ZMP

zrsr2

Ensembl ID:

ZFIN ID:

Human Orthologues:

ZRSR1, ZRSR2

Human Descriptions:

zinc finger (CCCH type), RNA-binding motif and serine/arginine rich 1 [Source:HGNC Symbol;Acc:12456]
zinc finger (CCCH type), RNA-binding motif and serine/arginine rich 2 [Source:HGNC Symbol;Acc:23019]

Mouse Orthologues:

Zrsr1, Zrsr2

Mouse Descriptions:

zinc finger (CCCH type), RNA binding motif and serine/arginine rich 1 Gene [Source:MGI Symbol;Acc:MG
zinc finger (CCCH type), RNA binding motif and serine/arginine rich 2 Gene [Source:MGI Symbol;Acc:MG

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa38832	Nonsense	Mutation detected in F1 DNA	Not yet available
sa41794	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa38832

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
ENSDART00000081319	Nonsense	307	635	10	11

Genomic Location (Zv9):

Chromosome 11 (position 12796837)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	12681246
GRCz11	11	12738905

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGAGCAATGCAAAGAAGCTTTTGTGATGTTTAATGGTCGCTGGTATGCT[G/T]GAAGACAACTGCAATGTGAATTCTCCCCTGTGACTAGATGGAAAACGGCC

Long Flanking Sequence:

TACGACACCGATGCCAGTCTGGAGTACAGTGAGGAGGAGTTGCACCAGCAGTTTCTGGATTTCTATGAAGACGCTCTGCCAGAGTTCAAGAACGCAGGGAGAGTGGTGCAGTTCAAGGTAACTCAAATAAAAGCCTGAAAAACCATCAACAAATAAAATCTCTCTTTATTTAGATGTTTCTTTAGATTTATCTCGTATGAAAGTCGTATTTTTTATTCTATCAGCTGCAGAAATGTAAATAAATATGTATATTTTTGTAAAATTAAATTGACAATGATTATTATTTGGCCATATTTTAATAGGTGAGCTGCAACTTTGAGCCTCACTTAAGAGGAAACGTTTACGTTCAGTATGAGACGTAAGTCCAGCATTATTATTTTGGAGATTTTTTTTGACAGCAGATTTATAAATGTACGTATATTTGGATATCTTTGTTTATATCCTGCAGAGAGGAGCAATGCAAAGAAGCTTTTGTGATGTTTAATGGTCGCTGGTATGCT[G/T]GAAGACAACTGCAATGTGAATTCTCCCCTGTGACTAGATGGAAAACGGCCATTTGTGGTAAGGAAAATATTAGTAGGTCACACTTACAATAAGGTTCCATTAGTTAATGTATTTACATGAATTTACATAAAAACATGAATATTAAACAATACTTTAGGCATTTATTAATTGTAGTTTGTGTTGAATTCAACATTTTATGACTCGTTTCCACTGATTGGTACAGTACGATACGGTTTAGGTCGGTACGGGTCATCTTTATCAGGCTTGCGTTTACACTACCAAGGGTACCTTTTGGTGGGTGTGGTGTATAACACAGTTTCAGTCGATGTAATTTTCGCTCGAGAAAATGTCTATAATAAAGCTGAACAGGTCGTTCACGAATCATATGAAAACAGACGCTTTTTACACATAAATACTTGTGTATAAATGTTTATTGCTAACTTTTCTATAAACAGGATTTGATTATAACTGCAGATCAATGACAGTGCGAAATAGCCTAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa41794

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
ENSDART00000081319	Nonsense	309	635	10	11

Genomic Location (Zv9):

Chromosome 11 (position 12796831)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	12681240
GRCz11	11	12738899

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATGCAAAGAAGCTTTTGTGATGTTTAATGGTCGCTGGTATGCTGGAAGA[C/T]AACTGCAATGTGAATTCTCCCCTGTGACTAGATGGAAAACGGCCATTTGT

Long Flanking Sequence:

ACCGATGCCAGTCTGGAGTACAGTGAGGAGGAGTTGCACCAGCAGTTTCTGGATTTCTATGAAGACGCTCTGCCAGAGTTCAAGAACGCAGGGAGAGTGGTGCAGTTCAAGGTAACTCAAATAAAAGCCTGAAAAACCATCAACAAATAAAATCTCTCTTTATTTAGATGTTTCTTTAGATTTATCTCGTATGAAAGTCGTATTTTTTATTCTATCAGCTGCAGAAATGTAAATAAATATGTATATTTTTGTAAAATTAAATTGACAATGATTATTATTTGGCCATATTTTAATAGGTGAGCTGCAACTTTGAGCCTCACTTAAGAGGAAACGTTTACGTTCAGTATGAGACGTAAGTCCAGCATTATTATTTTGGAGATTTTTTTTGACAGCAGATTTATAAATGTACGTATATTTGGATATCTTTGTTTATATCCTGCAGAGAGGAGCAATGCAAAGAAGCTTTTGTGATGTTTAATGGTCGCTGGTATGCTGGAAGA[C/T]AACTGCAATGTGAATTCTCCCCTGTGACTAGATGGAAAACGGCCATTTGTGGTAAGGAAAATATTAGTAGGTCACACTTACAATAAGGTTCCATTAGTTAATGTATTTACATGAATTTACATAAAAACATGAATATTAAACAATACTTTAGGCATTTATTAATTGTAGTTTGTGTTGAATTCAACATTTTATGACTCGTTTCCACTGATTGGTACAGTACGATACGGTTTAGGTCGGTACGGGTCATCTTTATCAGGCTTGCGTTTACACTACCAAGGGTACCTTTTGGTGGGTGTGGTGTATAACACAGTTTCAGTCGATGTAATTTTCGCTCGAGAAAATGTCTATAATAAAGCTGAACAGGTCGTTCACGAATCATATGAAAACAGACGCTTTTTACACATAAATACTTGTGTATAAATGTTTATTGCTAACTTTTCTATAAACAGGATTTGATTATAACTGCAGATCAATGACAGTGCGAAATAGCCTAAGGTAAC

Associated Phenotype:

Not determined