ZMP

frmd6

Ensembl ID:

ENSDARG00000002332

ZFIN ID:

ZDB-GENE-050522-354

Description:

Novel protein similar to H.sapiens FRMD6, FERM domain containing 6 (FRMD6, zgc:110114) [Source:UniPr

Human Orthologue:

FRMD6

Human Description:

FERM domain containing 6 [Source:HGNC Symbol;Acc:19839]

Mouse Orthologue:

Frmd6

Mouse Description:

FERM domain containing 6 Gene [Source:MGI Symbol;Acc:MGI:2442579]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa2703	Essential Splice Site	F2 line generated	Not yet available
sa9206	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa2703

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000024386	Essential Splice Site	116	616	5	14
ENSDART00000137328	None	None	186	None	6
ENSDART00000138104	Essential Splice Site	116	616	4	13

Genomic Location (Zv9):

Chromosome 13 (position 37378850)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	36855662
GRCz11	13	36981552

KASP Assay ID:

554-3068.1 (used for ordering genotyping assays)

KASP Sequence:

ATTGTTCACTTCAGAGCACAGTATTATGTTGAAAATGGCAGACTTATYAG[G/A]TGAGACACATGCACATCAAAAGGAAAGACRCAATAAAASAATTAAAAGTG

Long Flanking Sequence:

TGATCATTAAATATTAAAACTGTATTTTCATTGTCCATATATATATATTTTAAAGTAGCCATGTAGCTAGTGGAATAATGTATGGTTTGCTGGTTATTATCAAATTTTATGCTTTGATTTGGGGTTTTAATCATTCTGTCAGGGTTTATTTTGCGGTACTTACCGCAGTTATGCTTGTAATTTCCCCCATTATCCATTACACAGATAAACATTATAGACCTAAGCTTATGAGTTCTTTGTGCTTTTTTTCCTTTTAGACAATGAACACATATACATGGAACTGGGACAGAAACTGTCGAAATACTGCCCAAAAGAGTGGAAACGGGAAGCCAGCAAGGTATCACACATGCACTCTTTGATCTCCTTGGAATTTTAGTTAATTTGTTGTTTTTACATTTCGACTTAATTCTTGCCATTTTGCAGGGAATTGACCAGTTTGGACCTCCAATGATTGTTCACTTCAGAGCACAGTATTATGTTGAAAATGGCAGACTTATCAG[G/A]TGAGACACATGCACATCAAAAGGAAAGACGCAATAAAAGAATTAAAAGTGACAGTGCTGCCACTCACAAATGTTTTGGTCTTGTATAAAGCTTAGCTGCTTTTGGGACACTATTCTTAAAACTGCATGAATTTTTTTCGGTTATATCTATTTCTCCTTGCCCACTGATTGCCATTTTGTGGATTTTTTCCCATGTCAAATAATCTTACAAAGATCTGGGGTTCGTTCTTCGTACGTTGATTACTCAATTAACTGGATTTGGTTATTGATGATTTGACACGATCCAGGATTGTTTAGTTCGTCAAAACTCATTCGAGAGTTGTTGTCATAGCAACAGTTCTGGTAACTCAAACCTGCTCAGGAGCAGGCTCATTTCATATAAACAGGATTAGATCAGGTCAGTTCAAGCAAATACTAAAAGTATGTATCGAATGCTGATATTTTCGTTCAGTAGTAGTTAAGTTTAAAATAGTCAAATCTATAAATAAACTAATGCAAGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa9206

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
ENSDART00000024386	Nonsense	370	616	11	14
ENSDART00000137328	Nonsense	176	186	6	6
ENSDART00000138104	Nonsense	370	616	10	13

Genomic Location (Zv9):

Chromosome 13 (position 37387547)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	36864359
GRCz11	13	36990249

KASP Assay ID:

2260-6759.1 (used for ordering genotyping assays)

KASP Sequence:

ATTTGGAGCAGCGTTCGCGTGCCAGCGGCAGCAGTGCGGGAAGCACATCA[C/T]GACCCAATCCCTTTTCACGGCACTCCACCACCAGTCATGGCAGCTCCCGC

Long Flanking Sequence:

ATTTTGCTTTCTCAAATTATTTAAGAAATTTTCTATTGTTTCTGAGTGAAAATAATTTTTTGTTTTATATTTGTGCAACTTGGTTTGCTGATATACTTATTTTGTTTACAAGTAAATGTACTAATTAATTCACAGCACAAATGTATATTGATTTAGCATGAAAATATTCATTAACTGATTTCACAAACATCTCTATTTGACAGCAAGAACCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTGCTTGTACTACTACCATAACAACTGAACAACAACAGCAACAAAAAAAGAGAGAAAAGTTTCATGTTTTGCTTCACTAAGGACTTGGAGCATATGGTTGACATTAATCTCCGTGTGTGTTTGTGTGTGTGTGTGTCTTCTCAGAAAAGAAGCAGTACCGGGAGTCGTATATCAGTGATGCTCTGGAGGCGGACATGGATCATTTGGAGCAGCGTTCGCGTGCCAGCGGCAGCAGTGCGGGAAGCACATCA[C/T]GACCCAATCCCTTTTCACGGCACTCCACCACCAGTCATGGCAGCTCCCGCACATCCGGCGTCGACACAGACAGTTTCCGGACCCCTACAAACACACCCCACCGTCCGCTGAGAACACACTCGTCTTCCAACACCAGTCATGCCAGCACACACACGTCTGGCATCGAGAGCAGCAGCAAAGAGCACTGCCTGGATGAAGACGGTAGGAGACTGCATGAATGTGTTACTTATTATATTGGTAATACCAGTATGAACAAAAATGTGATGTGATTTAAGTGCGTACATTCTTCAAATCTTGTTGTGATGACGTTGTAACAGACTGACTGGTTAGGGGTGCCGACTTATACATTTTTATAATTGAAATAAATAGTAAATATATAATGTCAGTTCTACAAACACTACCCGACAAAAGCCTTGTCGTCGATTTCAGTTTTAAGAGCAACAAATAATAACTTGACTTCTAGTTAATTATTTGTAAAAGTGGCAGAAGGTAGATTTTTC

Associated Phenotype:

Not determined