ZMP

enc1l

Ensembl ID:

ENSDARG00000058322

ZFIN ID:

ZDB-GENE-030131-5742

Description:

ectodermal-neural cortex (with BTB-like domain) [Source:RefSeq peptide;Acc:NP_001001402]

Human Orthologues:

ENC1, KLHL25

Human Descriptions:

ectodermal-neural cortex 1 (with BTB-like domain) [Source:HGNC Symbol;Acc:3345]
kelch-like 25 (Drosophila) [Source:HGNC Symbol;Acc:25732]

Mouse Orthologues:

Enc1, Klhl25

Mouse Descriptions:

ectodermal-neural cortex 1 Gene [Source:MGI Symbol;Acc:MGI:109610]
kelch-like 25 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2668031]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa5968	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43781	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa5968

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:

G > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050171	None	None	273	3	4
ENSDART00000081183	Nonsense	424	589	2	3

Genomic Location (Zv9):

Chromosome 22 (position 10895030)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	10755198
GRCz11	22	10784880

KASP Assay ID:

554-3946.1 (used for ordering genotyping assays)

KASP Sequence:

ATCWGTGTCTCTCAAACAAGTGGAGCAATACAACCCCCAATCCAACAAGT[G/A]GACTCTGGTAGCTCCTCTTCGAGAGGGTGTGAGCAACGCTGCGGTCGTTG

Long Flanking Sequence:

GGGACACAAGGTGGGTCGTGAGATTGTGGAAGACGCAGTTCGTTGCAAAATGAAGATCTTGCAGAATGATGGAGTTGTCACAGGTTTCTGTGCCCGACCCCGGAAGGTGAGCCAAGCCCTTCTGCTTCTAGGGGGCCAAACTTTTATGTGCGACAAAGTATACATGATTGATCACAAGGCCAAGGAGATCACCCCTAAAACAGACCTTCCAAGCCCTCGTAAAGAGTGCAGTGCTTGTGCCATTGGCTGTAAGGTGTACGTCACAGGTGGTCGAGGCTCTGAAAATGGGGCTTCAAAAGACGTTTGGGTCTATGACACTCTGCATGATGAATGGTCCAAAGCTGCACAGATGCTTGTTGCTCGATTTGGGCATGGTTCGGCAGAACTTGACCACATCCTGTATGTAGTAGGTGGACACACATCCCTTGCAGGGTCATTTCCTGCTTCTCCATCTGTGTCTCTCAAACAAGTGGAGCAATACAACCCCCAATCCAACAAGT[G/A]GACTCTGGTAGCTCCTCTTCGAGAGGGTGTGAGCAACGCTGCGGTCGTTGGGGCCAAAAACAAACTCTTTGCTTTCGGAGGGACTAGTGTCAACAGGGACAAGTATCCCAAAGTTCAGTGCTTTGACCCCTGTGAGAACAGGTGGACAGTCCCGGCCACTTGCCCTCAGCTTTGGCGTTACACAGCGGCAGCAGTTGTTGGGAACCATGTTGTGGTCATCGGCGGAGATACAGAGTTCTCCGCCAGCTCTGCTTACCGCTTCAACAGTGAGACGTTCCAGTGGACCAAGTTTGGCGATGTGACCTCAAAGAGAATCAGCTGTCATGCAGTGGCGTCAGGGAATCGCCTGTATGTGGTCGGAGGCTACTTTGGGGCCCAGAGGTGTAAAACGTTGGACTGCTATGACCCCTCGACAGACTCATGGGACAGTATAACAAGCGTACCCTATTCGCTTATCCCGACAGCATTTGTCAGCACCTGGAAGTACCTCCCCTCTTGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43781

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050171	None	None	273	3	4
ENSDART00000081183	Nonsense	469	589	2	3

Genomic Location (Zv9):

Chromosome 22 (position 10895164)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	10755332
GRCz11	22	10785014

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTAGTGTCAACAGGGACAAGTATCCCAAAGTTCAGTGCTTTGACCCCTGT[G/T]AGAACAGGTGGACAGTCCCGGCCACTTGCCCTCAGCTTTGGCGTTACACA

Long Flanking Sequence:

GCCAAACTTTTATGTGCGACAAAGTATACATGATTGATCACAAGGCCAAGGAGATCACCCCTAAAACAGACCTTCCAAGCCCTCGTAAAGAGTGCAGTGCTTGTGCCATTGGCTGTAAGGTGTACGTCACAGGTGGTCGAGGCTCTGAAAATGGGGCTTCAAAAGACGTTTGGGTCTATGACACTCTGCATGATGAATGGTCCAAAGCTGCACAGATGCTTGTTGCTCGATTTGGGCATGGTTCGGCAGAACTTGACCACATCCTGTATGTAGTAGGTGGACACACATCCCTTGCAGGGTCATTTCCTGCTTCTCCATCTGTGTCTCTCAAACAAGTGGAGCAATACAACCCCCAATCCAACAAGTGGACTCTGGTAGCTCCTCTTCGAGAGGGTGTGAGCAACGCTGCGGTCGTTGGGGCCAAAAACAAACTCTTTGCTTTCGGAGGGACTAGTGTCAACAGGGACAAGTATCCCAAAGTTCAGTGCTTTGACCCCTGT[G/T]AGAACAGGTGGACAGTCCCGGCCACTTGCCCTCAGCTTTGGCGTTACACAGCGGCAGCAGTTGTTGGGAACCATGTTGTGGTCATCGGCGGAGATACAGAGTTCTCCGCCAGCTCTGCTTACCGCTTCAACAGTGAGACGTTCCAGTGGACCAAGTTTGGCGATGTGACCTCAAAGAGAATCAGCTGTCATGCAGTGGCGTCAGGGAATCGCCTGTATGTGGTCGGAGGCTACTTTGGGGCCCAGAGGTGTAAAACGTTGGACTGCTATGACCCCTCGACAGACTCATGGGACAGTATAACAAGCGTACCCTATTCGCTTATCCCGACAGCATTTGTCAGCACCTGGAAGTACCTCCCCTCTTGAAGAAAATACATCTCCTATTTGGTGAGTATTGTCCAGTGTAGGGCTGCACAGTATTTTTAAAAATGACATTCCGATATTTTGTGTTGTATATATTGAGATATGACATCTATTTCACCAGATGGATTGAATATCTCT

Associated Phenotype:

Not determined