ZMP

srrm1

Ensembl ID:

ENSDARG00000001244

ZFIN ID:

ZDB-GENE-040426-2789

Description:

serine/arginine repetitive matrix protein 1 [Source:RefSeq peptide;Acc:NP_998607]

Human Orthologue:

SRRM1

Human Description:

serine/arginine repetitive matrix 1 [Source:HGNC Symbol;Acc:16638]

Mouse Orthologue:

Srrm1

Mouse Description:

serine/arginine repetitive matrix 1 Gene [Source:MGI Symbol;Acc:MGI:1858303]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36419	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa7437	Missense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa36419

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121848	Essential Splice Site	78	929	3	17

Genomic Location (Zv9):

Chromosome 17 (position 25269954)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	25409873
GRCz11	17	25428264

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAGGATGATGTGGTCATTGAATTTGTCTTTAACCAGCTGGAGGAAAAGG[T/C]AGACCCCCACCTTGCACTTCCCGCTCTTGTTTTATTTTTTTATACACATG

Long Flanking Sequence:

ACATCGTATAAGTTTTATATAAATAGAGTGATTAAATACAATTCTGTAGCTCCTGCCAACTATAATTCAGACTCAACTATGCATATCTTGCAATGTGACTATTGCAGATGCACACATTGCAATATCGAAGCTGAAACTATATATTGTGCAGCCCTAGTGTACATGTAAAAACACATTTTATAGCAGTGAAAATGGGGCTTCTTTTTCTACAAGTAATATTAAGAAGAACTAAAAATTTAGGTATTTATACAAAGTAATTTTGCAAAGCAAATCATCATTTTAGGTTATTTCTGATTTGTAATTTGACAATAAACCATTTTTAGCTCAATACAAGTAAAGATCCTGTAATTATGATTATTTTTTGATGTGGTTTTAGGTGGATATGACCAAGGTCAACCTGGAAGTCATCAAGCCCTGGATCACCCAGCGTGTGACAGAGATACTTGGCTTCGAGGATGATGTGGTCATTGAATTTGTCTTTAACCAGCTGGAGGAAAAGG[T/C]AGACCCCCACCTTGCACTTCCCGCTCTTGTTTTATTTTTTTATACACATGCTGCAGTCTATATTAGATGTGTTGTGCTTTGGAAAGAAGAGAAGGTTTGAAGATCAATGAATAACCGCTGACAGTTATTTGAAACATTTGTCATGTGAAGATGTAACAGCAGAAACATCTAACATCACAGTGTTAAACTGTCTGCCTGATTTAAAAAAAGACAGAAAAGGGGGTAAAAAGATATATTTCTCTCTGAAGAAATGATTTGTGACACCGTTCCTTCTGAACAGCAATGTTCTAATGTTGATGTGATTTATGATTTAAAAGGCCTGAACCAATATGGATCTTATTCCTTGCATCTGAAGTATAGCACCAACTCCTAATTAGATCTCAACTGAGCCCAAAGTCTCTCTGAATCCAACTCTCCCTTGATGATGAGCTTTATTTTTTGAGGTGAGTTATGAGCAGGGCTTGACATTGTGCCAGTGGTAGAGTCATTTCAGCTTGATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7437

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:

T > C

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000121848	Missense	144	929	5	17

Genomic Location (Zv9):

Chromosome 17 (position 25273704)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	25413623
GRCz11	17	25432014

KASP Assay ID:

554-4035.1 (used for ordering genotyping assays)

KASP Sequence:

MAACTTTTCCTTCTGCTTGTTTCAGATTGAACAGGAGAAACTCGCCKCTC[T/C]AAAAAAAGTAGATGAAGATAAAAGGGAGAAGGAGAACAAAGAAAGAGCTC

Long Flanking Sequence:

ATTCTGTTGTGGCTGTTGGTTATAGAAACCATTTTGAGGCCCGCAGGTACTGGGCTCTTGTTGAAAAGCAGCTGTTTACTGATGTTCAGGAAAGGAAGGTCTAGGTAGACTATCAGAATTCTGTGCTCTTGTTCGGTGTCAGTATTAACTGCTTGGTTTTCTCCCCTTCTCTCTTCCTCCCCTGCTGTTTGTGTTGCAGAATCCAGATGGAAAGATGATGCAGATTAATTTGACAGGTTTTCTGAATGGAAAGAATGCTCGGGAGTTCATGAAAGACCTCTGGCCACTGTTGTTAAGCGCCCAGGAGAACATTGCCGGTATCCCATCAGCCTTCCTGGAGCAGAAGAAAGAGGAGATCAAACAGAGACAGGTGATAAAGAACTGGGTCTGATCTCATATGCACATTTTTATTGGTTTTGTGTTAACTGATGTTGTAATGATACTAAAATTCAACTTTTCCTTCTGCTTGTTTCAGATTGAACAGGAGAAACTCGCCTCTC[T/C]AAAAAAAGTAGATGAAGATAAAAGGGAGAAGGAGAACAAAGAAAGAGCTCAGTCAAAAAGCCCTAAACGGTTGGTTTTGCTCTAGATCCTTATTCATTGATTTTTCCATTATTTTTCTATTGTTTTTGTGGTGTCAGAATTTGAATTCATAAAATAAATATATATTCTAAAAAAAATGGCGACTAACAAATTGTCACAATTGTCTGTAAATGATATAAAATGTTGCATAACAATCAACTTTGTTCTAAACCGCTGTTTTTTTTCTGCTTCCCTTTTAATTGCAGGAGAAAGTCTCGCTCCCCTGTGAAGCGTGATCGTAAATCCAGTCCTTCTCGTTCTCGCTCTCCTCGACGAAAAATAAGCCCAGCCGCTTCACCACCTTCCAGTCCACCCAATCATAAAGAAGAACCGAAGCGAGAACCAGACCAGTCAGAGAGCTCTAAACCAGAGCCACTCATTCAGGAAGCTTCATCTACCAGGTGACTTTGGAAATCTGACAT

Associated Phenotype:

Not determined