATCCAGTTAAAAATGACATGCTTATATGAAGCTTTGTATATACTTCTCTGGCTTTAGGGATATTTTGAATTTCTTGCGCGAGGGTGAGCTGCCTCAGAGGGACCGTGTTCGTGCCGTGCACAGGGAAGCTCAATATTATGCTATTGGACCTCTTTTGGAAAACCTGGAAGACACACAGCCTCTCACTGGAGAGAAAGTGCGACAAGCTTTTCTTGATCTCTTGCCCTATTATAAAGGTAATATGAATAATTAGAGGCTTAACTACATAATAATGTATAGGTTTTTGTGAGAGCACAATTTTTTACATTAATATATACACTACCTAAGAAAAGGTCTTGTCACCTATCCAAGTTTTAGGAATAACAAATAATACTTTGACTTC

Associated Phenotype:

Not determined