ZMP

SLC44A4

Ensembl ID:

ENSDARG00000027875

Description:

solute carrier family 44, member 4 [Source:HGNC Symbol;Acc:13941]

Human Orthologue:

SLC44A4

Human Description:

solute carrier family 44, member 4 [Source:HGNC Symbol;Acc:13941]

Mouse Orthologue:

Slc44a4

Mouse Description:

solute carrier family 44, member 4 Gene [Source:MGI Symbol;Acc:MGI:1917379]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa23407	Essential Splice Site	Available for shipment	Available now
sa30707	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa23407

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:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000030030	Essential Splice Site	392	720	14	23

Genomic Location (Zv9):

Chromosome 19 (position 994824)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	KN150433.1	5706
GRCz11	19	958120

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGTTTGTGCTGCTGTTGGTGTGTGTGTCGTACTGGGGAATCACAGCGCTG[T/C]ATCCTTAATCAATAAACACACTGCAGATCTAAACAGAATGATTAATAATA

Long Flanking Sequence:

TGACTANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCACACACACACACACAAATGCAACGCTTATAAACATGCACACACAACACAAATAATCACAATCATACATTCATACACACACACACACACACACAATCACTTACTCACTCTTTTACACACAGTAGCACACGCACTCTCACATACATGCGCACATACACACACACACACACACACGCACGCACACACACACACACACACACATCACAAGTGTTACTCATCTATTAATTTAAATATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTGTGTGTGTGCGCGTGTGTGTGTGTGTGTACAGGGCTTTGGGTCACATGATGTCGACTCTCCTCTATCCCGTGGTGACGTTTGTGCTGCTGTTGGTGTGTGTGTCGTACTGGGGAATCACAGCGCTG[T/C]ATCCTTAATCAATAAACACACTGCAGATCTAAACAGAATGATTAATAATAACATCATCTATGTTAGATGACTAAAAACCTCAATAAATGTATTAATAAATGACTACTATATAATATTATTGATATTTCACATGACTAAAAGTGTACATGAATGTATTAATAAATGCTATCATTCATTTTAGAAGACTAAACTAAACATTACTGAACACTTAAATAAATAATGAATAATAATAATATATTAAATGTATAATTGATTTTTGTTTTGTTTTAGTTTTGAACATGGTTAACTGCCGATCTGGTCAGTATATAAATATACAGGTGTGTATTGATTATTGTTGTGTATCTTTGACTGAGTGTGTGTGTGTTCAGATATCTGGCCACATCAGGTGCTCCCATTTATAAAGTTGTGGCTCTGAACGCGACACAGGGAGACTGCAGCAACATACAAGCCAACCAGACCTGCGACCCTCAGGTACAGCCAGTCACTGACTTTTACAATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa30707

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
ENSDART00000030030	Nonsense	646	720	21	23

Genomic Location (Zv9):

Chromosome 19 (position 988955)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	1315507
GRCz11	19	952172

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATGCACAACATTGATATCATGAGCACATCAGAATATTGAACAATGCACAT[C/T]AATCCTTTGTGACAAATTTATTTACAACTTTTAATGTATTTAATGATCAT

Long Flanking Sequence:

AATTCATCAAGTTCATCAACAGAAACGCGTACATCATGGTAGATGAGCTCATAATGTTCATGTTTCTCAAATCCTCCTTCAGATGAACACACACTGTCAATAACGCCGCTGTTTCTCTGCTCTGCAGATCGCCATATACGGAAAAAACTTCTGCGTGTCGGCTAAAAACGCCTTCTTCCTGCTGATGAGGAACATCGTACGGTGAGACACGATTATTGATCGCCATTTAATAAGTGTCATCATGTGTGTGTGTGTGTGTATATGTATATTTATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGAGTGTGTATTTGTATATGTATATTTATGTGTGTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGGTGACAATGAGCATGCACAACATTGATATCATGAGCACATCAGAATATTGAACAATGCACAT[C/T]AATCCTTTGTGACAAATTTATTTACAACTTTTAATGTATTTAATGATCATGATGATACATGAAAAATCAATTTACCAAAAACTAACAACAAAAACTTTGTTATTTTTTATTTAAATTTATGAATGAATTTAATTTGGTAATCATCTACACTACCAGCAATATATATATATATATATATATATAATCCATCCCTTGCATATTACATGATTTCTGATTGATCATGTGACAATGAAGATTGAATTATCCATGCTAAAATATAAAAAAAATGGCATTTTACAAGACAATCGCATGGAAAACATGAAGATAATCAGGTGGAAATGCTCATTTAAAAATTAAAATTAAAATTAAAAAAAATTAAAAATATTTCAAAATATGTCGTTTTTATTCTGTTTTTTTTTTCTATCAAATTAATGAGCATGGGATTTTTTACACACAAAAGCAGTCTCCAGATTTCTGAATGTTACTGATGGATGTCTGATTAATATTTGGACTATTGTTGT

Associated Phenotype:

Not determined