ZMP

STRC (2 of 2)

Ensembl ID:

ENSDARG00000079336

Description:

stereocilin [Source:HGNC Symbol;Acc:16035]

Human Orthologue:

STRC

Human Description:

stereocilin [Source:HGNC Symbol;Acc:16035]

Mouse Orthologue:

Strc

Mouse Description:

stereocilin Gene [Source:MGI Symbol;Acc:MGI:2153816]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa17916	Essential Splice Site	Available for shipment	Available now
sa40926	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa17916

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC
Order Allele From EZRC

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110881	Essential Splice Site	59	576	2	13

Genomic Location (Zv9):

Chromosome 7 (position 32752481)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	31146821
GRCz11	7	31417971

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TTCTCAGATTTGCTTGGAGATTTGGGACCTCAGATTGCTCTGTCACTTCC[G/T]TGAGTCACAATTTAGTTCAGTTTTAATGTAATTTAATGTAATCATGTTTT

Long Flanking Sequence:

AATAACCTACCCAATGAAATATGAATTGCTTATTTTTCTTCTTCTTTCTCTGACAGATCTTTGGGCACAGTGGCTACAGGAGTGACATGTGTTGAACTTAAAAAAATGTTTGAAAGCCTGGCTTCTCTGTCTCCACTACGGGACATTCTATCATTTCTCAGAGAGCAGCCTGTGCCACTCCACCCCTCACTTGTATGCTAACGAAAGCTTAAATTCAATTGCAGATTACTTTTCTGTTTAGTCAATTCCTCACTAAATTCAGTCTTCTCATTGTTGACTTGATTGTTAAAGTTTTGTGTAGACCCAAATTGATGTGTTAAATTGTGAATGCTGGATCAATTATTGCCCAAACTGTATGAACAAATGTACATTTCTCATCAAAGAAGATGCATTGTCTTCTATGTATTACAGACACAGTGTATAAATGAGGAACTCTACAACTTTAACTTCTTCTCAGATTTGCTTGGAGATTTGGGACCTCAGATTGCTCTGTCACTTCC[G/T]TGAGTCACAATTTAGTTCAGTTTTAATGTAATTTAATGTAATCATGTTTTCACATTCAATTCCATACCATTCTTTAAGGCTGTCCACCATTAAGAAGTTTCCACCAGATAAAATGGATTCCCTCAGGAGAATGATAGTGGAAGACCCACATTACTTCCTATTGCTTCCAAGCACCAAACAAGCTGCACTTGTGGACAAGATGGTTCAAAGACTGGTAAAGATCGGTTTTGTTTTATTGTGGAGGGAACACACTTACTGAACAAAACAAATCCGTGTGAGAGTGAAGTCACATAATAGTGTATATAAAAATGTAAAGTTCTGAACATGACTTATTGACAGTGTAAAAGTTAAAGATCAGAGATGAAGCATAACTCATTTTCCTAATAACCAGTACAATCTACCAAGAATAGCCCAAGTTAAAACGACTGTGGCTTAAAAATGAATTCTACGAGTGAGTTCTACGTACTTCTTTGACAAGTTTCAGTTGCTGCTGGAGGATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40926

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110881	Nonsense	103	576	3	13

Genomic Location (Zv9):

Chromosome 7 (position 32752690)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	31147030
GRCz11	7	31418180

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATTGCTTCCAAGCACCAAACAAGCTGCACTTGTGGACAAGATGGTTCAA[A/T]GACTGGTAAAGATCGGTTTTGTTTTATTGTGGAGGGAACACACTTACTGA

Long Flanking Sequence:

TAAATTCAATTGCAGATTACTTTTCTGTTTAGTCAATTCCTCACTAAATTCAGTCTTCTCATTGTTGACTTGATTGTTAAAGTTTTGTGTAGACCCAAATTGATGTGTTAAATTGTGAATGCTGGATCAATTATTGCCCAAACTGTATGAACAAATGTACATTTCTCATCAAAGAAGATGCATTGTCTTCTATGTATTACAGACACAGTGTATAAATGAGGAACTCTACAACTTTAACTTCTTCTCAGATTTGCTTGGAGATTTGGGACCTCAGATTGCTCTGTCACTTCCGTGAGTCACAATTTAGTTCAGTTTTAATGTAATTTAATGTAATCATGTTTTCACATTCAATTCCATACCATTCTTTAAGGCTGTCCACCATTAAGAAGTTTCCACCAGATAAAATGGATTCCCTCAGGAGAATGATAGTGGAAGACCCACATTACTTCCTATTGCTTCCAAGCACCAAACAAGCTGCACTTGTGGACAAGATGGTTCAA[A/T]GACTGGTAAAGATCGGTTTTGTTTTATTGTGGAGGGAACACACTTACTGAACAAAACAAATCCGTGTGAGAGTGAAGTCACATAATAGTGTATATAAAAATGTAAAGTTCTGAACATGACTTATTGACAGTGTAAAAGTTAAAGATCAGAGATGAAGCATAACTCATTTTCCTAATAACCAGTACAATCTACCAAGAATAGCCCAAGTTAAAACGACTGTGGCTTAAAAATGAATTCTACGAGTGAGTTCTACGTACTTCTTTGACAAGTTTCAGTTGCTGCTGGAGGATGAATCTAAAGAACAATTGCTGCAAAATAGATAAATGCATATATTTTGGGTGCAAATAAAGTAAATTGACTCTCCTAACTTATTCATTTATTTTTGTTTGGCTTAATCCCTTTATTAATCAGGGGTCTCCTTAGTGAAATGAACTGCCAACTTATCCAGCATATGTTTTACACAGAGGAGCTGCAACCCAGTACTGGGAAACACTCATTAA

Associated Phenotype:

Not determined