Homo sapiens solute carrier family 39 (zinc transporter), member 4 (SL - Nucleotide

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Pick Primers
Design and test primers for this sequence using Primer-BLAST.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

Homo sapiens solute carrier family 39 (zinc transporter), member 4 (SLC39A4), Re...
Homo sapiens solute carrier family 39 (zinc transporter), member 4 (SLC39A4), RefSeqGene on chromosome 8
gi|238637281|ref|NG_012234.1|

Nucleotide
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Classic congenital adrenal hyperplasia due to 21-hydroxylase deficiency

MedGen
C2936858[conceptid] (1)
MedGen
Peritoneal mass
Peritoneal mass

MedGen
Retinal dystrophy with leukodystrophy
Retinal dystrophy with leukodystrophy

MedGen

Your browsing activity is empty.

Activity recording is turned off.

Nucleotide