ZMP

scxa

Ensembl ID:

ENSDARG00000035695

ZFIN ID:

ZDB-GENE-060503-414

Description:

scleraxis homolog A [Source:RefSeq peptide;Acc:NP_001076538]

Human Orthologues:

SCXA, SCXB

Human Descriptions:

scleraxis homolog A (mouse) [Source:HGNC Symbol;Acc:24312]
scleraxis homolog B (mouse) [Source:HGNC Symbol;Acc:32322]

Mouse Orthologue:

Scx

Mouse Description:

scleraxis Gene [Source:MGI Symbol;Acc:MGI:102934]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36755	Nonsense	Mutation detected in F1 DNA	Not yet available
sa23414	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa36755

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
ENSDART00000105192	Nonsense	50	204	1	2
ENSDART00000145363	Nonsense	45	199	1	2

Genomic Location (Zv9):

Chromosome 19 (position 3564418)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	3060991
GRCz11	19	3001889

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTT[A/T]AAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATT

Long Flanking Sequence:

TCCCACAACCTATAAAGCACAACCATACTGAAACACTCAGTGAAACCACACGTGGGTCTCAGCACGGGGGAGAGCCAGCGCTGCACAGAGACAGAAAGCCGGAGGAGTGTGTGTGTGCATGTGTATGTTTGAGGATACAAAACGTGGATTTCAGAGCTGATGGGATGTGAGTGAGGACAATCTCCAATATCAACCCGTCAGGATCAGTTCCCCAAGAGAAATGTAATACTGGAGCGCAACTGTACCAGAGGACCAAACAAGTGCAGGACTCATTGAGATTCATGCGTTTGGAACTTTAGAGCAATTGCAAGAAGCATTCGAGAGCCTTGTGGAGAGCGTTAGAAATCAAGTTGATGATGTCTTTTGCGATGGTGCGACCGGCTCCGAGCCGATACGTGTATTCTGACATCTCAATGATGTCGGAGGATGATGAAAACGGCAGCGAGAGCTCAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTT[A/T]AAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATTGGTGTAACACCAACCATTCCCACCGGGACAATCGGCCATGTGCCAGAGATCCGTCAACGCAATGCTGCCAATGCACGAGAGCGGGATCGCACCAACAGCGTCAACACGGCATTCACAGCATTGAGGACTCTCATCCCTACAGAGCCTGCTGACCGGAAGCTGTCCAAGATCGAGACCTTGCGGCTGGCGTCCAGTTACATCTCTCATCTGGGGAACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGCGGAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGGGACTCGGAGAACTCGCAGCCCAAACAGATCTGCACATTCTGCCTCAGCAACCAGAGGAAAATGGTAAGTCAGACACACGCAGGTGTTCTCCGTTAAAGGTTGTGCAATGATCTGGACAACTTCAAGTCCACAAAC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23414

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

Mutation:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000105192	Nonsense	155	204	1	2
ENSDART00000145363	Nonsense	150	199	1	2

Genomic Location (Zv9):

Chromosome 19 (position 3564733)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	3061306
GRCz11	19	3002204

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGC[G/T]GAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGG

Long Flanking Sequence:

ATTCGAGAGCCTTGTGGAGAGCGTTAGAAATCAAGTTGATGATGTCTTTTGCGATGGTGCGACCGGCTCCGAGCCGATACGTGTATTCTGACATCTCAATGATGTCGGAGGATGATGAAAACGGCAGCGAGAGCTCAGGCTCGGATGATCGCTCATTTCACCTGGACACTTCAGGGTATGATCTTAAAGTTGGAAGAAAGAGGAAATCCAGTGTAGGGGGTGGCGGACGGCTGATTGGTGTAACACCAACCATTCCCACCGGGACAATCGGCCATGTGCCAGAGATCCGTCAACGCAATGCTGCCAATGCACGAGAGCGGGATCGCACCAACAGCGTCAACACGGCATTCACAGCATTGAGGACTCTCATCCCTACAGAGCCTGCTGACCGGAAGCTGTCCAAGATCGAGACCTTGCGGCTGGCGTCCAGTTACATCTCTCATCTGGGGAACGTGCTGCTGGTGGGTGAAGCTTGCGGAGATGGACAGCCGTGCCACAGC[G/T]GAGGACCCTCCACCTCAAACTACTACCACCACCACGGCTCACCCAGCCGGGACTCGGAGAACTCGCAGCCCAAACAGATCTGCACATTCTGCCTCAGCAACCAGAGGAAAATGGTAAGTCAGACACACGCAGGTGTTCTCCGTTAAAGGTTGTGCAATGATCTGGACAACTTCAAGTCCACAAACAAGCTGGAGAAATAGTGACAGAGGTGTAAAATACTGCTGAACCTCAGGGAGGGATGAGAGCAGGTCTGATTTATTCCCTGCAAGTAAGGTCACTGAGGGCAATCACTATAGCAAGTCCAAAACTACTGAAGTTAACTTTAGCAGAGTATCTTTCAAACAAGTAGGACTTGACAAACAAGACTAAGCAGCTAACTTCTAAAAAGAGCACTGCAAAAACTTGATGATAATGTTTTGAGGCATGAGCAATCATGGCTGTAGACGGTCTGTCATTGATTTTCCTGAATTGGCCAACTGTCTTTTACTGAATCTGCGTCG

Associated Phenotype:

Not determined