ZMP

si:ch211-241j12.3

Ensembl ID:

ENSDARG00000043963

ZFIN ID:

ZDB-GENE-040724-72

Description:

actin-like [Source:RefSeq peptide;Acc:NP_001025380]

Human Orthologues:

AC078802.1, ACTL7A, ACTL7B, ACTL9, ACTRT1, ACTRT2

Human Descriptions:

Actin-related protein M1 [Source:UniProtKB/Swiss-Prot;Acc:Q9BYD9]
actin-like 7A [Source:HGNC Symbol;Acc:161]
actin-like 7B [Source:HGNC Symbol;Acc:162]
actin-like 9 [Source:HGNC Symbol;Acc:28494]
actin-related protein T1 [Source:HGNC Symbol;Acc:24027]
actin-related protein T2 [Source:HGNC Symbol;Acc:24026]

Mouse Orthologues:

4921517D21Rik, Actl7a, Actl7b, Actrt1, Actrt2, Arpm1, Gm498

Mouse Descriptions:

RIKEN cDNA 4921517D21 gene Gene [Source:MGI Symbol;Acc:MGI:1914972]
actin related protein M1 Gene [Source:MGI Symbol;Acc:MGI:1923902]
actin-like 7a Gene [Source:MGI Symbol;Acc:MGI:1343051]
actin-like 7b Gene [Source:MGI Symbol;Acc:MGI:1343053]
actin-related protein T1 Gene [Source:MGI Symbol;Acc:MGI:1920610]
actin-related protein T2 Gene [Source:MGI Symbol;Acc:MGI:1920603]
predicted gene 498 Gene [Source:MGI Symbol;Acc:MGI:2685344]

Alleles

There is 1 allele of this gene:

Allele Name	Consequence	Status	Availability
sa19222	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa19222

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
ENSDART00000064546	None	None	372	None	7
ENSDART00000123860	Nonsense	19	1239	1	12

Genomic Location (Zv9):

Chromosome 20 (position 191621)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	182216
GRCz11	20	170851

KASP Assay ID:

2261-3793.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCCTGAGGAGGATCCTGACCGCTCCTGGTGCCGTTCCCCTCCAAGACCTC[C/T]AGCTGGCCCTTCAGTGGCAGTACGAGTACCTGAAGGGCCACCGCTCGACC

Long Flanking Sequence:

TGAATGTGGATAACTCTGCTGTCGTATTTATATGTGTGATGTGTGTGTGCAGGCGCTAGTGCGGCGAGCAGAGGATGTGATGCACACACTAGCAGAGACTGTCCCACCAGCAGACAGGAGGCCTGCAGAGCCCTGGCTGGAGGAGCTGACCCGCCTAAAGGACCAGCTGAGCTCTGCAGTCCAGAACCAGCTCCAGACCCTCAACAGAGCCGCACACTTCCAACACTCCTGCAACAGGGTGGGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCTGAAATACACTCGCTGTGTTTACTGTGTTCTGACAGCTGAGGGGGCAATGTCATTACACCCCAAACCTAAACGTATGTCCTGTAGCAGTGCAGGTCCTGAACACAATCAAGCTCTCGTTCAGCATTAGTGTGTGTAATGAATGCTGATGTTTGTCCGCAGATGCATGACCCTGAGGAGGATCCTGACCGCTCCTGGTGCCGTTCCCCTCCAAGACCTC[C/T]AGCTGGCCCTTCAGTGGCAGTACGAGTACCTGAAGGGCCACCGCTCGACCTCTGACCTCTCCACTGCTGACCCTCCAGGCTCGGTGCAGTGCGGGAGCATCAGTGATCTCTCCAAGTGGCCCGCGGTCTCCTCCACACGAGCTGCGCCTAAACCTCCATCTCTCAGCTCCTTTGACTCTGGCTTTGATGGAGCGGGCAGCAGTCTCCTGGACCTCAGGGGCCGGAGAGACACGCCGGGTATTCTAGTTAATGGAGATCCTGTCTTTAAGCCGAGCCCCCTTCACGCGCAGATTCATGAAGAGATCATAGTGAGTGTGTCCGACTCTGAGGACCAGCAGGAGGAGCTGACGGGGTTCGGGCTGAAGCGGGACGCTGCTCATGCCAGCATTCAGATTGTCCCCAAAATCAGTTCTGACTCTGTGAACCTGGAAATCAAGGTGAAGCGCTCTGCAACGCTGCCCACCAACCCCTGGCTGAGCCTCCCCATAGAGGAGCTGGAG

Associated Phenotype:

Not determined