Busch Lab

ZMP

SRRM2 (2 of 2)

Ensembl ID:
ENSDARG00000090027
Description:
serine/arginine repetitive matrix 2 [Source:HGNC Symbol;Acc:16639]
Human Orthologue:
SRRM2
Human Description:
serine/arginine repetitive matrix 2 [Source:HGNC Symbol;Acc:16639]
Mouse Orthologue:
Srrm2
Mouse Description:
serine/arginine repetitive matrix 2 Gene [Source:MGI Symbol;Acc:MGI:1923206]

Alleles

There are 2 alleles of this gene:

Allele Name Consequence Status Availability
sa19924 Nonsense Mutation detected in F1 DNA Not yet available
sa39968 Nonsense Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa19924
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000129287 Nonsense 40 555 1 4
Genomic Location (Zv9):
Chromosome 3 (position 1936816)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 1395028
GRCz11 3 1163677
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGTTACGATTCTCCTACAGCTCGAAAACCAGACATAAAGAACCTTTCATA[T/A]GACCGACTGAACTCCTCCATCTCCACCAGCCGATATGATTCAAGAAGCCA
Long Flanking Sequence:
GATCTCACTGCAGAGATTGAGGCCCTCGCTGGACCCCGGGCCCTGAGCCCCACACCTTTTAAACAGGCTGAATCCTACAGTTCCTCCAGTCGAAGAGGTGGACAAAGTCGAAACACGTCTCCTTTACGACAGCCGGGGTCACTCAACACTTCCCACAGAGGCTCCAGTCTCCTGCAGTCCTCATCTCCCTCTCAAAGCCTTTCGCCATTCAGACGGGCTGAGTCCAGTTCCTCCATCAACACCGTGGGCTTACGCTCGAGTGGAGCGTCATATAGACAAGACCGGGCATCTGTCAGTCCAACACGGAGCAGTTACACTGCACAGAAAAATCTCAGATCATTGGCGAGTACGGTAGGCACGGTCAGCAAGTCTCTGTCCTACATGGATCTGAAAGGCTCTCAACAAAAACACGGAACCAGCAGCCGCAGCGGCTCGCCTCCATCTAGACGGAGTTACGATTCTCCTACAGCTCGAAAACCAGACATAAAGAACCTTTCATA[T/A]GACCGACTGAACTCCTCCATCTCCACCAGCCGATATGATTCAAGAAGCCAGTCCCCTTCCAGACAGAGTTATGAGGGTCGGAAAGCTGAGATAAAGAGCCCTTCACATGAGCGGAGCCATGACAGACAGAGCTCCTCCTTTTCCACGAAGGGTCGATACAGTTCCAGGAGCCAGTCCCCATCGGGGAGACCAGAGGATGGCCAGAGTCCAGAGGGGCGACGCAGCGCATCTCCAGTCAGGAAGGGCTATGGGACACCAAGCCAATCAGAACCAAGATCTGTCTCAAATAGGTGGAGAGATGAGAGAACAAGCCCTGCCCCCACTAGGAAAAACTATGAGGGACAAACCACAATGAAGAAAACAGAAGCAAATAGCCGACACTCTTCTCCAAATAGAGGCTCATCATTGTTTCGTAAGCCTGAAACATCATCAAACCATGGCCCCAAGAGCCGCAGTACATCCCCATTAGCCCCGAGTCCATCTGTCCTGCGTAACTCAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa39968
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
ENSDART00000129287 Nonsense 451 555 1 4
Genomic Location (Zv9):
Chromosome 3 (position 1938047)
Other Location(s):
Assembly Chromosome Position
GRCz10 3 1396259
GRCz11 3 1164908
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACCGTCTTCCAGAGGGAGAGTCCGAGCCACCCGATGAGGTCCGAGAAA[C/T]GAGAACAGTCCCGCTACAAACCCGCCAGGTGGAGAAAGCTTCATCACTGT
Long Flanking Sequence:
CCTTCACTCAGTCGGTCCCTGTGGGCTGGGGGGTGCCTCAGGACAGCGGCCGCAGGAGCAGCTCCAGACCAGGCCATCAGGAGCACACTTCCAGGACTTCACCCTTGAAGACACACACCTCCACCCCCAGTGGCCGGAGACACCGCAGCCCCTCTCCTCCAGTGCAGACACACACCTCCATCCCCAACAGCCGGAGACACCGCAGCCCCTCTCCCCCAGTGCAGACACACAACTCCACCCCTAGCAGGCAGAGACACCGCAGCCCCTCACCTCCAGTGCAGACACACAACTCCACCCCTAGCAGCCGGAGACACCGCAGCCCCTCACCTCCAGCGCAGACACACACATCTTCTCAGAGCTCCATGGACTCCGAGTCCAGCCATCTGTCTGCAGGGTCGTCGGGTCTCAACCGGGAGGAGTACGCCATGATGGCTGACCTTCCCAAAGTTAAAACCGTCTTCCAGAGGGAGAGTCCGAGCCACCCGATGAGGTCCGAGAAA[C/T]GAGAACAGTCCCGCTACAAACCCGCCAGGTGGAGAAAGCTTCATCACTGTACTAATCACTGTGTAATGCTGACATCAGACCAAACTTTATTATTTATTCTCCTCATTTATTTACAAATGAAATCATGTGTCTACAGTCACTCCCACAGCAAAGCTCCACACTCAGAATGGGAGGATCTGGAGGAGGATAGAGAGAGTGGCACACTATCACGGGCTCACTCGTCCAGCTCTCTACACACACAGGTAACCACACACTGGTCAGTGTGTTTGGCCTGCTTCTCCTCCACTGATTGGACGGCTGAGTGACAGTGACCAGTGCCTTTTTACCCAAAATCAAACAATAAAGAGCTCTACAAAACGAAAACAGACCAAACTGACTTGTGAATATTAATATTGATTTATTTTACTGTTATTAATTCTTCAGTGTTTCCGCAGGGATTGAGCCGCCCGGCTGCAGAGCACACACACTCCAGCAGGAGCTCAGGACAGAAGCAGGTACAG
Associated Phenotype:
Not determined